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List of PDF Full Texts available from EurekaMag Chapter 65342

Chapter 65342 contains a list of PDF Full Texts available from EurekaMag.

Opie, L.H., 1974:
Myocardial energy metabolism

Kim, P.Ki.; Hong, Y.Jin.; Sakuma, H.; Chawla, A.; Park, J.Kihyun.; Park, C.Hwan.; Hong, D.; Han, K.; Lee, J.Yeon.; Hur, J.; Lee, H-Jeong.; Kim, Y.Jin.; Suh, Y.Joo.; Choi, B.Wook., 2018:
Myocardial Extracellular Volume Fraction and Change in Hematocrit Level: MR Evaluation by Using T1 Mapping in an Experimental Model of Anemia

Scully, P.R.; Bastarrika, G.; Moon, J.C.; Treibel, T.A., 2018:
Myocardial Extracellular Volume Quantification by Cardiovascular Magnetic Resonance and Computed Tomography

Wiese, S.; Hove, J.; Mo, S.; Mookerjee, R.P.; Petersen, C.L.; Vester-Andersen, M.K.; Mygind, N.D.; Goetze, J.P.; Kjaer, A.; Bendtsen, F.; Møller, Søren., 2018:
Myocardial extracellular volume quantified by magnetic resonance is increased in cirrhosis and related to poor outcome

Tschöpe, C.; Díez, J., 2018:
Myocardial fibrosis as a matter of cell differentiation: opportunities for new antifibrotic strategies

Te Rijdt, W.P.; Ten Sande, J.N.; Gorter, T.M.; van der Zwaag, P.A.; van Rijsingen, I.A.; Boekholdt, S.Matthijs.; van Tintelen, J.Peter.; van Haelst, P.L.; Planken, R.Nils.; de Boer, R.A.; Suurmeijer, A.J.H.; van Veldhuisen, D.J.; Wilde, A.A.M.; Willems, T.P.; van Dessel, P.F.H.M.; van den Berg, M.P., 2018:
Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imaging

Monney, P.; Vincenti, G.; Masci, P-Giorgio.; Rutz, T.; Pavon, A.Giulia.; Pruvot, E.; Schwitter, J., 2018:
Myocardial fibrosis detected by cardiac MR : A substrate for ventricular arrhythmias and sudden cardiac death

Wu, R.; An, D-Aolei.; Shi, R-Yang.; Chen, B-Hua.; Jiang, M.; Bacyinski, A.; Han, T-Tong.; Hu, J.; Xu, J-Rong.; Wu, L-Ming., 2018:
Myocardial fibrosis evaluated by diffusion-weighted imaging and its relationship to 3D contractile function in patients with hypertrophic cardiomyopathy

Tahir, E.; Starekova, J.; Muellerleile, K.; von Stritzky, A.; Münch, J.; Avanesov, M.; Weinrich, J.M.; Stehning, C.; Bohnen, S.; Radunski, U.K.; Freiwald, E.; Blankenberg, S.; Adam, G.; Pressler, A.; Patten, M.; Lund, G.K., 2017:
Myocardial Fibrosis in Competitive Triathletes Detected by Contrast-Enhanced CMR Correlates With Exercise-Induced Hypertension and Competition History

Kitkungvan, D.; Nabi, F.; Kim, R.J.; Bonow, R.O.; Khan, M.A.; Xu, J.; Little, S.H.; Quinones, M.A.; Lawrie, G.M.; Zoghbi, W.A.; Shah, D.J., 2018:
Myocardial Fibrosis in Patients With Primary Mitral Regurgitation With and Without Prolapse

Iguchi, N.; Utanohara, Y.; Suzuki, Y.; Suzuki, M.; Hagiya, K.; Higuchi, R.; Takamisawa, I.; Tobaru, T.; Sumiyoshi, T.; Isobe, M., 2018:
Myocardial flow reserve derived by dynamic perfusion single-photon emission computed tomography reflects the severity of coronary atherosclerosis

Asthana, N.; Mantha, A.; Yang, E.H.; Suh, W.; Aksoy, O.; Shemin, R.J.; Vorobiof, G.; Benharash, P., 2017:
Myocardial functional changes in transfemoral versus transapical aortic valve replacement

Medina, G.; Gómez-Bañuelos, E.; Calderón-Aranda, E.; Cruz-Domínguez, Mía.Pilar.; Vera-Lastra, O.; Jara, L.J., 2018:
Myocardial function in primary antiphospholipid syndrome using speckle-tracking echocardiography

Roura, S.; Gálvez-Montón, C.; Bayes-Genis, A., 2018:
Myocardial healing using cardiac fat

Treibel, T.A.; Scully, P.Richard.; Moon, J.C., 2018:
Myocardial Hypertrophy, Matrix Expansion, and Focal Scar: Progression and Regression in Aortic Stenosis

Ruda, M.Y.; Barysheva, N.A.; Merkulova, I.N.; Shabanova, M.S.; Shariya, M.A.; Gaman, S.A.; Sukhinina, T.S.; Veselova, T.N., 2017:
Myocardial Hypoenhancement on Multidetector Computed Tomography in Patients With Non-ST Elevation Acute Coronary Syndrome

Toce, M.S.; Farias, M.; Powell, A.J.; Daly, K.P.; Vargas, S.O.; Burns, M.M., 2018:
Myocardial Infarct After Marijuana Inhalation in a 16-year-old Adolescent Boy

Tetreault, A., 1958:
Myocardial infarction

Polok, K.; Fronczek, J.; Szczeklik, W., 2018:
Myocardial Infarction After Vascular Surgery: A Systematic Troponin Surveillance and a Uniform Definition Is Needed

Ilic, M.; Grujicic Sipetic, S.; Ristic, B.; Ilic, I., 2018:
Myocardial infarction and alcohol consumption: A case-control study

Rothnie, K.J.; Connell, O.; Müllerová, H.; Smeeth, L.; Pearce, N.; Douglas, I.; Quint, J.K., 2018:
Myocardial Infarction and Ischemic Stroke after Exacerbations of Chronic Obstructive Pulmonary Disease

Michael, L.H.; Ballantyne, C.M.; Zachariah, J.P.; Gould, K.E.; Pocius, J.S.; Taffet, G.E.; Hartley, C.J.; Pham, T.T.; Daniel, S.L.; Funk, E.; Entman, M.L., 2018:
Myocardial infarction and remodeling in mice: effect of reperfusion

Hubert, A.; Guéret, P.; Leurent, G.; Martins, R.P.; Auffret, V.; Bedossa, M., 2017:
Myocardial infarction and thrombophilia: Do not miss the right diagnosis!

Lyon, R.M.Murray., 1938:
Myocardial Infarction-A Pathological Study

Buljević, B.Ana.; Trbušić, M.; Delić-Brkljačić, D.; Malčić, I., 2018:
Myocardial Infarction as a Consequence of Childhood Polyarteritis Nodosa – Case Report

Kechida, M.; Jomaa, W.; Hamda, K.Ben.; Klii, R.; Hammami, S.; Khochtali, I.; Maatouk, F., 2018:
Myocardial infarction as a first symptom of activated protein C resistance associated to hyperhomocyteinemia

Dahal, S.; Ghimire, D.K.C.; Sapkota, S.; Dahal, S.; Kafle, P.; Bhandari, M., 2018:
Myocardial Infarction as an Early Presentation in Thrombotic Thrombocytopenic Purpura: A Rare Case Series

Pina-Cabral, Lís.B.; Carvalhais, Vínia.; Mesquita, Bárbara.; Escórcio, Cáudia.; Silva, P.F.; Pinto, P.; Napoleão, Pícia.; Pinheiro, T.; Monteiro, M.C.; Almeida-Dias, Aónio.; Criado, Bña., 2018:
Myocardial infarction before and after the age of 45: Possible role of platelet receptor polymorphisms

Oyakawa, T.; Iida, K.; Urikura, A.; Kusuhara, M., 2018:
Myocardial Infarction Caused by Asymptomatic Spontaneous Coronary Dissection

Manchurov, V.N.; Anisimov, K.V.; Oskanov, M.B.; Skrypnik, D.V.; Vasilieva, E.Y.; Shpektor, A.V., 2018:
Myocardial Infarction Due to Coronary Artery Embolism

Makkonen, M.; Hietakorpi, S.; Orden, M.R.; Saarikoski, S., 1995:
Myocardial infarction during pregnancy

Streif, W., 2017:
Myocardial infarction in a neonate

Darki, A.; Masoumi, P.; Soleimani, A.; Naser Moghadasi, A., 2018:
Myocardial infarction in a patient with multiple sclerosis after receiving natalizumab

Santos, E.L.; Gonçalves, R.M.; Holanda, A.C.; Nogueira, Vícius.O.; Correia, Lís.C., 2018:
Myocardial Infarction in a Young Cocaine User with Atrial Myxoma: What is the Central Cause?

Brinkmann, M.; Tallone, E.Marcelo.; Würschmidt, F.; Wülfing, C.; Dieckmann, K-Peter., 2018:
Myocardial infarction in a young patient with seminoma during chemotherapy with cisplatinum, etoposide, and bleomycin

Sun, L-Lin.; Duan, M-Jing.; Ma, J-Chao.; Xu, L.; Mao, M.; Biddyut, D.; Wang, Q.; Yang, C.; Zhang, S.; Xu, Y.; Yang, L.; Tian, Y.; Liu, Y.; Xia, S-Nan.; Li, K-Xin.; Jin, Z.; Xiong, Q.; Ai, J., 2018:
Myocardial infarction-induced hippocampal microtubule damage by cardiac originating microRNA-1 in mice

Tian, C.; Gao, L.; Zimmerman, M.C.; Zucker, I.H., 2018:
Myocardial infarction-induced microRNA-enriched exosomes contribute to cardiac Nrf2 dysregulation in chronic heart failure

Sima, C.A.; Lau, B.C.; Taylor, C.M.; van Eeden, S.F.; Reid, W.Darlene.; Sheel, A.W.; Kirkham, A.R.; Camp, P.G., 2018:
Myocardial Infarction Injury in Patients with Chronic Lung Disease Entering Pulmonary Rehabilitation: Frequency and Association with Heart Rate Parameters

Onouchi, Z.; Tamiya, H.; Sonoda, T.; Inoue, S.; Fuyimoto, T.; Fujioka, K., 1988:
Myocardial infarction in Kawasaki disease

Y-Hassan, S., 2018:
Myocardial Infarction in Patients with Takotsubo Syndrome: Trigger and Consequence

Trouton, T.G.; Sidhu, H.; Adgey, A.A., 1988:
Myocardial infarction in pregnancy

Fowles, R.E., 1995:
Myocardial infarction in the 1990s

Zaleski, K.; Górska, A.; Kołodziej, M.; Witkowska, A.; Kujawa, A.; Przykaza, Z.; Szponar, J., 2018:
Myocardial infarction in the course of digoxin and

Hendel, R.C., 1990:
Myocardial infarction in women

Mendelson, M.A.; Hendel, R.C., 1995:
Myocardial infarction in women

Diebold, S.; Moellmann, J.; Kahles, F.; Haj-Yehia, E.; Liehn, E.A.; Nickel, A.; Lebherz, C.; Maack, C.; Marx, N.; Lehrke, M., 2018:
Myocardial infarction is sufficient to increase GLP-1 secretion, leading to improved left ventricular contractility and mitochondrial respiratory capacity

Ugalde, I.; Anjum, I.; Lo Presti, S.; Tolentino, A., 2018:
Myocardial Infarction Presenting as Ear Fullness and Pain

Moccetti, F.; Brown, E.; Xie, A.; Packwood, W.; Qi, Y.; Ruggeri, Z.; Shentu, W.; Chen, J.; López, J.A.; Lindner, J.R., 2018:
Myocardial Infarction Produces Sustained Proinflammatory Endothelial Activation in Remote Arteries

Mouton, A.J.; Rivera, O.J.; Lindsey, M.L., 2018:
Myocardial infarction remodeling that progresses to heart failure: a signaling misunderstanding

Marroush, T.S.; Sharma, A.V.; Saravolatz, L.D.; Takla, R.; Rosman, H.S., 2018:
Myocardial Infarction Secondary to Blunt Chest Trauma

Melly, L.; Cerino, G.; Frobert, Aélien.; Cook, Séphane.; Giraud, M-Noëlle.; Carrel, T.; Tevaearai Stahel, H.T.; Eckstein, F.; Rondelet, Bît.; Marsano, A.; Banfi, A., 2018:
Myocardial infarction stabilization by cell-based expression of controlled Vascular Endothelial Growth Factor levels

Marso, S.P.; Nauck, M.A.; Monk Fries, T.; Rasmussen, Søren.; Treppendahl, M.Bach.; Buse, J.B., 2018:
Myocardial Infarction Subtypes in Patients With Type 2 Diabetes Mellitus and the Effect of Liraglutide Therapy (from the LEADER Trial)

Ranjbar, A.; Ardalan, M.Reza., 2018:
Myocardial Infarction-triggered Thrombotic Microangiopathy

Lippi, G.; Favaloro, E.J., 2018:
Myocardial Infarction, Unstable Angina, and White Thrombi: Time to Move Forward?

Montenegro Sá, F.; Ruivo, C.; Santos, Lís.G.; Antunes, A.; Saraiva, Fátima.; Soares, F.; Morais, Jão., 2018:
Myocardial infarction with nonobstructive coronary arteries: a single-center retrospective study

Tamis-Holland, J.E.; Jneid, H., 2018:
Myocardial Infarction With Nonobstructive Coronary Arteries (MINOCA): It's Time to Face Reality!

Eggers, K.M.; Hadziosmanovic, N.; Baron, T.; Hambraeus, K.; Jernberg, T.; Nordenskjöld, A.; Tornvall, P.; Lindahl, B., 2017:
Myocardial Infarction with Nonobstructive Coronary Arteries: The Importance of Achieving Secondary Prevention Targets

Madias, J.E., 2018:
Myocardial Infarction With Nonobstructive Coronary Artery Disease in Patients Younger than 55 Years Old: How Many of Them Had Takotsubo Syndrome?

Raparelli, V.; Elharram, M.; Shimony, A.; Eisenberg, M.J.; Cheema, A.N.; Pilote, L., 2018:
Myocardial Infarction With No Obstructive Coronary Artery Disease: Angiographic and Clinical Insights in Patients With Premature Presentation

Budnik, M.; Kochanowski, J.; Piatkowski, R.; Kowalik, R.; Kochman, J.; Opolski, G., 2018:
Myocardial infarction with ST-segment elevation in old patient with history of takotsubo syndrome

Rossello, X.; He, Z.; Yellon, D.M., 2018:
Myocardial Infarct Size Reduction Provided by Local and Remote Ischaemic Preconditioning: References Values from the Hatter Cardiovascular Institute

Martins, D.; Ovaert, C.; Khraiche, D.; Boddaert, N.; Bonnet, D.; Raimondi, F., 2018:
Myocardial inflammation detected by cardiac MRI in Arrhythmogenic right ventricular cardiomyopathy: A paediatric case series

Alam, S.R.; Stirrat, C.; Spath, N.; Zamvar, V.; Pessotto, R.; Dweck, M.R.; Moore, C.; Semple, S.; El-Medany, A.; Manoharan, D.; Mills, N.L.; Shah, A.; Mirsadraee, S.; Newby, D.E.; Henriksen, P.A., 2018:
Myocardial inflammation, injury and infarction during on-pump coronary artery bypass graft surgery

Thackeray, J.T.; Hupe, H.C.; Wang, Y.; Bankstahl, J.P.; Berding, G.; Ross, T.L.; Bauersachs, J.; Wollert, K.C.; Bengel, F.M., 2018:
Myocardial Inflammation Predicts Remodeling and Neuroinflammation After Myocardial Infarction

Szczeklik, W.; Krzanowski, M.; Maga, Pł.; Partyka, Łukasz.; Kościelniak, J.; Kaczmarczyk, Pł.; Maga, Młaj.; Pieczka, P.; Suska, A.; Wachsmann, A.; Górka, J.; Biccard, B.; Devereaux, P.J., 2017:
Myocardial injury after endovascular revascularization in critical limb ischemia predicts 1-year mortality: a prospective observational cohort study

Miccichè, V.; Baldi, C.; De Robertis, E.; Piazza, O., 2018:
Myocardial injury after non-cardiac surgery: a perioperative affair?

George, R.; Menon, V.P.; Edathadathil, F.; Balachandran, S.; Moni, M.; Sathyapalan, D.; Prasanna, P.; S, G.; Paul, J.; K K, C.; Kumar, L.; Pillai, A., 2018:
Myocardial injury after noncardiac surgery-incidence and predictors from a prospective observational cohort study at an Indian tertiary care centre

Aboyans, V.; Kakisis, Y., 2018:
Myocardial Injury After Non-cardiac Surgery: What this "MINS" for the Vascular Surgeon?

Obokata, M.; Reddy, Y.N.V.; Melenovsky, V.; Kane, G.C.; Olson, T.P.; Jarolim, P.; Borlaug, B.A., 2018:
Myocardial Injury and Cardiac Reserve in Patients With Heart Failure and Preserved Ejection Fraction

Salter, M.; Kenney, A., 2018:
Myocardial Injury from Tranylcypromine-Induced Hypertensive Crisis Secondary to Excessive Tyramine Intake

Rezende, P.Cury.; Hueb, W.; Rahmi, R.Maria.; Scudeler, T.Luis.; de Azevedo, D.Freitas.Cardoso.; Garzillo, C.Larrosa.; Segre, C.Alexandre.Wainrober.; Ramires, J.Antonio.Franchini.; Filho, R.Kalil., 2017:
Myocardial injury in diabetic patients with multivessel coronary artery disease after revascularization interventions

Huang, S.; Peng, W.; Yang, N.; Yu, T.; Cui, H.Yuan.; Xu, J.Yong.; An, Q.; Yang, H.; Liu, Y.Nan.; Li, Z.; Zuo, M.Zhang., 2018:
Myocardial injury in elderly patients after abdominal surgery

Friedman, K.G.; Sleeper, L.A.; Fichorova, R.N.; Weilnau, T.; Tworetzky, W.; Wilkins-Haug, L.E., 2018:
Myocardial injury in fetal aortic stenosis: Insights from amniotic fluid analysis

Frencken, J.F.; Donker, D.W.; Spitoni, C.; Koster-Brouwer, M.E.; Soliman, I.W.; Ong, D.S.Y.; Horn, J.; van der Poll, T.; van Klei, W.A.; Bonten, M.J.M.; Cremer, O.L., 2018:
Myocardial Injury in Patients With Sepsis and Its Association With Long-Term Outcome

Górka, J.; Polok, K.; Fronczek, J.; Górka, K.; Kózka, M.; Iwaszczuk, Pł.; Frołow, M.; Devereaux, P.J.; Biccard, B.; Musiał, J.; Szczeklik, W., 2018:
Myocardial Injury is More Common than Deep Venous Thrombosis after Vascular Surgery and is Associated with a High One Year Mortality Risk

Lin, M-Sheng.; Lin, C-Chi.; Yang, C-Chang.; Weng, S-Chuan.; Wang, S-Mu.; Chen, C-Yu.; Huang, N.; Chou, Y-Hwa., 2018:
Myocardial injury was associated with neurological sequelae of acute carbon monoxide poisoning in Taiwan

González, A.; Schelbert, E.B.; Díez, J.; Butler, J., 2018:
Myocardial Interstitial Fibrosis in Heart Failure: Biological and Translational Perspectives

Brucato, A., 2018:
Myocardial involvement in patients with acute idiopathic pericarditis: Back to basics

Sekar, B.; Wheeler, R.; Masani, N.; Gallagher, S., 2018:
Myocardial ischaemia as a result of external coronary compression from infective aortic root aneurysm: atypical presentation of prosthetic valve endocarditis

Lefevre, C.; Mallett, L.H.; Wick, L., 2018:
Myocardial ischemia in an adolescent secondary to nutritional thiamine deficiency

Rajiah, P.; Maroules, C.D., 2017:
Myocardial ischemia testing with computed tomography: emerging strategies

Mehta, J.J.; Mahendran, A.K.; Bajaj, R.K.; Doshi, A.R., 2018:
Myocardial Ischemia with Cannabinoid Use in an Adolescent

Fan, H.; Li, S.; Lu, M.; Yin, G.; Yang, X.; Lan, T.; Dai, L.; Chen, X.; Li, J.; Zhang, Y.; Sirajuddin, A.; Kellman, P.; Arai, A.E.; Zhao, S., 2018:
Myocardial late gadolinium enhancement: a head-to-head comparison of motion-corrected balanced steady-state free precession with segmented turbo fast low angle shot

Eun, L.Youngmin.; Lee, Y.Mock., 2018:
Myocardial Layer-Specific Strain Analysis in Children with Mitochondrial Disease

Scheuer, J.; Shaver, J.A.; Kroetz, F.W.; Leonard, J.J., 1970:
Myocardial metabolism in cyanotic congenital heart disease

Wasfy, M.M.; Bibbo, C.Foster.; Brown, M.; DeLuca, J.R.; Wang, F.; Berkstresser, B.; Weiner, R.B.; Lewis, G.D.; Hutter, A.M.; Picard, M.H.; Di Carli, M.F.; Baggish, A.L., 2017:
Myocardial Metabolism in Endurance Exercise-Induced Left Ventricular Hypertrophy

Birkenfeld, A.L.; Jordan, J.; Dworak, M.; Merkel, T.; Burnstock, G., 2018:
Myocardial metabolism in heart failure: Purinergic signalling and other metabolic concepts

Tabata, D.; Isoda, H.; Kato, K.; Matsubara, H.; Kosugi, T.; Kosugi, T.; Terada, M.; Fukuyama, A.; Komori, Y.; Naganawa, S., 2018:
Myocardial motion analysis based on an optical flow method using tagged MR images

Orloff, E.; Fournier, P.; Bouisset, Fédéric.; Moine, T.; Cournot, M.; Elbaz, M.; Carrié, D.; Galinier, M.; Lairez, O.; Cognet, T., 2018:
Myocardial multilayer strain does not provide additional value for detection of myocardial viability assessed by SPECT imaging over and beyond standard strain

Rosmini, S.; Bulluck, H.; Captur, G.; Treibel, T.A.; Abdel-Gadir, A.; Bhuva, A.N.; Culotta, V.; Merghani, A.; Fontana, M.; Maestrini, V.; Herrey, A.S.; Chow, K.; Thompson, R.B.; Piechnik, S.K.; Kellman, P.; Manisty, C.; Moon, J.C., 2018:
Myocardial native T1 and extracellular volume with healthy ageing and gender

Ridouani, F.; Damy, T.; Tacher, V.; Derbel, H.; Legou, Fçois.; Sifaoui, I.; Audureau, E.; Bodez, D.; Rahmouni, A.; Deux, J-François., 2018:
Myocardial native T2 measurement to differentiate light-chain and transthyretin cardiac amyloidosis and assess prognosis

Arques, S., 2018:
Myocardial oedema and congestive heart failure: one piece of the puzzle?

Arai, A.E.; Kasserra, C.E.; Territo, P.R.; Gandjbakhche, A.H.; Balaban, R.S., 2018:
Myocardial oxygenation in vivo: optical spectroscopy of cytoplasmic myoglobin and mitochondrial cytochromes

Al-Humaidi, G.; Sarikaya, I.; Elgazzar, A.H.; Owunwanne, A., 2018:
Myocardial perfusion abnormalities in asymptomatic type 2 diabetic patients

Cai, X.; Zhang, S.; Deng, D.; Li, H.; Guan, X.; Fang, J.; Zhou, Q., 2018:
Myocardial perfusion at rest in uncomplicated type 2 diabetes patients without coronary artery disease evaluated by 320-multidetector computed tomography: A pilot study

Byrne, C.; Hasbak, P.; Kjær, A.; Thune, J.Jakob.; Køber, L., 2018:
Myocardial perfusion during atrial fibrillation in patients with non-ischaemic systolic heart failure: a cross-sectional study using Rubidium-82 positron emission tomography/computed tomography

Muthusami, P.; Luining, W.; McCrindle, B.; van der Geest, R.; Riesenkampff, E.; Yoo, S-Joon.; Seed, M.; Manlhiot, C.; Grosse-Wortmann, L., 2018:
Myocardial Perfusion, Fibrosis, and Contractility in Children With Kawasaki Disease

Proctor, P.; Al Solaiman, F.; Hage, F.G., 2018:
Myocardial perfusion imaging prior to coronary revascularization: From risk stratification to procedure guidance

Zaman, M.Uz.; Fatima, N., 2018:
Myocardial Perfusion Imaging: The Gatekeeper and Advisor

Byrne, C.; Hasbak, P.; Kjaer, A.; Thune, J.Jakob.; Køber, L., 2017:
Myocardial perfusion in patients with non-ischaemic systolic heart failure and type 2 diabetes: a cross-sectional study using Rubidium-82 PET/CT

Dantas, R.Nery.; Assuncao, A.Nascimento.; Marques, I.Aguiar.; Fahel, M.Guimaraes.; Nomura, C.Higa.; Avila, L.Francisco.Rodrigues.; Giorgi, M.Clementina.Pinto.; Soares, J.; Meneghetti, J.Claudio.; Parga, J.Rodrigues., 2018:
Myocardial perfusion in patients with suspected coronary artery disease: comparison between 320-MDCT and rubidium-82 PET

Kunze, K.P.; Nekolla, S.G.; Rischpler, C.; Zhang, S.HuaLei.; Hayes, C.; Langwieser, N.; Ibrahim, T.; Laugwitz, K-Ludwig.; Schwaiger, M., 2018:
Myocardial perfusion quantification using simultaneously acquired 13 NH 3 -ammonia PET and dynamic contrast-enhanced MRI in patients at rest and stress

Narang, A.; Blair, J.E.; Patel, M.B.; Mor-Avi, V.; Fedson, S.E.; Uriel, N.; Lang, R.M.; Patel, A.R., 2018:
Myocardial perfusion reserve and global longitudinal strain as potential markers of coronary allograft vasculopathy in late-stage orthotopic heart transplantation

Friesen, R.M.; Schäfer, M.; Jone, P-Ni.; Appiawiah, N.; Vargas, D.; Fonseca, B.; DiMaria, M.V.; Truong, U.; Malone, L.; Browne, L.P., 2017:
Myocardial Perfusion Reserve Index in Children With Kawasaki Disease

Sabra, M.Marta.Maggiotto.; Costa, F.Salomão.; de Azevedo, J.Cunha.; Mesquita, C.Tinoco.; Verberne, H.J., 2018:
Myocardial perfusion scintigraphy during chest pain: An atypical presentation of takotsubo cardiomyopathy?

Czaja, M.Z.; Wygoda, Z.; Duszańska, A.; Szczerba, D.; Głowacki, J.; Gąsior, M.; Wasilewski, Jław.P., 2018:
Myocardial perfusion scintigraphy - interpretation of gated imaging. Part 2

González-Rosa, J.Manuel.; Sharpe, M.; Field, D.; Soonpaa, M.H.; Field, L.J.; Burns, C.E.; Burns, C.Geoffrey., 2018:
Myocardial Polyploidization Creates a Barrier to Heart Regeneration in Zebrafish

Rossaint, J., 2018:
Myocardial Postconditioning by the Melatonin Receptor Agonist Ramelteon: Putting Pieces to the Puzzle

Lazar, H.L.; Painvin, G.A.; Roberts, A.J., 1986:
Myocardial preservation

Ellenberger, C.; Sologashvili, T.; Kreienbühl, L.; Cikirikcioglu, M.; Diaper, J.; Licker, M., 2018:
Myocardial Protection by Glucose-Insulin-Potassium in Moderate- to High-Risk Patients Undergoing Elective On-Pump Cardiac Surgery: A Randomized Controlled Trial

Bazylev, V.V.; Rosseĭkin, E.V.; Kobzev, E.E.; Evdokimov, M.E., 2018:
Myocardial protection during left-ventricular reconstruction in patients with an ejection fraction below 30

Panigrahi, D.; Roychowdhury, S.; Guhabiswas, R.; Rupert, E.; Das, M.; Narayan, P., 2018:
Myocardial protection following del Nido cardioplegia in pediatric cardiac surgery

Lebon, J-Sébastien.; Couture, P.; Fortier, A.; Rochon, A.G.; Ayoub, C.; Viens, C.; Laliberté, Éric.; Bouchard, D.; Pellerin, M.; Deschamps, A., 2017:
Myocardial Protection in Mitral Valve Surgery: Comparison Between Minimally Invasive Approach and Standard Sternotomy

López-Menéndez, Jé.; Miguelena, J.; Morales, C.; Callejo, F.; Silva, J., 2018:
Myocardial protection in on-pump coronary artery bypass grafting surgery: analysis of the effectiveness of the use of retrograde Celsior ®

Luptak, I.; Croteau, D.; Valentine, C.; Qin, F.; Siwik, D.; Remick, D.; Colucci, W.S.; Hobai, I., 2018:
Myocardial Redox Hormesis Protects the Heart of Female Mice in Sepsis

Banovic, M.; Pusnik-Vrckovnik, M.; Nakou, E.; Vardas, P., 2018:
Myocardial regeneration therapy in heart failure: Current status and future therapeutic implications in clinical practice

Maring, J.A.; Beez, C.M.; Falk, V.; Seifert, M.; Stamm, C., 2018:
Myocardial Regeneration via Progenitor Cell-Derived Exosomes

Lai, Y-Chen.; Li, N.; Lawrence, W.; Wang, S.; Levine, A.; Burchhardt, D.M.; Pautler, R.G.; Valderrábano, M.; Wehrens, X.H.; Anderson, A.E., 2018:
Myocardial remodeling and susceptibility to ventricular tachycardia in a model of chronic epilepsy

Pinelli, S.; Agrinier, N.; Bouchahda, N.; Metzdorf, P.Adrien.; Camenzind, E.; Popovic, B., 2018:
Myocardial reperfusion for acute myocardial infarction under an optimized antithrombotic medication: What can you expect in daily practice?

Zhang, Z.; Li, W.; Wu, W.; Xie, Q.; Li, J.; Zhang, W.; Zhang, Y., 2018:
Myocardial reperfusion with tirofiban injection via aspiration catheter : Efficacy and safety in STEMI patients with large thrombus burden

Topuz, M.; Genç, Ömer.; Acele, A.; Koc, Müt., 2018:
Myocardial repolarization is affected in patients with ascending aortic aneurysm

Arri, S.S.; Patterson, T.; Williams, R.P.; Moschonas, K.; Young, C.P.; Redwood, S.R., 2017:
Myocardial revascularisation in high-risk subjects

Ochsner, J.L.; Moore, C.B., 1966:
Myocardial revascularization

Shen, J.Q.; Ji, Q.; Ding, W.J.; Xia, L.M.; Song, K.; Wei, L.; Sun, Y.X.; Wang, C.S., 2018:
Myocardial revascularization among patients with severe left ventricular dysfunction: a comparison between on-pump beating-heart and off-pump coronary artery bypass grafting

Goldberg, H.L.; Hochreiter, C.; Borer, J.S., 1983:
Myocardial rupture

Rajiah, P., 2018:
Myocardial salvage imaging with computed tomography

Musa, T.A.; Treibel, T.A.; Vassiliou, V.S.; Captur, G.; Singh, A.; Chin, C.; Dobson, L.E.; Pica, S.; Loudon, M.; Malley, T.; Rigolli, M.; Foley, J.R.J.; Bijsterveld, P.; Law, G.R.; Dweck, M.R.; Myerson, S.G.; McCann, G.P.; Prasad, S.K.; Moon, J.C.; Greenwood, J.P., 2018:
Myocardial Scar and Mortality in Severe Aortic Stenosis

Mekkaoui, C.; Jackowski, M.P.; Kostis, W.J.; Stoeck, C.T.; Thiagalingam, A.; Reese, T.G.; Reddy, V.Y.; Ruskin, J.N.; Kozerke, S.; Sosnovik, D.E., 2018:
Myocardial Scar Delineation Using Diffusion Tensor Magnetic Resonance Tractography

Wei, J.; Bakir, M.; Darounian, N.; Li, Q.; Landes, S.; Mehta, P.K.; Shufelt, C.L.; Handberg, E.M.; Kelsey, S.F.; Sopko, G.; Pepine, C.J.; Petersen, J.W.; Berman, D.S.; Thomson, L.E.J.; Bairey Merz, C.Noel., 2018:
Myocardial Scar Is Prevalent and Associated With Subclinical Myocardial Dysfunction in Women With Suspected Ischemia But No Obstructive Coronary Artery Disease: From the Women's Ischemia Syndrome Evaluation-Coronary Vascular Dysfunction Study

Alexander, C.; Oberhausen, E., 1995:
Myocardial scintigraphy

Da Silva, F.; Massa, F.; Motamedi, F.Jian.; Vidal, V.; Rocha, A.Sofia.; Gregoire, E.P.; Cai, C-Leng.; Wagner, K.Dietrich.; Schedl, A., 2018:
Myocardial-specific R-spondin3 drives proliferation of the coronary stems primarily through the Leucine Rich Repeat G Protein coupled receptor LGR4

Villemain, O.; Correia, M.; Mousseaux, E.; Baranger, Jérome.; Zarka, S.; Podetti, I.; Soulat, G.; Damy, T.; Hagège, A.; Tanter, M.; Pernot, M.; Messas, E., 2018:
Myocardial Stiffness Evaluation Using Noninvasive Shear Wave Imaging in Healthy and Hypertrophic Cardiomyopathic Adults

Ong, G.; Brezden-Masley, C.; Dhir, V.; Deva, D.P.; Chan, K.K.W.; Chow, C-Ming.; Thavendiranathan, D.; Haq, R.; Barfett, J.J.; Petrella, T.M.; Connelly, K.A.; Yan, A.T., 2018:
Myocardial strain imaging by cardiac magnetic resonance for detection of subclinical myocardial dysfunction in breast cancer patients receiving trastuzumab and chemotherapy

Kim, H.Mee.; Cho, G-Yeong.; Hwang, I-Chang.; Choi, H-Mi.; Park, J-Bean.; Yoon, Y.E.; Kim, H-Kwan., 2018:
Myocardial Strain in Prediction of Outcomes After Surgery for Severe Mitral Regurgitation

Tsougos, E.; Angelidis, G.; Gialafos, E.; Tzavara, C.; Tzifos, V.; Tsougos, I.; Georgoulias, P., 2017:
Myocardial strain may predict exercise tolerance in patients with reduced and mid-range ejection fraction

Wang, X.; Su, L.; Yang, R.; Zhang, H.; Liu, D., 2018:
Myocardial strain/stress changes identified by echocardiography may reveal early sepsis-induced myocardial dysfunction

Siegel, B.; Olivieri, L.; Gordish-Dressman, H.; Spurney, C.F., 2017:
Myocardial Strain Using Cardiac MR Feature Tracking and Speckle Tracking Echocardiography in Duchenne Muscular Dystrophy Patients

Hernandez, L.E., 2018:
Myocardial stress perfusion magnetic resonance in children with hypertrophic cardiomyopathy

Noel, C.V.; Krishnamurthy, R.; Masand, P.; Moffett, B.; Schlingmann, T.; Cheong, B.Y.; Krishnamurthy, R., 2018:
Myocardial Stress Perfusion MRI: Experience in Pediatric and Young-Adult Patients Following Arterial Switch Operation Utilizing Regadenoson

Tahir, H.; Sachdev, S.; Nguyen, L.; Bardia, N.; Omar, B.; Cohen, M.V., 2018:
Myocardial Stunning After Electrocution With Complete Reversibility Within 24 Hours: Role of Repeat Transthoracic Echocardiograms in Potential Cardiac Transplant Donors

Jiang, Z.; Tang, H.; Shi, J.; Zhou, Y.; Wang, C.; Li, D.; Shan, Q.; Zhou, W., 2018:
Myocardial stunning-induced left ventricular dyssynchrony on gated single-photon emission computed tomography myocardial perfusion imaging

Nacif, M.Souto.; Raman, F.S.; Gai, N.; Jones, J.; van der Geest, R.J.; T Sibley, C.; Liu, S.; David, A.Bluemke., 2018:
Myocardial T1 mapping and determination of partition coefficients at 3 tesla: comparison between gadobenate dimeglumine and gadofosveset trisodium

Araujo-Filho, Jé.A.B.; Assuncao, A.N.; Tavares de Melo, M.D.; Bière, Lïc.; Lima, C.R.; Dantas, R.N.; Nomura, C.H.; Salemi, V.M.C.; Jerosch-Herold, M.; Parga, J.R., 2018:
Myocardial T1 mapping and extracellular volume quantification in patients with left ventricular non-compaction cardiomyopathy

Chen, S.S.M.; Leeton, L.; Castro, J.M.; Dennis, A.T., 2018:
Myocardial tissue characterisation and detection of myocardial oedema by cardiovascular magnetic resonance in women with pre-eclampsia: a pilot study

Schelbert, E.B.; Miller, C.A., 2018:
Myocardial tissue characteristics undoubtedly differ by gender but not age

Nii, M.; Ishida, M.; Dohi, K.; Tanaka, H.; Kondo, E.; Ito, M.; Sakuma, H.; Ikeda, T., 2018:
Myocardial tissue characterization and strain analysis in healthy pregnant women using cardiovascular magnetic resonance native T1 mapping and feature tracking technique

Suranyi, P.; Elgavish, G.A.; Schoepf, U.Joseph.; Ruzsics, B.; Kiss, P.; van Assen, M.; Jacobs, B.E.; Brott, B.C.; Elgavish, A.; Varga-Szemes, A., 2018:
Myocardial tissue characterization by combining late gadolinium enhancement imaging and percent edema mapping: a novel T2 map-based MRI method in canine myocardial infarction

Fujita, B.; Zimmermann, W-Hubertus., 2018:
Myocardial tissue engineering strategies for heart repair: current state of the art

Bergman, M.R.; Kao, R.H.; McCune, S.A.; Holycross, B.J., 2018:
Myocardial tumor necrosis factor-α secretion in hypertensive and heart failure-prone rats

Vergara-Uzcategui, C.Eduardo.; González, N.; Donís, Jé.Hipólito., 2017:
Myocardial tumour infiltration mimicking myocardial ischaemia in electrocardiogram

Hendel, R.C.; Chaudhry, F.A.; Bonow, R.O., 1996:
Myocardial viability

Löffler, Aán.I.; Kramer, C.M., 2018:
Myocardial Viability Testing to Guide Coronary Revascularization

Bonnemains, L.; Guerard, A.Sophie.; Soulié, P.; Odille, F.; Felblinger, J., 2018:
Myocardial volume change during cardiac cycle derived from three orthogonal systolic strains: towards a quality assessment of strains

Xiang, Y.; Liao, X-Hua.; Li, J-Peng.; Li, H.; Qin, H.; Yao, A.; Yu, C-Xi.; Hu, P.; Guo, W.; Gu, C-Jiang.; Zhang, T-Cun., 2017:
Myocardin and Stat3 act synergistically to inhibit cardiomyocyte apoptosis

Liu, L.; Wu, X.; Xu, H.; Yu, L.; Zhang, X.; Li, L.; Jin, J.; Zhang, T.; Xu, Y., 2018:
Myocardin-related transcription factor A (MRTF-A) contributes to acute kidney injury by regulating macrophage ROS production

Chen, B.; Li, Z.; Feng, Y.; Wu, X.; Xu, Y., 2018:
Myocardin-related transcription factor A (MRTF-A) mediates doxorubicin-induced PERP transcription in colon cancer cells

Lin, J.Z.; Rabhi, N.; Farmer, S.R., 2018:
Myocardin-Related Transcription Factor A Promotes Recruitment of ITGA5+ Profibrotic Progenitors during Obesity-Induced Adipose Tissue Fibrosis

Weinstein, C.; Fenoglio, J.J., 1987:

Kereiakes, D.J.; Parmley, W.W., 1984:
Myocarditis and cardiomyopathy

Buggey, J.; ElAmm, C.A., 2018:
Myocarditis and cardiomyopathy

Anonymous, 2018:
Myocarditis and Myocardial Disease-III

Anonymous, 2018:
Myocarditis and Myocardial Disease-IV

Anonymous, 2018:
Myocarditis and Myocardial Diseases-I

Anonymous, 2018:
Myocarditis and Myocardial Diseases-II

Kuntz, J.; Crane, B.; Weinmann, S.; Naleway, A.L., 2018:
Myocarditis and pericarditis are rare following live viral vaccinations in adults

Jepson, R.P.; Slavotinek, A.H.; Gilligan, J.E., 1972:
Myocarditis and Phaeochromocytomata

De Luca, G.; Cavalli, G.; Campochiaro, C.; Tresoldi, M.; Dagna, L., 2018:
Myocarditis: An Interleukin-1-Mediated Disease?

Martínez León, A.; Rugeles Niño, J.Paola.; Brandy García, A.María.; Morís de la Tassa, César.; Caminal Montero, L.; Rozado Castaño, Jé., 2018:
Myocarditis as a Form of Presentation of an Inflammatory Autoimmune Myopathy Associated With Anti-signal Recognition Particle Antibodies

Morikawa, D.; Hiraoka, E.; Obunai, K.; Norisue, Y., 2018:
Myocarditis Associated with Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome: A Case Report and Review of the Literature

Neilan, T.G.; Rothenberg, M.L.; Amiri-Kordestani, L.; Sullivan, R.J.; Steingart, R.M.; Gregory, W.; Hariharan, S.; Hammad, T.A.; Lindenfeld, J.; Murphy, M.J.; Moslehi, J.J.; Abdullah, H.; Amiri-Kordestani, L.; Bakker, C.; Boshoff, C.; Bringhurst, C.; Bucktrout, S.; Carlin, K.; Caubel, P.; Chen, R.; Chin, K.; Chudnovsky, A.; Davis, J.; Deutsch, J.; Dixit, R.; Gottfridsson, C.; Gregory, W.; Hammad, T.A.; Handelsman, D.; Hariharan, S.; Holmes, W.; Honig, P.; Hugh-Jones, C.; Kaufman, H.; Khan, N.; K, 2018:
Myocarditis Associated with Immune Checkpoint Inhibitors: An Expert Consensus on Data Gaps and a Call to Action

Aykac, K.; Ozsurekci, Y.; Kahyaoglu, P.; Basaranoglu, S.T.; Ertugrul, I.; Alp, A.; Cengiz, A.B.; Kara, A.; Ceyhan, M., 2018:
Myocarditis associated with influenza infection in five children

Tariq, S.; Garg, A.; Gass, A.; Aronow, W.S., 2018 :
Myocarditis due to systemic lupus erythematosus associated with cardiogenic shock

Kumar, V.; Sidhu, N.; Roy, S.; Gaurav, K., 2018:
Myocarditis following diphtheria, whole-cell pertussis, and tetanus toxoid vaccination in a young infant

Fukushima, M.; Shiba, T.; Yoshimura, S.; Doi, H.; Nambu, M., 2018:
Myocarditis in a girl with mixed connective tissue disease

Munjal, S.; Ferrando, S., 2018:
Myocarditis in a Patient on Clozapine: What did it?

Simon, R.; Perel-Winkler, A.; Bokhari, S.; Fazlollahi, L.; Nickerson, K., 2018:
Myocarditis in Giant Cell Arteritis Diagnosed With Fluorine 18-Labeled Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography: Case Report and Review of the Literature

Krishna, K.Sivarama., 2016:
Myocarditis in hair dye poisoning

Farinha, Iês.Teixeira.; Miranda, J.Oliveira., 2016:
Myocarditis in Paediatric Patients: Unveiling the Progression to Dilated Cardiomyopathy and Heart Failure

Mahmood, S.S.; Fradley, M.G.; Cohen, J.V.; Nohria, A.; Reynolds, K.L.; Heinzerling, L.M.; Sullivan, R.J.; Damrongwatanasuk, R.; Chen, C.L.; Gupta, D.; Kirchberger, M.C.; Awadalla, M.; Hassan, M.Z.O.; Moslehi, J.J.; Shah, S.P.; Ganatra, S.; Thavendiranathan, P.; Lawrence, D.P.; Groarke, J.D.; Neilan, T.G., 2018:
Myocarditis in Patients Treated With Immune Checkpoint Inhibitors

Myocarditis in poliomyelitis

Perel-Winkler, A.; Bokhari, S.; Perez-Recio, T.; Zartoshti, A.; Askanase, A.; Geraldino-Pardilla, L., 2018:
Myocarditis in systemic lupus erythematosus diagnosed by 18 F-fluorodeoxyglucose positron emission tomography

Tipoo Sultan, F.Ali.; Adnan, G., 2018:
Myocarditis mimicking acute coronary syndrome - the role of cardiac magnetic resonance imaging in the diagnosis

Okoro, K.U.; Roby, M.D.; Bankole, A.A., 2018:
Myocarditis Secondary to Mesalamine-Induced Cardiotoxicity in a Patient with Ulcerative Colitis

Keinath, K.; Church, T.; Kurth, B.; Hulten, E., 2018:
Myocarditis secondary to smallpox vaccination

Chang, A.; Nasti, T.H.; Khan, M.K.; Parashar, S.; Kaufman, J.L.; Boise, L.H.; Lonial, S.; Ahmed, R.; Nooka, A.K., 2018:
Myocarditis With Radiotherapy and Immunotherapy in Multiple Myeloma

Mahmood, S.S.; Chen, C.L.; Shapnik, N.; Krishnan, U.; Singh, H.S.; Makker, V., 2018:
Myocarditis with tremelimumab plus durvalumab combination therapy for endometrial cancer: A case report

Gardinal, M.Vitor.Buzete.; Faccioli, C.Kuhn.; Chedid, R.Alari.; Mori, R.Hideo.; Vicentini, I.Bastos.Franceschini.; Vicentini, C.Alberto., 2018:
Myocardium Arrangement and Coronary Vessel Distribution in the Ventricle of Three Neotropical Freshwater Teleosts

Villines, T.C., 2018:
Myocardium in jeopardy: The hemodynamic implications of stenosis proximity and severity on coronary CTA

Gil-Cayuela, C.; Ortega, A.; Tarazón, Eía.; Martínez-Dolz, L.; Cinca, J.; González-Juanatey, Jé.Ramón.; Lago, F.; Roselló-Lletí, E.; Rivera, M.; Portolés, M., 2018:
Myocardium of patients with dilated cardiomyopathy presents altered expression of genes involved in thyroid hormone biosynthesis

Liu, J.; Zhuang, X.; Xie, H.; Zhang, S.; Gu, L., 2018 :
Myocardium segmentation from DE MRI with guided random walks and sparse shape representation

Mueller, S.Manuel.; Aguayo, D.; Aeberli, D.; Vögelin, E.; Toigo, M., 2018:
Myocellular characteristics in rheumatoid arthritis and osteoarthritis patients

Myers, K.A.; Scheffer, I.E., 2018:
Myoclonic absence seizures with complex gestural automatisms

Endres, D.; Altenmüller, D-M.; Feige, B.; Maier, S.J.; Nickel, K.; Hellwig, S.; Rausch, Jördis.; Ziegler, C.; Domschke, K.; Doerr, J.P.; Egger, K.; Tebartz van Elst, L., 2018:
Myoclonic Jerks and Schizophreniform Syndrome: Case Report and Literature Review

Reyes, A.Jose.; Ramcharan, K.; Giddings, S.Lawrence.; Aboh, S.; Rampersad, F., 2018:
Myoclonic Jerks, Exposure to Many Cats, and Neurotoxoplasmosis in an Immunocompetent Male

Lee, J.Jin.; Lim, S.; Lee, Y.Sil.; Shin, H-Yong.; Baek, C-Wha.; Jung, Y.Hun.; Woo, Y.Cheol.; Park, Y-Hee., 2018:
Myoclonic movement after general anesthesia: A case report and review of the literature

Almallouhi, E.; Rahwan, M.; Kutluay, E., 2018:
Myoclonic status epilepticus as an initial presentation of acute biliary pancreatitis

Freund, B.; Kaplan, P.W., 2017:
Myoclonus After Cardiac Arrest: Where Do We Go From Here?

McFadzean, W.Jm.; Holopherne-Doran, D., 2018:
Myoclonus and hypersensitivity of the tail following intrathecal administration of morphine and bupivacaine in a cat

Isern de Val, Í.; Gazulla, J., 2018:
Myoclonus-dystonia and cerebellar ataxia in association with anti-glutamic acid decarboxylase autoimmunity

Roze, E.; Lang, A.E.; Vidailhet, M., 2018:
Myoclonus-dystonia: classification, phenomenology, pathogenesis, and treatment

Cardaioli, E.; Mignarri, A.; Cantisani, T.Anna.; Malandrini, A.; Nesti, C.; Rubegni, A.; Funel, N.; Federico, A.; Santorelli, F.Maria.; Dotti, M.Teresa., 2018:
Myoclonus epilepsy, retinitis pigmentosa, leukoencephalopathy and cerebral calcifications associated with a novel m.5513G>A mutation in the MT-TW gene

Ong, C.Yau.; Qin, Y., 2018:
Myoclonus from Antibiotic Therapy (Ceftazidime-induced Neurotoxicity): A Case Report and Review

Pollack, S.F.; Grocott, O.R.; Parkin, K.A.; Larson, A.M.; Thibert, R.L., 2018:
Myoclonus in Angelman syndrome

Kiziltan, M.E.; Gunduz, A.; Tutuncu, M.; Ertan, S.; Apaydin, H.; Kiziltan, G., 2018:
Myoclonus in the elderly: A retrospective analysis of clinical and electrophysiological characteristics of patients referred to an electrophysiology laboratory

Diab, K.M.; Naumova, I.V.; Balakireva, O.A.; Sokolova, V.N.; Terekhina, L.I., 2018:
Myoclonus of the middle ear

Hasinoff, B.B.; Patel, D., 2018:
Myocyte-Damaging Effects and Binding Kinetics of Boronic Acid and Epoxyketone Proteasomal-Targeted Drugs

Wang, Y-Ning.; Yang, W-Cai.; Li, P-Wei.; Wang, H-Bao.; Zhang, Y-Ying.; Zan, L-Sen., 2018:
Myocyte enhancer factor 2A promotes proliferation and its inhibition attenuates myogenic differentiation via myozenin 2 in bovine skeletal muscle myoblast

Russell, J.; Du Toit, E.F.; Peart, J.N.; Patel, H.H.; Headrick, J.P., 2018:
Myocyte membrane and microdomain modifications in diabetes: determinants of ischemic tolerance and cardioprotection

Zhang, L.; Wang, H.; Zhao, Y.; Wang, J.; Dubielecka, P.M.; Zhuang, S.; Qin, G.; Chin, Y.Eugene.; Kao, R.L.; Zhao, T.C., 2018:
Myocyte-specific overexpressing HDAC4 promotes myocardial ischemia/reperfusion injury

Awasthi, A.; Nain, V.; Puria, R., 2018:
MYOD and HAND transcription factors have conserved recognition sites in mTOR promoter: insights from in silico analysis

Schulberg, H.C., 2017:
My Odyssey Through the Changing World of Mental Health

Zhang, Y.; Long, C.; Bassel-Duby, R.; Olson, E.N., 2018:
Myoediting: Toward Prevention of Muscular Dystrophy by Therapeutic Genome Editing

Pan, L.; Crouch, D.L.; Huang, H., 2018:
Myoelectric Control Based on a Generic Musculoskeletal Model: Toward a Multi-User Neural-Machine Interface

Pan, L.; Crouch, D.L.; Huang, H.Helen., 2018:
Myoelectric Control Based on A Generic Musculoskeletal Model: Towards A Multi-User Neural-Machine Interface

Lu, Z.; Tong, R.Kai-Yu.; Zhang, X.; Li, S.; Zhou, P., 2018:
Myoelectric Pattern Recognition for Controlling a Robotic Hand: A Feasibility Study in Stroke

Raveh, E.; Portnoy, S.; Friedman, J., 2018:
Myoelectric Prosthesis Users Improve Performance Time and Accuracy Using Vibrotactile Feedback When Visual Feedback Is Disturbed

Miranda, H.; Maia, M.; de Oliveira, C.G.; Farias, Déborah.; da Silva, J.B.; Lima, V.P.; Willardson, J.M.; Paz, G.A., 2018:
Myoeletric indices of fatigue adopting different rest intervals during leg press sets

Chen, L.; Fu, Y.; Wang, H.; Yang, F.; Liu, J.; Xia, F.; Ma, X., 2018:
Myoepithelial carcinoma of the nasopharynx: Rare case report with clinicopathologic and immunohistochemical features review of literature

Guo, X.; Watanabe, J.; Ariyasu, S.; Sasaguri, Y.; Kurose, N.; Fukushima, K.; Yamada, S., 2018:
Myoepithelial carcinoma of the parotid gland: A case of adequate fine-needle aspiration cytology specimens rendering a conclusive diagnosis possible

Sharma, A.; Gogoi, P.; Arora, V.Kumar., 2018:
Myoepithelial carcinoma of the tongue- spindle cell morphology with high mitosis: A case report and review of literature

Khazeni, K.; LaBove, H.; Wilky, B.; Rosenberg, A.E.; Paulus, E.; Chim, H.; Pearson, J.M.; Yakoub, D., 2018:
Myoepithelial carcinoma or epithelioid sarcoma - A rare diagnosis with poor prognosis. A case report and review of literature

Sirka, O.Katarina.; Shamir, E.R.; Ewald, A.J., 2018:
Myoepithelial cells are a dynamic barrier to epithelial dissemination

Tata, A.; Kobayashi, Y.; Chow, R.D.; Tran, J.; Desai, A.; Massri, A.J.; McCord, T.J.; Gunn, M.Dee.; Tata, P.Rao., 2018:
Myoepithelial Cells of Submucosal Glands Can Function as Reserve Stem Cells to Regenerate Airways after Injury

Tomoda, T.; Kato, H.; Okada, H., 2018:
Myoepithelial Hamartoma in the Ampulla of Vater

Habu, T.; Soh, J.; Toji, T.; Shien, K.; Niman, E.; Namba, K.; Sato, H.; Yamamoto, H.; Sugimoto, S.; Yamane, M.; Toyooka, S., 2018:
Myoepithelioma occurring in the posterior mediastinum harboring EWSR1 rearrangement: a case report

Joob, B.; Wiwanitkit, V., 2018:
Myoepithelioma of soft tissue and diagnostic pitfall in cytology

Guo, L.; Zhou, F.; Zhang, N.; Dai, H.; Zeng, X.; Gong, H., 2018:
Myoepithelioma of the lateral abdominal wall: A case report

Klotz, S.G.R.; Ketels, G.; Löwe, B.; Brünahl, C.A., 2018:
Myofascial Findings and Psychopathological Factors in Patients with Chronic Pelvic Pain Syndrome

Tijs, C.; Bernabei, M.; van Dieën, J.H.; Maas, H., 2018:
Myofascial Loads Can Occur without Fascicle Length Changes

Massingill, J.; Jorgensen, C.; Dolata, J.; Sehgal, A.R., 2018:
Myofascial Massage for Chronic Pain and Decreased Upper Extremity Mobility After Breast Cancer Surgery

Moses, A.J., 2000:
Myofascial pain

Casale, R., 2018:
Myofascial pain: so common, and yet not understood

McClaflin, R.R., 1994:
Myofascial pain syndrome

Poveda-Roda, R.; Moreno, P.; Bagán, Jé.; Margaix, Mía., 2018:
Myofascial Pain: Ultrasound Width of the Masseter Muscle

Jazayeri, S.; Seffinger, M., 2018:
Myofascial Release Therapy Beneficial for Patients With Chronic Low Back Pain

Poluha, R.Lorenzi.; Grossmann, E.; Iwaki, L.Cristina.Vessoni.; Uchimura, T.Teruya.; Santana, Rângela.Getirana.; Iwaki Filho, L., 2018:
Myofascial trigger points in patients with temporomandibular joint disc displacement with reduction: a cross-sectional study

Kim, M.Hye.; Song, D.Hyun.; Ko, G.Hyuck.; Lee, J.Hee.; Kim, D.Chul.; Yang, J.Wook.; Lee, H.Im.; An, H.Jung.; Lee, J.Sil., 2018:
Myoferlin Expression and Its Correlation with FIGO Histologic Grading in Early-Stage Endometrioid Carcinoma

Barnhouse, V.R.; Weist, J.L.; Shukla, V.C.; Ghadiali, S.N.; Kniss, D.A.; Leight, J.L., 2018:
Myoferlin regulates epithelial cancer cell plasticity and migration through autocrine TGF-β1 signaling

Crupkin, A.C.; Iturburu, F.G.; Crupkin, M.; Menone, M.L., 2018:
Myofibrilar functional dysregulation in fish: A new biomarker of damage to pesticides

Koitka, K.; Dahiya, A.; Lo, A.; Scalia, G.M.; Atherton, J.J.; Prasad, S.B., 2017:
Myofibrillar Cardiomyopathy due to a Novel Desmin Gene Mutation: Complementary Role of Echocardiography, Cardiac Magnetic Resonance, and Genetic Testing in Delineating Diagnosis

Dhawan, P.S.; Liewluck, T.; Knapik, J.; Milone, M., 2017:
Myofibrillar myopathy due to dominant LMNA mutations: A report of 2 cases

Palethorpe, H.M.; Leach, D.A.; Need, E.F.; Drew, P.A.; Smith, E., 2018:
Myofibroblast androgen receptor expression determines cell survival in co-cultures of myofibroblasts and prostate cancer cells in vitro

Khatib, Y.; Pandey, V.; Khade, A.L.; Pandey, R., 2018:
Myofibroblastoma of the Breast: A Rare Cause of Breast Lump in a Postmenopausal Woman

Yilmaz, R.; Akkavak, G.; Ozgur, E.; Onder, S.; Ozkurt, E.; Dursun, M., 2018:
Myofibroblastoma of the Breast: Ultrasonography, Mammography, and Magnetic Resonance Imaging Features With Pathologic Correlation

Pereira, J.Dos.Santos.; de Oliveira Nóbrega, F.José.; Vasconcelos, R.Gadelha.; de Souza Martins Câmara, A.Costa.; de Souza, Lélia.Batista.; Queiroz, Lélia.Maria.Guedes., 2018 :
Myofibroblasts and mast cells: influences on biological behavior of odontogenic lesions

Powell, D.W.; Mifflin, R.C.; Valentich, J.D.; Crowe, S.E.; Saada, J.I.; West, A.B., 2018:
Myofibroblasts. II. Intestinal subepithelial myofibroblasts

Coletta, R.D.; Salo, T., 2018:
Myofibroblasts in oral potentially malignant disorders: Is it related to malignant transformation?

Powell, D.W.; Mifflin, R.C.; Valentich, J.D.; Crowe, S.E.; Saada, J.I.; West, A.B., 2018:
Myofibroblasts. I. Paracrine cells important in health and disease

Bagalad, B.S.; Mohan Kumar, K.P.; Puneeth, H.K., 2018:
Myofibroblasts: Master of disguise

Atarbashi-Moghadam, S.; Lotfi, A.; Shahrabi-Farahani, S.; Atarbashi-Moghadam, F., 2018:
Myofibroma as a Rapidly Growing Gingival Mass in a 4-year-old Boy: a Case Report

Fu, Y.; Guan, W.Y.; Wu, H.Y.; Wu, H.Y.; Fan, Z.W.; Ye, Q.; Meng, F.Q., 2018:
Myofibroma/myofibromatosis: a clinicopathologic analysis of 9 cases

Zhong, C.S.; Song, H.; Weiss, A.; Tan, W-H.; Coury, S.; Huang, J.T., 2018:
Myofibromatosis presenting as reticulated vascular changes and subcutaneous atrophy in a patient with somatic mosaicism of PDGFRB mutation

Huri, P.Yilgor.; Morrissette-McAlmon, J.; Grayson, W.L., 2018:
Myogenic Differentiation of ASCs Using Biochemical and Biophysical Induction

Venuti, J.M., 1996:
Myogenic Differentiation of Sea Urchin Secondary Mesenchyme Cells Is Dependent on an Intact Extracellular Matrix

Scirocco, A.; Pallotta, L.; Rengo, M.; Ignazzi, A.; Carabotti, M.; Cicenia, A.; Vona, R.; Chirletti, P.; Maselli, M.Antonietta.; Donghia, R.; Coluzzi, M.; Matarrese, P.; Silecchia, G.; Severi, C., 2018:
Myogenic oxidative imbalance interferes with antral motility in obese subjects

Milner, D.J.; Bionaz, M.; Monaco, E.; Cameron, J.Ann.; Wheeler, M.B., 2018:
Myogenic potential of mesenchymal stem cells isolated from porcine adipose tissue

Wang, H.Xin.; Davis, M.J.; Rajanayagam, M.A.Sharmini.; Potocnik, S.J.; Hill, M.A., 2018:
Myogenic reactivity of rat epineurial arterioles: potential role in local vasoregulatory events

Mortensen, H.Gavlshøj.; Madsen, J.Kvist.; Andersen, K.K.; Vosegaard, T.; Deen, G.Roshan.; Otzen, D.E.; Pedersen, J.Skov., 2018:
Myoglobin and α-Lactalbumin Form Smaller Complexes with the Biosurfactant Rhamnolipid Than with SDS

Vargas, D.A.; Tinoco, A.; Tyagi, V.; Fasan, R., 2018:
Myoglobin-Catalyzed C-H Functionalization of Unprotected Indoles

Molé, P.A.; Chung, Y.; Tran, T.Khanh.; Sailasuta, N.; Hurd, R.; Jue, T., 2018:
Myoglobin desaturation with exercise intensity in human gastrocnemius muscle

Stone, M.J.; Willerson, J.T., 1983:
Myoglobinemia in myocardial infarction

Jahanbakhshi, M., 2018:
Myoglobin immobilized on mesoporous carbon foam in a hydrogel (selep) dispersant for voltammetric sensing of hydrogen peroxide

Postnikova, G.B.; Shekhovtsova, E.A., 2018:
Myoglobin: Oxygen Depot or Oxygen Transporter to Mitochondria? A Novel Mechanism of Myoglobin Deoxygenation in Cells (review)

Servonnet, Aélie.; Dubost, Cément.; Martin, G.; Lefrère, B.; Fontan, Eéonore.; Ceppa, F.; Delacour, Hé., 2018:
Myoglobin: still a useful biomarker in 2017?

Rowland, L.P.; Penn, A.S., 1972:

Shirayama, Y.; Takahashi, M.; Osone, F.; Hara, A.; Okubo, T., 2018:
Myo-inositol, Glutamate, and Glutamine in the Prefrontal Cortex, Hippocampus, and Amygdala in Major Depression

Guo, X.; Guo, S.; Miao, Z.; Li, Z.; Zhang, H., 2018:
Myo-inositol lowers the risk of developing gestational diabetic mellitus in pregnancies: A systematic review and meta-analysis of randomized controlled trials with trial sequential analysis

Laganà, A.Simone.; Vitagliano, A.; Noventa, M.; Ambrosini, G.; D'Anna, R., 2018:
Myo-inositol supplementation reduces the amount of gonadotropins and length of ovarian stimulation in women undergoing IVF: a systematic review and meta-analysis of randomized controlled trials

Rao, C.; Fox, S.; Desai, S.S., 2018:
Myointimal Hyperplasia in a Patient with Neuromyelitis Optica (Devic's Disease) after the Creation of an Arteriovenous Graft

Duan, Y.; Li, F.; Tan, B.; Lin, B.; Kong, X.; Li, Y.; Yin, Y., 2015:
Myokine interleukin-15 expression profile is different in suckling and weaning piglets

Mazur-Bialy, A.I.; Kozlowska, K.; Pochec, E.; Bilski, J.; Brzozowski, T., 2018:
Myokine irisin-induced protection against oxidative stress in vitro. Involvement of heme oxygenase-1 and antioxidazing enzymes superoxide dismutase-2 and glutathione peroxidase

Miao, Y.; Hu, B.; Wang, Q.; Yang, Q.; Zhou, S., 2018:
Myokines related to leukocyte recruitment are down-regulated in osteosarcoma

Anonymous, 1934:
Myoma of the Rectum

Vlahos, N.F.; Theodoridis, T.D.; Partsinevelos, G.A., 2018:
Myomas and Adenomyosis: Impact on Reproductive Outcome

Anonymous, 2018:
Myoma Uteri and Its Treatment

Murray, H.Leith., 1930:
Myomectomy : A Record of 154 Consecutive Cases

Guo, Y.; Wang, P.; Wang, P.; Gao, W.; Li, F.; Yang, X.; Ni, H.; Shen, W.; Guo, Z., 2018:
Myometrial invasion and overall staging of endometrial carcinoma: assessment using fusion of T2-weighted magnetic resonance imaging and diffusion-weighted magnetic resonance imaging

Lucic, N.; Draganovic, D.; Sibincic, S.; Ecim-Zlojutro, V.; Milicevic, S., 2018:
Myometrium Invasion, Tumour Size and Lymphovascular Invasion as a Prognostic Factor in Dissemination of Pelvic Lymphatics at Endometrial Carcinoma

de Maio, Mício., 2018:
Myomodulation with Injectable Fillers: An Innovative Approach to Addressing Facial Muscle Movement

Gerhart, J.; Withers, C.; Gerhart, C.; Werner, L.; Mamalis, N.; Bravo-Nuevo, A.; Scheinfeld, V.; FitzGerald, P.; Getts, R.; George-Weinstein, M., 2018:
Myo/Nog cells are present in the ciliary processes, on the zonule of Zinn and posterior capsule of the lens following cataract surgery

Murach, K.A.; Englund, D.A.; Dupont-Versteegden, E.E.; McCarthy, J.J.; Peterson, C.A., 2018:
Myonuclear Domain Flexibility Challenges Rigid Assumptions on Satellite Cell Contribution to Skeletal Muscle Fiber Hypertrophy

Balakrishnan, M.; Baylies, M.K., 2018:
Myonuclear Positioning and Aneurysms Are LINC'd by Ariadne

Balakrishnan, M.; Baylies, M.K., 2018:
Myonuclear Positioning and Aneurysms Are LINC'd by Ariande

Srinivasan, J.; Amato, A.A., 2003:

O'Rourke, K.S., 2000:
Myopathies in the elderly

Anonymous, 2018:

Stöllberger, C.; Finsterer, J., 2017:
Myopathy and Noncompaction Detected After Malignant Hyperthermia During Cardiac Surgery

Finsterer, J.; Stöllberger, C., 2018:
Myopathy, athletism, pregnancy, race, and chromosomal defects need to be considered in noncompaction

Carvalho, A.Alves.de.Siqueira.; da Silva, V.Gomes.; Zanoteli, E.; Feder, D., 2018:
Myopathy due to HMGCR antibodies in adult mimicking muscular dystrophy associated with cancer and statin exposure - narrative review of the literature - case report

Anonymous, 2018:
Myopathy genes and SIDS

Wentink, G.H.; van der Linde-Sipman, J.S.; Meijer, A.E.F.H.; Kamphuisen, H.A.C.; van Vorstenbosch, C.J.A.H.V.; Hartman, W.; Hendriks, H.J., 1972:
Myopathy with a Possible Recessive X-Linked Inheritance in a Litter of Irish Terriers

Niu, Z.; Pontifex, C.Sabine.; Berini, S.; Hamilton, L.E.; Naddaf, E.; Wieben, E.; Aleff, R.A.; Martens, K.; Gruber, A.; Engel, A.G.; Pfeffer, G.; Milone, M., 2018:
Myopathy With SQSTM1 and TIA1 Variants: Clinical and Pathological Features

Yang, J.C.; Venteicher, A.S.; Koch, M.J.; Stapleton, C.J.; Friedman, G.N.; Venteicher, E.M.; Shin, J.H., 2018:
Myopericytoma at the Craniocervical Junction: Clinicopathological Report and Review of a Rare Perivascular Neoplasm

Ruiz-Arriaga, L.Felipe.; Ramirez Teran, A.Laura.; Ortiz-Hidalgo, C.; Fonte-Avalos, V.; Toussaint-Caire, S.; Vega-Memije, M.Elisa.; Anda-Juarez, M.CatalinaDe., 2018:
Myopericytoma in an unusual location

Peters, K.; Caracciolo, J.T.; Henderson-Jackson, E.; Binitie, O., 2018:
Myopericytoma/myopericytomatosis of the lower extremity in two young patients: a recently designated rare soft tissue neoplasm

Van Camp, L.; Goubau, J.; Van den Berghe, I.; Mermuys, K., 2018:
Myopericytoma of the Base of the Finger: Radiological and Pathological Description of a Rare Benign Entity

Strayer, E.; Throndson, R.; Clement, C.; McDaniel, K., 2018:
Myopericytoma of the Lip: A Case Report of This Rare Lesion

Schaeffel, F.; Howland, H.C., 1995:

Shapira, Y.; Vainer, I.; Mimouni, M.; Sela, T.; Munzer, G.; Kaiserman, I., 2018:
Myopia and myopic astigmatism photorefractive keratectomy: applying an advanced multiple regression-derived nomogram

Crim, N.; Esposito, E.; Monti, R.; Correa, L.J.; Serra, H.M.; Urrets-Zavalia, J.A., 2017:
Myopia as a risk factor for subsequent retinal tears in the course of a symptomatic posterior vitreous detachment

Asbell, P.A.; Tsubota, K., 2018:
Myopia Control: Current Thoughts and Future Research

Musolf, A.M.; Simpson, C.L.; Long, K.A.; Moiz, B.A.; Lewis, D.D.; Middlebrooks, C.D.; Portas, L.; Murgia, F.; Ciner, E.B.; Bailey-Wilson, J.E.; Stambolian, D., 2018:
Myopia in Chinese families shows linkage to 10q26.13

Carr, B.J.; Mihara, K.; Ramachandran, R.; Saifeddine, M.; Nathanson, N.M.; Stell, W.K.; Hollenberg, M.D., 2018:
Myopia-Inhibiting Concentrations of Muscarinic Receptor Antagonists Block Activation of Alpha2A-Adrenoceptors In Vitro

de Jong, P.T.V.M., 2018:
Myopia: its historical contexts

Logan, N.; Guggenheim, J.; To, C-Ho., 2018:
Myopia: mechanisms, manifestations and management

Wu, P-Chang.; Chen, C-Tan.; Lin, K-Kuo.; Sun, C-Chin.; Kuo, C-Neng.; Huang, H-Mei.; Poon, Y-Chieh.; Yang, M-Ling.; Chen, C-Yin.; Huang, J-Chen.; Wu, P-Chen.; Yang, I-Hui.; Yu, H-Ju.; Fang, P-Chiung.; Tsai, C-Ling.; Chiou, S-Ti.; Yang, Y-Hsin., 2018:
Myopia Prevention and Outdoor Light Intensity in a School-Based Cluster Randomized Trial

Rusnak, S.; Salcman, V.; Hecova, L.; Kasl, Z., 2018:
Myopia Progression Risk: Seasonal and Lifestyle Variations in Axial Length Growth in Czech Children

Galvis, V.; Tello, A.; Gomez, L.María.; Otero, J., 2017:
Myopia rates in a genetically isolated population

Mrugacz, M.; Gajecka, M.; Mrukwa-Kominek, E.; Witkowska, K.J., 2018:
Myopia: Risk Factors, Disease Mechanisms, Diagnostic Modalities, and Therapeutic Options

Díaz Llopis, M.; Cisneros Lanuza, A., 2018:
Myopia, the challenge of Ophthalmology and its worldwide "explosive epidemic"

Traquair, H.M., 1921:
Myopia, the Use of Concave Glasses for near Work in Low Degrees of

Bulgari, D.; Jha, A.; Deitcher, D.L.; Levitan, E.S., 2018:
Myopic (HD-PTP, PTPN23) selectively regulates synaptic neuropeptide release

Hwang, S.; Lim, D.Hui.; Hyun, J.; Kim, M.Joon.; Chung, T.Young., 2018:
Myopic Shift after Implantation of a Novel Diffractive Trifocal Intraocular Lens in Korean Eyes

Aker, J.; Dowling, J.; Halperin, L., 2018:
Myopic shift in a pseudophakic eye with an accommodating IOL following vitrectomy with gas tamponade

Cooke, M.B.; Rybalka, E.; Stathis, C.G.; Hayes, A., 2018:
Myoprotective Potential of Creatine Is Greater than Whey Protein after Chemically-Induced Damage in Rat Skeletal Muscle

Young, J.; Margaron, Y.; Fernandes, M.; Duchemin-Pelletier, E.; Michaud, J.; Flaender, Mélanie.; Lorintiu, O.; Degot, Sébastien.; Poydenot, P., 2018:
MyoScreen, a High-Throughput Phenotypic Screening Platform Enabling Muscle Drug Discovery

Liakath-Ali, K.; Vancollie, V.E.; Sequeira, Iês.; Lelliott, C.J.; Watt, F.M., 2018:
Myosin 10 is involved in murine pigmentation

Iuliano, O.; Yoshimura, A.; Prospéri, M-Thérèse.; Martin, Ré.; Knölker, H-Joachim.; Coudrier, E., 2018:
Myosin 1b promotes axon formation by regulating actin wave propagation and growth cone dynamics

Zhang, H-Rong.; Lai, S-Yu.; Huang, L-Jun.; Zhang, Z-Fei.; Liu, J.; Zheng, S-Rong.; Ding, K.; Bai, X.; Zhou, J-Yu., 2018:
Myosin 1b promotes cell proliferation, migration, and invasion in cervical cancer

Kannan, N.; Tang, V.W., 2018:
Myosin-1c promotes E-cadherin tension and force-dependent recruitment of α-actinin to the epithelial cell junction

Nevzorov, I.; Sidorenko, E.; Wang, W.; Zhao, H.; Vartiainen, M.K., 2018:
Myosin-1C uses a novel phosphoinositide-dependent pathway for nuclear localization

Salvermoser, M.; Pick, R.; Weckbach, L.T.; Zehrer, A.; Löhr, P.; Drechsler, M.; Sperandio, M.; Soehnlein, O.; Walzog, B., 2018:
Myosin 1f is specifically required for neutrophil migration in 3D environments during acute inflammation

López-Ortega, O.; Santos-Argumedo, L., 2018:
Myosin 1g Contributes to CD44 Adhesion Protein and Lipid Rafts Recycling and Controls CD44 Capping and Cell Migration in B Lymphocytes

Sato, N.; Fujishima, F.; Nakamura, Y.; Aoyama, Y.; Onodera, Y.; Ozawa, Y.; Ito, K.; Ishida, H.; Kamei, T.; Watanabe, M.; Sasano, H., 2018:
Myosin 5a regulates tumor migration and epithelial-mesenchymal transition in esophageal squamous cell carcinoma: utility as a prognostic factor

Yamashiro, S.; Tanaka, S.; McMillen, L.M.; Taniguchi, D.; Vavylonis, D.; Watanabe, N., 2018:
Myosin-dependent actin stabilization as revealed by single-molecule imaging of actin turnover

Titus, M.A., 2018:
Myosin-Driven Intracellular Transport

Hammer, J.A., 2018:
Myosin goes for blood

Coluccio, L.M., 1997:
Myosin I

Koshida, R.; Tome, S.; Takei, Y., 2018:
Myosin Id localizes in dendritic spines through the tail homology 1 domain

Norwood Toro, L.E.; Wang, Y.; Condeelis, J.S.; Jones, J.G.; Backer, J.M.; Bresnick, A.R., 2018:
Myosin-IIA heavy chain phosphorylation on S1943 regulates tumor metastasis

Smith, A.S.; Nowak, R.B.; Zhou, S.; Giannetto, M.; Gokhin, D.S.; Papoin, J.; Ghiran, I.C.; Blanc, L.; Wan, J.; Fowler, V.M., 2018:
Myosin IIA interacts with the spectrin-actin membrane skeleton to control red blood cell membrane curvature and deformability

Li, P.; Wei, G.; Cao, Y.; Deng, Q.; Han, X.; Huang, X.; Huo, Y.; He, Y.; Chen, L.; Luo, J., 2017:
Myosin IIa is critical for cAMP-mediated endothelial secretion of von Willebrand factor

Vijayan, K.Vinod., 2018:
Myosin IIa signal von Willebrand factor release

Jiao, M.; Wu, D.; Wei, Q., 2018:
Myosin II-interacting guanine nucleotide exchange factor promotes bleb retraction via stimulating cortex reassembly at the bleb membrane

Schulz, O.; Hanč, P.; Böttcher, J.P.; Hoogeboom, R.; Diebold, S.S.; Tolar, P.; Reis E Sousa, C., 2018:
Myosin II Synergizes with F-Actin to Promote DNGR-1-Dependent Cross-Presentation of Dead Cell-Associated Antigens

Iida, Y.; Senda, T.; Matsukawa, Y.; Onoda, K.; Miyazaki, J-Ichi.; Sakaguchi, H.; Nimura, Y.; Hidaka, H.; Niki, I., 1997:
Myosin light-chain phosphorylation controls insulin secretion at a proximal step in the secretory cascade

Coirault, C.; Lambert, F.; Marchand-Adam, S.; Attal, P.; Chemla, D.; Lecarpentier, Y., 2018:
Myosin molecular motor dysfunction in dystrophic mouse diaphragm

Horváth, Dániel.; Sipos, A.; Major, E.; Kónya, Zán.; Bátori, Róbert.; Dedinszki, Dóra.; Szöll Si, A.; Tamás, Ián.; Iván, J.; Kiss, A.; Erd di, F.; Lontay, Báta., 2018:
Myosin phosphatase accelerates cutaneous wound healing by regulating migration and differentiation of epidermal keratinocytes via Akt signaling pathway in human and murine skin

Kiss, A.; Erdődi, F.; Lontay, Báta., 2018:
Myosin phosphatase: Unexpected functions of a long-known enzyme

Bunda, J.; Gittings, W.; Vandenboom, R., 2018:
Myosin phosphorylation improves contractile economy of mouse fast skeletal muscle during staircase potentiation

Hecht, G.; Koutsouris, A., 2018:
Myosin regulation of NKCC1: effects on cAMP-mediated Cl- secretion in intestinal epithelia

Li, H.; Li, P.; Yan, J.; Xie, W.; Wang, P.; Wu, H.; Zhou, K., 2018:
Myosin Va from Eriocheir sinensis: cDNA cloning, expression and involvement in growth and development

Ripoll, Léa.; Heiligenstein, X.; Hurbain, I.; Domingues, L.; Figon, F.; Petersen, K.J.; Dennis, M.K.; Houdusse, A.; Marks, M.S.; Raposo, Gça.; Delevoye, Cédric., 2018:
Myosin VI and branched actin filaments mediate membrane constriction and fission of melanosomal tubule carriers

Kruppa, A.J.; Kishi-Itakura, C.; Masters, T.A.; Rorbach, J.E.; Grice, G.L.; Kendrick-Jones, J.; Nathan, J.A.; Minczuk, M.; Buss, F., 2018:
Myosin VI-Dependent Actin Cages Encapsulate Parkin-Positive Damaged Mitochondria

Majewski, L.; Nowak, J.; Sobczak, M.; Karatsai, O.; Havrylov, S.; Lenartowski, R.; Suszek, M.; Lenartowska, M.; Redowicz, M.Jolanta., 2018 :
Myosin VI in the nucleus of neurosecretory PC12 cells: Stimulation-dependent nuclear translocation and interaction with nuclear proteins

Abu-Abied, M.; Belausov, E.; Hagay, S.; Peremyslov, V.; Dolja, V.; Sadot, E., 2018:
Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division

Sun, H.; Furt, F.; Vidali, L., 2018:
Myosin XI localizes at the mitotic spindle and along the cell plate during plant cell division in Physcomitrella patens

Buschmann, H., 2018:
Myosin XI motors: back on the scene at the division machine

Kroon, J.; Schaefer, A.; Hoogenboezem, M.; Van Alphen, F.; Hordijk, P.; Strömblad, S.; Hoeben, K.; Van Rhenen, J.; Stroes, E.; Van Buul, J., 2018:
Myosin-X is required for ICAM-1-rich endothelial filopodia through the small gtpase CDC42 and PAK4 to functionally support leukocyte adhesion

Shah, M.; Tayar, J.H.; Abdel-Wahab, N.; Suarez-Almazor, M.E., 2018:
Myositis as an adverse event of immune checkpoint blockade for cancer therapy

Zampeli, E.; Venetsanopoulou, A.; Argyropoulou, O.D.; Mavragani, C.P.; Tektonidou, M.G.; Vlachoyiannopoulos, P.G.; Tzioufas, A.G.; Skopouli, F.N.; Moutsopoulos, H.M., 2018:
Myositis autoantibody profiles and their clinical associations in Greek patients with inflammatory myopathies

Lockney, D.T.; Jia, A.Y.; Lis, E.; Lockney, N.A.; Liu, C.; Hopkins, B.; Higginson, D.S.; Yamada, Y.; Laufer, I.; Bilsky, M.; Schmitt, A.M., 2018:
Myositis following spine radiosurgery for metastatic disease: a case series

Rossman, P.M.; Thomovsky, S.A.; Schafbuch, R.M.; Guo, L.T.; Shelton, G.D., 2018:
Myositis, Ganglioneuritis, and Myocarditis with Distinct Perifascicular Muscle Atrophy in a 2-Year-Old Male Boxer

Fujioka, S.; Kitajima, T.; Itotani, R., 2018:
Myositis in a Patient with Advanced Lung Cancer Treated with Osimertinib

Seo, M.; Cha, H.Jeong.; Choi, Y.; Park, S.Hoon., 2018:
Myositis in bilateral calves mimicking lymphoma on interim PET/CT in a patient with T-lymphoblastic lymphoma

Lim, J.; van Royen-Kerkhof, A.; Jonkers, R.E.; Starink, M.V.; Voskuyl, A.E.; van der Kooi, A.J., 2018:
Myositis: more than a muscle disease

Kaeding, C.C.; Sanko, W.A.; Fischer, R.A., 1995:
Myositis Ossificans

Bekers, E.M.; Eijkelenboom, A.; Grünberg, K.; Roverts, R.C.; de Rooy, J.W.J.; van der Geest, I.C.M.; van Gorp, J.M.; Creytens, D.; Flucke, U., 2018:
Myositis ossificans - Another condition with USP6 rearrangement, providing evidence of a relationship with nodular fasciitis and aneurysmal bone cyst

Shiono, S.; Matsumura, N.; Ogawa, K., 2014:
Myositis Ossificans Circumscripta Occurring in the Subacromial Space with Severe Mechanical Blocking of the Shoulder Joint: A Case Report

Mohamed, A.Wahab.Alassane.; Moussa, K.; Seyni, S.Badio.; Seyni, Z.Abassa.; Kasoumou, A.Sanoussi.; Ziberou, K., 2018:
Myositis ossificans circumscripta of the hip: about a case

Rossettini, G.; Ristori, D.; Testa, M., 2018:
Myositis Ossificans: Delayed Complication of Severe Muscle Contusion

Monteiro, D.I.; Nuñez Camarena, J.H.; Soldado, F., 2018:
Myositis ossificans of a lumbrical muscle in a child's hand

Lin, N.; Gao, N.; He, W., 2018:
Myositis ossificans progressia of lateral pterygoid muscle of both sides: a case report

Mair, W.Frederick., 1932:
Myositis Ossificans Progressiva

Stark, W.H., 1991:
Myositis ossificans progressiva

Karaali, S.; Emekli, U., 2018:
Myositis Ossificans Traumatica of the Medial Pterygoid Muscle After Third Molar Tooth Extraction: A Case Report and Review of Literature

Yoshii, T.; Nakai, O.; Hirai, T.; Sotome, S.; Shinomiya, K.; Okawa, A., 2012:
Myositis Ossificans Traumatica Secondary to Fracture of the Odontoid in a Five-Month-Old Infant: A Case Report

Eising, K.; Peitz, J.; Unterwalder, N.; Meisel, C.; Horneff, G., 2018:
Myositis-specific antibodies associated with juvenile dermatomyositis

Ueki, M.; Kobayashi, I.; Takezaki, S.; Tozawa, Y.; Okura, Y.; Yamada, M.; Kuwana, M.; Ariga, T., 2018:
Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathies

Carvalho, Lívia.Pinheiro.; Basso-Vanelli, R.Pedrolongo.; Di Thommazo-Luporini, L.; Mendes, R.Gonçalves.; Oliveira-Junior, M.Carneiro.; Vieira, R.de.Paula.; Bonjorno-Junior, Jé.Carlos.; Oliveira, Cáudio.Ricardo.; Luporini, R.; Borghi-Silva, A., 2017:
Myostatin and adipokines: The role of the metabolically unhealthy obese phenotype in muscle function and aerobic capacity in young adults

Ji, S.; Losinski, R.L.; Cornelius, S.G.; Frank, G.R.; Willis, G.M.; Gerrard, D.E.; Depreux, F.F.S.; Spurlock, M.E., 2018:
Myostatin expression in porcine tissues: tissue specificity and developmental and postnatal regulation

Tinklenberg, J.A.; Siebers, E.M.; Beatka, M.J.; Meng, H.; Yang, L.; Zhang, Z.; Ross, J.A.; Ochala, J.; Morris, C.; Owens, J.M.; Laing, N.G.; Nowak, K.J.; Lawlor, M.W., 2018:
Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice

Lin, Y-Shuen.; Lin, F-Yu.; Hsiao, Y-Hsin., 2018:
Myostatin Is Associated With Cognitive Decline in an Animal Model of Alzheimer's Disease

Cheewasopit, W.; Laird, M.; Glister, C.; Knight, P.G., 2018:
Myostatin is expressed in bovine ovarian follicles and modulates granulosal and thecal steroidogenesis

Hu, S-Lin.; Chang, A-Chen.; Huang, C-Chung.; Tsai, C-Hao.; Lin, C-Chieh.; Tang, C-Hsin., 2017:
Myostatin Promotes Interleukin-1β Expression in Rheumatoid Arthritis Synovial Fibroblasts through Inhibition of miR-21-5p

Bhanji, R.A.; Moctezuma-Velazquez, C.; Duarte-Rojo, A.; Ebadi, M.; Ghosh, S.; Rose, C.; Montano-Loza, A.J., 2018:
Myosteatosis and sarcopenia are associated with hepatic encephalopathy in patients with cirrhosis

Tachi, Y.; Kozuka, A.; Hirai, T.; Ishizu, Y.; Honda, T.; Kuzuya, T.; Hayashi, K.; Ishigami, M.; Goto, H., 2018:
Impact of myosteatosis on skeletal muscle volume loss in patients with chronic liver disease

van Dijk, D.P.J.; Bakers, F.C.H.; Sanduleanu, S.; Vaes, R.D.W.; Rensen, S.S.; Dejong, C.H.C.; Beets-Tan, R.G.H.; Olde Damink, S.W.M., 2018:
Myosteatosis predicts survival after surgery for periampullary cancer: a novel method using MRI

Mehta, H.K., 2018:
Myotarsal flap - a versatile entity for lower eyelid reconstructions

Rissatto Sierra, L.; Fávaro, G.; Cerri, B.Rubin.; Rocha, L.Caetano.; de Yokomizo de Almeida, S.Regina.; Watanabe, I-Sei.; Ciena, A.Polican., 2018:
Myotendinous junction plasticity in aged ovariectomized rats submitted to aquatic training

Draghi, F.; Draghi, A.G.; Gitto, S., 2018:
Myotendinous strains of the vastus lateralis as a result of sport-related trauma

Ramos-Fransi, A.; Martínez-Piñeiro, A.; Almendrote, Míriam.; Lucente, G.; Carrato, C.; Ballester-Lopez, A.; Lucia, A.; Pintos-Morell, G.; Nogales-Gadea, G.; Coll-Cantí, J., 2018:
Myotilinopathy unmasked by statin treatment: A case report

Kane, E.D.; Budhraja, V.; Desilets, D.J.; Romanelli, J.R., 2018:
Myotomy length informed by high-resolution esophageal manometry (HREM) results in improved per-oral endoscopic myotomy (POEM) outcomes for type III achalasia

HIRSCH, D.R.; DANCIS, J.; WARD, R.S., 1949:
Myotonia congenita

Kim, A.; Jang, M.; Kim, H-Joon.; Kim, Y.; Kim, D-Seong.; Shin, J-Hong.; Jeon, B., 2018:
Myotonia Congenita Can Be Mistaken as Paroxysmal Kinesigenic Dyskinesia

Quitt, P.R.; Hytönen, M.K.; Matiasek, K.; Rosati, M.; Fischer, A.; Lohi, H., 2018:
Myotonia congenita in a Labrador Retriever with truncated CLCN1

Partanen, J.; Isohanni, P.; Auranen, M., 2017:
Myotonia in ion channel diseases of muscle

Lehmann-Horn, F.; D'Amico, A.; Bertini, E.; Lomonaco, M.; Merlini, L.; Nelson, K.R.; Philippi, H.; Siciliano, G.; Spaans, F.; Jurkat-Rott, K., 2018:
Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life

Thomas, J.D.; Oliveira, R.; Sznajder, Łukasz.J.; Swanson, M.S., 2018:
Myotonic Dystrophy and Developmental Regulation of RNA Processing

Meinke, P.; Hintze, S.; Limmer, S.; Schoser, B., 2018:
Myotonic Dystrophy-A Progeroid Disease?

Bell, D.B.; Smith, D.W., 1972:
Myotonic dystrophy in the neonate

Heatwole, C.; Johnson, N.; Dekdebrun, J.; Dilek, N.; Eichinger, K.; Hilbert, J.; Luebbe, E.; Martens, W.; Mcdermott, M.P.; Thornton, C.; Moxley, R., 2018:
Myotonic dystrophy patient preferences in patient-reported outcome measures

Pelizzo, G.; Calcaterra, V.; Villanacci, V.; Mura, G.Battista.; Bassotti, G., 2018:
Myotonic dystrophy type 1 and pseudo-obstruction in a child with smooth muscle α-actin deficiency and eosinophilic myenteric plexitis

Ho, G.; Carey, K.A.; Cardamone, M.; Farrar, M.A., 2018:
Myotonic dystrophy type 1: clinical manifestations in children and adolescents

Gagnon, C.; Gallais, B.; Laberge, L., 2018:
Myotonic dystrophy type 1: reasons to be OPTIMISTIC

Filho, L.Huebra.Pimentel.; Gomes, A.Carolina.Dias.; Gonçalves, B.; Tufik, S.; Coelho, F.Morgadinho., 2018:
Myotonic dystrophytype 1 - report of non-24-h sleep-wake disorder with excessive daytime sleepiness

Takeshima, K.; Ariyasu, H.; Ishibashi, T.; Kawai, S.; Uraki, S.; Koh, J.; Ito, H.; Akamizu, T., 2018:
Myotonic dystrophy type 1 with diabetes mellitus, mixed hypogonadism and adrenal insufficiency

Otsuki, S.; Yasuda, T.; Mukaida, K.; Noda, Y.; Kanzaki, R.; Miyoshi, H.; Kondo, T.; Hamada, H.; Kawamoto, M., 2018:
Myotoxicity of local anesthetics is equivalent in individuals with and without predisposition to malignant hyperthermia

Urbański, A.; Lubawy, J.; Marciniak, Pł.; Rosiński, G., 2018:
Myotropic activity and immunolocalization of selected neuropeptides of the burying beetle Nicrophorus vespilloides (Coleoptera: Silphidae)

Lubawy, J.; Marciniak, Pł.; Kuczer, M.; Rosiński, G., 2018:
Myotropic activity of allatostatins in tenebrionid beetles

Chowanski, S.; Rosinski, G., 2018:
Myotropic Effects of Cholinergic Muscarinic Agonists and Antagonists in the Beetle Tenebrio molitor L

Nakasone, A.; Muramatsu, R.; Kato, Y.; Kawahara, Y.; Yamashita, T., 2018:
Myotube-derived factor promotes oligodendrocyte precursor cell proliferation

Narayanan, P.; Hütte, M.; Kudryasheva, G.; Taberner, F.J.; Lechner, S.G.; Rehfeldt, F.; Gomez-Varela, D.; Schmidt, M., 2018:
Myotubularin related protein-2 and its phospholipid substrate PIP 2 control Piezo2-mediated mechanotransduction in peripheral sensory neurons

Badurska, B.; Fidziańska, A.; Kamieniecka, Z.; Prot, J.; Strugalska, H., 1969:
Myotubular myopathy

Bender, K.; Begun, S.; Durbahn, R.; Ferguson, K.; Schau, N., 2018:
My Own Best Friend: Homeless Youths' Hesitance to Seek Help and Strategies for Coping Independently after Distressing and Traumatic Experiences

Osei-Tutu, A.; Dzokoto, V.Afi.; Adams, G.; Hanke, K.; Kwakye-Nuako, C.; Adu-Mensa, F.; Appiah-Danquah, R., 2018:
'My Own House, Car, My Husband, and Children': meanings of success among Ghanaians

Hilbert, G.; Vargas, Fédéric., 2018:
My paper 20 years later: NIV in immunocompromized patients

Panattoni, K.; Thomsen, D.Kirkegaard., 2018:
My partner's stories: relationships between personal and vicarious life stories within romantic couples

Komaki, R., 2018:
My Path from Hiroshima to Houston

Beauchamp, T.L.; Beauchamp, T.L., 2018:
My Path to Bioethics

Sanganyado, E., 2018:
My path to contentment

Heise, B.A.; Wing, D.K.; Hullinger, A.H.R., 2018:
My Patient Died: A National Study of Nursing Students' Perceptions After Experiencing a Patient Death

Anonymous, 2018:
My Patient Gave me a Second Chance at Life

Monnet, X.; Teboul, J-Louis., 2018:
My patient has received fluid. How to assess its efficacy and side effects?

Lal, N., 2018:
My Patient the Ex-Con-An Evolution of Perspective

Moore, A.Kenefick., 2018:
My People, 2014

Saini, I.; Bagri, N.; Gupta, N., 2018:
My Phenotype speaks: please do not harm me with biopsy needle

Hardison, B.; Leone, A.; Day, A., 2017:
MyPlate: Meeting Consumers Where They Are, Every Season

Postic, G.; Hamelryck, T.; Chomilier, J.; Stratmann, D., 2018:
MyPMFs: a simple tool for creating statistical potentials to assess protein structural models

Burgess, A.M.; Graves, L.M.; Frost, R.O., 2018:
My possessions need me: Anthropomorphism and hoarding

Sanada, S., 2017:
My Precious Memories in Preparation for RPT

Anonymous, 1879:
My Professional Peers at Cork

Murray Sherman, S., 2018:
My prolonged collaboration with Ray Guillery

Griffin, J.B.; Struempler, B.; Funderburk, K.; Parmer, S.M.; Tran, C.; Wadsworth, D.D., 2018:
My Quest, an Intervention Using Text Messaging to Improve Dietary and Physical Activity Behaviors and Promote Weight Loss in Low-Income Women

Soares, A.M.S.; Oliveira, J.T.A.; Rocha, Cáudia.Q.; Ferreira, Aé.T.S.; Perales, J.; Zanatta, A.Caroline.; Vilegas, W.; Silva, C.R.; Costa-Junior, L.M., 2018:
Myracrodruon urundeuva seed exudates proteome and anthelmintic activity against Haemonchus contortus

Saccol, E.M.H.; Jerez-Cepa, I.; Ourique, G.M.; Pês, T.S.; Gressler, L.T.; Mourão, R.H.V.; Martínez-Rodríguez, G.; Mancera, J.M.; Baldisserotto, B.; Pavanato, M.A.; Martos-Sitcha, J.A., 2017:
Myrcia sylvatica essential oil mitigates molecular, biochemical and physiological alterations in Rhamdia quelen under different stress events associated to transport

Kurahashi, H.; Azuma, Y.; Masuda, A.; Okuno, T.; Nakahara, E.; Imamura, T.; Saitoh, M.; Mizuguchi, M.; Shimizu, T.; Ohno, K.; Okumura, A., 2017:
MYRF is associated with encephalopathy with reversible myelin vacuolization

Pinder, T.; Price, I.; Allouni, K.; Rajagopalan, S., 2018:
Myriad manifestations of infective endocarditis

Post, R.M., 2018:
Myriad of implications of acetyl-l-carnitine deficits in depression

Carvajal-Rodríguez, A., 2017:
Myriads: P-value-based multiple testing correction

Sun, L.; Xu, P.; Fu, T.; Huang, X.; Song, J.; Chen, M.; Tian, X.; Yin, H.; Han, J., 2017:
Myricetin against ischemic cerebral injury in rat middle cerebral artery occlusion model

Fan, S.; Gao, X.; Chen, P.; Li, X., 2018:
Myricetin ameliorates glucocorticoid-induced osteoporosis through the ERK signaling pathway

Ren, R.; Yin, S.; Lai, B.; Ma, L.; Wen, J.; Zhang, X.; Lai, F.; Liu, S.; Li, L., 2018:
Myricetin antagonizes semen-derived enhancer of viral infection (SEVI) formation and influences its infection-enhancing activity

Zhang, N.; Feng, H.; Liao, H-Han.; Chen, S.; Yang, Z.; Deng, W.; Tang, Q-Zhu., 2017:
Myricetin attenuated LPS induced cardiac injury in vivo and in vitro

Hou, W.; Hu, S.; Su, Z.; Wang, Q.; Meng, G.; Guo, T.; Zhang, J.; Gao, P., 2018:
Myricetin attenuates LPS-induced inflammation in RAW 264.7 macrophages and mouse models

Dhanraj, V.; Karuppaiah, J.; Balakrishnan, R.; Elangovan, N., 2018:
Myricetin attenuates neurodegeneration and cognitive impairment in Parkinsonism

Tan, G.; Uson-Lopez, R.A.; Rahman, M.Mostafizur.; Hosokawa, T.; Saito, T.; Kurasaki, M., 2017 :
Myricetin enhances on apoptosis induced by serum deprivation in PC12 cells mediated by mitochondrial signaling pathway

Knickle, A.; Fernando, W.; Greenshields, A.L.; Rupasinghe, H.P.Vasantha.; Hoskin, D.W., 2018:
Myricetin-induced apoptosis of triple-negative breast cancer cells is mediated by the iron-dependent generation of reactive oxygen species from hydrogen peroxide

Ghassemi-Rad, J.; Maleki, M.; Knickle, A.F.; Hoskin, D.W., 2018:
Myricetin-induced oxidative stress suppresses murine T lymphocyte activation

Cao, J.; Chen, H.; Lu, W.; Wu, Y.; Wu, X.; Xia, D.; Zhu, J., 2017:
Myricetin Induces Protective Autophagy by Inhibiting the Phosphorylation of mTOR in HepG2 Cells

Kim, G.Dae., 2018:
Myricetin Inhibits Angiogenesis by Inducing Apoptosis and Suppressing PI3K/Akt/mTOR Signaling in Endothelial Cells

Khan, E.; Tawani, A.; Mishra, S.Kumar.; Verma, A.Kumar.; Upadhyay, A.; Kumar, M.; Sandhir, R.; Mishra, A.; Kumar, A., 2017:
Myricetin Reduces Toxic Level of CAG Repeats RNA in Huntington's Disease (HD) and Spino Cerebellar Ataxia (SCAs)

Ci, Y.; Zhang, Y.; Liu, Y.; Lu, S.; Cao, J.; Li, H.; Zhang, J.; Huang, Z.; Zhu, X.; Gao, J.; Han, M., 2018:
Myricetin suppresses breast cancer metastasis through down-regulating the activity of matrix metalloproteinase (MMP)-2/9

Park, H.; Park, S.; Bazer, F.W.; Lim, W.; Song, G., 2018:
Myricetin treatment induces apoptosis in canine osteosarcoma cells by inducing DNA fragmentation, disrupting redox homeostasis, and mediating loss of mitochondrial membrane potential

Gao, J.; Chen, S.; Qiu, Z.; Fang, L.; Zhang, L.; Guo, C.; Chen, T.; Qiu, L., 2018:
Myricitrin ameliorates ethanol-induced steatosis in mouse AML12 liver cells by activating AMPK, and reducing oxidative stress and expression of inflammatory cytokines

Iso-Mustajärvi, M.; Dietz, A.; Löppönen, H., 2018:
Myringoplasty Quality Control Is Necessary: Comparison of Surgical Results of Two Consecutive Series in A Single Institution

Anonymous, 2018:
Myringotomy: Incision of the Tympanic Membrane

Choi, S.; Snider, J.M.; Olakkengil, N.; Lambert, J.M.; Anderson, A.K.; Ross-Evans, J.S.; Cowart, L.Ashley.; Snider, A.J., 2018:
Myristate-induced endoplasmic reticulum stress requires ceramide synthases 5/6 and generation of C14-ceramide in intestinal epithelial cells

Speziali, G.; Liesinger, L.; Gindlhuber, J.; Leopold, C.; Pucher, B.; Brandi, J.; Castagna, A.; Tomin, T.; Krenn, P.; Thallinger, G.G.; Olivieri, O.; Martinelli, N.; Kratky, D.; Schittmayer, M.; Birner-Gruenberger, R.; Cecconi, D., 2018:
Myristic acid induces proteomic and secretomic changes associated with steatosis, cytoskeleton remodeling, endoplasmic reticulum stress, protein turnover and exosome release in HepG2 cells

Ying, M.; Wang, S.; Zhang, M.; Wang, R.; Zhu, H.; Ruan, H.; Ran, D.; Chai, Z.; Wang, X.; Lu, W., 2018:
Myristic Acid-Modified D A7R Peptide for Whole-Process Glioma-Targeted Drug Delivery

Lim, J.Mi.; Lim, J.Chae.; Kim, G.; Levine, R.L., 2018:
Myristoylated methionine sulfoxide reductase A is a late endosomal protein

Socas, L.B.P.; Ambroggio, E.E., 2018:
Myristoylation and Oligonucleotide Interaction Modulate Peptide and Protein Surface Properties: The Case of the HIV-1 Matrix Domain

Walton, T., 2018:
My road to discovering lymphoedema and beyond

Hijazi, A.; Al-Jaroudi, D., 2018:
Myrrh for treatment of severe vulvar edema in ovarian hyperstimulation syndrome

Britto, R.Moreira.de.; Silva-Neto, Júlio.Alves.da.; Mesquita, Tássio.Ricardo.Ribeiro.; Vasconcelos, C.Maria.Lins.de.; de Almeida, G.Kelly.Melo.; Jesus, I.Couto.Guedes.de.; Santos, Péligris.Henrique.Dos.; Souza, D.Santos.; Miguel-Dos-Santos, R.; de Sá, L.Andrade.; Dos Santos, F.Silva.Moraes.; Pereira-Filho, R.Nely.; Albuquerque-Júnior, R.Luiz.Cavalcanti.; Quintans-Júnior, L.José.; Guatimosim, S.; Lauton-Santos, S., 2017:
Myrtenol protects against myocardial ischemia-reperfusion injury through antioxidant and anti-apoptotic dependent mechanisms

Jabri, M-Amine.; Marzouki, L.; Sebai, H., 2018:
Myrtle berries seeds aqueous extract abrogates chronic alcohol consumption-induced erythrocytes osmotic stability disturbance, haematological and biochemical toxicity

Duan, L.; Zhang, W.; Zhang, F.; Cai, H., 2017:
Myrtol improves post-traumatic knee osteoarthritis by regulation of reactive oxygen species, transforming growth factor β1 and apoptosis in a mouse model

Anonymous, 2018:
"Myrtos in Kefalonia Island, Greece"

Yim, A.P., 2018:
My second career

Chandra, S., 2017:
My second-chance Ph.D

Phillips, C., 2018:
My second coming out

Waller, W.H., 2018:
My second life as a teacher

Henny, K.D.; Drumhiller, K.; Sutton, M.Y.; Nanín, Jé., 2018:
"My Sexuality…It Creates a Stress": HIV-Related Communication Among Bisexual Black and Latino Men, New York City

Tan, G.Hao., 2018:
My shoes are too small for me to fit in!

Parkes, E., 2018:
My Signature Scent

Seys, S.F.; Bousquet, J.; Bachert, C.; Fokkens, W.J.; Agache, I.; Bernal-Sprekelsen, M.; Callebaut, I.; Cardel, L.O.; Carrie, S.; Castelnuovo, P.; Cathcart, R.; Constantinidis, J.; Cools, L.; Cornet, M.; Clement, G.; de Sousa, J.C.; Cox, T.; Doulaptsi, M.; Gevaert, P.; Hopkins, C.; Hox, V.; Hummel, T.; Hosemann, W.; Jacobs, R.; Jorissen, M.; Landis, B.N.; Leunig, A.; Lund, V.J.; Mullol, J.; Onerci, M.; Palkonen, S.; Proano, I.; Prokopakis, E.; Ryan, D.; Riechelmann, H.; Saevels, J.; Segboer, C.;, 2018:
mySinusitisCoach: patient empowerment in chronic rhinosinusitis using mobile technology

Huo, Y.; Li, B-Yi.; Lin, Z-Feng.; Wang, W.; Jiang, X-Xia.; Chen, X.; Xi, W-Jin.; Yang, A-Gang.; Chen, S-Yi.; Wang, T., 2018:
MYSM1 Is Essential for Maintaining Hematopoietic Stem Cell (HSC) Quiescence and Survival

Macdonald, H., 2018:
My specialist training application

Lefrère, B., 2018:
Mysteries of a medicine chest

Yasui, K.; Tuziuti, T.; Kanematsu, W., 2018:
Mysteries of bulk nanobubbles (ultrafine bubbles); stability and radical formation

Mácová, A.; Hoblíková, A.; Hypša, Václav.; Stanko, M.; Martinů, J.; Kvičerová, J., 2018:
Mysteries of host switching: Diversification and host specificity in rodent-coccidia associations

Anonymous, 2018:
Mysterious Epidemie in Paris, Bearing Some Resemblance to the Dandy Fever

Iqbal, M.Zafar.; Cheng, M.; Zhao, Y.; Wen, X.; Ping Zhang; Zhang, L.; Ali, A.; Rong, T.; Tang, Q.Lin., 2018:
Mysterious meiotic behavior of autopolyploid and allopolyploid maize

Nakamura, T., 2018:
Mysterious Pisotriquetral Joint

Taxel, S.; Holtz, M., 2018:
Mysterious Weakness: Life-threatening condition can be managed in the field

Kesari, N.K.; Fleet, T.; Alenzi, B.; Goodman, J.Clay., 2018:
Mystery Case: A 48-year-old woman with bizarre behavior, neurologic symptoms, and progressive decline

Manners, J.; Jadhav, A.P.; Xia, Z., 2017:
Mystery Case: A 61-year-old woman with lower extremity paralysis and sensory loss

Lindegger, D.Josef.; Helfenstein, M.; Job, O.; Pless, M., 2018:
Mystery Case: Bilateral temporal crescent sparing after cardiac arrest

Joosten, I.B.T.; Hoeijmakers, J.G.J., 2018:
Mystery Case: Superior oblique myokymia: An uncommon cause of intermittent diplopia

Sharawat, I.Kumar.; Suthar, R.; Vyas, S.; Rawat, A.; Sankhyan, N., 2018:
Mystery Case: Tortuous hairs and tortuous blood vessels

Birkhead, G.S., 2018:
Mystery in the Pines

Nagaoka, S., 2018:
Mystery of Cholesterol-Lowering Peptides, Lactostatin and Soystatin

Li, W.; Zhang, X.; Li, X.; Lee, J.H.W., 2018:
Mystery of the high chlorine consumption in disinfecting a chemically enhanced primary saline sewage

Abdelsalam, M.; Vellanki, S.; Ashwini Kumar Trikannad, A.Kumar.; Degregorio, M., 2018:
Mystery ring: a case of TIPS stent migration

Collins, J.Charles.; Schneider, C.Richard.; Naughtin, C.Louise.; Wilson, F.; de Almeida Neto, A.Cesar.; Moles, R.Jane., 2018:
Mystery shopping and coaching as a form of audit and feedback to improve community pharmacy management of non-prescription medicine requests: an intervention study

Anonymous, 2018:
Mystery solved for mass mortality event

Ratto, C., 2018:
Mystifications in Methods Produce Fake Results!

Gordon, L.; Austin, P.; Rudzicz, F.; Grantcharov, T., 2018:
MySurgeryRisk and Machine Learning: A Promising Start to Real-time Clinical Decision Support

Bihorac, A.; Ozrazgat-Baslanti, T.; Ebadi, A.; Motaei, A.; Madkour, M.; Pardalos, P.M.; Lipori, G.; Hogan, W.R.; Efron, P.A.; Moore, F.; Moldawer, L.L.; Wang, D.Zhe.; Hobson, C.E.; Rashidi, P.; Li, X.; Momcilovic, P., 2018:
MySurgeryRisk: Development and Validation of a Machine-learning Risk Algorithm for Major Complications and Death After Surgery

Lee, J.; Lee, D.; Sim, M.; Kwon, D.; Kim, J.; Ko, Y.; Kim, J., 2018:
mySyntenyPortal: an application package to construct websites for synteny block analysis

Liang, X-Guang.; Tan, C.; Wang, C-Kun.; Tao, R-Rong.; Huang, Y-Jie.; Ma, K-Fen.; Fukunaga, K.; Huang, M-Zhu.; Han, F., 2018:
Myt1l induced direct reprogramming of pericytes into cholinergic neurons

Shi, Y.; Shao, Q.; Li, Z.; Gonzalez, G.A.; Lu, F.; Wang, D.; Pu, Y.; Huang, A.; Zhao, C.; He, C.; Cao, L., 2018:
Myt1L Promotes Differentiation of Oligodendrocyte Precursor Cells and is Necessary for Remyelination After Lysolecithin-Induced Demyelination

Drost, H-Georg.; Gabel, A.; Liu, J.; Quint, M.; Grosse, I., 2018:
myTAI: evolutionary transcriptomics with R

Dobkin, C.; Finkelstein, A.; Kluender, R.; Notowidigdo, M.J., 2018:
Myth and Measurement - The Case of Medical Bankruptcies

McLaren, E., 2018:
Myth-Busting Medicare for Long Term Care Skilled Services

Nunn, K., 2018:
Mythical truths for clinical practice

Berg, M., 2015:
Myth, Literature, and the Unconscious by Burnett, Leon, Bahun, Sanja, & Main, Roderick

Gershen, B.J., 2018:
Mythology in Medicine

Garcia-Ruiz, P.J.; Sanz-Cartagena, P.; Martinez-Castrillo, J.C.; Ares-Pensado, B.; Aviles-Olmos, I.; Blazquez-Estrada, M.; Fanjul-Arbos, S.; Garcia-Caldentey, J.; Gazulla, J.; Gutierrez-Garcia, J.; Huete-Anton, B.; Lucas-Rodenas, C.; Luquin, M.R.; Martinez-Torres, I.; Medialdea-Natera, P.; Mendoza-Rodriguez, A.; Mir-Rivera, P.; Posada, I.J.; Ruiz-Martinez, J.; Sanchez-Alonso, P.; Trejo-Gabriel Y Galan, J.M.; Vela, L.; Pena-Segura, J.L., 2018:
Myths and evidence on the use of botulinum toxin: neuropharmacology and dystonia

Bhatt, J.M.; Bush, A., 2018:
Myths and maxims in paediatric respiratory medicine

Sims, S.T.; Heather, A.K., 2018:
Myths and Methodologies: Reducing scientific design ambiguity in studies comparing sexes and/or menstrual cycle phases

Biesecker, L.G., 2018:
Myths and Misdiagnoses of Proteus Syndrome

Singhvi, A.; Yadav, D., 2018:
Myths and realities about alcohol and smoking in chronic pancreatitis

Cerantola, Y., 2017:
Myths and reality about immunonutrition in uro-oncology

Singh, S.; Mishra, V.Nath.; Rai, A.; Singh, R.; Chaurasia, R.Nath., 2018:
Myths and Superstition about Epilepsy: A Study from North India

Anagnostou, K.; Turner, P.J., 2018:
Myths, facts and controversies in the diagnosis and management of anaphylaxis

Maarouf, M.; Saberian, C.; Shi, V.Y., 2018:
Myths, Truths, and Clinical Relevance of Comedogenicity Product Labeling

Molinaro, A.M.; Pearson, B.J., 2018:
Myths vs. FACS: what do we know about planarian stem cell lineages?

Prieto, D.; Urrutxurtu, I.; Navarro, E.; Urrutia, M.B.; Ibarrola, I., 2018:
Mytilus galloprovincialis fast growing phenotypes under different restrictive feeding conditions: Fast feeders and energy savers

Piscopo, M.; Notariale, R.; Rabbito, D.; Ausió, J.; Olanrewaju, O.Sulaiman.; Guerriero, G., 2018:
Mytilus galloprovincialis (Lamarck, 1819) spermatozoa: hsp70 expression and protamine-like protein property studies

Zuykov, M.; Anderson, J.; Archambault, P.; Dufresne, F.; Pelletier, E., 2018:
Mytilus trossulus and hybrid (M. edulis-M. trossulus) - New hosts organisms for pathogenic microalgae Coccomyxa sp. from the Estuary and northwestern Gulf of St. Lawrence, Canada

Connolly, A.; Goepfert, A.; Blanchard, A.; Buys, E.; Donnellan, N.; Amundsen, C.L.; Galvin, S.L.; Kenton, K., 2018:
myTIPreport and Training for Independent Practice: A Tool for Real-Time Workplace Feedback for Milestones and Procedural Skills

Scherlag, B.J., 2018:
My tribute to Ralph Lazzara, MD

Goel, T.Chandra.; Goel, A.; Kumar, S., 2018:
My Tryst of Writing and Publishing a Comprehensive Medical Textbook in Vernacular Hindi and New Hindi Medical Terminology

Eck, K.M.; Delaney, C.L.; Leary, M.P.; Famodou, O.A.; Olfert, M.D.; Shelnutt, K.P.; Byrd-Bredbenner, C., 2018:
"My Tummy Tells Me" Cognitions, Barriers and Supports of Parents and School-Age Children for Appropriate Portion Sizes

Kappe, C.Oliver., 2018:
My Twenty Years in Microwave Chemistry: From Kitchen Ovens to Microwaves that aren't Microwaves

Oosawa, F., 2018:
My various thoughts on actin

Peters, P.; Carson, D.; Porter, R.; Vuin, A.; Carson, D.; Ensign, P., 2018:
My Village Is Dying? Integrating Methods from the Inside Out

Stewart, L.; Oates, J.; O'Halloran, P., 2018:
"My Voice Is My Identity": The Role of Voice for Trans Women's Participation in Sport

DeJonckheere, M.; Nichols, L.P.; Moniz, M.H.; Sonneville, K.R.; Vydiswaran, V.G.Vinod.; Zhao, X.; Guetterman, T.C.; Chang, T., 2017:
MyVoice National Text Message Survey of Youth Aged 14 to 24 Years: Study Protocol

Petretta, M.; Acampa, W.; Assante, R.; Zampella, E.; Nappi, C.; Petretta, A.; Cuocolo, A., 2018:
My warranty has expired: I need to be retested

Orth, K., 2018:
My winding trail while fulfilling my love for science and family

Dhingra, R.; Rai, P.; Sieker, J.; Roper, J., 2018:
Myxedema Ascites: An Unusual Presentation of Uncontrolled Hypothyroidism

Rizzo, L.F.L.; Mana, D.L.; Bruno, O.D.; Wartofsky, L., 2017:
Myxedema coma

Munir, A., 2018:
Myxedema Coma

Heksch, R.A.; Henry, R.K., 2018:
Myxedema Coma due to Hashimoto Thyroiditis: A Rare but Real Presentation of Failure to Thrive in Infancy

Gocho, N.; Aoki, E.; Okada, C.; Hirashima, T., 2018:
Myxedema Coma Following the Administration of Gonadotropin-releasing Hormone Agonist Complicated by Acute Pancreatitis

Sokolov, S.; Lebedeva, D., 2018:
Myxidium shedkoae Sokolov, 2013 (Myxozoa: Myxidiidae), a parasite of the gallbladder of Perccottus glenii Dybowski, 1877 (Actinoptrygii: Odontobutidae): Supplementary data on morphology and phylogenetic position based on 18s rDNA sequence analysis

Dehhaghi, M.; Mohammadipanah, F.; Guillemin, G.J., 2018:
Myxobacterial natural products: An under-valued source of products for drug discovery for neurological disorders

Vieira, D.Henrique.Mirandola.Dias.; Tagliavini, Vícius.Panciera.; Abdallah, V.Doro.; de Azevedo, R.Kozlowiski. , 2018:
Myxobolus imparfinis n. sp. (Myxozoa: Myxosporea), a new gill parasite of Imparfinis mirini Haseman (Siluriformes: Heptapteridae) in Brazil

Borzák, Réka.; Molnár, Kálmán.; Cech, Gábor.; Székely, C., 2018:
Myxobolus infection in the cornea of the roach (Rutilus rutilus) in Lake Balaton

Gupta, A.; Kaur, H., 2017:
Myxobolus okamurae sp. nov. (Myxosporea: Myxozoa) causing severe gill myxoboliosis in the cyprinid Labeo bata in a cold water wetland, Punjab (India)

De Vita, A.; Recine, F.; Mercatali, L.; Miserocchi, G.; Liverani, C.; Spadazzi, C.; Casadei, R.; Bongiovanni, A.; Pieri, F.; Riva, N.; Amadori, D.; Ibrahim, T., 2018:
Myxofibrosarcoma primary cultures: molecular and pharmacological profile

Cressey, B.D.; Jellinek, N.J., 2018:
Myxoid Cyst as a Probable Complication of Nail Surgery

AbdullGaffar, B.; Waslewski, K., 2018:
Myxoid Emboli

Solomon, D.A.; Korshunov, A.; Sill, M.; Jones, D.T.W.; Kool, M.; Pfister, S.M.; Fan, X.; Bannykh, S.; Hu, J.; Danielpour, M.; Li, R.; Johnston, J.; Cham, E.; Cooney, T.; Sun, P.P.; Oberheim Bush, N.Ann.; McDermott, M.; Van Ziffle, J.; Onodera, C.; Grenert, J.P.; Bastian, B.C.; Villanueva-Meyer, J.E.; Pekmezci, M.; Bollen, A.W.; Perry, A., 2018:
Myxoid glioneuronal tumor of the septum pellucidum and lateral ventricle is defined by a recurrent PDGFRA p.K385 mutation and DNT-like methylation profile

Zhang, L.; Li, Y.; Qu, Q.; Wen, K., 2016:
Myxoid leiomyosarcoma of the uterus: a case report and review of the literature

Cagaš, J.; Korbička, J.; Geršlová, A.; Vystrčilová, T., 2018:
Myxoid liposarcoma localised in the peritoneal cavity case report

Dürr, H.Roland.; Rauh, J.; Baur-Melnyk, A.; Knösel, T.; Lindner, L.; Roeder, F.; Jansson, V.; Klein, A., 2018:
Myxoid liposarcoma: local relapse and metastatic pattern in 43 patients

Farmer, R.P.; Schowinsky, J.T.; Lindeque, B.G.P., 2015:
Myxoid Liposarcoma of the Thigh with Metastasis to the Left Ventricle of the Heart: A Case Report

Muratori, F.; Bettini, L.; Frenos, F.; Mondanelli, N.; Greto, D.; Livi, L.; Franchi, A.; Roselli, G.; Scorianz, M.; Capanna, R.; Campanacci, D., 2018:
Myxoid Liposarcoma: Prognostic Factors and Metastatic Pattern in a Series of 148 Patients Treated at a Single Institution

Suzuki, K.; Yasuda, T.; Watanabe, K.; Hori, T.; Kanamori, M.; Kimura, T., 2017:
Myxoid liposarcoma with cartilaginous differentiation showing DDIT3 rearrangement

Kim, J.Hyun.; Kim, D.Chul.; Lee, R.; Shin, C.Ho.; Han, Y.Sik.; Chung, S.Hun.; Paik, S.Ya., 2018:
Myxoid Solitary Fibrous Tumor on the Scalp

Raut, M.S.; Dubey, S.; Maheshwari, A.; Sharma, M., 2018:
Myxoma in Left Atrium

Ataman, M.; Sarioglu, T.; Ayas, K., 1993:
Myxoma of the mandible

de Andrade Lima, E.Pinheiro.; de Moraes Ramos-Perez, Fávia.Maria.; de Hollanda Valente, Rômulo.Oliveira.; León, J.Esquiche.; Ferreti Bonan, P.Rogério.; da Cruz Perez, D.Elias., 2018:
Myxoma of the mandibular condyle: Report of a rare case and review of the literature

Olgun, Yüksel.; Közen, M.Arif.; Danyeli, Aça.Erşen.; Sarıoğlu, Sülen.; Güneri, E.Alpin., 2018:
Myxoma of the Middle Ear Mimicking Chronic Otitis Media

Andrews, T.; Kountakis, S.E.; Maillard, A.A., 2000:
Myxomas of the head and neck

Wolfe, A.M.; Dunlap, K.M.; Smith, A.C.; Bartee, M.Y.; Bartee, E., 2018:
Myxoma Virus M083 Is a Virulence Factor Which Mediates Systemic Dissemination

Shelekhova, K.V.; Egorenkov, V.V.; Kheinstein, V.A.; Konstantinova, A.M.; Iyevleva, A.; Imyanitov, E.N.; Matsko, M.V.; Matsko, D.E., 2017:
Myxopapillary Ependymoma of Lumbar Soft Tissue: A Case Report With Gene Expression Evaluation

Wang, H.; Xin, X.; Wang, M.; Han, L.; Li, J.; Hao, Y.; Zheng, C.; Shen, C., 2018:
Myxovirus resistance protein A inhibits hepatitis C virus replication through JAK-STAT pathway activation

Chakrabarty, P., 2018:
My year as a fed

Wheeler, L., 1988:
My Year in Hong Kong: Some Observations about Social Behavior

Miyake, K.; Mori, R.; Homma, Y.; Matsuyama, R.; Okayama, A.; Murakami, T.; Hirano, H.; Endo, I., 2017:
MZB1 in borderline resectable pancreatic cancer resected after neoadjuvant chemoradiotherapy

Fischer, B., 1889:
M. Zola on French Journalism and Its Health Results

Tan, W.W.; Hillman, D.W.; Salim, M.; Northfelt, D.W.; Anderson, D.M.; Stella, P.J.; Niedringhaus, R.; Bernath, A.M.; Gamini, S.S.; Palmieri, F.; Perez, E.A., 2018:
N0332 phase 2 trial of weekly irinotecan hydrochloride and docetaxel in refractory metastatic breast cancer: a North Central Cancer Treatment Group (NCCTG) Trial

Noel, S.; Sermet-Gaudelus, I.; Sheppard, D.N., 2018:
N1303K: Leaving no stone unturned in the search for transformational therapeutics

Greiser, J.; Kühnel, C.; Görls, H.; Weigand, W.; Freesmeyer, M., 2018:
N,1,4-Tri(4-alkoxy-2-hydroxybenzyl)-DAZA: efficient one-pot synthesis and labelling with 68 Ga for PET liver imaging in ovo

Martel, M-Jocelyne.; MacKinnon, C.Jane., 2018:
N° 155-Directive clinique sur l'accouchement vaginal chez les patientes ayant déjà subi une césarienne

Qiu, R.; Wang, H.; Fu, S., 2017:
N170 Reveals the Categorical Perception Effect of Emotional Valence

Liston, R.; Sawchuck, D.; Young, D., 2018:
N° 197a-Surveillance du bien-être fœtal : Directive consensus d'antepartum

Liston, R.; Sawchuck, D.; Young, D., 2018:
N° 197b-Surveillance du bien-être fœtal : Directive consensus d'intrapartum

Liston, R.; Sawchuck, D.; Young, D., 2018:
N° 197c-Maintien des normes dans le cadre de la surveillance fœtale intrapartum et prénatale : amélioration de la qualité et gestion du risque

Tripathi, A.C.; Upadhyay, S.; Paliwal, S.; Saraf, S.K., 2018:
N1-benzenesulfonyl-2-pyrazoline hybrids in neurological disorders: Syntheses, biological screening and computational studies

Nejabati, H.Reza.; Mihanfar, A.; Pezeshkian, M.; Fattahi, A.; Latifi, Z.; Safaie, N.; Valiloo, M.; Jodati, A.Reza.; Nouri, M., 2018:
N1-methylnicotinamide (MNAM) as a guardian of cardiovascular system

Le, T.; Giede, C., 2018:
N° 230-Prise en charge des masses pelviennes / ovariennes : Évaluation initiale et lignes directrices quant à l'orientation des patientes

Davies, G.A.L.; Maxwell, C.; McLeod, L., 2018:
N° 239 - Obésité et grossesse

Farine, D.; Shepherd, D., 2017:
N° 281-Classification des césariennes au Canada : Les critères modifiés de Robson

Singh, S.S.; Mehra, N.; Hopkins, L., 2018:
N° 286-Liste de contrôle de la sécurité chirurgicale en obstétrique-gynécologie

Sanchez-Lorente, D.; Guzman, R.; Boada, M.; Guirao, A.; Carriel, N.; Molins, L., 2018:
N2 disease in non-small-cell lung cancer: straight to surgery?

Bertoglio, P.; Ricciardi, S.; Alì, G.; Aprile, V.; Korasidis, S.; Palmiero, G.; Fontanini, G.; Mussi, A.; Lucchi, M., 2018:
N2 lung cancer is not all the same: an analysis of different prognostic groups

Benavides-Varela, S.; Basso Moro, S.; Brigadoi, S.; Meconi, F.; Doro, M.; Simion, F.; Sessa, P.; Cutini, S.; Dell'Acqua, R., 2018:
N2pc reflects two modes for coding the number of visual targets

Kessler, Y., 2018:
N-2 repetition leads to a cost within working memory and a benefit outside it

Bonapace, J.; Gagné, G-Paul.; Chaillet, N.; Gagnon, R.; Hébert, E.; Buckley, S., 2018:
N° 355-Fondements physiologiques de la douleur pendant le travail et l'accouchement: approche de soulagement basée sur les données probantes

Hashimoto, M., 2018:
n-3 fatty acids and the maintenance of neuronal functions

Healy-Stoffel, M.; Levant, B., 2018:
N-3 (Omega-3) Fatty Acids: Effects on Brain Dopamine Systems and Potential Role in the Etiology and Treatment of Neuropsychiatric Disorders

Bistrian, B.R., 2018:
n-3 Fatty Acid Supplementation and Dry Eye Disease

Asbell, P.A.; Maguire, M.G.; Pistilli, M.; Ying, G-shuang.; Szczotka-Flynn, L.B.; Hardten, D.R.; Lin, M.C.; Shtein, R.M.; Hom, M.M.; Quintana, M.; Zermeno, A.; Pendleton, R.; McCluskey, D.; Amador, D.; Corona, I.; Wechter, V.; Childs, C.; Do, U.; Lerma, M.; Li, W.; Young, Z.; Yuen, T.; Dubiner, H.; Ambrosia, H.; Bowser, M.; Chen, P.; Dubiner, H.; Fuller, C.; New, K.; Nguyen, T.Vy.; Seville, E.; Strait, D.; Wang, C.; Williams, S.; Weber, R.; Sutphin, J.; Bishara, M.; Bryan, A.; Ertel, A.; Green,, 2018:
n-3 Fatty Acid Supplementation for the Treatment of Dry Eye Disease

Shulkin, M.; Pimpin, L.; Bellinger, D.; Kranz, S.; Fawzi, W.; Duggan, C.; Mozaffarian, D., 2018:
n-3 Fatty Acid Supplementation in Mothers, Preterm Infants, and Term Infants and Childhood Psychomotor and Visual Development: A Systematic Review and Meta-Analysis

Kones, R.; Howell, S.; Rumana, U., 2017:
n-3 Polyunsaturated Fatty Acids and Cardiovascular Disease: Principles, Practices, Pitfalls, and Promises - A Contemporary Review

Wang, H.; Chen, J.; Zhao, L., 2018:
N-3 polyunsaturated fatty acids for prevention of postoperative atrial fibrillation: updated meta-analysis and systematic review

Ide, K.; Koshizaka, M.; Tokuyama, H.; Tokuyama, T.; Ishikawa, T.; Maezawa, Y.; Takemoto, M.; Yokote, K., 2018:
N-3 polyunsaturated fatty acids improve lipoprotein particle size and concentration in Japanese patients with type 2 diabetes and hypertriglyceridemia: a pilot study

Picou, Fédéric.; Debeissat, C.; Bourgeais, Jérôme.; Gallay, N.; Ferrié, E.; Foucault, Aélie.; Ravalet, Némie.; Maciejewski, A.; Vallet, N.; Ducrocq, E.; Haddaoui, L.; Domenech, J.; Hérault, O.; Gyan, E., 2018:
n-3 Polyunsaturated fatty acids induce acute myeloid leukemia cell death associated with mitochondrial glycolytic switch and Nrf2 pathway activation

Guo, Y-Ru.; Lee, H-Chuan.; Lo, Y-Chun.; Yu, S-Chuan.; Huang, S-Yi., 2018:
n-3 polyunsaturated fatty acids prevent d-galactose-induced cognitive deficits in prediabetic rats

Kim, J.Young.; Lim, K.; Kim, K.Hee.; Kim, J.Hyun.; Choi, J.Sun.; Shim, S-Cheol., 2018:
N-3 polyunsaturated fatty acids restore Th17 and Treg balance in collagen antibody-induced arthritis

Cieślak, A.; Trottier, J.; Verreault, Mélanie.; Milkiewicz, P.; Vohl, M-Claude.; Barbier, O., 2018:
N-3 Polyunsaturated Fatty Acids Stimulate Bile Acid Detoxification in Human Cell Models

Ciappolino, V.; Mazzocchi, A.; Enrico, P.; Syrén, M-Louise.; Delvecchio, G.; Agostoni, C.; Brambilla, P., 2018:
N-3 Polyunsatured Fatty Acids in Menopausal Transition: A Systematic Review of Depressive and Cognitive Disorders with Accompanying Vasomotor Symptoms

de Mello, A.Haas.; Uberti, M.Fornari.; de Farias, B.Xavier.; de Souza, N.Alberti.Ribas.; Rezin, G.Tezza., 2018:
n-3 PUFA and obesity: from peripheral tissues to the central nervous system

Morgese, M.G.; Schiavone, S.; Mhillaj, E.; Bove, M.; Tucci, P.; Trabace, L., 2017:
N-3 PUFA diet enrichment prevents amyloid beta-induced depressive-like phenotype

Huang, Y.; Jiang, M.; Guo, Q.; Yang, F-Pei.G., 2018:
N400 amplitude does not recover from disappearance after repetitions despite reinitiated semantic integration difficulty

Jakubovska, J.; Tauraite, D.; Birštonas, L.; Meškys, R., 2018:
N4-acyl-2'-deoxycytidine-5'-triphosphates for the enzymatic synthesis of modified DNA

Kumar, S.; Karmakar, B.C.; Nagarajan, D.; Mukhopadhyay, A.K.; Morgan, R.D.; Rao, D.N., 2018:
N4-cytosine DNA methylation regulates transcription and pathogenesis in Helicobacter pylori

Zhang, W.; Liu, Y.; Hureau, C.; Robert, A.; Meunier, B., 2018:
N 4 -Tetradentate Chelators Efficiently Regulate Copper Homeostasis and Prevent ROS Production Induced by Copper-Amyloid-β 1-16

Bowie, L.E.; Maiuri, T.; Alpaugh, M.; Gabriel, M.; Arbez, N.; Galleguillos, D.; Hung, C.L.K.; Patel, S.; Xia, J.; Hertz, N.T.; Ross, C.A.; Litchfield, D.W.; Sipione, S.; Truant, R., 2018:
N6-Furfuryladenine is protective in Huntington's disease models by signaling huntingtin phosphorylation

Hesser, C.R.; Karijolich, J.; Dominissini, D.; He, C.; Glaunsinger, B.A., 2018:
N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi's sarcoma-associated herpesvirus infection

Ianniello, Z.; Fatica, A., 2018:
N6-Methyladenosine Role in Acute Myeloid Leukaemia

Yoshioka, K.; Kurita, R., 2018:
N6-Methylation Assessment in Escherichia coli 23S rRNA Utilizing a Bulge Loop in an RNA-DNA Hybrid

Grasso, M.; Estrada, M.A.; Berrios, K.N.; Winkler, J.D.; Marmorstein, R., 2018:
N-(7-Cyano-6-(4-fluoro-3-(2-(3-(trifluoromethyl)phenyl)acetamido)phenoxy)benzo[d]thiazol-2-yl)cyclopropanecarboxamide (TAK632) Promotes Inhibition of BRAF through the Induction of Inhibited Dimers

Romański, Mł.; Girreser, U.; Teżyk, A.; Główka, F.K., 2018:
N-7-Guanine Adduct of the Active Monoepoxide of Prodrug Treosulfan: First Synthesis, Characterization, and Decomposition Profile Under Physiological Conditions

Soundharrajan, V.; Sambandam, B.; Kim, S.; Alfaruqi, M.H.; Putro, D.Yunianto.; Jo, J.; Kim, S.; Mathew, V.; Sun, Y-Kook.; Kim, J., 2018:
Na 2 V 6 O 16 ·3H 2 O Barnesite Nanorod: An Open Door to Display a Stable and High Energy for Aqueous Rechargeable Zn-Ion Batteries as Cathodes

McTiernan, N.; Støve, S.Isungset.; Aukrust, I.; Mårli, M.Torrisen.; Myklebust, L.M.; Houge, G.; Arnesen, T., 2018:
NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant - a case report

Drazic, A.; Aksnes, H.; Marie, Mël.; Boczkowska, M.; Varland, S.; Timmerman, E.; Foyn, Håvard.; Glomnes, N.; Rebowski, G.; Impens, F.; Gevaert, K.; Dominguez, R.; Arnesen, T., 2018:
NAA80 is actin's N-terminal acetyltransferase and regulates cytoskeleton assembly and cell motility

Gunaratne, G.S.; Yang, Y.; Li, F.; Walseth, T.F.; Marchant, J.S., 2018:
NAADP-dependent Ca 2+ signaling regulates Middle East respiratory syndrome-coronavirus pseudovirus translocation through the endolysosomal system

Crobach, M.J.T.; Duszenko, N.; Terveer, E.M.; Verduin, C.M.; Kuijper, E.J., 2017:
Nucleic Acid Amplification Test Quantitation as Predictor of Toxin Presence in Clostridium difficile Infection

Vajenine, G.V.; Simon, A., 2001:
NaBa 2 O: A Fresh Perspective in Suboxide Chemistry

Chai, Z.; Samulski, R.Jude.; Li, C., 2018:
Nab Escaping AAV Mutants Isolated from Mouse Muscles

Trigo, J.M.; Soliman, A.; Quilty, L.C.; Fischer, B.; Rehm, Jürgen.; Selby, P.; Barnes, A.J.; Huestis, M.A.; George, T.P.; Streiner, D.L.; Staios, G.; Le Foll, B., 2018:
Nabiximols combined with motivational enhancement/cognitive behavioral therapy for the treatment of cannabis dependence: A pilot randomized clinical trial

Katsaounis, P.; Kotsakis, A.; Kentepozidis, N.; Polyzos, A.; Bakogeorgos, M.; Koinis, F.; Vamvakas, L.; Vardakis, N.; Kalbakis, K.; Boukovinas, I.; Varthalitis, I.I.; Prinarakis, E.; Georgoulias, V.; Souglakos, J., 2018:
Nab-paclitaxel as second-line treatment in advanced gastric cancer: a multicenter phase II study of the Hellenic Oncology Research Group

Gridelli, C.; Chen, T.; Ko, A.; O'Brien, M.E.; Ong, T.Jin.; Socinski, M.A.; Postmus, P.E., 2018:
nab-Paclitaxel/carboplatin in elderly patients with advanced squamous non-small cell lung cancer: a retrospective analysis of a Phase III trial

Quinton, A.E.; Gwynne, S.H.; Yim, K.L., 2018:
Nab-paclitaxel in combination with gemcitabine for the treatment of metastatic pancreas cancer: the South Wales experience

Feng, R.; Morine, Y.; Ikemoto, T.; Imura, S.; Iwahashi, S.; Saito, Y.; Shimada, M., 2018:
Nab-paclitaxel interrupts cancer-stromal interaction through C-X-C motif chemokine 10-mediated interleukin-6 downregulation in vitro

Chang, P.Mu-Hsin.; Cheng, C-Tung.; Wu, R-Chin.; Chung, Y-Hsiu.; Chiang, K-Chun.; Yeh, T-Sen.; Liu, C-Yu.; Chen, M-Han.; Chen, M-Huang.; Yeh, C-Nan., 2018:
Nab-paclitaxel is effective against intrahepatic cholangiocarcinoma via disruption of desmoplastic stroma

Nakao, A.; Uchino, J.; Igata, F.; On, R.; Ikeda, T.; Yatsugi, H.; Hirano, R.; Sasaki, T.; Tanimura, K.; Imabayashi, T.; Tamiya, N.; Kaneko, Y.; Yamada, T.; Nagata, N.; Watanabe, K.; Kishimoto, J.; Takayama, K.; Fujita, M., 2018:
Nab-paclitaxel maintenance therapy following carboplatin + nab-paclitaxel combination therapy in chemotherapy naïve patients with advanced non-small cell lung cancer: multicenter, open-label, single-arm phase II trial

Niwa, H.; Otani, S.; Nakada, N.; Sasaki, J.; Saka, H.; Masuda, N., 2018:
Nab-paclitaxel plus carboplatin as an effective and safe chemotherapy regimen for pulmonary carcinosarcoma with interstitial lung disease: A case report

Yardley, D.A.; Coleman, R.; Conte, P.; Cortes, J.; Brufsky, A.; Shtivelband, M.; Young, R.; Bengala, C.; Ali, H.; Eakel, J.; Schneeweiss, A.; de la Cruz-Merino, L.; Wilks, S.; O'Shaughnessy, J.; Glück, S.; Li, H.; Miller, J.; Barton, D.; Harbeck, N., 2018:
nab-Paclitaxel plus carboplatin or gemcitabine versus gemcitabine plus carboplatin as first-line treatment of patients with triple-negative metastatic breast cancer: results from the tnAcity trial

Young, R.; Mainwaring, P.; Clingan, P.; Parnis, F.Xavier.; Asghari, G.; Beale, P.; Aly, A.; Botteman, M.; Romano, A.; Ferrara, S.; Margunato-Debay, S.; Harris, M., 2018:
nab-Paclitaxel plus gemcitabine in metastatic pancreatic adenocarcinoma: Australian subset analyses of the phase III MPACT trial

Kang, J.; Hwang, I.; Yoo, C.; Kim, K-Pyo.; Jeong, J.Ho.; Chang, H-Moon.; Lee, S.Soo.; Park, D.Hyun.; Song, T.Jun.; Seo, D.Wan.; Lee, S.Koo.; Kim, M-Hwan.; Hong, S-Mo.; Shin, S.Hyun.; Hwang, D.Wook.; Song, K.Byung.; Lee, J.Hoon.; Kim, S.Cheol.; Ryoo, B-Yeol., 2018:
Nab-paclitaxel plus gemcitabine versus FOLFIRINOX as the first-line chemotherapy for patients with metastatic pancreatic cancer: retrospective analysis

Zhang, W.; Du, C.; Sun, Y.; Yang, L.; Cui, C.; Jiang, Z.; Wang, C.; Wang, J.; Zhou, A., 2018:
Nab-paclitaxel plus S-1 as first-line followed by S-1 maintenance for advanced pancreatic adenocarcinoma: a single-arm phase II trial

Shi, Y.; Zhang, S.; Han, Q.; Li, J.; Yan, H.; Lv, Y.; Shi, H.; Liu, R.; Dai, G., 2017:
Nab-paclitaxel plus S-1 in advanced pancreatic adenocarcinoma (NPSPAC): a single arm, single center, phase II trial

Chen, F.; Yin, Y.; Yan, Z.; Cao, K.; Zhong, K., 2018:
NAC1 promotes the migration of prostate cancer cells and participates in osteoclastogenesis by negatively regulating IFNβ

Siddiqui, R.Ahmed.; Simjee, S.Usman.; Kabir, N.; Ateeq, M.; Shah, M.Raza.; Hussain, S.Saad., 2018:
N-(2-hydroxyphenyl)acetamide and its gold nanoparticle conjugation prevent glycerol-induced acute kidney injury by attenuating inflammation and oxidative injury in mice

Koch, K.S.; Moran, T.; Shier, W.Thomas.; Leffert, H.L., 2018:
N-Acetyl-2-Aminofluorene (AAF) Processing in Adult Rat Hepatocytes in Primary Culture Occurs by High-Affinity Low-Velocity and Low-Affinity High-Velocity AAF Metabolite-Forming Systems

Dong, H.; Wu, G.; Xu, H.; Zhang, C.; Wang, J.; Gao, M.; Pang, Y.; Zhang, H.; Zhang, B.; Tian, Y.; Li, Q., 2018:
N-acetylaminogalactosyl-decorated biodegradable PLGA-TPGS copolymer nanoparticles containing emodin for the active targeting therapy of liver cancer

Tang, J.; O'Neill, J.; Alger, J.R.; Shen, Z.; Johnson, M.C.; London, E.D., 2018:
N-Acetyl and Glutamatergic Neurometabolites in Perisylvian Brain Regions of Methamphetamine Users

Guo, M-Yin.; Wang, H.; Chen, Y-Hua.; Xia, M-Zhen.; Zhang, C.; Xu, D-Xiang., 2018:
N-acetylcysteine alleviates cadmium-induced placental endoplasmic reticulum stress and fetal growth restriction in mice

Zheng, J.; Yuan, X.; Zhang, C.; Jia, P.; Jiao, S.; Zhao, X.; Yin, H.; Du, Y.; Liu, H., 2018:
N-Acetylcysteine alleviates gut dysbiosis and glucose metabolic disorder in high-fat diet-fed mice

Rodriguez, B.Morales.; Khouzami, L.; Decostre, Vérie.; Varnous, S.; Pekovic-Vaughan, V.; Hutchison, C.J.; Pecker, Fçoise.; Bonne, Gèle.; Muchir, A., 2018:
N-acetyl cysteine alleviates oxidative stress and protects mice from dilated cardiomyopathy caused by mutations in nuclear A-type lamins gene

Xia, Q.; Liu, C.; Zheng, X., 2017:
N-acetylcysteine ameliorates contrast‑induced kidney injury in rats with unilateral hydronephrosis

Gao, X.; Lampraki, E-Maria.; Al-Khalidi, S.; Qureshi, M.Asif.; Desai, R.; Wilson, J.Beatrice., 2018:
N-acetylcysteine (NAC) ameliorates Epstein-Barr virus latent membrane protein 1 induced chronic inflammation

Moore, K., 2018:
N-Acetyl Cysteine and Curcumin in Pediatric Acute-Onset Neuropsychiatric Syndrome

di Michele, F.; Siracusano, A.; Talamo, A.; Niolu, C., 2018:
N-Acetyl Cysteine and Vitamin D Supplementation in Treatment Resistant Obsessive-compulsive Disorder Patients: A General Review

Polyak, E.; Ostrovsky, J.; Peng, M.; Dingley, S.D.; Tsukikawa, M.; Kwon, Y.Joon.; McCormack, S.E.; Bennett, M.; Xiao, R.; Seiler, C.; Zhang, Z.; Falk, M.J., 2018:
N-acetylcysteine and vitamin E rescue animal longevity and cellular oxidative stress in pre-clinical models of mitochondrial complex I disease

Mostajeran, F.; Tehrani, H.Ghasemi.; Rahbary, B., 2018:
N-Acetylcysteine as an Adjuvant to Letrozole for Induction of Ovulation in Infertile Patients with Polycystic Ovary Syndrome

Aldini, G.; Altomare, A.; Baron, G.; Vistoli, G.; Carini, M.; Borsani, L.; Sergio, F., 2018:
N-Acetylcysteine as an antioxidant and disulphide breaking agent: the reasons why

Allen, E.M.; Hughes, E.F.; Anderson, C.J.; Woehrle, N.S., 2018:
N-acetylcysteine blocks serotonin 1B agonist-induced OCD-related behavior in mice

Modarresi, A.; Nafar, M.; Sahraei, Z.; Salamzadeh, J.; Chaibakhsh, S.; Ziaie, S.; Parvin, M.; Panahi, Y.; Einollahi, B., 2018:
N-acetylcysteine decreases urinary level of neutrophil gelatinase-associated lipocalin in deceased-donor renal transplant recipients: a randomized clinical trial

Verdon, I.; Spahr, L.; Serratrice, J., 2018:
N-acetylcysteine : effective treatment in severe alcoholic hepatitis ?

Giustarini, D.; Galvagni, F.; Dalle Donne, I.; Milzani, A.; Severi, F.Maria.; Santucci, A.; Rossi, R., 2018:
N-acetylcysteine ethyl ester as GSH enhancer in human primary endothelial cells: A comparative study with other drugs

Oldham, J.M.; Witt, L.J.; Adegunsoye, A.; Chung, J.H.; Lee, C.; Hsu, S.; Chen, L.W.; Husain, A.; Montner, S.; Vij, R.; Strek, M.E.; Noth, I., 2018:
N-acetylcysteine exposure is associated with improved survival in anti-nuclear antibody seropositive patients with usual interstitial pneumonia

Zheng, W.; Zhang, Q-E.; Cai, D-B.; Yang, X-H.; Qiu, Y.; Ungvari, G.S.; Ng, C.H.; Berk, M.; Ning, Y-P.; Xiang, Y-T., 2018:
N-acetylcysteine for major mental disorders: a systematic review and meta-analysis of randomized controlled trials

Ezeriņa, D.; Takano, Y.; Hanaoka, K.; Urano, Y.; Dick, T.P., 2018:
N-Acetyl Cysteine Functions as a Fast-Acting Antioxidant by Triggering Intracellular H 2 S and Sulfane Sulfur Production

Conus, P.; Seidman, L.J.; Fournier, M.; Xin, L.; Cleusix, M.; Baumann, P.S.; Ferrari, C.; Cousins, A.; Alameda, L.; Gholam-Rezaee, M.; Golay, P.; Jenni, R.; Woo, T-U.Wilson.; Keshavan, M.S.; Eap, C.B.; Wojcik, J.; Cuenod, M.; Buclin, T.; Gruetter, R.; Do, K.Q., 2018:
N-acetylcysteine in a Double-Blind Randomized Placebo-Controlled Trial: Toward Biomarker-Guided Treatment in Early Psychosis

Moitra, S., 2018:
N-acetylcysteine (NAC) in COPD: benefits often lost in trials

Kókai, Dávid.; Mosolygó, Tímea.; Virók, Dő.P.; Endrész, Véria.; Burián, K., 2018:
N-acetyl-cysteine increases the replication of Chlamydia pneumoniae and prolongs the clearance of the pathogen from mice

Reyes, D.R.A.; Gomes, M.J.; Rosa, C.M.; Pagan, L.U.; Damatto, F.C.; Damatto, R.L.; Depra, I.; Campos, D.H.S.; Fernandez, A.A.H.; Martinez, P.F.; Okoshi, K.; Okoshi, M.P., 2017:
N-Acetylcysteine Influence on Oxidative Stress and Cardiac Remodeling in Rats During Transition from Compensated Left Ventricular Hypertrophy to Heart Failure

Guo, L.; Zhang, H.; Li, W.; Zhan, D.; Wang, M., 2018:
N-acetyl cysteine inhibits lipopolysaccharide-mediated induction of interleukin-6 synthesis in MC3T3-E1 cells through the NF-kB signaling pathway

Costa-Silva, D.Guilherme.da.; Leandro, L.Paganotto.; Vieira, Pícia.de.Brum.; de Carvalho, N.Rodrigues.; Lopes, A.Rubim.; Schimith, L.Emanueli.; Nunes, M.Eugênio.Medina.; de Mello, R.Siqueira.; Martins, I.Kemmerich.; de Paula, A.Alves.; Cañedo, Aés.Delgado.; Moreira, Jé.Cláudio.Fonseca.; Posser, T.; Franco, J.Luis., 2018:
N-acetylcysteine inhibits Mancozeb-induced impairments to the normal development of zebrafish embryos

Bhardwaj, J.Kumar.; Saraf, P.; Kumari, P.; Mittal, M.; Kumar, V., 2018:
N-Acetyl-cysteine mediated inhibition of spermatogonial cells apoptosis against malathion exposure in testicular tissue

Zhang, M.; Xia, H.; Yu, M.; Zhu, L.; Ju, L.; Chen, J.; Zhao, J.; Xiao, Y.; Chen, K., 2018:
N-acetylcysteine prevents cytotoxic effects induced by man-made mineral fibers in a human bronchial epithelial cell line

Robinson, B.; Dumas, M.; Gu, Q.; Kanungo, J., 2018:
N-acetylcysteine prevents ketamine-induced adverse effects on development, heart rate and monoaminergic neurons in zebrafish

Kim, T.Wan.; Moon, J.Woong.; Yu, H.Gon., 2018:
N-acetylcysteine protects against chorioretinal damage induced by photodynamic therapy for experimental choroidal neovascularization in a rat model

Nogueira, G.B.; Punaro, G.R.; Oliveira, C.S.; Maciel, F.R.; Fernandes, T.O.; Lima, D.Y.; Rodrigues, A.M.; Mouro, M.G.; Araujo, S.R.R.; Higa, E.M.S., 2018:
N-acetylcysteine protects against diabetic nephropathy through control of oxidative and nitrosative stress by recovery of nitric oxide in rats

Zhao, S.; Liu, Y.; Wang, F.; Xu, D.; Xie, P., 2018:
N-acetylcysteine protects against microcystin-LR-induced endoplasmic reticulum stress and germ cell apoptosis in zebrafish testes

Scheffel, M.J.; Scurti, G.; Wyatt, M.M.; Garrett-Mayer, E.; Paulos, C.M.; Nishimura, M.I.; Voelkel-Johnson, C., 2018:
N-acetyl cysteine protects anti-melanoma cytotoxic T cells from exhaustion induced by rapid expansion via the downmodulation of Foxo1 in an Akt-dependent manner

Calzetta, L.; Rogliani, P.; Facciolo, F.; Rinaldi, B.; Cazzola, M.; Matera, M.Gabriella., 2018:
N-Acetylcysteine protects human bronchi by modulating the release of neurokinin A in an ex vivo model of COPD exacerbation

Moss, H.G.; Brown, T.R.; Wiest, D.B.; Jenkins, D.D., 2018:
N-Acetylcysteine rapidly replenishes central nervous system glutathione measured via magnetic resonance spectroscopy in human neonates with hypoxic-ischemic encephalopathy

Mocelin, R.; Marcon, M.; D'ambros, S.; Mattos, J.; Sachett, A.; Siebel, A.M.; Herrmann, A.P.; Piato, A., 2018:
N-Acetylcysteine Reverses Anxiety and Oxidative Damage Induced by Unpredictable Chronic Stress in Zebrafish

Valdivieso, Ángel.G.; Dugour, A.V.; Sotomayor, Vónica.; Clauzure, Mángeles.; Figueroa, J.M.; Santa-Coloma, Tás.A., 2018:
N-acetyl cysteine reverts the proinflammatory state induced by cigarette smoke extract in lung Calu-3 cells

Aydın, A.Fatih.; Kondakçı, G.; Hatipoğlu, Sül.; Doğru-Abbasoğlu, S.; Uysal, Müjdat., 2018:
N-Acetylcysteine supplementation decreased brain lipid and protein oxidations produced by experimental homocysteine thiolactone exposure: Relevance to neurodegeneration

Paschalis, V.; Theodorou, A.A.; Margaritelis, N.V.; Kyparos, A.; Nikolaidis, M.G., 2017:
N-acetylcysteine supplementation increases exercise performance and reduces oxidative stress only in individuals with low levels of glutathione

Ceylan, B.; Ozansoy, M.; Kılıç, Ülkan.; Yozgat, Y.; Ercan, Çilem.; Yıldız, P.; Aslan, T., 2018:
N-acetylcysteine suppresses colistimethate sodium-induced nephrotoxicity via activation of SOD2, eNOS, and MMP3 protein expressions

Sancho-Martínez, S.M.; Prieto-García, L.; Prieto, M.; Fuentes-Calvo, I.; López-Novoa, Jé.M.; Morales, A.I.; Martínez-Salgado, C.; López-Hernández, F.J., 2018:
N-acetylcysteine transforms necrosis into apoptosis and affords tailored protection from cisplatin cytotoxicity

Marie, A.; Meunier, J.; Brun, E.; Malmstrom, S.; Baudoux, V.; Flaszka, E.; Naert, Gëlle.; Roman, Fçois.; Cosnier-Pucheu, S.; Gonzalez-Gonzalez, S., 2018:
N-acetylcysteine Treatment Reduces Age-related Hearing Loss and Memory Impairment in the Senescence-Accelerated Prone 8 (SAMP8) Mouse Model

Duryee, M.J.; Dusad, A.; Hunter, C.D.; Kharbanda, K.K.; Bruenjes, J.D.; Easterling, K.C.; Siebler, J.C.; Thiele, G.M.; Chakkalakal, D.A., 2018:
N-Acetyl Cysteine Treatment Restores Early Phase Fracture Healing in Ethanol-Fed Rats

Das, S.; Dey, P.; Roy, D.; Maiti, M.Kumar.; Sen, R., 2018:
N-Acetyl-D-glucosamine Production by a Chitinase of Marine Fungal Origin: a Case Study of Potential Industrial Significance for Valorization of Waste Chitins

Liang, Y.; Xu, W.; Liu, S.; Chi, J.; Zhang, J.; Sui, A.; Wang, L.; Liang, Z.; Li, D.; Chen, Y.; Niu, H., 2018:
N-Acetyl-Glucosamine Sensitizes Non-Small Cell Lung Cancer Cells to TRAIL-Induced Apoptosis by Activating Death Receptor 5

Maillard, Fçois.; Didion, M.; Fauchery, L.; Bach, C.; Buée, M., 2018:
N-Acetylglucosaminidase activity, a functional trait of chitin degradation, is regulated differentially within two orders of ectomycorrhizal fungi: Boletales and Agaricales

Krolicka, M.; Hinz, S.W.A.; Koetsier, M.J.; Eggink, G.; van den Broek, L.A.M.; Boeriu, C.G., 2018:
β-N-Acetylglucosaminidase MthNAG from Myceliophthora thermophila C1, a thermostable enzyme for production of N-acetylglucosamine from chitin

Yang, L.; Duan, Z.; Liu, X.; Yuan, Y., 2017:
N-acetyl-l-cysteine ameliorates the PM 2.5 -induced oxidative stress by regulating SIRT-1 in rats

Garg, G.; Singh, S.; Singh, A.Kumar.; Rizvi, S.Ibrahim., 2018:
N-acetyl-l-cysteine attenuates oxidative damage and neurodegeneration in rat brain during aging

Kong, Y.; Shi, M-Min.; Zhang, Y-Yuan.; Cao, X-Na.; Wang, Y.; Zhang, X-Hui.; Xu, L-Ping.; Huang, X-Jun., 2018:
N-acetyl-L-cysteine improves bone marrow endothelial progenitor cells in prolonged isolated thrombocytopenia patients post allogeneic hematopoietic stem cell transplantation

Kong, Y.; Song, Y.; Tang, F-Fei.; Zhao, H-Yan.; Chen, Y-Hong.; Han, W.; Yan, C-Hua.; Wang, Y.; Zhang, X-Hui.; Xu, L-Ping.; Huang, X-Jun., 2018:
N-acetyl-L-cysteine improves mesenchymal stem cell function in prolonged isolated thrombocytopenia post-allotransplant

Martacic, J.; Filipovic, M.Kovacevic.; Borozan, S.; Cvetkovic, Z.; Popovic, T.; Arsic, A.; Takic, M.; Vucic, V.; Glibetic, M., 2018:
N-acetyl-L-cysteine protects dental tissue stem cells against oxidative stress in vitro

Villagarcía, Hán.Gonzalo.; Castro, Mía.Cecilia.; Arbelaez, L.González.; Schinella, G.; Massa, Mía.Laura.; Spinedi, E.; Francini, F., 2018:
N-Acetyl-l-Cysteine treatment efficiently prevented pre-diabetes and inflamed-dysmetabolic liver development in hypothalamic obese rats

Fernandes, J.; Mudgal, J.; Rao, C.Mallikarjuna.; Arora, D.; Basu Mallik, S.; Pai, K.S.R.; Nampoothiri, M., 2017:
N-acetyl-L-tryptophan, a substance-P receptor antagonist attenuates aluminum-induced spatial memory deficit in rats

Zhang, L.; Xu, D.; Li, Q.; Yang, Y.; Xu, H.; Wei, Z.; Wang, R.; Zhang, W.; Liu, Y.; Geng, Y.; Li, S.; Gao, X.; Yang, F., 2018:
N-acetyl-seryl-aspartyl-lysyl-proline (Ac-SDKP) attenuates silicotic fibrosis by suppressing apoptosis of alveolar type II epithelial cells via mediation of endoplasmic reticulum stress

Chen, H.; Li, S.; Li, L.; Wu, W.; Ke, X.; Zou, W.; Zhao, J., 2018:
Nα-Acetyltransferases 10 and 15 are Required for the Correct Initiation of Endosperm Cellularization in Arabidopsis

Chien, M-Hsien.; Lee, W-Jiunn.; Yang, Y-Chieh.; Tan, P.; Pan, K-Fan.; Liu, Y-Cheng.; Tsai, H-Chi.; Hsu, C-Hua.; Wen, Y-Ching.; Hsiao, M.; Hua, K-Tai., 2018:
N-α-acetyltransferase 10 protein promotes metastasis by stabilizing matrix metalloproteinase-2 protein in human osteosarcomas

Aklillu, E.; Carrillo, J.Antonio.; Makonnen, E.; Bertilsson, L.; Djordjevic, N., 2018:
N-Acetyltransferase-2 (NAT2) phenotype is influenced by genotype-environment interaction in Ethiopians

Malhotra, P.; Gupta, A.K.; Singh, D.; Mishra, S.; Singh, S.K.; Kumar, R., 2018:
N-Acetyl-tryptophan glucoside (NATG) protects J774A.1 murine macrophages against gamma radiation-induced cell death by modulating oxidative stress

Laikowski, M.M.; Reisdorfer, F.; Moura, S., 2018:
NAChR α4β2 subtype and their relation with nicotine addiction, cognition, depression and hyperactivity disorder

Zhou, J.; Liu, F.; Yu, L.; Xu, D.; Li, B.; Zhang, G.; Huang, W.; Li, L.; Zhang, Y.; Zhang, W.; Wang, H., 2018:
nAChRs-ERK1/2-Egr-1 signaling participates in the developmental toxicity of nicotine by epigenetically down-regulating placental 11β-HSD2

Haneke, E.; Marsch, W., 2018:

Zimmermann, R.; Sollberg, S.; Emmert, S., 2017:
Nachruf für Prof. Dr. Heinz Flegel (geb. 26.10.1923 - gest. 28.10.2017)

Yang, J.; Feng, X.; Lu, G.; Li, Y.; Mao, C.; Wen, Z.; Yuan, W., 2018:
NaCl as a solid solvent to assist the mechanochemical synthesis and post-synthesis of hierarchical porous MOFs with high I 2 vapour uptake

Nja, R.Ben.; Merceron, B.; Faucher, M.; Fleurat-Lessard, P.; Béré, E., 2017:
NaCl - Changes stem morphology, anatomy and phloem structure in Lucerne (Medicago sativa cv. Gabès): Comparison of upper and lower internodes

Yamauchi, T.; Doi, S.; Nakashima, A.; Doi, T.; Sohara, E.; Uchida, S.; Masaki, T., 2018:
Na + -Cl - cotransporter-mediated chloride uptake contributes to hypertension and renal damage in aldosterone-infused rats

Liu, M.; Zhang, H.; Song, X.; Wei, C.; Xiong, Z.; Yu, F.; Li, C.; Ai, F.; Guo, G.; Wang, X., 2018:
NaCl: for the safer in vivo use of antibacterial silver based nanoparticles

Zhou, M-Xi.; Dailly, Hélène.; Renard, M-Eve.; Han, R-Ming.; Lutts, S., 2018:
NaCl impact on Kosteletzkya pentacarpos seedlings simultaneously exposed to cadmium and zinc toxicities

Zimmermann, N.E.R.; Vorselaars, B.; Espinosa, J.R.; Quigley, D.; Smith, W.R.; Sanz, E.; Vega, C.; Peters, B., 2018:
NaCl nucleation from brine in seeded simulations: Sources of uncertainty in rate estimates

Lee, C.J.D.; McMullan, P.E.; O'Kane, C.J.; Stevenson, A.; Santos, Iês.C.; Roy, C.; Ghosh, W.; Mancinelli, R.L.; Mormile, M.R.; McMullan, G.; Banciu, H.L.; Fares, M.A.; Benison, K.C.; Oren, A.; Dyall-Smith, M.L.; Hallsworth, J.E., 2018:
NaCl-saturated brines are thermodynamically moderate, rather than extreme, microbial habitats

Kumar, R.; Tamboli, V.; Sharma, R.; Sreelakshmi, Y., 2018:
NAC-NOR mutations in tomato Penjar accessions attenuate multiple metabolic processes and prolong the fruit shelf life

Jayasankar, V.; Vasudevan, S.Raghavan.; Poulose, S.C.; Divipala, I., 2018:
Nacre formation by epithelial cell cultures from mantle of the black-lip pearl oyster, Pinctada margaritifera

Chen, Z.; Zhao, S.; Zhou, Y.; Yu, C.; Zhong, W.; Yang, W., 2018:
Nacre-like laminate nitrogen-doped porous carbon/carbon nanotubes/graphene composite for excellent comprehensive performance supercapacitors

Kong, M.; Li, M.; Shang, R.; Wu, J.; Yan, P.; Xu, D.; Li, C., 2018:
Nacre-Templated Synthesis of Highly Dispersible Carbon Nanomeshes for Layered Membranes with High-Flux Filtration and Sensing Properties

O'Leary, J.G.; Reddy, K.Rajender.; Garcia-Tsao, G.; Biggins, S.W.; Wong, F.; Fallon, M.B.; Subramanian, R.M.; Kamath, P.S.; Thuluvath, P.; Vargas, H.E.; Maliakkal, B.; Tandon, P.; Lai, J.; Thacker, L.R.; Bajaj, J.S., 2018:
NACSELD acute-on-chronic liver failure (NACSELD-ACLF) score predicts 30-day survival in hospitalized patients with cirrhosis

Marchiolè, P.; Ferraioli, D.; Moran, E.; Mammoliti, S.; Tigaud, J-Dominique.; Beurrier, Fédéric.; Chopin, N.; Mathevet, P., 2018:
NACT and laparoscopic-assisted radical vaginal trachelectomy in young patients with large (2-5 cm) high risk cervical cancers: Safety and obstetrical outcome

Krammer, F.; Fouchier, R.A.M.; Eichelberger, M.C.; Webby, R.J.; Shaw-Saliba, K.; Wan, H.; Wilson, P.C.; Compans, R.W.; Skountzou, I.; Monto, A.S., 2018:
NAction! How Can Neuraminidase-Based Immunity Contribute to Better Influenza Virus Vaccines?

Xi, Y-Fei.; Zhou, L.; Bai, M.; Wang, J.; Lin, B.; Wang, X-Bo.; Huang, X-Xiao.; Song, S-Jiang., 2018:
N-acylanthranilic acid derivatives with anti-Aβ 1-42 aggregation activity from the leaves of Isatis indigotica fortune

Bottemanne, P.; Muccioli, G.G.; Alhouayek, M., 2018:
N-acylethanolamine hydrolyzing acid amidase inhibition: tools and potential therapeutic opportunities

Szostak, R.; Szostak, M., 2018:
N-Acyl-glutarimides: Resonance and Proton Affinities of Rotationally-Inverted Twisted Amides Relevant to N-C(O) Cross-Coupling

Chen, H.; Li, A.; Cui, D.; Wang, Q.; Wu, D.; Cui, C.; Ma, F., 2017:
N-Acyl-homoserine lactones and autoinducer-2-mediated quorum sensing during wastewater treatment

Thota, S.; Rodrigues, D.A.; Pinheiro, P.de.Sena.Murteira.; Lima, Lídia.M.; Fraga, C.A.M.; Barreiro, E.J., 2018:
N-Acylhydrazones as drugs

Stuyt, E.B.; Voyles, C.A.; Bursac, S., 2018:
NADA Protocol for Behavioral Health. Putting Tools in the Hands of Behavioral Health Providers: The Case for Auricular Detoxification Specialists

Zhang, K.; Chen, D.; Ma, K.; Wu, X.; Hao, H.; Jiang, S., 2018:
NAD(P)H:Quinone Oxidoreductase 1 (NQO1) as a Therapeutic and Diagnostic Target in Cancer

Rossi, F.; Geiszler, P.C.; Meng, W.; Barron, M.R.; Prior, M.; Herd-Smith, A.; Loreto, A.; Lopez, M.Yanez.; Faas, H.; Pardon, M-Christine.; Conforti, L., 2017:
NAD-biosynthetic enzyme NMNAT1 reduces early behavioral impairment in the htau mouse model of tauopathy

Grudzien-Nogalska, E.; Bird, J.G.; Nickels, B.E.; Kiledjian, M., 2018:
"NAD-capQ" detection and quantitation of NAD caps

Zhang, M.; Ying, W., 2018:
NAD + Deficiency Is a Common Central Pathological Factor of a Number of Diseases and Aging: Mechanisms and Therapeutic Implications

Rubio, L.; García-Pérez, D.; García-Sánchez, Mía.Jesús.; Fernández, Jé.A., 2018:
Na⁺-Dependent High-Affinity Nitrate, Phosphate and Amino Acids Transport in Leaf Cells of the Seagrass Posidonia oceanica (L.) Delile

Hsieh, C-Lu.; Huang, H-Min.; Hsieh, S-Ying.; Zheng, P-Xing.; Lin, Y-Shin.; Chiang-Ni, C.; Tsai, P-Jane.; Wang, S-Ying.; Liu, C-Chuan.; Wu, J-Jong., 2018:
NAD-Glycohydrolase Depletes Intracellular NAD + and Inhibits Acidification of Autophagosomes to Enhance Multiplication of Group A Streptococcus in Endothelial Cells

Sharma, M.; Mangas-Sanchez, J.; Turner, N.J.; Grogan, G., 2018:
NAD(P)H-Dependent Dehydrogenases for the Asymmetric Reductive Amination of Ketones: Structure, Mechanism, Evolution and Application

Afzal, M.; Shafeeq, S.; Kuipers, O.P., 2018:
NADH-Mediated Gene Expression in Streptococcus pneumoniae and Role of Rex as a Transcriptional Repressor of the Rex-Regulon

Yip, L.; Spyker, D.A., 2018:
NADH-methemoglobin reductase activity: adult versus child

Lindquist, R.L.; Bayat-Sarmadi, J.; Leben, R.; Niesner, R.; Hauser, A.E., 2018:
NAD(P)H Oxidase Activity in the Small Intestine Is Predominantly Found in Enterocytes, Not Professional Phagocytes

Wang, J-Ting.; Xie, W-Quan.; Liu, F-Quan.; Bi, Y.; Zhu, X-Jie.; Wang, Q-En.; Zheng, Y-Fang., 2018:
NADH protect against radiation enteritis by enhancing autophagy and inhibiting inflammation through PI3K/AKT pathway

Gaude, E.; Schmidt, C.; Gammage, P.A.; Dugourd, A.; Blacker, T.; Chew, S.Peak.; Saez-Rodriguez, J.; O'Neill, J.S.; Szabadkai, G.; Minczuk, M.; Frezza, C., 2018:
NADH Shuttling Couples Cytosolic Reductive Carboxylation of Glutamine with Glycolysis in Cells with Mitochondrial Dysfunction

Becker-Kettern, J.; Paczia, N.; Conrotte, J-François.; Zhu, C.; Fiehn, O.; Jung, P.P.; Steinmetz, L.M.; Linster, C.L., 2018:
NAD(P)HX repair deficiency causes central metabolic perturbations in yeast and human cells

Li, B-Bin.; Wang, X.; Tai, L.; Ma, T-Tian.; Shalmani, A.; Liu, W-Ting.; Li, W-Qiang.; Chen, K-Ming., 2018:
NAD Kinases: Metabolic Targets Controlling Redox Co-enzymes and Reducing Power Partitioning in Plant Stress and Development

Yaku, K.; Okabe, K.; Nakagawa, T., 2018:
NAD metabolism: Implications in aging and longevity

Gupte, S.A.; Rupawalla, T.; Phillibert, D.; Wolin, M.S., 2018:
NADPH and heme redox modulate pulmonary artery relaxation and guanylate cyclase activation by NO

Kuivanen, J.; Richard, P., 2017:
NADPH-dependent 5-keto-D-gluconate reductase is a part of the fungal pathway for D-glucuronate catabolism

Miller, C.G.; Holmgren, A.; Arnér, E.S.J.; Schmidt, E.E., 2018:
NADPH-dependent and -independent disulfide reductase systems

Collins, F.A.; Fisher, K.; Payne, K.A.P.; Gaytan Mondragon, S.; Rigby, S.E.J.; Leys, D., 2018:
NADPH-Driven Organohalide Reduction by a Nonrespiratory Reductive Dehalogenase

Xu, J-Zhong.; Yang, H-Kun.; Zhang, W-Guo., 2018:
NADPH metabolism: a survey of its theoretical characteristics and manipulation strategies in amino acid biosynthesis

Fuentes, E.; Gibbins, J.M.; Holbrook, L.M.; Palomo, Ián., 2018:
NADPH oxidase 2 (NOX2): A key target of oxidative stress-mediated platelet activation and thrombosis

Wang, J.; Ma, M.W.; Dhandapani, K.M.; Brann, D.W., 2018:
NADPH oxidase 2 deletion enhances neurogenesis following traumatic brain injury

Liao, Y.; Gou, L.; Chen, L.; Zhong, X.; Zhang, D.; Zhu, H.; Lu, X.; Zeng, T.; Deng, X.; Li, Y., 2017:
NADPH oxidase 4 and endothelial nitric oxide synthase contribute to endothelial dysfunction mediated by histone methylations in metabolic memory

Saez, F.; Hong, N.J.; Garvin, J.L., 2018:
NADPH oxidase 4-derived superoxide mediates flow-stimulated NKCC2 activity in thick ascending limbs

Mongue-Din, H.; Patel, A.S.; Looi, Y.H.; Grieve, D.J.; Anilkumar, N.; Sirker, A.; Dong, X.; Brewer, A.C.; Zhang, M.; Smith, A.; Shah, A.M., 2018:
NADPH Oxidase-4 Driven Cardiac Macrophage Polarization Protects Against Myocardial Infarction-Induced Remodeling

Nisimoto, Y.; Ogawa, H.; Kadokawa, Y.; Qiao, S., 2018:
NADPH oxidase 4 function as a hydrogen peroxide sensor

Sakai, Y.; Yamamori, T.; Yoshikawa, Y.; Bo, T.; Suzuki, M.; Yamamoto, K.; Ago, T.; Inanami, O., 2017:
NADPH oxidase 4 mediates ROS production in radiation-induced senescent cells and promotes migration of inflammatory cells

Antonescu, M-Loredana.; Manea, S-Adriana.; Simionescu, M.; Manea, A., 2018:
NADPH oxidase 5 expression is regulated by histone acetyltransferase 1 and P300- dependent in human macrophages

Montezano, A.C.; De Lucca Camargo, L.; Persson, P.; Rios, F.J.; Harvey, A.P.; Anagnostopoulou, A.; Palacios, R.; Gandara, A.Caroline.P.; Alves-Lopes, R.; Neves, K.B.; Dulak-Lis, M.; Holterman, C.E.; de Oliveira, P.Lagerblad.; Graham, D.; Kennedy, C.; Touyz, R.M., 2018:
NADPH Oxidase 5 Is a Pro-Contractile Nox Isoform and a Point of Cross-Talk for Calcium and Redox Signaling-Implications in Vascular Function

Andueza, A.; Garde, N.; García-Garzón, A.; Ansorena, E.; López-Zabalza, Mía.J.; Iraburu, Mía.J.; Zalba, G.; Martínez-Irujo, J.J., 2018:
NADPH oxidase 5 promotes proliferation and fibrosis in human hepatic stellate cells

Belambri, S.A.; Rolas, Lïc.; Raad, H.; Hurtado-Nedelec, M.; Dang, P.My-Chan.; El-Benna, J., 2018:
NADPH oxidase activation in neutrophils: Role of the phosphorylation of its subunits

Bagaitkar, J.; Huang, J.; Zeng, M.Yue.; Pech, N.K.; Monlish, D.A.; Perez-Zapata, L.J.; Miralda, I.; Schuettpelz, L.G.; Dinauer, M.C., 2018:
NADPH oxidase activation regulates apoptotic neutrophil clearance by murine macrophages

Petrovic, R.; Puskas, L.; Jevtic Dozudic, G.; Stojkovic, T.; Velimirovic, M.; Nikolic, T.; Zivkovic, M.; Djorovic, D.J.; Nenadovic, M.; Petronijevic, N., 2018:
NADPH oxidase and redox status in amygdala, hippocampus and cortex of male Wistar rats in an animal model of post-traumatic stress disorder

Giardino, G.; Cicalese, M.Pia.; Delmonte, O.; Migliavacca, M.; Palterer, B.; Loffredo, L.; Cirillo, E.; Gallo, V.; Violi, F.; Pignata, C., 2018:
NADPH Oxidase Deficiency: A Multisystem Approach

Li, W.; Young, J.F.; Sun, J., 2018:
NADPH oxidase-generated reactive oxygen species in mature follicles are essential for Drosophila ovulation

Obeso, A.; Gómez-Niño, A.; Gonzalez, C., 2018:
NADPH oxidase inhibition does not interfere with low[Formula: see text] transduction in rat and rabbit CB chemoreceptor cells

Loehr, J.Anthony.; Wang, S.; Cully, T.R.; Pal, R.; Larina, I.V.; Larin, K.V.; Rodney, G.G., 2018 :
NADPH oxidase mediates microtubule alterations and diaphragm dysfunction in dystrophic mice

Svegliati, S.; Spadoni, T.; Moroncini, G.; Gabrielli, A., 2018:
NADPH oxidase, oxidative stress and fibrosis in systemic sclerosis

Marrali, G.; Casale, F.; Salamone, P.; Fuda, G.; Ilardi, A.; Manera, U.; Calvo, A.; Zibetti, M.; Lopiano, L.; Chiò, A., 2018:
NADPH oxidases 2 activation in patients with Parkinson's disease

Salazar, G., 2018:
NADPH Oxidases and Mitochondria in Vascular Senescence

Huang, W-Yu.; Lin, S.; Chen, H-Ying.; Chen, Y-Ping.; Chen, T-Yu.; Hsu, K-Sen.; Wu, H-Ming., 2018:
NADPH oxidases as potential pharmacological targets against increased seizure susceptibility after systemic inflammation

Qiao, H.; Zhou, Y.; Qin, X.; Cheng, J.; He, Y.; Jiang, Y., 2018:
NADPH Oxidase Signaling Pathway Mediates Mesenchymal Stem Cell-Induced Inhibition of Hepatic Stellate Cell Activation

Ma, M.W.; Wang, J.; Dhandapani, K.M.; Wang, R.; Brann, D.W., 2018:
NADPH oxidases in traumatic brain injury - Promising therapeutic targets?

Miyahara, Y.; Oota, M.; Tsuge, T., 2018:
NADPH supply for poly(3-hydroxybutyrate) synthesis concomitant with enzymatic oxidation of phosphite

Guo, Y.; Song, Y.; Zheng, H.; Zhang, Y.; Guo, J.; Sui, N., 2018:
NADP-Malate Dehydrogenase of Sweet Sorghum Improves Salt Tolerance of Arabidopsis thaliana

Braidy, N.; Berg, J.; Clement, J.; Khorshidi, F.; Poljak, A.; Jayasena, T.; Grant, R.; Sachdev, P., 2018:
Role of Nicotinamide Adenine Dinucleotide and Related Precursors as Therapeutic Targets for Age-Related Degenerative Diseases: Rationale, Biochemistry, Pharmacokinetics, and Outcomes

Cho, H.Je.; Cho, H.Yeon.; Park, J-Woo.; Kwon, O-Shin.; Lee, H-Shik.; Huh, T.Lin.; Kang, B.Sik., 2018:
NADP + -dependent cytosolic isocitrate dehydrogenase provides NADPH in the presence of cadmium due to the moderate chelating effect of glutathione

Lin, J.B.; Apte, R.S., 2018:
NAD + and sirtuins in retinal degenerative diseases: A look at future therapies

Johnson, S.; Imai, S-Ichiro., 2018:
NAD + biosynthesis, aging, and disease

Porter, L.C.; Franczyk, M.P.; Pietka, T.; Yamaguchi, S.; Lin, J.B.; Sasaki, Y.; Verdin, E.; Apte, R.S.; Yoshino, J., 2018:
NAD + -dependent deacetylase SIRT3 in adipocytes is dispensable for maintaining normal adipose tissue mitochondrial function and whole body metabolism

Pajuelo, D.; Gonzalez-Juarbe, N.; Tak, U.; Sun, J.; Orihuela, C.J.; Niederweis, M., 2018:
NAD + Depletion Triggers Macrophage Necroptosis, a Cell Death Pathway Exploited by Mycobacterium tuberculosis

Yoshino, J.; Baur, J.A.; Imai, S-Ichiro., 2017:
NAD + Intermediates: The Biology and Therapeutic Potential of NMN and NR

Shimizu, M., 2018:
NAD + /NADH homeostasis affects metabolic adaptation to hypoxia and secondary metabolite production in filamentous fungi

Purhonen, J.; Rajendran, J.; Tegelberg, S.; Smolander, O-Pekka.; Pirinen, E.; Kallijärvi, J.; Fellman, V., 2018:
NAD + repletion produces no therapeutic effect in mice with respiratory chain complex III deficiency and chronic energy deprivation

Anonymous, 2018:
NAD+ Supplementation in Mouse AD Model

Carrasco-Yepez, M.M.; Campos-Rodríguez, R.; Reséndiz-Albor, A.A.; Peña-Juárez, C.; Contis-Montes de Oca, A.; Arciniega-Martínez, I.M.; Bonilla-Lemus, P.; Rojas-Hernandez, S., 2017:
Naegleria fowleri immunization modifies lymphocytes and APC of nasal mucosa

Wu, H.; Shabala, L.; Azzarello, E.; Huang, Y.; Pandolfi, C.; Su, N.; Wu, Q.; Cai, S.; Bazihizina, N.; Wang, L.; Zhou, M.; Mancuso, S.; Chen, Z.; Shabala, S., 2018:
Na+ extrusion from the cytosol and tissue-specific Na+ sequestration in roots confer differential salt stress tolerance between durum and bread wheat

Duan, H-Quan.; Wu, Q-Li.; Yao, X.; Fan, B-You.; Shi, H-Yu.; Zhao, C-Xi.; Zhang, Y.; Li, B.; Sun, C.; Kong, X-Hong.; Zhou, X-Fu.; Feng, S-Qing., 2018:
Nafamostat mesilate attenuates inflammation and apoptosis and promotes locomotor recovery after spinal cord injury

Mander, S.; You, D-Joo.; Park, S.; Kim, D.Hwi.; Yong, H.Jeong.; Kim, D-Sik.; Ahn, C.; Kim, Y-Hee.; Seong, J.Young.; Hwang, J-Ik., 2017:
Nafamostat mesilate negatively regulates the metastasis of triple-negative breast cancer cells

Rukma, P.; Mohsena, A.; Sunil, M., 2018:
Nafcillin-Associated Hypokalemia

Monogue, M.L.; Ortwine, J.K.; Wei, W.; Eljaaly, K.; Bhavan, K.P., 2018:
Nafcillin versus cefazolin for the treatment of methicillin-susceptible Staphylococcus aureus bacteremia

Dhull, V., 2018:
A Nafion/AChE-cSWCNT/MWCNT/Au-based amperometric biosensor for the determination of organophosphorous compounds

Yang, H.; Li, X.; Batchelor-McAuley, C.; Sokolov, S.V.; Compton, R.G., 2017:
Nafion particles doped with methyl viologen: electrochemistry

Jiang, S.; Lu, Y.; Lu, Y.; Han, M.; Li, H.; Tao, Z.; Niu, Z.; Chen, J., 2018:
Nafion/Titanium Dioxide-Coated Lithium Anode for Stable Lithium-Sulfur Batteries

Soti, S.; Corey, K.E.; Lake, J.E.; Erlandson, K.M., 2018:
NAFLD and HIV: Do Sex, Race, and Ethnicity Explain HIV-Related Risk?

Mantovani, A., 2018:
NAFLD and risk of cardiac arrhythmias: Is hyperuricemia a neglected pathogenic mechanism?

Castaño-Rodríguez, N.; Mitchell, H.M.; Kaakoush, N.O., 2018:
NAFLD, Helicobacter species and the intestinal microbiome

Tapper, E.B.; Loomba, R., 2017:
Nonalcoholic fatty liver disease, metabolic syndrome, and the fight that will define clinical practice for a generation of hepatologists

Radaelli, M.G.; Martucci, F.; Perra, S.; Accornero, S.; Castoldi, G.; Lattuada, G.; Manzoni, G.; Perseghin, G., 2017:
NAFLD/NASH in patients with type 2 diabetes and related treatment options

Banaszczak, M.; Stachowska, E., 2018:
NAFLD pathogenesis in the light of recent research

Jansen, J.C.; Wolthuis, D.; Van Scherpenzeel, M.; Ratziu, V.; Drenth, J.P.H.; Lefeber, D.J., 2018:
NAFLD Phenotype in Patients With V-ATPase Proton Pump Assembly Defects

Zhang, X., 2018:
NAFLD Related-HCC: The Relationship with Metabolic Disorders

Sliz, E.; Sebert, S.; Würtz, P.; Kangas, A.J.; Soininen, P.; Lehtimäki, T.; Kähönen, M.; Viikari, J.; Männikkö, M.; Ala-Korpela, M.; Raitakari, O.T.; Kettunen, J., 2018:
NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects

George, J.; Anstee, Q.; Ratziu, V.; Sanyal, A., 2017:
NAFLD: The evolving landscape

Li, J.; Wang, P.; Gao, J.; Fei, X.; Liu, Y.; Ruan, J., 2018:
NaF Reduces KLK4 Gene Expression by Decreasing Foxo1 in LS8 Cells

Goettsche, Z.S.; Ettinger, R.A.; Hogan, M.M.; Harless, J.D.; Qian, F., 2018:
NaF rinse and dentifrice concentrations on enamel lesion demineralization

Fotedar, R.; Kolecka, A.; Boekhout, T.; Fell, J.W.; Anand, A.; Al Malaki, A.; Zeyara, A.; Al Marri, M., 2018:
Naganishia qatarensis sp. nov., a novel basidiomycetous yeast species from a hypersaline marine environment in Qatar

Koncsos, Gábor.; Varga, Zán.V.; Baranyai, Tás.; Ferdinandy, Péter.; Schulz, R.; Giricz, Zán.; Boengler, K., 2018:
Nagarse treatment of cardiac subsarcolemmal and interfibrillar mitochondria leads to artefacts in mitochondrial protein quantification

Chaudhry, R.; Sharma, N.; Gupta, N.; Kant, K.; Bahadur, T.; Shende, T.M.; Kumar, L.; Kabra, S.K., 2017:
Nagging Presence of Clostridium difficile Associated Diarrhoea in North India

Anonymous, 2017:
Nagoya Gold and Silver Medals/Prelog Medal and Lectureship for Stephen B. H. Kent/And also in the News

Mercado, S., 2018:
NAHQ Is on the Move

Centurión, D.; de la Cruz, Súl.Huerta.; Castillo-Santiago, S.V.; Becerril-Chacón, Mía.Elena.; Torres-Pérez, Jé.A.; Sánchez-López, A., 2018:
NaHS prejunctionally inhibits the cardioaccelerator sympathetic outflow in pithed rats

Xu, K.; Wu, F.; Xu, K.; Li, Z.; Wei, X.; Lu, Q.; Jiang, T.; Wu, F.; Xu, X.; Xiao, J.; Chen, D.; Zhang, H., 2018:
NaHS restores mitochondrial function and inhibits autophagy by activating the PI3K/Akt/mTOR signalling pathway to improve functional recovery after traumatic brain injury

Linn, S.C.; Mustonen, A.M.; Silva, K.A.; Kennedy, V.E.; Sundberg, B.A.; Bechtold, L.S.; Alghamdi, S.; Hoehndorf, R.; Schofield, P.N.; Sundberg, J.P., 2018:
Nail abnormalities identified in an ageing study of 30 inbred mouse strains

Kaparos, N.; Norrenberg, S.; Al-Dhafiri, M.; Christen-Zaech, Séphanie., 2018:
Nail alterations in children

Hill, V.A.; Stowe, G.Neil.; Paulsen, R.B.; Schaffer, M., 2018:
Nail Analysis for Drugs: A Role in Workplace Testing?

Kanabur, P.; Sandilands, S.M.; Whitmer, K.K.; Owen, T.M.; Coniglione, F.M.; Shuler, T.E., 2018:
Nail and Locking Plate for Periprosthetic Fractures

Grover, C.; Bansal, S., 2018:
Nail Biopsy: A User's Manual

Shih, Y-Hsien.; Huang, C-Yu.; Lee, C-Chi.; Lee, W-Ruoh., 2018:
Nail Brace Application: A Noninvasive Treatment for Ingrown Nails in Pediatric Patients

Chelidze, K.; Lipner, S.R., 2018:
Nail changes in alopecia areata: an update and review

Gopal, V.; Shenoy, M.Mala.; Bejai, V.; Nargis, T., 2018:
Nail changes in autoimmune blistering disorders: A case-control study

Ehsani, A.Hooshang.; Nasimi, M.; Azizpour, A.; Noormohammadpoor, P.; Kamyab, K.; Seirafi, H.; Noori, M., 2018:
Nail Changes in Early Mycosis Fungoides

Romaszkiewicz, A.; Sławińska, M.; Sobjanek, Mł.; Nowicki, R.J., 2018:
Nail dermoscopy (onychoscopy) is useful in diagnosis and treatment follow-up of the nail mixed infection caused by Pseudomonas aeruginosa and Candida albicans

Borelli, S.; Lautenschlager, S., 2018:
Nail diseases

Mayeaux, E.J., 2000:
Nail disorders

Baeza, D.; Sola, Y.; Del Río, L.Alberto.; González, R., 2018:
Nail dryer devices: a measured spectral irradiance and labelling review

Lee, H.; Lee, W.S., 2017:
Nail-extracting behaviour as an unusual manifestation of adjustment disorder, confused with onychotillomania

Millar, M.J.; Wilkinson, A.; Navarre, P.; Steiner, J.; Vohora, A.; Hardidge, A.; Edwards, E., 2018:
Nail Fit: Does Nail Diameter to Canal Ratio Predict the Need for Exchange Nailing in the Setting of Aseptic, Hypertrophic Femoral Nonunions?

Rajaei, A.; Dehghan, P.; Amiri, A., 2017:
Nailfold capillaroscopy in 430 patients with rheumatoid arthritis

Cutolo, M.; Melsens, K.; Wijnant, S.; Ingegnoli, F.; Thevissen, K.; De Keyser, F.; Decuman, S.; Müller-Ladner, U.; Piette, Y.; Riccieri, V.; Ughi, N.; Vandecasteele, E.; Vanhaecke, A.; Smith, V., 2018:
Nailfold capillaroscopy in systemic lupus erythematosus: A systematic review and critical appraisal

Caetano, J.; Paula, F.S.; Amaral, M.; Oliveira, S.; Alves, Jé.D., 2018:
Nailfold Videocapillaroscopy Changes Are Associated With the Presence and Severity of Systemic Sclerosis-Related Interstitial Lung Disease

Midgley, G.; Moore, M.K., 1996:
Nail infections

Zou, Y.; Hu, W.; Zheng, J.; Pan, M., 2018:
Nail infestation: an atypical presentation of typical scabies

Palui, R.; Sahoo, J.Prakash.; Kamalanathan, S.; Sridharan, K., 2018:
Nailing septo-optic dysplasia

Jovanovich, A.J.; Chonchol, M.B., 2018:
Nail in the Coffin for Fibroblast Growth Factor 23 as a Predictor of Kidney Function Decline

Lee, J.Su.; Huh, C-Hun.; Kwon, O.; Yoon, H-Sun.; Cho, S.; Park, H-Sun., 2018:
Nail involvement in patients with moderate-to-severe alopecia areata treated with oral tofacitinib

Parker, M.; Raval, P.; Gjertsen, J-Erik., 2018:
Nail or plate fixation for A3 trochanteric hip fractures: A systematic review of randomised controlled trials

Bisaccia, M.; Cappiello, A.; Meccariello, L.; Rinonapoli, G.; Falzarano, G.; Medici, A.; Vicente, C.Ibáñez.; Piscitelli, L.; Stano, V.; Bisaccia, O.; Caraffa, A., 2018:
Nail or plate in the management of distal extra-articular tibial fracture, what is better? Valutation of outcomes

Aboobacker, I.N.; Krishnakumar, A.; Narayanan, S.; Hafeeque, B.; Gopinathan, J.C.; Aziz, F., 2018:
Nail-Patella Syndrome: A Rare Cause of Nephrotic Syndrome in Pregnancy

Price, A.; Cervantes, J.; Lindsey, S.; Aickara, D.; Hu, S., 2018:
Nail-patella syndrome: clinical clues for making the diagnosis

Gupta, S.; Singal, A.; Aggarwal, K.; Shankar Jangra, R., 2018:
Nail photography tricks for pediatric and geriatric patients

Saeedi, P.; Shavandi, A.; Meredith-Jones, K., 2018:
Nail Properties and Bone Health: A Review

Haneke, E., 2018:
Nail psoriasis: clinical features, pathogenesis, differential diagnoses, and management

Mazzeo, M.; Dattola, A.; Cannizzaro, M.V.; Bianchi, L., 2018:
Nail Psoriasis Treated With Certolizumab Pegol in Patients With Psoriatic Arthritis: Preliminary Observation

Peruzzo, J.; Garbin, G.Czarnobay.; Maldonado, G.; Cestari, T.Ferreira., 2018:
Nail psoriasis treated with pulsed dye laser

Paurobally, D.; Andre, J.; Richert, B., 2018:
Nail Pyogenic Granuloma following Treatment with Blinatumomab

Kourkoumelis, N.; Gaitanis, G.; Velegraki, A.; Bassukas, I.D., 2018:
Nail Raman spectroscopy: A promising method for the diagnosis of onychomycosis. An ex vivo pilot study

Koroglu, M.; Demiray, T.; Ozbek, A.; Guclu, E.; Karabay, O.; Altindis, M.; Durmaz, R., 2018:
Nail scissors and fingernails as reservoirs of hepatitis B virus DNA: Role of nail scissors in household transmission of hepatitis B virus

Clark, R.E.; Madani, S.; Bettencourt, M.S., 1998:
Nail surgery

Adhikari, S.; Sigdel, K.Raj.; Paudyal, B.; Basnyat, B., 2018:
Nail the Diagnosis

Zoltowska, D.M.; Agrawal, Y.; Kalavakunta, J.K.; Gupta, V., 2018:
Nail to the heart: no big deal. A rare case of post-traumatic pericarditis

Kaliyadan, F.; Ashique, K.T., 2018:
Nail Transillumination Combined with Dermoscopy for Enhancing Diagnosis of Subungual Hematoma

Da Silva, D.R.; Gaddis, K.J.; Hess, S.; Rubin, A.I., 2018:
Nail Unit Glomus Tumor with Myxoid and Symplastic Change Presenting with Longitudinal Erythronychia

Zhang, H-Hua.; Wang, Y-Qiang.; Huang, L-Tao.; Zhu, L-Qing.; Feng, Y-Yue.; Lu, Y-Mei.; Zhao, Q-Yi.; Wang, X-Qiang.; Wang, Z., 2018:
NaI-mediated divergent synthesis of isatins and isoindigoes: a new protocol enabled by an oxidation relay strategy

Miljkovic, D.; Psaltis, A.; Wormald, P-John.; Vreugde, S., 2018:
Naive and effector B-cell subtypes are increased in chronic rhinosinusitis with polyps

Zhang, N.; Wu, L.; Yang, J.; Guan, Y., 2018:
Naive Bayes Bearing Fault Diagnosis Based on Enhanced Independence of Data

Pape, K.A.; Maul, R.W.; Dileepan, T.; Paustian, A.Schmidt.; Gearhart, P.J.; Jenkins, M.K., 2018:
Naive B Cells with High-Avidity Germline-Encoded Antigen Receptors Produce Persistent IgM + and Transient IgG + Memory B Cells

Bandini, E.; Tennie, C., 2018:
Naive, captive long-tailed macaques ( Macaca fascicularis fascicularis ) fail to individually and socially learn pound-hammering, a tool-use behaviour

Ibrahim, M.; Scozzi, D.; Toth, K.A.; Ponti, D.; Kreisel, D.; Menna, C.; De Falco, E.; D'Andrilli, A.; Rendina, E.A.; Calogero, A.; Krupnick, A.S.; Gelman, A.E., 2017:
Naive CD4 + T Cells Carrying a TLR2 Agonist Overcome TGF-β-Mediated Tumor Immune Evasion

Han, M.; Wang, N.; Guo, S.; Chang, N.; Lu, S.; Wan, M., 2018:
Nakagami-m parametric imaging for characterization of thermal coagulation and cavitation erosion induced by HIFU

Sánchez-Aldehuelo, Rén.; Figueroa-Tubío, A.; García de la Filia, I.; González-Olivares, C.; García García de Paredes, A.; García-Cosío, Mónica.; Vázquez-Sequeiros, E.; Albillos, Aín., 2018:
Nakamura polyp: An unusual endoscopic finding

Khajah, M.A.; Mathew, P.M.; Luqmani, Y.A., 2018:
Na+/K+ ATPase activity promotes invasion of endocrine resistant breast cancer cells

Hansson, E.; Block, L.; Forshammar, J.; Lundborg, C.; Biber, Börn., 2018:
Na+/K+-ATPase dependent regulation of astrocyte Ca2+ signalling: A novel mechanism for modulation of long-term pain?

Lichtstein, D.; Ilani, A.; Rosen, H.; Horesh, N.; Singh, S.Vardan.; Buzaglo, N.; Hodes, A., 2018:
Na⁺, K⁺-ATPase Signaling and Bipolar Disorder

Marck, P.V.; Pierre, S.V., 2018:
Na/K-ATPase Signaling and Cardiac Pre/Postconditioning with Cardiotonic Steroids

Drummond, C.A.; Fan, X.; Haller, S.T.; Kennedy, D.J.; Liu, J.; Tian, J., 2018:
Na/K-ATPase signaling mediates miR-29b-3p regulation and cardiac fibrosis formation in mice with chronic kidney disease

Xie, J.X.; Zhang, S.; Cui, X.; Zhang, J.; Yu, H.; Khalaf, F.K.; Malhotra, D.; Kennedy, D.J.; Shapiro, J.I.; Tian, J.; Haller, S.T., 2018:
Na/K-ATPase/src complex mediates regulation of CD40 in renal parenchyma

Noe, T.; Vulkan, N., 2018:
Naked aggression: Personality and portfolio manager performance

Cong, P-Yun.; Harvey, T.H.P.; Williams, M.; Siveter, D.J.; Siveter, D.J.; Gabbott, S.E.; Li, Y-Jing.; Wei, F.; Hou, X-Guang., 2018:
Naked chancelloriids from the lower Cambrian of China show evidence for sponge-type growth

Hou, Y.L.; Ling, J.Q.; Chen, C.C.; Quan, J.J.; Du, Y., 2018:
Naked cuticle homolog 2 positively regulates the osteogenic differentiation of rat dental follicle cells

Islam, M.Nazmul.; Moriam, S.; Umer, M.; Phan, H-Phuong.; Salomon, C.; Kline, R.; Nguyen, N-Trung.; Shiddiky, M.J.A., 2018:
Naked-eye and electrochemical detection of isothermally amplified HOTAIR long non-coding RNA

Lin, C-Chi.; Huang, S-Chieh.; Lin, H-Hsin.; Huang, W.J.; Chen, W-Shone.; Yang, S-Haur., 2018:
Naked-eye box trainer and training box games have similar training effect as conventional video-based box trainer for novices: A randomized controlled trial

Santana-Jiménez, L.A.; Márquez-Lucero, A.; Osuna, V.; Estrada-Moreno, I.; Dominguez, R.B., 2018:
Naked-Eye Detection of Glucose in Saliva with Bienzymatic Paper-Based Sensor

Vidya, R.; Saji, A., 2018:
Naked eye detection of infertility based on sperm protamine-induced aggregation of heparin gold nanoparticles

Naderi, M.; Hosseini, M.; Ganjali, M.Reza., 2018:
Naked-eye detection of potassium ions in a novel gold nanoparticle aggregation-based aptasensor

Singpanomchai, N.; Akeda, Y.; Tomono, K.; Tamaru, A.; Santanirand, P.; Ratthawongjirakul, P., 2018:
Naked eye detection of the Mycobacterium tuberculosis complex by recombinase polymerase amplification-SYBR green I assays

Doytcheva, K.; Tan, T.; Guitart, J.; Gerami, P.; Yazdan, P., 2018:
Naked Hair Shafts as a Marker of Cicatricial Alopecia

Schuhmacher, L-Nadine.; Callejo, G.; Srivats, S.; Smith, E.St.John., 2017:
Naked mole-rat acid-sensing ion channel 3 forms nonfunctional homomers, but functional heteromers

Pamenter, M.E.; Lau, G.Y.; Richards, J.G.; Milsom, W.K., 2018:
Naked mole rat brain mitochondria electron transport system flux and H + leak are reduced during acute hypoxia

Evdokimov, A.; Kutuzov, M.; Petruseva, I.; Lukjanchikova, N.; Kashina, E.; Kolova, E.; Zemerova, T.; Romanenko, S.; Perelman, P.; Prokopov, D.; Seluanov, A.; Gorbunova, V.; Graphodatsky, A.; Trifonov, V.; Khodyreva, S.; Lavrik, O., 2018:
Naked mole rat cells display more efficient excision repair than mouse cells

Husson, Zé.; Smith, E.St.John., 2018:
Naked mole-rat cortical neurons are resistant to acid-induced cell death

Ruby, J.Graham.; Smith, M.; Buffenstein, R., 2018:
Naked Mole-Rat mortality rates defy gompertzian laws by not increasing with age

Zhao, Y.; Tyshkovskiy, A.; Muñoz-Espín, D.; Tian, X.; Serrano, M.; de Magalhaes, J.Pedro.; Nevo, E.; Gladyshev, V.N.; Seluanov, A.; Gorbunova, V., 2018:
Naked mole rats can undergo developmental, oncogene-induced and DNA damage-induced cellular senescence

Bens, M.; Szafranski, K.; Holtze, S.; Sahm, A.; Groth, M.; Kestler, H.A.; Hildebrandt, T.B.; Platzer, M., 2018:
Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging

Ito, T.; Okuda, T.; Takashima, Y.; Okamoto, H., 2018:
Naked pDNA inhalation powder composed of hyaluronic acid exhibits high gene expression in the lungs

Lo, H-Ming.; Ma, M-Chieh.; Shieh, J-Min.; Chen, H-Ling.; Wu, W-Bin., 2018:
Naked physically synthesized gold nanoparticles affect migration, mitochondrial activity, and proliferation of vascular smooth muscle cells

Abdelhamid, B.Mohamed.; Omar, H., 2018:
Nalbuphine as an adjuvant to 0.25% levobupivacaine in ultrasound-guided supraclavicular block provided prolonged sensory block and similar motor block durations (RCT)

Gong, Y.; Zhang, Y.; Tao, S., 2018:
Nalbuphine for analgesia after fracture surgery and its effect on circulating inflammatory factors

Gupta, M.; Gupta, P., 2018:
Nalbuphine pretreatment for prevention of etomidate induced myoclonus: A prospective, randomized and double-blind study

Ford, N.C.; Ren, D.; Baccei, M.L., 2018:
NALCN channels enhance the intrinsic excitability of spinal projection neurons

Campbell, J.; FitzPatrick, D.R.; Azam, T.; Gibson, N.A.; Somerville, L.; Joss, S.K.; Urquhart, D.S., 2018:
NALCN Dysfunction as a Cause of Disordered Respiratory Rhythm With Central Apnea

Anonymous, 2017:
Naldemedine (Symproic) for opioid-induced constipation

Reinl, E.L.; Zhao, P.; Wu, W.; Ma, X.; Amazu, C.; Bok, R.; Hurt, K.Joseph.; Wang, Y.; England, S.K., 2018:
Na+-Leak Channel, Non-Selective (NALCN) Regulates Myometrial Excitability and Facilitates Successful Parturition

Guzmán-Martín, Jé.Luis.; Navarro-Marí, Jé.María.; Expósito-Ruiz, M.; Gutiérrez-Fernández, Jé., 2018:
Nalidixic acid surrogate test for susceptibility to ciprofloxacin in Salmonella. Revisiting the question

Wang, S.; Liu, G.; Yuan, Z.; Da, C., 2017:
n-Alkanes in sediments from the Yellow River Estuary, China: Occurrence, sources and historical sedimentary record

Tamura, S.; Sato, K.; Kawano, T., 2018:
N-Alkylation Using Sodium Triacetoxyborohydride with Carboxylic Acids as Alkyl Sources

Toriumi, N.; Asano, N.; Miyamoto, K.; Muranaka, A.; Uchiyama, M., 2018:
N-Alkynylpyridinium Salts: Highly Electrophilic Alkyne-Pyridine Conjugates as Precursors of Cationic Nitrogen-Embedded Polycyclic Aromatic Hydrocarbons

Zheng, Q.; Xing, L.; Yang, X.; Li, X.; Ye, C.; Wang, K.; Huang, Q.; Li, W., 2018:
N-Allyl- N, N-Bis(trimethylsilyl)amine as a Novel Electrolyte Additive To Enhance the Interfacial Stability of a Ni-Rich Electrode for Lithium-Ion Batteries

Khegai, A.; Melkumov, M.; Riumkin, K.; Khopin, V.; Firstov, S.; Dianov, E., 2018:
NALM-based bismuth-doped fiber laser at 1.7  μm

Wu, Q.; Chen, X.; Wang, J.; Sun, P.; Weng, M.; Chen, W.; Sun, Z.; Zhu, M.; Miao, C., 2017:
Nalmefene attenuates malignant potential in colorectal cancer cell via inhibition of opioid receptor

Braillon, A.; Taiebi, F.; Bernoussi, A., 2018:
Nalmefene Phase IV Study: A Seeding Flying in the Face of Evidence?

Gelbrich, T.; Langes, C.; Stefinovic, M.; Griesser, U.J., 2018:
Naloxegol hydrogen oxalate displaying a hydrogen-bonded layer structure

Gálvez, R.; Maire, C.; Tovar, I.; Vargas, P., 2018:
Naloxegol to Treat Constipation in a Patient Taking Opioids for Cancer Pain: A Case Report

Abd-Elsayed, A.; Albert, C.Ann.; Fischer, M.; Anderson, B., 2018:
Naloxone Academic Detailing: Role of Community Outreach Teaching

Nikolaides, J.K.; Rizvanolli, L.; Rozum, M.; Aks, S.E., 2018:
Naloxone access among an urban population of opioid users

Cash, R.E.; Kinsman, J.; Crowe, R.P.; Rivard, M.K.; Faul, M.; Panchal, A.R., 2018:
Naloxone Administration Frequency During Emergency Medical Service Events - United States, 2012-2016

Wirth, S.R., 2017:
Naloxone Conundrum: Reduce risk in managing the opioid overdose patient

Madah-Amiri, D.; Gjersing, L.; Clausen, T., 2018:
Naloxone distribution and possession following a large-scale naloxone programme

Raffel, K.E.; Beach, L.Y.; Lin, J.; Berchuck, J.E.; Abram, S.; Markle, E.; Patel, S., 2018:
Naloxone Distribution and Training for Patients with High-Risk Opioid Use in a Veterans Affairs Community-Based Primary Care Clinic

Rzasa Lynn, R.; Galinkin, J.L., 2018:
Naloxone dosage for opioid reversal: current evidence and clinical implications

Dunn, K.E.; Barrett, F.S.; Bigelow, G.E., 2018:
Naloxone formulation for overdose reversal preference among patients receiving opioids for pain management

Toderika, Y.; Williams, S., 2018:
Naloxone for Opioid Overdose and the Role of the Pharmacist

Jiwa, N.; Sheth, H.; Silverman, R., 2018:
Naloxone-Induced Non-Cardiogenic Pulmonary Edema: A Case Report

Olsen, P.L.; Hoffman, C.R.; Green, M.Stuart., 2018:
Naloxone Infusion During Thoracic Endovascular Aortic Aneurysm Repair to Prevent Spinal Cord Injury

Carvalho, A-Maria.; Poirier, V., 2018:
Naloxone is becoming more available in airline medical kits

Lambdin, B.H.; Davis, C.S.; Wheeler, E.; Tueller, S.; Kral, A.H., 2018:
Naloxone laws facilitate the establishment of overdose education and naloxone distribution programs in the United States

Roy, K.; Bhattacharyya, P.; Deb, I., 2018:
Naloxone precipitated morphine withdrawal and clock genes expression in striatum: A comparative study in three different protocols for the development of morphine dependence

Verdier, M.; Routsolias, J.C.; Aks, S.E., 2018:
Naloxone prescriptions from the emergency department: An initiative in evolution

Seger, D.L.; Loden, J.K., 2018:
Naloxone reversal of clonidine toxicity: dose, dose, dose

Marco, C.A.; Trautman, W.; Cook, A.; Mann, D.; Rasp, J.; Perkins, O.; Ballester, M., 2018:
Naloxone Use Among Emergency Department Patients with Opioid Overdose

Date, Y.; Ebisawa, M.; Fukuda, S.; Shima, H.; Obata, Y.; Takahashi, D.; Kato, T.; Hanazato, M.; Nakato, G.; Williams, I.R.; Hase, K.; Ohno, H., 2017:
NALT M cells are important for immune induction for the common mucosal immune system

Nieto, S.J.; Quave, C.B.; Kosten, T.A., 2018:
Naltrexone alters alcohol self-administration behaviors and hypothalamic-pituitary-adrenal axis activity in a sex-dependent manner in rats

Lyu, X.; Du, J.; Zhan, G.; Wu, Y.; Su, H.; Zhu, Y.; Jarskog, F.; Zhao, M.; Fan, X., 2018:
Naltrexone and Bupropion Combination Treatment for Smoking Cessation and Weight Loss in Patients With Schizophrenia

Windisch, K.A.; Reed, B.; Kreek, M.Jeanne., 2018:
Naltrexone and nalmefene attenuate cocaine place preference in male mice

Azizi, H.; Mirzaeei, H.; Nasiri, A.Akbar.; Bazi, A.; Mirzapour, A.; Khatami, M.; Nahavandi, K.Hatam.; Azimi, A.; Yaghoobi, H., 2018:
Naltrexone; as an efficient adjuvant in induction of Th1 immunity and protection against Fasciola hepatica infection

Sakloth, F.; Negus, S.Stevens., 2018:
Naltrexone maintenance fails to alter amphetamine effects on intracranial self-stimulation in rats

Koyyada, R.; Latchooman, N.; Jonaitis, J.; Ayoub, S.S.; Corcoran, O.; Casalotti, S.O., 2018:
Naltrexone Reverses Ethanol Preference and Protein Kinase C Activation in Drosophila melanogaster

Anonymous, 2018:
Nalwanga Juliet Sekabunga

Nguyen, M-Nuong.Thi.; Ho-Huynh, T-Duong., 2017:
Nam Dia long, a Vietnamese folk formula, induces apoptosis in MCF-7 cells through various mechanisms of action

Good, M.; McElroy, S.J.; Berger, J.N.; Wynn, J.L., 2018:
Name and Characteristics of National Institutes of Health R01-Funded Pediatric Physician-Scientists: Hope and Challenges for the Vanishing Pediatric Physician-Scientists

Chang, B.S., 2018:
Name as Many AEDs as You Can in One Minute: Antiepileptic Drugs and the Disruption of Verbal Fluency Networks

Gorshenina, M.A.; Robustova, V.V., 2018:
Name is a term in clinical terminology

Pilcher, J., 2017:
Names and "Doing Gender": How Forenames and Surnames Contribute to Gender Identities, Difference, and Inequalities

Anonymous, 1982:
names and faces

Anonymous, 2017:
names and faces

Anonymous, 2018:
names and faces

Anonymous, 2018:
Names and Theories

Anonymous, 2018:
Names and Things: The Universal Craving for Euphemisms

Anonymous, 2018:
Names in Nursing: A Call for Definitions in Terms

Diesfeld, K.; Surgenor, L.J.; Ip, M.; Kersey, K., 2018:
Name Suppression Practices of New Zealand’s Health Practitioners Disciplinary Tribunal 2004-2014

Spezzano, L.Carmen.; Radanovic, Márcia., 2010:
Naming abilities: Differentiation between objects and verbs in aphasia

Hübner, L.Cristine.; Loureiro, F.; Tessaro, B.; Siqueira, E.Cristina.Gerner.; Jerônimo, G.Machado.; Gomes, Iênio.; Schilling, L.Porcello., 2018:
Naming and verbal learning in adults with Alzheimer's disease, mild cognitive impairment and in healthy aging, with low educational levels

Hardeman, R.R.; Murphy, K.A.; Karbeah, J'Mag.; Kozhimannil, K.Backes., 2018:
Naming Institutionalized Racism in the Public Health Literature: A Systematic Literature Review

Nilsson, J.; Lövdén, M., 2018:
Naming is not explaining: future directions for the "cognitive reserve" and "brain maintenance" theories

Maroske, S.; May, T.W., 2018:
Naming names: the first women taxonomists in mycology

Wilson, S., 2018:
Naming the drugs we use: neuroscience-based nomenclature, a helpful innovation

Lyubarova, R.; Schulman-Marcus, J., 2018:
Naming the misfits - MINOCA, ACSNNOCA, and the rest of the family

Fileborn, B., 2018:
Naming the Unspeakable Harm of Street Harassment: A Survey-Based Examination of Disclosure Practices

Anonymous, 2018:
"Nam Lake: A holy and beautiful lake"

Travelli, C.; Colombo, G.; Mola, S.; Genazzani, A.A.; Porta, C., 2018:
NAMPT: A pleiotropic modulator of monocytes and macrophages

Hassan, B.; Baroukh, B.; Llorens, A.; Lesieur, J.; Ribbes, S.; Chaussain, C.; Saffar, J-Louis.; Gosset, M., 2018:
NAMPT expression in osteoblasts controls osteoclast recruitment in alveolar bone remodeling

Lucena-Cacace, A.; Otero-Albiol, D.; Jiménez-García, M.P.; Muñoz-Galvan, S.; Carnero, A., 2017:
NAMPT Is a Potent Oncogene in Colon Cancer Progression that Modulates Cancer Stem Cell Properties and Resistance to Therapy through Sirt1 and PARP

Nielsen, K.Nørgaard.; Peics, J.; Ma, T.; Karavaeva, I.; Dall, M.; Chubanava, S.; Basse, A.L.; Dmytriyeva, O.; Treebak, J.T.; Gerhart-Hines, Z., 2018:
NAMPT-mediated NAD + biosynthesis is indispensable for adipose tissue plasticity and development of obesity

Lucena-Cacace, A.; Otero-Albiol, D.; Jiménez-García, M.P.; Peinado-Serrano, J.; Carnero, A., 2017:
NAMPT overexpression induces cancer stemness and defines a novel tumor signature for glioma prognosis

Pylaeva, E.; Harati, M.Dehghan.; Spyra, I.; Bordbari, S.; Strachan, S.; Thakur, B.Kumar.; Höing, B.; Franklin, C.; Skokowa, J.; Welte, K.; Schadendorf, D.; Bankfalvi, A.; Brandau, S.; Lang, S.; Jablonska, J., 2018:
NAMPT signaling is critical for the proangiogenic activity of tumor-associated neutrophils

Nakamae, S.; Toba, Y.; Takayama, K.; Sakurai, F.; Mizuguchi, H., 2018:
Nanaomycin A Treatment Promotes Hepatoblast Differentiation from Human iPS Cells

Queller, D.C., 2018:
Nancy A. Moran - Recipient of the 2017 Molecular Ecology Prize

Anonymous, 2018:
Nancy B. Esterly, MD: The mother of pediatric dermatology

Craig, J.M., 2018:
Nancy L. Segal and Yesika S. Monto: Accidental Brothers: The Story of Twins Exchanged at Birth and the Power of Nature and Nurture : St Martin's Press, New York, 2018, 325 pp, ISBN: 9781250101907

Anonymous, 2018:
Nancy Petry: 1 November 1968 - 17 July 2018

Mohamed, A.El.Ruby.; Barghi, S.; Rohani, S., 2018:
N- and C-Modified TiO₂ Nanotube Arrays: Enhanced Photoelectrochemical Properties and Effect of Nanotubes Length on Photoconversion Efficiency

Ziegler, C.Cathleen.; Lauderdale, J., 2016:
Nandi Traditional Healers: Sentinels in An Underserved Environment

Stavenhagen, K.; Kayili, H.Mehmet.; Holst, S.; Koeleman, C.A.M.; Engel, R.; Wouters, D.; Zeerleder, S.; Salih, B.; Wuhrer, M., 2017:
N- and O -glycosylation Analysis of Human C1-inhibitor Reveals Extensive Mucin-type O -Glycosylation

Ramasamy, D.Lakshmi.; Puhakka, V.; Iftekhar, S.; Wojtuś, A.; Repo, E.; Ben Hammouda, S.; Iakovleva, E.; Sillanpää, M., 2018:
N- and O- ligand doped mesoporous silica-chitosan hybrid beads for the efficient, sustainable and selective recovery of rare earth elements (REE) from acid mine drainage (AMD): Understanding the significance of physical modification and conditioning of the polymer

Melo Junior, A.F.; Dalpiaz, P.L.M.; Sousa, G.J.; Oliveira, P.Wendell.C.; Birocale, Aônio.M.; Andrade, T.U.; Abreu, Gáucia.R.; Bissoli, Né.S., 2018:
Nandrolone alter left ventricular contractility and promotes remodelling involving calcium-handling proteins and renin-angiotensin system in male SHR

Guzzoni, V.; Cunha, T.Sousa.; das Neves, V.José.; Briet, L.; Costa, R.; Moura, M.José.Costa.Sampaio.; Oliveira, V.; Franco, M.do.Carmo.Pinho.; Novaes, P.Duarte.; Marcondes, F.Klein., 2018:
Nandrolone combined with strenuous resistance training reduces vascular nitric oxide bioavailability and impairs endothelium-dependent vasodilation

Sretenovic, J.; Ajdzanovic, V.; Zivkovic, V.; Srejovic, I.; Corbic, M.; Milosevic, V.; Jakovljevic, V.; Milosavljevic, Z., 2018:
Nandrolone decanoate and physical activity affect quadriceps in peripubertal rats

Guimarães, A.Paula.Franttini.Garcia.Moreno.; Butezloff, M.Maloste.; Zamarioli, A.; Issa, Jão.Paulo.Mardegan.; Volpon, Jé.Batista., 2017:
Nandrolone decanoate appears to increase bone callus formation in young adult rats after a complete femoral fracture

Liu, X-Hua.; De Gasperi, R.; Bauman, W.A.; Cardozo, C.P., 2018:
Nandrolone-induced nuclear accumulation of MyoD protein is mediated by Numb, a Notch inhibitor, in C2C12 myoblasts

Riedl, C.A.; Hejl, M.; Klose, M.H.M.; Roller, A.; Jakupec, M.A.; Kandioller, W.; Keppler, B.K., 2018:
N- and S-donor leaving groups in triazole-based ruthena(ii)cycles: potent anticancer activity, selective activation, and mode of action studies

Xu, Y.; Xiao, H-Yun.; Zheng, N-Jian.; Zhang, Z-Yi.; Qu, L-Lu.; Zhao, J-Jing., 2016:
N% and S% in Leaves of Vascular Plants <i>Cinnamomum camphora</i> and <i>Pinus massoniana</i> Lamb. for Indicating the Spatial Variation of Atmospheric Nitrogen and Sulfur Deposition

Kamada, T.; Phan, C-Soon.; Vairappan, C.S., 2017:
Nangallenes A and B, halogenated nonterpenoid C 15 -acetogenins from the Bornean red alga Laurencia nangii

Li, J.; McClane, B.A., 2017:
NanI Sialidase Can Support the Growth and Survival of Clostridium perfringens Strain F4969 in the Presence of Sialyated Host Macromolecules (Mucin) or Caco-2 Cells

Anonymous, 2018:
NANNAHEIM Is the Place to Be This Fall!

Anonymous, 2017:
NANN Celebrates Neonatal Nurses Day

Mohr, K.I.; Moradi, A.; Glaeser, S.P.; Kämpfer, P.; Gemperlein, K.; Nübel, U.; Schumann, P.; Müller, R.; Wink, J., 2018:
Nannocystis konarekensis sp. nov., a novel myxobacterium from an Iranian desert

Li, Y.; Zhu, R.; Wang, J.; Li, Z-Sheng.; Xu, N.; Zhang, J.; Wang, P., 2017:
N-Annulated Perylene-Based Hole Transporters for Perovskite Solar Cells: The Significant Influence of Lateral Substituents

López-Marzo, A.M.; Hoyos-de-la-Torre, R.; Baldrich, E., 2018:
NaNO 3 /NaCl Oxidant and Polyethylene Glycol (PEG) Capped Gold Nanoparticles (AuNPs) as a Novel Green Route for AuNPs Detection in Electrochemical Biosensors

Zare, E.Nazarzadeh.; Motahari, A.; Sillanpää, M., 2018:
Nanoadsorbents based on conducting polymer nanocomposites with main focus on polyaniline and its derivatives for removal of heavy metal ions/dyes: A review

Fracasso, G.; Ghigna, P.; Nodari, L.; Agnoli, S.; Badocco, D.; Pastore, P.; Nicolato, E.; Marzola, P.; Mihajlović, Dšan.; Markovic, M.; Čolić, M.; Amendola, V., 2018:
Nanoaggregates of iron poly-oxo-clusters obtained by laser ablation in aqueous solution of phosphonates

Zhang, Y.; Liu, X.; Li, Z.; Zhu, S.; Yuan, X.; Cui, Z.; Yang, X.; Chu, P.K.; Wu, S., 2017:
Nano Ag/ZnO-Incorporated Hydroxyapatite Composite Coatings: Highly Effective Infection Prevention and Excellent Osteointegration

Fang, H.; Yang, J.; Wen, M.; Wu, Q., 2018:
Nanoalloy Materials for Chemical Catalysis

Sun, Y.; Wu, Q.; Shi, X.; Gao, J.; Dong, S.; Zhao, L., 2018:
Nano-amylose-2,3-bis(3,5-dimethylphenylcarbamate)-silica hybrid sol immobilized on open tubular capillary column for capillary electrochromatography enantioseparation

Faucher, Séphane.; Le Coustumer, P.; Lespes, Gëtane., 2018:
Nanoanalytics: history, concepts, and specificities

Ye, J-Hui.; Augustin, M.Ann., 2018:
Nano- and micro-particles for delivery of catechins: Physical and biological performance

Scharin-Mehlmann, M.; Häring, A.; Rommel, M.; Dirnecker, T.; Friedrich, O.; Frey, L.; Gilbert, D.F., 2018:
Nano- and Micro-Patterned S-, H-, and X-PDMS for Cell-Based Applications: Comparison of Wettability, Roughness, and Cell-Derived Parameters

Ma, Y.; Qiao, S-Lin.; Wang, Y.; Lin, Y-Xin.; An, H-Wei.; Wu, X-Chun.; Wang, L.; Wang, H., 2017:
Nanoantagonists with nanophase-segregated surfaces for improved cancer immunotherapy

Muzammil, S.; Hayat, S.; Fakhar-E-Alam, M.; Aslam, B.; Siddique, M.Hussnain.; Nisar, M.Atif.; Saqalein, M.; Atif, M.; Sarwar, A.; Khurshid, A.; Amin, N.; Wang, Z., 2018:
Nanoantibiotics: Future nanotechnologies to combat antibiotic resistance

Khurana, C.; Chudasama, B., 2018:
Nanoantibiotics: strategic assets in the fight against drug-resistant superbugs

Pu, M.; Li, X.; Guo, Y.; Ma, X.; Luo, X., 2017:
Nanoapertures with ordered rotations: symmetry transformation and wide-angle flat lensing

Nayak, A.; Unayama, S.; Tai, S.; Tsuruoka, T.; Waser, R.; Aono, M.; Valov, I.; Hasegawa, T., 2018:
Nanoarchitectonics for Controlling the Number of Dopant Atoms in Solid Electrolyte Nanodots

Ariga, K.; Mori, T.; Shrestha, L.Kumar., 2017:
Nanoarchitectonics from Molecular Units to Living-Creature-Like Motifs

Kim, Y.; Meade, S.M.; Chen, K.; Feng, H.; Rayyan, J.; Hess-Dunning, A.; Ereifej, E.S., 2018:
Nano-Architectural Approaches for Improved Intracortical Interface Technologies

Shaikh, J.S.; Shaikh, N.S.; Mali, S.S.; Patil, J.V.; Pawar, K.K.; Kanjanaboos, P.; Hong, C.Kook.; Kim, J.H.; Patil, P.S., 2018:
Nanoarchitectures in dye-sensitized solar cells: metal oxides, oxide perovskites and carbon-based materials

Zore, O.V.; Pande, P.; Okifo, O.; Basu, A.K.; Kasi, R.M.; Kumar, C.V., 2018:
Nanoarmoring: strategies for preparation of multi-catalytic enzyme polymer conjugates and enhancement of high temperature biocatalysis

Ly, J.; Li, Y.; Vu, M.N.; Moffat, B.A.; Jack, K.S.; Quinn, J.F.; Whittaker, M.R.; Davis, T.P., 2018:
Nano-assemblies of cationic mPEG brush block copolymers with gadolinium polyoxotungstate [Gd(W 5 O 18 ) 2 ] 9- form stable, high relaxivity MRI contrast agents

Misra, S.K.; Kampert, T.L.; Pan, D., 2018:
Nano-Assembly of Pamitoyl-Bioconjugated Coenzyme-A for Combinatorial Chemo-Biologics in Transcriptional Therapy

Nguyen, M.; Kim, S.; Tran, T.Trong.; Xu, Z-Quan.; Kianinia, M.; Toth, M.; Aharonovich, I., 2018:
Nanoassembly of quantum emitters in hexagonal boron nitride and gold nanospheres

Guo, Y.; Zhang, X.; Hao, W.; Xie, Y.; Chen, L.; Li, Z.; Zhu, B.; Feng, X., 2018:
Nano-bacterial cellulose/soy protein isolate complex gel as fat substitutes in ice cream model

Buss, J.Huch.; Begnini, K.Rech.; Bender, C.Bonemann.; Pohlmann, A.R.; Guterres, S.S.; Collares, T.; Seixas, F.Kömmling., 2018:
Nano-BCG: A Promising Delivery System for Treatment of Human Bladder Cancer

Yang, Y.; Li, Y.Gang.; Short, M.P.; Kim, C-Soo.; Berggren, K.K.; Li, J., 2018:
Nano-beam and nano-target effects in ion radiation

Zhu, Q.; Zhuang, W.; Chen, Y.; Wang, Z.; Villacorta Hernandez, B.; Wu, J.; Yang, P.; Liu, D.; Zhu, C.; Ying, H.; Zhu, Z., 2018:
Nano-Biocatalysts of Cyt c@ZIF-8/GO Composites with High Recyclability via a de Novo Approach

Hasan, A.; Waibhaw, G.; Saxena, V.; Pandey, L.M., 2018:
Nano-biocomposite scaffolds of chitosan, carboxymethyl cellulose and silver nanoparticle modified cellulose nanowhiskers for bone tissue engineering applications

Chander, N.Gopi., 2018:
Nano-bio interactions

Byrne, H.J.; Mukherjee, S.P.; Naha, P.C., 2018:
Nano⁻Bio Interactions: Nanomedicine and Nanotoxicology

Benetti, E.M.; Textor, M.; Duan, H., 2018:
Nanobiointerfaces: a themed collection

Cicciù, M., 2018:
Nanobiomaterials in dentistry: What's the consequent level

Timerbulatov, S.V.; Valiev, R.Z.; Timerbulatov, M.V., 2018:
Nanobiomedical technologies in surgery

Yang, N.; Zhang, W.; Ye, C.; Chen, X.; Ling, S., 2018:
Nanobiopolymers Fabrication and Their Life Cycle Assessments

Golichenari, B.; Nosrati, R.; Farokhi-Fard, A.; Abnous, K.; Vaziri, F.; Behravan, J., 2018:
Nano-biosensing approaches on tuberculosis: Defy of aptamers

Suhito, I.Rosalina.; Angeline, N.; Choo, S-Sik.; Woo, H.Young.; Paik, T.; Lee, T.; Kim, T-Hyung., 2018:
Nanobiosensing Platforms for Real-Time and Non-Invasive Monitoring of Stem Cell Pluripotency and Differentiation

Seifati, S.Morteza.; Nasirizadeh, N.; Azimzadeh, M., 2018:
Nano-biosensor based on reduced graphene oxide and gold nanoparticles, for detection of phenylketonuria-associated DNA mutation

Salahandish, R.; Ghaffarinejad, A.; Naghib, S.Morteza.; Majidzadeh-A, K.; Zargartalebi, H.; Sanati-Nezhad, A., 2018:
Nano-biosensor for highly sensitive detection of HER2 positive breast cancer

Moradi, S.; Khaledian, S.; Abdoli, M.; Shahlaei, M.; Kahrizi, D., 2018:
Nano-biosensors in cellular and molecular biology

Chamorro-Garcia, A.; Merkoçi, A., 2016 :
Nanobiosensors in diagnostics

Torres, L.M.F.C.; Braga, N.A.; Gomes, I.P.; Almeida, M.T.; Santos, T.L.; de Mesquita, J.P.; da Silva, L.M.; Martins, H.R.; Kato, K.C.; Dos Santos, W.T.P.; Resende, J.M.; Pereira, M.C.; Bemquerer, M.P.; Rodrigues, M.A.; Verly, R.M., 2018:
Nanobiostructure of fibrous-like alumina functionalized with an analog of the BP100 peptide: Synthesis, characterization and biological applications

Chen, S.; Liang, X-Jie., 2018:
Nanobiotechnology and nanomedicine: small change brings big difference

Barabadi, H., 2018:
Nanobiotechnology: A promising scope of gold biotechnology

Durán, N.; Simões, M.B.; de Moraes, A.C.M.; Fávaro, W.J.; Seabra, A.B., 2018:
Nanobiotechnology of Carbon Dots: A Review

Liu, P.; Fang, X.; Cao, H.; Gu, M.; Kong, J.; Deng, A., 2018:
Nano-biotinylated liposome-based immunoassay for the ultrasensitive detection of protein biomarker in urine

Rezaei, M.; Farhadian, M.; Rashidi, A.Mohammad.; Saeidipour, M.; Manshaei, M.; Rezaee, M., 2018:
Nano-Biphasic Calcium Phosphate Ceramic for the Repair of Bone Defects

Song, Y.; Lin, K.; He, S.; Wang, C.; Zhang, S.; Li, D.; Wang, J.; Cao, T.; Bi, L.; Pei, G., 2018:
Nano-biphasic calcium phosphate/polyvinyl alcohol composites with enhanced bioactivity for bone repair via low-temperature three-dimensional printing and loading with platelet-rich fibrin

Yang, X.; Liu, G.; Shi, Y.; Huang, W.; Shao, J.; Dong, X., 2018:
Nano-black phosphorus for combined cancer phototherapy: recent advances and prospects

Allegra, A.; Innao, V.; Gerace, D.; Vaddinelli, D.; Allegra, A.Gaetano.; Musolino, C., 2018 :
Nanobodies and Cancer: Current Status and New Perspectives

Bannas, P.; Hambach, J.; Koch-Nolte, F., 2017:
Nanobodies and Nanobody-Based Human Heavy Chain Antibodies As Antitumor Therapeutics