EurekaMag PDF full texts Chapter 32,460

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 Annual Meeting 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 Suppl 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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 36: 281

Matsuura, T.; Fang, P.; Tsai, T.F.; Sutcliffe, J.S.; Galjaard, R.J.; Jiang, Y.H.; Benton, C.S.; Meijers Heijboer, E.J.; Halley, D.J.; Kubota, T.; Christian, S.; Ledbetter, D.H.; Beaudet, A.L. 1997: Mutation analysis of the E6-AP ubiquitin-protein ligase gene in Angelman syndrome. American Journal of Human Genetics 61(4 Suppl): A314

Neerman Arbez, M.; Morris, M.A.; Nichols, W.C.; Ginsburg, D.; Tuddenham, E.G.D.; Antonarakis, S.E. 1998: Mutation analysis of the ERGIC53 gene in 39 families with combined deficiency of coagulation Factors V and VII. European Journal of Human Genetics 6(Suppl 1): 34

Auerbach, A.D.; Verlander, P.C. 1995: Mutation analysis of the Fanconi anemia gene FAC. Gluckman, E, Coulombel, L, INSERM Colloquium; Ontogeny of hematopoiesis: Aplastic anemia, Colloque INSERM; Ontogenie de l'hematopoiese: Aplasie medullaire 257-264

Monaghan, K.G.; Rybicki, B.; Shurafa, M.; Feldman, G.L. 1997: Mutation analysis of the HLA-H gene associated with hereditary hemochromatosis in African-Americans. American Journal of Human Genetics 61(4 Suppl): A387

Takeuchi, C.; Takeuchi, S.; Ikezoe, T.; Williamson, I.K.; Bartram, C.R.; Koeffler, H.P.; Taguchi, H. 1998: Mutation analysis of the Hel-N1 gene in childhood acute lymphoblastic leukemias with chromosome 9P21 deletion. Blood 92(10 Suppl 1 Part 1-2): 190B

Woodward, E.R.; Rose, S.; Schmidt, L.; Affara, N.A.; Maher, E.R. 1998: Mutation analysis of the MET proto-oncogene and the von Hippel-Lindau tumor suppressor gene in familial renal cell carcinoma. Proceedings of the American Association for Cancer Research Annual Meeting 39: 33

Woodward, E.; Rose, S.; Schmidt, L.; Affara, N.A.; Maher, E.R. 1997: Mutation analysis of the MET proto-oncogene and the von Hippel-Lindau tumour suppressor gene in familial renal cell carcinoma. Journal of Medical Genetics 34(Suppl 1): S39

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

Perez Cerda, C.; Merinero, B.; Marti, M.; Garcia, M.J.; Hoenicka, J.; Rodriguez Pombo, P.; Ugarte, M. 1997: Mutation analysis of the PCCB gene in a propionic acidemia patient with an unusual presentation of the disease. Journal of Inherited Metabolic Disease 20(Suppl 1): 35

Kumazawa, R.; Tomiyama, H.; Li, Y.; Imamichi, Y.; Funayama, M.; Yoshino, H.; Yokochi, F.; Fukusako, T.; Takehisa, Y.; Kashihara, K.; Kondo, T.; Elibol, B.; Bostantjopoulou, S.; Toda, T.; Takahashi, H.; Yoshii, F.; Mizuno, Y.; Hattori, N. 2008: Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease. Archives of Neurology 65(6): 802-808

Tyfield, L.A.; Stephenson, A.; Bidwell, J.; Wood, N.A.P.; Cockburn, F.; Harvie, A.; Smith, I. 1994: Mutation analysis of the PKU population in England and Scotland How and Why?. American Journal of Human Genetics 55(3 Suppl): A340

Negoro, K.; Takahashi, S.; Kinouchi, Y.; Takagi, S.; Iwabuchi, M.; Hiwatashi, N.; Toyota, T. 1998: Mutation analysis of the PTEN gene in Cowden disease and phenotypically Cowden-like diseases. Gastroenterology 114(4 Part 2): A653

Forgacs, E.; Biesterveld, E.J.; Sekido, Y.; Fong, K.; Muneer, S.; Wistuba, I.; Virmani, A.; Gazdar, A.F.; Minna, J.D. 1998: Mutation analysis of the PTEN/MMAC1 gene in human lung cancer. Proceedings of the American Association for Cancer Research Annual Meeting 39: 618-619

Iyengar, S.; Tallini, G.; Sirugo, G.; Bale, A.E.; Kidd, K.K. 1994: Mutation analysis of the RET gene in individuals with sporadic and familial pheochromocytoma. American Journal of Human Genetics 55(3 Suppl): A60

Morrison, P.J.; Hughes, A.E.; Nevin, N.C.; Powell, D.; Russell, C.J.F.; Hadden, D.R. 1995: Mutation analysis of the Ret proto-oncogene and disease phenotype in 3 large families with multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Journal of Endocrinology 144(Suppl ): RC2

Hageman, R.M.; Cameron, F.J.; Sinclair, A.H. 1998: Mutation analysis of the SOX9 gene in a patient with campomelic dysplasia. Human Mutation Suppl 1: S112-S113

Shah, A.B.; Petrukhin, K.; Chernov, I.; Zhang, H.T.; Ross, B.M.; Parano, E.; Pavano, L.; Evgrafov, O.; Ivanova Smolenkaya, I.A.; Anneren, G.; Westermark, K.; Penchaszadeh, G.K.; Sternlieb, I.; Scheinberg, J.H.; Gilliam, T.C. 1995: Mutation analysis of the Wilson disease gene in various ethnic populations. American Journal of Human Genetics 57(4 Suppl): A172

Zhu, O.; Zhang, M.; Blaese, R.M.; Derry, J.M.J.; Chen, S.H.; Francke, U.; Ochs, H.D. 1995: Mutation analysis of the Wiskott-Aldrich syndrome gene. FASEB Journal 9(4): A780

Sistermans, Erik A.; Van Beerendonk, Hetty M.; De Coo, Rene F.M.; Kleijer, Wim J.; Van Oost, Bernard A. 1997: Mutation analysis of the aspartoacylase gene in non-Ashkenazi Jewish patients with Canavan disease Identification of 6 new mutations. American Journal of Human Genetics 61(4 Suppl): A346

Dobbie, Z.; Mueller, H.J. 1998: Mutation analysis of the beta-catenin gene in FAP patients without an APC mutation. European Journal of Human Genetics 6(Suppl 1): 134

Stewart, H.; Ridgway, A.; Black, G.; Dixon, M. 1997: Mutation analysis of the beta-ig-h3 gene in corneal dystrophy. Journal of Medical Genetics 34(Suppl 1): S82

Planelles, V.; Leung, N.; Unger, R.; Haigwood, N.; Scandella, C.; Misher, L.; Gardner, M.; Luciw, P. 1992: Mutation analysis of the cd4 binding region of siv envelope. Journal of Cellular Biochemistry Suppl (16 Part E): 100

Williams, M.; Tyfield, L.A.; Turnpenny, P.D.; Stevens, D.L.; Lunt, P.W. 1997: Mutation analysis of the connexin 32 gene in HMSN1 patients in the southwest of England Identification of two potentially novel mutations. Journal of Medical Genetics 34(Suppl 1): S81

Lehesjoki, A.E.; Virtaneva, K.; D'amato, E.; Miao, J.; Pennacchio, L.; Myers, R.M. 1996: Mutation analysis of the cystatin B gene in progressive myoclonus epilepsy, EPM1 patients. Epilepsia 37(Suppl 5): 127

Beards, F.E.; Harris, A.; Flinter, F.A.; Mathew, C.G. 1990: Mutation analysis of the cystic fibrosis gene. Journal of Medical Genetics 27(10): 657-658

Van Vuuren, H.J.J.; Rai, R.; Cooper, T.G. 1990: Mutation analysis of the dal7 upstream induction sequence in saccharomyces cerevisiae. Yeast 6(SPEC ISSUE): S229

Hahn, S.H.; Krasnewich, D.M.; Gahl, W.A. 1994: Mutation analysis of the fumarylacetoacetate hydrolase gene in an American boy with tyrosinemia type 1. Clinical Research 42(2): 200A

Hagemann, T.L.; Assa'ad, A.H.; Kwan, S.P. 1995: Mutation analysis of the gene encoding Bruton's tyrosine kinase in a family with a sporadic case of X-linked agammaglobulinemia reveals three female carriers. American Journal of Medical Genetics 59(2): 188-192

Van Oost, B.A.; Ligtenberg, M.J.L.; Kemp, S.; Bolhuis, P.A. 1994: Mutation analysis of the gene involved in adrenoleukodystrophy. American Journal of Human Genetics 55(3 Suppl): A247

Jacobasch, G.; Gerth, C.; Ziemer, M.; Lenzner, C. 1998: Mutation analysis of the glucose-6-phosphate-dehydrogenase gene of German patients. Journal of Molecular Medicine 76(6): B34

Wieland, T.; Chen, C.K.; Simon, M.I. 1998: Mutation analysis of the interaction of RGS-r with transducin. Naunyn-Schmiedeberg's Archives of Pharmacology 357(4): R57

Ruppel, K.M.; Uyeda, T.Q.P.; Spudich, J.A. 1993: Mutation analysis of the molecular motor myosin. Biophysical Journal 64(2 Part 2): A2

Beier, D.; Deppisch, H.; Gross, R. 1996: Mutation analysis of the output domain of the unorthodox two components sensor protein BvgS of Bordetella pertussis. Zentralblatt fuer Bakteriologie Suppl 28: 46-47

Bergh, J.; Sjogren, S.; Norberg, T.; Jansson, T.; Nordgren, H.; Lindgren, A.; Inganas, M.; Holmberg, L. 1996: Mutation analysis of the p53 gene using cDNA based sequencing is superior to immunohistochemical analysis with Pab 1801 on a consecutive and population based primary breast cancer material regarding prognostic information and response to adjuvant therapy. Breast Cancer Research and Treatment 37(Suppl ): 39

Peral, B.; Ward, C.J.; Thomas, S.; Hughes, J.; Gamble, V.; Ratcliffe, P.J.; Harris, P.C. 1994: Mutation analysis of the polycystic kidney disease 1 gene. American Journal of Human Genetics 55(3 Suppl): A234

Cruts, M.; Backhovens, H.; Van Duijn, C.M.; Hofman, A.; Van Broeckhoven, C. 1996: Mutation analysis of the presenilin genes in families with early-onset Alzheimer disease. European Journal of Human Genetics 4(Suppl 1): 170

Cruts, M.; Backhovens, H.; Van Den Broeck, M.; Sernells, S.; Sherrington, R.; Hutton, M.; Hofman, A.; St Georges Hyslop, P.H.; Hardy, J.; Van Duijn, C.M.; Van Broeckhoven, C. 1997: Mutation analysis of the presenilin-1 and -2 genes in a population-based sample of early-onset Alzheimers disease. American Journal of Human Genetics 61(4 Suppl): A330

Braun, A.; Ambach, H.; Rabl, W.; Stockler, S.; Rolinski, B.; Strom, T.H.; Bernheimer, H.; Roscher, A.A. 1994: Mutation analysis of the putative adrenoleukodystrophy gene. European Journal of Pediatrics 153(3): 220

Gronskov, Karen; Vissing, Henrik; Shymko, Ronald M.; Tornqvist, Hans; De Meyts, Pierre 1993: Mutation analysis of the role of ser85 and arg86 of the insulin receptor in insulin binding and tyrosine kinase activity. Journal of Cellular Biochemistry Suppl 1993(17 Part A): 233

Amaral, Olga; Marcao, A.; Pinto, E.; Sa Miranda, M.C. 1998: Mutation analysis of the three most common lysosomal storage disorders in Portugal. European Journal of Human Genetics 6(Suppl 1): 50

Gilbert, J.R.; Kumar, A.; Kandt, R.S.; Wolpert, C.; Pufky, J.; Qiu, H.; Roses, A.D.; Pericak Vance, M.A. 1995: Mutation analysis of the tuberous sclerosis 2 gene. American Journal of Human Genetics 57(4 Suppl): A213

Iyengar, S.; Tallini, G.; Sirugo, G.; Bale, A.E.; Kidd, K.K. 1995: Mutation analysis of the vHL gene in individuals with sporadic and familial pheochromocytoma. American Journal of Human Genetics 57(4 Suppl): A67

Gilbert, J.; Wolpert, C.; Kumar, A.; Kandt, R.; Oiu, H.; Pufky, J.; Lennon, F.; Alysworth, A.; Nellist, M.; Sampson, J.; Roses, A.; Pericak Vance, M.A. 1994: Mutation analysis of tuberous sclerosis families using the chromosome 16 tuberin gene. American Journal of Human Genetics 55(3 Suppl): A370

Wallace, A.J.; Elles, R.G.; Hughes, H. 1991: Mutation analysis of two cystic fibrosis populations from northern england uk. Journal of Medical Genetics 28(8): 571

Adachi, M.; Mikami, B.; Utsumi, S. 1997: Mutation and X-ray crystallographic analysis of catalytic residues in soybean beta-amylase. Cereal Foods World 42(8): 620

Martinez, F.; Badia, L.; Montero, R.; Millan, J.M.; Prieto, F. 1996: Mutation and activation patterns in female carriers of fragile-X full mutation. European Journal of Human Genetics 4(Suppl 1): 117

Takahashi, H.; Ichimiya, S.; Watanabe, M.; Furusato, M.; Wakui, S.; Yantani, R.; Aizawa, S.; Nakagawara, A. 1998: Mutation and allelotyping analysis of p73 gene in clinical prostatic carcinoma. Proceedings of the American Association for Cancer Research Annual Meeting 39: 544-545

Chen-Yu; Lin-Jin-Ming; Liu-Guang-Fang 2008: Mutation and analysis of high lipid-content strains of Dunaliella bardawil. Xiamen Daxue Xuebao (Ziran Kexue Ban) 47(3): 397-401

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Dahia, P.L.M.; Marsh, D.J.; Zheng, Z.; Zedenius, J.; Komminoth, P.; Parsons, R.; Longy, M.; Larsson, C.; Eng, C. 1997: Mutation and deletion analysis of the Cowden disease gene, PTEN, in sporadic nonmedullary thyroid tumors. American Journal of Human Genetics 61(4 Suppl): A63

Zhou, X.L.; Suzuki, H.; Yin, J.; Tarmin, L.; Meltzer, S.J. 1995: Mutation and deletion of MTS1 in esophageal cancers and cell lines. Proceedings of the American Association for Cancer Research Annual Meeting 36: 145

Cheng, R.Y.S.; Tsao, S.W. 1996: Mutation and deletion of the p16 gene in esophageal squamous carcinoma. Proceedings of the American Association for Cancer Research Annual Meeting 37: 186

Stenzel, T.T.; Gallione, C.J.; Klaus, D.J.; Yeh, E.Y.; Lux, A.; Xue, Y.; Anthony, K.B.; Mcallister, K.A.; Baldwin, M.A.; Berg, J.N.; Smith, J.D.; Vary, C.P.H.; Craigen, W.J.; Lowry, R.B.; Westermann, C.J.J.; Warner, M.L.; Miller, Y.E.; Jackson, C. 1997: Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles A new model for pathogenesis. American Journal of Human Genetics 61(4 Suppl): A348

Chowdhury, P.; Lynn Cook, B.D.; Montague, D.C.; Doi, R.; Chang, L.W.; Takaori, K.; Rayford, P.L. 1993: Mutation and expression of H-ras gene in rat exocrine pancreas in response to nicotine. Pancreas 8(6): 752

Lang, P.; Kreuser, E.D.; Maurer, J.; Schueler, C.; Hoeher, D.; Montenarh, M.; Thiel, E. 1992: Mutation and expression of P53 in tumor cell lines Comparison of immunological methods and non-isotopic DNA sequencing. Annals of Hematology 65(Suppl ): A87

Fan, K.; Schutz, M. 1994: Mutation and expression of p53 gene in primary and metastatic prostatic adenocarcinoma. Modern Pathology 7(1): 74A

Witke, W.; Noegel, A.A. 1990: Mutation and expression of regulatory and functional domains of alpha actinin. Cell Biology International Reports 14(ABSTR Suppl): 49

Sheffield, L.; Sherman, S.; Morton, N.; Braun, J.; Duncan, B.; Lloyd, J. 1991: Mutation and genetic fitness of hemophilia a in south australia. American Journal of Human Genetics 49(4 Suppl): 493

Kalinsky, H.; Iyengar, S.; Weiss, S.; Sadeh, M.; Bonne Tamir, B.; Kidd, K.K. 1995: Mutation and haplotype analysis of a Druze pedigree with McArdles disease. American Journal of Human Genetics 57(4 Suppl): A331

Berger, D.; Pauer, H.D.; Hinze, R.; Taubert, H.; Meye, A.; Holzhausen, H.J.; Schmidt, H.; Rath, F.W. 1997: Mutation and immunohistochemical investigation of tumor suppressor genes p53 and p16 in malignant fibrous histiocytomas of the bone. European Journal of Cell Biology 72(Suppl 43): 87

Bennett, W.P.; Borkowski, A.; Colby, T.V.; Jones, R.T.; Lane, D.P.; Metcalf, R.A.; Samet, J.M.; Takeshima, Y.; Travis, W.D. 1993: Mutation and immunopositivity in the pathogenesis of human bronchogenic carcinoma. Laboratory Investigation 68(1): 129A

Mann, G.J.; Holland, E.A.; Becker, T.M.; Grulet, O.M.C.; Rizos, H.; Kefford, R.F. 1997: Mutation and linkage analysis of CDKN2A and CDK4 in 119 Australian melanoma kindreds. American Journal of Human Genetics 61(4 Suppl): A73

Stopper, H.; Eckert, I.; Spencer, D.L.; Caspary, W.J.; Schiffmann, D. 1994: Mutation and micronucleus induction in mouse L5178Y cells by substances that do not form DNA-adducts. Naunyn-Schmiedeberg's Archives of Pharmacology 349(Suppl): R122

Evans, H.J. 1996: Mutation and mutagenesis in inherited and acquired human disease. The first EEMS Frits Sobels Prize Lecture, Noordwijkerhout, The Netherlands, June 1995. Mutation Research 351(2): 89-103

Liu, F.S.; Boyd, J.; Berchuck, A. 1995: Mutation and over-expression on the P53 tumor suppressor gene frequently occurs in uterine and ovarian sarcomas. International Journal of Gynecology and Obstetrics 49(Suppl ): S91

Nishigori, C.; Takebe, H.; Matsumura, Y.; Imamura, S. 1993: Mutation and overexpression of p53 gene in human skin cancer of sun-exposed area. Journal of Investigative Dermatology 101(3): 406

Gamo, M.; Suzuki, T.; Niitani, T.; Kambe, M.; Kanamaru, R. 1993: Mutation and overexpression of p53 in gastric cancer. Proceedings of the American Association for Cancer Research Annual Meeting 34: 533

Gilbert, J.R.; Guy, V.; Kumar, A.; Kandt, R.; Wolpert, C.; Roses, A.D.; Pericak Vance, M.A. 1997: Mutation and polymorphism analysis of the tuberous sclerosis 2 gene. American Journal of Human Genetics 61(4 Suppl): A334

Wittmann, H.G. 1990: Mutation and protein structure studies on tobacco mosaic virus. Collection of Papers Presented at the Annual Symposium on Fundamental Cancer Research 19: 124-130

Zola, H.; Ridings, J.; Macardle, P.J.; Williams, R.; Robertson, D.; Elliott, S.; Lenton, K.; De Boer, N.; Van Der Horst, A.; Lodewijk, M.; Timens, W. 1998: Mutation and selection of Ig genes in the human infant. Immunology 95(Suppl 1): 38

Strauss, B.; Turkington, E.; Sahm, J.; Wang, J. 1990: Mutation and termination of dna synthesis studied in vitro ionizing radiation induced base damage and guanine aminofluorene adducts. Proceedings of the American Association for Cancer Research Annual Meeting 31: 102

Shimizu, Y.; Furukawa, Y. 1998: Mutation around the pore region of a voltage-gated K+ channel of Aplysia modifies the accumulative inactivation. Zoological Science 15(Suppl ): 101

Miwa, S.; Nakajima, T.; Murai, Y.; Takano, Y.; Sugiyama, T. 2008: Mutation assay of the novel gene DOG1 in gastrointestinal stromal tumors (GISTs). Journal of Gastroenterology 43(7): 531-537

Clare, C. 1995: Mutation assays in bacteria. Methods in Molecular Biology 43: 297-306

Kuryatov, A.; Gerzanich, V.; Nelson, M.; Olale, F.; Lindstrom, J. 1997: Mutation associated with autosomal dominant nocturnal frontal lobe epilepsy alters Ca++ permeability, conductance, and gating of the human alpha-4-beta-2 nicotinic receptor. Society for Neuroscience Abstracts 23(1-2): 389

Sunder Plassmann, G.; Foedinger, M.; Mannhalter, C.; Hoerl, W.H. 1995: Mutation at ARG-506 of coagulation factor V and access thrombosis in hemodialysis patients. Journal of the American Society of Nephrology 6(3): 503

Weiss, E.R.; Shi, W.; Dickerson, C.D.; Osawa, S. 1996: Mutation at ARG135 in rhodopsin alters its interaction with transducin, rhodopsin kinase and arrestin. IOVS Investigative Ophthalmology and Visual Science 37(3): S804

Wright, J. 1994: Mutation at VNTRs: Are minisatellites the evolutionary progeny of microsatellites?. Genome 37(2): 345-347

Yoshida, L.S.; Saruta, F.; Yoshikawa, K.; Tatsuzawa, O.; Tsunawaki, S. 1998: Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase. Journal of Biological Chemistry 273(43): 27879-27886

Grant, B.W.; Trombley, L.; Nicklas, J.A.; Hunter, T.; Albertini, R.J. 1996: Mutation at hprt in CD34+ cells from patients at risk for AML. Blood 88(10 Suppl 1 Part 1-2): 83A

Thakker, N.S.; Tassabehji, M.; Colley, A.; Sharland, M.; Donnai, D.; Harris, R.; Strachan, T. 1992: Mutation at the NF1 locus in a Watson syndrome family. Journal of Pathology 168(Suppl): 112A

Kitamura, Y.; Kasugal, T.; Tsujimura, T.; Hirota, S.; Morii, E.; Nomura, S.; Niwa, Y.; Kondo, K.; Nishimune, Y. 1991: Mutation at the c kit locus of rats results in anemia and mast cell deficiency. Experimental Hematology 19(6): 466

Fujimori, A.; Harker, W.G.; Hoki, Y.; Kohlhagen, G.; Pommier, Y. 1994: Mutation at the catalytic site of topoisomerase I in a human leukemia cell line resistant to camptothecin. Proceedings of the American Association for Cancer Research Annual Meeting 35: 363

Ko, K.W.Y.; Mcleod, R.S.; Avramoglu, K.K.; Nimpf, J.; Fitzgerald, D.J.; Vukmirica, J.; Yao, Y. 1998: Mutation at the furin cleavage site of LRP impairs exit from the ER but does not affect endocytosis. Molecular Biology of the Cell 9(Suppl ): 78A

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Tsujimura, T.; Morimoto, M.; Kanno, H.; Asai, H.; Miwa, S.; Kitamura, Y. 1996: Mutation at the pyruvate kinase gene of mice An animal model of nonspherocytic hemolytic anemia. Experimental Hematology 24(9): 1064

Akhmaloka; Susilowati, P.Endang.; Subandi; Madayanti, F. 2008: Mutation at tyrosine in AMLRY (GILRY like) motif of yeast eRF1 on nonsense codons suppression and binding affinity to eRF3. International Journal of Biological Sciences 4(2): 87-95

ZhuHong; XuJingZao; ShiJun; ZhangRui; SunXiaoYu; ZhuRongRong; YaoSide; WangShiLong 2008: Mutation breeding for productive yeast strains through a novel method high-energy-pulse-electron-beam. Annals Of Microbiology: 3, 549-553

Love, S.L.; Thompson Johns, A.; Werner, B.K. 1995: Mutation breeding for quality improvements in Russet Burbank. American Potato Journal 72(10): 638

Kaveri,S.B.; Nadaf,H.L. 2008: Mutation breeding for quantitative characters in groundnut. Crop Research (hisar): 1 2, 91-94

ZhangShuFei; SongJiaHuan; WuMinChen; ShengJinPing; LiJianFang 2008: Mutation breeding of Aspergillus niger strain LW-1 for high-yield beta -mannanase production. Chinese Journal Of Agricultural Biotechnology: 2, 153-158

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Parija, S.C.; Khairnar, K. 2008: Mutation detection analysis of a region of 16S-like ribosomal RNA gene of Entamoeba histolytica, Entamoeba dispar and Entamoeba moshkovskii. Bmc Infectious Diseases 8: 131

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Dry, K.L.; Manson, F.D.C.; Edgar, A.J.; Lennon, A.A.; Bergen, A.A.B.; Bird, A.C.; Wright, A. 1997: Mutation detection and characterization of RPGR, the gene for X-linked retinitis pigmentosa. IOVS Investigative Ophthalmology and Visual Science 38(4 Part 1-2): S679

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Chauveau, D.; Rossetti, S.; Strmecki, L.; Gamble, V.; Burton, S.; Winearls, C.; Harris, P.C. 1998: Mutation detection at PKD1 by PTT and direct sequencing. Journal of the American Society of Nephrology 9(Program and Abstr. Issue): 372A

Grompe, M.; Caskey, C.T. 1989: Mutation detection by chemical cleavage of amplified dna in ornithine transcarbamylase deficiency. Pediatric Research 25(4 Part 2): 141A

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A.Biochem (Usa) 1994: Mutation detection by heteroduplex analysis. FASEB Journal 8(7): A1475

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Afzal, A.R.; Hand, M.; Pereira, E.T.; Malik, A.S.; Taylor, R.; Jeffery, S. 1998: Mutation detection in 3 region of the polycystic kidney disease 1 gene reveals four novel mutations. Journal of the American Society of Nephrology 9(Program and Abstr. Issue): 370A

Plant, K.E.; Vetrie, D.; Green, P.; Flinter, F.A. 1997: Mutation detection in Alport syndrome A large scale screen of all 51 exons of COL4A5. American Journal of Human Genetics 61(4 Suppl): A343

Hollway, G.E.; Suthers, G.K.; Haan, E.A.; Thompson, E.; David, D.J.; Gecz, J.; Mulley, J.C. 1996: Mutation detection in FGFR2 craniosynostosis syndromes Recurrent mutations and a novel splice site mutation. American Journal of Human Genetics 59(4 Suppl): A396

Van Bakel, I.; Yates, J.R.W.; Green, A.J. 1996: Mutation detection in Tuberous Sclerosis using the Protein Truncation Test. American Journal of Human Genetics 59(4 Suppl): A290

Forrest, S.M.; Rosenthal, A.; Balnaves, M.E. 1994: Mutation detection in X-linked hydrocephalus. American Journal of Human Genetics 55(3 Suppl): A219

Angrist, M.; Bolk, S.; Chakravarti, A. 1994: Mutation detection in autosomal dominant Hirschsprung disease SSCP analysis of the RET proto-oncogene. American Journal of Human Genetics 55(3 Suppl): A209

Yasuda, K. 1994: Mutation detection in diabetes mellitus. Japanese Journal of Electrophoresis 38(6): 371-375

Tuohy, T.M.F.; White, R.; Groden, J. 1994: Mutation detection in large genes Use of overlapping PCR fragments for double screening of the APC gene and a PCR modification to concatenate multiple exons. American Journal of Human Genetics 55(3 Suppl): A246

Ficsor, G.; Goodwin, J.T.; Leon, J.H.; Rank, K.; Ginsberg, L.C. 1993: Mutation detection in mammalian sperm without progeny testing An in vitro model for method development. Environmental and Molecular Mutagenesis 21(Suppl 22): 19

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Lester, T.; Genet, S.; Bradley, L.A.D.; Fontan, G.; Lovering, R.; Middleton Price, H.R. 1996: Mutation detection in patients with X-linked agammaglobulinaemia and detection of grandpaternal germline mosaicism. European Journal of Human Genetics 4(Suppl 1): 140

Peral, B.; Gamble, V.; Ong, A.C.M.; San Millan, J.L.; Harris, P.C. 1996: Mutation detection in polycystic kidney disease 1 gene. Journal of the American Society of Nephrology 7(9): 1620

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Lishanskaya, A.I.; Ostrander, E.A.; Rine, J. 1992: Mutation detection in the cystic fibrosis gene using an Escherichia coli mismatch binding protein. American Journal of Human Genetics 51(4 Suppl): A385

Smeitink, J.; Loeffen, J.; Ruitenbeek, W.; Smeets, R.; Janssen, A.; Rubio Gozalbo, E.; Mariman, E.; Sengers, R.; Trijbels, F.; Van Den Heuvel, B. 1997: Mutation detection in the nuclear encoded complex I subunit NDUFA1 in patients with multisystemic complex I deficiency. Journal of Inherited Metabolic Disease 20(Suppl 1): 59

Roelfsema, J.; Peters, D.J.M.; Spruit, L.; Breuning, M.H. 1996: Mutation detection in the repeated part of the polycystic kidney disease 1 gene by the protein truncation test. Journal of the American Society of Nephrology 7(9): 1605

Van Bakel, I.; Yates, J.R.W.; Green, A.J. 1996: Mutation detection in tuberous sclerosis Restriction endonuclease fingerprinting and protein truncation test. European Journal of Human Genetics 4(Suppl 1): 63

Yandava, C.N.; Cooper, D.M.; Pillari, A.; Liggett, S.B.; Drazen, J.M. 1997: Mutation detection methods and preferential amplification of wild type allele of the human beta2-adrenergic receptor gene. American Journal of Human Genetics 61(4 Suppl): A389

Zhu, D.; Brown, D.R.; Li, Y.; Mitchell, T.N.; Hussels, I.E.M.umenee 1996: Mutation detection of OA1 gene in X-linked ocular albinism. IOVS Investigative Ophthalmology and Visual Science 37(3): S996

Watnick, T.; Phakdeekitcharoen, B.; Gandolph, M.; Johnson, A.; Gabow, P.; Kimberling, W.; Overbeck, L.; Landes, G.; Klinger, K.; Germino, G.G. 1998: Mutation detection of PKD1 exons 15-21 using locus specific reagents. Journal of the American Society of Nephrology 9(Program and Abstr. Issue): 384A

Vrolijk, L.P.; Rader, D.J.; Addelston, M.B.; Smith, P.N.; Boyce Jacino, M. 1997: Mutation detection of four atherosclerosis high-risk genes and correlations to coronary artery disease. American Journal of Human Genetics 61(4 Suppl): A225

Dao, D.D.; Beattie, W.G.; Meng, L.; Larry, L.A.; Bishop, C.A.; Abbruzzese, J.L.; Evans, D.B.; Frazier, M.L.; Hansen, J.F.; Beattie, K.L. 1995: Mutation detection of single base changes in oncogenes and tumor suppressor genes by matrix hybridization. Proceedings of the American Association for Cancer Research Annual Meeting 36: 561

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Ledley, F.D.; Jansen, R.; Nham, S.U.; Fenton, W.A.; Rosenberg, L.E. 1989: Mutation eliminating mitochondrial targeting sequence of methylmalonyl coenzyme a mutase causes mut o methylmalonic acidemia. American Journal of Human Genetics 45(4 Suppl): A9

Masters, J.R.W.; Parris, C.N. 1989: Mutation frequencies and resistance to cisplatin. Investigational New Drugs 7(4): 445

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Mcqueen, M.J.; Bamford, K.; Nazir, D.J.; Hill, S.A. 1996: Mutation frequencies of cholesterol ester transfer protein and hepatic lipase in a North American population. Clinical Chemistry 42(6 Part 2): S298

Woo, S.L.C.; Martinez, D.; Kouzmine, A.; Goltsov, A.; Brown, A.; Singh, R.; Elsas, L.J.; Eisensmith, R.C. 1994: Mutation frequency and genotype/phenotype correlation among phenylketonuria patients from Georgia. American Journal of Human Genetics 55(3 Suppl): A250

Wang, Z.; Zhang, W.Q.; Safe, S.; Goldstein, L.; Rodriguez, L.V. 1997: Mutation frequency and spectrum in relation to dose and exposure length in coal tar carcinogenesis. Proceedings of the American Association for Cancer Research Annual Meeting 38: 461

Wojcik, A.; Janion, C. 1997: Mutation frequency decline and DNA repair in halogen light irradiated Escherichia coli K-12 strains. Mutation Research 379(1 Suppl 1): S38

Bockrath, R.; Li, B.H. 1995: Mutation frequency decline and transcription-coupled excision repair in E coli. Journal of Cellular Biochemistry Suppl 1995(21A): 311

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Pignatti, P.F.; Bombieri, C.; Benetazzo, M.G.; Malerba, G.; Saccomani, A.; Gile, L.S.; Luisetti, M. 1996: Mutation frequency in CFTR, alpha-1AT and alpha-1ACT genes in obstructive pulmonary disease. American Journal of Human Genetics 59(4 Suppl): A278

Shane, B.S.; Winston, G.W.; Reilly, P.A.; Schaeffer, D.O.; Battista, J.R.; Swenson, D.H.; Chang, S.H.; Lee, W.R. 1993: Mutation frequency of benzo pyrene in rapidly dividing cells of the liver of C57BL/6 transgenic mice. Environmental and Molecular Mutagenesis 21(Suppl 22): 64

Zheng, N.; Monckton, D.G.; Wilson, G.; Ramagli, L.; Siciliano, M.J.; Meistrich, M.L. 1998: Mutation frequency of minisatellite repeat number changes in human sperm before and after mitoxantrone, vincristine, vinblastine and prednisone chemotherapy. Environmental and Molecular Mutagenesis 31(Suppl 29): 61

Kobayashi, T. 1993: Mutation from multi-polar to bi-polar state in C6 glioma cells is related to content of cytoskeletal proteins, especially vimentin. Zoological Science (Tokyo) 10(Suppl ): 6

Risinger, J.I.; Umar, A.; Berchuck, A.; Kunkel, T.A.; Barrett, J.C.rl 1996: Mutation hMRP1/DUG1, the human homolog of yMSH3, in human endometrial cancers with microsatellite instability. Proceedings of the American Association for Cancer Research Annual Meeting 37: 554

Berg, M.A.; Argente, J.; Chernausek, S.; Gracia, R.; Guevara Aguirre, J.; Hopp, M.; Perez Jurado, L.; Rosenbloom, A.L.; Toledo, S.P.A.; Francke, U. 1992: Mutation heterogeneity in Laron syndrome. American Journal of Human Genetics 51(4 Suppl): A208

Rathmann, M.; Popowska, E.; Bunge, S.; Beck, M.; Hopwood, J.J.; Schwinger, E.; Gal, A. 1994: Mutation hot spots in the iduronated-sulfatase gene, and evidence for a pseudogene. American Journal of Human Genetics 55(3 Suppl): A238

Gallie, B.; Rushlow, D.; Han, L.; Pittman, J.; Sutherland, J.; Liu, S.; Hui, M.; Zamora, J.; Dunn, J.M. 1997: Mutation identification in the retinoblastoma gene. IOVS Investigative Ophthalmology and Visual Science 38(4 Part 1-2): S470

Wu, S.J.; Locy, R.D.; Shaw, J.J.; Cherry, J.H.; Singh, N.K. 1998: Mutation in Arabidopsis HIT1 locus causing heat and osmotic hypersensitivity. Plant Biology (Rockville) : 103-104

Wang, L.; Recupero, A.; Harter, M.L.; Banerjee, S. 1993: Mutation in DNA polymerase beta of renal cell carcinoma. Proceedings of the American Association for Cancer Research Annual Meeting 34: 535

Gottschalk, S.; Ng, C.Y.C.; Perez, M.; Brenner, M.K.; Heslop, H.E.; Rooney, C.M. 1998: Mutation in EBV produces immunoblastic lymphoma unresponsive to CTL immunotherapy. Blood 92(10 Suppl 1 Part 1-2): 321A

Bailey, C.H.; Kaang, B.K.; Chen, M.; Kandel, E.R. 1996: Mutation in MAP kinase phosphorylation sites blocks learning-related internalization of apCAM in Aplysia sensory neurons. Society for Neuroscience Abstracts 22(1-3): 1446

Schimmenti, L.A.; Byerly, K.A.; Braddock, S.R.; Eccles, M.R.; Zhang, Y.H.; Shim, H.H. 1996: Mutation in PAX 2 in a patient with coloboma-ureteral-renal syndrome. American Journal of Human Genetics 59(4 Suppl): A9

Souza, R.F.; Yin, J.; Smolinski, K.N.; Wang, S.; Zou, T.T.; Abraham, J.M.; Powell, S.M.; Sugimura, H.; Matsubara, N.; Meltzer, S.J. 1997: Mutation in a coding region microsatellite of E2F-4 in genetically unstable gastric tumors. Proceedings of the American Association for Cancer Research Annual Meeting 38: 358

Eissenberg, J.C.; James, T.C.; Foster Hartnett, D.M.; Hartnett, T.; Ngan, V.; Craig, C.; Elgin, S.C.R. 1990: Mutation in a heterochromatin specific chromosomal protein are associated with suppression of position effect variegation in a drosophila melanogaster. Journal of Cell Biology 111(5 Part 2): 5A

Puk, O.; Löster, J.; Dalke, C.; Soewarto, D.; Fuchs, H.; Budde, B.; Nürnberg, P.; Wolf, E.; de Angelis, M.Hrabé.; Graw, J. 2008: Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype. IOVS Investigative Ophthalmology and Visual Science 49(4): 1525-1532

Denison, S.; May, G. 1991: Mutation in a protein containing a leucine zipper like motif results in a mitotic block in aspergillus nidulans. Journal of Cell Biology 115(3 Part 2): 346A

Lefebvre, S.E.; Rollins, S.L.; Melera, P.W. 1995: Mutation in a putative reduced folate carrier contributes to methotrexate resistance in the methotrexate resistant cell line DC-3F/A55. Proceedings of the American Association for Cancer Research Annual Meeting 36: 376

Boissy, R.E.; Zhao, H.; Oetting, W.S.; Kobayashi, T.; Austin, L.M.; Wildenberg, S.C.; Boissy, Y.L.; Zhao, Y.; Hearing, V.J.; King, R.A.; Nordlund, J.J. 1995: Mutation in and lack of expression of tyrosinase related protein-1 in melanocytes from an individual with tyrosinase-positive oculocutaneous albinism A new subtype of albinism classified as OCA3. Journal of Investigative Dermatology 104(4): 597

Kishnani, P.; Bao, Y.; Wu, J.Y.; Brix, A.E.; Chen, Y.T. 1994: Mutation in canine glucose-6-phosphatase deficiency. Pediatric Research 37(4 Part 2): 149A

Stamato, T.; Denko, N.; Giaccia, A.; Maclaren, R.; Richardson, E. 1989: Mutation in chinese hamster cells can be delayed at least 9 cell divisions after uv light treatment. Journal of Cellular Biochemistry Suppl (13 Part B): 23

Aerts H.; Sa C.M.; Tager J.M.; Weiler S.; Tomich J.A.; Ohashi T.; Barranger J.A. 1991: Mutation in codon 370 of human glucocerebrosidase a ph sensitive mutation associated with mild presentation of gaucher disease. American Journal of Human Genetics 49(4 Suppl): 93

Berglund, E.O.; Murai, K.; Fredette, B.; Marturano, B.; Ranscht, B. 1997: Mutation in contactin gene causes ataxia and early postnatal death. Society for Neuroscience Abstracts 23(1-2): 1956

Lichtenauer Kaligis, E.G.R.; Thijssen, J.C.P.; Den Dulk, H.; Van, D.P.tte, P.; Giphart Gassler, M.; Tasseron, D.J.ng, J.G. 1992: Mutation in different positions on the human chromosome. Mutagenesis 7(5): 367-368

Tanizawa, A.; Tabuchi, A.; Bertrand, R.; Pommier, Y. 1992: Mutation in dna topoisomerase i cdna from a camptothecin resistant chinese hamster cell line. Proceedings of the American Association for Cancer Research Annual Meeting 33: 450

WuShengLong; Musa,H.H.; BaoWenBin; WangKeHua; ZhuGuoQian; ChenGuoHong 2008: Mutation in exon 4 of apoVLDL-II gene is a candidate for meat tenderness in chicken. Journal Of Animal And Veterinary Advances: 12, 1624-1627

Mayr, B.; Reifinger, M. 1994: Mutation in exon 8 of tumour suppressor gene p53 in a feline osteosarcoma. Animal Genetics 25(Suppl 2): 35

Sood, S.; Eldadah, Z.A.; Krause, W.L.; Mcintosh, I.; Dietz, H.C. 1996: Mutation in fibrillin-1 and the Marfanoid-craniosynostosis syndrome. Nature Genetics 12(2): 209-211

Biery, B.J.; Goodman, S.I. 1992: Mutation in glutaryl-CoA dehydrogenase in glutaric acidemia type I. American Journal of Human Genetics 51(4 Suppl): A165

Horikawa, Y.kio; Iwasaki, Naoko; Hara, Manami; Furuta, Hiroto; Hinokio, Yoshinori; Cockburn, Brian, N.; Lindner, Tom; Yamagata, Kazuya; Ogata, Makiko; Tomonaga, Osamu; Kuroki, Hiroyuki; Kasahara, Tadasu; Iwamoto, Yasuhiko; Bell, Graeme, I. 1997: Mutation in hepatocyte nuclear factor-1beta gene associated with MODY. Nature Genetics 17(4): 384-385

Takebe, H.; Ohtsu, S.; Tachiiri, S.; Kitagawa, K.; Tsukada, T.; Miyakoshi, J. 1997: Mutation in human cells and enhanced gene expression in rodent cells induced by electro-magnetic fields. Mutation Research 379(1 Suppl 1): S92

Accili, D.; Frapier, C.; Mosthaf, L.; Mckeon, C.; Ullrich, A.; Taylor, S.I. 1989: Mutation in insulin receptor gene causes insulin resistance by impairing receptor transport to cell surface. Clinical Research 37(2): 568A

Wittrup, H.H.; Tybjaerg Hansen, A.; Steffensen, R.; Reeler, S.; Schnohr, P.; Nordestgaard, B.G. 1996: Mutation in lipoprotein lipase associated with increased risk of ischemic heart disease in women, but not in men. Circulation 94(8): I92-I93

Dreyer, S.; Chen, H.; Zhou, G.; Baldini, A.; Winterpacht, A.; Zabel, B.; Cole, W.; Oberg, K.C.; Johnson, R.L.; Lee, B. 1998: Mutation in lmx1b causes skeletal and renal dysplasia in mice and nail patella syndrome in humans. Pediatric Research 43(4 Part 2): 123A

Lemkes, H.H.P.J.; Jansen, J.J.; Van Den Ouweland, J.M.W.; Van Der Woude, F.J.; Hart, L.M. 't.; Bruyn, J.A.; Maassen, J.A. 1995: Mutation in mitochondrial tRNA-LEU gene associated with diabetes and severe non-diabetic kidney disease. Diabetologia 38(Suppl 1): A229

Wang, L.; Bukowski, R.; Church, J.; Milsom, J.; Banerjee, S. 1992: Mutation in nm23 a putative metastasis suppressor gene in human colorectal cancer. Proceedings of the American Association for Cancer Research Annual Meeting 33: 384

Chou, S.; Marousek, G.; Parenti, D.; Lalezari, J.; Miner, R.; Drew, L. 1997: Mutation in region III of the DNA polymerase gene associated with dual ganciclovir-foscarnet resistance in cytomegalovirus isolates from three subjects receiving prolonged antiviral therapy. Clinical Infectious Diseases 25(2): 449

Bridges, B.A. 1996: Mutation in resting cells: the role of endogenous DNA damage. Cancer Surveys 28: 155-167

Renjifo, B.; Essex, M. 1994: Mutation in tax of HTLV-I is associated with TSP/HAM. AIDS Research and Human Retroviruses 10(4): 446

Poulat, F.; Desclozeaux, M.; Tuffery, S.; Jay, P.; Boizet, B.; Berta, P. 1998: Mutation in the 5' noncoding region of the SRY gene in an XY sex-reversed patient. Human Mutation Suppl 1: S192-S194

Dudani, R.; Russell, M.; van Faassen, H.; Krishnan, L.; Sad, S. 2008: Mutation in the Fas pathway impairs CD8+ T cell memory. Journal of Immunology 180(5): 2933-2941

Wang, H.L.; Bren, N.; Auerbach, A.; Engel, A.G.; Sine, S.M. 1996: Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases both the rate of agonist dissociation and rate constants for channel gating. Society for Neuroscience Abstracts 22(1-3): 1260

Thakker, N.; Tassabehji, M.; Sharland, M.; Colley, A.; Donnai, D.; Harris, R.; Strachan, T. 1992: Mutation in the NF1 gene in a Watson syndrome family. American Journal of Human Genetics 51(4 Suppl): A73

Shastry, B.S.; Trese, M.T. 1996: Mutation in the Norrie disease gene associated with one X-linked and four sporadic cases of familial exudative vitreoretinopathy. IOVS Investigative Ophthalmology and Visual Science 37(3): S996

Ogata, H.; Tsuji, H.; Hashiguchi, M.; Shimono, J.; Fujishima, M.; Sato, H. 1998: Mutation in the TATA box in the family with Crigler-Najjar syndrome type 2. Hepatology 28(4 Part 2): 617A

Matsui, T.; Higuchi, S.; Arai, H.; Matsushita, S.; Higuchi, M.; Okamura, N.; Muramatsu, T.; Sasaki, H. 1998: Mutation in the alpha-synuclein gene among sporadic Parkinsons disease, Alzheimers disease and dementia with Lewy bodies. Society for Neuroscience Abstracts 24(1-2): 967

Levy, E.; Carman, M.D.; Fernandez Madrid, I.J.; Lieberburg, I.; Power, M.D.; Van Duinen, S.G.; Bots, G.T.A.M.; Luyendijk, W.; Frangione, B. 1990: Mutation in the alzheimers disease amyloid gene in patients with hereditary cerebral hemorrhage with amyloidosis dutch type. Neurobiology of Aging 11(3): 300

Norrgard, K.J.; Swango, K.L.; Wolf, B. 1996: Mutation in the biotinidase gene causes approximately 50 percent loss of enzyme activity and is common in the general population. American Journal of Human Genetics 59(4 Suppl): A275

Fuhrer, C.; Geffen, I.; Spiess, M. 1989: Mutation in the cytoplasmic tail of the human asialoglycoprotein receptor affects endocytosis and cellular distribution. Experientia 45(ABSTR): A59

Warner, L.E.; Mancias, P.; Butler, I.; Lupski, J.R. 1997: Mutation in the early growth response 2 transcription factor associated with recessive congenital hypomyelinating neuropathy. American Journal of Human Genetics 61(4 Suppl): A350

Dianzani, I.; Garelli, E.; Dompe, C.; Crescenzio, N.; Olivieri, N.; Gabutti, V.; Ramenghi, U. 1995: Mutation in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. American Journal of Human Genetics 57(4 Suppl): A210

Bonaventure, J.; Legeal Mallet, L.; Benoist Lasselin, C.; Rousseau, F.; Munnich, A. 1997: Mutation in the fibroblast growth factor receptor genes result in defective endochondral or membranous ossification. Bone (New York) 20(4 Suppl): 2S

Ridker, P.M.; Hennekens, C.H.; Lindpaintner, K.; Stampfer, M.J.; Eisenberg, P.R.; Miletich, J.P. 1995: Mutation in the gene coding for coagulation factor V and risks of future myocardial infarction, stroke, and venous thrombosis in apparently healthy men. Journal of Investigative Medicine 43(Suppl 2): 269A

Schorderet, D.F.; Nichini, O.; Boisset, G.ël.; Polok, B.; Tiab, L.; Mayeur, H.él.èn.; Raji, B.; de la Houssaye, G.; Abitbol, M.M.; Munier, F.L. 2008: Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome. American Journal of Human Genetics 82(5): 1178-1184

Bonneau, D.; Leneuve, P.; Beaumont, C. 1996: Mutation in the iron responsive element of L ferritin mRNA in a family with dominant cataract and hyperferritinemia. European Journal of Human Genetics 4(Suppl 1): 11

Bonneau, D.; Leneuve, P.; Beaumont, C. 1995: Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant cataract and hyperferritinemia. American Journal of Human Genetics 57(4 Suppl): A7

Kimura, T.; Sho, M.; Kinoshita, M.; Ishida, Y.; Nakata, K.; Niiyama, G.; Kinoyama, S.; Ito, T.; Yamada, G. 1998: Mutation in the nonstructural protein 5A gene in chronic hepatitis C virus 2A infection patients with interferon treatment. Hepatology 28(4 Part 2): 699A

Semina, E.V.; Reiter, R.; Hittner, H.; Ferrell, R.; Bitoun, P.; Alward, W.L.; Funkhauser, C.; Daack Hirsh, S.; Murray, J.C. 1998: Mutation in the novel homeobox gene PITX3 causes anterior segment mesenchymal dysgenesis and cataracts in humans. IOVS Investigative Ophthalmology and Visual Science 39(4): S950

Fujita, M.; Enomoto, T.; Inoue, M.; Nomura, T.; Tanizawa, O. 1992: Mutation in the p53 gene in primary human cervical carcinoma with and without human papilloma virus infection. Proceedings of the American Association for Cancer Research Annual Meeting 33: 248

Kimbrough, J.; Gingrich, K.J. 1998: Mutation in the putative local anesthetic receptor in IVS6 of rat skeletal muscle MU1 Na+ channels alters single channel interactions. Biophysical Journal 74(2 Part 2): A32

Krzysztof, K.; Kobielak, A.; Trzeciak, W.H. 1998: Mutation in the regulatory region of the EDA gene coincides with the symptoms. European Journal of Human Genetics 6(Suppl 1): 159

Knauber, T.; Doss, S.D.; Gerth, K.; Perlova, O.; Müller, R.; Treuner-Lange, A. 2008: Mutation in the rel gene of Sorangium cellulosum affects morphological and physiological differentiation. Molecular Microbiology 69(1): 254-266

Fletcher, J.E.; Tripolitis, L.; Rosenberg, H. 1994: Mutation in the ryanodine receptor in patients referred for MH testing. Anesthesiology 81(3A): A429

Burger, M.; Hoch, R.; Oades, Z.; Schraufstatter, I.U. 1998: Mutation in the second intracellular loop of CXCR2 leads to constitutive activation similar to KSRV-GPCR. Blood 92(10 Suppl 1 Part 1-2): 383A

Vilalta, A.; Trivedi, A.; Johnson, D.L. 1996: Mutation in the tata-binding protein selectively abolishes both RNA polymerase III transcription and the interaction of TBP with A TFIIIB subunit. Molecular Biology of the Cell 7(Suppl ): 465A

Marui, S.; Latronico, A.C.; Amhold, I.J.P.; Castro, M.; Elias, L.L.K.; Moreira, A.C.; Mendonca, B.B. 1997: Mutation in the type II 3-beta-hydroxysteroid dehydrogenase gene in girls with premature pubarche. Hormone Research 48(Suppl 2): 104

Isnard, R.; Richard, P.; Flavigny, J.; Charron, P.; Carrie, L.; Bonne, G.; Schwartz, K.; Komajda, M.; Hainque, B. 1997: Mutation in ventricular myosin regulatory light chain in a Caribbean family with hypertrophic cardiomyopathy and hypertension. European Heart Journal 18(ABSTR Suppl ): 406

Echols, H.; Goodman, M.F. 1990: Mutation induced by DNA damage: a many protein affair. Mutation Research 236(2-3): 301-311

Vrieling, H.; Wijnhoven, S.; Van Sloun, P.; Bol, S.; Van Steeg, H.; Slater, R.; Weeda, G. 1997: Mutation induction at the HPRT and APRT loci in wild type and repair deficient mice. Mutation Research 379(1 Suppl 1): S77

Furuno Fukushi, I.; Matsudaira, H. 1993: Mutation induction by low dose rate gamma rays and tritiated water in near-diploid mouse cells m5S. Journal of Radiation Research 34(4): 335

Hei, T.K.; Waldren, C.A. 1990: Mutation induction by radiation and asbestos fibers. Proceedings of the American Association for Cancer Research Annual Meeting 31: 99

Kiefer, J.; Stoll, U.; Schneider, E.; Kranert, T. 1994: Mutation induction in Chinese hamster V79 cells after heavy ion exposure. International Journal of Radiation Biology 65(1): 132

Steenwinkel, M.J.se S.T.; Van Asten, J.G.; Van Delft, J.H.M. 1996: Mutation induction in relation to formation of DNA adducts in organs of lambda-LacZ transgenic mice treated with benzo pyrene. Mutation Research 360(3): 221-222

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Kawanishi, C.; Shimoda, Y.; Fujimaki, J.; Onishi, H.; Suzuki, K.; Hanihara, T.; Sugiyama, N.; Kosaka, K. 1998: Mutation involving cytochrome P450IID6 in two Japanese patients with neuroleptic malignant syndrome. Journal of the Neurological Sciences 160(1): 102-104

Sesta, D.; Lenicek, S.; Papes, D. 1994: Mutation ju of Drosophila melanogaster Research between 1983 and 1993. Periodicum Biologorum 96(4): 375-376

Schoppa, N.E.; Mccormack, K.; Tanouye, M.A.; Sigworth, F.J. 1992: Mutation l370v in shaker 29 4 alters the voltage sensitivity of activation without altering total single channel charge movement. Biophysical Journal 61(2 Part 2): A426

Petersen Jones, S.M.; Entz, D.; Sargan, D.R. 1998: Mutation linked to cGMP-phosphodiesterase alpha gene causes generalized progressive retinal atrophy in the Cardigan Welsh Corgi. IOVS Investigative Ophthalmology and Visual Science 39(4): S880

Beutler, E.; McKusick, V.A.; Motulsky, A.G.; Scriver, C.R.; Hutchinson, F. 1996: Mutation nomenclature: nicknames, systematic names, and unique identifiers. Human Mutation 8(3): 203-206

Page, K.M.; Curtis, C.A.M.; Hulme, E.C. 1993: Mutation of ASP to GLU in the third transmembrane helix of the muscarinic receptors. Life Sciences 52(5-6): 560

Page, K.M.; Curtis, C.A.M.; Hulme, E.C. 1992: Mutation of Asp to Glu in transmembrane helix 3 of the muscarinic receptors. Society for Neuroscience Abstracts 18(1-2): 254

Kennedy, M.E.; Limbird, L.E. 1992: Mutation of Cys-442 of the alpha-2-adrenergic receptor eliminates tritiated palmitate incorporation but does not perturb receptor G-protein coupling. Molecular Biology of the Cell 3(Suppl ): 122A

Cho, W.; Taylor, L.P.; Akil, H.; Mansour, A. 1993: Mutation of D2 phenylalanine residues important for linking ligand binding and G-protein coupling. Society for Neuroscience Abstracts 19(1-3): 734

Millette, L.A.; Tepperman, K.; Wallick, E.T. 1996: Mutation of D925 in the alpha subunit of Na+,K+-ATPase alters the external cation binding pocket. FASEB Journal 10(6): A1245

Leith, M.K.; Begleiter, A. 1998: Mutation of DT-diaphorase in human breast cancer cell lines. Proceedings of the American Association for Cancer Research Annual Meeting 39: 428

Omi, N.; Kiyokawa, E.; Matsuda, M.; Kinoshita, K.; Yamada, S.; Yamada, K.; Matsushima, Y.; Wang, Y.; Kawai, J.; Suzuki, M.; Hayashizaki, Y.; Hiai, H. 2008: Mutation of Dock5, a member of the guanine exchange factor Dock180 superfamily, in the rupture of lens cataract mouse. Experimental Eye Research 86(5): 828-834

Ueda, A.; Grabbe, C.; Lee, J.; Lee, J.; Palmer, R.H.; Wu, C.-F. 2008: Mutation of Drosophila focal adhesion kinase induces bang-sensitive behavior and disrupts glial function, axonal conduction and synaptic transmission. European Journal of Neuroscience 27(11): 2860-2870

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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 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 Annual Meeting 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

Reitz, M.S.; Guo H G.; Veronese, F.D.; Pal, R.; Kalyanaraman, V.S.; Gallo, R.C. 1989: Mutation of the carboxyl terminal arginine residue of the hiv 1 gp120 blocks envelope protein cleavage. Journal of Cellular Biochemistry Suppl (13 Part B): 288

Marshak, D.R.; Russo, G.L.; Sutton, A. 1994: Mutation of the casein kinase II phosphorylation site in CDC28 causes premature entry into S phase in the budding yeast Saccharomyces cerevisiae. FASEB Journal 8(7): A1239

Wallner, E.I.; Martin, G.J.; Lomasney, J.W. 1996: Mutation of the catalytic domain of phospholipase C delta in human essential hypertension. Journal of Investigative Medicine 44(7): 379A

Murray, E.W.; Prevost, J.; Pihl, C.; Jackson, T.; Brown, C.B. 1996: Mutation of the cysteine in the soluble GM-CSF receptor alpha tail affects the interaction of solGMR-alpha with GMR-BETA on the cell surface. Blood 88(10 Suppl 1 Part 1-2): 546A

Attié, T.; Till, M.; Pelet, A.; Amiel, J.; Edery, P.; Boutrand, L.; Munnich, A.; Lyonnet, S. 1995: Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease. Human Molecular Genetics 4(12): 2407-2409

Schwan, W.R.; Langhorne, M.H.; Warrener, P.; Stover, C.K.; Folger, K.R. 1998: Mutation of the fiu gene from Pseudomonas aeruginosa affects in vivo survival. Abstracts of the General Meeting of the American Society for Microbiology 98: 93

Putkey, J.A.; Sweeney, H.L.; Negele, J. 1990: Mutation of the four calcium binding sites in cardiac troponin c. FASEB Journal 4(7): A1963

Bourgeron, T.; Chretien, D.; Poggi-Bach, J.; Doonan, S.; Rabier, D.; Letouzé, P.; Munnich, A.; Rötig, A.; Landrieu, P.; Rustin, P. 1994: Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency. Journal of Clinical Investigation 93(6): 2514-2518

Martin, A.; Hunter, E.; Gallaher, W. 1992: Mutation of the fusion peptide of human immunodeficiency virus. Abstracts of the General Meeting of the American Society for Microbiology 92: 419

Cvitanovic Sojat, L.; Jurcic, Z.; Mucic Pucic, B.; Shin, Y.; Podskarbi, T. 1997: Mutation of the glucose-6-phosphatase gene in a Croatian girl with glycogen storage disease type Ia. Journal of Inherited Metabolic Disease 20(Suppl 1): 91

Mayo, K.E.; Dealmeida, V.I.; Wu, K.C.; Godfrey, P.A. 1998: Mutation of the growth hormone-releasing hormone receptor in the little mouse. Spiegel, A M Contemporary Endocrinology; G proteins, receptors, and disease 217-229

Bressler, B.H.; Morishita, L.; Gauthier, L.; Borgford, T. 1994: Mutation of the high affinity calcium binding site of skeletal muscle troponin C. Biophysical Journal 66(2 Part 2): A310

Dotson, D.G.; Dotson, G.; Negele, J.; Liu, W.; Sweeney, H.L.; Putkey, J.A. 1992: Mutation of the high affinity calcium magnesium binding sites in cardiac troponin c. Biophysical Journal 61(2 Part 2): A280

Scheer, A.; Fanelli, F.; De Benedetti, P.G.; Cotecchia, S. 1996: Mutation of the highly conserved dry motif constitutively activates the alpha-1B-adrenergic receptor. Experientia 52(ABSTR ): A33

Clauser, E.; Auzan, C.; Debant, A.; Ponzio, G.; Rossi, B. 1989: Mutation of the human insulin receptor cleavage site modifies the alpha beta chain structure but does not impair the receptor functions. Diabetologia 32(7): 476A

Marsh, B.J.; Alm, R.A.; Mcintosh, S.R.; James, D.E. 1996: Mutation of the major phosphorylation site in GLUT-4 does not impair its insulin-stimulated movement in 3T3-L1 adipocytes. Molecular Biology of the Cell 7(Suppl ): 259A

Miller, T.; Sheng, Z.; Kong, Y.; Potter, J.D. 1992: Mutation of the metal binding sites in skeletal tnc. Biophysical Journal 61(2 Part 2): A280

Linsdell, P.; Rommens, J.M.; Hou, Y.X.; Chang, X.B.; Tsui, L.C.; Riordan, J.R.; Hanrahan, J.W. 1996: Mutation of the narrow region of the CFTR channel pore. Biophysical Journal 70(2 Part 2): A72

Ohta, M.; Nagai, H.; Shimizu, M.; Rasio, D.; Berd, D.; Mastrangelo, M.; Croce, C.M.; Huebner, K. 1995: Mutation of the p16 gene in familial and sporadic melanoma cases. Proceedings of the American Association for Cancer Research Annual Meeting 36: 579

Casson A.G.; Mukhopadhyay T.; Cleary K.; Ro J.; Levin B.; Roth J.A. 1991: Mutation of the p53 gene detected in barretts epithelium squamous cell and adenocarcinoma of the esophagus. Clinical and Investigative Medicine 14(4 Suppl): A42

Onda, M.; Fukushima, T.; Ono, T.; Kimijima, I.; Tsutiya, A.; Abe, R. 1994: Mutation of the p53 gene do not occur in male breast cancer. International Journal of Oncology 5(Suppl ): 366

Imamura, J.; Bartram, C.R.; Miyoshi, I.; Koeffler, H.P. 1993: Mutation of the p53 gene in nephroblastoma. Blood 82(10 Suppl 1): 526A

Eastham, J.A.; Gousse, A.E.; Slawin, K.M.; Wheeler, T.M.; Scardino, P.T.; Thompson, T.C. 1995: Mutation of the p53 tumor suppressor gene in metastatic prostate cancer. Journal of Urology 153(4 Suppl): 272A

Kraus, J.; Garbutt, K.G.; Geller, B.L. 1996: Mutation of the pip locus in three strains of Lactococcus lactis. Journal of Dairy Science 79(Suppl 1): 121

Satoh, H.; Shibahara, K.; Tokunaga, T.; Nishi, A.; Tasaki, M.; Hwang, S.-K.; Okita, T.W.; Kaneko, N.; Fujita, N.; Yoshida, M.; Hosaka, Y.; Sato, A.; Utsumi, Y.; Ohdan, T.; Nakamura, Y. 2008: Mutation of the plastidial alpha-glucan phosphorylase gene in rice affects the synthesis and structure of starch in the endosperm. Plant Cell 20(7): 1833-1849

Banks, S.D.; Lee, C.J. 1993: Mutation of the pneumolysin gene of type 19F Streptococcus pneumoniae. Abstracts of the General Meeting of the American Society for Microbiology 93: 108

Voets, T.; Buyse, G.; Droogmans, G.; Eggermont, J.; Nilius, B. 1998: Mutation of the putative nucleotide-binding site of pICln does not alter the nucleotide sensitivity and Ca2+ dependence of the chloride current ICln after expression in Xenopus oocytes. Journal of Physiology (Cambridge) 506P: 47P

Steiner, M.S.; Anthony, C.T.; Moses, H.L. 1994: Mutation of the retinoblastoma susceptibility protein correlates with resistance to TGF-beta inhibition in prostate cancer. Proceedings of the American Association for Cancer Research Annual Meeting 35: 127

Qi, J.; Qian, Q.; Bu, Q.; Li, S.; Chen, Q.; Sun, J.; Liang, W.; Zhou, Y.; Chu, C.; Li, X.; Ren, F.; Palme, K.; Zhao, B.; Chen, J.; Chen, M.; Li, C. 2008: Mutation of the rice Narrow leaf1 gene, which encodes a novel protein, affects vein patterning and polar auxin transport. Plant Physiology 147(4): 1947-1959

Sturm, N.R.; Fleischmann, J.; Campbell, D.A. 1997: Mutation of the spliced leader RNA gene affects transcript termination, processing and trans-splicing in Leishmania tarentolae. Memorias do Instituto Oswaldo Cruz 92(Suppl 1): 174

Ono, K.; Tomasiewicz, H.; Magnuson, T.; Rutishauser, U. 1994: Mutation of the subependymal layer in the NCAM-180 deficient mouse and its phenocopy by enzymatic removal of polysialic acid. Society for Neuroscience Abstracts 20(1-2): 1491

Rothstein, R.; Gangloff, S.; Bailis, A.; Rolfe, M.; Arthur, L. 1991: Mutation of the top3 gene from saccharomyces cerevisiae which encodes a bacterial like type i topoisomerase causes hyper recombination and genomic rearrangements. Journal of Cellular Biochemistry Suppl (15 Part D): 87

Erdman, S.H.; Wu, D.H.; Ahnen, D.J.; Hixson, L.; Gerner, E.W. 1994: Mutation of the tumor suppressor gene p53 in dimethylhydrazine induced rat colon adenocarcinomas. Gastroenterology 106(4 Suppl): A383

Gottlieb, T.; Kruppa, J.; Kruppa, A.; Adesnik, M.; Sabatini, D. 1992: Mutation of the tyrosine-containing endocytic signal in the VSV G protein impairs basolateral but not apical endocytosis in MDCK cells. Molecular Biology of the Cell 3(Suppl ): 303A

Burgess, D.L.; Jones, J.M.; Meisler, M.H.; Zilinski, C.A.; Noebels, J.L. 1997: Mutation of the voltage-dependent calcium channel beta subunit gene Cchb4 is associated with absence seizures and ataxia in the lethargic mouse. Epilepsia 38(Suppl 8): 126

Suzuki, Y.; Tamura, G.; Sakata, K.; Maesawa, C.; Fujioka, T.; Satodate, R. 1995: Mutation of the von Hippel-Lindau disease gene in human renal cell carcinoma. Proceedings of the American Association for Cancer Research Annual Meeting 36: 584

Brownlie, A.; Donovan, A.; Paw, B.; Ransom, D.; Witkowska, H.E.; Zon, L.I. 1997: Mutation of the zebrafish genes sauternes and chardonnay causes identical defects in globin chain expression. Blood 90(10 Suppl 1 Pt 1): 275A

Storey, A.; Almond, N.; Crawford, L. 1989: Mutation of the zinc finger of hpv16 e7 does not abolish co transformation with ras. Journal of Cellular Biochemistry Suppl (13 Part C): 215

Friebe, A.; Wedel, B.; Harteneck, C.; Schultz, G.; Koesling, D. 1996: Mutation of two cysteines of the beta subunit of soluble guanylyl cyclase yields NO-insensitive enzymes. Naunyn-Schmiedeberg's Archives of Pharmacology 353(4): R35

Niitsu, Y.; Sakamaki, S.; Kuroda, H.; Matsunaga, T.; Hirayama, Y.; Kusakabe, T.; Akiyama, T.; Sasaki, K. 1998: Mutation of type II TGF-beta receptor gene in patients with essential thrombocythemia may cause an escape from suppression of megakaryopoiesis by TGF-beta. Blood 92(10 Suppl 1 Part 1-2): 422A-423A

Nakamori, S.; Shimada, M.; Tamura, S.; Kameyama, M.; Yasuda, T.; Hiratsuka, M.; Kabuto, T.; Furkukawa, H.; Imaoka, S. 1997: Mutation of type II transforming growth factor beta receptor gene is uncommon in sporadic colorectal cancer and independent of loss of heterozygosity. Gastroenterology 112(4 Suppl): A624

Patel, P.S.; Rose, P.M.; Krystek, S.; Fisher, S.M.; Lach, D.A.; Liu, E.; Lynch, J.S.; Webb, M. 1994: Mutation of tyrosine 129 of the endothelin subtype a receptor confers subtype B receptor -like binding. FASEB Journal 8(4-5): A388

Das, T.K.; Pecoraro, C.; Tomson, F.L.; Gennis, R.B.; Rousseau, D.L. 1998: Mutation of tyrosine-288 located near the binuclear center impairs electron transfer in cytochrome C oxidase. Biophysical Journal 74(2 Part 2): A146

Valiquette, M.; Bonin, H.; Bouvier, M. 1992: Mutation of tyrosine-350 impairs the coupling of beta-2-adrenergic receptor to Gs without interfering with normal receptor down-regulation. Molecular Biology of the Cell 3(Suppl ): 244A

Fang, F.; Ahmad, S.; Lei, J.; Smithgall, T.E.; Glazer, R.I. 1993: Mutation of tyrosine-713 in the p93-c-fes proto-oncogene tyrosine kinase attenuates some of its catalytic and myeloid differentiating activities. Proceedings of the American Association for Cancer Research Annual Meeting 34: 519

Knowlton, A.A.; Grenier, M.; Kirchhoff, S.R.; Salfity, M. 1998: Mutation of tyrosine524 alters HSP 72sS stress response and viability. Journal of Molecular and Cellular Cardiology 30(7): A264

Urakami, S.; Tokuzen, R.; Tsuda, H.; Igawa, M.; Hino, O. 1997: Mutation on the tuberous sclerosis gene in chemically induced rat renal cell carcinomas. Journal of Urology 157(4 Suppl): 106

Abraham, E.H.; Okunieff, P.; Ding, I.; Kahn, J.; Wood, K.; Grubman, S.A.; Jefferson, D.M. 1996: Mutation or knockout of the cystic fibrosis gene inhibits breast cancer growth through modulation of extracellular ATP. Proceedings of the American Association for Cancer Research Annual Meeting 37: 569-570

Santos, C.; Montiel, R.; Arruda, A.; Alvarez, L.; Aluja, M.P.; Lima, M. 2008: Mutation patterns of mtDNA: empirical inferences for the coding region. Bmc Evolutionary Biology 8: 167

Osterholm, A.M.; Podlutsky, A.; Hou, S.M.; Lambert, B. 1997: Mutation profile at the HPRT locus in T-cells by healthy non-smoking males. Mutation Research 379(1 Suppl 1): S79

Wei, S.C.; Chang, R.L.; Hennig, E.; Merkler, K.; Cui, X.; Wong, C.Q.; Yagi, H.; Sayer, J.M.; Jerina, D.M.; Conney, A.H. 1993: Mutation profile induced by -7S,8R-dihydroxy-9R,10S-epoxy-7,8,9,10-tetrahydrobenzo pyrene in Chinese hamster V-79 cells. Proceedings of the American Association for Cancer Research Annual Meeting 34: 130

Gumerlock, P.H.; Devere White, R.W.; Chi, S.G.; Meyers, F.; Lee, F.; Siders, D.B. 1994: Mutation rate of p53 in prostate cancer and benign prostatic hypertrophy. Journal of Urology 151(5 Suppl): 470A

Quillardet, P. 1990: Mutation rate, transcription and gene position. Research in Microbiology 141(4): 403-405

Woodruff, R.C.; ThompsonJ.N.Jr.; Huai, H. 1997: Mutation rate vs genetic damage rate The influence of premeiotic clusters of mutation on our view of genetic damage. Environmental and Molecular Mutagenesis 29(Suppl 28): 57

Jaffrezou, J.P.; Chen, G.; Duran, G.E.; Ross, K.; Sikic, B.I. 1993: Mutation rates and mechanisms of resistance to etoposide, determined from Luria-Delbruck fluctuation analysis. Proceedings of the American Association for Cancer Research Annual Meeting 34: 329

Domingo, E.; Holland, J.J. 1994: Mutation rates and rapid evolution of RNA viruses. Morse, S S The evolutionary biology of viruses 161-184

Andersson, D.I.; Hughes, D. 1997: Mutation rates in Salmonella typhimurium during starvation. Abstracts of the General Meeting of the American Society for Microbiology 97: 362

Drost, J.B. 1990: Mutation rates in metazoa and their relationship to germ line characteristics. 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 : 55

Kowalchuk, G.; Houghton, J.E.; Ornston, L.N. 1992: Mutation repair and codon usage in catc the structural gene for muconolactone isomerase in pseudomonas putida. Abstracts of the General Meeting of the American Society for Microbiology 92: 212

Carrano, A.V. 1997: Mutation research genomics: a blending two of disciplines. Mutation Research 382(1-2): 1-4

Shah, M.; Coon, H.; Holik, J.; Hoff, M.; Helmer, V.; Panos, P.; Byerley, W. 1995: Mutation scan of the D1 dopamine receptor gene in 22 cases of bipolar i disorder. American Journal of Medical Genetics 60(2): 150-153

Shah, M.; Hoff, M.; Holik, J.; Coon, H.; Byerley, W. 1994: Mutation scan of the D1 dopamine receptor gene in 22 cases of manic-depression. Clinical Research 42(1): 78A

Larsen, Z.M.; Johannesen, J.; Kristiansen, O.P.; Nerup, J.; Pociot, F. 1998: Mutation scanning of an IDDM candidate gene, galectin-3. Diabetologia 41(Suppl 1): A81