+ Site Statistics
References:
52,654,530
Abstracts:
29,560,856
PMIDs:
28,072,755
+ Search Articles
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ PDF Full Text
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Translate
+ Recently Requested

Get PDF Full Texts from EurekaMag Chapter 55340

Chapter 55340 provides scholary research titles of which PDF Full Texts are available through EurekaMag.





Ismael, O.; Shimada, A.; Elmahdi, S.; Elshazley, M.; Muramatsu, H.; Hama, A.; Takahashi, Y.; Yamada, M.; Yamashita, Y.; Horide, K.; Kojima, S., 2014:
RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22)

Schnittger, S.; Dicker, F.; Kern, W.; Wendland, N.; Sundermann, J.; Alpermann, T.; Haferlach, C.; Haferlach, T., 2011:
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis

Butcher, C.M.; Neufing, P.J.; Eriksson, L.; Carmichael, C.L.; Wilkins, E.J.; Melo, J.V.; Lewis, I.D.; Bardy, P.G.; Scott, H.S.; D'Andrea, R.J., 2011:
RUNX1 mutations are rare in chronic phase polycythaemia vera

Gaidzik, V.I.; Bullinger, L.; Schlenk, R.F.; Zimmermann, A.S.; Röck, Jürgen.; Paschka, P.; Corbacioglu, A.; Krauter, Jürgen.; Schlegelberger, B.; Ganser, A.; Späth, D.; Kündgen, A.; Schmidt-Wolf, I.G.H.; Götze, K.; Nachbaur, D.; Pfreundschuh, M.; Horst, H.A.; Döhner, H.; Döhner, K., 2011:
RUNX1 mutations in acute myeloid leukemia: results from a comprehensive genetic and clinical analysis from the AML study group

Mangan, J.K.; Speck, N.A., 2012:
RUNX1 mutations in clonal myeloid disorders: from conventional cytogenetics to next generation sequencing, a story 40 years in the making

Greif, P.A.; Konstandin, N.P.; Metzeler, K.H.; Herold, T.; Pasalic, Z.; Ksienzyk, B.; Dufour, A.; Schneider, F.; Schneider, S.; Kakadia, P.M.; Braess, J.; Sauerland, M.Cristina.; Berdel, W.E.; Büchner, T.; Woermann, B.J.; Hiddemann, W.; Spiekermann, K.; Bohlander, S.K., 2013:
RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes

Mok, M.Meng.Huang.; Du, L.; Wang, C.Qiuxia.; Tergaonkar, V.; Liu, T.Chih.; Yin Kham, S.Kow.; Sanda, T.; Yeoh, A.Eng-Juh.; Osato, M., 2014:
RUNX1 point mutations potentially identify a subset of early immature T-cell acute lymphoblastic leukaemia that may originate from differentiated T-cells

Lie-A-Ling, M.; Marinopoulou, E.; Li, Y.; Patel, R.; Stefanska, M.; Bonifer, C.; Miller, C.; Kouskoff, V.; Lacaud, G., 2014:
RUNX1 positively regulates a cell adhesion and migration program in murine hemogenic endothelium prior to blood emergence

Hu, Z.; Gu, X.; Baraoidan, K.; Ibanez, V.; Sharma, A.; Kadkol, S.; Munker, R.; Ackerman, S.; Nucifora, G.; Saunthararajah, Y., 2011:
RUNX1 regulates corepressor interactions of PU.1

Edwards, H.; Xie, C.; LaFiura, K.M.; Dombkowski, A.A.; Buck, S.A.; Boerner, J.L.; Taub, J.W.; Matherly, L.H.; Ge, Y., 2009:
RUNX1 regulates phosphoinositide 3-kinase/AKT pathway: role in chemotherapy sensitivity in acute megakaryocytic leukemia

Liang, X-Lei.; Wang, X-Yan.; Gao, J.; Yao, H-Yu.; Chen, C.; Liu, Y-Lin.; Wu, Y.; Mao, N., 2012:
RUNX1 regulates transcription activity of WNT5A in mouse bone marrow derived mesenchymal stem cells

Hyde, R.Katherine.; Liu, P.Paul., 2010:
RUNX1 repression-independent mechanisms of leukemogenesis by fusion genes CBFB-MYH11 and AML1-ETO (RUNX1-RUNX1T1)

D.B.aekeleer, E.; Douet-Guilbert, N.; Morel, Fédéric.; L.B.is, M-Josée.; Férec, C.; D.B.aekeleer, M., 2011:
RUNX1 translocations and fusion genes in malignant hemopathies

D.B.aekeleer, E.; Férec, C.; D.B.aekeleer, M., 2009:
RUNX1 translocations in malignant hemopathies

van Bragt, M.P.A.; Hu, X.; Xie, Y.; Li, Z., 2015:
RUNX1, a transcription factor mutated in breast cancer, controls the fate of ER-positive mammary luminal cells

DeKelver, R.C.; Lewin, B.; Weng, S.; Yan, M.; Biggs, J.; Zhang, D-Er., 2015:
RUNX1-ETO induces a type I interferon response which negatively effects t(8;21)-induced increased self-renewal and leukemia development

Athanasiadou, A.; Stalika, E.; Sidi, V.; Papaioannou, M.; Gaitatzi, M.; Anagnostopoulos, A., 2011:
RUNX1-MTG16 fusion gene in de novo acute myeloblastic leukemia with t(16;21)(q24;q22)

Cieslak, A.; L.N.ir, S.; Trinquand, Aélie.; Lhermitte, L.; Franchini, D-Marc.; Villarese, P.; Gon, Séphanie.; Bond, J.; Simonin, M.; Vanhille, L.; Vanhile, L.; Reimann, C.; Verhoeyen, E.; Larghero, J.; Six, E.; Spicuglia, S.; André-Schmutz, I.; Langerak, A.; Nadel, B.; Macintyre, E.; Payet-Bornet, D.; Asnafi, V., 2014:
RUNX1-dependent RAG1 deposition instigates human TCR-δ locus rearrangement

Yan, M.; Ahn, E-Young.; Hiebert, S.W.; Zhang, D-Er., 2008:
RUNX1/AML1 DNA-binding domain and ETO/MTG8 NHR2-dimerization domain are critical to AML1-ETO9a leukemogenesis

Kaur, G.; Jalagadugula, G.; Mao, G.; Rao, A.Koneti., 2010:
RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency

Rossetti, S.; Sacchi, N., 2013:
RUNX1: A microRNA hub in normal and malignant hematopoiesis

Binato, R.; Mencalha, A.; Pizzatti, L.; Scholl, V.; Zalcberg, I.; Abdelhay, E., 2009:
RUNX1T1 is overexpressed in imatinib mesylate-resistant cells

Huynh, M.Tuan.; Béri-Dexheimer, Mène.; Bonnet, Céline.; Bronner, M.; Khan, A.Ali.; Allou, L.; Philippe, C.; Vigneron, J.; Jonveaux, P., 2012:
RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability

Migas, A.A.; Mishkova, O.A.; Ramanouskaya, T.V.; Ilyushonak, I.M.; Aleinikova, O.V.; Grinev, V.V., 2014 :
RUNX1T1/MTG8/ETO gene expression status in human t(8;21)(q22;q22)-positive acute myeloid leukemia cells

Nasir, A.; Helm, J.; Turner, L.; Chen, D-Tsa.; Strosberg, J.; Hafez, N.; Henderson-Jackson, E.B.; Hodul, P.; Bui, M.M.; Nasir, N.A.; Hakam, A.; Malafa, M.P.; Yeatman, T.J.; Coppola, D.; Kvols, L.K., 2011:
RUNX1T1: a novel predictor of liver metastasis in primary pancreatic endocrine neoplasms

Hansen, L.; Riis, A.K.; Silahtaroglu, A.; Hove, H.; Lauridsen, E.; Eiberg, H.; Kreiborg, S., 2011:
RUNX2 analysis of Danish cleidocranial dysplasia families

McDonald, L.; Ferrari, N.; Terry, A.; Bell, M.; Mohammed, Z.M.; Orange, C.; Jenkins, A.; Muller, W.J.; Gusterson, B.A.; Neil, J.C.; Edwards, J.; Morris, J.S.; Cameron, E.R.; Blyth, K., 2014:
RUNX2 correlates with subtype-specific breast cancer in a human tissue microarray, and ectopic expression of Runx2 perturbs differentiation in the mouse mammary gland

Boregowda, R.K.; Olabisi, O.O.; Abushahba, W.; Jeong, B-Seon.; Haenssen, K.K.; Chen, W.; Chekmareva, M.; Lasfar, A.; Foran, D.J.; Goydos, J.S.; Cohen-Solal, K.A., 2014:
RUNX2 is overexpressed in melanoma cells and mediates their migration and invasion

Li, Y.; Pan, W.; Xu, W.; He, N.; Chen, X.; Liu, H.; Darryl Quarles, L.; Zhou, H.; Xiao, Z., 2009:
RUNX2 mutations in Chinese patients with cleidocranial dysplasia

Lin, W-De.; Lin, S-Pei.; Wang, C-Hsing.; Tsai, Y.; Chen, C-Ping.; Tsai, F-Jen., 2011:
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia

Lee, K-E.; Seymen, F.; Ko, J.; Yildirim, M.; Tuna, E.B.; Gencay, K.; Kim, J-W., 2014:
RUNX2 mutations in cleidocranial dysplasia

Ryoo, H-M.; Kang, H-Y.; Lee, S-K.; Lee, K-E.; Kim, J-W., 2010:
RUNX2 mutations in cleidocranial dysplasia patients

Liu, Y.; Zhao, Y.; Chen, Y.; Shi, G.; Yuan, W., 2010:
RUNX2 polymorphisms associated with OPLL and OLF in the Han population

Greives, M.R.; Odessey, E.A.; Waggoner, D.J.; Shenaq, D.S.; Aradhya, S.; Mitchell, A.; Whitcomb, E.; Warshawsky, N.; He, T-Chuan.; Reid, R.R., 2014:
RUNX2 quadruplication: additional evidence toward a new form of syndromic craniosynostosis

Olfa, G.; Christophe, C.; Philippe, L.; Romain, S.; Khaled, H.; Pierre, H.; Odile, B.; Jean-Christophe, D., 2010:
RUNX2 regulates the effects of TNFalpha on proliferation and apoptosis in SaOs-2 cells

Pointer, M.A.; Kamilar, J.M.; Warmuth, V.; Chester, S.G.B.; Delsuc, Fédéric.; Mundy, N.I.; Asher, R.J.; Bradley, B.J., 2012:
RUNX2 tandem repeats and the evolution of facial length in placental mammals

Park, E-Sil.; Lind, A-Karin.; Dahm-Kähler, P.; Brännström, M.; Carletti, M.Z.; Christenson, L.K.; Curry, T.E.; Jo, M., 2010:
RUNX2 transcription factor regulates gene expression in luteinizing granulosa cells of rat ovaries

Huang, X.; Hao, C.; Shen, X.; Zhang, Y.; Liu, X., 2014:
RUNX2, GPX3 and PTX3 gene expression profiling in cumulus cells are reflective oocyte/embryo competence and potentially reliable predictors of embryo developmental competence in PCOS patients

Ito, K.; Lim, A.Chee-Beng.; Salto-Tellez, M.; Motoda, L.; Osato, M.; Chuang, L.Shyue.Huey.; Lee, C.Wei.Lin.; Voon, D.Chih-Cheng.; Koo, J.Kin.Wai.; Wang, H.; Fukamachi, H.; Ito, Y., 2008:
RUNX3 attenuates beta-catenin/T cell factors in intestinal tumorigenesis

Watanabe, T.; Kobunai, T.; Ikeuchi, H.; Yamamoto, Y.; Matsuda, K.; Ishihara, S.; Nozawa, K.; Iinuma, H.; Kanazawa, T.; Tanaka, T.; Yokoyama, T.; Konishi, T.; Eshima, K.; Ajioka, Y.; Hibi, T.; Watanabe, M.; Muto, T.; Nagawa, H., 2011:
RUNX3 copy number predicts the development of UC-associated colorectal cancer

Gao, J.; Chen, Y.; Wu, K-Chun.; Liu, J.; Zhao, Y-Qiu.; Pan, Y-Lin.; Du, R.; Zheng, G-Rong.; Xiong, Y-Min.; Xu, H-Lin.; Fan, D-Ming., 2010:
RUNX3 directly interacts with intracellular domain of Notch1 and suppresses Notch signaling in hepatocellular carcinoma cells

Ge, M-Hua.; Ling, Z-Qiang.; Tan, Z.; Chen, C.; Zheng, C-Ming.; Xu, J-Jie.; Zhu, X., 2011:
RUNX3 expression and its methylation of 5'-CpG island in salivary gland adenoid cystic carcinoma cell lines ACC-2, ACC-3 and ACC-M

Ogasawara, N.; Tsukamoto, T.; Mizoshita, T.; Inada, K-I.; Ban, H.; Kondo, S.; Takasu, S.; Ushijima, T.; Ito, K.; Ito, Y.; Ichinose, M.; Ogawa, T.; Joh, T.; Tatematsu, M., 2008:
RUNX3 expression correlates with chief cell differentiation in human gastric cancers

Zheng, Z.; Zhu, L.; Zhang, X.; Li, L.; Moon, S.; Roh, M.Ryung.; Jin, Z., 2015:
RUNX3 expression is associated with sensitivity to pheophorbide a-based photodynamic therapy in keloids

Bledsoe, K.L.; McGee-Lawrence, M.E.; Camilleri, E.T.; Wang, X.; Riester, S.M.; van Wijnen, A.J.; Oliveira, A.M.; Westendorf, J.J., 2014:
RUNX3 facilitates growth of Ewing sarcoma cells

Zhang, S.; Wei, L.; Zhang, A.; Zhang, L.; Yu, H., 2009:
RUNX3 gene methylation in epithelial ovarian cancer tissues and ovarian cancer cell lines

Kang, H-Feng.; Dai, Z-Jun.; Bai, H-Ping.; Lu, W-Feng.; Ma, X-Bin.; Bao, X.; Lin, S.; Wang, X-Jing., 2013:
RUNX3 gene promoter demethylation by 5-Aza-CdR induces apoptosis in breast cancer MCF-7 cell line

Tsunematsu, T.; Kudo, Y.; Iizuka, S.; Ogawa, I.; Fujita, T.; Kurihara, H.; Abiko, Y.; Takata, T., 2009:
RUNX3 has an oncogenic role in head and neck cancer

Ito, K., 2011:
RUNX3 in oncogenic and anti-oncogenic signaling in gastrointestinal cancers

Subramaniam, M.Mani.; Chan, J.Yongsheng.; Soong, R.; Ito, K.; Ito, Y.; Yeoh, K.Guan.; Salto-Tellez, M.; Putti, T.Choudary., 2008:
RUNX3 inactivation by frequent promoter hypermethylation and protein mislocalization constitute an early event in breast cancer progression

Tong, D-Dan.; Jiang, Y.; Li, M.; Kong, D.; Meng, X-Nin.; Zhao, Y-Zhen.; Jin, Y.; Bai, J.; Fu, S-Bin.; Geng, J-Shu., 2009:
RUNX3 inhibits cell proliferation and induces apoptosis by TGF-beta-dependent and -independent mechanisms in human colon carcinoma cells

Li, X.; Zhang, Y.; Zhang, Y.; Qiao, T.; Wu, K.; Ding, J.; Liu, J.; Fan, D., 2008:
RUNX3 inhibits growth of HCC cells and HCC xenografts in mice in combination with adriamycin

Liu, Z.; Zhang, X.; Xu, X.; Chen, L.; Li, W.; Yu, H.; Sun, Y.; Zeng, J.; Jia, J., 2014:
RUNX3 inhibits survivin expression and induces cell apoptosis in gastric cancer

Chuang, L.Shyue.Huey.; Lai, S.Kuan.; Murata-Hori, M.; Yamada, A.; Li, H-Yeung.; Gunaratne, J.; Ito, Y., 2012:
RUNX3 interactome reveals novel centrosomal targeting of RUNX family of transcription factors

Bai, J.; Yong, H-Mei.; Chen, F-Fei.; Song, W-Bo.; Li, C.; Liu, H.; Zheng, J-Nian., 2013:
RUNX3 is a prognostic marker and potential therapeutic target in human breast cancer

Ito, Y., 2012:
RUNX3 is expressed in the epithelium of the gastrointestinal tract

Guo, C.; Ren, F.; Wang, D.; Li, Y.; Liu, K.; Liu, S.; Chen, P., 2015:
RUNX3 is inactivated by promoter hypermethylation in malignant transformation of ovarian endometriosis

Fu, Y.; Chang, A.Chia.Yu.; Fournier, Mèle.; Chang, L.; Niessen, K.; Karsan, A., 2011 :
RUNX3 maintains the mesenchymal phenotype after termination of the Notch signal

He, L.; Zhao, X.; Wang, H.; Zhang, P.; Guo, C.; Huang, C.; Liu, X.; Yao, F.; Chen, Y.; Lou, W.; Sun, S.; Fan, D., 2012:
RUNX3 mediates suppression of tumor growth and metastasis of human CCRCC by regulating cyclin related proteins and TIMP-1

Li, W-Qing.; Pan, K-Feng.; Zhang, Y.; Dong, C-Xuan.; Zhang, L.; Ma, J-Ling.; Zhou, T.; Li, J-You.; You, W-Cheng., 2011:
RUNX3 methylation and expression associated with advanced precancerous gastric lesions in a Chinese population

Knapp, D.W., 2008:
RUNX3 methylation and the potential to predict the behavior of bladder cancer

Yan, C.; Kim, Y-Won.; Ha, Y-Sok.; Kim, I.Yi.; Kim, Y-June.; Yun, S-Joong.; Moon, S-Kwon.; Bae, S-Chul.; Kim, W-Jae., 2012:
RUNX3 methylation as a predictor for disease progression in patients with non-muscle-invasive bladder cancer

Jeong, P.; Min, B.D.; Ha, Y.S.; Song, P.H.; Kim, I.Y.; Ryu, K.H.; Kim, J.H.; Yun, S.J.; Kim, W.J., 2013:
RUNX3 methylation in normal surrounding urothelium of patients with non-muscle-invasive bladder cancer: potential role in the prediction of tumor progression

Wolff, E.M.; Liang, G.; Cortez, C.C.; Tsai, Y.C.; Castelao, J.Esteban.; Cortessis, V.K.; Tsao-Wei, D.D.; Groshen, S.; Jones, P.A., 2008:
RUNX3 methylation reveals that bladder tumors are older in patients with a history of smoking

Yamada, C.; Ozaki, T.; Ando, K.; Suenaga, Y.; Inoue, K-ichi.; Ito, Y.; Okoshi, R.; Kageyama, H.; Kimura, H.; Miyazaki, M.; Nakagawara, A., 2010:
RUNX3 modulates DNA damage-mediated phosphorylation of tumor suppressor p53 at Ser-15 and acts as a co-activator for p53

Tang, Y.; Wu, F.; Hu, C., 2012:
RUNX3 promoter hypermethylation and prognosis of early surgically resected non-small cell lung cancers

Nishio, M.; Sakakura, C.; Nagata, T.; Komiyama, S.; Miyashita, A.; Hamada, T.; Kuryu, Y.; Ikoma, H.; Kubota, T.; Kimura, A.; Nakanishi, M.; Ichikawa, D.; Fujiwara, H.; Okamoto, K.; Ochiai, T.; Kokuba, Y.; Sonoyama, T.; Ida, H.; Ito, K.; Chiba, T.; Ito, Y.; Otsuji, E., 2010:
RUNX3 promoter methylation in colorectal cancer: its relationship with microsatellite instability and its suitability as a novel serum tumor marker

Nevadunsky, N.S.; Barbieri, J.S.; Kwong, J.; Merritt, M.A.; Welch, W.R.; Berkowitz, R.S.; Mok, S.C., 2008:
RUNX3 protein is overexpressed in human epithelial ovarian cancer

Estecha, A.; Aguilera-Montilla, Ní.; Sánchez-Mateos, P.; Puig-Kröger, A., 2012:
RUNX3 regulates intercellular adhesion molecule 3 (ICAM-3) expression during macrophage differentiation and monocyte extravasation

Liu, Z.; Chen, L.; Zhang, X.; Xu, X.; Xing, H.; Zhang, Y.; Li, W.; Yu, H.; Zeng, J.; Jia, J., 2015:
RUNX3 regulates vimentin expression via miR-30a during epithelial-mesenchymal transition in gastric cancer cells

Chen, F.; Bai, J.; Li, W.; Mei, P.; Liu, H.; Li, L.; Pan, Z.; Wu, Y.; Zheng, J., 2013:
RUNX3 suppresses migration, invasion and angiogenesis of human renal cell carcinoma

Dalcq, J.; Pasque, V.; Ghaye, Aélie.; Larbuisson, A.; Motte, P.; Martial, J.A.; Muller, M., 2013:
RUNX3, EGR1 and SOX9B form a regulatory cascade required to modulate BMP-signaling during cranial cartilage development in zebrafish

Brady, G.; Farrell, P.J., 2009:
RUNX3-mediated repression of RUNX1 in B cells

Parrella, J.; Wu, Y.; Kahn, D.W.; Genest, P., 2010:
RUNspike, a complementary virus filter spiking method: a solution to the problem of reduced throughput due to the addition of the virus spike

Zhang, H.; Balasubramanian, S.; Wei, R.; Austin, H.; Buchanan, S.; Herman, R.; He, J., 2011:
RUPERT closed loop control design

Magee, R., 1935:
RUPTURE OF THE DIAPHRAGM : (With report of two cases)

Beven, J.O., 1920:
RUPTURE OF VEIN OF DERMOID CYST: Intraperitoneal Haemorrhage: Operation: Recovery

Anonymous, 1946:
RURAL medicine, community hospitals and metropolitan assistance

Anonymous, 1948:
RURAL sewage disposal

Shetty, R.M.; Dixit, U.; Hegde, R.; Shivprakash, P.K., 2011:
RURS' elbow guard: an innovative treatment of the thumb-sucking habit in a child with Hurler's syndrome

Brown, J.R.; Zetsche, B.; Jackson-Grusby, L., 2014:
RUSH and CRUSH: a rapid and conditional RNA interference method in mice

Nottingham, R.M.; Ganley, I.G.; Barr, F.A.; Lambright, D.G.; Pfeffer, S.R., 2011:
RUTBC1 protein, a Rab9A effector that activates GTP hydrolysis by Rab32 and Rab33B proteins

Nottingham, R.M.; Pusapati, G.V.; Ganley, I.G.; Barr, F.A.; Lambright, D.G.; Pfeffer, S.R., 2012:
RUTBC2 protein, a Rab9A effector and GTPase-activating protein for Rab36

De, N.C., 2010:
RUTF: imported or indigenous

Anonymous, 1947:
RUTIN in the treatment of capillary fragility

Anonymous, 2010:
RUTIN to be commercially available for hypertension

Anonymous, 1947:
RUTIN; its clinical value

Taniuchi, K.; Furihata, M.; Iwasaki, S.; Tanaka, K.; Shimizu, T.; Saito, M.; Saibara, T., 2014:
RUVBL1 directly binds actin filaments and induces formation of cell protrusions to promote pancreatic cancer cell invasion

Drew, R.J.; Boyle, B., 2009:
RUWA scoring system: a novel predictive tool for the identification of patients at high risk for complications from Clostridium difficile infection

Pratali, L.; Allemann, Y.; Rimoldi, S.F.; Faita, F.; Hutter, D.; Rexhaj, E.; Brenner, R.; Bailey, D.M.; Sartori, C.; Salmon, C.Salinas.; Villena, M.; Scherrer, U.; Picano, E.; Sicari, R., 2014:
RV contractility and exercise-induced pulmonary hypertension in chronic mountain sickness: a stress echocardiographic and tissue Doppler imaging study

Bernier, M.; Josephson, M.E., 2010:
RV electrical activation in heart failure during right, left, and biventricular pacing

Sengupta, P.P.; Narula, J., 2013:
RV form and function: a piston pump, vortex impeller, or hydraulic ram?

Naeije, R., 2014:
RV is doing well at high altitudes!--Always?

D.M.ria, M.V.; Younoszai, A.K.; Mertens, L.; Landeck, B.F.; Ivy, D.Dunbar.; Hunter, K.S.; Friedberg, M.K., 2014:
RV stroke work in children with pulmonary arterial hypertension: estimation based on invasive haemodynamic assessment and correlation with outcomes

Fratz, S.; Stern, H., 2012:
RV volume measurements by CMR

Cooper, J.M.; Patel, R.K.; Emmi, A.; Wang, Y.; Kirkpatrick, J.N., 2014:
RV-only pacing can produce a Q wave in lead 1 and an R wave in V1: implications for biventricular pacing

Vanderpool, R.R.; Pinsky, M.R.; Naeije, R.; Deible, C.; Kosaraju, V.; Bunner, C.; Mathier, M.A.; Lacomis, J.; Champion, H.C.; Simon, M.A., 2015:
RV-pulmonary arterial coupling predicts outcome in patients referred for pulmonary hypertension

Meng, X.Lian.; Yang, J.Yu.; Chen, G.Liang.; Zhang, L.Jia.; Wang, L.Hui.; Li, J.; Wang, J.Ming.; Wu, C.Fu., 2008:
RV09, a novel resveratrol analogue, inhibits NO and TNF-alpha production by LPS-activated microglia

Weiner, D.B., 2013:
RV144: old vs. new

Jha, S.; Dutta, A., 2009:
RVB1/RVB2: running rings around molecular biology

Anonymous, 2014:
RVC academic features in diversity project

Anonymous, 2011:
RVC appoints its next principal

Anonymous, 2012:
RVC becomes an FAO reference centre for veterinary epidemiology

Anonymous, 2014:
RVC launches an exotics service for animals and their owners

Anonymous, 2014:
RVC opens dedicated clinic for brachycephalic dogs

Anonymous, 2011:
RVC opens second regional centre

Anonymous, 2013:
RVC reaccredited by the AVMA

Anonymous, 2014:
RVC recognised for its commitment to the environment

Cushing, A.; Flaherty, P.; Hopmans, E.; Bell, J.M.; Ji, H.P., 2013:
RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencing

Rohn, S.; Suttkus, A.; Arendt, T.; Ueberham, U., 2012:
RVG peptide as transfection reagent for specific cdk4 gene silencing in vitro and in vivo

Son, S.; Hwang, D.Won.; Singha, K.; Jeong, J.Hoon.; Park, T.Gwan.; Lee, D.Soo.; Kim, W.Jong., 2012:
RVG peptide tethered bioreducible polyethylenimine for gene delivery to brain

Gao, Y.; Wang, Z-You.; Zhang, J.; Zhang, Y.; Huo, H.; Wang, T.; Jiang, T.; Wang, S., 2014:
RVG-peptide-linked trimethylated chitosan for delivery of siRNA to the brain

Li, X-Ru.; Hu, Z-Yi.; Zhao, Y-Heng.; Li, X-Ming., 2009:
RVM supervised feature extraction and Seyfert spectra classification

Anonymous, 2013:
RVN to be removed from the nurses' register

Watson, H.G., 2011:
RVO--real value obscure

Carter, K.A.; Dawson, B.C.; Brewer, K.; Lawson, L., 2009:
RVU ready? Preparing emergency medicine resident physicians in documentation for an incentive-based work environment

Martin, R.B., 2007:
RVUCOM: striving to meet the needs of the osteopathic medical profession

Rubenstein, D.; Friedman, G.; Bateman, D., 2013:
RVUs and DRGs: do they fairly reimburse physicians and hospitals and incentivize improved care?

Bendix, J., 2014:
RVUs: a valuable tool for aiding practice management. Understanding the basics of the RVU can assist physicians and practice managers in a wide variety of finance and management-related tasks

McNeill, E., 2010:
RVX-208, a stimulator of apolipoprotein AI gene expression for the treatment of cardiovascular diseases

McLure, K.G.; Gesner, E.M.; Tsujikawa, L.; Kharenko, O.A.; Attwell, S.; Campeau, E.; Wasiak, S.; Stein, A.; White, A.; Fontano, E.; Suto, R.K.; Wong, N.C.W.; Wagner, G.S.; Hansen, H.C.; Young, P.R., 2014:
RVX-208, an inducer of ApoA-I in humans, is a BET bromodomain antagonist

Picaud, S.; Wells, C.; Felletar, I.; Brotherton, D.; Martin, S.; Savitsky, P.; Diez-Dacal, B.; Philpott, M.; Bountra, C.; Lingard, H.; Fedorov, O.; Müller, S.; Brennan, P.E.; Knapp, S.; Filippakopoulos, P., 2014:
RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain

Bailey, D.; Jahagirdar, R.; Gordon, A.; Hafiane, A.; Campbell, S.; Chatur, S.; Wagner, G.S.; Hansen, H.C.; Chiacchia, F.S.; Johansson, J.; Krimbou, L.; Wong, N.C.W.; Genest, J., 2010:
RVX-208: a small molecule that increases apolipoprotein A-I and high-density lipoprotein cholesterol in vitro and in vivo

Wang, C.; Davila, J.I.; Baheti, S.; Bhagwate, A.V.; Wang, X.; Kocher, J-Pierre.A.; Slager, S.L.; Feldman, A.L.; Novak, A.J.; Cerhan, J.R.; Thompson, E.Aubrey.; Asmann, Y.W., 2015:
RVboost: RNA-seq variants prioritization using a boosting method

Grötsch, H.; Kunert, M.; Mooslehner, K.A.; Gao, Z.; Struve, D.; Hughes, I.A.; Hiort, O.; Werner, R., 2012:
RWDD1 interacts with the ligand binding domain of the androgen receptor and acts as a coactivator of androgen-dependent transactivation

Verbyla, Aūnas.P.; Taylor, J.D.; Verbyla, K.L., 2013:
RWGAIM: an efficient high-dimensional random whole genome average (QTL) interval mapping approach

Anonymous, 2008:
RWJF launches national program to build next generation of academic nurse leaders

Johnson, J.E., 2012:
RWJUH--New Brunswick wins quality award

Bateman, C., 2013:
RWOPS abuse 'eroding ethical standards of juniors'

Bateman, C., 2013:
RWOPS abuse - government's had enough

Bateman, C., 2013:
RWOPS abuse could cost, or even ruin, offenders

Bateman, C., 2013:
RWOPS clampdown - a crisis in the offing

Bateman, C., 2014:
RWOPS- light at the end of a dusty tunnel?

Chen, X.; Liu, M-Xi.; Yan, G-Ying., 2013:
RWRMDA: predicting novel human microRNA-disease associations

Colyer, W.R., 2012:
RX Herculink Elite(®) renal stent system: a review of its use for the treatment of renal artery stenosis

Newman, B.Y., 2011:
RX for a healthy life: pets

Miñano, J.C.; Benítez, P.; González, J.C., 1995:
RX: a nonimaging concentrator

David, D.S., 2007:
RX: professional integrity (PRN)

Halls, M.L.; Papaioannou, M.; Wade, J.D.; Evans, B.A.; Bathgate, R.A.D.; Summers, R.J., 2009:
RXFP1 couples to the Galpha-Gbetagamma-PI3K-PKCzeta pathway via the final 10 amino acids of the receptor C-terminal tail

Lewandowski, R.; Procida, K.; Vaidyanathan, R.; Coombs, W.; Jalife, Jé.; Nielsen, M.S.; Taffet, S.M.; Delmar, M., 2008:
RXP-E: a connexin43-binding peptide that prevents action potential propagation block

Kakuta, H.; Yakushiji, N.; Shinozaki, R.; Ohsawa, F.; Yamada, S.; Ohta, Y.; Kawata, K.; Nakayama, M.; Hagaya, M.; Fujiwara, C.; Makishima, M.; Uno, S.; Tai, A.; Maehara, A.; Nakayama, M.; Oohashi, T.; Yasui, H.; Yoshikawa, Y., 2012:
RXR Partial Agonist CBt-PMN Exerts Therapeutic Effects on Type 2 Diabetes without the Side Effects of RXR Full Agonists

Ning, R.B.; Zhu, J.; Chai, D.J.; Xu, C.S.; Xie, H.; Lin, X.Y.; Zeng, J.Z.; Lin, J.X., 2014:
RXR agonists inhibit high glucose-induced upregulation of inflammation by suppressing activation of the NADPH oxidase-nuclear factor-κB pathway in human endothelial cells

Shan, P.; Pu, J.; Yuan, A.; Shen, L.; Shen, L.; Chai, D.; He, B., 2008:
RXR agonists inhibit oxidative stress-induced apoptosis in H9c2 rat ventricular cells

Nakatsuka, A.; Wada, J.; Hida, K.; Hida, A.; Eguchi, J.; Teshigawara, S.; Murakami, K.; Kanzaki, M.; Inoue, K.; Terami, T.; Katayama, A.; Ogawa, D.; Kagechika, H.; Makino, H., 2012:
RXR antagonism induces G0 /G1 cell cycle arrest and ameliorates obesity by up-regulating the p53-p21(Cip1) pathway in adipocytes

Halftermeyer, J.; L.B.as, M.; D.T.é, H., 2012:
RXR, a key member of the oncogenic complex in acute promyelocytic leukemia

Desvergne, Béatrice., 2007:
RXR: from partnership to leadership in metabolic regulations

López-Díaz, F.; Nores, R.; Panzetta-Dutari, G.; Slavin, D.; Prieto, C.; Koritschoner, N.P.; Bocco, J.L., 2007:
RXRalpha regulates the pregnancy-specific glycoprotein 5 gene transcription through a functional retinoic acid responsive element

Papi, A.; Rocchi, P.; Ferreri, A.Maria.; Orlandi, M., 2010:
RXRgamma and PPARgamma ligands in combination to inhibit proliferation and invasiveness in colon cancer cells

Gilardi, F.; Desvergne, Béatrice., 2014:
RXRs: collegial partners

Chen, Y.; Moradin, A.; Schlessinger, D.; Nagaraja, R., 2012:
RXRα and LXR activate two promoters in placenta- and tumor-specific expression of PLAC1

Ocadiz-Delgado, R.; Castañeda-Saucedo, E.; Indra, A.K.; Hernandez-Pando, R.; Flores-Guizar, P.; Cruz-Colin, J.Luis.; Recillas-Targa, F.; Perez-Ishiwara, G.; Covarrubias, L.; Gariglio, P., 2012:
RXRα deletion and E6E7 oncogene expression are sufficient to induce cervical malignant lesions in vivo

Wang, H.; Liu, K.; Geng, M.; Gao, P.; Wu, X.; Hai, Y.; Li, Y.; Li, Y.; Luo, L.; Hayes, J.D.; Wang, X.Jun.; Tang, X., 2013:
RXRα inhibits the NRF2-ARE signaling pathway through a direct interaction with the Neh7 domain of NRF2

Pushpakom, S.P.; Owen, A.; Back, D.J.; Pirmohamed, M., 2014:
RXRγ gene variants are associated with HIV lipodystrophy

Ishikawa, S.A.; Inagaki, Y.; Hashimoto, T., 2012:
RY-Coding and Non-Homogeneous Models Can Ameliorate the Maximum-Likelihood Inferences From Nucleotide Sequence Data with Parallel Compositional Heterogeneity

Liu, Z.; Liu, Z.; Zhang, X.; Xue, P.; Zhang, H., 2015:
RY10-4 suppressed metastasis of MDA-MB-231 by stabilizing ECM and E-cadherin

Liu, Z.; Yuan, Q.; Zhang, X.; Xiong, C.; Xue, P.; Ruan, J., 2012:
RY10-4, a novel anti-tumor compound, exhibited its anti-angiogenesis activity by down-regulation of the HIF-1α and inhibition phosphorylation of AKT and mTOR

Scherer, M.R.J.; Muresan, N.M.; Steiner, U.; Reisner, E., 2013:
RYB tri-colour electrochromism based on a molecular cobaloxime

Morey, L.; Aloia, L.; Cozzuto, L.; Benitah, S.Aznar.; D.C.oce, L., 2013:
RYBP and Cbx7 define specific biological functions of polycomb complexes in mouse embryonic stem cells

Wang, W.; Cheng, J.; Qin, J-Jiang.; Voruganti, S.; Nag, S.; Fan, J.; Gao, Q.; Zhang, R., 2015:
RYBP expression is associated with better survival of patients with hepatocellular carcinoma (HCC) and responsiveness to chemotherapy of HCC cells in vitro and in vivo

Mazzeu, J.F., 2013:
RYK is not mutated in autosomal dominant Robinow syndrome

Wilmshurst, J.M.; Lillis, S.; Zhou, H.; Pillay, K.; Henderson, H.; Kress, W.; Müller, C.R.; Ndondo, A.; Cloke, V.; Cullup, T.; Bertini, E.; Boennemann, C.; Straub, V.; Quinlivan, R.; Dowling, J.J.; Al-Sarraj, S.; Treves, S.; Abbs, S.; Manzur, A.Y.; Sewry, C.A.; Muntoni, F.; Jungbluth, H., 2010:
RYR1 mutations are a common cause of congenital myopathies with central nuclei

Shaaban, S.; Ramos-Platt, L.; Gilles, F.H.; Chan, W-Man.; Andrews, C.; D.G.rolami, U.; Demer, J.; Engle, E.C., 2014:
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia

Chan, B.; Chen, S.P.L.; Wong, W.C.; Mak, C.M.; Wong, S.; Chan, K.Y.; Chan, A.Y.W., 2011:
RYR1-related central core myopathy in a Chinese adolescent boy

Illingworth, M.A.; Main, M.; Pitt, M.; Feng, L.; Sewry, C.A.; Gunny, R.; Vorstman, E.; Beeson, D.; Manzur, A.; Muntoni, F.; Robb, S.A., 2015:
RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimine

Akilzhanova, A.; Guelly, C.; Nuralinov, O.; Nurkina, Z.; Nazhat, D.; Smagulov, S.; Tursunbekov, A.; Alzhanova, A.; Rashbayeva, G.; Abdrakhmanov, A.; Dosmagambet, S.; Trajanoski, S.; Zhumadilov, Z.; Sharman, A.; Bekbosynova, M., 2015:
RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort

Shendre, A.; Irvin, M.R.; Aouizerat, B.E.; Wiener, H.W.; Vazquez, A.I.; Anastos, K.; Lazar, J.; Liu, C.; Karim, R.; Limdi, N.A.; Cohen, M.H.; Golub, E.T.; Zhi, D.; Kaplan, R.C.; Shrestha, S., 2014:
RYR3 gene variants in subclinical atherosclerosis among HIV-infected women in the Women's Interagency HIV Study (WIHS)

Menant, A.; Karess, R., 2010:
RZZ finds its ancestral roots

Krause, D.P., 2014:
Ra-228 (mesothorium I) in midwest well waters

Yadav, D.N.; Sarin, M.M., 2008:
Ra-Po-Pb isotope systematics in waters of Sambhar Salt Lake, Rajasthan (India): geochemical characterization and particulate reactivity

Slobodin, B.; Gerst, J.E., 2011:
RaPID: an aptamer-based mRNA affinity purification technique for the identification of RNA and protein factors present in ribonucleoprotein complexes

Horton, P.B.; Kiseleva, L.; Fujibuchi, W., 2007:
RaPiDS: an algorithm for rapid expression profile database search

Torchala, M.; Chelminiak, P.; Kurzynski, M.; Bates, P.A., 2014:
RaTrav: a tool for calculating mean first-passage times on biochemical networks

Furman, C.A.; Lo, C.B.; Stokes, S.; Esteban, J.A.; Gnegy, M.E., 2009:
Rab 11 regulates constitutive dopamine transporter trafficking and function in N2A neuroblastoma cells

Huang, T-Hao.; Shui, H-Ai.; Ka, S-Man.; Tang, B-Luen.; Chao, T-Kuang.; Chen, J-Shuen.; Lin, Y-Feng.; Chen, A., 2008:
Rab 23 is expressed in the glomerulus and plays a role in the development of focal segmental glomerulosclerosis

Suda, Y.; Kurokawa, K.; Hirata, R.; Nakano, A., 2014:
Rab GAP cascade regulates dynamics of Ypt6 in the Golgi traffic

Barr, F.; Lambright, D.G., 2010:
Rab GEFs and GAPs

Pfeffer, S.R., 2013:
Rab GTPase localization and Rab cascades in Golgi transport

Nabavi, N.; Pustylnik, S.; Harrison, R.E., 2013:
Rab GTPase mediated procollagen trafficking in ascorbic acid stimulated osteoblasts

Köhnke, M.; Delon, C.; Hastie, M.L.; Nguyen, U.T.T.; Wu, Y-Wen.; Waldmann, H.; Goody, R.S.; Gorman, J.J.; Alexandrov, K., 2014:
Rab GTPase prenylation hierarchy and its potential role in choroideremia disease

Jopling, H.M.; Odell, A.F.; Hooper, N.M.; Zachary, I.C.; Walker, J.H.; Ponnambalam, S., 2009:
Rab GTPase regulation of VEGFR2 trafficking and signaling in endothelial cells

Liu, T-Ting.; Gomez, T.S.; Sackey, B.K.; Billadeau, D.D.; Burd, C.G., 2012:
Rab GTPase regulation of retromer-mediated cargo export during endosome maturation

Roland, J.T.; Bryant, D.M.; Datta, A.; Itzen, A.; Mostov, K.E.; Goldenring, J.R., 2011:
Rab GTPase-Myo5B complexes control membrane recycling and epithelial polarization

Guo, P.; Wang, X., 2011:
Rab GTPases act in sequential steps to regulate phagolysosome formation

Horgan, C.P.; McCaffrey, M.W., 2012:
Rab GTPases and microtubule motors

Lachmann, J.; Ungermann, C.; Engelbrecht-Vandré, S., 2011:
Rab GTPases and tethering in the yeast endocytic pathway

Ng, E.Ling.; Tang, B.Luen., 2008:
Rab GTPases and their roles in brain neurons and glia

Rasineni, K.; McVicker, B.L.; Tuma, D.J.; McNiven, M.A.; Casey, C.A., 2014:
Rab GTPases associate with isolated lipid droplets (LDs) and show altered content after ethanol administration: potential role in alcohol-impaired LD metabolism

Esseltine, J.L.; Dale, L.B.; Ferguson, S.S.G., 2011 :
Rab GTPases bind at a common site within the angiotensin II type I receptor carboxyl-terminal tail: evidence that Rab4 regulates receptor phosphorylation, desensitization, and resensitization

Mitra, S.; Cheng, K.W.; Mills, G.B., 2011:
Rab GTPases implicated in inherited and acquired disorders

Nayak, R.C.; Keshava, S.; Esmon, C.T.; Pendurthi, U.R.; Rao, L.Vijaya.Mohan., 2013:
Rab GTPases regulate endothelial cell protein C receptor-mediated endocytosis and trafficking of factor VIIa

Seto, S.; Tsujimura, K.; Koide, Y., 2011:
Rab GTPases regulating phagosome maturation are differentially recruited to mycobacterial phagosomes

Li, G., 2012:
Rab GTPases, membrane trafficking and diseases

Aloisi, A.Laura.; Bucci, C., 2014:
Rab GTPases-cargo direct interactions: fine modulators of intracellular trafficking

Kawauchi, T.; Sekine, K.; Shikanai, M.; Chihama, K.; Tomita, K.; Kubo, K-ichiro.; Nakajima, K.; Nabeshima, Y-Ichi.; Hoshino, M., 2010:
Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking

Bastin, G.; Heximer, S.P., 2013:
Rab family proteins regulate the endosomal trafficking and function of RGS4

Nishimura, N.; Sasaki, T., 2009:
Rab family small G proteins in regulation of epithelial apical junctions

Gutkowska, M.; Wnuk, M.; Nowakowska, J.; Lichocka, M.; Stronkowski, M.M.; Swiezewska, E., 2016:
Rab geranylgeranyl transferase β subunit is essential for male fertility and tip growth in Arabidopsis

Baron, R.A.; Seabra, M.C., 2008:
Rab geranylgeranylation occurs preferentially via the pre-formed REP-RGGT complex and is regulated by geranylgeranyl pyrophosphate

Brighouse, A.; Dacks, J.B.; Field, M.C., 2010:
Rab protein evolution and the history of the eukaryotic endomembrane system

Wandinger-Ness, A.; Zerial, M., 2015:
Rab proteins and the compartmentalization of the endosomal system

Vázquez-Martínez, R.; Malagón, M.M., 2011:
Rab proteins and the secretory pathway: the case of rab18 in neuroendocrine cells

Kiss, R.Scott.; Nilsson, T., 2014:
Rab proteins implicated in lipid storage and mobilization

Ortiz Sandoval, C.; Simmen, T., 2013:
Rab proteins of the endoplasmic reticulum: functions and interactors

Bhuin, T.; Roy, J.Kumar., 2014:
Rab proteins: the key regulators of intracellular vesicle transport

Tatebe, H.; Shiozaki, K., 2011:
Rab small GTPase emerges as a regulator of TOR complex 2

Itoh, T.; Fukuda, M., 2011:
Rab small GTPases and their effectors

Torres, V.A., 2015:
Rab'ing tumor cell migration and invasion: focal adhesion disassembly driven by Rab5

Wada, M.; Fukui, K.; Sasaki, T.; Imazumi, K.; Matsuura, Y.; Nakanishi, H.; Takai, Y., 1997:
Rab, GAP and GEP make three

Johnson, J.R.; Kashyap, S.; Rankin, K.; Barclay, J.W., 2015:
Rab-3 and unc-18 interactions in alcohol sensitivity are distinct from synaptic transmission

Chow, C-Ming.; Neto, Hélia.; Foucart, C.; Moore, I., 2008:
Rab-A2 and Rab-A3 GTPases define a trans-golgi endosomal membrane domain in Arabidopsis that contributes substantially to the cell plate

Malagnac, F.; Fabret, Céline.; Prigent, M.; Rousset, J-Pierre.; Namy, O.; Silar, P., 2014:
Rab-GDI complex dissociation factor expressed through translational frameshifting in filamentous ascomycetes

Caswell, P.T.; Chan, M.; Lindsay, A.J.; McCaffrey, M.W.; Boettiger, D.; Norman, J.C., 2008:
Rab-coupling protein coordinates recycling of alpha5beta1 integrin and EGFR1 to promote cell migration in 3D microenvironments

Tatebe, H.; Morigasaki, S.; Murayama, S.; Zeng, C.Tracy.; Shiozaki, K., 2011:
Rab-family GTPase regulates TOR complex 2 signaling in fission yeast

Arora, D.K.; Syed, I.; Machhadieh, B.; McKenna, C.E.; Kowluru, A., 2013:
Rab-geranylgeranyl transferase regulates glucose-stimulated insulin secretion from pancreatic β cells

Baskys, A.; Bayazitov, I.; Zhu, E.; Fang, L.; Wang, R., 2007:
Rab-mediated endocytosis: linking neurodegeneration, neuroprotection, and synaptic plasticity?

Villarroel-Campos, D.; Gastaldi, L.; Conde, C.; Caceres, A.; Gonzalez-Billault, C., 2014:
Rab-mediated trafficking role in neurite formation

Houalla, T.; Shi, L.; van Meyel, D.J.; Rao, Y., 2010:
Rab-mediated vesicular transport is required for neuronal positioning in the developing Drosophila visual system

Liu, P.; Bartz, Ré.; Zehmer, J.K.; Ying, Y.; Anderson, R.G.W., 2008:
Rab-regulated membrane traffic between adiposomes and multiple endomembrane systems

Zhang, X.; Wang, G.; Dupré, D.J.; Feng, Y.; Robitaille, Mélanie.; Lazartigues, E.; Feng, Y-Hong.; Hébert, T.E.; Wu, G., 2009:
Rab1 GTPase and dimerization in the cell surface expression of angiotensin II type 2 receptor

Li, Y.; Wang, G.; Lin, K.; Yin, H.; Zhou, C.; Liu, T.; Wu, G.; Qian, G., 2010:
Rab1 GTPase promotes expression of beta-adrenergic receptors in rat pulmonary microvascular endothelial cells

Yin, H.; Li, Q.; Qian, G.; Wang, Y.; Li, Y.; Wu, G.; Wang, G., 2011:
Rab1 GTPase regulates phenotypic modulation of pulmonary artery smooth muscle cells by mediating the transport of angiotensin II type 1 receptor under hypoxia

Brombacher, E.; Urwyler, S.; Ragaz, C.; Weber, S.S.; Kami, K.; Overduin, M.; Hilbi, H., 2009:
Rab1 guanine nucleotide exchange factor SidM is a major phosphatidylinositol 4-phosphate-binding effector protein of Legionella pneumophila

Hammad, M.M.; Kuang, Y-Qun.; Morse, A.; Dupré, D.J., 2012:
Rab1 interacts directly with the β2-adrenergic receptor to regulate receptor anterograde trafficking

Zhuang, X.; Adipietro, K.A.; Datta, S.; Northup, J.K.; Ray, K., 2010:
Rab1 small GTP-binding protein regulates cell surface trafficking of the human calcium-sensing receptor

Chen, Y.; Wang, Y.; Zhang, J.; Deng, Y.; Jiang, L.; Song, E.; Wu, X.S.; Hammer, J.A.; Xu, T.; Lippincott-Schwartz, J., 2012:
Rab10 and myosin-Va mediate insulin-stimulated GLUT4 storage vesicle translocation in adipocytes

Babbey, C.M.; Bacallao, R.L.; Dunn, K.W., 2010:
Rab10 associates with primary cilia and the exocyst complex in renal epithelial cells

Chen, Y.; Lippincott-Schwartz, J., 2013:
Rab10 delivers GLUT4 storage vesicles to the plasma membrane

Cardoso, C.M.P.; Jordao, L.; Vieira, O.V., 2010:
Rab10 regulates phagosome maturation and its overexpression rescues Mycobacterium-containing phagosomes maturation

Deen, A.Jawahar.; Rilla, K.; Oikari, S.; Kärnä, R.; Bart, G.; Häyrinen, J.; Bathina, A.Rahul.; Ropponen, A.; Makkonen, K.; Tammi, R.H.; Tammi, M.I., 2014:
Rab10-mediated endocytosis of the hyaluronan synthase HAS3 regulates hyaluronan synthesis and cell adhesion to collagen

Castillo-Romero, A.; Leon-Avila, G.; Wang, C.C.; Perez Rangel, A.; Camacho Nuez, M.; Garcia Tovar, C.; Ayala-Sumuano, J.Tonatiuh.; Luna-Arias, J.Pedro.; Hernandez, J.Manuel., 2010:
Rab11 and actin cytoskeleton participate in Giardia lamblia encystation, guiding the specific vesicles to the cyst wall

Eva, R.; Dassie, E.; Caswell, P.T.; Dick, G.; ffrench-Constant, C.; Norman, J.C.; Fawcett, J.W., 2010:
Rab11 and its effector Rab coupling protein contribute to the trafficking of beta 1 integrins during axon growth in adult dorsal root ganglion neurons and PC12 cells

Giorgini, F.; Steinert, J.R., 2014:
Rab11 as a modulator of synaptic transmission

Hehnly, H.; Doxsey, S., 2014:
Rab11 endosomes contribute to mitotic spindle organization and orientation

Szatmári, Z.; Kis, V.; Lippai, Mónika.; Hegedus, K.; Faragó, Tás.; Lorincz, Péter.; Tanaka, T.; Juhász, Gábor.; Sass, Mós., 2015 :
Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization

Roeth, J.F.; Sawyer, J.K.; Wilner, D.A.; Peifer, M., 2010:
Rab11 helps maintain apical crumbs and adherens junctions in the Drosophila embryonic ectoderm

Bhuin, T.; Kumar Roy, J., 2012:
Rab11 is Required for Maintenance of Cell Shape Via βPS Integrin Mediated Cell Adhesion in Drosophila

Pavarotti, Mín.; Capmany, Aí.; Vitale, N.; Colombo, Mía.Isabel.; Damiani, Mía.Teresa., 2013:
Rab11 is phosphorylated by classical and novel protein kinase C isoenzymes upon sustained phorbol ester activation

Bhuin, T.; Roy, J.K., 2011:
Rab11 is required for cell adhesion, maintenance of cell shape and actin-cytoskeleton organization during Drosophila wing development

Bhuin, T.; Roy, J.K., 2008:
Rab11 is required for embryonic nervous system development in Drosophila

Xu, J.; Lan, L.; Bogard, N.; Mattione, C.; Cohen, R.S., 2011:
Rab11 is required for epithelial cell viability, terminal differentiation, and suppression of tumor-like growth in the Drosophila egg chamber

Breda, C.; Nugent, M.L.; Estranero, J.G.; Kyriacou, C.P.; Outeiro, T.F.; Steinert, J.R.; Giorgini, F., 2015:
Rab11 modulates α-synuclein-mediated defects in synaptic transmission and behaviour

Singh, D.; Kumar Roy, J., 2014:
Rab11 plays an indispensable role in the differentiation and development of the indirect flight muscles in Drosophila

Kelly, E.E.; Horgan, C.P.; McCaffrey, M.W., 2013:
Rab11 proteins in health and disease

Chung, Y-Chiang.; Wei, W-Chen.; Huang, S-Han.; Shih, C-Min.; Hsu, C-Ping.; Chang, K-Jen.; Chao, W-Ting., 2015:
Rab11 regulates E-cadherin expression and induces cell transformation in colorectal carcinoma

Bhuin, T.; Roy, J.K., 2011:
Rab11 regulates JNK and Raf/MAPK-ERK signalling pathways during Drosophila wing development

Takahashi, S.; Kubo, K.; Waguri, S.; Yabashi, A.; Shin, H-Won.; Katoh, Y.; Nakayama, K., 2013:
Rab11 regulates exocytosis of recycling vesicles at the plasma membrane

Parent, A.; Hamelin, E.; Germain, P.; Parent, J-Luc., 2008:
Rab11 regulates the recycling of the beta2-adrenergic receptor through a direct interaction

Niyogi, S.; Mucci, J.; Campetella, O.; Docampo, R., 2015:
Rab11 regulates trafficking of trans-sialidase to the plasma membrane through the contractile vacuole complex of Trypanosoma cruzi

Matthies, H.J.G.; Moore, J.L.; Saunders, C.; Matthies, D.Signor.; Lapierre, L.A.; Goldenring, J.R.; Blakely, R.D.; Galli, A., 2010:
Rab11 supports amphetamine-stimulated norepinephrine transporter trafficking

Park, S.Won.; Schonhoff, C.M.; Webster, C.R.L.; Anwer, M.Sawkat., 2014:
Rab11, but not Rab4, facilitates cyclic AMP- and tauroursodeoxycholate-induced MRP2 translocation to the plasma membrane

Qi, M.; Williams, J.A.; Chu, H.; Chen, X.; Wang, J-Jiun.; Ding, L.; Akhirome, E.; Wen, X.; Lapierre, L.A.; Goldenring, J.R.; Spearman, P., 2014:
Rab11-FIP1C and Rab14 direct plasma membrane sorting and particle incorporation of the HIV-1 envelope glycoprotein complex

Ducharme, N.A.; Ham, A-Joan.L.; Lapierre, L.A.; Goldenring, J.R., 2011:
Rab11-FIP2 influences multiple components of the endosomal system in polarized MDCK cells

Schafer, J.C.; Baetz, N.W.; Lapierre, L.A.; McRae, R.E.; Roland, J.T.; Goldenring, J.R., 2014:
Rab11-FIP2 interaction with MYO5B regulates movement of Rab11a-containing recycling vesicles

Horgan, C.P.; Hanscom, S.R.; Jolly, R.S.; Futter, C.E.; McCaffrey, M.W., 2010:
Rab11-FIP3 binds dynein light intermediate chain 2 and its overexpression fragments the Golgi complex

Horgan, C.P.; Oleksy, A.; Zhdanov, A.V.; Lall, P.Y.; White, I.J.; Khan, A.R.; Futter, C.E.; McCaffrey, J.G.; McCaffrey, M.W., 2007:
Rab11-FIP3 is critical for the structural integrity of the endosomal recycling compartment

Horgan, C.P.; Hanscom, S.R.; Jolly, R.S.; Futter, C.E.; McCaffrey, M.W., 2010:
Rab11-FIP3 links the Rab11 GTPase and cytoplasmic dynein to mediate transport to the endosomal-recycling compartment

Baetz, N.W.; Goldenring, J.R., 2013:
Rab11-family interacting proteins define spatially and temporally distinct regions within the dynamic Rab11a-dependent recycling system

Leiva, N.; Capmany, Aí.; Damiani, Mía.Teresa., 2013:
Rab11-family of interacting protein 2 associates with chlamydial inclusions through its Rab-binding domain and promotes bacterial multiplication

Agop-Nersesian, C.; Naissant, B.; Ben Rached, F.; Rauch, M.; Kretzschmar, A.; Thiberge, S.; Menard, R.; Ferguson, D.J.P.; Meissner, M.; Langsley, G., 2009:
Rab11A-controlled assembly of the inner membrane complex is required for completion of apicomplexan cytokinesis

Liu, J.; Zhang, J-Peng.; Shi, M.; Quinn, T.; Bradner, J.; Beyer, R.; Chen, S.; Zhang, J., 2009:
Rab11a and HSP90 regulate recycling of extracellular alpha-synuclein

Gardner, L.A.; Hajjhussein, H.; Frederick-Dyer, K.C.; Bahouth, S.W., 2011:
Rab11a and its binding partners regulate the recycling of the ß1-adrenergic receptor

Khandelwal, P.; Ruiz, W.G.; Balestreire-Hawryluk, E.; Weisz, O.A.; Goldenring, J.R.; Apodaca, G., 2008:
Rab11a-dependent exocytosis of discoidal/fusiform vesicles in bladder umbrella cells

Mattila, P.E.; Raghavan, V.; Rbaibi, Y.; Baty, C.J.; Weisz, O.A., 2014:
Rab11a-positive compartments in proximal tubule cells sort fluid-phase and membrane cargo

Oehlke, O.; Martin, H.W.; Osterberg, N.; Roussa, E., 2011:
Rab11b and its effector Rip11 regulate the acidosis-induced traffic of V-ATPase in salivary ducts

Silvis, M.R.; Bertrand, C.A.; Ameen, N.; Golin-Bisello, F.; Butterworth, M.B.; Frizzell, R.A.; Bradbury, N.A., 2009:
Rab11b regulates the apical recycling of the cystic fibrosis transmembrane conductance regulator in polarized intestinal epithelial cells

Rydell, G.E.; Renard, H-François.; Garcia-Castillo, M-Daniela.; Dingli, F.; Loew, D.; Lamaze, C.; Römer, W.; Johannes, L., 2015:
Rab12 localizes to Shiga toxin-induced plasma membrane invaginations and controls toxin transport

Nishikimi, A.; Ishihara, S.; Ozawa, M.; Etoh, K.; Fukuda, M.; Kinashi, T.; Katagiri, K., 2015:
Rab13 acts downstream of the kinase Mst1 to deliver the integrin LFA-1 to the cell surface for lymphocyte trafficking

Hirvonen, M.J.; Mulari, M.T.K.; Büki, Kálmán.G.; Vihko, P.; Härkönen, P.L.; Väänänen, H.Kalervo., 2012:
Rab13 is upregulated during osteoclast differentiation and associates with small vesicles revealing polarized distribution in resorbing cells

Nokes, R.L.; Fields, I.C.; Collins, R.N.; Fölsch, H., 2008:
Rab13 regulates membrane trafficking between TGN and recycling endosomes in polarized epithelial cells

Sakane, A.; Honda, K.; Sasaki, T., 2010:
Rab13 regulates neurite outgrowth in PC12 cells through its effector protein, JRAB/MICAL-L2

Sakane, A.; Abdallah, A.Alamir.Mahmoud.; Nakano, K.; Honda, K.; Ikeda, W.; Nishikawa, Y.; Matsumoto, M.; Matsushita, N.; Kitamura, T.; Sasaki, T., 2013:
Rab13 small G protein and junctional Rab13-binding protein (JRAB) orchestrate actin cytoskeletal organization during epithelial junctional development

Wu, C.; Agrawal, S.; Vasanji, A.; Drazba, J.; Sarkaria, S.; Xie, J.; Welch, C.M.; Liu, M.; Anand-Apte, B.; Horowitz, A., 2011:
Rab13-dependent trafficking of RhoA is required for directional migration and angiogenesis

Linford, A.; Yoshimura, S-ichiro.; Nunes Bastos, R.; Langemeyer, L.; Gerondopoulos, A.; Rigden, D.J.; Barr, F.A., 2012:
Rab14 and its exchange factor FAM116 link endocytic recycling and adherens junction stability in migrating cells

Uno, T.; Moriwaki, T.; Isoyama, Y.; Uno, Y.; Kanamaru, K.; Yamagata, H.; Nakamura, M.; Takagi, M., 2010:
Rab14 from Bombyx mori (Lepidoptera: Bombycidae) shows ATPase activity

Kitt, K.N.; Hernández-Deviez, D.; Ballantyne, S.D.; Spiliotis, E.T.; Casanova, J.E.; Wilson, J.M., 2008:
Rab14 regulates apical targeting in polarized epithelial cells

Lu, R.; Johnson, D.L.; Stewart, L.; Waite, K.; Elliott, D.; Wilson, J.M., 2015:
Rab14 regulation of claudin-2 trafficking modulates epithelial permeability and lumen morphogenesis

Pham, T.Van.Huyen.; Hartomo, T.Budi.; Lee, M.Jin.; Hasegawa, D.; Ishida, T.; Kawasaki, K.; Kosaka, Y.; Yamamoto, T.; Morikawa, S.; Yamamoto, N.; Kubokawa, I.; Mori, T.; Yanai, T.; Hayakawa, A.; Takeshima, Y.; Iijima, K.; Matsuo, M.; Nishio, H.; Nishimura, N., 2012:
Rab15 alternative splicing is altered in spheres of neuroblastoma cells

Nishimura, N.; Van Huyen Pham, T.; Hartomo, T.Budi.; Lee, M.Jin.; Hasegawa, D.; Takeda, H.; Kawasaki, K.; Kosaka, Y.; Yamamoto, T.; Morikawa, S.; Yamamoto, N.; Kubokawa, I.; Mori, T.; Yanai, T.; Hayakawa, A.; Takeshima, Y.; Nishio, H.; Matsuo, M., 2011:
Rab15 expression correlates with retinoic acid-induced differentiation of neuroblastoma cells

Haobam, B.; Nozawa, T.; Minowa-Nozawa, A.; Tanaka, M.; Oda, S.; Watanabe, T.; Aikawa, C.; Maruyama, F.; Nakagawa, I., 2015:
Rab17-mediated recycling endosomes contribute to autophagosome formation in response to Group A Streptococcus invasion

Dejgaard, S.Y.; Murshid, A.; Erman, Aül.; Kizilay, O.; Verbich, D.; Lodge, R.; Dejgaard, K.; Ly-Hartig, T.Bach.Nga.; Pepperkok, R.; Simpson, J.C.; Presley, J.F., 2008:
Rab18 and Rab43 have key roles in ER-Golgi trafficking

Gerondopoulos, A.; Bastos, R.Nunes.; Yoshimura, S-Ichiro.; Anderson, R.; Carpanini, S.; Aligianis, I.; Handley, M.T.; Barr, F.A., 2014:
Rab18 and a Rab18 GEF complex are required for normal ER structure

Salloum, S.; Wang, H.; Ferguson, C.; Parton, R.G.; Tai, A.W., 2014:
Rab18 binds to hepatitis C virus NS5A and promotes interaction between sites of viral replication and lipid droplets

Pulido, M.R.; Diaz-Ruiz, A.; Jiménez-Gómez, Y.; Garcia-Navarro, S.; Gracia-Navarro, F.; Tinahones, F.; López-Miranda, Jé.; Frühbeck, G.; Vázquez-Martínez, R.; Malagón, M.M., 2011:
Rab18 dynamics in adipocytes in relation to lipogenesis, lipolysis and obesity

Tang, W-Chun.; Lin, R-Jye.; Liao, C-Len.; Lin, Y-Ling., 2014:
Rab18 facilitates dengue virus infection by targeting fatty acid synthase to sites of viral replication

Vazquez-Martinez, R.; Cruz-Garcia, D.; Duran-Prado, M.; Peinado, J.R.; Castaño, J.P.; Malagon, M.M., 2007:
Rab18 inhibits secretory activity in neuroendocrine cells by interacting with secretory granules

Dansako, H.; Hiramoto, H.; Ikeda, M.; Wakita, T.; Kato, N., 2014:
Rab18 is required for viral assembly of hepatitis C virus through trafficking of the core protein to lipid droplets

Coune, P.G.; Bensadoun, J.C.; Aebischer, P.; Schneider, B.L., 2014:
Rab1A over-expression prevents Golgi apparatus fragmentation and partially corrects motor deficits in an alpha-synuclein based rat model of Parkinson's disease

Kirsten, M.L.; Baron, R.A.; Seabra, M.C.; Ces, O., 2013:
Rab1a and Rab5a preferentially bind to binary lipid compositions with higher stored curvature elastic energy

Mukhopadhyay, A.; Quiroz, J.A.; Wolkoff, A.W., 2014:
Rab1a regulates sorting of early endocytic vesicles

Monetta, P.; Slavin, I.; Romero, N.; Alvarez, C., 2007:
Rab1b interacts with GBF1 and modulates both ARF1 dynamics and COPI association

Romero, N.; Dumur, C.I.; Martinez, Hán.; García, I.A.; Monetta, P.; Slavin, I.; Sampieri, L.; Koritschoner, N.; Mironov, A.A.; D.M.tteis, M.Antonietta.; Alvarez, C., 2013:
Rab1b overexpression modifies Golgi size and gene expression in HeLa cells and modulates the thyrotrophin response in thyroid cells in culture

García, I.A.; Martinez, Hán.E.; Alvarez, C., 2012:
Rab1b regulates COPI and COPII dynamics in mammalian cells

Hutt, D.M.; Balch, W.E., 2008:
Rab1b silencing using small interfering RNA for analysis of disease-specific function

Tisdale, E.J.; Azizi, F.; Artalejo, C.R., 2009:
Rab2 utilizes glyceraldehyde-3-phosphate dehydrogenase and protein kinase C{iota} to associate with microtubules and to recruit dynein

Egami, Y.; Araki, N., 2012:
Rab20 regulates phagosome maturation in RAW264 macrophages during Fc gamma receptor-mediated phagocytosis

Wang, L.; Liang, Z.; Li, G., 2012:
Rab22 controls NGF signaling and neurite outgrowth in PC12 cells

Ng, E.Ling.; Ng, J.Jie.; Liang, F.; Tang, B.Luen., 2009:
Rab22B is expressed in the CNS astroglia lineage and plays a role in epidermal growth factor receptor trafficking in A431 cells

Lumb, J.H.; Field, M.C., 2011:
Rab23 is a flagellar protein in Trypanosoma brucei

Liu, Y-Jian.; Wang, Q.; Li, W.; Huang, X-Hui.; Zhen, M-Chuan.; Huang, S-Hong.; Chen, L-Zhou.; Xue, L.; Zhang, H-Wei., 2007:
Rab23 is a potential biological target for treating hepatocellular carcinoma

Chi, S.; Xie, G.; Liu, H.; Chen, K.; Zhang, X.; Li, C.; Xie, J., 2012:
Rab23 negatively regulates Gli1 transcriptional factor in a Su(Fu)-dependent manner

Huang, T-Hao.; Ka, S-Man.; Hsu, Y-Juei.; Shui, H-Ai.; Tang, B-Luen.; Hu, K-Yu.; Chang, J-Liang.; Chen, A., 2011:
Rab23 plays a role in the pathophysiology of mesangial cells--a proteomic analysis

Fuller, K.; O'Connell, J.T.; Gordon, J.; Mauti, O.; Eggenschwiler, J., 2014:
Rab23 regulates Nodal signaling in vertebrate left-right patterning independently of the Hedgehog pathway

Caswell, P.T.; Spence, H.J.; Parsons, M.; White, D.P.; Clark, K.; Cheng, K.Wa.; Mills, G.B.; Humphries, M.J.; Messent, A.J.; Anderson, K.I.; McCaffrey, M.W.; Ozanne, B.W.; Norman, J.C., 2007:
Rab25 associates with alpha5beta1 integrin to promote invasive migration in 3D microenvironments

Liu, L.; Ding, G., 2014:
Rab25 expression predicts poor prognosis in clear cell renal cell carcinoma

Mitra, S.; Cheng, K.W.; Mills, G.B., 2013:
Rab25 in cancer: a brief update

Tong, M.; Chan, K.Wah.; Bao, J.Y.J.; Wong, K.Yau.; Chen, J-Na.; Kwan, P.Shing.; Tang, K.Ho.; Fu, L.; Qin, Y-Ru.; Lok, S.; Guan, X-Yuan.; Ma, S., 2013:
Rab25 is a tumor suppressor gene with antiangiogenic and anti-invasive activities in esophageal squamous cell carcinoma

Brusegard, K.; Stavnes, H.Tuft.; Nymoen, D.André.; Flatmark, K.; Trope, C.G.; Davidson, B., 2012:
Rab25 is overexpressed in Müllerian serous carcinoma compared to malignant mesothelioma

Fan, Y.; Wang, L.; Han, X.; Liu, X.; Ma, H., 2015:
Rab25 is responsible for phosphoinositide 3-kinase/AKT‑mediated cisplatin resistance in human epithelial ovarian cancer cells

Krishnan, M.; Lapierre, L.A.; Knowles, B.C.; Goldenring, J.R., 2013:
Rab25 regulates integrin expression in polarized colonic epithelial cells

Amornphimoltham, P.; Rechache, K.; Thompson, J.; Masedunskas, A.; Leelahavanichkul, K.; Patel, V.; Molinolo, A.; Gutkind, J.Silvio.; Weigert, R., 2013:
Rab25 regulates invasion and metastasis in head and neck cancer

Li, C.; Fan, Y.; Lan, T-Hung.; Lambert, N.A.; Wu, G., 2013:
Rab26 modulates the cell surface transport of α2-adrenergic receptors from the Golgi

Hendrix, A.; D.W.ver, O., 2013:
Rab27 GTPases distribute extracellular nanomaps for invasive growth and metastasis: implications for prognosis and treatment

Bustos, Mías.A.; Lucchesi, O.; Ruete, Mía.C.; Mayorga, L.S.; Tomes, C.N., 2012:
Rab27 and Rab3 sequentially regulate human sperm dense-core granule exocytosis

Yasuda, T.; Saegusa, C.; Kamakura, S.; Sumimoto, H.; Fukuda, M., 2012:
Rab27 effector Slp2-a transports the apical signaling molecule podocalyxin to the apical surface of MDCK II cells and regulates claudin-2 expression

Li, W.; Hu, Y.; Jiang, T.; Han, Y.; Han, G.; Chen, J.; Li, X., 2014:
Rab27A regulates exosome secretion from lung adenocarcinoma cells A549: involvement of EPI64

Nightingale, T.D.; Pattni, K.; Hume, A.N.; Seabra, M.C.; Cutler, D.F., 2009:
Rab27a and MyRIP regulate the amount and multimeric state of VWF released from endothelial cells

Kariya, Y.; Honma, M.; Hanamura, A.; Aoki, S.; Ninomiya, T.; Nakamichi, Y.; Udagawa, N.; Suzuki, H., 2011:
Rab27a and Rab27b are involved in stimulation-dependent RANKL release from secretory lysosomes in osteoblastic cells

Johnson, J.L.; Brzezinska, A.A.; Tolmachova, T.; Munafo, D.B.; Ellis, B.A.; Seabra, M.C.; Hong, H.; Catz, S.D., 2010:
Rab27a and Rab27b regulate neutrophil azurophilic granule exocytosis and NADPH oxidase activity by independent mechanisms

Booth, A.E.G.; Seabra, M.C.; Hume, A.N., 2013:
Rab27a and melanosomes: a model to investigate the membrane targeting of Rabs

Kawakami, T.; He, J.; Morita, H.; Yokoyama, K.; Kaji, H.; Tanaka, C.; Suemori, S-ichiro.; Tohyama, K.; Tohyama, Y., 2014:
Rab27a is essential for the formation of neutrophil extracellular traps (NETs) in neutrophil-like differentiated HL60 cells

Fraile-Ramos, A.; Cepeda, V.; Elstak, E.; van der Sluijs, P., 2011:
Rab27a is required for human cytomegalovirus assembly

Yokoyama, K.; Kaji, H.; He, J.; Tanaka, C.; Hazama, R.; Kamigaki, T.; Ku, Y.; Tohyama, K.; Tohyama, Y., 2011:
Rab27a negatively regulates phagocytosis by prolongation of the actin-coating stage around phagosomes

Herrero-Turrión, M.Javier.; Calafat, J.; Janssen, H.; Fukuda, M.; Mollinedo, F., 2008:
Rab27a regulates exocytosis of tertiary and specific granules in human neutrophils

Bobrie, Aélique.; Krumeich, S.; Reyal, F.; Recchi, C.; Moita, L.F.; Seabra, M.C.; Ostrowski, M.; Théry, C., 2012:
Rab27a supports exosome-dependent and -independent mechanisms that modify the tumor microenvironment and can promote tumor progression

Wang, H.; Zhao, Y.; Zhang, C.; Li, M.; Jiang, C.; Li, Y., 2015:
Rab27a was identified as a prognostic biomaker by mRNA profiling, correlated with malignant progression and subtype preference in gliomas

Kimura, T.; Niki, I., 2011:
Rab27a, actin and beta-cell endocytosis

Singh, R.K.; Liao, W.; Tracey-White, D.; Recchi, C.; Tolmachova, T.; Rankin, S.M.; Hume, A.N.; Seabra, M.C., 2013:
Rab27a-mediated protease release regulates neutrophil recruitment by allowing uropod detachment

Suda, J.; Zhu, L.; Okamoto, C.T.; Karvar, S., 2011:
Rab27b localizes to the tubulovesicle membranes of gastric parietal cells and regulates acid secretion

Tanaka, C.; Kaji, H.; He, J.; Hazama, R.; Yokoyama, K.; Kinoshita, E.; Tsujioka, T.; Tohyama, K.; Yamamura, H.; Nishio, H.; Tohyama, Y., 2012:
Rab27b regulates c-kit expression by controlling the secretion of stem cell factor

Mizuno, K.; Tolmachova, T.; Ushakov, D.S.; Romao, M.; Abrink, M.; Ferenczi, M.A.; Raposo, Gça.; Seabra, M.C., 2007:
Rab27b regulates mast cell granule dynamics and secretion

Lumb, J.H.; Leung, K.Fai.; Dubois, K.N.; Field, M.C., 2012:
Rab28 function in trypanosomes: interactions with retromer and ESCRT pathways

Giagtzoglou, N.; Mahoney, T.; Yao, C-Kuang.; Bellen, H.J., 2010:
Rab3 GTPase lands Bruchpilot

Graf, E.R.; Daniels, R.W.; Burgess, R.W.; Schwarz, T.L.; DiAntonio, A., 2010:
Rab3 dynamically controls protein composition at active zones

Schonn, J-Sébastien.; van Weering, J.R.T.; Mohrmann, R.; Schlüter, O.M.; Südhof, T.C.; de Wit, H.; Verhage, M.; Sørensen, J.B., 2011:
Rab3 proteins involved in vesicle biogenesis and priming in embryonic mouse chromaffin cells

Müller, M.; Pym, E.C.G.; Tong, A.; Davis, G.W., 2011:
Rab3-GAP controls the progression of synaptic homeostasis at a late stage of vesicle release

Uriu, Y.; Kiyonaka, S.; Miki, T.; Yagi, M.; Akiyama, S.; Mori, E.; Nakao, A.; Beedle, A.M.; Campbell, K.P.; Wakamori, M.; Mori, Y., 2010:
Rab3-interacting molecule gamma isoforms lacking the Rab3-binding domain induce long lasting currents but block neurotransmitter vesicle anchoring in voltage-dependent P/Q-type Ca2+ channels

Kelly, E.E.; Giordano, F.; Horgan, C.P.; Jollivet, F.; Raposo, Gça.; McCaffrey, M.W., 2013:
Rab30 is required for the morphological integrity of the Golgi apparatus

Chua, C.En.Lin.; Goh, E.Lay.Keow.; Tang, B.Luen., 2014:
Rab31 is expressed in neural progenitor cells and plays a role in their differentiation

Hou, L.; Wang, J-Xing.; Zhao, X-Fan., 2011:
Rab32 and the remodeling of the imaginal midgut in Helicoverpa armigera

Bui, M.; Gilady, S.Y.; Fitzsimmons, R.E.B.; Benson, M.D.; Lynes, E.M.; Gesson, K.; Alto, N.M.; Strack, S.; Scott, J.D.; Simmen, T., 2010:
Rab32 modulates apoptosis onset and mitochondria-associated membrane (MAM) properties

Nakazawa, H.; Sada, T.; Toriyama, M.; Tago, K.; Sugiura, T.; Fukuda, M.; Inagaki, N., 2012:
Rab33a mediates anterograde vesicular transport for membrane exocytosis and axon outgrowth

Starr, T.; Sun, Y.; Wilkins, N.; Storrie, B., 2010:
Rab33b and Rab6 are functionally overlapping regulators of Golgi homeostasis and trafficking

Goldenberg, N.M.; Silverman, M., 2009:
Rab34 and its effector munc13-2 constitute a new pathway modulating protein secretion in the cellular response to hyperglycemia

Zhang, J.; Fonovic, M.; Suyama, K.; Bogyo, M.; Scott, M.P., 2009:
Rab35 controls actin bundling by recruiting fascin as an effector protein

Zhu, Y.; Shen, T.; Liu, J.; Zheng, J.; Zhang, Y.; Xu, R.; Sun, C.; Du, J.; Chen, Y.; Gu, L., 2013:
Rab35 is required for Wnt5a/Dvl2-induced Rac1 activation and cell migration in MCF-7 breast cancer cells

Kobayashi, H.; Etoh, K.; Fukuda, M., 2015:
Rab35 is translocated from Arf6-positive perinuclear recycling endosomes to neurite tips during neurite outgrowth

Shim, J.; Lee, S-Min.; Lee, M.Sup.; Yoon, J.; Kweon, H-Seok.; Kim, Y-Joon., 2010:
Rab35 mediates transport of Cdc42 and Rac1 to the plasma membrane during phagocytosis

Kobayashi, H.; Etoh, K.; Ohbayashi, N.; Fukuda, M., 2014:
Rab35 promotes the recruitment of Rab8, Rab13 and Rab36 to recycling endosomes through MICAL-L1 during neurite outgrowth

Kobayashi, H.; Fukuda, M., 2012:
Rab35 regulates Arf6 activity through centaurin-β2 (ACAP2) during neurite outgrowth

Charrasse, S.; Comunale, F.; D.R.ssi, S.; Echard, A.; Gauthier-Rouvière, Cécile., 2013:
Rab35 regulates cadherin-mediated adherens junction formation and myoblast fusion

Egami, Y.; Fukuda, M.; Araki, N., 2012:
Rab35 regulates phagosome formation through recruitment of ACAP2 in macrophages during FcγR-mediated phagocytosis

Miyamoto, Y.; Yamamori, N.; Torii, T.; Tanoue, A.; Yamauchi, J., 2015:
Rab35, acting through ACAP2 switching off Arf6, negatively regulates oligodendrocyte differentiation and myelination

Chua, C.En.Lin.; Lim, Y.Shan.; Tang, B.Luen., 2010:
Rab35--a vesicular traffic-regulating small GTPase with actin modulating roles

Chen, L.; Hu, J.; Yun, Y.; Wang, T., 2010:
Rab36 regulates the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34

Becker, C.E.; Creagh, E.M.; O'Neill, L.A.J., 2010:
Rab39a binds caspase-1 and is required for caspase-1-dependent interleukin-1beta secretion

Seto, S.; Sugaya, K.; Tsujimura, K.; Nagata, T.; Horii, T.; Koide, Y., 2014:
Rab39a interacts with phosphatidylinositol 3-kinase and negatively regulates autophagy induced by lipopolysaccharide stimulation in macrophages

Xie, C.; Li, J.; Guo, T.; Yan, Y.; Tang, C.; Wang, Y.; Chen, P.; Wang, X.; Liang, S., 2014:
Rab3A is a new interacting partner of synaptotagmin I and may modulate synaptic membrane fusion through a competitive mechanism

Tian, M.; Xu, C.Shan.; Montpetit, R.; Kramer, R.H., 2012:
Rab3A mediates vesicle delivery at photoreceptor ribbon synapses

Rotondo, F.; Scheithauer, B.W.; Kovacs, K.; Bell, D.C., 2009:
Rab3B immunoexpression in human pituitary adenomas

Kögel, T.; Rudolf, Rüdiger.; Hodneland, E.; Copier, J.; Regazzi, R.; Tooze, S.A.; Gerdes, H-Hermann., 2013:
Rab3D is critical for secretory granule maturation in PC12 cells

Figueiredo, A.C.; Wasmeier, C.; Tarafder, A.K.; Ramalho, Jé.S.; Baron, R.A.; Seabra, M.C., 2008:
Rab3GEP is the non-redundant guanine nucleotide exchange factor for Rab27a in melanocytes

Wong, F.K.; Stanley, E.F., 2010:
Rab3a interacting molecule (RIM) and the tethering of pre-synaptic transmitter release site-associated CaV2.2 calcium channels

Sedej, S.; Klemen, Mša.Skelin.; Schlüter, O.M.; Rupnik, M.Slak., 2014:
Rab3a is critical for trapping alpha-MSH granules in the high Ca²⁺-affinity pool by preventing constitutive exocytosis

Kim, J-Kyum.; Lee, S-Yup.; Park, C-Won.; Park, S-Hwang.; Yin, J.; Kim, J.; Park, J-Bong.; Lee, J-Yong.; Kim, H.; Kim, S-Chan., 2015:
Rab3a promotes brain tumor initiation and progression

Schonhoff, C.M.; Thankey, K.; Webster, C.R.L.; Wakabayashi, Y.; Wolkoff, A.W.; Anwer, M.Sawkat., 2008:
Rab4 facilitates cyclic adenosine monophosphate-stimulated bile acid uptake and Na+-taurocholate cotransporting polypeptide translocation

Ferrándiz-Huertas, C.; Fernández-Carvajal, A.; Ferrer-Montiel, A., 2010:
Rab4 interacts with the human P-glycoprotein and modulates its surface expression in multidrug resistant K562 cells

D'Souza, R.S.; Semus, R.; Billings, E.A.; Meyer, C.B.; Conger, K.; Casanova, J.E., 2015:
Rab4 orchestrates a small GTPase cascade for recruitment of adaptor proteins to early endosomes

Jacob, A.; Jing, J.; Lee, J.; Schedin, P.; Gilbert, S.M.; Peden, A.A.; Junutula, J.R.; Prekeris, R., 2014:
Rab40b regulates trafficking of MMP2 and MMP9 during invadopodia formation and invasion of breast cancer cells

Liu, S.; Hunt, L.; Storrie, B., 2014:
Rab41 is a novel regulator of Golgi apparatus organization that is needed for ER-to-Golgi trafficking and cell growth

Sack, M.N., 2011:
Rab4a signaling unmasks a pivotal link between myocardial homeostasis and metabolic remodeling in the diabetic heart

Perrin, L.; Laura, P.; Lacas-Gervais, S.; Sandra, L-Gervais.; Gilleron, Jérôme.; Jérôme, G.; Ceppo, F.; Franck, C.; Prodon, Fçois.; François, P.; Benmerah, A.; Alexandre, B.; Tanti, J-François.; Jean-François, T.; Cormont, M.; Mireille, C., 2014:
Rab4b controls an early endosome sorting event by interacting with the γ-subunit of the clathrin adaptor complex 1

Kaddai, V.; Gonzalez, T.; Keslair, Fédérique.; Grémeaux, T.; Bonnafous, Séphanie.; Gugenheim, J.; Tran, A.; Gual, P.; L.M.rchand-Brustel, Y.; Cormont, M., 2009:
Rab4b is a small GTPase involved in the control of the glucose transporter GLUT4 localization in adipocyte

Maganto-Garcia, E.; Punzon, C.; Terhorst, C.; Fresno, M., 2008:
Rab5 activation by Toll-like receptor 2 is required for Trypanosoma cruzi internalization and replication in macrophages

Mendoza, P.; Ortiz, R.; Díaz, J.; Quest, A.F.G.; Leyton, L.; Stupack, D.; Torres, V.A., 2014:
Rab5 activation promotes focal adhesion disassembly, migration and invasiveness in tumor cells

Tessneer, K.L.; Jackson, R.M.; Griesel, B.A.; Olson, A.Louise., 2014:
Rab5 activity regulates GLUT4 sorting into insulin-responsive and non-insulin-responsive endosomal compartments: a potential mechanism for development of insulin resistance

Hagiwara, M.; Kobayashi, K-Ichi.; Tadokoro, T.; Yamamoto, Y., 2009:
Rab5 affinity chromatography without nonhydrolyzable GTP analogues

Li, Y.; Low, L-Hian.; Putz, U.; Goh, C-Peng.; Tan, S-Seng.; Howitt, J., 2015:
Rab5 and Ndfip1 are involved in Pten ubiquitination and nuclear trafficking

Falk, J.; Konopacki, F.A.; Zivraj, K.H.; Holt, C.E., 2014:
Rab5 and Rab4 regulate axon elongation in the Xenopus visual system

Torres, V.A.; Stupack, D.G., 2011:
Rab5 in the regulation of cell motility and invasion

Azouz, N.P.; Zur, N.; Efergan, A.; Ohbayashi, N.; Fukuda, M.; Amihai, D.; Hammel, I.; Rothenberg, M.E.; Sagi-Eisenberg, R., 2014:
Rab5 is a novel regulator of mast cell secretory granules: impact on size, cargo, and exocytosis

Díaz, J.; Mendoza, P.; Ortiz, R.; Díaz, N.; Leyton, L.; Stupack, D.; Quest, A.F.G.; Torres, V.A., 2015:
Rab5 is required in metastatic cancer cells for Caveolin-1-enhanced Rac1 activation, migration and invasion

Chen, P-I.; Kong, C.; Su, X.; Stahl, P.D., 2009:
Rab5 isoforms differentially regulate the trafficking and degradation of epidermal growth factor receptors

Chen, P-I.; Schauer, K.; Kong, C.; Harding, A.R.; Goud, B.; Stahl, P.D., 2014:
Rab5 isoforms orchestrate a "division of labor" in the endocytic network; Rab5C modulates Rac-mediated cell motility

Torres, V.A.; Mielgo, A.; Barbero, S.; Hsiao, R.; Wilkins, J.A.; Stupack, D.G., 2010:
Rab5 mediates caspase-8-promoted cell motility and metastasis

Bridges, D.; Fisher, K.; Zolov, S.N.; Xiong, T.; Inoki, K.; Weisman, L.S.; Saltiel, A.R., 2012:
Rab5 proteins regulate activation and localization of target of rapamycin complex 1

Yoshida, H.; Okumura, N.; Kitagishi, Y.; Shirafuji, N.; Matsuda, S., 2010:
Rab5(Q79L) interacts with the carboxyl terminus of RUFY3

Hagemann, A.I.; Xu, X.; Nentwich, O.; Hyvonen, M.; Smith, J.C., 2009:
Rab5-mediated endocytosis of activin is not required for gene activation or long-range signalling in Xenopus

Ma, R.; Hou, X.; Zhang, L.; Sun, S-Chen.; Schedl, T.; Moley, K.; Wang, Q., 2015:
Rab5a is required for spindle length control and kinetochore-microtubule attachment during meiosis in oocytes

Zhao, Z.; Liu, X-Fan.; Wu, H-Cheng.; Zou, S-Biao.; Wang, J-Yi.; Ni, P-Hua.; Chen, X-Hua.; Fan, Q-Shi., 2010:
Rab5a overexpression promoting ovarian cancer cell proliferation may be associated with APPL1-related epidermal growth factor signaling pathway

Kageyama-Yahara, N.; Suehiro, Y.; Yamamoto, T.; Kadowaki, M., 2011:
Rab5a regulates surface expression of FcεRI and functional activation in mast cells

Asaka, M.; Hirase, T.; Hashimoto-Komatsu, A.; Node, K., 2011:
Rab5a-mediated localization of claudin-1 is regulated by proteasomes in endothelial cells

Onodera, Y.; Nam, J-Min.; Hashimoto, A.; Norman, J.C.; Shirato, H.; Hashimoto, S.; Sabe, H., 2012:
Rab5c promotes AMAP1-PRKD2 complex formation to enhance β1 integrin recycling in EGF-induced cancer invasion

Rejman Lipinski, A.; Heymann, J.; Meissner, C.; Karlas, A.; Brinkmann, V.; Meyer, T.F.; Heuer, D., 2010:
Rab6 and Rab11 regulate Chlamydia trachomatis development and golgin-84-dependent Golgi fragmentation

Johns, H.L.; Gonzalez-Lopez, C.; Sayers, C.L.; Hollinshead, M.; Elliott, G., 2014:
Rab6 dependent post-Golgi trafficking of HSV1 envelope proteins to sites of virus envelopment

Elfrink, H.Lim.; Zwart, R.; Cavanillas, Mía.L.; Schindler, A.Jay.; Baas, F.; Scheper, W., 2012:
Rab6 is a modulator of the unfolded protein response: implications for Alzheimer's disease

Sun, Y.; Shestakova, A.; Hunt, L.; Sehgal, S.; Lupashin, V.; Storrie, B., 2007:
Rab6 regulates both ZW10/RINT-1 and conserved oligomeric Golgi complex-dependent Golgi trafficking and homeostasis

Jeong, K.; Kwon, H.; Lee, J.; Jang, D.; Hwang, E.Mi.; Park, J-Yong.; Pak, Y., 2012:
Rab6-mediated retrograde transport regulates inner nuclear membrane targeting of caveolin-2 in response to insulin

Micaroni, M.; Stanley, A.C.; Khromykh, T.; Venturato, J.; Wong, C.X.F.; Lim, J.P.; Marsh, B.J.; Storrie, B.; Gleeson, P.A.; Stow, J.L., 2013:
Rab6a/a' are important Golgi regulators of pro-inflammatory TNF secretion in macrophages

Romero Rosales, K.; Peralta, E.R.; Guenther, G.G.; Wong, S.Y.; Edinger, A.L., 2009:
Rab7 activation by growth factor withdrawal contributes to the induction of apoptosis

Javier-Reyna, R.; Hernández-Ramírez, V.I.; González-Robles, A.; Galván-Mendoza, I.; Osorio-Trujillo, C.; Talamás-Rohana, P., 2012:
Rab7 and actin cytoskeleton participate during mobilization of β1EHFNR in fibronectin-stimulated Entamoeba histolyticatrophozoites

Cogli, L.; Piro, F.; Bucci, C., 2009:
Rab7 and the CMT2B disease

Hida, T.; Sohma, H.; Kokai, Y.; Kawakami, A.; Hirosaki, K.; Okura, M.; Tosa, N.; Yamashita, T.; Jimbow, K., 2011:
Rab7 is a critical mediator in vesicular transport of tyrosinase-related protein 1 in melanocytes

Girard, E.; Chmiest, D.; Fournier, N.; Johannes, L.; Paul, J-Louis.; Vedie, Bît.; Lamaze, C., 2014:
Rab7 is functionally required for selective cargo sorting at the early endosome

BasuRay, S.; Mukherjee, S.; Romero, E.G.; Seaman, M.N.J.; Wandinger-Ness, A., 2013:
Rab7 mutants associated with Charcot-Marie-Tooth disease cause delayed growth factor receptor transport and altered endosomal and nuclear signaling

BasuRay, S.; Mukherjee, S.; Romero, E.; Wilson, M.C.; Wandinger-Ness, A., 2011:
Rab7 mutants associated with Charcot-Marie-Tooth disease exhibit enhanced NGF-stimulated signaling

Vanlandingham, P.A.; Ceresa, B.P., 2009:
Rab7 regulates late endocytic trafficking downstream of multivesicular body biogenesis and cargo sequestration

Mousa, S.A.; Shaqura, M.; Khalefa, B.I.; Zöllner, C.; Schaad, L.; Schneider, J.; Shippenberg, T.S.; Richter, J.F.; Hellweg, R.; Shakibaei, M.; Schäfer, M., 2013:
Rab7 silencing prevents μ-opioid receptor lysosomal targeting and rescues opioid responsiveness to strengthen diabetic neuropathic pain therapy

Wang, T.; Ming, Z.; Xiaochun, W.; Hong, W., 2011:
Rab7: role of its protein interaction cascades in endo-lysosomal traffic

Zhang, M.; Chen, L.; Wang, S.; Wang, T., 2009:
Rab7: roles in membrane trafficking and disease

Caillet, M.; Janvier, K.; Pelchen-Matthews, A.; Delcroix-Genête, D.; Camus, Gégory.; Marsh, M.; Berlioz-Torrent, C., 2012:
Rab7A is required for efficient production of infectious HIV-1

Bucci, C.; Bakke, O.; Progida, C., 2010:
Rab7b and receptors trafficking

Progida, C.; Cogli, L.; Piro, F.; D.L.ca, A.; Bakke, O.; Bucci, C., 2010:
Rab7b controls trafficking from endosomes to the TGN

Peränen, J., 2012:
Rab8 GTPase as a regulator of cell shape

Banton, M.C.; Inder, K.L.; Valk, E.; Rudd, C.E.; Schneider, H., 2014:
Rab8 binding to immune cell-specific adaptor LAX facilitates formation of trans-Golgi network-proximal CTLA-4 vesicles for surface expression

Dong, C.; Yang, L.; Zhang, X.; Gu, H.; Lam, M.L.; Claycomb, W.C.; Xia, H.; Wu, G., 2010:
Rab8 interacts with distinct motifs in alpha2B- and beta2-adrenergic receptors and differentially modulates their transport

Faust, F.; Gomez-Lazaro, M.; Borta, H.; Agricola, B.; Schrader, M., 2008:
Rab8 is involved in zymogen granule formation in pancreatic acinar AR42J cells

Esseltine, J.L.; Ribeiro, F.M.; Ferguson, S.S.G., 2013:
Rab8 modulates metabotropic glutamate receptor subtype 1 intracellular trafficking and signaling in a protein kinase C-dependent manner

Linder, M.D.; Mäyränpää, M.I.; Peränen, J.; Pietilä, T.E.; Pietiäinen, V.M.; Uronen, R-Liisa.; Olkkonen, V.M.; Kovanen, P.T.; Ikonen, E., 2009:
Rab8 regulates ABCA1 cell surface expression and facilitates cholesterol efflux in primary human macrophages

Henry, L.; Sheff, D.R., 2008:
Rab8 regulates basolateral secretory, but not recycling, traffic at the recycling endosome

Chibalina, M.V.; Roberts, R.C.; Arden, S.D.; Kendrick-Jones, J.; Buss, F., 2008:
Rab8-optineurin-myosin VI: analysis of interactions and functions in the secretory pathway

Sun, Y.; Bilan, P.J.; Liu, Z.; Klip, A., 2010:
Rab8A and Rab13 are activated by insulin and regulate GLUT4 translocation in muscle cells

Sato, T.; Iwano, T.; Kunii, M.; Matsuda, S.; Mizuguchi, R.; Jung, Y.; Hagiwara, H.; Yoshihara, Y.; Yuzaki, M.; Harada, R.; Harada, A., 2014:
Rab8a and Rab8b are essential for several apical transport pathways but insufficient for ciliogenesis

Essid, M.; Gopaldass, N.; Yoshida, K.; Merrifield, C.; Soldati, T., 2012:
Rab8a regulates the exocyst-mediated kiss-and-run discharge of the Dictyostelium contractile vacuole

Wu, L.; Xu, D.; Zhou, L.; Xie, B.; Yu, L.; Yang, H.; Huang, L.; Ye, J.; Deng, H.; Yuan, Y.Adam.; Chen, S.; Li, P., 2014:
Rab8a-AS160-MSS4 regulatory circuit controls lipid droplet fusion and growth

Heidrych, P.; Zimmermann, U.; Bress, A.; Pusch, C.M.; Ruth, P.; Pfister, M.; Knipper, M.; Blin, N., 2008:
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form

Chia, P.Zhi.Cheryl.; Gasnereau, I.; Lieu, Z.Zhao.; Gleeson, P.A., 2011:
Rab9-dependent retrograde transport and endosomal sorting of the endopeptidase furin

Roos, J.; Bejai, S.; Oide, S.; Dixelius, C., 2014:
RabGAP22 is required for defense to the vascular pathogen Verticillium longisporum and contributes to stomata immunity

Schoebel, S.; Oesterlin, L.Katharina.; Blankenfeldt, W.; Goody, R.Sidney.; Itzen, A., 2010:
RabGDI displacement by DrrA from Legionella is a consequence of its guanine nucleotide exchange activity

Thomas, C.; Strutt, D., 2014:
Rabaptin-5 and Rabex-5 are neoplastic tumour suppressor genes that interact to modulate Rab5 dynamics in Drosophila melanogaster

Rios, E.J.; Piliponsky, A.M.; Ra, C.; Kalesnikoff, J.; Galli, S.J., 2008:
Rabaptin-5 regulates receptor expression and functional activation in mast cells

Goldman, N.S., 1978:
Rabbinic theology and the unconscious

Endo, S.; Matsunaga, T.; Matsumoto, A.; Arai, Y.; Ohno, S.; El-Kabbani, O.; Tajima, K.; Bunai, Y.; Yamano, S.; Hara, A.; Kitade, Y., 2013:
Rabbit 3-hydroxyhexobarbital dehydrogenase is a NADPH-preferring reductase with broad substrate specificity for ketosteroids, prostaglandin D₂, and other endogenous and xenobiotic carbonyl compounds

Dufour, C.; Bacigalupo, A.; Oneto, R.; Socie, G.; Tichelli, A.; Passweg, J.R.; Risitano, A.M.; Schrezenmeier, H.; Locasciulli, A.; Aljurf, M.; Marsh, J.C.W., 2012:
Rabbit ATG for aplastic anaemia treatment: a backward step?

de Roodt, A.R., 2008:
Rabbit IgG antibodies against phospholipase A2 from Crotalus durisms terrificus neutralize the lethal activity of the venom

Qiao, X.B.; Xu, K.Y.; Li, B.; Luan, X.; Xia, T.; Fan, X.Z., 2014:
Rabbit MSTN gene polymorphisms and genetic effect analysis

Kong, M.Ho.; Do, D.H.; Miyazaki, M.; Wei, F.; Yoon, S-Hwan.; Wang, J.C., 2009:
Rabbit Model for in vivo Study of Intervertebral Disc Degeneration and Regeneration

Sinha, R.K.; Santos, A.V.; Smith, J.W.; Horsewood, P.; Andrew, M.; Kelton, J.G., 1992:
Rabbit Platelets do not Express Fc Receptors for IgG

Greene, H.S., 1935:
Rabbit Pox : Iii. Report Of An Epidemic With Especial Reference To Epidemiological Factors

D.Kruif, P.H., 1922:
Rabbit Septicemia Bacillus, Types D And G, In Normal Rabbits

Rhee, T.K.; Ryu, R.K.; Bangash, A.K.; Wang, D.; Szolc-Kowalska, B.; Harris, K.R.; Sato, K.T.; Chrisman, H.B.; Vogelzang, R.L.; Paunesku, T.; Woloschak, G.E.; Larson, A.C.; Omary, R.A., 2007:
Rabbit VX2 tumors as an animal model of uterine fibroids and for uterine artery embolization

Barter, L.S., 2011:
Rabbit analgesia

Webre, J.M.; Hill, J.M.; Nolan, N.M.; Clement, C.; McFerrin, H.E.; Bhattacharjee, P.S.; Hsia, V.; Neumann, D.M.; Foster, T.P.; Lukiw, W.J.; Thompson, H.W., 2013:
Rabbit and mouse models of HSV-1 latency, reactivation, and recurrent eye diseases

Xie, M.; Yang, S.; Win, H.Latt.; Xiong, L.; Huang, J.; Zhou, J., 2013:
Rabbit annulus fibrosus cell apoptosis induced by mechanical overload via a mitochondrial apoptotic pathway

Grüllich, C.; Ziegler, C.; Finke, Jürgen., 2009:
Rabbit anti T-lymphocyte globulin induces apoptosis in peripheral blood mononuclear cell compartments and leukemia cells, while hematopoetic stem cells are apoptosis resistant

Pan, R.; Sampson, J.M.; Chen, Y.; Vaine, M.; Wang, S.; Lu, S.; Kong, X-Peng., 2013:
Rabbit anti-HIV-1 monoclonal antibodies raised by immunization can mimic the antigen-binding modes of antibodies derived from HIV-1-infected humans

Ziegler, C.; Finke, Jürgen.; Grüllich, C., 2015:
Rabbit anti-T-lymphocyte globulin (ATG) persists with differential reactivity in patients' sera after full hematopoetic regeneration from allogeneic stem cell transplantation

Zhu, L.; Fang, Y.; Liu, Z.; Wang, P.; Wang, Y.; Xu, H., 2008:
Rabbit anti-human leukocyte polyclonal antibody inhibits xenogeneic cell-mediated immune responses

Liu, X.; Liu, Q.; Feng, X.; Tang, Q.; Wang, Z.; Li, S.; Feng, Z.; Zhu, J.; Guan, X., 2011:
Rabbit anti-rabies immunoglobulins production and evaluation

Berenguer, M.; Pons, Jé-Antonio., 2012:
Rabbit anti-thymocyte globulin in liver transplantation: all that glitters is not gold, but 1000 patients are so many to dazzle

Coceres, V.M.; Alonso, Aés.M.; Alomar, M.Lis.; Corvi, Mía.M., 2012:
Rabbit antibodies against Toxoplasma Hsp20 are able to reduce parasite invasion and gliding motility in Toxoplasma gondii and parasite invasion in Neospora caninum

Rocha, R.Malagoli.; Nunes, C.Buzelin.; Sanches, F.Squarcio.Fernandes.; Rocha, G.Fátima.Silva.; Oliveira, Fávio.Nepomuceno.de.; Reis-Filho, J.Sérgio.; Lambros, M.B.; Gobbi, H., 2010:
Rabbit antibodies for hormone receptors and HER2 evaluation in breast cancer

Cong, Y.; Cui, L.; Zhang, Z.; Xi, J.; Wang, M., 2014:
Rabbit antiserum to mouse embryonic stem cells delays compaction of mouse preimplantation embryos

Na, I-Kang.; Wittenbecher, F.; Dziubianau, M.; Herholz, A.; Mensen, A.; Kunkel, Désirée.; Blau, O.; Blau, I.; Thiel, E.; Uharek, L.; Scheibenbogen, C.; Rieger, K.; Thiel, A., 2014:
Rabbit antithymocyte globulin (thymoglobulin) impairs the thymic output of both conventional and regulatory CD4+ T cells after allogeneic hematopoietic stem cell transplantation in adult patients

Gaber, A.Osama.; Monaco, A.P.; Russell, J.A.; Lebranchu, Y.; Mohty, M., 2010:
Rabbit antithymocyte globulin (thymoglobulin): 25 years and new frontiers in solid organ transplantation and haematology

Deeks, E.D.; Keating, G.M., 2009 :
Rabbit antithymocyte globulin (thymoglobulin): a review of its use in the prevention and treatment of acute renal allograft rejection

Takahashi, Y.; Muramatsu, H.; Sakata, N.; Hyakuna, N.; Hamamoto, K.; Kobayashi, R.; Ito, E.; Yagasaki, H.; Ohara, A.; Kikuchi, A.; Morimoto, A.; Yabe, H.; Kudo, K.; Watanabe, K-ichiro.; Ohga, S.; Kojima, S., 2013:
Rabbit antithymocyte globulin and cyclosporine as first-line therapy for children with acquired aplastic anemia

Wittenbecher, F.; Rieger, K.; Dziubianau, M.; Herholz, A.; Mensen, A.; Blau, I.Wolfgang.; Uharek, L.; Dörken, B.; Thiel, A.; Na, I-Kang., 2013:
Rabbit antithymocyte globulin induces rapid expansion of effector memory CD8 T cells without accelerating acute graft versus host disease

Hardinger, K.L.; Brennan, D.C.; Schnitzler, M.A., 2009:
Rabbit antithymocyte globulin is more beneficial in standard kidney than in extended donor recipients

Karapinar, D.Yilmaz.; Karadaş, N.; Ay, Yılmaz.; Akin, M.; Balkan, C.; Aydinok, Yşim.; Kavakli, K., 2014:
Rabbit antithymocyte globulin treatment in childhood acquired severe aplastic anemia

Patel, S.J.; Knight, R.J.; Suki, W.N.; Abdellatif, A.; Duhart, B.T.; Krauss, A.G.; Mannan, S.; Nezakatgoo, N.; Osama Gaber, A., 2011:
Rabbit antithymocyte induction and dosing in deceased donor renal transplant recipients over 60 yr of age

Cheng, X.; Wang, S.; Dai, X.; Shi, C.; Wen, Y.; Zhu, M.; Zhan, S.; Meng, J., 2013:
Rabbit as a novel animal model for hepatitis E virus infection and vaccine evaluation

Mapara, M.; Thomas, B.Sara.; Bhat, K.M., 2012:
Rabbit as an animal model for experimental research

Schoondermark-van de Ven, E.; Van Ranst, M.; de Bruin, W.; van den Hurk, P.; Zeller, M.; Matthijnssens, J.; Heylen, E., 2014:
Rabbit colony infected with a bovine-like G6P[11] rotavirus strain

Wu, Q.; Yeh, A.T., 2008:
Rabbit cornea microstructure response to changes in intraocular pressure visualized by using nonlinear optical microscopy

Isaksson, H.; Malkiewicz, M.; Nowak, R.; Helminen, H.J.; Jurvelin, J.S., 2011:
Rabbit cortical bone tissue increases its elastic stiffness but becomes less viscoelastic with age

Jekl, V.; Redrobe, S., 2014:
Rabbit dental disease and calcium metabolism--the science behind divided opinions

Sprague, R.S.; Hanson, M.S.; Achilleus, D.; Bowles, E.A.; Stephenson, A.H.; Sridharan, M.; Adderley, S.; Procknow, J.; Ellsworth, M.L., 2009:
Rabbit erythrocytes release ATP and dilate skeletal muscle arterioles in the presence of reduced oxygen tension

Sandrini, F.Aurelio.Lucchesi.; Pereira-Júnior, E.Dourado.; Gay-Escoda, C., 2007:
Rabbit facial nerve anastomosis with fibrin glue: nerve conduction velocity evaluation

Withers, W.A., 1948:
Rabbit fever in North Carolina

Høstmark, K.; Moritz, J., 2010:
Rabbit fever--a neck tumor

Maeng, J.Hee.; Lee, E.; Lee, D.Haeng.; Yang, S-Geun., 2013:
Rabbit gastric ulcer models: comparison and evaluation of acetic acid-induced ulcer and mucosectomy-induced ulcer

Carneiro, M.; Rubin, C-Johan.; Di Palma, F.; Albert, F.W.; Alföldi, J.; Martinez Barrio, A.; Pielberg, G.; Rafati, N.; Sayyab, S.; Turner-Maier, J.; Younis, S.; Afonso, S.; Aken, B.; Alves, J.M.; Barrell, D.; Bolet, G.; Boucher, S.; Burbano, Hán.A.; Campos, R.; Chang, J.L.; Duranthon, V.; Fontanesi, L.; Garreau, Hé.; Heiman, D.; Johnson, J.; Mage, R.G.; Peng, Z.; Queney, G.; Rogel-Gaillard, C.; Ruffier, M.; Searle, S.; Villafuerte, R.; Xiong, A.; Young, S.; Forsberg-Nilsson, K.; Good, J.M.; L, 2014:
Rabbit genome analysis reveals a polygenic basis for phenotypic change during domestication

Elsworth, P.G.; Kovaliski, J.; Cooke, B.D., 2012:
Rabbit haemorrhagic disease: are Australian rabbits (Oryctolagus cuniculus) evolving resistance to infection with Czech CAPM 351 RHDV?

Esteves, P.J.; Lopes, A.M.; Magalhães, M.J.; Pinheiro, A.; Gonçalves, D.; Abrantes, J., 2015:
Rabbit hemorrhagic disease virus detected in Pico, Azores, Portugal, revealed a unique endemic strain with more than 17 years of independent evolution

Tam, A.L.; Melancon, M.P.; Ensor, J.; Liu, Y.; Dixon, K.; McWatters, A.; Gupta, S., 2015:
Rabbit hepatic arterial anatomy variations: implications on experimental design

Katiyar, R.D., 1947:
Rabbit husbandry

Nussenblatt, R.B.; Calogero, D.; Buchen, S.Y.; Leder, H.A.; Goodkin, M.; Eydelman, M.B., 2012:
Rabbit intraocular reactivity to endotoxin measured by slit-lamp biomicroscopy and laser flare photometry

Püschel, B.; Viebahn, C., 2010:
Rabbit mating and embryo isolation

Kim, Y-Sung.; Kim, S-Hwan.; Kim, K-Hwa.; Jhin, M-Ju.; Kim, W-Kyung.; Lee, Y-Kyoo.; Seol, Y-Jo.; Lee, Y-Moo., 2013:
Rabbit maxillary sinus augmentation model with simultaneous implant placement: differential responses to the graft materials

Gómez Galán, C.; Ferré Ybarz, L.; Sansosti Viltes, A.; de la Borbolla Morán, J.M.; Peña Peloche, M.A.; Duocastella Selvas, P.; Llusá Serra, A.; Torredemer Palau, A.; Ledesma, A.; Nevot Falcó, S., 2014:
Rabbit meat anaphylaxis

Jordan, D.G., 2007:
Rabbit medicine

Soares, Jão.Henrique.Neves.; Brosnan, R.J.; Smith, A.; Mayhew, P.D., 2015:
Rabbit model of chest wall rigidity induced by fentanyl and the effects of apomorphine

Kang, S.Jeong.; Grossniklaus, H.E., 2011:
Rabbit model of retinoblastoma

Rezende-Neto, J.B.; Rizoli, S.B.; Andrade, M.V.; Lisboa, T.A.; Cunha-Melo, J.R., 2011:
Rabbit model of uncontrolled hemorrhagic shock and hypotensive resuscitation

Fan, J.; Kitajima, S.; Watanabe, T.; Xu, J.; Zhang, J.; Liu, E.; Chen, Y.Eugene., 2015:
Rabbit models for the study of human atherosclerosis: from pathophysiological mechanisms to translational medicine

McCanna, D.J.; Driot, J-Yves.; Hartsook, R.; Ward, K.W., 2008:
Rabbit models of contact lens--associated corneal hypoxia: a review of the literature

van der Laarse, A.; van der Wall, E.E., 2009:
Rabbit models: ideal for imaging purposes?

Rüter, C.; Silva, M.Ruiz.; Grabowski, B.; Lubos, M-Luise.; Scharnert, J.; Poceva, M.; von Tils, D.; Flieger, A.; Heesemann, Jürgen.; Bliska, J.B.; Schmidt, M.Alexander., 2014:
Rabbit monoclonal antibodies directed at the T3SS effector protein YopM identify human pathogenic Yersinia isolates

Feng, L.; Wang, X.; Jin, H., 2011:
Rabbit monoclonal antibody: potential application in cancer therapy

Vicente, J.S.; Saenz-de-Juano, M.D.; Jiménez-Trigos, E.; Viudes-de-Castro, M.P.; Peñaranda, D.S.; Marco-Jiménez, F., 2014:
Rabbit morula vitrification reduces early foetal growth and increases losses throughout gestation

de Almeida, Aé.Martinho., 2014:
Rabbit muscle proteomics: a great leap forward

Dehghan, S.; Tafaghodi, M.; Bolourieh, T.; Mazaheri, V.; Torabi, A.; Abnous, K.; Tavassoti Kheiri, M., 2015:
Rabbit nasal immunization against influenza by dry-powder form of chitosan nanospheres encapsulated with influenza whole virus and adjuvants

Sinding, C.; Thomas-Danguin, T.; Chambault, A.; Béno, N.; Dosne, T.; Chabanet, C.; Schaal, B.; Coureaud, Gérard., 2013:
Rabbit neonates and human adults perceive a blending 6-component odor mixture in a comparable manner

Alley, P., 1997:
Rabbit news and research

Alley, P.E., 2007:
Rabbit news and research quarterly

Kim, J.Han.; Moon, H.Joo.; Lee, J.Hoon.; Kim, J.Hyun.; Kwon, T.Hyun.; Park, Y.Kwan., 2013:
Rabbit notochordal cells modulate the expression of inflammatory mediators by human annulus fibrosus cells cocultured with activated macrophage-like THP-1 cells

Buchen, S.Y.; Calogero, D.; Hilmantel, G.; Eydelman, M.B., 2012:
Rabbit ocular reactivity to bacterial endotoxin contained in aqueous solution and ophthalmic viscosurgical devices

Okabe, T.; Hoshiga, M.; Negoro, N.; Nakakoji, T.; Arishiro, K.; Ishihara, T.; Ueno, H.; Hanafusa, T., 2011:
Rabbit plaque models closely resembling lesions in human coronary artery disease

Huang, Y.; Parker, M.; Xia, C.; Peng, R.; Wasserfall, C.; Clarke, T.; Wu, L.; Chowdhry, T.; Campbell-Thompson, M.; Williams, J.; Clare-Salzler, M.; Atkinson, M.A.; Womer, K.L., 2009:
Rabbit polyclonal mouse antithymocyte globulin administration alters dendritic cell profile and function in NOD mice to suppress diabetogenic responses

Rosario, C.M.; Fry, K.R.; Madison, R., 1989:
Rabbit retinal ganglion cells survive optic nerve transection and entubulation repair with type I collagen nerve guide tubes

Sampaio, R.B.; Mendonca, R.J.; Simioni, A.R.; Costa, R.A.; Siqueira, R.C.; Correa, V.M.; Tedesco, A.C.; Haddad, A.; Coutinho Netto, J.; Jorge, R., 2010:
Rabbit retinal neovascularization induced by latex angiogenic-derived fraction: an experimental model

Paula, J.S.; Ribeiro, V.R.C.; Sampaio, R.B.; Mendonca, R.J.; Haddad, A.; Tedesco, A.C.; Coutinho-Netto, J.; Haendchen, H.A.; Jorge, R., 2012:
Rabbit rubeosis iridis induced by intravitreal latex-derived angiogenic fraction

Xu, H.; Wang, D.; Peng, C.; Huang, X.; Ou, M.; Wang, N.; Wang, P.; Zhou, L.; Ye, X., 2014:
Rabbit sera containing compound danshen dripping pill attenuate leukocytes adhesion to TNF-alpha--activated human umbilical vein endothelial cells by suppressing endothelial ICAM-1 and VCAM-1 expression through NF-kappaB signaling pathway

Diaz-Soto, J.Camilo.; Lasso, P.; Guzmán, F.; Forero-Shelton, M.; Thomas, M.Del.Carmen.; López, M.Carlos.; Guhl, F.; Cuellar, A.; Puerta, Cón.Judith.; González, J.M., 2012:
Rabbit serum against K1 peptide, an immunogenic epitope of the Trypanosoma cruzi KMP-11, decreases parasite invasion to cells

Fallas-López, M.; Rodríguez-D.L.ra, R.; Bárcena-Gama, R.; Sánchez-Torres Esqueda, M.T.; Hernández-Sánchez, D.; Martínez-Hernández, P.A.; Aguilar-Romero, O., 2012:
Rabbit sexual behavior, semen and sperm characteristics when supplemented with sprouted wheat

Swindle-Reilly, K.E.; Shah, M.; Hamilton, P.D.; Eskin, T.A.; Kaushal, S.; Ravi, N., 2009:
Rabbit study of an in situ forming hydrogel vitreous substitute

Culp, B.C.; Culp, W.C., 2008:
Rabbit subselective angiography stroke model

Deshmukh, D.K., 1997:
Rabbit syndrome

Sethi, S., 2001:
Rabbit syndrome - an acute complication of neuroleptic medication

Pandey, S.K., 1998:
Rabbit syndrome - an uncommon side effect of neuroleptic therapy

Gada, M., 1997:
Rabbit syndrome : an uncommon side effect of neuroleptics

Liang, C-Sung.; Yang, F-Wen.; Huang, Y-Chin., 2013:
Rabbit syndrome following discontinuation of paliperidone in a patient with schizoaffective disorder

Jain, R., 2001:
Rabbit syndrome: an acute complication of neurouliptic medication

Gangadhar, B.N.; John, C.J.; Chattergi, S.; Keshavan, M.S.; Narayanan, H.S., 1981:
Rabbit syndrome: patchy disapperance in stage 1 nrem sleep

Han, D.; Guan, X.; Wang, J.; Wei, J.; Li, Q., 2014:
Rabbit tibial periosteum and saphenous arteriovenous vascular bundle as an in vivo bioreactor to construct vascularized tissue-engineered bone: a feasibility study

To, N.; Curtiss, S.; Neu, C.P.; Salgado, C.J.; Jamali, A.A., 2012:
Rabbit trochlear model of osteochondral allograft transplantation

Kim, D.Young.; Reilly, T.J.; Schommer, S.K.; Spagnoli, S.T., 2011:
Rabbit tularemia and hepatic coccidiosis in wild rabbit

Dunea, G., 1987:
Rabbit two

Alcayaga, J.; Del Rio, R.; Moya, E.A.; Freire, Mías.; Iturriaga, R., 2013:
Rabbit ventilatory responses to peripheral chemoexcitators: effects of chronic hypoxia

Alexandre, J.; Schiariti, M.; Rouet, Ré.; Puddu, P.Emilio., 2013:
Rabbit ventricular myocardium undergoing simulated ischemia and reperfusion in a double compartment tissue bath: a model to investigate both antiarrhythmic and arrhythmogenic likelihood

Marshall, V.A.; Carney, E.W., 2012:
Rabbit whole embryo culture

Stetson, I.; Izquierdo-Rico, M.J.; Moros, C.; Chevret, P.; Lorenzo, P.L.; Ballesta, J.; Rebollar, P.G.; Gutiérrez-Gallego, R.; Avilés, M., 2013:
Rabbit zona pellucida composition: a molecular, proteomic and phylogenetic approach

Anonymous, 1915:
Rabbit's Vertebra in the Right Lower Bronchus removed by Superior Bronchoscopy

Olah, Z.; Veselovsky, J., 2007:
Rabbit's intraocular pressure after instillation of timolol and aminoacid lysine, arginine, glycine or taurine mixture

Audigane, L.; Kerfant, Bît-Gilles.; E.H.rchi, A.; Lorenzen-Schmidt, I.; Toumaniantz, G.; Cantereau, A.; Potreau, D.; Charpentier, F.; Noireaud, J.; Gauthier, C., 2009:
Rabbit, a relevant model for the study of cardiac beta 3-adrenoceptors

Hart, E.; Tauschek, M.; Bennett-Wood, V.; Hartland, E.L.; Robins-Browne, R.M., 2009:
Rabbit-specific fimbriae, Ral, alter the patterns of in vitro adherence and intestinal colonisation of rabbits by human-specific enteropathogenic E. coli

Li, T.; Wu, S-Mian.; Xu, Z-Yuan.; Ou-Yang, S., 2015:
Rabbiteye blueberry prevents osteoporosis in ovariectomized rats

Nalca, A.; Nichols, D.K., 2011:
Rabbitpox: a model of airborne transmission of smallpox

Chianini, F.; Fernández-Borges, N.; Vidal, E.; Gibbard, L.; Pintado, Bén.; de Castro, J.; Priola, S.A.; Hamilton, S.; Eaton, S.L.; Finlayson, J.; Pang, Y.; Steele, P.; Reid, H.W.; Dagleish, M.P.; Castilla, Jín., 2012:
Rabbits are not resistant to prion infection

Djasim, U.M.; Hekking-Weijma, J.M.; Wolvius, E.B.; van Neck, J.W.; van der Wal, K.G.H., 2008:
Rabbits as a model for research into craniofacial distraction osteogenesis

Stein, G., 1967:
Rabbits first-then humans

Toni, M.Carolina.; Meirelles, A.Érica.Wilkes.Burton.; Gava, Fábio.Nelson.; Camacho, A.Antônio.; Laus, Jé.Luiz.; Canola, Júlio.Carlos., 2011:
Rabbits' eye globe sonographic biometry

Anonymous, 2011:
Rabbits' feet and four-leaf clovers II. By Caveman

Sethi, N.; Yan, Y.; Quek, D.; Schupbach, T.; Kang, Y., 2010:
Rabconnectin-3 is a functional regulator of mammalian Notch signaling

Tuttle, A.M.; Hoffman, T.L.; Schilling, T.F., 2015:
Rabconnectin-3a regulates vesicle endocytosis and canonical Wnt signaling in zebrafish neural crest migration

Einhorn, Z.; Trapani, J.G.; Liu, Q.; Nicolson, T., 2012:
Rabconnectin3α promotes stable activity of the H+ pump on synaptic vesicles in hair cells

Feng, T.; Pu, J.; Hu, Z.; Liu, D.; Sun, H.; Zhou, G., 2011:
Rabdocoetsin B, a diterpenoid isolated from Isodon coetsa, is a potential proteasome inhibitor and induced apoptosis of t(8;21) leukemia cells

Díaz-Pérez, J.Alexander.; Gómez-Arbeláez, D.; Hurtado-Gomez, G.Alexander., 2015:
Rabdomiosarcoma primario de corazón como causa de síncope recurrente en el adulto

Chu, C-Jun.; Xu, N-Yu.; Li, X-Lun.; Xia, L.; Zhang, J.; Liang, Z-Tao.; Zhao, Z-Zhen.; Chen, D-Feng., 2014:
Rabdosia japonica var. glaucocalyx Flavonoids Fraction Attenuates Lipopolysaccharide-Induced Acute Lung Injury in Mice

Lindgren, C.; Rabelais, F.; Celine, L-Ferdinand., 2008:
Rabelais and Celine. Physicians, writers and language revolters 400 years apart

Vanbeuren, F.T., 1937:
Rabelais as a Physician

Sugimoto, M.; Shirai, N.; Nishino, M.; Kodaira, C.; Uotani, T.; Yamade, M.; Sahara, S.; Ichikawa, H.; Sugimoto, K.; Miyajima, H.; Furuta, T., 2013:
Rabeprazole 10 mg q.d.s. decreases 24-h intragastric acidity significantly more than rabeprazole 20 mg b.d. or 40 mg o.m., overcoming CYP2C19 genotype

Zhu, H-di.; Wang, H.; Xia, X-ming.; Xu, S-man.; Lan, Y., 2014:
Rabeprazole 10 mg versus 20 mg in preventing relapse of gastroesophageal reflux disease: a meta-analysis

Cutler, A.; Robinson, M.; Murthy, A.; Delemos, B., 2010:
Rabeprazole 20 mg for erosive esophagitis-associated symptoms in a large, community-based study: additional results

Maiti, R.; Jaida, J.; Israel, P.L.John.; Koyagura, N.; Mukkisa, S.; Palani, A., 2011:
Rabeprazole and esomeprazole in mild-to-moderate erosive gastroesophageal reflux disease: A comparative study of efficacy and safety

Kuo, C-Hung.; Wang, S.S.W.; Hsu, W-Hung.; Kuo, F-Chen.; Weng, B-Chuang.; Li, C-Jung.; Hsu, P-I.; Chen, A.; Hung, W-Chun.; Yang, Y-Chieh.; Wang, W-Ming.; Wu, D-Chyang., 2010:
Rabeprazole can overcome the impact of CYP2C19 polymorphism on quadruple therapy

Chen, H.; Li, X.; Ge, Z.; Gao, Y.; Chen, X.; Cui, Y., 2010:
Rabeprazole combined with hydrotalcite is effective for patients with bile reflux gastritis after cholecystectomy

Gu, M.; Zhang, Y.; Zhou, X.; Ma, H.; Yao, H.; Ji, F., 2014:
Rabeprazole exhibits antiproliferative effects on human gastric cancer cell lines

Yuan, Y.; Hunt, R.H., 2011:
Rabeprazole extended-release 50 mg compared with esomeprazole 40 mg and rabeprazole delayed release 20 mg

Marelli, S.; Pace, F., 2013:
Rabeprazole for the treatment of acid-related disorders

Miyashita, T.; Shah, F.A.; Marti, G.P.; Wang, J.; Bonde, P.; Gibson, M.K.; Ohta, T.; Montgomery, E.A.; Duncan, M.; Harmon, J.W., 2011:
Rabeprazole impedes the development of reflux-induced esophageal cancer in a surgical rat model

Lebedenko, O.B., 2007:
Rabeprazole in the treatment of acid-dependent diseases in children

Baudeau, C.; Dard, S.; Zylberberg, H.; Patey-Mariaud de Serre, N., 2008:
Rabeprazole induced acute interstitial nephritis

Lam, P.K.Y.; Ng, M.L.; Cheung, T.K.; Wong, B.Y.H.; Tan, V.P.Y.; Fong, D.Y.T.; Wei, W.I.; Wong, B.C.Y., 2010:
Rabeprazole is effective in treating laryngopharyngeal reflux in a randomized placebo-controlled trial

Shahani, S.; Sawant, P.; Dabholkar, P., 2008:
Rabeprazole plus domperidone: the answer for gastro-oesophageal reflux disease

Tirpude, R.N.; Puranik, P.K., 2011:
Rabeprazole sodium delayed-release multiparticulates: Effect of enteric coating layers on product performance

Maev, I.V.; Iurenev, G.L.; Burkov, S.G.; V'iuchnova, E.S., 2007:
Rabeprazole test and comparison of the effectiveness of course treatment with rabeprazole in patients with gastroesophageal reflux disease and non-coronary chest pain

Onyekwere, C.Asabamaka.; Odiagah, J.Nwabuaku.; Igetei, R.; Emanuel, A.Olufunmilayo.Duro.; Ekere, F.; Smith, S., 2015:
Rabeprazole, clarithromycin, and amoxicillin Helicobacter pylori eradication therapy: report of an efficacy study

Wu, I-Chen.; Wu, D-Chyang.; Hsu, P-I.; Lu, C-Yu.; Yu, F-Jung.; Wang, T-En.; Chang, W-Hsiung.; Chen, J-Jon.; Kuo, F-Chen.; Wu, J-Yih.; Wang, W-Ming.; Bair, M-Jong., 2007:
Rabeprazole- versus esomeprazole-based eradication regimens for H. pylori infection

Kekilli, M.; Tanoglu, A.; Ocal, S.; Beyazit, Y., 2014:
Rabeprazole-Induced Tinnitus

Aktaş, B.; Başar, Ömer.; Altinbaş, A.; Ekiz, F.; Yüksel, O., 2013:
Rabeprazole-induced acute cholestatic liver injury

Dadabhai, A.; Friedenberg, F.K., 2009:
Rabeprazole: a pharmacologic and clinical review for acid-related disorders

Baldwin, C.M.; Keam, S.J., 2009:
Rabeprazole: a review of its use in the management of gastric acid-related diseases in adults

Pallotta, S.; Pace, F.; Marelli, S., 2009:
Rabeprazole: a second-generation proton pump inhibitor in the treatment of acid-related disease

Ghosh, A.; Halder, S.; Mandal, S.; Mandal, A.; Basu, M.; Dabholkar, P., 2009:
Rabeto plus: a valuable drug for managing functional dyspepsia

Mori, Y.; Fukuda, M., 2013:
Rabex-5 determines the neurite localization of its downstream Rab proteins in hippocampal neurons

Zhu, H.; Liang, Z.; Li, G., 2010:
Rabex-5 is a Rab22 effector and mediates a Rab22-Rab5 signaling cascade in endocytosis

Mori, Y.; Matsui, T.; Fukuda, M., 2013:
Rabex-5 protein regulates dendritic localization of small GTPase Rab17 and neurite morphogenesis in hippocampal neurons

Aikawa, Y., 2012:
Rabex-5 protein regulates the endocytic trafficking pathway of ubiquitinated neural cell adhesion molecule L1

Yan, H.; Jahanshahi, M.; Horvath, E.A.; Liu, H-Yu.; Pfleger, C.M., 2010:
Rabex-5 ubiquitin ligase activity restricts Ras signaling to establish pathway homeostasis in Drosophila

Hultqvist, M.; Nandakumar, K.Selva.; Björklund, U.; Holmdahl, R., 2010:
Rabeximod reduces arthritis severity in mice by decreasing activation of inflammatory cells

Abbasnejad, F.; Shoja, M.M.; Agutter, P.S.; Alakbarli, F.; Loukas, M.; Shokouhi, G.; Khalili, M.; Tubbs, R.Shane.; Rashidi, R., 2013:
Rabi Rashidi (Rashidi Quarters): a late thirteen to early fourteenth century Middle Eastern Medical School

Prescott, D.W.; Malone, M.W.; Douglass, S.P.; Sauer, K.L., 2012:
Rabi and Larmor nuclear quadrupole double resonance of spin-1 nuclei

Nicklas, E.; Strobel, H.; Zibold, T.; Gross, C.; Malomed, B.A.; Kevrekidis, P.G.; Oberthaler, M.K., 2011:
Rabi flopping induces spatial demixing dynamics

Hsu, C.J., 1982:
Rabi frequency splitting in stimulated Raman scattering

Reetz-Lamour, M.; Amthor, T.; Deiglmayr, J.; Weidemüller, M., 2008:
Rabi oscillations and excitation trapping in the coherent excitation of a mesoscopic frozen Rydberg gas

Ruggenthaler, M.; Bauer, D., 2009:
Rabi oscillations and few-level approximations in time-dependent density functional theory

Karni, O.; Capua, A.; Eisenstein, G.; Sichkovskyi, V.; Ivanov, V.; Reithmaier, J.Peter., 2013:
Rabi oscillations and self-induced transparency in InAs/InP quantum dot semiconductor optical amplifier operating at room temperature

Dietz, B.; Friedrich, T.; Metz, J.; Miski-Oglu, M.; Richter, A.; Schäfer, F.; Stafford, C.A., 2007:
Rabi oscillations at exceptional points in microwave billiards

Yan, M.; DeSalvo, B.J.; Huang, Y.; Naidon, P.; Killian, T.C., 2013:
Rabi oscillations between atomic and molecular condensates driven with coherent one-color photoassociation

Johnson, T.A.; Urban, E.; Henage, T.; Isenhower, L.; Yavuz, D.D.; Walker, T.G.; Saffman, M., 2008:
Rabi oscillations between ground and Rydberg states with dipole-dipole atomic interactions

Dóra, Bázs.; Ziegler, K.; Thalmeier, P.; Nakamura, M., 2009:
Rabi oscillations in Landau-quantized graphene

D.Marchi, A., 1987:
Rabi pulling and long-term stability in cesium beam frequency standards

Layton, K.J.; Tahayori, B.; Mareels, I.M.Y.; Farrell, P.M.; Johnston, L.A., 2014:
Rabi resonance in spin systems: theory and experiment

Calero, C.; Chudnovsky, E.M., 2007:
Rabi spin oscillations generated by ultrasound in solids

Zhang, L.; Zhang, Y.; Zhao, Y.; Zhai, J.; Li, L., 2010:
Rabi splitting induced by a metamaterial plasmon cavity

Jiang, H-Tao.; Chen, H.; Zhu, S-Yao., 2007:
Rabi splitting with excitons in effective (near) zero-index media

Mailles, A.; Boisseleau, D.; Dacheux, L.; Michalewiscz, C.; Gloaguen, C.; Ponçon, N.; Bourhy, H.; Callon, H.; Vaillant, V.; Dabosville, I.; Morineau-L.H.ussine, P., 2011:
Rabid dog illegally imported to France from Morocco, August 2011

Brown, K., 2011:
Rabid epidemiologies: the emergence and resurgence of rabies in twentieth century South Africa

Madhusudana, S.N.; Mani, R.; Ashwin, Y.B.; Desai, A., 2015:
Rabid fox bites and human rabies in a village community in southern India: epidemiological and laboratory investigations, management and follow-up

van Rijckevorsel, G.G.; Swaan, C.M.; van den Bergh, J.P.; Goorhuis, A.; Baayen, D.; Isken, L.; Timen, A.; van den Hoek, A., 2012 :
Rabid puppy-dog imported into the Netherlands from Morocco via Spain, February 2012

Ribadeau-Dumas, F.; Dacheux, L.; Bourhy, Hé., 2013:
Rabies

Jackson, A.C., 2014:
Rabies

Lackenbach, F.I., 1912:
Rabies And The Pasteur Treatment

Anonymous, 1940:
Rabies Controlled

Denison, G.A.; McAlpine, J.G.; Gill, D.G., 1937:
Rabies Deaths in Alabama: Analysis of Case Histories With Regard to Treatment

Swartout, H.O.; Harvey, C.O., 1942:
Rabies Epidermiology And Control In Los Angeles Country

McLean, D.M.; Krause, V.W.; Wilson, W.M.; Hawke, W.A., 1960:
Rabies Following Skunk Bite

Anonymous, 1956:
Rabies In Canada

Anonymous, 1919:
Rabies In England

Anonymous, 1910:
Rabies In Southern California

Frothingham, L., 1899:
Rabies In The Vicinity Of Boston

Berger, F.; Desplanches, Nëlle.; Baillargeaux, S.; Joubert, M.; Miller, M.; Ribadeau-Dumas, F.; Spiegel, Aé.; Bourhy, Hé., 2013:
Rabies Risk: Difficulties Encountered during Management of Grouped Cases of Bat Bites in 2 Isolated Villages in French Guiana

Wiwanitkit, V., 2014:
Rabies Vaccination in a Pediatric Patient with Acute Myeloid Leukemia during the Course of Chemotherapy: a Case report

Reichel, J.; Schneider, J.E., 1934:
Rabies Vaccine Protection Tests

Gluska, S.; Zahavi, E.Erez.; Chein, M.; Gradus, T.; Bauer, A.; Finke, S.; Perlson, E., 2015:
Rabies Virus Hijacks and accelerates the p75NTR retrograde axonal transport machinery

Bhaumik, S., 2013:
Rabies after corneal transplantation: non-canine rabies and eye banking

Wiwanitkit, S.; Wiwanitkit, V., 2012:
Rabies after lung transplantation: Existed evidence

D.Lange, K., 2008:
Rabies also concerns cats

Warrell, M., 2011:
Rabies and African bat lyssavirus encephalitis and its prevention

Nouvellet, P.; Donnelly, C.A.; D.N.rdi, M.; Rhodes, C.J.; D.B.nedictis, P.; Citterio, C.; Obber, F.; Lorenzetto, M.; Pozza, M.Dalla.; Cauchemez, S.; Cattoli, G., 2013:
Rabies and canine distemper virus epidemics in the red fox population of northern Italy (2006-2010)

Hambolu, S.Emmanuel.; Dzikwi, A.A.; Kwaga, J.K.P.; Kazeem, H.M.; Umoh, J.U.; Hambolu, D.A., 2014 :
Rabies and dog bites cases in lagos state Nigeria: a prevalence and retrospective studies (2006-2011)

Mutinelli, F., 2010:
Rabies and feral cat colonies in Italy

Wang, L.; Tang, Q.; Liang, G., 2015:
Rabies and rabies virus in wildlife in mainland China, 1990-2013

Morris, J.; Crowcroft, N.S.; Fooks, A.R.; Brookes, S.M.; Andrews, N., 2007:
Rabies antibody levels in bat handlers in the United Kingdom: immune response before and after purified chick embryo cell rabies booster vaccination

Fayaz, A.; Simani, S.; Fallahian, V.; Eslamifar, A.; Hazrati, M.; Farahtaj, F.; Howaizi, N.; Biglari, P., 2012:
Rabies antibody levels in pregnant women and their newborns after rabies post-exposure prophylaxis

Stapleton, S.F., 2014:
Rabies as encountered in general practice

Koprowski, H., 2008:
Rabies at the dawn of the twenty-first century

Anonymous, 2014:
Rabies confirmed in an imported kitten in France

Cleaveland, S.; Lankester, F.; Townsend, S.; Lembo, T.; Hampson, K., 2015:
Rabies control and elimination: a test case for One Health

Imnadze, P.; Surguladze, V.; Tushishvili, T.; Baidoshvili, L., 2008:
Rabies control and prevention in Georgia: current status and perspectives

Starr, L.E., 1947 :
Rabies control in Georgia

Fagan, R., 1948:
Rabies control in Indiana

Lucas, C.H.Alvarez.; Pino, F.Vargas.; Baer, G.; Morales, P.Kuri.; Cedillo, V.Gutiérrez.; Blanco, M.A.Llanas.; Avila, M.Hernández., 2008:
Rabies control in Mexico

Tang, Q.; Yu, Y-Xin., 2008:
Rabies control should be done from their origin

Anonymous, 2015:
Rabies death attributed to exposure in Central America with symptom onset in a US detention facility—Texas, 2013

Almeida, M.Fernandes.de.; Martorelli, L.Fátima.Alves.; Sodré, M.Martos.; Kataoka, A.Paula.Arruda.Geraldes.; Rosa, A.Ruckert.da.; Oliveira, M.Lucia.de.; Amatuzzi, E., 2011:
Rabies diagnosis and serology in bats from the State of São Paulo, Brazil

Dürr, S.; Naïssengar, S.; Mindekem, R.; Diguimbye, C.; Niezgoda, M.; Kuzmin, I.; Rupprecht, C.E.; Zinsstag, J., 2008:
Rabies diagnosis for developing countries

Alarcón, A.Morales., 2011:
Rabies encephalitis caused by bat bite in a urban area in Colombia

Santhoshkumar, A.; Kalpana, D.; Sowrabha, R., 2012:
Rabies encephalomyelitis vs. ADEM: Usefulness of MR imaging in differential diagnosis

Acharya, A.S.; Kaur, R.; Lakra, K., 2014:
Rabies epidemiology and control in India: a review

Johnson, N.; Un, H.; Fooks, A.R.; Freuling, C.; Müller, T.; Aylan, O.; Vos, A., 2010:
Rabies epidemiology and control in Turkey: past and present

Green, A.L.; Carpenter, L.Rand.; Dunn, J.R., 2012:
Rabies epidemiology, risk assessment, and pre- and post exposure vaccination

Piyaphanee, W.; Shantavasinkul, P.; Phumratanaprapin, W.; Udomchaisakul, P.; Wichianprasat, P.; Benjavongkulchai, M.; Ponam, T.; Tantawichian, T., 2010:
Rabies exposure risk among foreign backpackers in Southeast Asia

Miller, E.T.; Marsh, R.H.; Harris, N.Stuart., 2009:
Rabies exposure--implications for wilderness travelers

Roy, S.; Tyagi, A.; Tiwari, S.; Singh, A.; Sawant, S.V.; Singh, P.K.; Tuli, R., 2010:
Rabies glycoprotein fused with B subunit of cholera toxin expressed in tobacco plants folds into biologically active pentameric protein

Anonymous, 2007:
Rabies has its day

Ogawa, T.; Gamoh, K.; Kanda, K.; Suzuki, T.; Kawashima, A.; Narushima, R.; Shimazaki, T., 2009:
Rabies immune status of dogs brought into the Hyogo Prefecture Animal Well-being Center, Japan

Wang, C.; Wang, Y.; Du, X.; Zeng, L.; Dong, G.; Wu, Y.; Lu, J.; Wei, D.; Zhu, X.; Liu, G.; Zhao, T.; Chen, Z., 2011:
Rabies immunization status of dogs, Beijing, China

Williams, R.B., 1949:
Rabies in Alaska

Anonymous, 1959:
Rabies in Animals Confirmed by Laboratory Examination

Carneiro, Nídia.Francisca.de.Figueiredo.; Caldeira, Aônio.Prates.; Antunes, Lícia.Alves.; Carneiro, Vícius.Figueiredo.; Carneiro, G.Figueiredo., 2010:
Rabies in Artibeus lituratus bats in Montes Claros, State of Minas Gerais

Wilde, H.; Hemachudha, T.; Wacharapluesadee, S.; Lumlertdacha, B.; Tepsumethanon, V., 2014:
Rabies in Asia: the classical zoonosis

Anonymous, 1899:
Rabies in Boston

Anonymous, 1938:
Rabies in California

Whitney, H.G., 1988:
Rabies in Canada

Favi, C.M.; Rodríguez A.L.; Espinosa, M.C.; Yung, P.V.nica., 2008:
Rabies in Chile: 1989-2005

Hu, R.; Tang, Q.; Tang, J.; Fooks, A.R., 2008:
Rabies in China: an update

Niin, E.; Laine, M.; Guiot, A.L.; Demerson, J.M.; Cliquet, F., 2008:
Rabies in Estonia: situation before and after the first campaigns of oral vaccination of wildlife with SAG2 vaccine bait

Cliquet, F.; Picard-Meyer, E.; Robardet, E., 2015:
Rabies in Europe: what are the risks?

Li, G-Wei.; Qu, Z-Yu.; Lam, A.King-Yin.; Wang, J-Guo.; Gao, F-Lan.; Deng, T-Xing.; Lu, J-Hai., 2014:
Rabies in Henan province, China, 2010-2012

Menezes, R., 2008:
Rabies in India

Horton, D.L.; Ismail, M.Z.; Siryan, E.S.; Wali, A.Raheem.A.; Ab-dulla, H.E.; Wise, E.; Voller, K.; Harkess, G.; Marston, D.A.; McElhinney, L.M.; Abbas, S.F.; Fooks, A.R., 2013:
Rabies in Iraq: trends in human cases 2001-2010 and characterisation of animal rabies strains from Baghdad

Ruiz, M.; Chávez, C.Briones., 2010:
Rabies in Latin America

Peters, A., 1907:
Rabies in Massachusetts-Symptoms, Importance of early Diagnosis and Practical Methods for its Suppression

Corner, A.H.; Beauregard, M.; Mitchell, H.K., 1960:
Rabies in Piglets

Sadkowska-Todys, Młgorzata.; Kucharczyk, B., 2009:
Rabies in Poland in 2007

Sadkowska-Todys, Młgorzata.; Kucharczyk, B., 2010:
Rabies in Poland in 2008

Sadkowska-Todys, Młgorzata.; Kucharczyk, B., 2011:
Rabies in Poland in 2009

Sadkowska-Todys, Młgorzata.; Kucharczyk, B., 2012:
Rabies in Poland in 2010

Sadkowska-Todys, M.; Kucharczyk, B., 2014:
Rabies in Poland in 2011

Sadkowska-Todys, Młgorzata.; Kucharczyk, Bżena., 2015 :
Rabies in Poland in 2012

Vargas-Linares, E.; Romaní-Romaní, F.; López-Ingunza, R.; Arrasco-Alegre, J.; Yagui-Moscoso, Mín., 2015:
Rabies in Potos flavus identified in Madre de Dios, Peru

Brodrick, R.G., 1914:
Rabies in San Francisco, With Notes on Some Recent Additions to Our Knowledge of the Disease

Malerczyk, C.; Nel, L.H.; Gniel, D.; Blumberg, L., 2011:
Rabies in South Africa and the FIFA Soccer World Cup: travelers' awareness for an endemic but neglected disease

Gummow, B.; Roefs, Y.A.A.; de Klerk, G., 2010:
Rabies in South Africa between 1993 and 2005--what has been achieved?

Singh, C.K.; Sandhu, B.S., 2008:
Rabies in South Asia: epidemiological investigations and clinical perspective

Ben Néfissa, K.; Moulin, A.Marie.; Dellagi, K., 2008:
Rabies in Tunisia during the 19th century: case increase or disease emergence?

Kretzler, H.H., 2010:
Rabies in Washington state

Mema, S.C.; Friesen, B.; Desai, S.; Rock, M.; McIntyre, L., 2014:
Rabies in a Calgary puppy adopted from the Arctic

Ramesh Masthi, N.R.; Raviprakash, D.; Gangasagara, S.B.; Sriprakash, K.S.; Ashwin, B.Y.; Ullas, P.T.; Madhusudhana, S.N., 2012:
Rabies in a blind patient: confusion after corneal transplantation

Christensen, L.Siig.; Jacobsen, K.; Maersk-Møller, E., 2008:
Rabies in a cat in Greenland

Anonymous, 2008:
Rabies in a dog imported from Iraq--New Jersey, June 2008

Despond, O.; Tucci, M.; Decaluwe, Hélène.; Grégoire, M-Claude.; S Teitelbaum, J.; Turgeon, N., 2007:
Rabies in a nine-year-old child: The myth of the bite

Mondal, P.Chandra.; Char, D.; Mandal, D.; Das, S., 2015:
Rabies in a pregnant woman and delivery of a live fetus

Bailey, J.W., 1948:
Rabies in a steer

D.B.nedictis, P.; Mutinelli, F.; Veggiato, C.; Capua, I.; Squecco, G.; Coassin, R.; Ferri, G., 2009:
Rabies in a vaccinated dog in Italy

Orpetveit, I.; Ytrehus, B.; Vikoren, T.; Handeland, K.; Mjos, A.; Nissen, S.; Blystad, H.; Lund, A., 2011:
Rabies in an Arctic fox on the Svalbard archipelago, Norway, January 2011

Kooi, E.A.; Bouwstra, R.J.; D.R.sa, M., 2012:
Rabies in bats: be alert

Petersen, B.W.; Tack, D.M.; Longenberger, A.; Simeone, A.; Moll, Mària.E.; Deasy, M.P.; Blanton, J.D.; Rupprecht, C.E., 2012:
Rabies in captive deer, Pennsylvania, USA, 2007-2010

Zhang, S.; Tang, Q.; Wu, X.; Liu, Y.; Zhang, F.; Rupprecht, C.E.; Hu, R., 2009:
Rabies in ferret badgers, southeastern China

Vos, A.; Freuling, C.; Eskiizmirliler, S.; Un, H.; Aylan, O.; Johnson, N.; Gürbüz, S.; Müller, W.; Akkoca, N.; Müller, T.; Fooks, A.R.; Askaroglu, H., 2010:
Rabies in foxes, Aegean region, Turkey

Fernandes, M.Emanuel.Barroncas.; Costa, L.Jamile.Corrêa.da.; Andrade, F.Atanaena.Gonçalves.de.; Silva, L.Pereira., 2014:
Rabies in humans and non-human in the state of Pará, Brazilian Amazon

Scott, T.; Hasse, R.; Nel, L., 2012:
Rabies in kudu (Tragelaphus strepsiceros)

Dalfardi, B.; Esnaashary, M.Hosein.; Yarmohammadi, H., 2014:
Rabies in medieval Persian literature - the Canon of Avicenna (980-1037 AD)

Bhatia, H.M., 1949:
Rabies in mongoose

Gautret, P.; Blanton, J.; Dacheux, L.; Ribadeau-Dumas, F.; Brouqui, P.; Parola, P.; Esposito, D.H.; Bourhy, Hé., 2015:
Rabies in nonhuman primates and potential for transmission to humans: a literature review and examination of selected French national data

Singer, A.; Kauhala, K.; Holmala, K.; Smith, G.C., 2010:
Rabies in northeastern Europe--the threat from invasive raccoon dogs

Fitzpatrick, J.L.; Dyer, J.L.; Blanton, J.D.; Kuzmin, I.V.; Rupprecht, C.E., 2015:
Rabies in rodents and lagomorphs in the United States, 1995-2010

Čertíková Chábová, Věra.; Kujal, P.; Škaroupková, P.; Varňourková, Zňka.; Vacková, Šárka.; Husková, Z.; Kikerlová, Sňa.; Sadowski, J.; Kompanowska-Jezierska, E.; Baranowska, I.; Hwang, S.Hee.; Hammock, B.D.; Imig, J.D.; Tesař, Vír.; Červenka, L., 2018:
Combined Inhibition of Soluble Epoxide Hydrolase and Renin-Angiotensin System Exhibits Superior Renoprotection to Renin-Angiotensin System Blockade in 5/6 Nephrectomized Ren-2 Transgenic Hypertensive Rats with Established Chronic Kidney Disease

Wunner, W.H.; Briggs, D.J., 2010:
Rabies in the 21 century

Ward, M.P., 2014:
Rabies in the Dutch East Indies a century ago - a spatio-temporal case study in disease emergence

van Sittert, S.J.; Raath, J.; Akol, G.W.; Miyen, J.M.; Mlahlwa, B.; Sabeta, C.T., 2011:
Rabies in the Eastern Cape Province of South Africa--where are we going wrong?

Botvinkin, A.D.; Otgonbaatar, D.; Tsoodol, S.; Kuzmin, I.V., 2008:
Rabies in the Mongolian steppes

Jackson, A.C., 2011:
Rabies in the critical care unit: diagnostic and therapeutic approaches

Koprowski, H., 2011:
Rabies in the face of the 21st century

Rietz, J.H., 2014:
Rabies in the fox

de Araújo, J.Leal.; Nascimento, E.Melo.; Dantas, Aônio.Flávio.M.; Galiza, G.José.N.; Pedroso, P.Miguel.Ocampos.; Silva, M.Luana.Cristiny.Rodrigues.; Riet-Correa, F., 2015:
Rabies in the insectivorous Pallas's mastiff bat (Molossus molossus) in northeastern Brazil

Barcat, J.Antonio., 2011:
Rabies in the river plate

Gautret, P.; Parola, P., 2014:
Rabies in travelers

David, D.; Bellaiche, M.; Yakobson, B.A., 2011:
Rabies in two vaccinated dogs in Israel

Murray, K.O.; Holmes, K.C.; Hanlon, C.A., 2009:
Rabies in vaccinated dogs and cats in the United States, 1997-2001

Anonymous, 2013:
Rabies mission ready to roll

Numan, M.; Qureshi, Z.A.; Shauket, M.; Hashmi, H.A.; Iqbal, M.; Gill, Z.J.; Habib, M.; Siddique, M., 2011:
Rabies out-break in mules at Mansehra, Pakistan

Weinstein, S., 2013:
Rabies post-exposure prophylaxis

Thomas, E.; Jallow, B.J.; Carayol, I.; Ideh, R.C.; Anderson, S.T., 2016:
Rabies post-exposure prophylaxis at a clinic in Fajara, The Gambia

Quiambao, B.P.; Dytioco, H.Z.; Dizon, R.M.; Crisostomo, M.E.; Laot, T.M.; Teuwen, D.E., 2008:
Rabies post-exposure prophylaxis in the Philippines: health status of patients having received purified equine F(ab')(2) fragment rabies immunoglobulin (Favirab)

Gautret, P.; Lim, P.L.; Shaw, M.; Leder, K., 2011:
Rabies post-exposure prophylaxis in travellers returning from Bali, Indonesia, November 2008 to March 2010

Park, J.Hyun.; Lee, C.Hyu.; Won, Y.Kyoung.; Chin, B.Sik.; Shin, H.Sik.; Kim, J.Yoon., 2014:
Rabies post-exposure prophylaxis of overseas travelers in the international travel clinic of the national medical center from 2006 to 2012, Korea

Quiambao, B.P.; Dy-Tioco, H.Z.; Dizon, R.M.; Crisostomo, M.E.; Teuwen, D.E., 2010:
Rabies post-exposure prophylaxis with purified equine rabies immunoglobulin: one-year follow-up of patients with laboratory-confirmed category III rabies exposure in the Philippines

Shaw, M.T.M.; Visser, J.; Edwards, C., 2015:
Rabies postexposure consultations in New Zealand from 1998 to 2012

Shaw, M.T.M.; O'Brien, B.; Leggat, P.A., 2009:
Rabies postexposure management of travelers presenting to travel health clinics in Auckland and Hamilton, New Zealand

Gautret, P.; Shaw, M.; Gazin, P.; Soula, G.; Delmont, J.; Parola, P.; Soavi, M.José.; Brouqui, P.; Matchett, D.Elizabeth.; Torresi, J., 2008:
Rabies postexposure prophylaxis in returned injured travelers from France, Australia, and New Zealand: a retrospective study

Uwanyiligira, M.; Landry, P.; Genton, B.; de Valliere, S., 2013:
Rabies postexposure prophylaxis in routine practice in view of the new Centers for Disease Control and Prevention and World Health Organization recommendations

Suganuma, A.; Takayama, N.; Yanagisawa, N.; Nishimura, M., 2010:
Rabies pre-exposure immunization effects on rabies post-exposure prophylaxis

Malerczyk, C.; Vakil, H.B.; Bender, W., 2014:
Rabies pre-exposure vaccination of children with purified chick embryo cell vaccine (PCECV)

Gautret, P.; Parola, P.; Shaw, M.; Torresi, J., 2007:
Rabies preexposure vaccination in travelers

Gautret, P.; Parola, P., 2012:
Rabies pretravel vaccination

Roebling, A.D.; Johnson, D.; Blanton, J.D.; Levin, M.; Slate, D.; Fenwick, G.; Rupprecht, C.E., 2014:
Rabies prevention and management of cats in the context of trap-neuter-vaccinate-release programmes

Anderson, J., 2013:
Rabies prevention in people who travel overseas

Xu, H-bin.; Wang, X-tai.; Zhuang, H., 2010:
Rabies prevention strategies and challenges in the United States

Anonymous, 2013:
Rabies project short-listed for charity award

Holzer, M.P.; Solomon, K.D., 2010:
Rabies prophylaxis after an animal attack that caused a ruptured eye and traumatic cataract: a case report

Abazeed, M.E.; Cinti, S., 2008:
Rabies prophylaxis for pregnant women

Topp, R.C., 1981:
Rabies prophylaxis in humans - latest recommendations

Bailey, A.M.; Holder, M.C.; Baker, S.N.; Weant, K.A., 2013:
Rabies prophylaxis in the emergency department

Wilde, H.; Lumlertdacha, B., 2011:
Rabies research in resource-poor countries

D.Q.inzio, M.; McCarthy, A., 2008:
Rabies risk among travellers

Anonymous, 2013:
Rabies risk assessment of exposures to a bat on a commercial airliner

Anonymous, 2012:
Rabies risk assessment of exposures to a bat on a commercial airliner - United States, August 2011

Singer, A.; Kauhala, K.; Holmala, K.; Smith, G.C., 2008:
Rabies risk in raccoon dogs and foxes

Feldmann, B.M., 1974:
Rabies shots

De Marco, G.; McGonagle, D.; Mathieson, H.R.; Merashli, M.; Magee, C.; FitzGerald, O.; Goodfield, M.; Marzo-Ortega, H., 2018:
Combined inhibition of tumour necrosis factor-alpha and interleukin-12/23 for long-standing, refractory psoriatic disease: a differential role for cytokine pathways?

Ly, S.; Buchy, P.; Heng, N.Yim.; Ong, S.; Chhor, N.; Bourhy, Hé.; Vong, S., 2010:
Rabies situation in Cambodia

Munang'andu, H.M.; Mweene, A.S.; Siamudaala, V.; Muma, J.B.; Matandiko, W., 2011:
Rabies status in Zambia for the period 1985-2004

Smreczak, M.; Trebas, P.; Orłowska, A.; mudziński, J.F., 2008:
Rabies surveillance in Poland (1992-2006)

Blanton, J.D.; Robertson, K.; Palmer, D.; Rupprecht, C.E., 2009:
Rabies surveillance in the United States during 2008

Blanton, J.D.; Palmer, D.; Rupprecht, C.E., 2010:
Rabies surveillance in the United States during 2009

Blanton, J.D.; Palmer, D.; Dyer, J.; Rupprecht, C.E., 2012:
Rabies surveillance in the United States during 2010

Blanton, J.D.; Dyer, J.; McBrayer, J.; Rupprecht, C.E., 2013 :
Rabies surveillance in the United States during 2011

Dyer, J.L.; Wallace, R.; Orciari, L.; Hightower, D.; Yager, P.; Blanton, J.D., 2016:
Rabies surveillance in the United States during 2012

Dyer, J.L.; Yager, P.; Orciari, L.; Greenberg, L.; Wallace, R.; Hanlon, C.A.; Blanton, J.D., 2015:
Rabies surveillance in the United States during 2013

Wohlsein, P.; Baumgärtner, W.; Kreipe, H.H.; Haverich, A.; Hori, A.; Stan, A.C., 2012:
Rabies transmission through organ transplantation

Schneider, M.Cristina.; Romijn, P.Catharina.; Uieda, W.; Tamayo, H.; da Silva, D.Fernandes.; Belotto, A.; da Silva, J.Barbosa.; Leanes, L.Fernando., 2009:
Rabies transmitted by vampire bats to humans: an emerging zoonotic disease in Latin America?

Si, H.; Guo, Z-Min.; Hao, Y-Tao.; Liu, Y-Ge.; Zhang, D-Mei.; Rao, S-Qi.; Lu, J-Hai., 2008:
Rabies trend in China (1990-2007) and post-exposure prophylaxis in the Guangdong province

Vigilato, M.A.N.; Cosivi, O.; Knöbl, T.; Clavijo, A.; Silva, H.M.T., 2013:
Rabies update for Latin America and the Caribbean

Skeet, J., 2007:
Rabies vaccination and post-exposure prophylaxis

Rogers, C.L., 2011:
Rabies vaccination compliance following introduction of the triennial vaccination interval--the Texas experience

Parola, P.; Gautret, P., 2013:
Rabies vaccination in travelers: a global perspective

Chrisphonte, Y.; Borja-Hart, N.L., 2010:
Rabies vaccination update

Wieten, R.W.; Leenstra, T.; van Thiel, P.P.A.M.; van Vugt, M.; Stijnis, C.; Goorhuis, A.; Grobusch, M.P., 2013:
Rabies vaccinations: are abbreviated intradermal schedules the future?

Hermann, J.; Fry, A.; Reising, M.; Patterson, P.; Siev, D.; Gatewood, D., 2013:
Rabies vaccine standards: comparison of the 5th and 6th WHO international reference standards to the USDA veterinary reference standard

Kadikoylu, G.; Yavasoglu, I.; Bolaman, Z., 2015:
Rabies vaccine-associated thrombotic thrombocytopenic purpura

Harish, R., 2007:
Rabies vaccine: a case for optional childhood vaccination

Anonymous, 2007:
Rabies vaccines. WHO position paper

Anonymous, 2011:
Rabies vaccines: WHO position paper--recommendations

Tsiang, H., 2007:
Rabies vaccines: a review of progress towards improved efficacy and safety

Kaur, M.; Garg, R.; Singh, S.; Bhatnagar, R., 2015:
Rabies vaccines: where do we stand, where are we heading?

Shankar, S.K.; Mahadevan, A.; Sapico, S.Dias.; Ghodkirekar, M.S.G.; Pinto, R.G.W.; Madhusudana, S.N., 2012:
Rabies viral encephalitis with proable 25 year incubation period!

Gadre, G.; Satishchandra, P.; Mahadevan, A.; Suja, M.S.; Madhusudana, S.N.; Sundaram, C.; Shankar, S.K., 2010:
Rabies viral encephalitis: clinical determinants in diagnosis with special reference to paralytic form

Wirblich, C.; Schnell, M.J., 2011:
Rabies virus (RV) glycoprotein expression levels are not critical for pathogenicity of RV

Carneiro, A.J.B.; Franke, C.R.; Stocker, A.; Dos Santos, F.; Ungar de Sa, J.E.; Moraes-Silva, E.; Alves, J.N.M.; Brunink, S.; Corman, V.M.; Drosten, C.; Drexler, J.F., 2011:
Rabies virus RNA in naturally infected vampire bats, northeastern Brazil

Tobiume, M.; Sato, Y.; Katano, H.; Nakajima, N.; Tanaka, K.; Noguchi, A.; Inoue, S.; Hasegawa, H.; Iwasa, Y.; Tanaka, J.; Hayashi, H.; Yoshida, S.; Kurane, I.; Sata, T., 2009:
Rabies virus dissemination in neural tissues of autopsy cases due to rabies imported into Japan from the Philippines: immunohistochemistry

Allendorf, S.Dora.; Cortez, A.; Heinemann, M.Bryan.; Harary, C.M.Appolinário.; Antunes, Jão.Marcelo.A.P.; Peres, M.Gea.; Vicente, Aácia.Ferreira.; Sodré, M.Martos.; da Rosa, A.Ruckert.; Megid, J., 2012:
Rabies virus distribution in tissues and molecular characterization of strains from naturally infected non-hematophagous bats

Hislop, J.N.; Islam, T.A.; Eleftheriadou, I.; Carpentier, D.C.J.; Trabalza, A.; Parkinson, M.; Schiavo, G.; Mazarakis, N.D., 2014:
Rabies virus envelope glycoprotein targets lentiviral vectors to the axonal retrograde pathway in motor neurons

Wen, Y.; Wang, H.; Wu, H.; Yang, F.; Tripp, R.A.; Hogan, R.J.; Fu, Z.F., 2011:
Rabies virus expressing dendritic cell-activating molecules enhances the innate and adaptive immune response to vaccination

Astray, R.M.; Ventini, D.C.; Boldorini, V.L.L.; Silva, F.G.; Rocca, M.P.; Pereira, C.A., 2014:
Rabies virus glycoprotein and immune response pattern using recombinant protein or recombinant RNA viral vectors

Lemos, M.Alexandre.Nobre.; Santos, A.Souza.Dos.; Astray, R.Mancini.; Pereira, C.Augusto.; Jorge, S.Attie.Calil., 2009:
Rabies virus glycoprotein expression in Drosophila S2 cells. I: design of expression/selection vectors, subpopulations selection and influence of sodium butyrate and culture medium on protein expression

Dos Santos, A.Souza.; Lemos, M.Alexandre.Nobre.; Pereira, C.Augusto.; Jorge, S.Attie.Calil., 2010:
Rabies virus glycoprotein expression in Drosophila S2 cells: influence of re-selection on protein expression

Zhang, G.; Wang, H.; Mahmood, F.; Fu, Z.F., 2014:
Rabies virus glycoprotein is an important determinant for the induction of innate immune responses and the pathogenic mechanisms

Mori, T.; Morimoto, K., 2014:
Rabies virus glycoprotein variants display different patterns in rabies monosynaptic tracing

Ross, B.A.s.; Favi, C.M.; Vásquez V.A., 2008:
Rabies virus glycoprotein: structure, immunogenicity and pathogenic role

Silva, L.Augustinho.Menezes.da.; Machado, Jé.Lindemberg.Martins.; Melo, M.de.Lima.; Alencar, Vônica.Isabel.de.Brito.; Melo, R.Soares.de.; Andrade, L.Pimentel.de.; Silva, E.Messias.Vilar.Gonçalves.da., 2012:
Rabies virus in Molossus molossus (Chiroptera: Molossidae) in the State of Pernambuco, Northeastern Brazil

Oliveira, R.de.Novaes.; de Souza, S.Pinheiro.; Lobo, R.Spinelli.Vaz.; Castilho, J.Galera.; Macedo, C.Isabel.; Carnieli, P.; Fahl, W.Oliveira.; Achkar, S.Maria.; Scheffer, K.Corrêa.; Kotait, I.; Carrieri, M.Luiza.; Brandão, P.Eduardo., 2010:
Rabies virus in insectivorous bats: implications of the diversity of the nucleoprotein and glycoprotein genes for molecular epidemiology

Scheffer, K.Corrêa.; Carrieri, M.Luiza.; Albas, A.; Santos, H.Cristina.Pires.dos.; Kotait, I.; Ito, F.Honma., 2007:
Rabies virus in naturally infected bats in the State of São Paulo, Southeastern Brazil

Davis, A.D.; Jarvis, J.A.; Pouliott, C.; Rudd, R.J., 2014:
Rabies virus infection in Eptesicus fuscus bats born in captivity (naïve bats)

Faul, E.J.; Wanjalla, C.N.; Suthar, M.S.; Gale, M.; Wirblich, C.; Schnell, M.J., 2010:
Rabies virus infection induces type I interferon production in an IPS-1 dependent manner while dendritic cell activation relies on IFNAR signaling

Lawrence, T.M.; Hudacek, A.W.; de Zoete, M.R.; Flavell, R.A.; Schnell, M.J., 2013:
Rabies virus is recognized by the NLRP3 inflammasome and activates interleukin-1β release in murine dendritic cells

Reddy, R.V.Chandrasekhar.; Mohana Subramanian, B.; Surendra, K.S.N.L.; Babu, R.P.Aravindh.; Rana, S.K.; Manjari, K.Sunitha.; Srinivasan, V.A., 2016:
Rabies virus isolates of India - simultaneous existence of two distinct evolutionary lineages

Gury Dohmen, F.; Beltrán, F., 2010:
Rabies virus isolation in the salivary glands of insectivorous bats

Yin, X.; Li, Z.; Li, J.; Yi, Y.; Zhang, Y.; Li, X.; Li, B.; Yang, B.; Lan, X.; Li, Y.; Jiao, W.; Zhang, Z.; Liu, J., 2013:
Rabies virus nucleoprotein expressed in silkworm pupae at high-levels and evaluation of immune responses in mice

Masatani, T.; Ito, N.; Shimizu, K.; Ito, Y.; Nakagawa, K.; Sawaki, Y.; Koyama, H.; Sugiyama, M., 2010:
Rabies virus nucleoprotein functions to evade activation of the RIG-I-mediated antiviral response

Franka, R.; Wu, X.; Jackson, F.R.; Velasco-Villa, A.; Palmer, D.P.; Henderson, H.; Hayat, W.; Green, D.B.; Blanton, J.D.; Greenberg, L.; Rupprecht, C.E., 2010:
Rabies virus pathogenesis in relationship to intervention with inactivated and attenuated rabies vaccines

Tenzin; Wacharapluesadee, S.; Denduangboripant, J.; Dhand, N.K.; Dorji, R.; Tshering, D.; Rinzin, K.; Raika, V.; Dahal, N.; Ward, M.P., 2011 :
Rabies virus strains circulating in Bhutan: implications for control

Evans, J.S.; Horton, D.L.; Easton, A.J.; Fooks, A.R.; Banyard, A.C., 2013:
Rabies virus vaccines: is there a need for a pan-lyssavirus vaccine?

Ohara, S.; Sato, S.; Oyama, K.; Tsutsui, K-Ichiro.; Iijima, T., 2014:
Rabies virus vector transgene expression level and cytotoxicity improvement induced by deletion of glycoprotein gene

Fontana, D.; Kratje, R.; Etcheverrigaray, M.; Prieto, C., 2014:
Rabies virus-like particles expressed in HEK293 cells

Case, G.I., 1947:
Rabies with atypical course and symptoms

McCall, B.; Davison, R., 2011:
Rabies – prevention in travellers

Sawyer, W.A., 1912:
Rabies, And Its Present Status In California

Scull, A.J., 1949:
Rabies, a community problem in Texas

Paulke-Korinek, M.; Kollaritsch, H., 2008:
Rabies, a neglected threat

Berentsen, A.R.; Dunbar, M.R.; Becker, M.S.; M'soka, J.; Droge, E.; Sakuya, N.M.; Matandiko, W.; McRobb, R.; Hanlon, C.A., 2015:
Rabies, canine distemper, and canine parvovirus exposure in large carnivore communities from two Zambian ecosystems

Dainty, L.A.; Morgan, S.A.; Parker, M.E.; Burke, R.L., 2014:
Rabies, readiness, and role 1 medical care

Bourhy, Hé.; Dautry-Varsat, A.; Hotez, P.J.; Salomon, Jérôme., 2011:
Rabies, still neglected after 125 years of vaccination

Murthy, J.M.K.; Dastur, F.D.; Khadilkar, S.V.; Kochar, D.K., 2014:
Rabies, tetanus, leprosy, and malaria

Steffens, I.; Ekdahl, K., 2008:
Rabies--a recurrent danger to European countries from dogs introduced from endemic countries

Müller, T.; Freuling, C.M., 2012:
Rabies--research towards elimination

Brückner, G., 2010:
Rabies--the role of the World Organisation for animal health in mobilising global control

Records, E., 1932:
Rabies-Its History in Nevada

Kinyoun, J.J., 1891:
Rabies-Its Prevention and Treatment

Matouch, O.; Vitasek, J.; Semerad, Z.; Malena, M., 2008:
Rabies-free status of the Czech Republic after 15 years of oral vaccination

Brady, M.T.; Bernstein, H.H.; Byington, C.L.; Edwards, K.M.; Fisher, M.C.; Glode, M.P.; Jackson, M.Anne.; Keyserling, H.L.; Kimberlin, D.W.; Maldonado, Y.A.; Orenstein, W.A.; Schutze, G.E.; Willoughby, R.E.; Bortolussi, R.; Fischer, M.A.; Gellin, B.; Gorman, R.L.; Lee, L.; Pratt, R.Douglas.; Read, J.S.; Seward, J.; Starke, J.R.; Swanson, J.; Tan, T.Q.; Baker, C.J.; Long, S.S.; Meissner, H.Cody.; Pickering, L.K.; Rubin, L.G.; Frantz, J., 2011:
Rabies-prevention policy update: new reduced-dose schedule

Robertson, K.; Lumlertdacha, B.; Franka, R.; Petersen, B.; Bhengsri, S.; Henchaichon, S.; Peruski, L.F.; Baggett, H.C.; Maloney, S.A.; Rupprecht, C.E., 2011:
Rabies-related knowledge and practices among persons at risk of bat exposures in Thailand

Moore, S.M.; Hanlon, C.A., 2010:
Rabies-specific antibodies: measuring surrogates of protection against a fatal disease

Swormink, B.Klein., 2014:
Rabies-suspicion difficult for veterinarians

Wyatt, J., 2007:
Rabies-update on a global disease

Wu, Q.; Yu, F.; Xu, J.; Li, Y.; Chen, H.; Xiao, S.; Fu, Z.F.; Fang, L., 2014:
Rabies-virus-glycoprotein-pseudotyped recombinant baculovirus vaccine confers complete protection against lethal rabies virus challenge in a mouse model

Anonymous, 1937:
Rabies: An All-Year Hazard

Anonymous, 1954:
Rabies: Introduction

Anonymous, 1939:
Rabies: Its Present-Day Problems

Peters, A., 1891:
Rabies: Its Prevalence and Suppression

Jain, S.; Parwar, V.R., 2010:
Rabies: Post exposure prophylaxis for the health care workers

Nicolle, L., 2007 :
Rabies: Still with us

Ernst, H.C., 1891:
Rabies: With an Account of Pasteur's Work and Methods

Anonymous, 2014:
Rabies: a deadly viral disease

Senior, K., 2008:
Rabies: a preventable killer

Chatterjee, S.; Riaz, H., 2014:
Rabies: beware of the dog

Panda, A.K.; Thakur, S.D.; Katoch, R.C., 2009:
Rabies: control strategies for Himalayan states of the Indian subcontinent

Leung, A.K.C.; Davies, H.Dele.; Hon, K-Lun.Ellis., 2008:
Rabies: epidemiology, pathogenesis, and prophylaxis

Haider, S., 2008:
Rabies: old disease, new challenges

Pye, J., 2015:
Rabies: prevention strategies for overseas travellers

Hatz, C.F.R.; Kuenzli, E.; Funk, M., 2013:
Rabies: relevance, prevention, and management in travel medicine

Driver, C., 2014:
Rabies: risk, prognosis and prevention

Dodet, B.; Durrheim, D.N.; Rees, H., 2014 :
Rabies: underused vaccines, unnecessary deaths

DUFFY, C.E.; WOOLLEY, P.V.; NOLTING, W.S., 1947:
Rabies; a case report with notes on the isolation of the virus from saliva

Schlotthauer, C.F., 2010:
Rabies; a general consideration

Chant, H.L., 2014:
Rabies; a national public health problem

Parkhitko, C.A.Cyrillic.А.; Favorova, C.O.Cyrillic.О.; Henske, E.P., 2012:
Rabin8 Protein Interacts with GTPase Rheb and Inhibits Phosphorylation of Ser235/Ser236 in Small Ribosomal Subunit Protein S6

Ghosh, S.; Tagore, R., 2014:
Rabindranath Tagore and his vision and thought in health perspectives

Narita, R.; Kitaura, H.; Torii, A.; Tashiro, E.; Miyazawa, M.; Ariga, H.; Iguchi-Ariga, S.M.M., 2012:
Rabring7 degrades c-Myc through complex formation with MM-1

Zhang, J.; Naslavsky, N.; Caplan, S., 2012:
Rabs and EHDs: alternate modes for traffic control

Tang, B.Luen.; Ng, E.Ling., 2009:
Rabs and cancer cell motility

Lim, Y.Shan.; Chua, C.En.Lin.; Tang, B.Luen., 2011:
Rabs and other small GTPases in ciliary transport

Chua, C.En.Lin.; Tang, B.Luen., 2012:
Rabs, SNAREs and α-synuclein--membrane trafficking defects in synucleinopathies

Parveen, B.Ahamed.; Sindhuja, R., 2008:
Rabson-Mendenhall syndrome

Aguado Lobo, I.; Garcia Cuartero, B.; González Vergaz, A., 2012:
Rabson-Mendenhall syndrome

Gupta, J.; Daniel, J.M.; Vasudevan, V., 2014:
Rabson-Mendenhall syndrome

Bathi, R.J.; Parveen, S.; Mutalik, S.; Rao, R., 2010:
Rabson-Mendenhall syndrome: two case reports and a brief review of the literature

Sann, S.B.; Crane, M.M.; Lu, H.; Jin, Y., 2012:
Rabx-5 regulates RAB-5 early endosomal compartments and synaptic vesicles in C. elegans

Birukova, A.A.; Burdette, D.; Moldobaeva, N.; Xing, J.; Fu, P.; Birukov, K.G., 2010:
Rac GTPase is a hub for protein kinase A and Epac signaling in endothelial barrier protection by cAMP

Guo, F.; Cancelas, J.A.; Hildeman, D.; Williams, D.A.; Zheng, Y., 2008:
Rac GTPase isoforms Rac1 and Rac2 play a redundant and crucial role in T-cell development

Labouesse, M., 2012:
Rac GTPase signaling in mechanotransduction during embryonic morphogenesis

Marland, J.R.K.; Pan, D.; Buttery, P.C., 2011:
Rac GTPase-activating protein (Rac GAP) α1-Chimaerin undergoes proteasomal degradation and is stabilized by diacylglycerol signaling in neurons

Sato, Y.; Oda, H.; Patrick, M.S.; Baba, Y.; Rus'd, A.A.; Azuma, Y.; Abe, T.; Shirai, M.; Suzuki, H., 2010:
Rac GTPases are involved in development, survival and homeostasis of T cells

Konstantinidis, D.G.; George, A.; Kalfa, T.A., 2011:
Rac GTPases in erythroid biology

Pai, S-Yun.; Kim, C.; Williams, D.A., 2011:
Rac GTPases in human diseases

Dumont, C.; Corsoni-Tadrzak, A.; Ruf, S.; de Boer, J.; Williams, A.; Turner, M.; Kioussis, D.; Tybulewicz, V.L.J., 2009:
Rac GTPases play critical roles in early T-cell development

Ji, P.; Lodish, H.F., 2011:
Rac GTPases play multiple roles in erythropoiesis

Cernuda-Morollón, E.; Millán, J.; Shipman, M.; Marelli-Berg, F.M.; Ridley, A.J., 2010:
Rac activation by the T-cell receptor inhibits T cell migration

Aslan, J.E.; McCarty, O.J.T., 2013:
Rac and Cdc42 team up for platelets

Knaus, U.G.; Bamberg, A.; Bokoch, G.M., 2008:
Rac and Rap GTPase activation assays

Parri, M.; Chiarugi, P., 2010:
Rac and Rho GTPases in cancer cell motility control

Symons, M.; Segall, J.E., 2009:
Rac and Rho driving tumor invasion: who's at the wheel?

Kawashima, T.; Kitamura, T., 2008:
Rac and nuclear translocation of signal transducers and activators of transcription factors

Halstead, J.R.; Savaskan, N.E.; van den Bout, I.; Van Horck, F.; Hajdo-Milasinovic, A.; Snell, M.; Keune, W-Jan.; Ten Klooster, J-Paul.; Hordijk, P.L.; Divecha, N., 2011:
Rac controls PIP5K localisation and PtdIns(4,5)P₂ synthesis, which modulates vinculin localisation and neurite dynamics

Croke, M.; Ross, F.Patrick.; Korhonen, M.; Williams, D.A.; Zou, W.; Teitelbaum, S.L., 2012:
Rac deletion in osteoclasts causes severe osteopetrosis

Steffen, A.; Ladwein, M.; Dimchev, G.A.; Hein, A.; Schwenkmezger, L.; Arens, S.; Ladwein, K.I.; Margit Holleboom, J.; Schur, F.; Victor Small, J.; Schwarz, J.; Gerhard, R.; Faix, J.; Stradal, T.E.B.; Brakebusch, C.; Rottner, K., 2014:
Rac function is crucial for cell migration but is not required for spreading and focal adhesion formation

Davis, R.L., 2010:
Rac in the act of forgetting

Xu, S-wen.; Liu, S.; Eastwood, M.; Sonnylal, S.; Denton, C.P.; Abraham, D.J.; Leask, A., 2010:
Rac inhibition reverses the phenotype of fibrotic fibroblasts

Williams, L.M.; Lali, F.; Willetts, K.; Balague, C.; Godessart, N.; Brennan, F.; Feldmann, M.; Foxwell, B.M.J., 2008:
Rac mediates TNF-induced cytokine production via modulation of NF-kappaB

Kuiper, J.W.P.; Sun, C.; Magalhães, M.A.O.; Glogauer, M., 2012:
Rac regulates PtdInsP₃ signaling and the chemotactic compass through a redox-mediated feedback loop

Kageyama, Y.; Doi, T.; Akamatsu, S.; Kuroyanagi, G.; Kondo, A.; Mizutani, J.; Otsuka, T.; Tokuda, H.; Kozawa, O.; Ogura, S., 2014:
Rac regulates collagen-induced HSP27 phosphorylation via p44/p42 MAP kinase in human platelets

Parsons, M.; Adams, J.C., 2008:
Rac regulates the interaction of fascin with protein kinase C in cell migration

Sebe, A.; Masszi, Aás.; Zulys, M.; Yeung, T.; Speight, P.; Rotstein, O.D.; Nakano, H.; Mucsi, Ián.; Szászi, K.; Kapus, Aás., 2007:
Rac, PAK and p38 regulate cell contact-dependent nuclear translocation of myocardin-related transcription factor

Rao, G.K.; Bender, J.R., 2008:
Rac, PAK, and eNOS ACTion

Del Pozo, M.A.; Schwartz, M.A., 2007:
Rac, membrane heterogeneity, caveolin and regulation of growth by integrins

Freret, M.; Gouel, F.; Buquet, C.; Legrand, E.; Vannier, J-Pierre.; Vasse, M.; Dubus, I., 2011:
Rac-1 GTPase controls the capacity of human leukaemic lymphoblasts to migrate on fibronectin in response to SDF-1α (CXCL12)

Carrizzo, A.; Forte, M.; Lembo, M.; Formisano, L.; Puca, A.A.; Vecchione, C., 2015:
Rac-1 as a new therapeutic target in cerebro- and cardio-vascular diseases

Diebold, I.; Djordjevic, T.; Hess, J.; Görlach, A., 2009:
Rac-1 promotes pulmonary artery smooth muscle cell proliferation by upregulation of plasminogen activator inhibitor-1: role of NFkappaB-dependent hypoxia-inducible factor-1alpha transcription

Chiu, T.Ting.; Sun, Y.; Koshkina, A.; Klip, A., 2013:
Rac-1 superactivation triggers insulin-independent glucose transporter 4 (GLUT4) translocation that bypasses signaling defects exerted by c-Jun N-terminal kinase (JNK)- and ceramide-induced insulin resistance

Tivodar, S.; Kalemaki, K.; Kounoupa, Z.; Vidaki, M.; Theodorakis, K.; Denaxa, M.; Kessaris, N.; de Curtis, I.; Pachnis, V.; Karagogeos, D., 2016:
Rac-GTPases Regulate Microtubule Stability and Axon Growth of Cortical GABAergic Interneurons

Halpert, M.; Abu-Abied, M.; Avisar, D.; Moskovitz, Y.; Altshuler, O.; Cohen, A.; Weissberg, M.; Riov, J.; Gottlieb, H.E.; Perl, A.; Sadot, E., 2012 :
Rac-dependent doubling of HeLa cell area and impairment of cell migration and cell cycle by compounds from Iris germanica

Elnakish, M.T.; Hassona, M.D.H.; Alhaj, M.A.; Moldovan, L.; Janssen, P.M.L.; Khan, M.; Hassanain, H.H., 2013:
Rac-induced left ventricular dilation in thyroxin-treated ZmRacD transgenic mice: role of cardiomyocyte apoptosis and myocardial fibrosis

Bustelo, Xé.R.; Ojeda, V.; Barreira, Mía.; Sauzeau, V.; Castro-Castro, A., 2013:
Rac-ing to the plasma membrane: the long and complex work commute of Rac1 during cell signaling

Fumoto, S.; Nishi, J.; Ishii, H.; Wang, X.; Miyamoto, H.; Yoshikawa, N.; Nakashima, M.; Nakamura, J.; Nishida, K., 2009:
Rac-mediated macropinocytosis is a critical route for naked plasmid DNA transfer in mice

Sima, C.; Gastfreund, S.; Sun, C.; Glogauer, M., 2014:
Rac-null leukocytes are associated with increased inflammation-mediated alveolar bone loss

Laurin, Mélanie.; Huber, J.; Pelletier, A.; Houalla, T.; Park, M.; Fukui, Y.; Haibe-Kains, B.; Muller, W.J.; Côté, J-François., 2013:
Rac-specific guanine nucleotide exchange factor DOCK1 is a critical regulator of HER2-mediated breast cancer metastasis

Yang, H-Young.; Kim, J.; Lee, K-Yeol.; Jang, Y-Suk., 2010:
Rac/ROS-related protein kinase C and phosphatidylinositol-3-kinase signaling are involved in a negative regulating cascade in B cell activation by antibody-mediated cross-linking of MHC class II molecules

Buongiorno, P.; Pethe, V.V.; Charames, G.S.; Esufali, S.; Bapat, B., 2008:
Rac1 GTPase and the Rac1 exchange factor Tiam1 associate with Wnt-responsive promoters to enhance beta-catenin/TCF-dependent transcription in colorectal cancer cells

Park, H.Tae.; Feltri, M.Laura., 2011:
Rac1 GTPase controls myelination and demyelination

Shibata, S.; Mu, S.; Kawarazaki, H.; Muraoka, K.; Ishizawa, K-ichi.; Yoshida, S.; Kawarazaki, W.; Takeuchi, M.; Ayuzawa, N.; Miyoshi, J.; Takai, Y.; Ishikawa, A.; Shimosawa, T.; Ando, K.; Nagase, M.; Fujita, T., 2011:
Rac1 GTPase in rodent kidneys is essential for salt-sensitive hypertension via a mineralocorticoid receptor-dependent pathway

Tan, T.Lin.; Fang, N.; Neo, T.Ling.; Singh, P.; Zhang, J.; Zhou, R.; Koh, C-Gee.; Chan, V.; Lim, S.Gee.; Chen, W.Ning., 2007:
Rac1 GTPase is activated by hepatitis B virus replication--involvement of HBX

Guignandon, A.; Faure, Céline.; Neutelings, T.; Rattner, A.; Mineur, P.; Linossier, M-Thérèse.; Laroche, N.; Lambert, C.; Deroanne, C.; Nusgens, B.; Demets, Ré.; Colige, A.; Vico, L., 2015:
Rac1 GTPase silencing counteracts microgravity-induced effects on osteoblastic cells

Fritz, G.; Kaina, B., 2014:
Rac1 GTPase, a multifunctional player in the regulation of genotoxic stress response

Maddala, R.; Chauhan, B.K.; Walker, C.; Zheng, Y.; Robinson, M.L.; Lang, R.A.; Rao, P.V., 2012:
Rac1 GTPase-deficient mouse lens exhibits defects in shape, suture formation, fiber cell migration and survival

Bosco, E.E.; Mulloy, J.C.; Zheng, Y., 2009:
Rac1 GTPase: a "Rac" of all trades

Zhang, P.; Zhang, X.; Fan, J-Li.; Hao, X-Feng.; Wang, Y-Sheng.; Hui, Y-Nian.; Hu, D.; Zhou, J., 2011:
Rac1 activates HIF-1 in laser induced choroidal neovascularization

Zhang, P.; Zhang, X.; Hao, X.; Wang, Y.; Hui, Y.; Wang, H.; Hu, D.; Zhou, J., 2009:
Rac1 activates HIF-1 in retinal pigment epithelium cells under hypoxia

Goc, A.; Abdalla, M.; Al-Azayzih, A.; Somanath, P.R., 2013:
Rac1 activation driven by 14-3-3ζ dimerization promotes prostate cancer cell-matrix interactions, motility and transendothelial migration

Yu, H.; Suleiman, H.; Kim, A.H.J.; Miner, J.H.; Dani, A.; Shaw, A.S.; Akilesh, S., 2014:
Rac1 activation in podocytes induces rapid foot process effacement and proteinuria

Zhang, T.; Lu, X.; Beier, F.; Feng, Q., 2011:
Rac1 activation induces tumour necrosis factor-α expression and cardiac dysfunction in endotoxemia

Hage, B.; Meinel, K.; Baum, I.; Giehl, K.; Menke, A., 2009:
Rac1 activation inhibits E-cadherin-mediated adherens junctions via binding to IQGAP1 in pancreatic carcinoma cells

Johanna, Gérrez-Vargas.; Fredy, C-Alvarez.John.; David, Vásquez-Carvajal.; Natalia, Mñez-Velásquez.Maria.; Angel, Céspedes-Rubio.; Patricia, C-Gómez.Gloria., 2011:
Rac1 activity changes are associated with neuronal pathology and spatial memory long-term recovery after global cerebral ischemia

Nethe, M.; de Kreuk, B-Jan.; Tauriello, D.V.F.; Anthony, E.C.; Snoek, B.; Stumpel, T.; Salinas, P.C.; Maurice, M.M.; Geerts, D.; Deelder, Aé.M.; Hensbergen, P.J.; Hordijk, P.L., 2013:
Rac1 acts in conjunction with Nedd4 and dishevelled-1 to promote maturation of cell-cell contacts

Braun, A.; Dang, K.; Buslig, F.; Baird, M.A.; Davidson, M.W.; Waterman, C.M.; Myers, K.A., 2014:
Rac1 and Aurora A regulate MCAK to polarize microtubule growth in migrating endothelial cells

Appledorn, D.M.; Dao, K-Hien.T.; O'Reilly, S.; Maher, V.M.; McCormick, J.Justin., 2010:
Rac1 and Cdc42 are regulators of HRasV12-transformation and angiogenic factors in human fibroblasts

Kalfa, T.A.; Pushkaran, S.; Zhang, X.; Johnson, J.F.; Pan, D.; Daria, D.; Geiger, H.; Cancelas, J.A.; Williams, D.A.; Zheng, Y., 2011:
Rac1 and Rac2 GTPases are necessary for early erythropoietic expansion in the bone marrow but not in the spleen

Baier, A.; Ndoh, V.N.E.; Lacy, P.; Eitzen, G., 2014:
Rac1 and Rac2 control distinct events during antigen-stimulated mast cell exocytosis

Wang, Y.; Belsham, D.D.; Glogauer, M., 2009:
Rac1 and Rac2 in osteoclastogenesis: a cell immortalization model

Pennucci, R.; Tavano, S.; Tonoli, D.; Gualdoni, S.; de Curtis, I., 2012:
Rac1 and Rac3 GTPases regulate the development of hilar mossy cells by affecting the migration of their precursors to the hilus

Deplazes, Jëlle.; Fuchs, M.; Rauser, S.; Genth, H.; Lengyel, E.; Busch, R.; Luber, B., 2009:
Rac1 and Rho contribute to the migratory and invasive phenotype associated with somatic E-cadherin mutation

Verma, S.K.; Lal, H.; Golden, H.B.; Gerilechaogetu, F.; Smith, M.; Guleria, R.S.; Foster, D.M.; Lu, G.; Dostal, D.E., 2011:
Rac1 and RhoA differentially regulate angiotensinogen gene expression in stretched cardiac fibroblasts

Wigerius, M.; Melik, W.; Elväng, A.; Johansson, M., 2010:
Rac1 and Scribble are targets for the arrest of neurite outgrowth by TBE virus NS5

Chen, S.; Zhao, H.; Zou, C.; Li, Y.; Chen, Y.; Wang, Z.; Jiang, Y.; Liu, A.; Zhao, P.; Wang, M.; Ahammed, G.J., 2018:
Combined Inoculation with Multiple Arbuscular Mycorrhizal Fungi Improves Growth, Nutrient Uptake and Photosynthesis in Cucumber Seedlings

Adorni, M.Pia.; Ronda, N.; Bernini, F.; Favari, E., 2014:
Rac1 and cholesterol metabolism in macrophage

Liao, J.K., 2010:
Rac1 and connective tissue growth factor. The missing link between atrial remodeling and the pathogenesis of atrial fibrillation?

Vaghi, V.; Pennucci, R.; Talpo, F.; Corbetta, S.; Montinaro, V.; Barone, C.; Croci, L.; Spaiardi, P.; Consalez, G.Giacomo.; Biella, G.; de Curtis, I., 2014:
Rac1 and rac3 GTPases control synergistically the development of cortical and hippocampal GABAergic interneurons

D'Ambrosi, N.; Rossi, S.; Gerbino, V.; Cozzolino, M., 2014:
Rac1 at the crossroad of actin dynamics and neuroinflammation in Amyotrophic Lateral Sclerosis

Boo, J.Hyun.; Sohn, J.Hoon.; Kim, J.Eun.; Song, H.; Mook-Jung, I., 2008:
Rac1 changes the substrate specificity of gamma-secretase between amyloid precursor protein and Notch1

Attias, O.; Jiang, R.; Aoudjit, L.; Kawachi, H.; Takano, T., 2010:
Rac1 contributes to actin organization in glomerular podocytes

Dokmanovic, M.; Hirsch, D.S.; Shen, Y.; Wu, W.Jin., 2009:
Rac1 contributes to trastuzumab resistance of breast cancer cells: Rac1 as a potential therapeutic target for the treatment of trastuzumab-resistant breast cancer

Guo, L.; Moon, C.; Niehaus, K.; Zheng, Y.; Ratner, N., 2013:
Rac1 controls Schwann cell myelination through cAMP and NF2/merlin

Li, A.; Machesky, L.M., 2013:
Rac1 cycling fast in melanoma with P29S

Hunziker, L.; Benitah, S.Aznar.; Aznar Benitah, S.; Braun, K.M.; Jensen, K.; McNulty, K.; Butler, C.; Potton, E.; Nye, E.; Boyd, R.; Laurent, G.; Glogauer, M.; Wright, N.A.; Watt, F.M.; Janes, S.M., 2011:
Rac1 deletion causes thymic atrophy

Myant, K.B.; Scopelliti, A.; Haque, S.; Vidal, M.; Sansom, O.J.; Cordero, J.B., 2014:
Rac1 drives intestinal stem cell proliferation and regeneration

Vauchelles, R.; Stalder, Dèle.; Botton, T.; Arkowitz, R.A.; Bassilana, M., 2011:
Rac1 dynamics in the human opportunistic fungal pathogen Candida albicans

Liu, S.; Kapoor, M.; Leask, A., 2009:
Rac1 expression by fibroblasts is required for tissue repair in vivo

Muzzy, R.A.; Hable, W.E., 2009:
Rac1 function during fucoid development

Kassai, H.; Terashima, T.; Fukaya, M.; Nakao, K.; Sakahara, M.; Watanabe, M.; Aiba, A., 2008:
Rac1 in cortical projection neurons is selectively required for midline crossing of commissural axonal formation

Geny, B.; Grassart, A.; Manich, M.; Chicanne, Gëtan.; Payrastre, B.; Sauvonnet, N.; Popoff, M.R., 2010:
Rac1 inactivation by lethal toxin from Clostridium sordellii modifies focal adhesions upstream of actin depolymerization

Tovell, V.E.; Chau, C.Y.; Khaw, P.T.; Bailly, M., 2012:
Rac1 inhibition prevents tissue contraction and MMP mediated matrix remodeling in the conjunctiva

Sawada, N.; Kim, H-Hwan.; Moskowitz, M.A.; Liao, J.K., 2009:
Rac1 is a critical mediator of endothelium-derived neurotrophic activity

Sylow, L.; Jensen, T.E.; Kleinert, M.; Mouatt, J.R.; Maarbjerg, S.J.; Jeppesen, J.; Prats, C.; Chiu, T.T.; Boguslavsky, S.; Klip, A.; Schjerling, P.; Richter, E.A., 2013:
Rac1 is a novel regulator of contraction-stimulated glucose uptake in skeletal muscle

Jacquemet, G.; Morgan, M.R.; Byron, A.; Humphries, J.D.; Choi, C.K.; Chen, C.S.; Caswell, P.T.; Humphries, M.J., 2014:
Rac1 is deactivated at integrin activation sites through an IQGAP1-filamin-A-RacGAP1 pathway

He, X.; Liu, J.; Qi, Y.; Brakebusch, C.; Chrostek-Grashoff, A.; Edgar, D.; Yurchenco, P.D.; Corbett, S.A.; Lowry, S.F.; Graham, A.M.; Han, Y.; Li, S., 2010:
Rac1 is essential for basement membrane-dependent epiblast survival

Ghiaur, G.; Ferkowicz, M.J.; Milsom, M.D.; Bailey, J.; Witte, D.; Cancelas, J.A.; Yoder, M.C.; Williams, D.A., 2007:
Rac1 is essential for intraembryonic hematopoiesis and for the initial seeding of fetal liver with definitive hematopoietic progenitor cells

Pleines, I.; Elvers, M.; Strehl, A.; Pozgajova, M.; Varga-Szabo, D.; May, F.; Chrostek-Grashoff, A.; Brakebusch, C.; Nieswandt, B., 2008:
Rac1 is essential for phospholipase C-gamma2 activation in platelets

Shen, E.; Li, Y.; Li, Y.; Shan, L.; Zhu, H.; Feng, Q.; Arnold, J.Malcolm.O.; Peng, T., 2009:
Rac1 is required for cardiomyocyte apoptosis during hyperglycemia

Castilho, R.M.; Squarize, C.H.; Leelahavanichkul, K.; Zheng, Y.; Bugge, T.; Gutkind, J.Silvio., 2010:
Rac1 is required for epithelial stem cell function during dermal and oral mucosal wound healing but not for tissue homeostasis in mice

Long, D.L.; Willey, J.S.; Loeser, R.F., 2013:
Rac1 is required for matrix metalloproteinase 13 production by chondrocytes in response to fibronectin fragments

Chen, J.; Zheng, W.; Zheng, S.; Zhang, D.; Sang, W.; Chen, X.; Li, G.; Lu, G.; Wang, Z., 2008:
Rac1 is required for pathogenicity and Chm1-dependent conidiogenesis in rice fungal pathogen Magnaporthe grisea

Silva, G.B.; Garvin, J.L., 2010:
Rac1 mediates NaCl-induced superoxide generation in the thick ascending limb

Park, J.; Stanley, D.; Kim, Y., 2013:
Rac1 mediates cytokine-stimulated hemocyte spreading via prostaglandin biosynthesis in the beet armyworm, Spodoptera exigua

Huang, X.; Shen, Y.; Zhang, Y.; Wei, L.; Lai, Y.; Wu, J.; Liu, X.; Liu, X., 2014:
Rac1 mediates laminar shear stress-induced vascular endothelial cell migration

Shim, J.W.; Hamamura, K.; Chen, A.; Wan, Q.; Na, S.; Yokota, H., 2014:
Rac1 mediates load-driven attenuation of mRNA expression of nerve growth factor beta in cartilage and chondrocytes

Migeotte, I.; Grego-Bessa, J.; Anderson, K.V., 2011:
Rac1 mediates morphogenetic responses to intercellular signals in the gastrulating mouse embryo

Nomura, N.; Nomura, M.; Mizuki, N.; Hamada, J-Ichiro., 2008:
Rac1 mediates phorbol 12-myristate 13-acetate-induced migration of glioblastoma cells via paxillin

Zhu, H.; Shan, L.; Peng, T., 2009:
Rac1 mediates sex difference in cardiac tumor necrosis factor-alpha expression via NADPH oxidase-ERK1/2/p38 MAPK pathway in endotoxemia

Lai, Y.; Liu, X.; Wu, J.; Zeng, Y.; Yue, A.; He, X., 2008:
Rac1 mediates the migration of endothelial cells induced by IL-8

Santibáñez, J.F.; Kocić, J.; Fabra, A.; Cano, A.; Quintanilla, M., 2010:
Rac1 modulates TGF-beta1-mediated epithelial cell plasticity and MMP9 production in transformed keratinocytes

Zhang, X-Feng.; Forscher, P., 2009:
Rac1 modulates stimulus-evoked Ca(2+) release in neuronal growth cones via parallel effects on microtubule/endoplasmic reticulum dynamics and reactive oxygen species production

Lee, S-Kyu.; Thomas, G.H., 2011:
Rac1 modulation of the apical domain is negatively regulated by β (Heavy)-spectrin

Gungor, B.; Gombos, I.; Crul, T.; Ayaydin, F.; Szabó, László.; Török, Z.; Mátés, L.; Vígh, László.; Horváth, I., 2015:
Rac1 participates in thermally induced alterations of the cytoskeleton, cell morphology and lipid rafts, and regulates the expression of heat shock proteins in B16F10 melanoma cells

Dipaolo, B.C.; Davidovich, N.; Kazanietz, M.G.; Margulies, S.S., 2013:
Rac1 pathway mediates stretch response in pulmonary alveolar epithelial cells

Hubchak, S.C.; Sparks, E.E.; Hayashida, T.; Schnaper, H.William., 2009:
Rac1 promotes TGF-beta-stimulated mesangial cell type I collagen expression through a PI3K/Akt-dependent mechanism

Rao, J.N.; Liu, S.V.; Zou, T.; Liu, L.; Xiao, L.; Zhang, X.; Bellavance, E.; Yuan, J.X-J.; Wang, J-Ying., 2008:
Rac1 promotes intestinal epithelial restitution by increasing Ca2+ influx through interaction with phospholipase C-(gamma)1 after wounding

Arrizabalaga, O.; Lacerda, H.M.; Zubiaga, A.M.; Zugaza, Jé.L., 2012:
Rac1 protein regulates glycogen phosphorylase activation and controls interleukin (IL)-2-dependent T cell proliferation

Chan, D.; Citro, A.; Cordy, J.M.; Shen, G.C.; Wolozin, B., 2011:
Rac1 protein rescues neurite retraction caused by G2019S leucine-rich repeat kinase 2 (LRRK2)

Huelsenbeck, S.C.; Schorr, A.; Roos, W.P.; Huelsenbeck, J.; Henninger, C.; Kaina, B.; Fritz, G., 2013:
Rac1 protein signaling is required for DNA damage response stimulated by topoisomerase II poisons

van Duijn, T.J.; Anthony, E.C.; Hensbergen, P.J.; Deelder, Aé.M.; Hordijk, P.L., 2010:
Rac1 recruits the adapter protein CMS/CD2AP to cell-cell contacts

Fiedler, L.R., 2009:
Rac1 regulates cardiovascular development and postnatal function of endothelium

Tahirovic, S.; Hellal, F.; Neukirchen, D.; Hindges, R.; Garvalov, B.K.; Flynn, K.C.; Stradal, T.E.; Chrostek-Grashoff, A.; Brakebusch, C.; Bradke, F., 2010:
Rac1 regulates neuronal polarization through the WAVE complex

Greiner, T.U.; Kesavan, G.; Ståhlberg, A.; Semb, H., 2009:
Rac1 regulates pancreatic islet morphogenesis

Chen, R.; Fu, M.; Zhang, G.; Zhou, Y.; Zhu, S.; Liu, J.; Wang, D.; Deng, A.; Wang, Z., 2015:
Rac1 regulates skin tumors by regulation of keratin 17 through recruitment and interaction with CD11b+Gr1+ cells

Eitel, J.; Meixenberger, K.; van Laak, C.; Orlovski, C.; Hocke, A.; Schmeck, B.; Hippenstiel, S.; N'Guessan, P.Dje.; Suttorp, N.; Opitz, B., 2012:
Rac1 regulates the NLRP3 inflammasome which mediates IL-1beta production in Chlamydophila pneumoniae infected human mononuclear cells

Saci, A.; Cantley, L.C.; Carpenter, C.L., 2011:
Rac1 regulates the activity of mTORC1 and mTORC2 and controls cellular size

Lorenzetto, E.; Ettorre, M.; Pontelli, V.; Bolomini-Vittori, M.; Bolognin, S.; Zorzan, S.; Laudanna, C.; Buffelli, M., 2014:
Rac1 selective activation improves retina ganglion cell survival and regeneration

Leung, C.; Lu, X.; Liu, M.; Feng, Q., 2015:
Rac1 signaling is critical to cardiomyocyte polarity and embryonic heart development

Sylow, L.; Jensen, T.E.; Kleinert, M.; Højlund, K.; Kiens, B.; Wojtaszewski, Jørgen.; Prats, C.; Schjerling, P.; Richter, E.A., 2013:
Rac1 signaling is required for insulin-stimulated glucose uptake and is dysregulated in insulin-resistant murine and human skeletal muscle

Barros, Pícia.; Jordan, P.; Matos, P., 2009 :
Rac1 signaling modulates BCL-6-mediated repression of gene transcription

Woods, A.; Pala, D.; Kennedy, L.; McLean, S.; Rockel, J.S.; Wang, G.; Leask, A.; Beier, F., 2008:
Rac1 signaling regulates CTGF/CCN2 gene expression via TGFbeta/Smad signaling in chondrocytes

Yu, C.; Zhang, S.; Song, L.; Wang, Y.; Hwaiz, R.; Luo, L.; Thorlacius, H., 2015:
Rac1 signaling regulates neutrophil-dependent tissue damage in experimental colitis

Barros, Pícia.; Lam, E.W-F.; Jordan, P.; Matos, P., 2012:
Rac1 signalling modulates a STAT5/BCL-6 transcriptional switch on cell-cycle-associated target gene promoters

Wertheimer, E.; Kazanietz, M.G., 2011:
Rac1 takes center stage in pancreatic cancer and ulcerative colitis: quantity matters

Akunuru, S.; Palumbo, J.; Zhai, Q.James.; Zheng, Y., 2012:
Rac1 targeting suppresses human non-small cell lung adenocarcinoma cancer stem cell activity

Bosco, E.E.; Ni, W.; Wang, L.; Guo, F.; Johnson, J.F.; Zheng, Y., 2010:
Rac1 targeting suppresses p53 deficiency-mediated lymphomagenesis

Zhang, B.; Sun, J.; Yu, S-ping.; Chen, C.; Liu, B.; Liu, Z-feng.; Ren, B-cheng.; Ming, H-lang.; Yang, X-jun., 2013:
Rac1+ cells distributed in accordance with CD 133+ cells in glioblastomas and the elevated invasiveness of CD 133+ glioma cells with higher Rac1 activity

Braet, F., 2008:
Rac1, caveolin-1 and vascular endothelial growth factor -mediated liver sinusoidal endothelial cell angiogenesis

Sylow, L.; Møller, L.L.V.; Kleinert, M.; Richter, E.A.; Jensen, T.E., 2015:
Rac1--a novel regulator of contraction-stimulated glucose uptake in skeletal muscle

Vidaki, M.; Tivodar, S.; Doulgeraki, K.; Tybulewicz, V.; Kessaris, N.; Pachnis, V.; Karagogeos, D., 2012:
Rac1-dependent cell cycle exit of MGE precursors and GABAergic interneuron migration to the cortex

Migeotte, I.; Omelchenko, T.; Hall, A.; Anderson, K.V., 2010:
Rac1-dependent collective cell migration is required for specification of the anterior-posterior body axis of the mouse

Li, S-min.; Zeng, L-wen.; Feng, L.; Chen, D-bao., 2010:
Rac1-dependent intracellular superoxide formation mediates vascular endothelial growth factor-induced placental angiogenesis in vitro

Kato, T.; Kawai, K.; Egami, Y.; Kakehi, Y.; Araki, N., 2015:
Rac1-dependent lamellipodial motility in prostate cancer PC-3 cells revealed by optogenetic control of Rac1 activity

May, M.; Schelle, I.; Brakebusch, C.; Rottner, K.; Genth, H., 2015:
Rac1-dependent recruitment of PAK2 to G2 phase centrosomes and their roles in the regulation of mitotic entry

Adam, O.; Lavall, D.; Theobald, K.; Hohl, M.; Grube, M.; Ameling, S.; Sussman, M.A.; Rosenkranz, S.; Kroemer, H.K.; Schäfers, H-Joachim.; Böhm, M.; Laufs, U., 2010:
Rac1-induced connective tissue growth factor regulates connexin 43 and N-cadherin expression in atrial fibrillation

Takemura, Y.; Goodson, P.; Bao, H.Fang.; Jain, L.; Helms, M.N., 2010:
Rac1-mediated NADPH oxidase release of O2- regulates epithelial sodium channel activity in the alveolar epithelium

Adam, O.; Laufs, U., 2014:
Rac1-mediated effects of HMG-CoA reductase inhibitors (statins) in cardiovascular disease

Hikita, T.; Ohno, A.; Sawada, M.; Ota, H.; Sawamoto, K., 2014 :
Rac1-mediated indentation of resting neurons promotes the chain migration of new neurons in the rostral migratory stream of post-natal mouse brain

Murthy, S.; Ryan, A.; He, C.; Mallampalli, R.K.; Carter, A.Brent., 2010:
Rac1-mediated mitochondrial H2O2 generation regulates MMP-9 gene expression in macrophages via inhibition of SP-1 and AP-1

Dwivedi, S.; Pandey, D.; Khandoga, A.L.; Brandl, R.; Siess, W., 2011:
Rac1-mediated signaling plays a central role in secretion-dependent platelet aggregation in human blood stimulated by atherosclerotic plaque

Tan, A.M.; Chang, Y-Wen.; Zhao, P.; Hains, B.C.; Waxman, S.G., 2011:
Rac1-regulated dendritic spine remodeling contributes to neuropathic pain after peripheral nerve injury

Hamalukic, M.; Huelsenbeck, J.; Schad, A.; Wirtz, S.; Kaina, B.; Fritz, G., 2012:
Rac1-regulated endothelial radiation response stimulates extravasation and metastasis that can be blocked by HMG-CoA reductase inhibitors

Zhou, X.; Izumi, Y.; Burg, M.B.; Ferraris, J.D., 2011:
Rac1/osmosensing scaffold for MEKK3 contributes via phospholipase C-gamma1 to activation of the osmoprotective transcription factor NFAT5

Perez, S.E.; Getova, D.P.; He, B.; Counts, S.E.; Geula, C.; Desire, L.; Coutadeur, S.; Peillon, H.; Ginsberg, S.D.; Mufson, E.J., 2012:
Rac1b increases with progressive tau pathology within cholinergic nucleus basalis neurons in Alzheimer's disease

Ungefroren, H.; Sebens, S.; Giehl, K.; Helm, O.; Groth, S.; Fändrich, F.; Röcken, C.; Sipos, B.; Lehnert, H.; Gieseler, F., 2014:
Rac1b negatively regulates TGF-β1-induced cell motility in pancreatic ductal epithelial cells by suppressing Smad signalling

Pethe, V.V.; Charames, G.S.; Bapat, B., 2012:
Rac1b recruits Dishevelled and β-catenin to Wnt target gene promoters independent of Wnt3A stimulation