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Section 33

EurekaMag Full Text Articles Chapter 32,460



References:

Karunaratne, S.H.P.P.; Hawkes, N.J.; Perera, M.D.B.; Ranson, H.; Hemingway, J. 2000: Mutated sodium channel genes and elevated monooxygenases are found in pyrethroid resistant populations of Sri Lankan malaria vectors. Pesticide Biochemistry and Physiology 88(1): 108-113
Gelfand, D.H.; Lawyer, F.C.; Stoffel, S. 1995: Mutated thermostable nucleic acid polymerase enzyme from thermotoga maritima. Official Gazette of the United States Patent and Trademark Office Patents 1174(5): 3334
Abramson, R.D.; Gelfand, D.H.; Greenfield, I.L. 1995: Mutated thermostable nucleic acid polymerase enzyme from thermus species Z05. Official Gazette of the United States Patent and Trademark Office Patents 1179(1): 357
Kochli, O.R.; Schar, G.; Schenk, V.; Fink, D.; Hornung, R.; Eppenberger, U.; Muller, H.; Haller, U. 1995: Mutated tumor suppressor protein p53 Another factor with influences the chemoresistance of breast carcinomas. Archives of Gynecology and Obstetrics 256(Suppl ): S242
Dirksen, R.T.; Beam, K. 1996: Mutating a pore region glutamate in repeat III of the skeletal L-type Ca-2+ channel abolishes Ca-2+ permeation but not E-C coupling. Biophysical Journal 70(2 Part 2): A146
Arts, E.J.; Miller, J.T.; Ehresmann, B.; Le Grice, S.F. 1998: Mutating a region of HIV-1 reverse transcriptase implicated in tRNA(Lys-3) binding and the consequences for (-)-strand DNA synthesis. Journal of Biological Chemistry 273(23): 14523-14532
Jaenisch, R. 1991: Mutating genes in the germ line of mice. Lindsten, J And U Pettersson (Ed ) Nobel Symposium, Vol 80 Etiology Of Human Disease at The Dna Level; Karlskoga, Sweden, June 11-14, 1990 Xv+316p Raven Press: New York, New York, Usa Illus 191-198
Gasparini, P.; Fortina, P.; Surrey, S.; Rabionet, R.; Melchionda, S.; D'agruma, L.; Rappaport, E.; Govea, N.; Montse Mila, M.; Zelante, L.; Estivill, X. 1998: Mutation 35delG in the connexin-26 gene is the major cause of sporadic and familial congenital deafness in mediterranean patients. European Journal of Human Genetics 6(Suppl 1): 153
Brooimans, R.A.; Rijkers, G.T.; Tilanus, M.; Kuis, W.; Zegers, B.J.M. 1995: Mutation Analysis of the Brutons Tyrosine Kinase Gene in X-Linked Agammaglobulinemia Patients. 9TH INTERNATIONAL CONGRESS OF IMMUNOLOGY The 9th International Congress of Immunology : 380
Mcguire, S.L.; Bajt, M.L. 1994: Mutation Analysis of the I Domain of CD11b Defines a Potential Ligand Binding Site in Integrin CD11b/CD18. Molecular Biology of the Cell 5(Suppl ): 183A
Jacquemin, M.G.; Peerlinck, K.; Gilles, J.G.; Benhida, A.; Desqueper, B.; Lavend'homme, R.; Vermylen, J.; Saint Remy, J.M.R. 1998: Mutation Arg2150 -fwdarw His in the factor VIII C1 domain alters the binding of factor VIII to von Willebrand factor and is responsible for a mild hemophilia A phenotype. Blood 92(10 Suppl 1 Part 1-2): 710A
Orendac, M.; Muskova, B.; Richterova, F.; Zvarova, J.; Stefek, M.; Zaykova, E.; Stribny, J.; Hyanek, J.; Kraus, J.P.; Kozich, V. 1998: Mutation C6577T in the MTHFR gene and polymorphism 844ins68bp in the CBS gene Risk factors for peripheral arterial occlusive disease?. Netherlands Journal of Medicine 52(Suppl ): S47
Li, F.; Wang, S.; Gao, C.; Liu, S.; Zhao, B.; Zhang, M.; Huang, S.; Zhu, S.; Ma, X. 2008: Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts. Molecular Vision 14: 378-386
Désilets, A.; Béliveau, F.ço.; Vandal, G.; McDuff, F.ço.-O.; Lavigne, P.; Leduc, R. 2008: Mutation G827R in matriptase causing autosomal recessive ichthyosis with hypotrichosis yields an inactive protease. Journal of Biological Chemistry 283(16): 10535-10542
Sorensen, T.; Andersen, J.P.ter 1996: Mutation Lys758 fwdarw ILE of the SR Ca-2+-ATPase uncouples ATP hydrolysis from Ca-2+ transport. Biophysical Journal 70(2 Part 2): A330
Diaz, L.F.; Wallner, M.; Stefani, E.; Toro, L.; Latorre, R. 1996: Mutation R207Q in the S4 segment increases Ca-2+ sensitivity of a cloned maxi K+ channel. Biophysical Journal 70(2 Part 2): A193
Lelonek, M.; Pietrucha, T.; Matyjaszczyk, M.; Goch, J.Henryk. 2008: Mutation T/C,Ile 131 of the gene encoding the alfa subunit of the human Gs protein and predisposition to vasovagal syncope. Circulation Journal: Official Journal of the Japanese Circulation Society 72(4): 558-562
Andersen, Jens Peter 1995: Mutation Tyr763 fwdarw Gly of the SR Ca-2+-ATPase uncouples ATP hydrolysis from Ca-2+ transport. Biophysical Journal 68(2 Part 2): A317
Staub, J.E.; Braunschweig, K. 1990: Mutation a microcomputer module designed for plant breeding and genetics. HortScience 25(9): 1106
Mueller, L.D. 1990: Mutation accumulation and the evolution of drosophila ageing. University Of Maryland And The Smithsonian Institute Fourth International Congress Of Systematic And Evolutionary Biology; College Park, Maryland, Usa, July 1-7, Pagination Varies University Of Maryland: College Park, Maryland, Usa Illus Paper : 354
Lynch, M. 1997: Mutation accumulation and the extinction of small populations. Environmental and Molecular Mutagenesis 29(Suppl 28): 32
Platz, A.; Ringborg, U.; Lagerlof, B. 1993: Mutation activation and expression of N-ras in malignant melanoma. Proceedings of the American Association for Cancer Research 34: 99
Tsai, F.J.; Lin, S.P.; Chang, J.G.; Peng, C.T.; Tsai, C.H. 1996: Mutation analyses of Wilson disease in Taiwan. American Journal of Human Genetics 59(4 Suppl): A402
Mcandrew, S.; Chen, N.; Dicaprio, L.; Kopchick, J. 1989: Mutation analyses of bovine growth hormone secretion. Abstracts of the Annual Meeting of the American Society for Microbiology 89: 211
Wang, P.; Wang, X.; Cong, S.; Ma, H.; Zhang, X. 2008: Mutation analyses of integrated HBV genome in hepatitis B patients. Journal of Genetics and Genomics 35(2): 85-90
Clermont, O.; Burlet, P.; Cruaud, C.; Bertrandy, S.; Melki, J.; Munnich, A.; Lefebvre, S. 1997: Mutation analyses of the SMN gene in undeleted SMA patients. American Journal of Human Genetics 61(4 Suppl): A329
Nguyen, T.D.; Chen, H.; Chen, P.; Hetherington, J.; Lieberman, M.; Nguyen, N.; Yen, D.; Richards, J.E.; Polansky, J.R. 1997: Mutation analyses of the TIGR promoter in a POAG pedigree. American Journal of Human Genetics 61(4 Suppl): A341
Li, P.; Thompson, J.N.; Hug, G.; Chuck, G. 1994: Mutation analysis and carrier detection of Hunter syndrome. American Journal of Human Genetics 55(3 Suppl): A229
Plourde, M.; Manhes, C.; Leblanc, G.; Durocher, F.; Dumont, M.; Sinilnikova, O.; Simard, J.; Bessette, P.; Chiquette, J.; Laframboise, R.; Lespérance, B.; Plante, M. 2008: Mutation analysis and characterization of HSD17B2 sequence variants in breast cancer cases from French Canadian families with high risk of breast and ovarian cancer. Journal of Molecular Endocrinology 40(4): 161-172
Onadim, Z.; Hogg, A.; Hungerford, J.; Cowell, J.K. 1991: Mutation analysis and genetic linkage in retinoblastoma patients. American Journal of Human Genetics 49(4 Suppl): 123
Tyfield, L.; Stephenson, A.; Holton, J.B. 1997: Mutation analysis and psychometric assessments in the galactosaemia population of the British Isles. Journal of Medical Genetics 34(Suppl 1): S18
Will, A.; Caspari, T.; Robl, I.; Tanner, W. 1996: Mutation analysis and purification of the Chlorella monosaccharide/H+ symporter HUP1. European Journal of Cell Biology 69(Suppl 42): 84
Fodde, R.; Losekoot, M. 1996: Mutation analysis by denaturing gradient gel electrophoresis. Pfeifer, G P Technologies for detection of DNA damage and mutations 253-265
Loda, M. 1991: Mutation analysis by pcr. Pathology Research and Practice 187(6): 716
Waldren, C.; Sinclair, J.; Wood, S.; Puck, T.; Webb, P.; Doolittle, D.; Smith, C.; Ueno, A. 1990: Mutation analysis by the human hamster hybrid cell primary embryonic chick hepatocyte a l pech method. Environmental and Molecular Mutagenesis. Supplement 15(17): 62
Traystman, M.D.; Schulte, N.; Macdonald, M.; Sanger, W.G. 1992: Mutation analysis for cystic fibrosis for 167 sperm donors from the Nebraska Genetic Semen Bank. American Journal of Human Genetics 51(4 Suppl): A391
Guffon, N.; Froissart, R.; Chevalier-Porst, F.; Maire, I. 1998: Mutation analysis in 11 French patients with Fabry disease. Human Mutation Suppl 1: S288-S290
Goldenfum, S.L.; Young, E.; Michelakakis, H.; Tsagarakis, S.; Winchester, B. 1996: Mutation analysis in 20 patients with Hunter disease. Human Mutation 7(1): 76-78
Heptinstall, L.E.; Loftus, H.M.; Till, J.; Walter, J.H.; Wraith, J.E.; Besley, G.T.N. 1997: Mutation analysis in Asian patients with propionic acidaemia. Journal of Inherited Metabolic Disease 20(Suppl 1): 36
Gaspar, H.B.; Bradley, L.A.; Katz, F.; Lovering, R.C.; Roifman, C.M.; Morgan, G.; Levinsky, R.J.; Kinnon, C. 1995: Mutation analysis in Bruton's tyrosine kinase, the X-linked agammaglobulinaemia gene, including identification of an insertional hotspot. Human Molecular Genetics 4(4): 755-757
Tomkins, J.; Ince, P.G.; Jackson, T.; Slade, J.Y.; Usher, P.; Curtis, A.; Bushby, K.; Shaw, P.J. 1997: Mutation analysis in CNS tissue from motor neuron disease patients. Journal of Medical Genetics 34(Suppl 1): S82
Kakiuchi, H.; Makino, H.; Ushijima, T.; Tsujimoto, A.; Weisburger, J.H.; Ronai, Z.; Sugimura, T.; Nagao, M. 1993: Mutation analysis in IQ-induced rat colon cancers. Environmental and Molecular Mutagenesis 21(Suppl 22): 34
Shiono, Y.; Okada, T.; Takeda, Y.; Hayashi, H.; Hamano, H.; Suzuki, A.; Morise, T.; Mabuchi, H.; Yano, M. 1998: Mutation analysis in Japanese patients with Wilsons disease. Gastroenterology 114(4 Part 2): A1342
Aronovich, E.L.; Zhao, H.G.; Neufeld, E.F.; Whitley, C.B. 1996: Mutation analysis in Sanfilippo syndrome type B by automated sequencing of the NAGLU coding region. American Journal of Human Genetics 59(4 Suppl): A246
O'rawe, A.; Munroe, P.B.; Mitchison, H.M.; Gardiner, R.M.; Mole, S.E. 1996: Mutation analysis in a European Batten disease resource. European Journal of Human Genetics 4(Suppl 1): 66
Marie, S.; Cuppens, H.; Heuterspreute, M.; Jaspers, M.; Tola, E.Z.; Gu, X.X.; Legius, E.; Vincent, M.F.; Jaeken, J.; Cassiman, J.J.; Van Den Berghe, G. 1998: Mutation analysis in adenylosuccinate lyase deficiency. Journal of Inherited Metabolic Disease 21(Suppl 2): 124
Anonymous 1990: Mutation analysis in cystic fibrosis. New England Journal of Medicine 323(1): 62-63
Maier Dobersberger, T.; Nazer, H.; Ferenci, P.; Cox, D.W. 1998: Mutation analysis in exon 8 of the Wilson disease gene. Hepatology 28(4 Part 2): 617A
Tarpey, P.; Phillimore, H.; Murday, V.; Eeles, R.; Taylor, R. 1997: Mutation analysis in familial breast cancer Results of the first 18 months of a diagnostic service. Journal of Medical Genetics 34(Suppl 1): S33
Lin, S.P.; Tsai, F.J.; Wu, J.Y.; Peng, C.T.; Tsai, C.H. 1998: Mutation analysis in fibroblast growth factor receptor genes Chinese data. European Journal of Human Genetics 6(Suppl 1): 164
Bidichandani, S.I.; Lanyon, W.G.; Shiach, C.; Lowe, G.D.O.; Connor, J.M. 1994: Mutation analysis in haemophilia A. Journal of Cellular Biochemistry Suppl 1994(18 Part A): 236
Vosberg, H.P.; Jeschke, B.; Sakthivel, S.; Waldmueller, S. 1998: Mutation analysis in hypertrophic cardiomyopathy Causes and pathogenesis. Journal of Molecular and Cellular Cardiology 30(6): A28
Ellard, S.; Bulman, M.P.; Frayling, T.M.; Beards, F.E.; Appleton, M.; Hattersley, A.T. 1997: Mutation analysis in maturity-onset diabetes of the young. Journal of Medical Genetics 34(Suppl 1): S17
Mahadevan, M.; Sabourin, L.A.; O'hoy, K.; Earle Macdonald, J.; Hag, R.; Jansen, G.; Wieringa, B.; Amemiya, C.; De Jong, P.; Korneluk, R.G. 1992: Mutation analysis in myotonic dystrophy families exhibiting no CTG repeat amplification at the DM locus. American Journal of Human Genetics 51(4 Suppl): A328
Rood Breithaupt, J.A.; Dodson, L.A.; Williams, T.M.; Kant, J.A. 1991: Mutation analysis in neurofibromatosis 1 patients. American Journal of Human Genetics 49(4 Suppl): 203
Krakow, D.; Wilcox, W.R.; Lachman, R.S.; King, L.M.; Cohn, D.H. 1996: Mutation analysis in osteogenesis imperfecta patients with normal type I procollagen biochemical studies. American Journal of Human Genetics 59(4 Suppl): A266
Duke, V.M.; De Zoysa, P.A.; Quinton, R.; Bouloux, P.M.G. 1995: Mutation analysis in patient with Kallmanns syndrome using the polymerase chain reaction. Clinical Science 89(1): 19P
Santer, R.; Schneppenheim, R.; Dombrowski, A.; Bakker, H.D.; Brodehl, J.; Burlina, A.; Chen, Y.T.; Gellissen, K.; Leonard, J.; Moses, S.; Pronicka, E.; Shin, Y.; Van T'hoff, W.; Steinmann, S.; Schaub, J. 1998: Mutation analysis in patients with Fanconi-Bickel syndrome. Journal of Inherited Metabolic Disease 21(Suppl 2): 86
Lenzner, C.; Nuernberg, P.; Jacobasch, G.; Thiele, B. 1996: Mutation analysis in patients with pyruvate kinase deficiency and haplotype backgrounds on normal and mutant PK genes. American Journal of Human Genetics 59(4 Suppl): A268
Davies, J.P.; Winchester, B.G.; Malcolm, S. 1993: Mutation analysis in patients with the typical form of Anderson-Fabry disease. Human Molecular Genetics 2(7): 1051-1053
Weiss, M.; Schindelhauer, D.; Hellebrand, H.; Meindl, A.; Belohradsky, B.H. 1996: Mutation analysis in patients with variable phenotype expression of the Wiskott-Aldrich syndrome. European Journal of Pediatrics 155(2): 153
Michels Rautenstrauss, K.; Mardin, C.Y.; Budde, W.M.; Ozbey, S.; Grasser, J.; Liehr, T.; Naumann, G.O.H.; Pfeiffer, R.A.; Rautenstrauss, B. 1998: Mutation analysis in primary open angle glaucoma patients. European Journal of Human Genetics 6(Suppl 1): 143
Heptinstall, L.E.; Gillaspy, E.E.; Loftus, H.M.; Till, J.; Walter, J.H.; Wraith, J.E.; Besley, G.T.N. 1998: Mutation analysis in propionic acidaemia. Journal of Inherited Metabolic Disease 21(Suppl 2): 40
Arnheim, N. 1997: Mutation analysis in sperm. Journal of Assisted Reproduction and Genetics 14(8): 423-424
Schindler, D.; Baumer, A.; Bernthaler, U.; Sennefelder, H.; Brohm, M.; Weber, B.H.F.; Sandoval, N.; Platzer, M.; Rosenthal, A.; Shiloh, H.; Wegner, R.D.; Sperling, K.; Doerk, T.; Bendix, R.; Skawran, B.; Stuhrmann Spangenberg, M. 1998: Mutation analysis in the ATM gene of 67 ataxia-telangiectasia patients in Germany. European Journal of Human Genetics 6(Suppl 1): 160
Koch, M.C.; Mecklenbeck, S.; Meyer Kleine, C. 1997: Mutation analysis in the CLCN1 gene leading to dominant Thomsens and recessive Beckers disease. Greger, R , Jentsch, T J Nova Acta Leopoldina; Ion channels and disease : 129-131
Fogli, A.; Lo Nigro, C.; Renieri, R.; Fernandez, E.; Pilz, D.; Ledbetter, D.H.; Guerrini, R.; Carrozzo, R. 1997: Mutation analysis in the LIS1 gene of 14 patients with isolated lissencephaly sequence. American Journal of Human Genetics 61(4 Suppl): A333
Yapijakis, C.; Vassilopoulos, D.; Kladi, A.; Panas, M.; Youroukos, S.; Panteliadis, C.; Papageorgiou, C. 1996: Mutation analysis in the NF1 gene in Greek families with neurofibromatosis type 1. European Journal of Human Genetics 4(Suppl 1): 74
Hill, A.J.M.; Graham, C.A.; Goon, P.K.C.; Magee, A.C.; Redmond, A.O.; Nevin, N.C. 1991: Mutation analysis in the cftr gene and genotype phenotype comparisons. Cytogenetics and Cell Genetics 58(1-4): 1921
Hill, A.J.M.; Graham, C.A.; Goon, P.K.C.; Magee, A.C.; Redmond, A.; Nevin, N.C. 1991: Mutation analysis in the cftr gene in northern ireland uk and genotype phenotype comparisons. Journal of Medical Genetics 28(8): 566
Boehmer, A.L.M.; Koper, J.W.; Otten, B.J.; Noordam, C.; Drop, S.L.S.; De Jong, F.H. 1998: Mutation analysis in the diagnosis 17-hydroxylase/17,20-lyase deficiency. Hormone Research (Basel) 50(Suppl 3): 117
Hergersburg, M.; Boltshauser, E.; Schinzel, A.; Spiegel, R.; Landau, K.; Kato, R. 1998: Mutation analysis in the neurofibromatosis 2 gene. European Journal of Human Genetics 6(Suppl 1): 151
Lewis, B.D.; Nelson, P.V.; Robertson, E.F.; Morris, C.P. 1994: Mutation analysis of 28 Gaucher disease patients: the Australasian experience. American Journal of Medical Genetics 49(2): 218-223
Schaffner, C.; Stilgenbauer, S.; Doehner, H.; Lichter, P. 1998: Mutation analysis of ATM in lymphoproliferative diseases reveals a pathogenic role for ATM not only in T-PLL but also in B-CLL. Blood 92(10 Suppl 1 Part 1-2): 310A
Davidson, H.R.; Renwick, A.A.; Douglas, S.F.; Irvine, L.; Whiteford, M.L.; Crow, Y.; Black, D.; Trainer, A.H. 1997: Mutation analysis of BRCA1 and 2 What do the results mean?. American Journal of Human Genetics 61(4 Suppl): A63
San Agustin, T.; Schofield, A.; Haites, N.E. 1997: Mutation analysis of BRCA1 and BRCA2 through the use of PTT. Journal of Medical Genetics 34(Suppl 1): S83
Zhu, O.; Zhang, M.; Rawlings, D.J.; Witte, O.N.; Chen, S.H.; Ochs, H.D. 1995: Mutation analysis of Brutons tyrosine kinase Genotypic and phenotypic heterogeneity. Journal of Investigative Medicine 43(Suppl 1): 185A
Holland, E.A.; Becker, T.M.; Kefford, R.F.; Mann, G.J. 1997: Mutation analysis of CDKN2A and CDK4 in familial melanoma. Melanoma Research 7(Suppl 1): S133
Kusic, J.; Radojkovic, D.; Maletic, V.; Niksic, S.; Savic, A. 1998: Mutation analysis of CFTR gene in men with azoospermia. European Journal of Human Genetics 6(Suppl 1): 118
Vieira, P.P.; Zalis, M.G.; Oliveira, R.; Pereira, T.; Marques, C.; Azevedo, A.; Cerruti, C.; Wirth, D.F.; Alwen, A. 1998: Mutation analysis of CG2- chloroquine resistance related gene in Plasmodium falciparum isolates from the Brazilian Amazon region Evidence of clonal expansion of chloroquine resistant parasite. Memorias do Instituto Oswaldo Cruz 93(Suppl 2): 308-309
Tsai, F.J.; Wu, J.Y.; Chang, J.G.; Lin, S.P.; Peng, C.T.; Tsai, C.H. 1998: Mutation analysis of Chinese patients with Wilson disease. European Journal of Human Genetics 6(Suppl 1): 165
Gosling, A.; Myers, S.M.; Von Deimling, A.; Mulligan, L.M. 1997: Mutation analysis of GDNFR-alpha in Hirschsprung disease patients. American Journal of Human Genetics 61(4 Suppl): A410
Nguyen, N.J.; Henneberger, M.W.; Smolec, J.M.; Mcpherson, R.A.; Beutler, E. 1992: Mutation analysis of Gaucher disease by multiplex PCR. American Journal of Human Genetics 51(4 Suppl): A354
Nomura, S.; Kashiwabara, H.; Fujita, S.; Ohkura, H.; Sugano, K. 1997: Mutation analysis of HNPCC susceptibility genes using long RT-PCR and auto sequencer. Proceedings of the American Association for Cancer Research 38: 518
Rosenblatt, H.M.; Belmont, J.; Lewandowski, R.; Rothschild, B.; Simonsen, R.; Puck, J. 1995: Mutation analysis of IL-2 receptor gamma chain gene for prenatal diagnosis of X-linked severe combined immunodeficiency. Journal of Allergy and Clinical Immunology 95(1 Part 2): 232
Sharp, J.; Parker, K.; Hutchings, S.; Gardiner, R.M.; Chung, E. 1996: Mutation analysis of NOS1, a candidate gene for infantile pyloric stenosis. European Journal of Human Genetics 4(Suppl 1): 96
Braverman, N.; Yahraus, T.; Moser, A.; Gordon, D.; Gould, S.J.; Valle, D. 1996: Mutation analysis of PXAAA1, a new peroxisome assembly gene responsible for a subgroup of the peroxisome biogenesis disorders. American Journal of Human Genetics 59(4 Suppl): A4
Ciccodicola, A.; Miano, M.G.; Testa, F.; Simonelli, F.; Antinolo, M.B.iget G.; Del Porto, G.; Danesino, C.; Rinaldi, E.; Ventruto, V.; D'urso, M. 1997: Mutation analysis of RPGR gene in patients with X-linked retinitis pigmentosa. American Journal of Human Genetics 61(4 Suppl): A328
Weber, B.; Xiao Hui, G.; Kleijer, W.J.; Hopwood, J.J. 1998: Mutation analysis of Sanfilippo B syndrome patients reveals strong allelic heterogeneity. European Journal of Human Genetics 6(Suppl 1): 163
Hilgert, N.; Alasti, F.; Dieltjens, N.; Pawlik, B.; Wollnik, B.; Uyguner, O.; Delmaghani, S.; Weil, D.; Petit, C.; Danis, E.; Yang, T.; Pandelia, E.; Petersen, M.B.; Goossens, D.; Favero, J.D.; Sanati, M.H.; Smith, R.J.H.; Van Camp, G. 2008: Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clinical Genetics 74(3): 223-232
Malzac, P.; Voelckel, M.A.; Wagstaff, J.; Livet, M.O.; Vovan, C.; Pedeillier, K.; Moncla, A. 1998: Mutation analysis of UBE3A in Angelman syndrome patients A description of 8 different mutations. European Journal of Human Genetics 6(Suppl 1): 145-146
Schuster, V.; Brandau, O.; Weiss, M.; Seidenspinner, S.; Hellebrand, H.; Kreth, H.W.; Meindl, A. 1998: Mutation analysis of a novel SH2-domain encoding gene, SH2D1A, in five patients with X-linked lymphoproliferative disease. Blood 92(10 Suppl 1 Part 1-2): 169A
Bhattacharya, S. 1992: Mutation analysis of autosomal dominant retinitis pigmentosa. Experimental Eye Research 55(Suppl 1): S16
Goldblatt, Jack; Boyer, S.J.; Pereira, E.; Palmer, L.; Gibson, N.; Rye, P.; Le Souef, P.N.; Sanderson, C.J. 1996: Mutation analysis of candidate genes with the chromosome 5 interleukin cluster in an asthmatic cohort. European Journal of Human Genetics 4(Suppl 1): 103
Hart, E.J.; Powers-Lee, S.G. 2008: Mutation analysis of carbamoyl phosphate synthetase: does the structurally conserved glutamine amidotransferase triad act as a functional dyad?. Protein Science: a Publication of the Protein Society 17(7): 1120-1128
Taggart, R.T.; Apolito, C.; Smail, D.; Vladutiu, G.D. 1997: Mutation analysis of carnitine palmitoyl transferase deficiency. American Journal of Human Genetics 61(4 Suppl): A27
Chen, J.S.; Nordstrom, J.L. 1991: Mutation analysis of downstream sequences of the mouse beta globin poly a signal. FASEB Journal 5(4): A827
Lee, S.H.; Kim, U.K.; Kay, C.W.; Kim, J.W.; Cha, S.H.; Kim, S.J.; Cha, K.Y. 1994: Mutation analysis of fragile X syndrome by Southern blot, radio-active PCR, silver-stained polyacrylamide gel and DIG DNA labeling/detection technique. American Journal of Human Genetics 55(3 Suppl): A361
Sidransky, E.; Stubblefield, B.; Tsuji, S.; Ginns, E. 1991: Mutation analysis of gaucher patients with oculomotor abnormalities. American Journal of Human Genetics 49(4 Suppl): 106
Tsai Wu, J.J.; Wu, C.H.; Liu, T.; Chang, K.J. 1998: Mutation analysis of hMLH1 and hMSH2 in Taiwanese breast cancer patients with early onset. Proceedings of the American Association for Cancer Research 39: 637
Chang, C.C.; Gould, S.J. 1997: Mutation analysis of human PEX12 in group 3 patients of the peroxisome biogenesis disorders. Molecular Biology of the Cell 8(Suppl ): 114A
Glustein, J.Z.; Shaag, A.; Anikster, Y.; Saada, A.B.; Joseph, A.; Ruitenbeek, W.; Elpeleg, O.N. 1994: Mutation analysis of lipoamide dehydrogenase deficiency in Ashkenazi-Jews with a favourable clinical course. Pediatric Research 37(4 Part 2): 148A
Rupar, C.A.; Atkison, P.; Gordon, B.A.; Kronick, J. 1991: Mutation analysis of medium chain acyl coa dehydrogenase mcad deficiency. Clinical and Investigative Medicine 14(4 Suppl): A85
Ju, T.; Qi, Y.; Bao, X.; Wu, X. 1996: Mutation analysis of mitochondrial DNAs of 15 children with Rett syndrome and 14 their mothers. Journal of Neurochemistry 67(Suppl ): S40
Jaksch, M.; Hofmann, S.; Hedblom, A.; Kleinle, S.; Meitinger, T.; Gerbitz, K.D. 1998: Mutation analysis of mitochondrial and nuclear encoded cytochrome C oxidase subunit genes in patients with COX-deficiency. Journal of Molecular Medicine 76(6): B42
Nelis, Eva; Warner, L.E.; De Vriendt, E.; Timmerman, V.; Chance, P.; Lupski, J.R.; Van Broeckhoven, C. 1996: Mutation analysis of myelin genes in nonduplicated Charcot-Marie-Tooth type 1 patients Comparison of single strand conformational polymorphism analysis and heteroduplex analysis. European Journal of Human Genetics 4(Suppl 1): 2
Pérez, B.; Desviat, L.R.; De Lucca, M.; Schmidt, B.; Loghin-Grosso, N.; Giugliani, R.; Pires, R.F.; Ugarte, M. 1996: Mutation analysis of phenylketonuria in south Brazil. Human Mutation 8(3): 262-264
Leandro, P.; Rivera, I.; Ribeiro, V.; de Almeida, I.T.; da Silveira, C.; Lechner, M.C. 1995: Mutation analysis of phenylketonuria in south and central Portugal: prevalence of V388M mutation. Human Mutation 6(2): 192-194
Gelb, B.D.; Wilner, J.P.; Verloes, A.; Herens, C.; Desnick, R.J. 1997: Mutation analysis of pycnodysostosis reveals uniparental disomy of chromosome 1. American Journal of Human Genetics 61(4 Suppl): A39
Driessen, A.; Tierens, A.; Ectors, N.; Pittaluga, S.; Geboes, K.; Delabie, J.; De Wolf Peeters, C. 1997: Mutation analysis of rearranged heavy chain variable genes in gastrointestinal diffuse large B-cell lymphoma indicates positive antigen selection of the neoplastic cells. Gut 41(Suppl 1): A46
Goldfarb, L.G.; Lunkes, A.; Vasconcelos, O.; Plantonov, F.A.; Nagle, J.; Cervenakova, L.; Kononova, S.K.; Penn, M.; Aliprandis, E.; Higgins, J.J.; Vladimirtsev, V.A.; Dubnick, M.; Alexeev, V.P.; Gajdusek, D.C. 1994: Mutation analysis of spinocerebellar ataxia type 1 in a large iakut kinship of eastern Siberia. American Journal of Human Genetics 55(3 Suppl): A221
Small, K.W.; Udar, N.; Gislason, S.; Silva, R.M.; Yelchits, L. 1998: Mutation analysis of the ABCR gene in age-related macular degeneration. IOVS Investigative Ophthalmology and Visual Science 39(4): S963
Tonin, P.T.; Simard, J.; Leblanc, J.; Goldgar, D.J.F.; Morgan, K.; Narod, S. 1995: Mutation analysis of the BRCA1 gene in 26 Canadian breast, ovarian, breast and ovarian cancer families. Proceedings of the American Association for Cancer Research 36: 281
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Zhu, D.; Maumenee, I.H.ssels 1994: Mutation analysis of the Norrie disease gene in eleven families. IOVS Investigative Ophthalmology and Visual Science 35(4): 1265
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Zhang, X.; Chow, C.Y.; Sahenk, Z.; Shy, M.E.; Meisler, M.H.; Li, J. 2008: Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration. Brain: a Journal of Neurology 131(Part 8): 1990-2001
Marques, J.; Luzzatto, L.; Vulliamy, T.; Barretto, O.C.O.; Nonoyama, K. 1993: Mutation of G6PD gene in Brazilian blood samples. Blood 82(10 Suppl 1): 465A
Wallick, E.T.; Millette, L.A.; Johnson, C.L.; Lingrel, J.B.; Tepperman, K. 1995: Mutation of Glu-327 and Asp-925 of Na+, K+-ATPase reveals positive cooperativity in Rb+ uptake. Biophysical Journal 68(2 Part 2): A256
Nabedryk, E.; Breton, J.; Okamura, M.Y.; Paddock, M.L. 1998: Mutation of Glu-H173 to Gln affects the protonation state of Glu-L212 in Rb sphaeroides. Biophysical Journal 74(2 Part 2): A134
Sampietro, M.; Piperno, A.; Vergani, A.; Arosio, C.; Malosio, I.; Lupica, L.; Fracanzani, A.L.; Cappellini, M.D.; Molteni, V.; Fiorelli, G.; Fargion, S. 1997: Mutation of HLA-H is rare in Italian patients with porphyria cutanea tarda and iron overload. Journal of Hepatology 26(Suppl 1): 173
Elsea, S.H.; Hsiung, Y.; Nitiss, J.L.; Osheroff, N. 1994: Mutation of His-1012 to Tyr confers resistance to quinolones in yeast topoisomerase II. FASEB Journal 8(7): A1331
Ito, H.; Klugbauer, N.; Hofmann, F. 1997: Mutation of IIIS5 segment of L-type Ca channel markedly decreases the sensitivity to dihydropyridines. Biophysical Journal 72(2 Part 2): A244
Nounou, R.; Estey, E.; Beran, M.; Kantarjian, H.; Freireich, E.J.; Albitar, H. 1996: Mutation of K-, N-, and H-ras oncogenes in patients with myelodysplastic syndrome. Blood 88(10 Suppl 1 Part 1-2): 208B
Yadrandji, S.; Visscher, D.W.; Madan, S.K.; Valdivieso, M.; Sarkar, F.H. 1996: Mutation of K-ras and p53 in pulmonary adenocarcinoma Histologic correlations. Modern Pathology 9(1): 164A
Horiuchi, F.; Maeda, Y.; Tatsumi, Y.; Miyatake, J.; Tohno, T.; Shirakawa, C.; Koyama, A.; Hamazaki, H.; Irimajiri, K.; Horiuchi, A. 1994: Mutation of M-BCR gene is induced by X-irradiation with repair. Blood 84(10 Suppl 1): 607A
Collins, D.M.; Wilson, T.M.; Wards, B.J. 1997: Mutation of Mycobacterium bovis by illegitimate recombination after high efficiency electroporation with suicide plasmids. Abstracts of the General Meeting of the American Society for Microbiology 97: 565
Sanyanusin, P.; McNoe, L.A.; Sullivan, M.J.; Weaver, R.G.; Eccles, M.R. 1995: Mutation of PAX2 in two siblings with renal-coloboma syndrome. Human Molecular Genetics 4(11): 2183-2184
Swaroop, M.; Kaufman, R.J. 1996: Mutation of PHE309SER, a putative BiP binding site, enhances secretion of coagulation factor VIII. Blood 88(10 Suppl 1 Part 1-2): 441A
Cheng, X.J.; Hoog, J.O.; Fisone, G.; Nairn, A.C.; Jornvall, H.; Greengard, P.; Aperia, A. 1993: Mutation of PKA phosphorylated site changes sodium affinity of rat sodium, potassium ATPase transfectal into COS cells. Journal of the American Society of Nephrology 4(3): 865
Holmberg, L.; Dent, J.A.; Ware, J.; Ruggeri, Z.M. 1992: Mutation of Pro503 fwdarw -leu in patients with increased von Willebrand factor affinity for platelets but not alteration of its multimeric structure of von Willebrand factor. Circulation 86(4 Suppl 1): I416
Ichimura, K.; Bondesson, M.; Moshref, A.; Goike, H.M.; Schmidt, E.E.; Collins, V.P. 1997: Mutation of RB1 preferentially occurs in glioblastomas with p53 abnormalities. Proceedings of the American Association for Cancer Research 38: 256
Bendahhou, S.; Cummins, T.R.; Potts, J.F.; Sigworth, F.J.; Agnew, W.S. 1994: Mutation of S1321 alters the inactivation kinetics of mu-1 sodium channel expressed in HEK 293 cells. Society for Neuroscience Abstracts 20(1-2): 66
Zu, L.Z.; Pilkis, S.J. 1995: Mutation of SER-151 converts glucokinase to a low K-M enzyme. FASEB Journal 9(6): A1294
Togo, G.; Toda, N.; Kanai, F.; Kato, N.; Yoshida, H.; Shiratori, Y.; Omata, M. 1996: Mutation of TGF-beta type II receptor gene in gastrointestinal and hepatobiliary carcinomas. Gastroenterology 110(4 Suppl): A604
Togo, G.; Toda, N.; Okamoto, S.; Kanai, F.; Kato, N.; Matsumura, M.; Tada, M.; Yoshida, H.; Shiratori, Y.; Omata, M. 1997: Mutation of TGF-beta type II receptor in cecum cancer. Gastroenterology 112(4 Suppl): A669
Shen, K.Z.; Lagrutta, A.; Adelman, J.P.; North, R.A. 1993: Mutation of TYR residues at the external mouth of the slowpoke channel pore. Society for Neuroscience Abstracts 19(1-3): 705
Guan, X.; Middlebrooks, B.W.; Alexander, S.; Wasserman, S.A. 2006: Mutation of TweedleD, a member of an unconventional cuticle protein family, alters body shape in Drosophila. Proceedings of the National Academy of Sciences of the United States of America 103(45): 16794-16799
Martinat, L.; Denamur, E.; Mougenot, B.; Ronco, P.; Bensman, A. 1998: Mutation of WT1 gene in a family with Denys-Drash syndrome and focal segmental glomerulosclerosis. Pediatric Nephrology 12(7): C89
Gabilondo, A.M.; Krasel, C.; Hegler, J.; Jahns, V.; Hein, L.; Lohse, M.J. 1997: Mutation of a Leu-Leu motif in the C-terminus of the beta2-adrenoceptor impairs receptor internalization. Methods and Findings in Experimental and Clinical Pharmacology 19(Suppl A): 146
Fackler, M.J.; Boyles, S.L.; Huang, F.Y. 1997: Mutation of a PKC target domain of full-length CD34 prevents CD34-mediated negative regulation of M1 cell differentiation. Blood 90(10 Suppl 1 Pt 1): 427A
Souza, R.F.; Yin, J.; Smolinski, K.N.; Wang, S.; Zou, T.T.; Abraham, J.M.; Biden, K.; Simms, L.; Leggett, B.; Shimizu, K.; Powell, S.M.; Sugimura, H.; Harpaz, N.; Young, J.; Matsubara, N.; Meltzer, S.J. 1997: Mutation of a coding region microsatellite within E2F-4 in genetically unstable gastrointestinal tumors. Gastroenterology 112(4 Suppl): A661
Rasmussen, S.G.F.; Jensen, A.D.; Ghanouni, P.; Liapakis, G.; Hjorth, S.A.; Javitch, J.; Gether, U. 1998: Mutation of a conserved aspartic acid in the beta2 adrenergic receptor Constitutive activation, structural instability, and conformational rearrangement of helix VI. Society for Neuroscience Abstracts 24(1-2): 23
Kazmi, M.A.; Sakmar, T.P.; Ostrer, H. 1996: Mutation of a conserved cysteine in the X-linked cone opsins disrupts targeting and causes color vision deficiencies. American Journal of Human Genetics 59(4 Suppl): A266
Chang, Y.; Weiss, D.S. 1996: Mutation of a conserved leucine in the M2 region of homomeric pi-1 GABA receptors. Society for Neuroscience Abstracts 22(1-3): 1295
Wojcik, S.; Rothnagel, J.A.; Hohl, D.; Roop, D.R. 1994: Mutation of a critical arginine residue within the 1A segment of keratin 9 in epidermolytic palmoplantar keratoderma. Journal of Investigative Dermatology 102(4): 541
Andresson, T.; Sparkowski, J.; Goldstein, D.; Schlegel, R. 1994: Mutation of a critical glutamic acid residue in the 16KDa pore forming component of the vacuolar H+-ATPase reduces virus E5 protein and converts it into a transforming protein. Journal of Cellular Biochemistry Suppl 1994(18C): 219
Elliott, C.E.; Harjono; Howlett, B.J. 2008: Mutation of a gene in the fungus Leptosphaeria maculans allows increased frequency of penetration of stomatal apertures of Arabidopsis thaliana. Molecular Plant 1(3): 471-481
Gallagher, P.G.; Petruzzi, M.J.; Marchesi, S.L.; Forget, B.G. 1994: Mutation of a highly conserved residue of erythrocyte beta-spectrin associated with fatal and near-fatal neonatal hemolytic anemia. Blood 84(10 Suppl 1): 112A
Brooke, J., S.; Albert-Vo; Watts, P.; Davis, N., A. 2008: Mutation of a lipopolysaccharide synthesis gene results in increased biofilm of Stenotrophomonas maltophilia, on plastic and glass surfaces. Annals of Microbiology 58(1): 35-40
Banerjei, L.; Davidson, J.N. 1995: Mutation of a proposed phosphorylation site of hamster carbamyl phosphate synthetase II. FASEB Journal 9(6): A1284
Guthmiller, J.M.; Kolodrubetz, D.; Kraig, E. 1993: Mutation of a putative leukotoxin transport gene in Actinobacillus actinomycetemcomitans. Journal of Dental Research 72(Special Issue): 300
Judge, S.I.V.; Monteiro, M.J.; Bever, C.T. 1997: Mutation of a single amino acid in human brain K+ channel Kv14 alters gating and increases 4-AP sensitivity by two orders of magnitude. Biophysical Journal 72(2 Part 2): A27
Kaye, F.J.; Kratzke, R.; Gerster, J.; Horowitz, J. 1990: Mutation of a single amino acid of the retinoblastoma protein blocks phosphorylation and oncoprotein binding. Journal of Cellular Biochemistry Suppl (14 Part C): 283
Calero, G.A.; Ek Vitorin, J.F.; Taffet, S.M.; Delmar, M. 1996: Mutation of a single amino acid prevents pH regulation of connexin43. Biophysical Journal 70(2 Part 2): A208
Schofield, P.R.; Ragendra, S.; Lynch, J.W.; Pierce, K.D.; French, C.R.; Barry, P.H. 1995: Mutation of a single amino acid residue in the human glycine receptor transforms B-alanine and taurine from agonists into competitive antagonists. Journal of Cellular Biochemistry Suppl 1995(19B): 182
West, J.W.; Numann, R.; Scheuer, T.; Catterall, W.A. 1991: Mutation of a single phosphorylation site blocks the action of protein kinase c on rat brain type iia sodium channels. Society for Neuroscience Abstracts 17(1-2): 953
Welch, A.R.; Brenner, M.C.; Huber, M.; Van Wart, H.E. 1995: Mutation of a single tyrosine residue in matrilysin alters the P-1 specificity to resemble that of stromelysin-1. FASEB Journal 9(6): A1344
Millar, R.P.; Flanagan, C.A.; Becker, I.I.; Davidson, J.S.; Wakefield, I.K.; Zhou, W.; Sealfon, S.C. 1994: Mutation of acidic amino acids in the mouse GnRH receptor reveals that GLU-301 determines binding specificity for ARG-8 in mammalian GnRH. Neuroendocrinology 60(Suppl 1): 25
Ueno, S.; Wick, M.J.; Harrison, N.L.; Harris, R.A. 1998: Mutation of amino acids in TM2/TM3 GABAA receptor subunits reduces the ethanol sensitivity of heteromeric receptors expressed in Xenopus oocytes. Alcoholism Clinical and Experimental Research 22(3 ABSTR Suppl ): 157A
O'shea, S.M.; Harrison, N.L. 1997: Mutation of an arginine residue in the alpha subunit M2-M3 loop alters apparent GABA-A receptor affinity. Society for Neuroscience Abstracts 23(1-2): 110
Stanfield, P.R.; Davies, N.W.; Shelton, P.A.; Khan, I.A.; Brammar, W.J.; Standen, N.B.; Conley, E.C. 1994: Mutation of an aspartate residue in the inward rectifier potassium channel encoded by the murine IRK1 gene alters its voltage- and K+-dependent gating. Journal of Physiology (Cambridge) 477P: 86P-87P
Supp, D.M.; Potter, S.S.; Brueckner, M. 1997: Mutation of an axonemal dynein in the mouse left-right asymmetry mutant IV. Molecular Biology of the Cell 8(Suppl ): 7A
Lynch, H.T.; Drouhard, T.; Lanspa, S.; Smyrk, T.; Lynch, P.; Lynch, J.; Vogelstein, B.; Nyström-Lahti, M.; Sistonen, P.; Peltomäki, P. 1994: Mutation of an mutL homologue in a Navajo family with hereditary nonpolyposis colorectal cancer. Journal of the National Cancer Institute 86(18): 1417-1419
Chandrasekaran, L.; Roberts, D.D. 1998: Mutation of anti-angiogenic sequences in the type I repeats of thrombospondin-1. Molecular Biology of the Cell 9(Suppl ): 298A
Spencer, C.J.; Schwarz, R.D.; Moreland, D.W.; Thomas, A.J.; Tecle, H. 1993: Mutation of aspartate 103 to asparagine or glutamate in human muscarinic receptor subtype Hm2 Effect of subtype selectivity versus pK-a on receptor binding. Society for Neuroscience Abstracts 19(1-3): 1768
Wang, C.J.; Hosford, D.A. 1998: Mutation of beta4 subunit of voltage-dependent Ca2+ channels decreases the frequency of spontaneous EPSCs in thalamic neurons of lethargic mice. Society for Neuroscience Abstracts 24(1-2): 1314
Barakat, R.R.; O'connor, B.; Banerjee, D.; Bertino, J. 1995: Mutation of c-Ki-ras in tamoxifen-associated endometrial carcinoma. Proceedings of the American Association for Cancer Research 36: 186
Sweeney, H.L.; Putkey, J.A. 1991: Mutation of calcium binding sites i and ii in cardiac troponin c. Biophysical Journal 59(2 Part 2): 218A
Putkey, J.A.; Sweeney, H.L.; Negele, J. 1991: Mutation of calcium binding sites iii and iv in cardiac troponin c. Biophysical Journal 59(2 Part 2): 218A
Wallick, E.T.; Millette, L.A.; Lingrel, J.B.; Tepperman, K. 1998: Mutation of cationic residues in the the alpha subunit of Na,K-ATPase. Biophysical Journal 74(2 Part 2): A43
Smith, R.A.; Cohen, S.M.; Lawson, T.A. 1989: Mutation of chinese hamster v79 cells by acrolein. Proceedings of the American Association for Cancer Research 30: 141
Nochur, S.V.; Roberts, M.F.; Demain, A.L. 1990: Mutation of clostridium thermocellum in the presence of certain carbon sources. FEMS Microbiology Letters 71(1-2): 199-204
Dent, G.A.; Smith, G.J.; Grisham, J.W. 1990: Mutation of codon 12 of c ki ras in c 3h 10t 1 2 cells morphologically transformed by mnng. Proceedings of the American Association for Cancer Research 31: 128
Hulme, E.C.; Page, K.M.; Jones, P.; Curtis, C.A.M.; Morris, R. 1993: Mutation of conserved aspartate and arginine residues in transmembrane helix 3 of the muscarinic acetylcholine receptors. Society for Neuroscience Abstracts 19(1-3): 1768
Gupta, M.L.; Dougherty, C.A.; Himes, R.H. 1998: Mutation of conserved cysteines in beta-tubulin. Molecular Biology of the Cell 9(Suppl ): 150A
Yoshida, T.; Sone, M.; Satou, A.; Nishida, E.; Omae, S.; Shirota, S.; Mihune, N.; Nihei, H. 1998: Mutation of endothelial nitric oxide synthase is related to renal hypertension and probably to non-dipper hypertension. Journal of the American Society of Nephrology 9(Program and Abstr. Issue): 332A
Kotlar, T.J.; Albanese, C.; Crowley, W.F.; Scully, R.E.; Young, R.H.; Jameson, J.L. 1996: Mutation of follicle FSH stimulating hormone receptor in human ovarian sex cord tumors. Journal of Investigative Medicine 44(3): 267A
Sinha, D.; Kozak, C.; Jaworski, C.; Lyon, M.; Wistow, G. 1997: Mutation of gammas-crystallin in the Opj cataract. Molecular Biology of the Cell 8(Suppl ): 313A
Mullauer, L.; Fujita, H.; Ogiso, Y.; Kuzumaki, N. 1992: Mutation of gelsolin gene and ras tumor suppression. Cell Structure and Function 17(6): 484
Liu, Y.C.; Chen, G.S.; Chang, C.C. 1995: Mutation of gene required for cell spreading is corrected by serum or factor secreted by normal cells. In Vitro Cellular and Developmental Biology. Animal 31(8): 571-573
Alper, S.L.K.S.range; Jiang, L.; Hand, M.; Gola, M.; Crest, M.; Chernova, M.N. 1995: Mutation of glutamate 699 to glutamine in mouse bank 3 induces extracellular Cl-dependent inward sulfate currents in Xenopus oocytes. Journal of the American Society of Nephrology 6(3): 303
Schulze, J.; Lehnerer, M.; Hlavica, P. 1998: Mutation of glutamic acid at position 250 changes stability of cytochrome P450 2B4. Naunyn-Schmiedeberg's Archives of Pharmacology 357(4): R19
Latinwo, L.M.; Silver, S.; Donald, C. 1992: Mutation of glutathione gene confers arsenite and mercury sensitivity to escherichia coli. Abstracts of the General Meeting of the American Society for Microbiology 92: 349
Carman, W.F.; Mcintyre, G.; Hadziyannis, S.; Fattovich, G.; Alberti, A. 1992: Mutation of hbcag after loss of hbeag and association with progressive disease. Journal of Hepatology 16(Suppl 1): S25
Carman, W.F.; Mcintyre, G.; Klein, H.; Muller, R.; Thomas, H.C. 1992: Mutation of hbsag in homograft recipients receiving hyperimmune globulin. Journal of Hepatology 16(Suppl 1): S9
Bhandari, S.; Hunter, M. 1997: Mutation of histidine residue 280 affects the intracellular pH sensitivity of ROMK1. Nephrology Dialysis Transplantation 12(9): A9
Bowden, P.E.; Watts, C.E.; Marks, R. 1994: Mutation of human keratin 9 gene in epidermolytic tylosis. Journal of Investigative Dermatology 102(4): 576
Chang, P.-C.; Chang, Y.-J.; Wu, H.-L.; Chang, C.-W.; Lin, C.-I.; Wang, W.-C.; Shi, G.-Y. 2008: Mutation of human plasminogen kringle 1-5 enhances anti-angiogenic action via increased interaction with integrin alpha(v)beta(3). Thrombosis and Haemostasis 99(4): 729-738
MaXin; ZhengYuJian 2008: Mutation of influenza virus and monitoring technology of influenza. Disease Surveillance: 8, 518-521
Zou, T.T.; Kong, D.; Yin, J.; Wang, S.; Smolinski, K.N.; Souza, R.F.; Abraham, J.M.; Meltzer, S.J. 1998: Mutation of insulin-like growth factor binding protein-3 gene in colon, gastric and esophageal cancers. Proceedings of the American Association for Cancer Research 39: 284
Emara, M.M.; Liu, H.; Davis, W.G.; Brinton, M.A. 2008: Mutation of mapped TIA-1/TIAR binding sites in the 3' terminal stem-loop of West Nile virus minus-strand RNA in an infectious clone negatively affects genomic RNA amplification. Journal of Virology 82(21): 10657-10670
Tsutsumi, M.; Tsuchishima, M.; Ueshima, Y.; Kawahara, H.; Takase, S.; Okubo, T.; Harada, S. 1997: Mutation of mitochondrial DNA encoding ATPase region in patients with liver disease. Hepatology 26(4 Part 2): 618A
Tanamura, A.; Iwai, T.; Kawashima, O.; Takeda, N.; Nagano, M. 1993: Mutation of mitochondrial DNA in human autopsied myocardium. Japanese Circulation Journal 57(7): 587-588
Iwai, T.; Tanamura, A.; Arino, T.; Kato, M.; Takeda, N.; Nagano, M. 1993: Mutation of mitochondrial DNA in human myocardium. Journal of Molecular and Cellular Cardiology 25(Suppl 2): S32
Macdonald, R.I.; Pantazatos, D.P. 1995: Mutation of nearly invariant tryptophan of repeating unit of spectrin to histidine or tyrosine-but not phenylalanine-yields little change in DELTA G-H20 of urea-induced unfolding. FASEB Journal 9(6): A1431
Wang, Jun Jie 1995: Mutation of p-53 gene as it related with the radiosensitivity to radiation. Zhongguo Zhongliu Linchuang 22(7): 510-512
Clarke, A.R.; Purdie, C.A.; Peter, A.; Dobbie, L.; Hooper, M.L.; Wyllie, A.H. 1992: Mutation of p53 by homologous recombination. Journal of Cellular Biochemistry Suppl (16 Part B): 131
Namba, M.; Noguchi, M.; Hirohashi, S.; Kawai, A. 1992: Mutation of p53 gene in immortalized human fibroblasts. Cell Structure and Function 17(6): 516
Winter, M.C.; Welsh, M.J. 1996: Mutation of phosphorylation sites alters ATP dependent regulation of CFTR. Biophysical Journal 70(2 Part 2): A71
Yun, T.J.; Hansen, M.; Allen, K.; Pease, L.R. 1993: Mutation of pocket B in the K-b class I antigen binding cleft influence peptide binding. Journal of Immunology 150(8 Part 2): 40A
Doll, B.A.; Bond, J.S. 1998: Mutation of proposed zinc ligands in the protease domain of the meprin alpha subunit. FASEB Journal 12(8): A1429
Gawronski, S.W.; Sugita, M.; Sugiura, M. 1992: Mutation of psbA gene in herbicide resistant populations of Erigeron canadensis. Murata, N Research in photosynthesis, Vol III: 405-407
Manahan, C.L.; Patnana, M.; Blumer, K.J.; Linder, M.E. 1996: Mutation of putative palmitoylation site of Gpa1p disrupts protein function. FASEB Journal 10(6): A1118
Coultrap, S.J.; Machu, T.K. 1997: Mutation of putative phosphorylation sites in the 5-HT-3 receptor does not eliminate its modulation by ethanol. Alcoholism Clinical and Experimental Research 21(3): 7A
Baum, M.; Biemesderfer, D.; Gentry, D.; Aronson, P.S. 1994: Mutation of rabbit renal cortical NHE-3 and NHE-1 Effect of glucocorticoids. Journal of the American Society of Nephrology 5(3): 247
Shivapurkar, N.; Clayton, T.; Iype, P.T. 1991: Mutation of ras proto oncogenes in liver cell cultures by sub cytotoxic doses of carcinogens. Proceedings of the American Association for Cancer Research 32: 100
Kaji, A. 1996: Mutation of repa protein. Official Gazette of the United States Patent and Trademark Office Patents 1193(2): 1245
Choesmel, V.ér.; Fribourg, S.éb.; Aguissa-Touré, A.-H.; Pinaud, N.ël.; Legrand, P.; Gazda, H.T.; Gleizes, P.-E. 2008: Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder. Human Molecular Genetics 17(9): 1253-1263
Xu, J.; Lin, Y.; Xi, Y.; Jiang, X.; Li, J. 1995: Mutation of rice seeds in high space environment. International Rice Research Notes 20(2): 5-6
Starr, S.; Watts, V.J.; Vu, M.N.; Neve, K.A. 1996: Mutation of serine 167 of the D2L receptor modulates receptor regulation. Society for Neuroscience Abstracts 22(1-3): 1044
Woodward, R.; Strange, P.G.; Naylor, L.H. 1994: Mutation of serine residues 194 and 197 in the rat D-2 dopamine receptor affects the binding of antagonist drugs. British Journal of Pharmacology 112(Proceedings Suppl ): 289P
Stock, K.; Spearman, P. 1997: Mutation of serine residues within the matrix protein region of Pr55-Gag leads to disruption of replication at distinct stages of the HIV lifecycle. Clinical Infectious Diseases 25(2): 391
Anderson, J.W.; Waygood, E.B. 1993: Mutation of serine-46 to aspartate in the histidine-containing protein of Escherichia coli mimics the inactivation by phosphorylation of serine-46 in HPr from gram-positive bacteria. Biochemistry and Cell Biology 71(11-12): AX-AXI
Sardini, A.; Goodfellow, H.R.; Higgins, C.F.; Mcnaughton, P.A. 1996: Mutation of sites phosphorylated by protein kinase C in the human multidrug resistance P-glycoprotein has no effect on drug transport. Journal of Physiology (Cambridge) 491P: 97P-98P
Meyer, R.A.Jr.; Morgan, P.L.; Mcdonald, A.G.; Meyer, M.H.; Price, D.K. 1998: Mutation of spermine synthase in the X-linked hypophosphatemic, Gyro mouse. FASEB Journal 12(5): A753
Jiang, Y.H.; Armstrong, D.; Albrecht, U.; Atkins, C.M.; Noebels, J.L.; Eichele, G.; Sweatt, J.D.; Beaudet, A.L. 1998: Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation. Neuron 21(4): 799-811
Lin, S.-H.; Kuo, H.-F.; Canivenc, G.èv.; Lin, C.-S.; Lepetit, M.; Hsu, P.-K.; Tillard, P.; Lin, H.-L.; Wang, Y.-Y.; Tsai, C.-B.; Gojon, A.; Tsay, Y.-F. 2008: Mutation of the Arabidopsis NRT1.5 nitrate transporter causes defective root-to-shoot nitrate transport. Plant Cell 20(9): 2514-2528
Risinger, J.I.; Kohler, M.F.; Berchuck, A.; Boyd, J. 1993: Mutation of the E-cadherin gene in endometrial carcinoma. Proceedings of the American Association for Cancer Research 34: 540
Moehlig, M.; Ristow, M.; Rifai, M.; Schatz, H.; Feldmann, K.; Pfeiffer, A. 1996: Mutation of the InhA gene in Mycobacterium tuberculosis resistant against isoniazid/ethionamide. Atemwegs- und Lungenkrankheiten 22(8): 419
Marszalek, J.R.; Ruiz Lozano, P.; Roberts, E.; Chien, K.R.; Goldstein, L.S.B. 1998: Mutation of the Kif3A kinesin gene in mouse results in embryonic cardiac situs inversus. Molecular Biology of the Cell 9(Suppl ): 436A
Haynes, T.; Valerius, T.; Potter, S.; Wiginton, D. 1994: Mutation of the LEF-1 binding site in the enhancer of the adenosine deaminase gene disrupts position independent expression in transgenic mice. FASEB Journal 8(7): A1271
Zhang, M.; Atherton, S.S. 1998: Mutation of the MCMV Fc receptor reduces incidence of retinitis following supraciliary inoculation. IOVS Investigative Ophthalmology and Visual Science 39(4): S1063
Molano, A.; Tucek Szabo, C.; Nikolic Zugic, J. 1995: Mutation of the MHC class I H-2K-b pockets reveals a role for both major pocket C and minor pocket B in peptide binding and class I stability. 9TH INTERNATIONAL CONGRESS OF IMMUNOLOGY Author The 9th International Congress of Immunology : 707
Zhu, D.; Li, Y.; Traboulsi, E.I.; Maumenee, I.H.ssels 1994: Mutation of the PAX6 gene in a sporadic patient with atypical aniridia. American Journal of Human Genetics 55(3 Suppl): A368
Bayascas, J.R.; Wullschleger, S.; Sakamoto, K.; García-Martínez, J.M.; Clacher, C.; Komander, D.; van Aalten, D.M.F.; Boini, K.M.; Lang, F.; Lipina, C.; Logie, L.; Sutherland, C.; Chudek, J.A.; van Diepen, J.A.; Voshol, P.J.; Lucocq, J.M.; Alessi, D.R. 2008: Mutation of the PDK1 PH domain inhibits protein kinase B/Akt, leading to small size and insulin resistance. Molecular and Cellular Biology 28(10): 3258-3272
Bermingham, J.R.Jr; O'connell, S.; Arroyo, E.; Powell, F.; Kalla, K.; Mcevilly, R.; Scherer, S.S.; Rosenfeld, M.G. 1995: Mutation of the POU domain transcription factor TST-1/Oct6/SCIP in mice produces neuronal and myelinating Schwann cell defects. Society for Neuroscience Abstracts 21(1-3): 5
Amiel, J.; Attie, T.; Simeoni, J.; Edery, P.; Gaultier, C.; Munnich, A.; Lyonnet, S. 1995: Mutation of the RET proto-oncogene in a patient with congenital central hypoventilation syndrome Hirschsprung disease. American Journal of Human Genetics 57(4 Suppl): A206
Kulak, S.C.; Kozlowski, K.; Semina, E.V.; Pearce, W.G.; Walter, M.A. 1997: Mutation of the RIEG1 gene in patients with Iridogoniodysgenesis syndrome. American Journal of Human Genetics 61(4 Suppl): A337
Ongkeko, W.M.; Harris, A.L.; Norbury, C.J. 1997: Mutation of the Ser 315 cdk phosphorylation site of human p53 Functional consequences in vivo contrast with those seen in vitro. Proceedings of the American Association for Cancer Research 38: 198
Hanley, K.; Jiang, Y.; Crumrine, D.; Devaskar, U.; Hicks, S.J.; Elias, P.M.; Williiams, M.L.; Feingold, K.R. 1997: Mutation of the TSH receptor leading to hypothyroidism results in delayed fetal SC formation. Journal of Investigative Dermatology 108(4): 593
Kozam, M.L.; Karpaz, N.; Chan, O.; Kinzler, K.W.; Meltzer, S.J. 1994: Mutation of the adenomatous polyposis coli gene in ulcerative colitis. Gastroenterology 106(4 Suppl): A1033
Meili, R.; Ballmer Hofer, K. 1994: Mutation of the amino-terminal PKC phosphorylation site alters activation of c-Src during mitosis. Experientia (Basel) 50(ABSTR ): A32
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