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List of PDF Full Texts available from EurekaMag Chapter 11030

Chapter 11030 contains a list of PDF Full Texts available from EurekaMag.

Perren, A.; Komminoth, P.; Saremaslani, P.; Matter, C.; Feurer, S.; Lees, J.A.; Heitz, P.U.; Eng, C., 2000:
Mutation and expression analyses reveal differential subcellular compartmentalization of PTEN in endocrine pancreatic tumors compared to normal islet cells

Myrie, K.A.; Percy, M.J.; Azim, J.N.; Neeley, C.K.; Petty, E.M., 2000:
Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines

A.Y.ng; L.C.ong; Ren Qun; Jiang Li; Wang Zhen Ning; Luo Yang; X.H.i Mian; Zhang Xue, 2002:
Mutation and expression analysis of the AGO gene in cancer cell lines and primary gastric carcinomas

Kehrer-Sawatzki, H.; Wilda, M.; Braun, V.M.; Richter, H-Peter.; Hameister, H., 2002:
Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1)

Yokomizo, A.; Mai, M.; Bostwick, D.G.; Tindall, D.J.; Qian, J.; Cheng, L.; Jenkins, R.B.; Smith, D.I.; Liu, W., 1999:
Mutation and expression analysis of the p73 gene in prostate cancer

Gray, I.C.; Stewart, L.M.D.; Phillips, S.M.A.; Hamilton, J.A.; Gray, N.E.; Watson, G.J.; Spurr, K.N.; Snary, D., 1998:
Mutation and expression analysis of the putative prostate tumour-supressor gene PTEN

Ai, Yun Can; Wilson, David, B., 2002:
Mutation and expression of N233C-D506C of cellulase Cel6B from Thermobifida fusca in Escherichia coli

Sun Miao; Qiu Guangrong; Sun Guifeng; Yuan Yihua; Sun Kailai, 2001 :
Mutation and expression of Nkx 2-5 gene in human simple congenital heart disease

Wan Hong; W.M.ngming; Y.S.ngting; E.A., 2000:
Mutation and expression of nm23 - H1 gene in bladder carcinomas

Koyama, T.; Tago, K-Ichi.; Nakamura, T.; Ohwada, S.; Morishita, Y.; Yokota, J.; Akiyama, T., 2002:
Mutation and expression of the beta-catenin-interacting protein ICAT in human colorectal tumors

Miyazaki, T.; Kato, H.; Shitara, Y.; Yoshikawa, M.; Tajima, K.; Masuda, N.; Shouji, H.; Tsukada, K.; Nakajima, T.; Kuwano, H., 2000:
Mutation and expression of the metastasis suppressor gene KAI1 in esophageal squamous cell carcinoma

Fu, Y.; Deng, W.; Kawarada, Y.; Kawagoe, M.; Ma, Y.Z.e; Li, X.; Guo, N.; Kameda, T.; Terada, K.; Sugiyama, T., 2003:
Mutation and expression of the p53 gene during chemical hepatocarcinogenesis in F344 rats

Li-Chao-Xuan; Zhou-Pei, 2002:
Mutation and fermentation studies on S. laurentii

Monahan, B.J.; Unkles, S.E.; Tsing I, T.; Kinghorn, J.R.; Hynes, M.J.; Davis, M.A., 2002:
Mutation and functional analysis of the Aspergillus nidulans ammonium permease MeaA and evidence for interaction with itself and MepA

Chabas, A.; Montfort, M.; Martinez Campos, M.; Diaz, A.; Coll, M.J.sep; Grinberg, D.; Vilageliu, L., 2001:
Mutation and haplotype analyses in 26 Spanish Sanfilippo syndrome type A patients: Possible single origin for 1091delC mutation

Nayak, B.K.; Das, B.R., 1999:
Mutation and methylation status of p53 gene promoter in human breast tumours

Cui, J.; Zhou, X.; Liu, Y.; Tang, Z., 2001:
Mutation and overexpression of the beta-catenin gene may play an important role in primary hepatocellular carcinoma among Chinese people

Toyosawa, K.; Tanaka, K.; Imai, T.; Yasuhara, K.; Koujitani, T.; Hirose, M.; Mitsumori, K., 2003:
Mutation and overexpression of the transgene in ethylnitrosourea-induced tumors in mice carrying a human prototype c-Ha-ras gene

Woodruff, R.; Thompson, J.,. Jr.;, 2002:
Mutation and premating isolation

Nijman, I.J.; Lenstra, J.A., 2001:
Mutation and recombination in cattle satellite DNA: a feedback model for the evolution of satellite DNA repeats

Beletskaia, T.S.; Samoĭlovich, E.O.; Korotkova, E.A.; Scheslenok, E.P.; Fel'dman, E.V., 2002:
Mutation and recombination variability of vaccine polioviruses isolated in Belarus (1960-1999)

Baake, Ellen, 2001:
Mutation and recombination with tight linkage

Hong, Wen Rong, 1998:
Mutation and selection of tobramycins producing strains

Nishi, H.; Isaka, K.; Sagawa, Y.; Usuda, S.; Fujito, A.; Ito, H.; Senoo, M.; Kato, H.; Takayama, M., 1999:
Mutation and transcription analyses of the p63 gene in cervical carcinoma

Ferlini, A.; Obici, L.; Manzati, E.; Biadi, O.; Tarantino, E.; Conigli, P.; Merlini, G.; D'alessandro, M.; Mazzaferro, V.; Tassinari, C.A.; Salvi, F., 2000:
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: A putative novel 'hot spot' in codon 47

Okumura, A.; Ishikawa, T.; Yoshioka, K.; Yuasa, R.; Fukuzawa, Y.; Kakumu, S., 2001:
Mutation at codon 130 in hepatitis B virus (HBV) core region increases markedly during acute exacerbation of hepatitis in chronic HBV carriers

Mouillet-Richard, S.; Teil, C.; Lenne, M.; Hugon, S.; Taleb, O.; Laplanche, J.-Louis, 1999:
Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease

Andreassen, R.; Lundsted, J.; Olaisen, Børnar., 2002:
Mutation at minisatellite locus DYF155S1: allele length mutation rate is affected by age of progenitor

Russo, G.L.igi; Van Den Bos, C.; Marshak, D.R., 2001:
Mutation at the CK2 phosphorylation site on Cdc28 affects kinase activity and cell size in Saccharomyces cerevisiae

Datta, B.; Datta, R., 2003:
Mutation at the acidic residue-rich domain of eukaryotic initiation factor 2 (eIF2alpha)-associated glycoprotein p67 increases the protection of eIF2alpha phosphorylation during heat shock

Reddy, V.R.K., 2001:
Mutation breeding in hexaploid triticales: Desirable mutants

Soeranto, H.; Nakanishi, T.M.; Razzak, M.T., 2001:
Mutation breeding in sorghum in Indonesia

Xing-Wei-Ling; Zhou-Xi-Gui; Wang-He-Xiang; Xiao-Xi-Long; Song-Yuan; Zhang-Hong, 2002:
Mutation breeding of high colistin producing strains

Presneau, N.; Laplace-Marieze, V.; Sylvain, V.; Lortholary, A.; Hardouin, A.; Bernard-Gallon, D.; Bignon, Y.J., 1999:
Mutation by deletion-insertion in BRCA-1 gene in three unrelated French breast/ovarian cancer families: possible implication of a mobile element

Quiram, P.A.; Ohno, K.; Milone, M.; Patterson, M.C.; Pruitt, N.J.; Brengman, J.M.; Sine, S.M.; Engel, A.G., 1999:
Mutation causing congenital myasthenia reveals acetylcholine receptor beta/delta subunit interaction essential for assembly

Shen, X-Ming.; Ohno, K.; Tsujino, A.; Brengman, J.M.; Gingold, M.; Sine, S.M.; Engel, A.G., 2003:
Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating

Venta, P.J.; Li, J.; Yuzbasiyan-Gurkan, V.; Brewer, G.J.; Schall, W.D., 2000:
Mutation causing von Willebrand's disease in Scottish Terriers

Groves, C.; Lamlum, H.; Crabtree, M.; Williamson, J.; Taylor, C.; Bass, S.; Cuthbert-Heavens, D.; Hodgson, S.; Phillips, R.; Tomlinson, I., 2002:
Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis

Cotton, R.G., 1998:
Mutation detection and mutation databases

Frenzel, H.; Hampe, J.; Huse, K.; Mascheretti, S.M.; Croucher, P.P.; Lynch, N.J.; Siebert, R.; Platzer, M.; Schreiber, S., 2002:
Mutation detection and physical mapping of the CD11 gene cluster in association with inflammatory bowel disease

Hecker, K.H.; Taylor, P.D.; Gjerde, D.T., 1999:
Mutation detection by denaturing DNA chromatography using fluorescently labeled polymerase chain reaction products

Gunderson, K.L.; Huang, X.C.; Morris, M.S.; Lipshutz, R.J.; Lockhart, D.J.; Chee, M.S., 1998:
Mutation detection by ligation to complete n-mer DNA arrays

Garcia, C.A.; Ahmadian, A.; Gharizadeh, B.; Lundeberg, J.; Ronaghi, M.; Nyren, P., 2000:
Mutation detection by pyrosequencing: Sequencing of exons 5-8 of the p53 tumor suppressor gene

Matsubara, Yoichi, 2001 :
Mutation detection by sequencing and TaqMan-allele specific amplification

Maldonado-Rodriguez, R.; Espinosa-Lara, M.; Loyola-Abitia, P.; Beattie, W.G.; Beattie, K.L., 1999:
Mutation detection by stacking hybridization on genosensor arrays

Genet, S.; Cranston, T.; Middleton Price, H.R., 2000:
Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations

Bjørheim, J.; Minarik, M.; Gaudernack, G.; Ekstrøm, P.Olaf., 2002:
Mutation detection in KRAS Exon 1 by constant denaturant capillary electrophoresis in 96 parallel capillaries

Syrris, P.; Murray, A.; Carter, N.D.; McKenna, W.M.; Jeffery, S., 2001:
Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions

Lodewyckx, L.; Vandevyver, C.; Vandervorst, C.; Van Steenbergen, W.; Raus, J.; Michiels, L., 2001:
Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis

Moore, W.; Bogdarina, I.; Patel, U.A.; Perry, M.; Crane-Robinson, C., 2000:
Mutation detection in the breast cancer gene BRCA1 using the protein truncation test

McCluskey, M.; Schiavello, T.; Hunter, M.; Hantke, J.; Angelicheva, D.; Bogdanova, N.; Markoff, A.; Thomas, M.; Dworniczak, B.; Horst, J.; Kalaydjieva, L., 2002:
Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families

Lianchun, P.; Goto, M.; Furusaki, S., 2002:
Mutation detection of DNA by reversed micelles

Bardwell, P.D.; Martin, A.; Scharff, M.D., 2002 :
Mutation detection of immunoglobulin V-regions by DHPLC

Tsolakidou, A.F.; Coulocheri, S.A.; Sekeris, C.E.; Moutsatsou, P., 2002:
Mutation detection of the human glucocorticoid receptor alpha gene area coding for the hormone-binding domain by denaturing gradient gel electrophoresis

Babon, J.J.; McKenzie, M.; Cotton, R.G., 1999:
Mutation detection using fluorescent enzyme mismatch cleavage with T4 endonuclease VII

Paulino, L.C.; Araujo, M.; Guerra, G.Jr.; Marini, S.H.V.L.; D.M.llo, M.P., 1999:
Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency

Obayashi, E.; Shimizu, H.; Park, S.-Yong; Shoun, H.; Shiro, Y., 2000:
Mutation effects of a conserved threonine (Thr243) of cytochrome P450nor on its structure and function

Ogi, T.; Kato, T., J.; Kato, T.; Ohmori, H., 1999:
Mutation enhancement by DINB1, a mammalian homologue of the Escherichia coli mutagenesis protein DinB

Zhang-Wenhui; Zhou-Yijun; Fan-Yongjian; Cheng-Zhaobang; Wu-Shuhua, 2002:
Mutation for pathogenicity of Magnaporthe grisea by Restriction Enzyme Mediated Integration (REMI)

Martinez, J.L.; Baquero, F., 2000:
Mutation frequencies and antibiotic resistance

O'Neill, A.J.; Cove, J.H.; Chopra, I., 2001:
Mutation frequencies for resistance to fusidic acid and rifampicin in Staphylococcus aureus

Seki, H.; Kubota, T.; Ikegawa, S.; Haga, N.; Fujioka, F.; Ohzeki, S.; Wakui, K.; Yoshikawa, H.; Takaoka, K.; Fukushima, Y., 2001:
Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses

Stuart, G.R.; Oda, Y.; de Boer, J.G.; Glickman, B.W., 2000:
Mutation frequency and specificity with age in liver, bladder and brain of lacI transgenic mice

Martin, S.L.; Hopkins, C.L.; Naumer, A.; Dolle, M.E.T.; Vijg, J., 2001:
Mutation frequency and type during ageing in mouse seminiferous tubules

Davies, R.; Clothier, B.; Smith, A.G., 2000:
Mutation frequency in the lacI gene of liver DNA from lambda/lacI transgenic mice following the interaction of PCBs with iron causing hepatic cancer and porphyria

Forster, Brian, P., 2001:
Mutation genetics of salt tolerance in barley: An assessment of Golden Promise and other semi-dwarf mutants

Bazar, L.S.; Collier, G.B.; Vanek, P.G.; Siles, B.A.; Kow, Y.W.; Doetsch, P.W.; Cunningham, R.P.; Chirikjian, J.G., 1999:
Mutation identification DNA analysis system (MIDAS) for detection of known mutations

Ng, L-King.; Martin, I.; Liu, G.; Bryden, L., 2002:
Mutation in 23S rRNA associated with macrolide resistance in Neisseria gonorrhoeae

Depardieu, F.; Courvalin, P., 2000:
Mutation in 23S rRNA responsible for resistance to 16-membered macrolides and streptogramins in Streptococcus pneumoniae

Tutt, A.; Bertwistle, D.; Valentine, J.; Gabriel, A.; Swift, S.; Ross, G.; Griffin, C.; Thacker, J.; Ashworth, A., 2001:
Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences

Boursalian, T.E.; Fink, P.J., 2003:
Mutation in fas ligand impairs maturation of thymocytes bearing moderate affinity T cell receptors

Murray, A.; Potet, F.; Bellocq, C.; Baró, I.; Reardon, W.; Hughes, H.E.; Jeffery, S., 2002:
Mutation in KCNQ1 that has both recessive and dominant characteristics

Park, S.Y.; Seo, S.B.; Lee, S.J.; Na, J.G.; Kim, Y.J., 2001:
Mutation in PMR1, a Ca(2+)-ATPase in Golgi, confers salt tolerance in Saccharomyces cerevisiae by inducing expression of PMR2, an Na(+)-ATPase in plasma membrane

Raimondi, A.; Sisto, F.; Nikaido, H., 2001:
Mutation in Serratia marcescens AmpC beta-lactamase producing high-level resistance to ceftazidime and cefpirome

El-Hashemite, N.; Zhang, H.; Henske, E.P.; Kwiatkowski, D.J., 2003:
Mutation in TSC2 and activation of mammalian target of rapamycin signalling pathway in renal angiomyolipoma

Nozawa, S.R.; May, G.S.; Martinez Rossi, N.M.; Ferreira Nozawa, M.S.; Coutinho Netto, J.; Maccheroni, W.J.; Rossi, A., 2003:
Mutation in a calpain-like protease affects the posttranslational mannosylation of phosphatases in Aspergillus nidulans

Wurch, T.; Colpaert, F.C.; Pauwels, P.J., 2003:
Mutation in a protein kinase C phosphorylation site of the 5-HT1A receptor preferentially attenuates Ca2+ responses to partial as opposed to higher-efficacy 5-HT1A agonists

Quillet, E.; Aubard, G.; Quéau, I., 2002:
Mutation in a sex-determining gene in rainbow trout: detection and genetic analysis

Hayward, C.; Shu, X.; Cideciyan, A.V.; Lennon, A.; Barran, P.; Zareparsi, S.; Sawyer, L.; Hendry, G.; Dhillon, B.; Milam, A.H.; Luthert, P.J.; Swaroop, A.; Hastie, N.D.; Jacobson, S.G.; Wright, A.F., 2003:
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

Hamada, Y.; Kadokawa, Y.; Okabe, M.; Ikawa, M.; Coleman, J.R.; Tsujimoto, Y., 1999:
Mutation in ankyrin repeats of the mouse Notch2 gene induces early embryonic lethality

Telegeev, G.D.; Dubrovska, A.N.; Dybkov, M.V.; Maliuta, S.S., 2000:
Mutation in bcr/abl hybrid gene as a possible factor of tumor progression during CML

Miller, A., D.; Tyagi, S., C., 2002:
Mutation in collagen gene induces cardiomyopathy in transgenic mice

Jadoun, J.; Sela, S., 2000:
Mutation in csrR global regulator reduces Streptococcus pyogenes internalization

Matsuda, S.; Yuzaki, M., 2002:
Mutation in hotfoot-4J mice results in retention of delta2 glutamate receptors in ER

Rampazzo, A.; Nava, A.; Malacrida, S.; Beffagna, G.; Bauce, B.; Rossi, V.; Zimbello, R.; Simionati, B.; Basso, C.; Thiene, G.; Towbin, J.A.; Danieli, G.A., 2002:
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

McCright, I.J.; Tsunoda, I.; Libbey, J.E.; Fujinami, R.S., 2002:
Mutation in loop I of VP1 of Theiler's virus delays viral RNA release into cells and enhances antibody-mediated neutralization: a mechanism for the failure of persistence by the mutant virus

Moroni, A.; Gazzarrini, S.; Cerana, R.; Colombo, R.; Sutter, J.U.; DiFrancesco, D.; Gradmann, D.; Thiel, G., 2000:
Mutation in pore domain uncovers cation- and voltage-sensitive recovery from inactivation in KAT1 channel

Kitayama, S.; Narumi, I.; Kikuchi, M.; Watanabe, H., 2000:
Mutation in recR gene of Deinococcus radiodurans and possible involvement of its product in the repair of DNA interstrand cross-links

Muradov, K.G.; Granovsky, A.E.; Artemyev, N.O., 2003:
Mutation in rod PDE6 linked to congenital stationary night blindness impairs the enzyme inhibition by its gamma-subunit

Al-Kateb, H.; Bähring, S.; Hoffmann, K.; Strauch, K.; Busjahn, A.; Nürnberg, G.; Jouma, M.; Bautz, E.K.F.; Dresel, H.A.; Luft, F.C., 2002:
Mutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemia

Ricci, C.; Scappini, B.; Divoky, V.; Gatto, S.; Onida, F.; Verstovsek, S.; Kantarjian, H.M.; Beran, M., 2002:
Mutation in the ATP-binding pocket of the ABL kinase domain in an STI571-resistant BCR/ABL-positive cell line

Barthe, C.; Gharbi, M.J.see; Lagarde, V.; Chollet, C.; Cony Makhoul, P.; Reiffers, J.; Goldman, J.M.; Melo, J.V.; Mahon, F.X.vier, 2002:
Mutation in the ATP-binding site of BCR-ABL in a patient with chronic myeloid leukaemia with increasing resistance to STI571

Carbone, I.; Bruno, C.; Sotgia, F.; Bado, M.; Broda, P.; Masetti, E.; Panella, A.; Zara, F.; Bricarelli, F.D.; Cordone, G.; Lisanti, M.P.; Minetti, C., 2000:
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia

Friedman, S.M.; Lu, T.; Drlica, K., 2001:
Mutation in the DNA gyrase A Gene of Escherichia coli that expands the quinolone resistance-determining region

Wang, T.J.; Huang, C.B.; Tsai, F.J.; Wu, J.Y.; Lai, R.B.; Hsiao, M., 2002:
Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome

Lehto, M.; Bitzén, P.O.; Isomaa, B.; Wipemo, C.; Wessman, Y.; Forsblom, C.; Tuomi, T.; Taskinen, M.R.; Groop, L., 1999:
Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism

Papa, S.; Scacco, S.; Sardanelli, A.M.ria; Vergari, R.; Papa, F.; Budde, S.; Van Den Heuvel, L.; Smeitink, J., 2001:
Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndrome

Chao, L.Y.; Huff, V.; Strong, L.C.; Saunders, G.F., 2000:
Mutation in the PAX6 gene in twenty patients with aniridia

Hung, C.H.in; Wu, H.C.i; Tseng, Y.H.iung, 2002:
Mutation in the Xanthomonas campestris xanA gene required for synthesis of xanthan and lipopolysaccharide drastically reduces the efficiency of bacteriophage variant phiL7 adsorption

Dougherty, C.A.; Sage, C.R.; Davis, A.; Farrell, K.W., 2001:
Mutation in the beta-tubulin signature motif suppresses microtubule GTPase activity and dynamics, and slows mitosis

Graw, J.; Jung, M.; Löster, J.; Klopp, N.; Soewarto, D.; Fella, C.; Fuchs, H.; Reis, A.; Wolf, E.; Balling, R.; Hrabé de Angelis, M., 1999:
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse

Faiyaz-Ul-Haque, M.; Ahmad, W.; Zaidi, S.H.E.; Haque, S.; Teebi, A.S.; Ahmad, M.; Cohn, D.H.; Tsui, L.C., 2002:
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

Tateyama, M.; Aoki, M.; Nishino, I.; Hayashi, Y.K.; Sekiguchi, S.; Shiga, Y.; Takahashi, T.; Onodera, Y.; Haginoya, K.; Kobayashi, K.; Iinuma, K.; Nonaka, I.; Arahata, K.; Itoyama, Y.; Itoyoma, Y., 2002:
Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy

Newman, J.H.; Wheeler, L.; Lane, K.B.; Loyd, E.; Gaddipati, R.; Phillips, J.A.; Loyd, J.E., 2001:
Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred

Wang, X.; Moylan, B.; Leopold, D.A.; Kim, J.; Rubenstein, R.C.; Togias, A.; Proud, D.; Zeitlin, P.L.; Cutting, G.R., 2000:
Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population

Ayene, I.S.; Stamato, T.D.; Mauldin, S.K.; Biaglow, J.E.; Tuttle, S.W.; Jenkins, S.F.; Koch, C.J., 2002:
Mutation in the glucose-6-phosphate dehydrogenase gene leads to inactivation of Ku DNA end binding during oxidative stress

Hufnagel, C.; Eiden, S.; Nuesslein-Hildesheim, B.; Zhang, Y.; Leibel, R.; Schmidt, I., 1999:
Mutation in the leptin receptor (Leprfa) causes fat-storage-independent hyperleptinaemia in neonatal rats

Iaccarino, I.; Marra, G.; Dufner, P.; Jiricny, J., 2000:
Mutation in the magnesium binding site of hMSH6 disables the hMutSalpha sliding clamp from translocating along DNA

Korn-Lubetzki, I.; Gillis, S.; Steiner, I., 2001:
Mutation in the methylenetetrahydrofolate reductase gene might be a risk factor for cerebrovascular disease in peripartum and under oral contraceptive use

Gubkina, O.; Cremer, H.; Rougon, G., 2001:
Mutation in the neural cell adhesion molecule interferes with the differentiation of anterior pituitary secretory cells

Blake, G.J.; Schmitz, C.; Lindpaintner, K.; Ridker, P.M., 2001:
Mutation in the promoter region of the beta-fibrinogen gene and the risk of future myocardial infarction, stroke and venous thrombosis

Habara, Y.; Urushiyama, S.; Shibuya, T.; Ohshima, Y.; Tani, T., 2001:
Mutation in the prp12+ gene encoding a homolog of SAP130/SF3b130 causes differential inhibition of pre-mRNA splicing and arrest of cell-cycle progression in Schizosaccharomyces pombe

Kiefer, J.; Schreiber, A.; Gutermuth, F.; Koch, S.; Schmidt, P., 1999:
Mutation induction by different types of radiation at the Hprt locus

Ikehata, H.; Ono, T., 2002:
Mutation induction with UVB in mouse skin epidermis is suppressed in acute high-dose exposure

Sasaki, A.; Nowak, M.A., 2003:
Mutation landscapes

Schoen, D.J.; Brownstein, J.S.; White, P.A., 2002:
Mutation load in natural populations of the sensitive fern Onoclea sensibilis exposed to soil mutagens

Kamb, Alexander, 2003:
Mutation load, functional overlap, and synthetic lethality in the evolution and treatment of cancer

den Dunnen, J.T.; Antonarakis, S.E., 1999:
Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

Hearn, T.; Renforth, G.L.; Spalluto, C.; Hanley, N.A.; Piper, K.; Brickwood, S.; White, C.; Connolly, V.; Taylor, J.F.N.; Russell Eggitt, I.; Bonneau, D.; Walker, M.; Wilson, D.I., 2002:
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstrom syndrome

Galés, C.; Kowalski-Chauvel, A.; Dufour, M.N.; Seva, C.; Moroder, L.; Pradayrol, L.; Vaysse, N.; Fourmy, D.; Silvente-Poirot, S., 2000:
Mutation of Asn-391 within the conserved NPXXY motif of the cholecystokinin B receptor abolishes Gq protein activation without affecting its association with the receptor

Hannawacker, A.; Krasel, C.; Lohse, M.J., 2002:
Mutation of Asn293 to Asp in transmembrane helix VI abolishes agonist-induced but not constitutive activity of the beta(2)-adrenergic receptor

Hatse, S.; Princen, K.; Gerlach, L.O.; Bridger, G.; Henson, G.; De Clercq, E.; Schwartz, T.W.; Schols, D., 2001:
Mutation of Asp(171) and Asp(262) of the chemokine receptor CXCR4 impairs its coreceptor function for human immunodeficiency virus-1 entry and abrogates the antagonistic activity of AMD3100

Adachi, M.; Zhang, Y.B.n; Imai, K., 2003:
Mutation of BAD within the BH3 domain impairs its phosphorylation-mediated regulation

Gaidano, G.; Vivenza, D.; Forconi, F.; Capello, D.; Gloghini, A.; Bhatia, K.; Gutierrez, M.; Gallicchio, M.; Avanzi, G.C.rlo; Fassone, L.; Ariatti, C.; Buonaiuto, D.; Cingolani, A.; Saglio, G.; Tirelli, U.; Larocca, L.M.; Dalla Favera, R.; Car, 2000:
Mutation of BAX occurs infrequently in acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas

Curtin, J.A.; Quint, E.; Tsipouri, V.; Arkell, R.M.; Cattanach, B.; Copp, A.J.; Henderson, D.J.; Spurr, N.; Stanier, P.; Fisher, E.M.; Nolan, P.M.; Steel, K.P.; Brown, S.D.M.; Gray, I.C.; Murdoch, J.N., 2003:
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse

Diagana, T.T.; Thomas, U.; Prokopenko, S.N.; Xiao, B.; Worley, P.F.; Thomas, J.B., 2002:
Mutation of Drosophila homer disrupts control of locomotor activity and behavioral plasticity

Murga, M.; Fernandez Capetillo, O.; Field, S.J.; Moreno, B.; R.Borlado, L.; Fujiwara, Y.; Balomenos, D.; Vicario, A.; Carrera, A.C.; Orkin, S.H.; Greenberg, M.E.; Zubiaga, A.M., 2001:
Mutation of E2F2 in mice causes enhanced T lymphocyte proliferation, leading to the development of autoimmunity

Neye, Holger, 2001:
Mutation of FKBP associated protein 48 (FAP48) at proline 219 disrupts the interaction with FKBP12 and FKBP52

Liu, Z.; Deng, H.; Tang, W-Li., 2003:
Mutation of GCK gene of Chinese patients with late-onset type 2 diabetes

Degrève, B.; Esnouf, R.; D.C.ercq, E.; Balzarini, J., 2001:
Mutation of Gln125 to Asn selectively abolishes the thymidylate kinase activity of herpes simplex virus type 1 thymidine kinase

Booden, M.A.; Sakaguchi, D.S.; Buss, J.E., 2000:
Mutation of Ha-Ras C terminus changes effector pathway utilization

Suzuki, M.; Saito, S.; Saga, Y.; Ohwada, M.; Sato, I., 2000:
Mutation of K-RAS protooncogene and loss of heterozygosity on 6q27 in serous and mucinous ovarian carcinomas

Angeles, R.; Devine, J.; Barton, K.; Smith, M.; Mccauley, R., 1999:
Mutation of K234 and K236 in the voltage-dependent anion channel 1 impairs its insertion into the mitochondrial outer membrane

Gerstin, K.M.; Gong, D.H.; Abdallah, M.; Winegar, B.D.; Eger, E.I.; Gray, A.T., 2003:
Mutation of KCNK5 or Kir3.2 potassium channels in mice does not change minimum alveolar anesthetic concentration

Grewal, P.K.; Hewitt, J.E., 2002:
Mutation of Large, which encodes a putative glycosyltransferase, in an animal model of muscular dystrophy

Zhao, C.; Koide, A.; Abrams, J.; Deighton-Collins, S.; Martinez, A.; Schwartz, J.A.; Koide, S.; Skafar, D.F., 2003:
Mutation of Leu-536 in human estrogen receptor-alpha alters the coupling between ligand binding, transcription activation, and receptor conformation

Medvedeva, M.V.; Polyakova, O.V.; Watterson, D.M.rtin; Gusev, N.B., 1999:
Mutation of Lys-75 affects calmodulin conformation

Pelpel, K.; Leibovitch, M.P.erre; Fernandez, A.; Leibovitch, S.A., 2000:
Mutation of MyoD-Ser237 abolishes its up-regulation by c-Mos

Chin, H.S.; Sim, J.; Sim, T.S., 2001:
Mutation of N304 to leucine in Streptomyces clavuligerus deacetoxycephalosporin C synthase creates an enzyme with increased penicillin analogue conversion

Sakamoto, T.; Mishina, M.; Niki, H., 2002:
Mutation of NMDA receptor subunit epsilon 1: Effects on audiogenic-like seizures induced by electrical stimulation of the inferior colliculus in mice

Yamamoto, K.; Jigami, Y., 2002:
Mutation of TRS130, which encodes a component of the TRAPP II complex, activates transcription of OCH1 in Saccharomyces cerevisiae

Larigauderie, G.; Laalami, S.; Nyengaard, N.R.; Grunberg Manago, M.; Cenatiempo, Y.; Mortensen, K.K.; Sperling Petersen, H.U., 2000:
Mutation of Thr445 and Ile500 of initiation factor 2 G-domain affects Escherichia coli growth rate at low temperature

Ito, K.; Oleschuk, C.J.; Westlake, C.; Vasa, M.Z.; Deeley, R.G.; Cole, S.P., 2001:
Mutation of Trp1254 in the multispecific organic anion transporter, multidrug resistance protein 2 (MRP2) (ABCC2), alters substrate specificity and results in loss of methotrexate transport activity

Powe, A.C.; A.N.kkash, L.; Li, M.; Hwang, T.C.ang, 2002:
Mutation of Walker-A lysine 464 in cystic fibrosis transmembrane conductance regulator reveals functional interaction between its nucleotide-binding domains

Bhalla, N.; Biggins, S.; Murray, A.W., 2002:
Mutation of YCS4, a budding yeast condensin subunit, affects mitotic and nonmitotic chromosome behavior

Moore, D.J.; Taylor, R.M.; Clements, P.; Caldecott, K.W., 2000:
Mutation of a BRCT domain selectively disrupts DNA single-strand break repair in noncycling Chinese hamster ovary cells

Barbosa, V.; Yamamoto, R.R.; Henderson, D.S.; Glover, D.M., 2000:
Mutation of a Drosophila gamma tubulin ring complex subunit encoded by discs degenerate-4 differentially disrupts centrosomal protein localization

Talts, J.F.; Timpl, R., 1999:
Mutation of a basic sequence in the laminin alpha2LG3 module leads to a lack of proteolytic processing and has different effects on beta1 integrin-mediated cell adhesion and alpha-dystroglycan binding

Pomerening, J.R.; Valente, L.; Kinzy, T.G.; Jacobs, T.W., 2003:
Mutation of a conserved CDK site converts a metazoan Elongation Factor 1Bbeta subunit into a replacement for yeast eEF1Balpha

Liu, L.X.; Heveker, N.; Fackler, O.T.; Arold, S.; L.G.ll, S.; Janvier, K.; Peterlin, B.M.; Dumas, C.; Schwartz, O.; Benichou, S.; Benarous, R., 2000:
Mutation of a conserved residue (D123) required for oligomerization of human immunodeficiency virus type 1 Nef protein abolishes interaction with human thioesterase and results in impairment of Nef biological functions

Strumberg, D.; Nitiss, J.L.; Rose, A.; Nicklaus, M.C.; Pommier, Y., 1999:
Mutation of a conserved serine residue in a quinolone-resistant type II topoisomerase alters the enzyme-DNA and drug interactions

Laitinen, O.H.; Airenne, K.J.; Marttila, A.T.; Kulik, T.; Porkka, E.; Bayer, E.A.; Wilchek, M.; Kulomaa, M.S., 1999:
Mutation of a critical tryptophan to lysine in avidin or streptavidin may explain why sea urchin fibropellin adopts an avidin-like domain

Denlinger, L.C.; Sommer, J.A.; Parker, K.; Gudipaty, L.; Fisette, P.L.; Watters, J.W.; Proctor, R.A.; Dubyak, G.R.; Bertics, P.J., 2003:
Mutation of a dibasic amino acid motif within the C terminus of the P2X7 nucleotide receptor results in trafficking defects and impaired function

Cole, L.A.; Zirngibl, R.; Craig, A.W.; Jia, Z.; Greer, P., 1999:
Mutation of a highly conserved aspartate residue in subdomain IX abolishes Fer protein-tyrosine kinase activity

Rasmussen, S.G.; Jensen, A.D.; Liapakis, G.; Ghanouni, P.; Javitch, J.A.; Gether, U., 1999:
Mutation of a highly conserved aspartic acid in the beta2 adrenergic receptor: constitutive activation, structural instability, and conformational rearrangement of transmembrane segment 6

Marie, S.; Race, V.; Nassogne, M-C.; Vincent, M-F.; Van den Berghe, G., 2002 :
Mutation of a nuclear respiratory factor 2 binding site in the 5' untranslated region of the ADSL gene in three patients with adenylosuccinate lyase deficiency

Allikmets, R.; Raskind, W.H.; Hutchinson, A.; Schueck, N.D.; Dean, M.; Koeller, D.M., 1999:
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)

Kappen, C.; Yaworsky, P.J., 2003:
Mutation of a putative nuclear receptor binding site abolishes activity of the nestin midbrain enhancer

Street, V.A.; Bennett, C.L.; Goldy, J.D.; Shirk, A.J.; Kleopa, K.A.; Tempel, B.L.; Lipe, H.P.; Scherer, S.S.; Bird, T.D.; Chance, P.F., 2003:
Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C

Chen, S.; Lin, F.; Xu, M.; Riek, R.Peter.; Novotny, J.; Graham, R.M., 2002:
Mutation of a single TMVI residue, Phe(282), in the beta(2)-adrenergic receptor results in structurally distinct activated receptor conformations

Ito, K.; Olsen, S.L.; Qiu, W.; Deeley, R.G.; Cole, S.P., 2001:
Mutation of a single conserved tryptophan in multidrug resistance protein 1 (MRP1/ABCC1) results in loss of drug resistance and selective loss of organic anion transport

Crary, J.I.; Dean, D.M.; Maroof, F.; Zimmerman, A.L., 2000:
Mutation of a single residue in the S2-S3 loop of CNG channels alters the gating properties and sensitivity to inhibitors

Peters, L.M.; Anderson, D.W.; Griffith, A.J.; Grundfast, K.M.; San Agustin, T.B.; Madeo, A.C.; Friedman, T.B.; Morell, R.J., 2002:
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

Roy, R.; Biswas, T.; Lee, J.C.; Mitra, S., 2000:
Mutation of a unique aspartate residue abolishes the catalytic activity but not substrate binding of the mouse N-methylpurine-DNA glycosylase (MPG)

Thompson, M.W.; Govindaswami, M.; Hersh, L.B., 2003:
Mutation of active site residues of the puromycin-sensitive aminopeptidase: Conversion of the enzyme into a catalytically inactive binding protein

Costas, E.; Carrillo, E.; Ferrero, L., M.; Agrelo, M.; Garcia-Villada, L.; Juste, J.; Lopez-Rodas, V., 2001:
Mutation of algae from sensitivity to resistance against environmental selective agents: The ecological genetics of Dictyosphaerium chlorelloides (Chlorophyceae) under lethal doses of 3-(3,4-dichlorophenyl)-1, 1-dimethylurea herbicide

Sun, D.; Chen, Z-wei.; Mathews, F.Scott.; Davidson, V.L., 2002:
Mutation of alphaPhe55 of methylamine dehydrogenase alters the reorganization energy and electronic coupling for its electron transfer reaction with amicyanin

Gupta, S.; Quirk, P., G.; Venning, J., D.; Slade, J.; Bizouarn, T.; Grimley, R., L.; Cotton, N., P.J.; Jackson, J.B.z, 1998:
Mutation of amino acid residues in the mobile loop region of the NAD(H)-binding domain of proton-translocating transhydrogenase

Knowlton, A.A., 1999:
Mutation of amino acids 246-251 alters nuclear accumulation of human heat shock protein (HSP) 72 with stress, but does not reduce viability

Knowlton, A.A., 2001:
Mutation of amino acids 566-572 (KKKVLDK) inhibits nuclear accumulation of heat shock protein 72 after heat shock

Julias, J.G.; McWilliams, M.Jane.; Sarafianos, S.G.; Alvord, W.Gregory.; Arnold, E.; Hughes, S.H., 2003:
Mutation of amino acids in the connection domain of human immunodeficiency virus type 1 reverse transcriptase that contact the template-primer affects RNase H activity

Bhattacharyya, R.; Wedegaertner, P.B., 2003:
Mutation of an N-terminal acidic-rich region of p115-RhoGEF dissociates alpha13 binding and alpha13-promoted plasma membrane recruitment

Ni, H.; Blajchman, M.A.; Ananthanarayanan, V.S.; Smith, I.J.; Sheffield, W.P., 2000:
Mutation of any site of N-linked glycosylation accelerates the in vivo clearance of recombinant rabbit antithrombin

Bennett, E.R.; Su, H.; Kanner, B.I., 2000:
Mutation of arginine 44 of GAT-1, a (Na(+) + Cl(-))-coupled gamma-aminobutyric acid transporter from rat brain, impairs net flux but not exchange

Wang, Y-Hua.; Zeng, W-Yong.; Shi, Y-Yu., 2003:
Mutation of arginines near the active site Cys124 of human dual-specificity phosphatase and its effect on the enzymatic activity

Yamanaka, H.; Okamoto, K., 2000:
Mutation of aromatic amino acid residues located at the amino- and carboxy-termini of Escherichia coli heat-stable enterotoxin Ip reduces the efficiency of the toxin to cross the outer membrane

Song, D.D.; Jacques, N.A., 1999:
Mutation of aspartic acid residues in the fructosyltransferase of Streptococcus salivarius ATCC 25975

Yamaguchi, H.; Inokuchi, K.; Tarusawa, M.; Dan, K., 2002:
Mutation of bcl-x gene in non-Hodgkin's lymphoma

Miao, J.; Kusafuka, T.; Kuroda, S.; Yoneda, A.; Zhou, Z.; Okada, A., 2003:
Mutation of beta-catenin and its protein accumulation in solid and cystic tumor of the pancreas associated with metastasis

Ashihara, K.; Saito, T.; Mizumoto, H.; Nishimura, M.; Tanaka, R.; Kudo, R., 2002:
Mutation of beta-catenin gene in endometrial cancer but not in associated hyperplasia

Tunbridge, E.; Dingwall, C.; Edge, C.; Konduri, M.; DeMarini, D.J.; Livi, G.P.; Maycox, P.R., 2002:
Mutation of charged residues in the TR3 death domain does not perturb interaction with TRADD

Stolz, M.; Hornemann, T.; Schlattner, U.; Wallimann, T., 2002:
Mutation of conserved active-site threonine residues in creatine kinase affects autophosphorylation and enzyme kinetics

Yu, G.; Chen, F.; Nishimura, M.; Steiner, H.; Tandon, A.; Kawarai, T.; Arawaka, S.; Supala, A.; Song, Y.Q.; Rogaeva, E.; Holmes, E.; Zhang, D.M.; Milman, P.; Fraser, P.; Haass, C.; St-George-Hyslop, P., 2000:
Mutation of conserved aspartates affect maturation of presenilin 1 and presenilin 2 complexes

Yu, G.; Chen, F.; Nishimura, M.; Steiner, H.; Tandon, A.; Kawarai, T.; Arawaka, S.; Supala, A.; Song, Y.Q.; Rogaeva, E.; Holmes, E.; Zhang, D.M.; Milman, P.; Fraser, P.E.; Haass, C.; George-Hyslop, P.S., 2000:
Mutation of conserved aspartates affects maturation of both aspartate mutant and endogenous presenilin 1 and presenilin 2 complexes

Evans, D.J.; Kuo, T.C.; Kwong, M.; Van, R.; Fleiszig, S.M.J., 2002:
Mutation of csk, encoding the C-terminal Src kinase, reduces Pseudomonas aeruginosa internalization by mammalian cells and enhances bacterial cytotoxicity

Herbig, U.; Griffith, J.W.; Fanning, E., 2000:
Mutation of cyclin/cdk phosphorylation sites in HsCdc6 disrupts a late step in initiation of DNA replication in human cells

Lee, Y.S.n; Cho, Y.D.ng, 2001:
Mutation of cysteine-115 to alanine in Nicotiana glutinosa ornithine decarboxylase reduces enzyme activity

Du, G.G.; Khanna, V.K.; MacLennan, D.H., 2000:
Mutation of divergent region 1 alters caffeine and Ca(2+) sensitivity of the skeletal muscle Ca(2+) release channel (ryanodine receptor)

Vonderlinden, D.; Ma, X.; Sandberg, E.M.; Gernert, K.; Bernstein, K.E.; Sayeski, P.P., 2002:
Mutation of glutamic acid residue 1046 abolishes Jak2 tyrosine kinase activity

Seol, S.Y.ng; Chang, H.K.ung; Lee, Y.C.ul, 1999:
Mutation of gyrA in quinolone-resistant clinical isolates of Escherichia coli

Clarke, C.E.; Benham, C.D.; Bridges, A.; George, A.R.; Meadows, H.J., 2000:
Mutation of histidine 286 of the human P2X4 purinoceptor removes extracellular pH sensitivity

Lee, W.M.; Ishikawa, M.; Ahlquist, P., 2001:
Mutation of host delta9 fatty acid desaturase inhibits brome mosaic virus RNA replication between template recognition and RNA synthesis

Tomita, Y.; Mizuno, T.; Díez, J.; Naito, S.; Ahlquist, P.; Ishikawa, M., 2003:
Mutation of host DnaJ homolog inhibits brome mosaic virus negative-strand RNA synthesis

Yuan-Ying; Huang-Jian; Zheng-Shu, 1999:
Mutation of human mismatch repair genes in hereditary nonpolyposis colorectal cancer (HNPCC) families

Ichida, K.; Matsumura, T.; Sakuma, R.; Hosoya, T.; Nishino, T., 2001:
Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II

Wada, Y.; Abe, T.; Takeshita, T.; Sato, H.; Yanashima, K.; Tamai, M., 2001:
Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa

Moreau-Fauvarque, C.; Taillebourg, E.; Préat, T.; Dura, J-Maurice., 2002:
Mutation of linotte causes behavioral defects independently of pigeon in Drosophila

Merritt, J.; Qi, F.; Goodman, S.D.; Anderson, M.H.; Shi, W., 2003:
Mutation of luxS affects biofilm formation in Streptococcus mutans

Lyon, W.R.; Madden, J.C.; Levin, J.C.; Stein, J.L.; Caparon, M.G., 2001:
Mutation of luxS affects growth and virulence factor expression in Streptococcus pyogenes

Stroeher, U.H.; Paton, A.W.; Ogunniyi, A.David.; Paton, J.C., 2003:
Mutation of luxS of Streptococcus pneumoniae affects virulence in a mouse model

Rorison, K.A.; Lee, D.J.; Baldwin, G.S., 2001:
Mutation of lysine residues of the 78-kDa gastrin-binding protein reduces gastrin binding

Dobbins, D.E.; Sood, R.; Hashiramoto, A.; Hansen, C.T.; Wilder, R.L.; Remmers, E.F., 2002:
Mutation of macrophage colony stimulating factor (Csf1) causes osteopetrosis in the tl rat

Wu, Z.; Earle, J.; Saito, S'ichi.; Anderson, C.W.; Appella, E.; Xu, Y., 2002:
Mutation of mouse p53 Ser23 and the response to DNA damage

Basler, C.F.; García-Sastre, A.; Palese, P., 1999:
Mutation of neuraminidase cysteine residues yields temperature-sensitive influenza viruses

Qari, M.H.; Khalil, S.H.; Kambouris, M.; Meyer, B.F., 1998:
Mutation of p16, p21 or cyclin dependent kinase 4 is rare in acute lymphoblastic leukaemia

Chen Guang Yu; Yuan, S.B.; M.H.a Zhi; Liao Ming Yang, 2002:
Mutation of p16INK4a and p15INK4b genes of human bronchial epithelial cells malignantly transformed by cyclophosphamide and thiotepa

Kang, Y.K.; Kim, W.H.; Lee, H.W.; Lee, H.K.; Kim, Y.I., 1999:
Mutation of p53 and K-ras, and loss of heterozygosity of APC in intrahepatic cholangiocarcinoma

Minouchi, K.; Kaneko, S.; Kobayashi, K., 2002:
Mutation of p53 gene in regenerative nodules in cirrhotic liver

Chen, G.G.; Merchant, J.L.; Lai, P.B.S.; Ho, R.L.K.; Hu, X.; Okada, M.; Huang, S.F.; Chui, A.K.K.; Law, D.J.; Li, Y.G.; Lau, W.Y.; Li, A.K.C., 2003:
Mutation of p53 in recurrent hepatocellular carcinoma and its association with the expression of ZBP-89

Grote, H.J.; Schneider Stock, R.; Neumann, W.; Roessner, A., 2000:
Mutation of p53 with loss of heterozygosity in the osteosarcomatous component of a dedifferentiated chondrosarcoma

Hertzler, S.; Luo, M.; Lipton, H.L., 2000:
Mutation of predicted virion pit residues alters binding of Theiler's murine encephalomyelitis virus to BHK-21 cells

Ito, K.-Ichi; Weigl, K., E.; Deeley, R., G.; Cole, S., P.C., 2003:
Mutation of proline residues in the NH2-terminal region of the multidrug resistance protein, MRP1 (ABCC1): Effects on protein expression, membrane localization, and transport function

Ariyama, K.-Ichirou; Nagasawa, S., 1999:
Mutation of proto-oncogenes in rat free-cell type tumor (CTS) cells

Machu, T.K.; Coultrap, S.J.; Waugh, M.D.; Hamilton, M.E., 1999:
Mutation of putative phosphorylation sites in the 5-hydroxytryptamine3 receptor does not eliminate its modulation by ethanol

Kobayashi, Y.; Kawaoi, A.; Katoh, R., 2002:
Mutation of ras oncogene in di-isopropanolnitrosamine-induced rat thyroid carcinogenesis

Chaillot, D.; Declerck, N.; Niefind, K.; Schomburg, D.; Chardot, T.; Meunier, J.C., 2000:
Mutation of recombinant catalytic subunit alpha of the protein kinase CK2 that affects catalytic efficiency and specificity

Visser, F.; Vickers, M.F.; Ng, A.M.L.; Baldwin, S.A.; Young, J.D.; Cass, C.E., 2001:
Mutation of residue 33 of human equilibrative nucleoside transporters 1 and 2 alters sensitivity to inhibition of transport by dilazep and dipyridamole

Wallace, T.J.; Kodsi, E.M.; Langston, T.B.; Gergis, M.R.; Grogan, W.M., 2001:
Mutation of residues 423 (Met/Ile), 444 (Thr/Met), and 506 (Asn/Ser) confer cholesteryl esterase activity on rat lung carboxylesterase. Ser-506 is required for activation by cAMP-dependent protein kinase

Howes, B.D.; Heering, H.A.; Roberts, T.O.; Schneider-Belhadadd, F.; Smith, A.T.; Smulevich, G., 2001:
Mutation of residues critical for benzohydroxamic acid binding to horseradish peroxidase isoenzyme C

Bertoldi, M.; Castellani, S.; Voltattorni, C.B.rri, 2001:
Mutation of residues in the coenzyme binding pocket of Dopa decarboxylase. Effects on catalytic properties

Beenken, K.E.; Blevins, J.S.; Smeltzer, M.S., 2003:
Mutation of sarA in Staphylococcus aureus limits biofilm formation

Sheeler, C.Q.; Singleton, D.W.; Khan, S.A., 2003:
Mutation of serines 104, 106, and 118 inhibits dimerization of the human estrogen receptor in yeast

Walters, J.N.; Sexton, G.L.; McCaffery, J.Michael.; Desai, P., 2003:
Mutation of single hydrophobic residue I27, L35, F39, L58, L65, L67, or L71 in the N terminus of VP5 abolishes interaction with the scaffold protein and prevents closure of herpes simplex virus type 1 capsid shells

Ballarè, E.; Persani, L.; Lania, A.G.; Filopanti, M.; Giammona, E.; Corbetta, S.; Mantovani, S.; Arosio, M.; Beck-Peccoz, P.; Faglia, G.; Spada, A., 2001:
Mutation of somatostatin receptor type 5 in an acromegalic patient resistant to somatostatin analog treatment

Pei, S.; Doye, A.; Boquet, P., 2001:
Mutation of specific acidic residues of the CNF1 T domain into lysine alters cell membrane translocation of the toxin

Zheng, X.; Zhang, L.; Wang, A.P.; Araneda, R.C.; Lin, Y.; Zukin, R.S.; Bennett, M.V.L., 1999 :
Mutation of structural determinants lining the N-methyl-D-aspartate receptor channel differentially affects phencyclidine block and spermine potentiation and block

Zaveckas, M.; Luksa, V.; Zvirblis, G.; Chmieliauskaite, V.; Bumelis, V.; Pesliakas, H., 2003:
Mutation of surface-exposed histidine residues of recombinant human granulocyte-colony stimulating factor (Cys17Ser) impacts on interaction with chelated metal ions and refolding in aqueous two-phase systems

Bianchi, M.T.; Macdonald, R.L., 2001:
Mutation of the 9' leucine in the GABA(A) receptor gamma2L subunit produces an apparent decrease in desensitization by stabilizing open states without altering desensitized states

McClellan, A.J.; Brodsky, J.L., 2000:
Mutation of the ATP-binding pocket of SSA1 indicates that a functional interaction between Ssa1p and Ydj1p is required for post-translational translocation into the yeast endoplasmic reticulum

Evans, D.R.H.; Hemmings, B.A., 2000:
Mutation of the C-terminal leucine residue of PP2Ac inhibits PR55/B subunit binding and confers supersensitivity to microtubule destabilization in Saccharomyces cerevisiae

Skålhegg, Børn.S.; Huang, Y.; Su, T.; Idzerda, R.L.; McKnight, G.Stanley.; Burton, K.A., 2002:
Mutation of the Calpha subunit of PKA leads to growth retardation and sperm dysfunction

Andronis, C.; Merry, S.A.P.; Durrant, J.R.; Klug, D.R.; Barber, J.; Nixon, P.J., 1999:
Mutation of the Chlamydomonas reinhardtii analogue of residue M210 of the Rhodobacter sphaeroides reaction center slows primary electron transfer in Photosystem II

Kanai, Y.; Ushijima, S.; Nakanishi, Y.; Sakamoto, M.; Hirohashi, S., 2003:
Mutation of the DNA methyltransferase (DNMT) 1 gene in human colorectal cancers

Jeng, Yung Ming; Hsu, Hey Chi, 2002:
Mutation of the DR5/TRAIL receptor 2 gene is infrequent in hepatocellular carcinoma

Cummings, C.J.; Reinstein, E.; Sun, Y.; Antalffy, B.; Jiang, Y.H.i; Ciechanover, A.; Orr, H.T.; Beaudet, A.L.; Zoghbi, H.Y., 1999:
Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice

Greenfield, L.John.; Zaman, S.H.; Sutherland, M.L.; Lummis, S.C.R.; Niemeyer, Mía-Isabel.; Barnard, E.A.; Macdonald, R.L., 2002:
Mutation of the GABAA receptor M1 transmembrane proline increases GABA affinity and reduces barbiturate enhancement

Kumagai, T.; Hibino, R.; Kawano, Y.; Sugiyama, M., 1999:
Mutation of the N-terminal proline 9 of BLMA from Streptomyces verticillus abolishes the binding affinity for bleomycin

Dixon, M.J.; Gazzard, J.; Chaudhry, S.S.; Sampson, N.; Schulte, B.A.; Steel, K.P., 1999:
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice

Ladogana, A.; Almonti, S.; Petraroli, R.; Giaccaglini, E.; Ciarmatori, C.; Liu, Q.G.; Bevivino, S.; Squitieri, F.; Pocchiari, M., 2001:
Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease

Harima, Y.; Sawada, S.; Nagata, K.; Sougawa, M.; Ostapenko, V.; Ohnishi, T., 2001:
Mutation of the PTEN gene in advanced cervical cancer correlated with tumor progression and poor outcome after radiotherapy

Damjanovich, J.; Adany, R.; Berta, A.; Beck, Z.; Balazs, M., 2000:
Mutation of the RB1 gene caused unilateral retinoblastoma in early age

Eng, C.; Thomas, G.A.; Neuberg, D.S.; Mulligan, L.M.; Healey, C.S.; Houghton, C.; Frilling, A.; Raue, F.; Williams, E.D.; Ponder, B.A., 1998:
Mutation of the RET proto-oncogene is correlated with RET immunostaining in subpopulations of cells in sporadic medullary thyroid carcinoma

Hoeflich, A.; Reisinger, R.; Vargas, G.A.; Elmlinger, M.W.; Schuett, B.; Jehle, P.M.; Renner Mueller, I.; Lahm, H.; Russo, V.C.; Wolf, E., 2002:
Mutation of the RGD sequence does not affect plasma membrane association and growth inhibitory effects of elevated IGFBP-2 in vivo

Planas, J.V.; Cummings, D.E.; Idzerda, R.L.; McKnight, G.S., 1999:
Mutation of the RIIbeta subunit of protein kinase A differentially affects lipolysis but not gene induction in white adipose tissue

Schreyer, S.A.; Cummings, D.E.; McKnight, G.S.; LeBoeuf, R.C., 2001:
Mutation of the RIIbeta subunit of protein kinase A prevents diet-induced insulin resistance and dyslipidemia in mice

Senderek, J.; Bergmann, C.; Weber, S.; Ketelsen, U.P.ter; Schorle, H.; Rudnik Schoeneborn, S.; Buettner, R.; Buchheim, E.; Zerres, K., 2003:
Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15

Stofega, M.R.; Herrington, J.; Billestrup, N.; Carter-Su, C., 2000:
Mutation of the SHP-2 binding site in growth hormone (GH) receptor prolongs GH-promoted tyrosyl phosphorylation of GH receptor, JAK2, and STAT5B

Sugimura, M.; Kobayashi, K.; Sagae, S.; Nishioka, Y.; Ishioka, S.I.hi; Terasawa, K.; Tokino, T.; Kudo, R., 2000:
Mutation of the SRC gene in endometrial carcinoma

Nichols, P.; Croxen, R.; Vincent, A.; Rutter, R.; Hutchinson, M.; Newsom-Davis, J.; Beeson, D., 1999:
Mutation of the acetylcholine receptor epsilon-subunit promoter in congenital myasthenic syndrome

Franowicz, J.S.; Kessler, L.E.; Borja, C.M.Dailey.; Kobilka, B.K.; Limbird, L.E.; Arnsten, A.F.T., 2002:
Mutation of the alpha2A-adrenoceptor impairs working memory performance and annuls cognitive enhancement by guanfacine

Peschard, P.; Fournier, T.M.; Lamorta, L.; Naujokas, M.A.; Band, H.; Langdon, W.Y.; Park, M., 2001:
Mutation of the c-Cbl TKB domain binding site on the Met receptor tyrosine kinase converts it into a transforming protein

Rinke, C.S.; Boyer, P.L.; Sullivan, M.D.; Hughes, S.H.; Linial, M.L., 2002:
Mutation of the catalytic domain of the foamy virus reverse transcriptase leads to loss of processivity and infectivity

Maeno, K.; Ito, K-ichi.; Hama, Y.; Shingu, K.; Kimura, M.; Sano, M.; Nakagomi, H.; Tsuchiya, S-ichi.; Fujimori, M., 2003:
Mutation of the class I beta-tubulin gene does not predict response to paclitaxel for breast cancer

West, J.T.; Weldon, S.K.; Wyss, S.; Lin, X.; Yu, Q.; Thali, M.; Hunter, E., 2002:
Mutation of the dominant endocytosis motif in human immunodeficiency virus type 1 gp41 can complement matrix mutations without increasing Env incorporation

Kato, M.; Kanai, M.; Soma, O.; Takusa, Y.; Kimura, T.; Numakura, C.; Matsuki, T.; Nakamura, S.; Hayasaka, K., 2001:
Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis

Hill, N.L.; Laib, A.; Duncan, M.K., 2002:
Mutation of the ectodysplasin-A gene results in bone defects in mice

Rodríguez-Crespo, I.; Nishida, C.R.; Knudsen, G.M.; de Montellano, P.R., 1999:
Mutation of the five conserved histidines in the endothelial nitric-oxide synthase hemoprotein domain. No evidence for a non-heme metal requirement for catalysis

Ernst, O.P.; Meyer, C.K.; Marin, E.P.; Henklein, P.; Fu, W.Y.; Sakmar, T.P.; Hofmann, K.P., 2000:
Mutation of the fourth cytoplasmic loop of rhodopsin affects binding of transducin and peptides derived from the carboxyl-terminal sequences of transducin alpha and gamma subunits

Rippere-Lampe, K.E.; O'Brien, A.D.; Conran, R.; Lockman, H.A., 2001:
Mutation of the gene encoding cytotoxic necrotizing factor type 1 (cnf(1)) attenuates the virulence of uropathogenic Escherichia coli

Chaudhry, S.S.; Gazzard, J.; Baldock, C.; Dixon, J.; Rock, M.J.; Skinner, G.C.; Steel, K.P.; Kielty, C.M.; Dixon, M.J., 2001:
Mutation of the gene encoding fibrillin-2 results in syndactyly in mice

Rajpar, M.H.; Harley, K.; Laing, C.; Davies, R.M.; Dixon, M.J., 2001:
Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

Visalli, R.J.; Brandt, C.R., 2002:
Mutation of the herpes simplex virus 1 KOS UL45 gene reveals dose dependent effects on central nervous system growth

Agaphonov, M.O.; Packeiser, A.N.; Chechenova, M.B.; Choi, E.S.; Ter-Avanesyan, M.D., 2001:
Mutation of the homologue of GDP-mannose pyrophosphorylase alters cell wall structure, protein glycosylation and secretion in Hansenula polymorpha

Krittanai, C.; Bourchookarn, A.; Pathaichindachote, W.; Panyim, S., 2003:
Mutation of the hydrophobic residue on helix alpha5 of the Bacillus thuringiensis Cry4B affects structural stability

Marttila, A.T.; Hytönen, V.P.; Laitinen, O.H.; Bayer, E.A.; Wilchek, M.; Kulomaa, M.S., 2002:
Mutation of the important Tyr-33 residue of chicken avidin: functional and structural consequences

Frauwirth, K.; Shastri, N., 2001:
Mutation of the invariant chain transmembrane region inhibits II degradation, prolongs association with MHC class II, and selectively disrupts antigen presentation

Mitchem, K.L.; Hibbard, E.; Beyer, L.A.; Bosom, K.; Dootz, G.A.; Dolan, D.F.; Johnson, K.R.; Raphael, Y.; Kohrman, D.C., 2002:
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

Li, J.; Ahvazi, B.; Szittner, R.; Meighen, E., 2000:
Mutation of the nucleophilic elbow of the Lux-specific thioesterase from Vibrio harveyi

Montesinos-Rongen, M.; Roers, A.; Küppers, R.; Rajewsky, K.; Hansmann, M.L., 1999:
Mutation of the p53 gene is not a typical feature of Hodgkin and Reed-Sternberg cells in Hodgkin's disease

Minamisawa, S.; Sato, Y.; Tatsuguchi, Y.; Fujino, T.; Imamura, S.I.hiro; Uetsuka, Y.; Nakazawa, M.; Matsuoka, R., 2003:
Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy

Chatterjee, R.; Millard, C.S.; Champion, K.; Clark, D.P.; Donnelly, M.I., 2001:
Mutation of the ptsG gene results in increased production of succinate in fermentation of glucose by Escherichia coli

D'Cruz, P.M.; Yasumura, D.; Weir, J.; Matthes, M.T.; Abderrahim, H.; LaVail, M.M.; Vollrath, D., 2000:
Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat

Mertens, G.; Gielis, M.; Mommers, N.; Mularoni, A.; Lamartine, J.; Heylen, H.; Muylle, L.; Vandenberghe, A., 1999:
Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles

Rajpar, M.Helen.; Koch, M.J.; Davies, R.M.; Mellody, K.T.; Kielty, C.M.; Dixon, M.J., 2002:
Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization

Shiga, K.; Fukuyama, R.; Kimura, S.; Nakajima, K.; Fushiki, S., 1999:
Mutation of the sterol 27-hydroxylase gene (CYP27) results in truncation of mRNA expressed in leucocytes in a Japanese family with cerebrotendinous xanthomatosis

Lee, M-Jen.; Huang, Y-Chung.; Sweeney, M.G.; Wood, N.W.; Reilly, M.M.; Yip, P-Keung., 2002:
Mutation of the sterol 27-hydroxylase gene ( CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis

Dawson, J.F.; Luu, H.A.; Bagu, J.R.; Holmes, C.F., 2001:
Mutation of the toxin binding site of PP-1c: comparison with PP-2B

Moon, Y.W.n; Park, W.S.ng; Vortmeyer, A.O.; Weil, R.J.; Lee, Y.S.o; Winters, T.A.; Zhuang, Z.; Fuller, B.G., 1998:
Mutation of the uracil DNA glycosylase gene detected in glioblastoma

Kimata, Y.; Lim, C.R.; Kiriyama, T.; Nara, A.; Hirata, A.; Kohno, K., 1999:
Mutation of the yeast epsilon-COP gene ANU2 causes abnormal nuclear morphology and defects in intracellular vesicular transport

Buckway, C.K.; Wilson, E.M.; Ahlsén, M.; Bang, P.; Oh, Y.; Rosenfeld, R.G., 2001:
Mutation of three critical amino acids of the N-terminal domain of IGF-binding protein-3 essential for high affinity IGF binding

Blencke, S.; Ullrich, A.; Daub, H., 2003:
Mutation of threonine 766 in the epidermal growth factor receptor reveals a hotspot for resistance formation against selective tyrosine kinase inhibitors

Sciotti, M.A.; Nakajin, S.; Wermuth, B.; Baker, M.E., 2000:
Mutation of threonine-241 to proline eliminates autocatalytic modification of human carbonyl reductase

Lin, H-lien.; Kent, U.M.; Zhang, H.; Waskell, L.; Hollenberg, P.F., 2003:
Mutation of tyrosine 190 to alanine eliminates the inactivation of cytochrome P450 2B1 by peroxynitrite

Kramer, H.K.; Andria, M.L.; Kushner, S.A.; Esposito, D.H.; Hiller, J.M.; Simon, E.J., 2000:
Mutation of tyrosine 318 (Y318F) in the delta-opioid receptor attenuates tyrosine phosphorylation, agonist-dependent receptor internalization, and mitogen-activated protein kinase activation

Bertoldi, M.; Gonsalvi, M.; Contestabile, R.; Voltattorni, C.Borri., 2002:
Mutation of tyrosine 332 to phenylalanine converts dopa decarboxylase into a decarboxylation-dependent oxidative deaminase

Chaika, O.V.; Chaika, N.; Volle, D.J.; Hayashi, H.; Ebina, Y.; Wang, L.M.; Pierce, J.H.; Lewis, R.E., 1999:
Mutation of tyrosine 960 within the insulin receptor juxtamembrane domain impairs glucose transport but does not inhibit ligand-mediated phosphorylation of insulin receptor substrate-2 in 3T3-L1 adipocytes

Hamazaki, S.; Yoshida, M.; Yao, M.; Nagashima, Y.; Taguchi, K.; Nakashima, H.; Okada, S., 2001:
Mutation of von Hippel-Lindau tumor suppressor gene in a sporadic endolymphatic sac tumor

Nørgaard, P.; Winther, J.R., 2001:
Mutation of yeast Eug1p CXXS active sites to CXXC results in a dramatic increase in protein disulphide isomerase activity

Fernando, P.; Abdulle, R.; Mohindra, A.; Guillemette, J.G.; Heikkila, J.J., 2002:
Mutation or deletion of the C-terminal tail affects the function and structure of Xenopus laevis small heat shock protein, hsp30

Tavankar, G.Reza.; Mossialos, D.; Williams, H.D., 2002:
Mutation or overexpression of a terminal oxidase leads to a cell division defect and multiple antibiotic sensitivity in Pseudomonas aeruginosa

Wu, T.D.; Schiffer, C.A.; Gonzales, M.J.; Taylor, J.; Kantor, R.; Chou, S.; Israelski, D.; Zolopa, A.R.; Fessel, W.Jeffrey.; Shafer, R.W., 2003:
Mutation patterns and structural correlates in human immunodeficiency virus type 1 protease following different protease inhibitor treatments

Mizokami, M.; Imanishi, T.; Ikeo, K.; Suzuki, Y.; Orito, E.; Kumada, T.; Ueda, R.; IIno, S.; Nakano, T., 1999:
Mutation patterns for two flaviviruses: Hepatitis C virus and GB virus C/hepatitis G virus

Chaudhry, U.; Ray, K.; Bala, M.; Saluja, D., 2002:
Mutation patterns in gyrA and parC genes of ciprofloxacin resistant isolates of Neisseria gonorrhoeae from India

Bielawski, J.P.; Gold, J.R., 2002:
Mutation patterns of mitochondrial H- and L-strand DNA in closely related cyprinid fishes

Hovde, L.B.; Rotschafer, S.E.; Ibrahim, K.H.; Gunderson, B.; Hermsen, E.D.; Rotschafer, J.C., 2003:
Mutation prevention concentration of ceftriaxone, meropenem, imipenem, and ertapenem against three strains of Streptococcus pneumoniae

Chernoff, Yury, O., 2001:
Mutation processes at the protein level: Is Lamarck back?

Kannan, K.; Krishnamurthy, J.; Feng, J.; Nakajima, T.; Tsuchida, N.; Shanmugam, G., 2000:
Mutation profile of the p53, fhit, p16INK4a/p19ARF and H-ras genes in Indian breast carcinomas

Park, J.; Betel, D.; Gryfe, R.; Michalickova, K.; D.N.cola, N.; Gallinger, S.; Hogue, C.W.V.; Redston, M., 2002:
Mutation profiling of mismatch repair-deficient colorectal cancers using an in silico genome scan to identify coding microsatellites

Lindgren, P.K.mp; Karlsson, A.; Hughes, D., 2003:
Mutation rate and evolution of fluoroquinolone resistance in Escherichia coli isolates from patients with urinary tract infections

Eckert, K.A.; Yan, G.; Hile, S.E., 2002:
Mutation rate and specificity analysis of tetranucleotide microsatellite DNA alleles in somatic human cells

Holtkemper, U.; Rolf, B.; Hohoff, C.; Forster, P.; Brinkmann, B., 2001:
Mutation rates at two human Y-chromosomal microsatellite loci using small pool PCR techniques

Saunders, N.J.; Moxon, E.Richard.; Gravenor, M.B., 2003:
Mutation rates: estimating phase variation rates when fitness differences are present and their impact on population structure

Ahmed, R.; Kannan, M.; Choudhry, V.Prakash.; Saxena, R., 2003:
Mutation reports: intron 1 and 22 inversions in Indian haemophilics

Oberacher, H.; Huber, C.G.; Oefner, P.J., 2002:
Mutation scanning by ion-pair reversed-phase high-performance liquid chromatography-electrospray ionization mass spectrometry (ICEMS)

Lu, J.; Chen, Y.; Zhang, Y.; Pan, H.; Wu, H.; Xu, K.; Liu, X.; Jiang, Y.; Bao, X.; Ding, K.; Shen, Y.; Wu, X., 2002:
Mutation screen of the GABAA receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy

Alvi, A.J.; Hogg, R.; Rader, J.S.; Kuo, M.J.; Maher, E.R.; Latif, F., 2002:
Mutation screening analysis of the retinoblastoma related gene RB2/p130 in sporadic ovarian cancer and head and neck squamous cell cancer

Suzuki, Y.; Sasagawa, I.; Tateno, T.; Ashida, J.; Nakada, T.; Muroya, K.; Ogata, T., 2001:
Mutation screening and CAG repeat length analysis of the androgen receptor gene in Klinefelter's syndrome patients with and without spermatogenesis

Peng, R.; Gou, Y.; Yuan, Q.; Li, T.; Latsoudis, H.; Yuan, G.; Luo, D.; Liu, X.; Collier, D.A., 2003:
Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China

Wang, H.; Chu, W.; Hemphill, C.; Hasstedt, S.J.; Elbein, S.C., 2002:
Mutation screening and association of human retinoid X receptor gamma variation with lipid levels in familial type 2 diabetes

Otabe, S.; Clement, K.; Dubois, S.; Lepretre, F.; Pelloux, V.; Leibel, R.; Chung, W.; Boutin, P.; Guy-Grand, B.; Froguel, P.; Vasseur, F., 1999:
Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients

Bost, M.; Lachaux, A.; Accominotti, M.; Vandenberghe, A., 1999 :
Mutation screening and genotype-phenotype correlation in 32 families with Wilson disease

Graham, C.A.; Mcclean, E.; Ward, A.J.M.; Beattie, E.D.ane; Martin, S.; O'kane, M.; Young, I.S.; Nicholls, D.P.ul, 1999:
Mutation screening and genotype:phenotype correlation in familial hypercholesterolaemia

Conway, G.S.; Conway, E.; Walker, C.; Hoppner, W.; Gromoll, J.; Simoni, M., 1999:
Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome

Kim, S.J.ong; Herzing, L.B.K.; Veenstra Vanderweele, J.; Lord, C.; Courchesne, R.; Leventhal, B.L.; Ledbetter, D.H.; Courchesne, E.; Cook, E.H.Jr, 2002:
Mutation screening and transmission disequilibrium study of ATP10C in autism

Ganesh, S.; Shoda, K.; Amano, K.; Uchiyama, A.; Kumada, S.; Moriyama, N.; Hirose, S.; Yamakawa, K., 2001:
Mutation screening for Japanese Lafora's disease patients: identification of novel sequence variants in the coding and upstream regulatory regions of EPM2A gene

Stuhrmann, M.; Graf, N.; Doerk, T.; Schmidtke, J., 2000:
Mutation screening for prenatal and presymptomatic diagnosis: Cystic fibrosis and haemochromatosis

Lako, M.; Ramsden, S.; Campbell, R.D.; Strachan, T., 1999:
Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis

Xiang, F.; Buervenich, S.; Nicolao, P.; Bailey, M.E.; Zhang, Z.; Anvret, M., 2000:
Mutation screening in Rett syndrome patients

Sacconi, S.; Salviati, L.; Sue, C.M.; Shanske, S.; Davidson, M.M.; Bonilla, E.; Naini, A.B.; De Vivo, D.C.; DiMauro, S., 2003:
Mutation screening in patients with isolated cytochrome c oxidase deficiency

Rueffert, H.; Olthoff, D.; Deutrich, C.; Meinecke, C.D.; Froster, U.G., 2002:
Mutation screening in the ryanodine receptor 1 gene (RYR1) in patients susceptible to malignant hyperthermia who show definite IVCT results: Identification of three novel mutations

Gauthier, J.; Joober, R.; Mottron, L.; Laurent, S.; Fuchs, M.; De Kimpe, V.; Rouleau, G.A., 2003:
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

Khaliq, S.; Abid, A.; Hameed, A.; Anwar, K.; Mohyuddin, A.; Azmat, Z.; Shami, S.A.; Ismail, M.; Mehdi, S.Q.sim, 2003:
Mutation screening of Pakistani families with congenital eye disorders

Bennett, P.J.; Hoff, M.; Rosenthal, J.; Zhao, M.; Coon, H.; Myles-Worsley, M.; Byerley, W.F., 2000:
Mutation screening of a neutral amino acid transporter, ASCT1, and its potential role in schizophrenia

Noguchi, E.; Shibasaki, M.; Arinami, T.; Yamakawa-Kobayashi, K.; Yokouchi, Y.; Takeda, K.; Matsui, A.; Hamaguchi, H., 2000:
Mutation screening of interferon regulatory factor 1 gene (IRF-1) as a candidate gene for atopy/asthma

Tomkins, J.; Banner, S.J.; McDermott, C.J.; Shaw, P.J., 2001:
Mutation screening of manganese superoxide dismutase in amyotrophic lateral sclerosis

Acar, C.; Mears, A.J.; Yashar, B.M.; Maheshwary, A.S.; Andreasson, S.; Baldi, A.; Sieving, P.A.; Iannaccone, A.; Musarella, M.A.; Jacobson, S.G.; Swaroop, A., 2003:
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene

Sueoka, H.; Moshinetsky, A.; Nagao, M.; Chiba, S., 1999:
Mutation screening of phenylketonuria in the Far East of Russia

Harland, M.; Holland, E.A.; Ghiorzo, P.; Mantelli, M.; Bianchi Scarra, G.; Goldstein, A.M.; Tucker, M.A.; Ponder, B.A.J.; Mann, G.J.; Bishop, D.T.mothy; Bishop, J.N.wton, 2000:
Mutation screening of the CDKN2A promoter in melanoma families

Steinlein, O.K.; Stoodt, J.; de Vos, R.A.; Steur, E.N.; Wevers, A.; Schütz, U.; Schröder, H., 1999:
Mutation screening of the CHRNA4 and CHRNB2 nicotinic cholinergic receptor genes in Alzheimer's disease

Shi, Y-Ru.; Wu, J-Yuarn.; Hsu, Y-An.; Lee, C-Chun.; Tsai, C-Hai.; Tsai, F-Jen., 2002:
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan

Norton, N.; Williams, H.J.; Williams, N.M.; Spurlock, G.; Zammit, S.; Jones, G.; Jones, S.; Owen, R.; O'Donovan, M.C.; Owen, M.J., 2003:
Mutation screening of the Homer gene family and association analysis in schizophrenia

Hunter, M.; Bernard, Rëlle.; Freitas, E.; Boyer, A.; Morar, B.; Martins, I.J.; Tournev, I.; Jordanova, A.; Guergelcheva, V.; Ishpekova, B.; Kremensky, I.; Nicholson, G.; Schlotter, B.; Lochmüller, H.; Voit, T.; Colomer, J.; Thomas, P.K.; Levy, N.; Kalaydjieva, L., 2003:
Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease

Burtey, S.; Lossi, A.M.; Bayle, J.; Berland, Y.; Fontés, M., 2002:
Mutation screening of the PKD1 transcript by RT-PCR

Lacquemant, C.; Lepretre, F.; Pineda Torra, I.; Manraj, M.; Charpentier, G.; Ruiz, J.; Staels, B.; Froguel, P., 2000:
Mutation screening of the PPARalpha gene in type 2 diabetes associated with coronary heart disease

Barone, V.; Massa, O.; Intravaia, E.; Bracco, A.; D.M.rtino, A.; Tegazzin, V.; Cozzolino, S.; Sorrentino, V., 1999:
Mutation screening of the RYR1 gene and identification of two novel mutations in Italian malignant hyperthermia families

Lutwyche, J.K.; Keough, R.A.; Hughes, T.P.; Gonda, T.J., 2001:
Mutation screening of the c-MYB negative regulatory domain in acute and chronic myeloid leukaemia

Haug, K.; Kremerskothen, J.; Hallmann, K.; Sander, T.; Dullinger, J.; Rau, B.; Beyenburg, S.; Lentze, M.J.; Barnekow, A.; Elger, C.E.; Propping, P.; Heils, A., 2000:
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy

Todd, R.D.; Lobos, E.A., 2002:
Mutation screening of the dopamine D2 receptor gene in attention-deficit hyperactivity disorder subtypes: Preliminary report of a research strategy

Christiansen, L.; Bygum, A.; Käehne, M.; Jensen, A.; Hørder, M.; Petersen, N.E., 2001:
Mutation screening of the entire coding region of the protoporphyrinogen oxidase gene using denaturing gradient gel electrophoresis and denaturing hplc

Mayer, K.; Ballhausen, W.; Rott, H.D., 1999:
Mutation screening of the entire coding regions of the TSC1 and the TSC2 gene with the protein truncation test (PTT) identifies frequent splicing defects

Zhu, Q.; Yamagata, K.; Tsukahara, Y.; Yang, Q.; Liu, W.; Hanafusa, T.; Miyagawa, J.; Matsuzawa, Y., 2001:
Mutation screening of the hepatocyte nuclear factor (HNF)-6 gene in Japanese subjects with diabetes mellitus

Iwase, T.; Kajimura, N.; Uchiyama, M.; Ebisawa, T.; Yoshimura, K.; Kamei, Y.; Shibui, K.; Kim, K.; Kudo, Y.; Katoh, M.; Watanabe, T.; Nakajima, T.; Ozeki, Y.; Sugishita, M.; Hori, T.; Ikeda, M.; Toyoshima, R.; Inoue, Y.; Yamada, N.; Mishima, K., 2002:
Mutation screening of the human Clock gene in circadian rhythm sleep disorders

Kang, B.Y.ng; Bae, J.S.ol; Kim, K.T.e; Lee, K.H.; Shin, J.H.e; Lee, C.C.oo, 2002:
Mutation screening of the human lipoprotein lipase gene in Korean individuals with essential hypertension

Shiino, Y.; Nakajima, S.; Ozeki, Y.; Isono, T.; Yamada, N., 2003:
Mutation screening of the human period 2 gene in bipolar disorder

Giedraitis, V.; He, B.; Hillert, J., 1999:
Mutation screening of the interferon-gamma gene as a candidate gene for multiple sclerosis

Ohtsuki, T.; Toru, M.; Arinami, T., 2001:
Mutation screening of the metabotropic glutamate receptor mGluR4 (GRM4) gene in patients with schizophrenia

Yamamoto, T.; Yamashita, N.; Kuwabara, M.; Nakano, J.; Sugimoto, H.; Akiyama, K.; Hirai, K.; Ishii, A.; Uehara, Y.; Ohta, K., 2002:
Mutation screening of the muscarinic m2 and m3 receptor genes in asthmatics, outgrow subjects, and normal controls

Kim, S.H.; Warram, J.H.; Krolewski, A.S.; Doria, A., 2001:
Mutation screening of the neurogenin-3 gene in autosomal dominant diabetes

Roks, G.; Dermaut, B.; Heutink, P.; Julliams, A.; Backhovens, H.; Van, D.B.oeck, M.; Serneels, S.; Hofman, A.; Van Broeckhoven, C.; Van Duijn, C.M.; Cruts, M., 1999:
Mutation screening of the tau gene in patients with early-onset Alzheimer's disease

Delplanque, J.; Vasseur, F.; Durand, E.; Abderrahmani, A.; Dina, C.; Waeber, G.; Guy-Grand, B.; Clement, K.; Weill, J.; Boutin, P.; Froguel, P., 2002:
Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians

Maheshwari, M.; Christian, S.L.; Liu, C.; Badner, J.A.; Detera-Wadleigh, S.; Gershon, E.S.; Gibbs, R., A., 2002:
Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: Human peptide transporter (SLC15A1) and human glypican5 (GPC5)

Shevchenko, Y.O.; Bale, S.J.; Compton, J.G., 2000:
Mutation screening using automated bidirectional dideoxy fingerprinting

Wei-Sai-Jin; Fu-Xue-Qin; Cheng-Xin; Tu-Guo-Quan, 2002:
Mutation selection by 60Cogamma treatment of nanchangmycin producing Streptomyces nanchangensis

Ohe, T.; Shaughnessy, D., T.; Landi, S.; Terao, Y.; Sawanishi, H.; Nukaya, H.; Wakabayashi, K.; Demarini, D., M., 1999:
Mutation spectra in Salmonella TA98, TA100, and TA104 of two phenylbenzotriazole mutagens (PBTA-1 and PBTA-2) detected in the Nishitakase River in Kyoto, Japan

Demarini, D.M.; Landi, S.; Ohe, T.; Shaughnessy, D.T.; Franzen, R.; Richard, A.M., 2000:
Mutation spectra in Salmonella of analogues of MX: Implications of chemical structure for mutational mechanisms

Canella, K.A.; Seidman, M.M., 2000:
Mutation spectra in supF: Approaches to elucidating sequence context effects

Gentil, A.; L.P.ge, F.; Cadet, J.; Sarasin, A., 2000:
Mutation spectra induced by replication of two vicinal oxidative DNA lesions in mammalian cells

Ohta, T.; Watanabe Akanuma, M.; Tokishita, S.I.hi; Yamagata, H., 1999:
Mutation spectra of chemical mutagens determined by Lac+ reversion assay with Escherichia coli WP3101P-WP3106P tester strains

Lu, Q.; Hwang, Y.T.; Hwang, C.B.C., 2002:
Mutation spectra of herpes simplex virus type 1 thymidine kinase mutants

Granville, C.A.; Hanley, N.M.; Mumford, J.L.; Demarini, D.M., 2003:
Mutation spectra of smoky coal combustion emissions in Salmonella reflect the TP53 and KRAS mutations in lung tumors from smoky coal-exposed individuals

Shaughnessy, D., T.; Ohe, T.; Landi, S.; Warren, S., H.; Richard, A., M.; Munter, T.; Franzen, R.; Kronberg, L.; Demarini, D., M., 2000:
Mutation spectra of the drinking water mutagen 3-chloro-4-methyl-5-hydroxy-2(5H)-furanone (MCF) in salmonella TA100 and TA104: Comparison to MX

Kondo, I.; Yamagata, H., 2002:
Mutation spectrum and genotype-phenotype correlation of MECP2 in patients with Rett syndrome

Minassian, B.A.; Ianzano, L.; Meloche, M.; Andermann, E.; Rouleau, G.A.; Delgado Escueta, A.V.; Scherer, S.W., 2000:
Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy

Delettre, C.; Griffoin, J.M.; Kaplan, J.; Dollfus, H.; Lorenz, B.; Faivre, L.; Lenaers, G.; Belenguer, P.; Hamel, C.P., 2002:
Mutation spectrum and splicing variants in the OPA1 gene

Mcleod, J.L.; Craig, J.; Gumley, S.; Roberts, S.; Kirkland, M.A., 2002:
Mutation spectrum in Australian pedigrees with hereditary hyperferritinaemia-cataract syndrome reveals novel and de novo mutations

Zhou, R.; Yu, G.; Zhou, Y.; Zeng, X., 1999:
Mutation spectrum in Salmonella induced by environmental tobacco smoke

Laccone, F.; Huppke, P.; Hanefeld, F.; Meins, M., 2001:
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions

Herzog, B.; Morris, A.A.M.; Saunders, C.; Eschrich, K., 2001:
Mutation spectrum in patients with fructose-1,6-bisphosphatase deficiency

Beltcheva, O.; Martin, P.; Lenkkeri, U.; Tryggvason, K., 2001:
Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome

Agnez Lima, L.F.; D.M.scio, P.; Napolitano, R.L.; Fuchs, R.P.; Menck, C.F.M., 1999:
Mutation spectrum induced by singlet oxygen in Escherichia coli deficient in exonuclease III

Ryu, J-Chun.; Kim, Y-Jung.; Chai, Y-Gyu., 2002:
Mutation spectrum of 1,2-dibromo-3-chloropropane, an endocrine disruptor, in the lacI transgenic Big Blue Rat2 fibroblast cell line

Komatireddy, S.; Chakrabarti, S.; Mandal, A.Kumar.; Reddy, A.Bindu.Madhava.; Sampath, S.; Panicker, S.George.; Balasubramanian, D., 2003:
Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India

Tauchi, H.; Komatsu, K.; Ishizaki, K.; Yatagai, F.; Kato, T., 2000:
Mutation spectrum of MSH3-deficient HHUA/chr.2 cells reflects in vivo activity of the MSH3 gene product in mismatch repair

Rihet, S.; Vielh, P.; Camonis, J.; Goud, B.; Chevillard, S.; D.G.nzburg, J., 2001:
Mutation status of genes encoding RhoA, Rac1, and Cdc42 GTPases in a panel of invasive human colorectal and breast tumors

Hoyes, K.P.; Wadeson, P.J.; Sharma, H.L.; Hendry, J.H.; Morris, I.D., 1998:
Mutation studies in lacI transgenic mice after exposure to radiation or cyclophosphamide

Ono, T.; Uehara, Y.; Saito, Y.; Ikehata, H., 2002:
Mutation theory of aging, assessed in transgenic mice and knockout mice

Arimoto-Kobayashi, S.; Ando, Y.; Horai, Y.; Okamoto, K.; Hayatsu, H.; Lowe, J.E.; Green, M.H.L., 2002:
Mutation, DNA strand cleavage and nitric oxide formation caused by N-nitrosoproline with sunlight: a possible mechanism of UVA carcinogenicity

Parsian, A.; Racette, B.; Zhang, Z.H.; Chakraverty, S.; Rundle, M.; Goate, A.; Perlmutter, J.S., 1998:
Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease

Rizzu, P.; Joosse, M.; Ravid, R.; Hoogeveen, A.; Kamphorst, W.; van Swieten, J.C.; Willemsen, R.; Heutink, P., 2000:
Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients

Hanemann, C.O.iver; D'urso, D.; Gabreeels Festen, A.A.W.M.; Mueller, H.W., 2000:
Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot-Marie-Tooth type 1A

Piau, D., 2003:
Mutation-replication statistics of polymerase chain reactions

Chasnov, J.R., 2000:
Mutation-selection balance, dominance and the maintenance of sex

Hermisson, J.; Redner, O.; Wagner, H.; Baake, E., 2002:
Mutation-selection balance: ancestry, load, and maximum principle

Baake, E.; Wagner, H., 2001:
Mutation-selection models solved exactly with methods of statistical mechanics

Komarova, N.L.; Sengupta, A.; Nowak, M.A., 2003:
Mutation-selection networks of cancer initiation: Tumor suppressor genes and chromosomal instability

Moller, P.; Borg, A.; Evans, G.; Haites, N.; Steel, C.M.; Vasen, H.; Gregory, H.; Hodgson, S.; Apold, J.; Lalloo, F.; Maehle, L.; Anderson, E.; Heimdal, K.; The Biomed 2 Demonstration Programme, O.I.herited Breast Cancer, 1999:
Mutation-specific survival of inherited breast cancer

Pevzner, P.A.; Dancík, V.; Tang, C.L., 2001:
Mutation-tolerant protein identification by mass spectrometry

Chi, S.G.l; Kim, H.J.ng; Park, B.J.on; Min, H.J.ng; Park, J.H.on; Kim, Y.W.a; Dong, S.H.; Kim, B.H.; Lee, J.I.; Chang, Y.W.on; Chang, R.; Kim, W.K.p; Yang, M.H., 1998:
Mutational abrogation of the PTEN/MMAC1 gene in gastrointestinal polyps in patients with Cowden disease

Berger, D.H.; Chang, H.; Wood, M.; Huang, L.; Heath, C.W.; Lehman, T.; Ruggeri, B.A., 1999:
Mutational activation of K-ras in nonneoplastic exocrine pancreatic lesions in relation to cigarette smoking status

Yang, Q.; Borkovich, K.A., 1999:
Mutational activation of a Galphai causes uncontrolled proliferation of aerial hyphae and increased sensitivity to heat and oxidative stress in Neurospora crassa

Koesters, R.; Ridder, R.; Kopp-Schneider, A.; Betts, D.; Adams, V.; Niggli, F.; Briner, J.; von Knebel Doeberitz, M., 1999:
Mutational activation of the beta-catenin proto-oncogene is a common event in the development of Wilms' tumors

Park, Y.K.; Chi, S.G.; Kim, Y.W.; Park, H.R.; Unni, K.K., 1999:
Mutational alteration of the p16CDKN2a tumor suppressor gene is infrequent in Ewing's sarcoma

Murén, E.M.; Suciu, D.; Topping, T.B.; Kumamoto, C.A.; Randall, L.L., 1999:
Mutational alterations in the homotetrameric chaperone SecB that implicate the structure as dimer of dimers

Bae, D.K.; Park, Y.K.; Chi, S.G.; Lee, C.W.; Unni, K.K., 2000:
Mutational alterations of the p16CDKN2A tumor suppressor gene have low incidence in mesenchymal chondrosarcoma

Hirono, H.; Shoji, Y.; Takahashi, T.; Sato, W.; Takeda, E.; Nishijo, T.; Kuroda, Y.; Nishigaki, T.; Inui, K.; Takada, G., 1998:
Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1

Lim, J.H.; Choi, J.; Kim, W.; Ahn, B.Y.; Han, Y.S., 2001:
Mutational analyses of Aquifex pyrophilus DNA ligase define essential domains for self-adenylation and DNA binding activity

Shiri-Sverdlov, R.; Oefner, P.; Green, L.; Baruch, R.G.; Wagner, T.; Kruglikova, A.; Haitchick, S.; Hofstra, R.M.; Papa, M.Z.; Mulder, I.; Rizel, S.; Bar Sade, R.B.; Dagan, E.; Abdeen, Z.; Goldman, B.; Friedman, E., 2000:
Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

Sakurai, M.; Adachi, H.; Sutoh, K., 2001:
Mutational analyses of Dictyostelium IQGAP-related protein GAPA: Possible interaction with small GTPases in cytokinesis

Terada, T.; Fujita, N.; Adachi, H.; Nanjo, H.; Sato, R.; Takagi, T.; Maeda, M., 2001:
Mutational analyses of cysteine residues of bovine dihydrodiol dehydrogenase 3

Eckert, K.A.; Yan, G., 2000:
Mutational analyses of dinucleotide and tetranucleotide microsatellites in Escherichia coli: influence of sequence on expansion mutagenesis

Nicholson, S.E.; Willson, T.A.; Farley, A.; Starr, R.; Zhang, J.G.; Baca, M.; Alexander, W.S.; Metcalf, D.; Hilton, D.J.; Nicola, N.A., 1999:
Mutational analyses of the SOCS proteins suggest a dual domain requirement but distinct mechanisms for inhibition of LIF and IL-6 signal transduction

Xu, G.; Rich, R.L.; Steegborn, C.; Min, T.; Huang, Y.; Myszka, D.G.; Wu, H., 2002:
Mutational analyses of the p35-caspase interaction. A bowstring kinetic model of caspase inhibition by p35

Pfister, S.C.istina; Machado Santelli, G.M.ria; Han, S.W.n; Henrique Silva, F., 2002:
Mutational analyses of the signals involved in the subcellular location of DSCRI

Pei, Y.; Ho, C.K.; Schwer, B.; Shuman, S., 1999:
Mutational analyses of yeast RNA triphosphatases highlight a common mechanism of metal-dependent NTP hydrolysis and a means of targeting enzymes to pre-mRNAs in vivo by fusion to the guanylyltransferase component of the capping apparatus

Kloiber, K.; Weiskirchen, R.; Kräutler, B.; Bister, K.; Konrat, R., 1999:
Mutational analysis and NMR spectroscopy of quail cysteine and glycine-rich protein CRP2 reveal an intrinsic segmental flexibility of LIM domains

Orimo, H.; Girschick, H.J.; Goseki-Sone, M.; Ito, M.; Oda, K.; Shimada, T., 2002:
Mutational analysis and functional correlation with phenotype in German patients with childhood-type hypophosphatasia

Grigorescu-Sido, A.; Schulze, E.; Grigorescu-Sido, P.; Heinrich, U.; Nistor, T.; Duncea, I., 2002:
Mutational analysis and genotype-phenotype correlation in patients with classic 21-hydroxylase deficiency from transylvania (north-west Romania)

Takano, H.; Koike, R.; Onodera, O.; Sasaki, R.; Tsuji, S., 1999:
Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy

Holm, I.A.; Nelson, A.E.; Robinson, B.G.; Mason, R.S.; Marsh, D.J.; Cowell, C.T.; Carpenter, T.O., 2001:
Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic rickets

Bissar Tadmouri, N.; Parman, Y.; Boutrand, L.; Deymeer, F.; Serdaroglu, P.; Vandenberghe, A.; Battaloglu, E., 2000:
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients

Malherbe, P.; Kratochwil, N.; Knoflach, Fédéric.; Zenner, M-Thérèse.; Kew, J.N.C.; Kratzeisen, C.; Maerki, H.P.; Adam, G.; Mutel, V., 2003:
Mutational analysis and molecular modeling of the allosteric binding site of a novel, selective, noncompetitive antagonist of the metabotropic glutamate 1 receptor

Rössle, S.C.; Bisch, P.M.; Lone, Y-Chun.; Abastado, J-Pierre.; Kourilsky, P.; Bellio, M., 2002:
Mutational analysis and molecular modeling of the binding of Staphylococcus aureus enterotoxin C2 to a murine T cell receptor Vbeta10 chain

Malherbe, P.; Kratochwil, N.; Zenner, M-Thérèse.; Piussi, J.; Diener, C.; Kratzeisen, C.; Fischer, C.; Porter, R.H.P., 2003:
Mutational analysis and molecular modeling of the binding pocket of the metabotropic glutamate 5 receptor negative modulator 2-methyl-6-(phenylethynyl)-pyridine

Gouldson, P.; Calandra, B.; Legoux, P.; Kerneis, A.; Rinaldi Carmona, M.; Barth, F.; L.F.r, G.; Ferrara, P.; Shire, D., 2000:
Mutational analysis and molecular modelling of the antagonist SR 144528 binding site on the human cannabinoid CB2 receptor

Yu, T.W.; Muller, R.; Muller, M.; Zhang, X.; Draeger, G.; Kim, C.G.; Leistner, E.; Floss, H.G., 2001:
Mutational analysis and reconstituted expression of the biosynthetic genes involved in the formation of 3-amino-5-hydroxybenzoic acid, the starter unit of rifamycin biosynthesis in amycolatopsis Mediterranei S699

Adhikari, P.; Bachhawat-Sikder, K.; Thomas, C.J.; Ravishankar, R.; Jeyaprakash, A.A.; Sharma, V.; Vijayan, M.; Surolia, A., 2001:
Mutational analysis at Asn-41 in peanut agglutinin. A residue critical for the binding of the tumor-associated Thomsen-Friedenreich antigen

Wang, L.Kai.; Shuman, S., 2002:
Mutational analysis defines the 5'-kinase and 3'-phosphatase active sites of T4 polynucleotide kinase

Friedrich, T.; Breiderhoff, T.; Jentsch, T.J., 1999:
Mutational analysis demonstrates that ClC-4 and ClC-5 directly mediate plasma membrane currents

Bacíková, D.; Horowitz, D.S., 2002:
Mutational analysis identifies two separable roles of the Saccharomyces cerevisiae splicing factor Prp18

Delague, V.; Souraty, N.; Khallouf, E.; Tardy, V.; Chouery, E.; Halaby, G.; Loiselet, J.; Morel, Y.; Mégarbané, A., 2000:
Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylase

Decourt, C.; Rocca, A.; Bridoux, F.; Vrtovsnik, F.; Preud'homme, J.L.; Cogné, M.; Touchard, G., 1999:
Mutational analysis in murine models for myeloma-associated Fanconi's syndrome or cast myeloma nephropathy

Laurans, M.S.H.; DiLuna, M.L.; Shin, D.; Niazi, F.; Voorhees, J.R.; Nelson-Williams, C.; Johnson, E.W.; Siegel, A.M.; Steinberg, G.K.; Berg, M.J.; Scott, R.Michael.; Tedeschi, G.; Enevoldson, T.Peter.; Anson, J.; Rouleau, G.A.; Ogilvy, C.; Awad, I.A.; Lifton, R.P.; Gunel, M., 2003:
Mutational analysis of 206 families with cavernous malformations

Stuible, H.P.ter; Buettner, D.; Ehlting, J.; Hahlbrock, K.; Kombrink, E., 2000:
Mutational analysis of 4-coumarate:CoA ligase identifies functionally important amino acids and verifies its close relationship to other adenylate-forming enzymes

Beesley, C.E.; Meaney, C.A.; Greenland, G.; Adams, V.; Vellodi, A.; Young, E.P.; Winchester, B.G., 2001:
Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations

Eroglu, B.; Powers Lee, S.G., 2002:
Mutational analysis of ATP-grasp residues in the two ATP sites of Saccharomyces cerevisiae carbamoyl phosphate synthetase

Okada, T.; Shiono, Y.; Hayashi, H.; Satoh, H.; Sawada, T.; Suzuki, A.; Takeda, Y.; Yano, M.; Michitaka, K.; Onji, M.; Mabuchi, H., 2000:
Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease

Crespo, J.L.; Guerrero, M.G.; Florencio, F.J., 1999:
Mutational analysis of Asp51 of Anabaena azollae glutamine synthetase. D51E mutation confers resistance to the active site inhibitors L-methionine-DL-sulfoximine and phosphinothricin

Popat, S.; Hearle, N.; Bevan, S.; Hogberg, L.; Stenhammar, L.; Houlston, R.S., 2002:
Mutational analysis of CD28 in coeliac disease

Saridaki, Z.; Liloglou, T.; Zafiropoulos, A.; Koumantaki, E.; Zoras, O.; Spandidos, D.A., 2003:
Mutational analysis of CDKN2A genes in patients with squamous cell carcinoma of the skin

Cheong, H.I.; Park, H.W.n; Ha, I.S.o; Choi, Y., 2000:
Mutational analysis of COL4A5 gene in Korean Alport syndrome

Turner, R.L.; Buck, K.W., 1999:
Mutational analysis of cis-acting sequences in the 3'- and 5'-untranslated regions of RNA2 of red clover necrotic mosaic virus

Ogura, M.; Liu, L.; Lacelle, M.; Nakano, M.M.; Zuber, P., 1999:
Mutational analysis of ComS: Evidence for the interaction of ComS and MecA in the regulation of competence development in Bacillus subtilis

Hwang, J.; Tai, P.C., 1999:
Mutational analysis of CvaA in the highly conserved domain of the membrane fusion protein family

Achermann, J.C.; Gu, W.X.; Kotlar, T.J.; Meeks, J.J.; Sabacan, L.P.; Seminara, S.B.; Habiby, R.L.; Hindmarsh, P.C.; Bick, D.P.; Sherins, R.J.; Crowley, W.F.; Layman, L.C.; Jameson, J.L., 1999:
Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay

Ji, Y.S.an; Johnson, B.H.; Webb, M.S.ott; Thompson, E.B.ad, 2002:
Mutational analysis of DBD: A unique antileukemic gene sequence

Kibel, A.S.; Faith, D.A.; Bova, G.Steven.; Isaacs, W.B., 2002:
Mutational analysis of ETV6 in prostate carcinoma

Sriskanda, V.; Schwer, B.; Ho, C.K.; Shuman, S., 1999:
Mutational analysis of Escherichia coli DNA ligase identifies amino acids required for nick-ligation in vitro and for in vivo complementation of the growth of yeast cells deleted for CDC9 and LIG4

Mossessova, E.; Levine, C.; Peng, H.; Nurse, P.; Bahng, S.; Marians, K.J., 2000:
Mutational analysis of Escherichia coli topoisomerase IV. I. Selection of dominant-negative parE alleles

Nurse, P.; Bahng, S.; Mossessova, E.; Marians, K.J., 2000:
Mutational analysis of Escherichia coli topoisomerase IV. II. ATPase negative mutants of parE induce hyper-DNA cleavage

Bahng, S.; Mossessova, E.; Nurse, P.; Marians, K.J., 2000:
Mutational analysis of Escherichia coli topoisomerase IV. III. Identification of a region of parE involved in covalent catalysis

Manchak, J.; Anthony, K.G.; Frost, L.S., 2002:
Mutational analysis of F-pilin reveals domains for pilus assembly, phage infection and DNA transfer

Kim, H.S.g; Lee, S.H.ung; Lee, J.W.o; Soung, Y.H.a; Lee, J.H.un; Park, J.Y.ung; Cho, Y.G.; Kim, C.J.e; Kim, S.Y.ung; Lee, Y.S.l; Park, W.S.ng; Kim, S.H.; Lee, J.Y.ung; Yoo, N.J.n, 2003:
Mutational analysis of Fas ligand gene in human non-Hodgkin lymphoma

Wang, D.; Kranz-Eble, P.; De Vivo, D.C., 2000:
Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome

Mantovani, G.; Romoli, R.; Weber, G.; Brunelli, V.; D.M.nis, E.; Beccio, S.; Beck-Peccoz, P.; Spada, A., 2000:
Mutational analysis of GNAS1 in patients with pseudohypoparathyroidism: identification of two novel mutations

Carman, C.V.; Barak, L.S.; Chen, C.; Liu-Chen, L.Y.; Onorato, J.J.; Kennedy, S.P.; Caron, M.G.; Benovic, J.L., 2000:
Mutational analysis of Gbetagamma and phospholipid interaction with G protein-coupled receptor kinase 2

Miyaura, M.; Yoshida, A.; Sakurai, A.; Fujita, M.; Koyama, A.H.; Adachi, A., 2000:
Mutational analysis of HIV-1 gag proteins (review)

O'Neil, P.K.; Sun, G.; Yu, H.; Ron, Y.; Dougherty, J.P.; Preston, B.D., 2002:
Mutational analysis of HIV-1 long terminal repeats to explore the relative contribution of reverse transcriptase and RNA polymerase II to viral mutagenesis

Pérez-Cabrera, A.; Kofman-Alfaro, S.; Zenteno, J.C., 2002:
Mutational analysis of HOXD13 and HOXA13 genes in the triphalangeal thumb-brachyectrodactyly syndrome

Scheiber, Dóra.; Barta, C.; Halász, Z.; Sallai, A.; Rácz, Károly.; Ságodi, László.; Fekete, Görgy.; Hiort, O.; Sólyom, János., 2003:
Mutational analysis of Hungarian patients with androgen insensitivity syndrome

Weber, M.; Stockhammer, F.; Schmitz, U.; Von Deimling, A., 2001:
Mutational analysis of INI1 in sporadic human brain tumors

Hatta, Y.; Arima, N.; Machino, T.; Itoh, T.; Hashimoto, S.; Takeuchi, J.; Sawada, U.; Hayakawa, S.; Yamamoto, T.; Horie, T., 2003:
Mutational analysis of IkappaBalpha in hematologic malignancies

Sluis-Cremer, N.; Arion, D.; Kaushik, N.; Lim, H.; Parniak, M.A., 2000:
Mutational analysis of Lys65 of HIV-1 reverse transcriptase

Inui, K.; Akagi, M.; Ono, J.; Tsukamoto, H.; Shimono, K.; Mano, T.; Imai, K.; Yamada, M.; Muramatsu, T.; Sakai, N.; Okada, S., 2001:
Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome

Alekshun, M.N.; Kim, Y.S.o; Levy, S.B., 2000:
Mutational analysis of MarR, the negative regulator of marRAB expression in Escherichia coli, suggests the presence of two regions required for DNA binding

Sun, Yun Fu; Yu, L.Y.ng; Saarma, Mart; Arumae, Urmas, 2003:
Mutational analysis of N-Bak reveals different structural requirements for antiapoptotic activity in neurons and proapoptotic activity in nonneuronal cells

Papp, T.; Schipper, H.; Pemsel, H.; Bastrop, R.; Muller, K.M.; Wiethege, T.; Weiss, D.G.; Dopp, E.; Schiffmann, D.; Rahman, Q., 2001:
Mutational analysis of N-ras, p53, p16INK4a, p14ARF and CDK4 genes in primary human malignant mesotheliomas

Lee, S.H.ung; Soung, Y.H.a; Lee, J.W.o; Kim, H.S.g; Lee, J.H.un; Park, J.Y.ung; Cho, Y.G.; Kim, C.J.e; Kim, S.Y.ung; Park, W.S.ng; Kim, S.H.; Lee, J.Y.ung; Yoo, N.J.n, 2003:
Mutational analysis of Noxa gene in human cancers

Arcuri, P.; D.S.irito, P.; D.V.lerio, A.; Palmirotta, R.; Creati, B.; Mammarella, S.; Esposito, D.L.; Caramia, F.G.; Mariani-Costantini, R.; Cama, A.; Battista, P., 2000:
Mutational analysis of OB gene in obese and type 2 diabetes affected subjects

Segerman, B.; Larsson, N.; Holmfeldt, P.; Gullberg, M., 2000:
Mutational analysis of op18/stathmin-tubulin-interacting surfaces. Binding cooperativity controls tubulin GTP hydrolysis in the ternary complex

Gutiérrez-Rivas, M.; Ibáñez, A.; Martínez, M.A.; Domingo, E.; Menéndez-Arias, L., 1999:
Mutational analysis of Phe160 within the "palm" subdomain of human immunodeficiency virus type 1 reverse transcriptase

Ishino, S.; Oyama, T.; Yuasa, M.; Morikawa, K.; Ishino, Y., 2003:
Mutational analysis of Pyrococcus furiosus replication factor C based on the three-dimensional structure

Inoue, K.; Shimotake, T.; Iwai, N., 2000:
Mutational analysis of RET/GDNF/NTN genes in children with total colonic aganglionosis with small bowel involvement

Improta Brears, T.; Ghosh, S.; Bell, R.M., 1999:
Mutational analysis of Raf-1 cysteine rich domain: Requirement for a cluster of basic aminoacids for interaction with phosphatidylserine

Paget, M.S.B.; Bae, J.B.m; Hahn, M.Y.ung; Li, W.; Kleanthous, C.; Roe, J.H.e; Buttner, M.J., 2001:
Mutational analysis of RsrA, a zinc-binding anti-sigma factor with a thiol-disulphide redox switch

Nishioka, Y.; Kobayashi, K.; Sagae, S.; Sugimura, M.; Ishioka, S.; Nagata, M.; Terasawa, K.; Tokino, T.; Kudo, R., 1999:
Mutational analysis of STK11 gene in ovarian carcinomas

Beesley, C., E.; Young, E., P.; Vellodi, A.; Winchester, B., G., 2000:
Mutational analysis of Sanfilippo syndrome type A (MPS IIIA): Identification of 13 novel mutations

Schüler, H.; Korenbaum, E.; Schutt, C.E.; Lindberg, U.; Karlsson, R., 1999:
Mutational analysis of Ser14 and Asp157 in the nucleotide-binding site of beta-actin

Shattuck, T.M.; Costa, J.; Bernstein, M.; Jensen, R.T.; Chung, D.C.; Arnold, A., 2002:
Mutational analysis of Smad3, a candidate tumor suppressor implicated in TGF-beta and menin pathways, in parathyroid adenomas and enteropancreatic endocrine tumors

Stigliano, A.; Caiola, S.; Siniscalchi, E.; Papini, E.; Crescenzi, A.; Monti, S.; Arnaldi, G.; Mantero, F.; Sciarra, F.; Toscano, V., 2002:
Mutational analysis of StAR gene in adrenal tumors

Zhang, H.; Nanba, E.; Yamamoto, T.; Ninomiya, H.; Ohno, K.; Mizuguchi, M.; Takeshita, K., 1999:
Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex

Becker, A.J.; Loebach, M.; Klein, H.; Normann, S.; Noethen, M.M.; Von Deimling, A.; Mizuguchi, M.; Elger, C.E.; Schramm, J.; Wiestler, O.D.; Bluemcke, I., 2001:
Mutational analysis of TSC1 and TSC2 genes in gangliogliomas

Luo, Z-Qing.; Smyth, A.J.; Gao, P.; Qin, Y.; Farrand, S.K., 2003:
Mutational analysis of TraR. Correlating function with molecular structure of a quorum-sensing transcriptional activator

Pelemans, H.; Esnouf, R.; D.C.ercq, E.; Balzarini, J., 2000:
Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors

Arion, D.; Sluis-Cremer, N.; Min, K-Lyum.; Abram, M.E.; Fletcher, R.S.; Parniak, M.A., 2001:
Mutational analysis of Tyr-501 of HIV-1 reverse transcriptase. Effects on ribonuclease H activity and inhibition of this activity by N-acylhydrazones

Chen, M.; Elder, R.T.; Yu, M.; O'Gorman, M.G.; Selig, L.; Benarous, R.; Yamamoto, A.; Zhao, Y., 1999:
Mutational analysis of Vpr-induced G2 arrest, nuclear localization, and cell death in fission yeast

Takano, H.; Koike, R.; Onodera, O.; Tsuji, S., 2000:
Mutational analysis of X-linked adrenoleukodystrophy gene

Hart, S.; Hart, T.; Gibson, C.; Wright, J.T., 2000:
Mutational analysis of X-linked amelogenesis imperfecta in multiple families

Pflegerl, K.; Hahn, R.; Berger, E.; Jungbauer, A., 2002:
Mutational analysis of a blood coagulation factor VIII-binding peptide

Psaridi, L.; Georgopoulou, U.; Varaklioti, A.; Mavromara, P., 1999:
Mutational analysis of a conserved tetraloop in the 5' untranslated region of hepatitis C virus identifies a novel RNA element essential for the internal ribosome entry site function

Munro, T.P.; Magee, R.J.; Kidd, G.J.; Carson, J.H.; Barbarese, E.; Smith, L.M.; Smith, R., 1999:
Mutational analysis of a heterogeneous nuclear ribonucleoprotein A2 response element for RNA trafficking

Mottus, R.; Sobel, R.E.; Grigliatti, T.A., 2000:
Mutational analysis of a histone deacetylase in Drosophila melanogaster: missense mutations suppress gene silencing associated with position effect variegation

Park, J.; Ryu, J.; Kim, K-Ae.; Lee, H.Joo.; Bahn, J.Hoon.; Han, K.; Choi, E.Yul.; Lee, K.Soo.; Kwon, H.Yil.; Choi, S.Young., 2002:
Mutational analysis of a human immunodeficiency virus type 1 Tat protein transduction domain which is required for delivery of an exogenous protein into mammalian cells

Luongo, C.L., 2002:
Mutational analysis of a mammalian reovirus mRNA capping enzyme

Julien, B.; Pountye, D.; Christie, G.E.; Calendar, R., 1998:
Mutational analysis of a satellite phage activator

Lessard, I.A.; Walsh, C.T., 1999:
Mutational analysis of active-site residues of the enterococcal D-ala-D-Ala dipeptidase VanX and comparison with Escherichia coli D-ala-D-Ala ligase and D-ala-D-Ala carboxypeptidase VanY

D'Abronzo, F.H.; Swearingen, B.; Klibanski, A.; Alexander, J.M., 1999:
Mutational analysis of activin/transforming growth factor-beta type I and type II receptor kinases in human pituitary tumors

Davis, M.D.; Wu, J.; Owens, R.A., 2000:
Mutational analysis of adeno-associated virus type 2 Rep68 protein endonuclease activity on partially single-stranded substrates

Huye, L.E.; Purugganan, M.M.; Jiang, M-Ming.; Roth, D.B., 2002:
Mutational analysis of all conserved basic amino acids in RAG-1 reveals catalytic, step arrest, and joining-deficient mutants in the V(D)J recombinase

Laughery, M.D.; Todd, M.L.; Kaplan, J.H., 2003:
Mutational analysis of alpha-beta subunit interactions in the delivery of Na,K-ATPase heterodimers to the plasma membrane

Chakraborty, A.R.; Davidson, A.; Howell, P.L., 1999:
Mutational analysis of amino acid residues involved in argininosuccinate lyase activity in duck delta II crystallin

Teng, B.B.; Ochsner, S.; Zhang, Q.; Soman, K.V.; Lau, P.P.; Chan, L., 1999:
Mutational analysis of apolipoprotein B mRNA editing enzyme (APOBEC1). structure-function relationships of RNA editing and dimerization

Schüler, H.; Nyåkern, M.; Schutt, C.E.; Lindberg, U.; Karlsson, R., 2000:
Mutational analysis of arginine 177 in the nucleotide binding site of beta-actin

Kim, M.H.; Lu, M.; Lim, E.J.; Chai, Y.G.; Hersh, L.B., 1999:
Mutational analysis of aspartate residues in the transmembrane regions and cytoplasmic loops of rat vesicular acetylcholine transporter

Sharma, U.K.; Praveen, P.V.K.; Balganesh, T.S., 2002:
Mutational analysis of bacteriophage T4 AsiA: involvement of N- and C-terminal regions in binding to sigma(70) of Escherichia coli in vivo

Wang, L.Kai.; Ho, C.Kiong.; Pei, Y.; Shuman, S., 2003:
Mutational analysis of bacteriophage T4 RNA ligase 1. Different functional groups are required for the nucleotidyl transfer and phosphodiester bond formation steps of the ligation reaction

Martins, A.; Shuman, S., 2001:
Mutational analysis of baculovirus capping enzyme Lef4 delineates an autonomous triphosphatase domain and structural determinants of divalent cation specificity

Martins, A.; Shuman, S., 2002:
Mutational analysis of baculovirus phosphatase identifies structural residues important for triphosphatase activity in vitro and in vivo

Kim, M.H.; Lu, M.; Kelly, M.; Hersh, L.B., 2000:
Mutational analysis of basic residues in the rat vesicular acetylcholine transporter. Identification of a transmembrane ion pair and evidence that histidine is not involved in proton translocation

Sagae, S.; Kobayashi, K.; Nishioka, Y.; Sugimura, M.; Ishioka, S.; Nagata, M.; Terasawa, K.; Tokino, T.; Kudo, R., 1999 :
Mutational analysis of beta-catenin gene in Japanese ovarian carcinomas: frequent mutations in endometrioid carcinomas

Kim, H.A.n, J.; Gorlach, J.; Caprari, C.S.ott-Craig, J.; Walton, J., 2001:
Mutational analysis of beta-glucanase genes from the plant-pathogenic fungus Cochliobolus carbonum

Shida, T.; Hattori, H.; Ise, F.; Sekiguchi, J., 2001:
Mutational analysis of catalytic sites of the cell wall lytic N-acetylmuramoyl-L-alanine amidases CwlC and CwlV

Meredith, J.E.; Kiosses, W.B.; Takada, Y.; Schwartz, M.A., 1999:
Mutational analysis of cell cycle inhibition by integrin beta1C

Abu-Duhier, F., M.; Goodeve, A., C.; Care, R., S.; Gari, M.; Wilson, G., A.; Peake, I., R.; Reilly, J., T., 2003:
Mutational analysis of class III receptor tyrosine kinases (C-KIT, C-FMS, FLT3) in idiopathic myelofibrosis

Bhatnagar, A.; Gülland, S.; Bascand, M.; Palmer, E.; Gardner, T.G.; Kearse, K.P.; Bäckström, B.Thomas., 2003:
Mutational analysis of conserved amino acids in the T cell receptor alpha-chain transmembrane region: a critical role of leucine 112 and phenylalanine 127 for assembly and surface expression

Urbatsch, I.L.; Julien, M.; Carrier, I.; Rousseau, M.E.ienne; Cayrol, R.; Gros, P., 2000:
Mutational analysis of conserved carboxylate residues in the nucleotide binding sites of P-glycoprotein

Piller, S.C.; Dubay, J.W.; Derdeyn, C.A.; Hunter, E., 2000:
Mutational analysis of conserved domains within the cytoplasmic tail of gp41 from human immunodeficiency virus type 1: effects on glycoprotein incorporation and infectivity

Loke, P.; Sim, T.S., 2001:
Mutational analysis of conserved glycines 42 and 256 in Cephalosporium acremonium isopenicillin N synthase

Koterasawa, M.; Mima, S.; Makise, M.; Tsuchiya, T.; Mizushima, T., 2002:
Mutational analysis of conserved hydrophobic amino acid residues in the N-terminal region of DnaA protein

Sankpal, U.T.; Rao, D.N., 2002:
Mutational analysis of conserved residues in HhaI DNA methyltransferase

Langer, M.R.; Tanner, K.G.; Denu, J.M., 2001:
Mutational analysis of conserved residues in the GCN5 family of histone acetyltransferases

Hatt, J.K.; Youngman, P., 2000:
Mutational analysis of conserved residues in the putative DNA-binding domain of the response regulator Spo0A of Bacillus subtilis

Reichstetter, S.; Papadopoulos, G.K.; Moustakas, A.K.; Swanson, E.; Liu, A.W.; Beheray, S.; Ettinger, R.A.; Nepom, G.T.; Kwok, W.W., 2002:
Mutational analysis of critical residues determining antigen presentation and activation of HLA-DQ0602 restricted T-cell clones

You, J.S.m; Baik, H.S.k; Paek, K.H.e, 1999:
Mutational analysis of cucumber mosaic virus movement protein gene

Firsov, D.; Robert-Nicoud, M.; Gruender, S.; Schild, L.; Rossier, B.C., 1999:
Mutational analysis of cysteine-rich domains of the epithelium sodium channel (ENaC). Identification of cysteines essential for channel expression at the cell surface

Zhang, H.; Kelley, W.L.; Chamberlain, L.H.; Burgoyne, R.D.; Lang, J., 1999:
Mutational analysis of cysteine-string protein function in insulin exocytosis

Schmidt, H.; Stiefel, K.M.; Racay, P.; Schwaller, B.; Eilers, J., 2003:
Mutational analysis of dendritic Ca2+ kinetics in rodent Purkinje cells: Role of parvalbumin and calbindin D28k

Takahashi, Y.; Ueno, A.; Mihara, H., 2000:
Mutational analysis of designed peptides that undergo structural transition from alpha helix to beta sheet and amyloid fibril formation

Los, M.; Kerckhaert, O.A.; Zewald, R.; van Amstel, H.K.; Voest, E.E., 2000:
Mutational analysis of endothelial cells derived from von Hippel-Lindau-related renal cancer

Hasegawa, S.; Miyoshi, Y.; Ikeda, N.; Egawa, C.; Tamaki, Y.; Monden, M.; Noguchi, S., 2003:
Mutational analysis of estrogen receptor-beta gene in human breast cancers

Hara, K.; Lewohl, J.M.; Yamakura, T.; Harris, R.A.ron, 2001:
Mutational analysis of ethanol interactions with G-protein-coupled inwardly rectifying potassium channels

Breedveld, M.; Bonting, K.; Dijkhuizen, L., 1998:
Mutational analysis of exopolysaccharide biosynthesis by Lactobacillus sakei 0-1

Jobling, M.G.; Holmes, R.K., 2002:
Mutational analysis of ganglioside GM(1)-binding ability, pentamer formation, and epitopes of cholera toxin B (CTB) subunits and CTB/heat-labile enterotoxin B subunit chimeras

Yoshihara, S.; Geng, X.; Okamoto, S.; Yura, K.; Murata, T.; Go, M.; Ohmori, M.; Ikeuchi, M., 2001:
Mutational analysis of genes involved in pilus structure, motility and transformation competency in the unicellular motile cyanobacterium Synechocystis sp. PCC 6803

Zafrullah, M.; Ozdener, M.H.; Kumar, R.; Panda, S.K.; Jameel, S., 1999:
Mutational analysis of glycosylation, membrane translocation, and cell surface expression of the hepatitis E virus ORF2 protein

Paolini, C.; Lahm, A.; De Francesco, R.; Gallinari, P., 2000:
Mutational analysis of hepatitis C virus NS3-associated helicase

Fuda, H.; Lee, Y.C.; Shimizu, C.; Javitt, N.B.; Strott, C.A., 2002:
Mutational analysis of human hydroxysteroid sulfotransferase SULT2B1 isoforms reveals that exon 1B of the SULT2B1 gene produces cholesterol sulfotransferase, whereas exon 1A yields pregnenolone sulfotransferase

Sakai, K.; Horiuchi, M.; Iida, S.; Fukumori, T.; Akari, H.; Adachi, A., 1999:
Mutational analysis of human immunodeficiency virus type 1 vif gene

Lambrechts, A.; Jonckheere, V.; Dewitte, D.; Vandekerckhove, J.; Ampe, C., 2002:
Mutational analysis of human profilin I reveals a second PI(4,5)-P2 binding site neighbouring the poly(L-proline) binding site

Ma, X.; Hu, J.; Lindner, D.J.; Kalvakolanu, D.V., 2002:
Mutational analysis of human thioredoxin reductase 1. Effects on p53-mediated gene expression and interferon and retinoic acid-induced cell death

Semrad, T.J.; Kenny, T.P.; Malyj, W.; Robbins, D.L., 2001:
Mutational analysis of immunoglobulin germline derived Vlambda4A light chains in rheumatoid arthritis

Kenny, T.P.; Semrad, T.J.; Malyj, W.; Robbins, D.L., 2001:
Mutational analysis of immunoglobulin germline derived Vlambda4B light chains in rheumatoid arthritis

Bellón, T.; Kitzig, F.; Sayós, J.; López-Botet, M., 2002:
Mutational analysis of immunoreceptor tyrosine-based inhibition motifs of the Ig-like transcript 2 (CD85j) leukocyte receptor

Mena, I.; Jambrina, E.; Albo, C.; Perales, B.; Ortín, J.; Arrese, M.; Vallejo, D.; Portela, A., 1999:
Mutational analysis of influenza A virus nucleoprotein: identification of mutations that affect RNA replication

Shirotani, K.; Takahashi, K.; Araki, W.; Maruyama, K.; Tabira, T., 2000:
Mutational analysis of intrinsic regions of presenilin 2 that determine its endoproteolytic cleavage and pathological function

Nakagawa, S.H.; Tager, H.S.; Steiner, D.F., 2000:
Mutational analysis of invariant valine B12 in insulin: Implications for receptor binding

Juan, S.H.; Aust, S.D., 1999:
Mutational analysis of loading of iron into rat liver ferritin by ceruloplasmin

Subden, R.E.; Krizus, A.; Osothsilp, C.; Viljoen, M.; Van Vuuren, H.J.J., 1998:
Mutational analysis of malate pathways in Schizosaccharomyces pombe

Das, S.; Maitra, U., 2000:
Mutational analysis of mammalian translation initiation factor 5 (eIF5): role of interaction between the beta subunit of eIF2 and eIF5 in eIF5 function in vitro and in vivo

Dubern, B.; Clément, K.; Pelloux, V.; Froguel, P.; Girardet, J.P.; Guy-Grand, B.; Tounian, P., 2001:
Mutational analysis of melanocortin-4 receptor, agouti-related protein, and alpha-melanocyte-stimulating hormone genes in severely obese children

Yanchak, M.P.; Taylor, R.A.; Crowder, M.W., 2000:
Mutational analysis of metallo-beta-lactamase CcrA from Bacteroides fragilis

Duga, S.; Asselta, R.; Bonati, M.Teresa.; Malcovati, M.; Dalprà, L.; Oldani, A.; Zucconi, M.; Ferini-Strambi, L.; Tenchini, M.Luisa., 2002:
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy

Sato, B.; Ito, H.; Hinchliffe, S.; Sommer, M.H.; Zerboni, L.; Arvin, A.M., 2003:
Mutational analysis of open reading frames 62 and 71, encoding the varicella-zoster virus immediate-early transactivating protein, IE62, and effects on replication in vitro and in skin xenografts in the SCID-hu mouse in vivo

Vazquez, N.; Lehrnbecher, T.; Chen, R.; Christensen, B., L.; Gallin, J., I.; Malech, H.; Holland, S.; Zhu, S.; Chanock, S., J., 2001:
Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

McTaggart, K.E.; Tran, M.; Mah, D.Y.; Lai, S.W.; Nesslinger, N.J.; MacDonald, I.M., 2002:
Mutational analysis of patients with the diagnosis of choroideremia

Nock, S.; Liang, W.; Warrick, H.M.; Spudich, J.A., 2000:
Mutational analysis of phosphorylation sites in the Dictyostelium myosin II tail: Disruption of myosin function by a single charge change

Ueda, K.; Lipkind, G.M.; Zhou, A.; Zhu, X.; Kuznetsov, A.; Philipson, L.; Gardner, P.; Zhang, C.; Steiner, D.F., 2003:
Mutational analysis of predicted interactions between the catalytic and P domains of prohormone convertase 3 (PC3/PC1)

Shin, K-Hyuk.; Shin, J-Ho.; Kim, J-Hwa.; Park, J-Gahb., 2002:
Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene

Polyak, S.W.; Chapman-Smith, A.; Mulhern, T.D.; Cronan, J.E.; Wallace, J.C., 2000:
Mutational analysis of protein substrate presentation in the post-translational attachment of biotin to biotin domains

Petmitr, S.; Wongsommart, D.; Chaksangchaichot, P.; Pakeetoot, T.; Sutinont, P.; Sirivaidyapong, P.; Karalak, A., 2003:
Mutational analysis of ras gene family in lung cancer in Thai

Yamamoto, I.; Ujiiye, T.; Ohshima, Y.; Satoh, T., 2001:
Mutational analysis of regulatory cis-acting elements for the transcriptional activation of the dmsCBA operon in Rhodobacter sphaeroides f. sp. denitrificans

Ross, J.J.; Gryczynski, U.; Schleif, R., 2003:
Mutational analysis of residue roles in AraC function

Weng, Y.; Weiss, C.D., 1998:
Mutational analysis of residues in the coiled-coil domain of human immunodeficiency virus type 1 transmembrane protein gp41

Liu, J.; Tsukuba, T.; Okamoto, K.; Ohishi, M.; Yamamoto, K., 2002:
Mutational analysis of residues in two consensus motifs in the active sites of cathepsin E

Phin, S.; Kupferwasser, D.; Lam, J.; Lee-Fruman, K.K., 2003:
Mutational analysis of ribosomal S6 kinase 2 shows differential regulation of its kinase activity from that of ribosomal S6 kinase 1

Yoo, N.J.n; Soung, Y.H.a; Lee, J.W.o; Park, W.S.ng; Kim, S.Y.ung; Nam, S.W.o; Han, J.H.; Kim, S.H.; Lee, J.Y.ung; Lee, S.H.ung, 2003:
Mutational analysis of salvador gene in human carcinomas

Edmunds, S.C.; Kelsell, D.P.; Hungerford, J.L.; Cree, I.A., 2002:
Mutational analysis of selected genes in the TGFbeta, Wnt, pRb, and p53 pathways in primary uveal melanoma

Li, X.; Himanen, J.-Pekka; Martin-De-Llano, J.-Javier; Padovan, J.-Cesar; Chait, B., T.; Manning, J., M., 1999:
Mutational analysis of sickle haemoglobin (Hb) gelation

Ott, R.D.; Wang, Y.; Fanning, E., 2002:
Mutational analysis of simian virus 40 T-antigen primosome activities in viral DNA replication

Fujimoto, K.; Takahashi, S.Y.; Katoh, S., 2002:
Mutational analysis of sites in sepiapterin reductase phosphorylated by Ca2+/calmodulin-dependent protein kinase II

Yang, D.; Brunn, G.J.; Lawrence, J.C.Jr, 1999:
Mutational analysis of sites in the translational regulator, PHAS-I, that are selectively phosphorylated by mTOR

Rudrabhatla, P.; Rajasekharan, R., 2003:
Mutational analysis of stress-responsive peanut dual specificity protein kinase. Identification of tyrosine residues involved in regulation of protein kinase activity

Charsky, C.M.; Schumann, N.J.; Kane, P.M., 2000:
Mutational analysis of subunit G (Vma10p) of the yeast vacuolar H+-ATPase

Bowen, M.E.; Engelman, D.M.; Brunger, A.T., 2002:
Mutational analysis of synaptobrevin transmembrane domain oligomerization

Jeltsch, A.; Roth, M.; Friedrich, T., 1999:
Mutational analysis of target base flipping by the EcoRV adenine-N6 DNA methyltransferase

Lewis, G.S.ane; Jewell, J.E.; Phang, T.; Miller, K.W., 2002:
Mutational analysis of tetracycline resistance protein transmembrane segment insertion

Borgione, E.; Sturnio, M.; Spalletta, A.; Angela Lo Giudice, M.; Castiglia, L.; Galesi, O.; Ragusa, A.; Fichera, M., 2003:
Mutational analysis of the ATRX gene by DGGE: a powerful diagnostic approach for the ATRX syndrome

Rutter, J.L.; Smith, A.M.; Dávila, M.R.; Sigurdson, A.J.; Giusti, R.M.; Pineda, M.A.; Doody, M.M.; Tucker, M.A.; Greene, M.H.; Zhang, J.; Struewing, J.P., 2003:
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals

Preston, A.; Thomas, R.; Maskell, D.J., 2002:
Mutational analysis of the Bordetella pertussis wlb LPS biosynthesis locus

Bergendahl, V.; Linne, U.; Marahiel, M.A., 2002:
Mutational analysis of the C-domain in nonribosomal peptide synthesis

Lee, S.F.; Gao, L., 2000:
Mutational analysis of the C-terminal anchoring domains of Streptococcus mutans P1 antigen: role of the LPXTGX motif in P1 association with the cell wall

Ikeda, T.; Yoshinaga, K.; Semba, S.; Kondo, E.; Ohmori, H.; Horii, A., 2000:
Mutational analysis of the CTNNB1 (beta-catenin) gene in human endometrial cancer: frequent mutations at codon 34 that cause nuclear accumulation

Paquet, Y.; Trottier, E.; Beaudet, M.J.; Anderson, A., 2000:
Mutational analysis of the CYP2B2 phenobarbital response unit and inhibitory effect of the constitutive androstane receptor on phenobarbital responsiveness

Schaumburg, C.S.; Tan, M., 2003:
Mutational analysis of the Chlamydia trachomatis dnaK promoter defines the optimal -35 promoter element

Wohlschlegel, J.A.; Dwyer, B.T.; Takeda, D.Y.; Dutta, A., 2001:
Mutational analysis of the Cy motif from p21 reveals sequence degeneracy and specificity for different cyclin-dependent kinases

Auner, H.W.; Olipitz, W.; Hoefler, G.; Bodner, C.; Konrad, D.; Crevenna, R.; Linkesch, W.; Sill, H., 1999:
Mutational analysis of the DNA mismatch repair gene hMLH1 in myeloid leukaemias

Rijnbrand, R.; Abell, G.; Lemon, S.M., 2000:
Mutational analysis of the GB virus B internal ribosome entry site

Lim, S.H.M.; Poh, L.K.S.; Cowell, C.T.; Tey, B-Hea.; Loke, K-Yin., 2002:
Mutational analysis of the GNAS1 exons encoding the stimulatory G protein in five patients with pseudohypoparathyroidism type 1a

Veugelers, M.; Cat, B.D.; Muyldermans, S.Y.; Reekmans, G.; Delande, N.; Frints, S.; Legius, E.; Fryns, J.P.; Schrander-Stumpel, C.; Weidle, B.; Magdalena, N.; David, G., 2000:
Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene

Beltrán-Valero de Bernabé, D.; Peterson, P.; Luopajärvi, K.; Matintalo, P.; Alho, A.; Konttinen, Y.; Krohn, K.; Rodríguez de Córdoba, S.; Ranki, A., 1999:
Mutational analysis of the HGO gene in Finnish alkaptonuria patients

McShane, M.P.; Mullen, M.M.; Haan, K.M.; Jardetzky, T.S.; Longnecker, R., 2003:
Mutational analysis of the HLA class II interaction with Epstein-Barr virus glycoprotein 42

Ye, D.; Blanke, S.R., 2000:
Mutational analysis of the Helicobacter pylori vacuolating toxin amino terminus: identification of amino acids essential for cellular vacuolation

Helm, R.M.; Cockrell, G.; Connaughton, C.; West, C.M.chael; Herman, E.; Sampson, H.A.; Bannon, G.A.; Burks, A.W.sley, 2000:
Mutational analysis of the IgE-binding epitopes of P34/Gly m Bd 30K

Fuchs, K.-Peter; Bommer, G.; Dumont, E.; Christoph, B.; Vidal, M.; Kremmer, E.; Kempkes, B., 2001:
Mutational analysis of the J recombination signal sequence binding protein (RBP-J)/Epstein-Barr virus nuclear antigen 2 (EBNA2) and RBP-J/Notch interaction

Sutherland, K.D.; Visvader, J.E.; Choong, D.Y.H.; Sum, E.Y.M.; Lindeman, G.J.; Campbell, I.G., 2003:
Mutational analysis of the LMO4 gene, encoding a BRCA1-interacting protein, in breast carcinomas

Amano, K.; Nomura, Y.; Segawa, M.; Yamakawa, K., 2000:
Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

Voskoboinik, I.; Mar, J.; Camakaris, J., 2003 :
Mutational analysis of the Menkes copper P-type ATPase (ATP7A)

Krementsova, E.; Giffin, M.J.; Pincus, D.; Baker, T.A., 1998:
Mutational analysis of the Mu transposase. Contributions of two distinct regions of domain II to recombination

Loh, T.; Murphy, K.C.; Marinus, M.G., 2001:
Mutational analysis of the MutH protein from Escherichia coli

Shenoy, A.R.; Srinivasan, N.; Subramaniam, M.; Visweswariah, S.S., 2003:
Mutational analysis of the Mycobacterium tuberculosis Rv1625c adenylyl cyclase: Residues that confer nucleotide specificity contribute to dimerization

Elleman, T.C.; Frenkel, M.J.; Hoyne, P.A.; McKern, N.M.; Cosgrove, L.; Hewish, D.R.; Jachno, K.M.; Bentley, J.D.; Sankovich, S.E.; Ward, C.W., 2000:
Mutational analysis of the N-linked glycosylation sites of the human insulin receptor

Hacker, C.; Glinski, M.; Hornbogen, T.; Doller, A.; Zocher, R., 2000:
Mutational analysis of the N-methyltransferase domain of the multifunctional enzyme enniatin synthetase

Papp, T.; Pemsel, H.; Zimmermann, R.; Bastrop, R.; Weiss, D.G.; Schiffmann, D., 1999:
Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naevi

Joseph, J.; Savithri, H.S., 2000:
Mutational analysis of the NIa protease from pepper vein banding potyvirus

Cipollini, G.; Moretti, A.; Ghimenti, C.; Viacava, P.; Bevilacqua, G.; Caligo, M.A.elaide, 2000:
Mutational analysis of the NM23.H1 gene in human breast cancer

Basil, J.B.; Swisher, E.M.; Herzog, T.J.; Rader, J.S.; Elbendary, A.; Mutch, D.G.; Goodfellow, P.J., 1999:
Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability

Glasow, A.; Horn, L.C.; Taymans, S.E.; Stratakis, C.A.; Kelly, P.A.; Kohler, U.; Gillespie, J.; Vonderhaar, B.K.; Bornstein, S.R., 2001:
Mutational analysis of the PRL receptor gene in human breast tumors with differential PRL receptor protein expression

Sun, H.; Enomoto, T.; Fujita, M.; Wada, H.; Yoshino, K.; Ozaki, K.; Nakamura, T.; Murata, Y., 2001:
Mutational analysis of the PTEN gene in endometrial carcinoma and hyperplasia

Zhou, X.P.ng; Li, Y.J.n; Hoang Xuan, K.; Laurent Puig, P.; Mokhtari, K.; Longy, M.; Sanson, M.; Delattre, J.Y.es; Thomas, G.; Hamelin, R., 1999:
Mutational analysis of the PTEN gene in gliomas: Molecular and pathological correlations

Lancaster, J.M.; Risinger, J.I.; Carney, M.E.; Barrett, J.C.; Berchuck, A., 2001:
Mutational analysis of the PTEN gene in human uterine sarcomas

Hu, Y.C.; Lam, K.Y.; Tang, J.C.; Srivastava, G., 2000:
Mutational analysis of the PTEN/MMAC1 gene in primary oesophageal squamous cell carcinomas

Papp, T.; Schipper, H.; Pemsel, H.; Unverricht, M.; Muller, K.M.; Wiethege, T.; Schiffmann, D.; Rahman, Q., 2001:
Mutational analysis of the PTEN/MMAC1 tumour suppressor gene in primary human malignant mesotheliomas

Xia, Y.; Uhlin, B.E.ic, 1999:
Mutational analysis of the PapB transcriptional regulator in Escherichia coli

Komori, K.; Sakae, S.; Daiyasu, H.; Toh, H.; Morikawa, K.; Shinagawa, H.; Ishino, Y., 2000:
Mutational analysis of the Pyrococcus furiosus holliday junction resolvase hjc revealed functionally important residues for dimer formation, junction DNA binding, and cleavage activities

Kubo, Y.; Amanuma, H., 2003:
Mutational analysis of the R peptide cleavage site of Moloney murine leukaemia virus envelope protein

Shadel, G.S.; Buckenmeyer, G.A.; Clayton, D.A.; Schmitt, M.E., 2000:
Mutational analysis of the RNA component of Saccharomyces cerevisiae RNase MRP reveals distinct nuclear phenotypes

Matera, I.; Bachetti, T.; Cinti, R.; Lerone, M.; Gagliardi, L.; Morandi, F.; Motta, M.; Mosca, F.; Ottonello, G.; Piumelli, R.; Schober, J.G.; Ravazzolo, R.; Ceccherini, I., 2002:
Mutational analysis of the RNX gene in congenital central hypoventilation syndrome

Fukuhara, Noriko, 2002:
Mutational analysis of the Sendai virus V protein: Importance of the conserved residues for virus pathogenesis and efficient RNA editing

Hegde, P.; Gu, G.G.; Chen, D.; Free, S.J.; Singh, S., 1999:
Mutational analysis of the Shab-encoded delayed rectifier K(+) channels in Drosophila

Kawate, S.; Ohwada, S.; Hamada, K.; Koyama, T.; Takenoshita, S.; Morishita, Y.; Hagiwara, K., 2001:
Mutational analysis of the Smad6 and Smad7 genes in hepatocellular carcinoma

Orioli, I., M.; Vieira, A., R.; Castilla, E., E.; Ming, J., E.; Muenke, M., 2002:
Mutational analysis of the Sonic Hedgehog gene in 220 newborns with oral clefts in a South American (ECLAMC) population

Flick, R.; Elgh, F.; Pettersson, R.F., 2002:
Mutational analysis of the Uukuniemi virus (Bunyaviridae family) promoter reveals two elements of functional importance

Jo, E-Kyeong.; Futatani, T.; Kanegane, H.; Kubota, T.; Lee, Y-Ho.; Jung, J-A.; Song, C-Hwa.; Park, J-Kyu.; Nonoyama, S.; Miyawaki, T., 2003:
Mutational analysis of the WASP gene in 2 Korean families with Wiskott-Aldrich syndrome

Evans, K.L.; Lawson, D.; Meitinger, T.; Blackwood, D.H.R.; Porteous, D.J., 2000:
Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

Laustsen, P.G.; Vang, S.; Kristensen, T., 2001:
Mutational analysis of the active site of human insulin-regulated aminopeptidase

Wu, P.; Xiao, W.; Conlon, T.; Hughes, J.; Agbandje-McKenna, M.; Ferkol, T.; Flotte, T.; Muzyczka, N., 2000:
Mutational analysis of the adeno-associated virus type 2 (AAV2) capsid gene and construction of AAV2 vectors with altered tropism

Yang, P.L.; Schultz, P.G., 1999:
Mutational analysis of the affinity maturation of antibody 48G7

Slagsvold, T.; Kraus, I.; Bentzen, T.; Palvimo, J.; Saatcioglu, F., 2000:
Mutational analysis of the androgen receptor AF-2 (activation function 2) core domain reveals functional and mechanistic differences of conserved residues compared with other nuclear receptors

Matsuo, H.; Kamakura, K.; Matsushita, S.; Ohmori, T.; Okano, M.; Tadano, Y.; Tsuji, S.; Higuchi, S., 1999:
Mutational analysis of the anion exchanger 3 gene in familial paroxysmal dystonic choreoathetosis linked to chromosome 2q

Wieland, K.; Laak, A.M.; Smit, M.J.; Kühne, R.; Timmerman, H.; Leurs, R., 1999:
Mutational analysis of the antagonist-binding site of the histamine H(1) receptor

Ananvoranich, S.; Lafontaine, D.A.; Perreault, J.P., 1999:
Mutational analysis of the antigenomic trans-acting delta ribozyme: the alterations of the middle nucleotides located on the P1 stem

Kalliampakou, K.I.; Psaridi Linardaki, L.; Mavromara, P., 2002:
Mutational analysis of the apical region of domain II of the HCV IRES

Bøe, A.S.; Knappskog, P.M.; Myhre, A.Grethe.; Sørheim, J.I.; Husebye, E.S., 2002:
Mutational analysis of the autoimmune regulator (AIRE) gene in sporadic autoimmune Addison's disease can reveal patients with unidentified autoimmune polyendocrine syndrome type I

Chang, Y-Shin.; Liaw, S-Huey.; Mei, H-Ching.; Hsu, C-Chieh.; Wu, C-Yu.; Tsai, Y-Chieh., 2002:
Mutational analysis of the autoprocessing site of subtilisin YaB-G124A

Michou, A.I.; Lehrmann, H.; Saltik, M.; Cotten, M., 1999:
Mutational analysis of the avian adenovirus CELO, which provides a basis for gene delivery vectors

Ason, B.; Reznikoff, W.S., 2002:
Mutational analysis of the base flipping event found in Tn5 transposition

Jiang, Y.L.n; Stivers, James, T., 2002:
Mutational analysis of the base-flipping mechanism of uracil DNA glycosylase

Sylvius, N.; Duboscq-Bidot, L.; Bouchier, C.; Charron, P.; Benaiche, A.; Sébillon, P.; Komajda, M.; Villard, E., 2003:
Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

Marasco, R.; Muscariello, L.; Rigano, M.; Sacco, M., 2002:
Mutational analysis of the bglH catabolite-responsive element (cre) in Lactobacillus plantarum

Olson, L.J.; Hancock, M.K.; Dix, D.; Kim, J.J.; Dahms, N.M., 1999:
Mutational analysis of the binding site residues of the bovine cation-dependent mannose 6-phosphate receptor

Takai, E.; Akita, H.; Shiga, N.; Kanazawa, K.; Yamada, S.; Terashima, M.; Matsuda, Y.; Iwai, C.; Kawai, K.; Yokota, Y.; Yokoyama, M., 1999:
Mutational analysis of the cardiac actin gene in familial and sporadic dilated cardiomyopathy

Corringer, P.J.; Bertrand, S.; Galzi, J.L.; Devillers-Thiéry, A.; Changeux, J.P.; Bertrand, D., 1999:
Mutational analysis of the charge selectivity filter of the alpha7 nicotinic acetylcholine receptor

Hasegawa, S.; Miyoshi, Y.; Egawa, C.; Ishitobi, M.; Tamaki, Y.; Monden, M.; Noguchi, S., 2002:
Mutational analysis of the class I beta-tubulin gene in human breast cancer

Hansen, L.; Fjordvang, H.; Rasmussen, S.K.; Vestergaard, H.; Echwald, S.M.; Hansen, T.; Alessi, D.; Shenolikar, S.; Saltiel, A.R.; Barbetti, F.; Pedersen, O., 1999:
Mutational analysis of the coding regions of the genes encoding protein kinase B-alpha and -beta, phosphoinositide-dependent protein kinase-1, phosphate targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin: Lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients

Teufel, D.P.; Kao, R.Y.T.; Acharya, K.Ravi.; Shapiro, R., 2003:
Mutational analysis of the complex of human RNase inhibitor and human eosinophil-derived neurotoxin (RNase 2)

Meyer, J.; Mai, M.; Ortega, G.; Moessner, R.; Lesch, K.-Peter, 2002:
Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree

Clyne, J.Dylan.; Wang, L-Fang.; Hume, R.I., 2002:
Mutational analysis of the conserved cysteines of the rat P2X2 purinoceptor

Hathaway, H.J.; Evans, S.C.; Dubois, D.H.; Foote, C.I.; Elder, B.H.; Shur, B.D., 2003:
Mutational analysis of the cytoplasmic domain of beta1,4-galactosyltransferase I: influence of phosphorylation on cell surface expression

Odreman-Macchioli, F.; Baralle, F.E.; Buratti, E., 2001:
Mutational analysis of the different bulge regions of hepatitis C virus domain II and their influence on internal ribosome entry site translational ability

Gardiol, D.; Galizzi, S.; Banks, L., 2002:
Mutational analysis of the discs large tumour suppressor identifies domains responsible for human papillomavirus type 18 E6-mediated degradation

Connolly, J.P.; Augustine, J.G.; Francklyn, C., 1999:
Mutational analysis of the engrailed homeodomain recognition helix by phage display

Xiang, L.; Kalaitzis, J.A.; Nilsen, G.; Chen, L.; Moore, B.S., 2002:
Mutational analysis of the enterocin Favorskii biosynthetic rearrangement

Stachelhaus, T.; Walsh, C.T., 2000:
Mutational analysis of the epimerization domain in the initiation module PheATE of gramicidin S synthetase

Kikuchi, Y.; Kojima, H.; Tanaka, T., 1999:
Mutational analysis of the feedback sites of lysine-sensitive aspartokinase of Escherichia coli

Simoni, M.; Gromoll, J.; Höppner, W.; Kamischke, A.; Krafft, T.; Stähle, D.; Nieschlag, E., 1999:
Mutational analysis of the follicle-stimulating hormone (FSH) receptor in normal and infertile men: identification and characterization of two discrete FSH receptor isoforms

Harrison, J.K.; Fong, A.M.; Swain, P.A.; Chen, S.; Yu, Y.R.; Salafranca, M.N.; Greenleaf, W.B.; Imai, T.; Patel, D.D., 2001:
Mutational analysis of the fractalkine chemokine domain. Basic amino acid residues differentially contribute to CX3CR1 binding, signaling, and cell adhesion

Iwasaki, H.; Han, Y.W.on; Okamoto, T.; Ohnishi, T.; Yoshikawa, M.; Yamada, K.; Toh, H.; Daiyasu, H.; Ogura, T.; Shinagawa, H., 2000:
Mutational analysis of the functional motifs of RuvB, an AAA+ class helicase and motor protein for Holliday junction branch migration

Sharina, I.G.; Zhao, R.; Wang, Y.; Babani, S.; Goldman, I.D., 2001 :
Mutational analysis of the functional role of conserved arginine and lysine residues in transmembrane domains of the murine reduced folate carrier

Heck, I.S.; Schrag, J.D.; Sloan, J.; Millar, L.J.; Kanan, G.; Kinghorn, J.R.; Unkles, S.E., 2002:
Mutational analysis of the gephyrin-related molybdenum cofactor biosynthetic gene cnxE from the lower eukaryote Aspergillus nidulans

Perret, J.; Van Craenenbroeck, Mélanie.; Langer, I.; Vertongen, P.; Gregoire, Fçoise.; Robberecht, P.; Waelbroeck, M., 2002:
Mutational analysis of the glucagon receptor: similarities with the vasoactive intestinal peptide (VIP)/pituitary adenylate cyclase-activating peptide (PACAP)/secretin receptors for recognition of the ligand's third residue

Figer, A.; Kaplan, A.; Geva, R.; Flex, D.; Yaron, M.; Levy, T.; Sapir, E.Even.; Fidder, H.H.; Friedman, E., 2003:
Mutational analysis of the hMSH6 gene in familial and early-onset colorectal and endometrial cancer in Israeli patients

Dickson, P.W.; Wong, Z.Y.; Harrap, S.B.; Abramson, M.J.; Walters, E.H., 1999:
Mutational analysis of the high affinity immunoglobulin E receptor beta subunit gene in asthma

Boucher, P.E.; Yang, M.S.in; Stibitz, S., 2001:
Mutational analysis of the high-affinity BvgA binding site in the fha promoter of Bordetella pertussis

Manzanera, M.; Marques, S.; Ramos, J.L., 2000:
Mutational analysis of the highly conserved C-terminal residues of the XylS protein, a member of the AraC family of transcriptional regulators

Matsushika, A.; Mizuno, T., 1998:
Mutational analysis of the histidine-containing phosphotransfer (HPt) signaling domain of the ArcB sensor in Escherichia coli

Olesen, C.; Silber, J.; Eiberg, H.; Ernst, E.; Petersen, K.; Lindenberg, S.; Tommerup, N., 2003:
Mutational analysis of the human FATE gene in 144 infertile men

Fischer, J.; Schwab, M.; Eichelbaum, M.; Zanger, U.M., 2003:
Mutational analysis of the human dihydropyrimidine dehydrogenase gene by denaturing high-performance liquid chromatography

Simon, J.H.; Sheehy, A.M.; Carpenter, E.A.; Fouchier, R.A.; Malim, M.H., 1999:
Mutational analysis of the human immunodeficiency virus type 1 Vif protein

Chen, J.M.; Mercier, B.; Audrezet, M.P.; Ferec, C., 2000:
Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis

Bobkova, E.V.; Habib, N.; Alexander, G.; Hall, B.D., 1999:
Mutational analysis of the hydrolytic activity of yeast RNA polymerase III

Linhult, M.; Binz, H.Kaspar.; Uhlén, M.; Hober, S., 2002:
Mutational analysis of the interaction between albumin-binding domain from streptococcal protein G and human serum albumin

Bonaccorsi, D.P.tti, M.C.rmela; Paronetto, M.P.ola; Dolci, V.; Felice, M.R.sa; Lania, A.; Musci, G., 2001:
Mutational analysis of the iron binding site of Saccharomyces cerevisiae ferroxidase Fet3. An in vivo study

Profant, D.A.; Roberts, C.J.; Wright, R.L., 2000:
Mutational analysis of the karmellae-inducing signal in Hmg1p, a yeast HMG-CoA reductase isozyme

Canto, P.; Soderlund, D.; Ramon, G.; Nishimura, E.; Mendez, J.P.blo, 2002:
Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumors

Weiss, G.A.; Wells, J.A.; Sidhu, S.S., 2000:
Mutational analysis of the major coat protein of M13 identifies residues that control protein display

Mårdberg, K.; Trybala, E.; Glorioso, J.C.; Bergström, T., 2001:
Mutational analysis of the major heparan sulfate-binding domain of herpes simplex virus type 1 glycoprotein C

Uchihashi, K.; Misawa, T.; Takeo, M.; Negoro, S., 2003:
Mutational analysis of the metabolism of 2,6-naphthalenedisulfonate by Pigmentiphaga sp. NDS-2

Heaton, D.; Nittis, T.; Srinivasan, C.; Winge, D.R., 2000:
Mutational analysis of the mitochondrial copper metallochaperone Cox17

Manga, P.; Sato, K.; Ye, L.; Beermann, F.; Lamoreux, M.L.nn; Orlow, S.J., 2000:
Mutational analysis of the modulation of tyrosinase by tyrosinase-related proteins 1 and 2 in vitro

Minsavage, G.D.; Vorojeikina, D.P.; Gasiewicz, T.A., 2003:
Mutational analysis of the mouse aryl hydrocarbon receptor tyrosine residues necessary for recognition of dioxin response elements

Yamagata, A.; Hirota, R.; Kato, J.; Kuroda, A.; Ikeda, T.; Takiguchi, N.; Ohtake, H., 2000:
Mutational analysis of the multicopy hao gene coding for hydroxylamine oxidoreductase in Nitrosomonas sp. strain ENI-11

Schipper, H.; Papp, T.; Johnen, G.; Pemsel, H.; Bastrop, R.; Müller, K-Michael.; Wiethege, T.; Jaworska, M.; Krismann, M.; Schiffmann, D.; Rahman, Q., 2003:
Mutational analysis of the nf2 tumour suppressor gene in three subtypes of primary human malignant mesotheliomas

Shao, E.; Nishi, T.; Kawasaki-Nishi, S.; Forgac, M., 2003:
Mutational analysis of the non-homologous region of subunit A of the yeast V-ATPase

Koehler, P.; Marahiel, M.A., 1998:
Mutational analysis of the nucleoid-associated protein HBsu of Bacillus subtilis

Chen, T.C.ing; Ng, K.F.ng; Lien, J.M.n; Jeng, L.B.n; Chen, M.F.; Hsieh, L.L.ng, 2000:
Mutational analysis of the p27kip1 gene in hepatocellular carcinoma

Hagiwara, K.; McMenamin, M.G.; Miura, K.; Harris, C.C., 1999:
Mutational analysis of the p63/p73L/p51/p40/CUSP/KET gene in human cancer cell lines using intronic primers

Shishikura, T.; Ichimiya, S.; Ozaki, T.; Nimura, Y.; Kageyama, H.; Nakamura, Y.; Sakiyama, S.; Miyauchi, M.; Yamamoto, N.; Suzuki, M.; Nakajima, N.; Nakagawara, A., 1999:
Mutational analysis of the p73 gene in human breast cancers

Kuwata, K.; Hirota, M.; Nishimori, I.; Otsuki, M.; Ogawa, M., 2003:
Mutational analysis of the pancreatic secretory trypsin inhibitor gene in familial and juvenile pancreatitis in Japan

Ikezoe, T.; Miller, C.W.; Kawano, S.; Heaney, A.; Williamson, E.A.; Hisatake, J.; Green, E.; Hofmann, W.; Taguchi, H.; Koeffler, H.P., 2001:
Mutational analysis of the peroxisome proliferator-activated receptor gamma gene in human malignancies

Chen, S-Hu.; Tang, T.K., 2002:
Mutational analysis of the phosphorylation sites of the Aie1 (Aurora-C) kinase in vitro

Xu, Y.; Circolo, A.; Jing, H.; Wang, Y.; Narayana, S.V.; Volanakis, J.E., 2000:
Mutational analysis of the primary substrate specificity pocket of complement factor B. Asp(226) is a major structural determinant for p(1)-Arg binding

Sawaya, R.; Arhin, F.F.; Moreau, F.; Coulton, J.W.; Mills, E.L., 1999:
Mutational analysis of the promoter region of the porA gene of Neisseria meningitidis

Chiti, F.; Taddei, N.; Bucciantini, M.; White, P.; Ramponi, G.; Dobson, C.M., 2000:
Mutational analysis of the propensity for amyloid formation by a globular protein

Boldt, H.B.; Overgaard, M.T.; Laursen, L.S.; Weyer, K.; Sottrup-Jensen, L.; Oxvig, C., 2001:
Mutational analysis of the proteolytic domain of pregnancy-associated plasma protein-A (PAPP-A): classification as a metzincin

Asano, S.; Furumoto, R.; Tega, Y.; Matsuda, S.; Takeguchi, N., 2000:
Mutational analysis of the putative K(+)-binding site on the fourth transmembrane segment of the gastric H(+),K(+)-ATPase

Ito, H.; Watanabe, S.; Sanchez, A.; Whitt, M.A.; Kawaoka, Y., 1999:
Mutational analysis of the putative fusion domain of Ebola virus glycoprotein

Hiraga, K.; Seeram, S.S.; Tate, S.; Tanaka, N.; Kainosho, M.; Oda, K., 1999:
Mutational analysis of the reactive site loop of Streptomyces metalloproteinase inhibitor, SMPI

Yoshinaga, C.; Mukai, H.; Toshimori, M.; Miyamoto, M.; Ono, Y., 1999:
Mutational analysis of the regulatory mechanism of PKN: the regulatory region of PKN contains an arachidonic acid-sensitive autoinhibitory domain

Sommer, M.H.; Zagha, E.; Serrano, O.K.; Ku, C.C.; Zerboni, L.; Baiker, A.; Santos, R.; Spengler, M.; Lynch, J.; Grose, C.; Ruyechan, W.; Hay, J.; Arvin, A.M., 2001:
Mutational analysis of the repeated open reading frames, ORFs 63 and 70 and ORFs 64 and 69, of varicella-zoster virus

Satyanarayana, T.; Gowda, S.; Ayllón, Mía.A.; Albiach-Martí, Mía.R.; Dawson, W.O., 2002:
Mutational analysis of the replication signals in the 3'-nontranslated region of citrus tristeza virus

Christensen, D.P.; Benson, A.K.; Hutkins, R.W., 1999:
Mutational analysis of the role of HPr in Listeria monocytogenes

Mentesana, P.E.; Konopka, J.B., 2001:
Mutational analysis of the role of N-glycosylation in alpha-factor receptor function

Kazazic, M.; Nissen-Meyer, J.; Fimland, G., 2002:
Mutational analysis of the role of charged residues in target-cell binding, potency and specificity of the pediocin-like bacteriocin sakacin P

Liang, Y.; Gillam, S., 2000:
Mutational analysis of the rubella virus nonstructural polyprotein and its cleavage products in virus replication and RNA synthesis