Section 41

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Lambden, P.R.; Guest, J.R. 1976: Mutants of Escherichia coli K12 unable to use fumarate as an anaerobic electron acceptor. Journal of General Microbiology 97(2): 145-160
Whitfield, C.; Schoenhals, G.; Graham, L. 1989: Mutants of Escherichia coli O9:K30 with altered synthesis and expression of the capsular K30 antigen. Journal of General Microbiology 135(10): 2589-2599
Clark, D.P.; Cunningham, P.R.; Reams, S.G.; Mat-Jan, F.; Mohammedkhani, R.; Williams, C.R. 1988: Mutants of Escherichia coli defective in acid fermentation. Applied Biochemistry and Biotechnology 17: 163-173
McIntyre, T.M.; Bell, R.M. 1975: Mutants of Escherichia coli defective in membrane phospholipid synthesis. Effect of cessation of net phospholipid synthesis on cytoplasmic and outer membranes. Journal of Biological Chemistry 250(23): 9053-9059
McIntyre, T.M.; Chamberlain, B.K.; Webster, R.E.; Bell, R.M. 1977: Mutants of Escherichia coli defective in membrane phospholipid synthesis. Effects of cessation and reinitiation of phospholipid synthesis on macromolecular synthesis and phospholipid turnover. Journal of Biological Chemistry 252(13): 4487-4493
Bell, R.M.; Cronan, J.E. 1975: Mutants of Escherichia coli defective in membrane phospholipid synthesis. Phenotypic suppression of sn-glycerol-3-phosphate acyltransferase Km mutants by loss of feedback inhibition of the biosynthetic sn-glycerol-3-phosphate dehydrogenase. Journal of Biological Chemistry 250(18): 7153-7158
Bell, R.M. 1975: Mutants of Escherichia coli defective in membrane phospholipid synthesis. Properties of wild type and Km defective sn-glycerol-3-phosphate acyltransferase activities. Journal of Biological Chemistry 250(18): 7147-7152
Somerville, C.R.; Ahmed, A. 1979: Mutants of Escherichia coli defective in the degradation of guanosine 5'-triphosphate, 3'-diphosphate (pppGpp). Molecular and General Genetics: Mgg 169(3): 315-323
Thomas, G.; Favre, A. 1977: Mutants of Escherichia coli deficient in 4-thiouridine in which growth is insensitive to illumination at 365 nm. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences. Serie D: Sciences Naturelles 284(14): 1345-1347
Markiewicz, Z.; Kwiatkowski, Z. 1975: Mutants of Escherichia coli excreting deoxyribonucleases. Acta Microbiologica Polonica. Series A: Microbiologia Generalis 7(2): 107-111
Seong, B.L.; RajBhandary, U.L. 1987: Mutants of Escherichia coli formylmethionine tRNA: a single base change enables initiator tRNA to act as an elongator in vitro. Proceedings of the National Academy of Sciences of the United States of America 84(24): 8859-8863
Matsuhashi, M.; Takagaki, Y.; Maruyama, I.N.; Tamaki, S.; Nishimura, Y.; Suzuki, H.; Ogino, U.; Hirota, Y. 1977: Mutants of Escherichia coli lacking in highly penicillin-sensitive D-alanine carboxypeptidase activity. Proceedings of the National Academy of Sciences of the United States of America 74(7): 2976-2979
Hafner, E.W.; Tabor, C.W.; Tabor, H. 1979: Mutants of Escherichia coli that do not contain 1,4-diaminobutane (putrescine) or spermidine. Journal of Biological Chemistry 254(24): 12419-12426
Hidaka, S.; Matsubara, K. 1975: Mutants of Escherichia coli which block head formation of lambda. Japanese Journal of Microbiology 19(5): 363-371
Spratt, B.G.; Jobanputra, V. 1977: Mutants of Escherichia coli which lack a component of penicillin-binding protein 1 are viable. Febs Letters 79(2): 374-378
Beacham, I.R.; Haas, D.; Yagil, E. 1977: Mutants of Escherichia coli "cryptic" for certain periplasmic enzymes: evidence for an alteration of the outer membrane. Journal of Bacteriology 129(2): 1034-1044
Gill, G.; Ptashne, M. 1987: Mutants of GAL4 protein altered in an activation function. Cell 51(1): 121-126
Michaeli, T.; Field, J.; Ballester, R.; O'Neill, K.; Wigler, M. 1989: Mutants of H-ras that interfere with RAS effector function in Saccharomyces cerevisiae. EMBO Journal 8(10): 3039-3044
Sibirnyĭ, A.A.; Shavlovskiĭ, G.M.; Goloshchapova, G.V. 1977: Mutants of Pichia guilliermondii yeasts with multiple sensitivity to antibiotics and antimetabolites. I. The selection and properties of the mutants. Genetika 13(5): 872-879
Lehrbach, P.R.; Kung, A.H.; Lee, B.T. 1976: Mutants of Pseudomonas aeruginosa deficient in DNA polymerase i. Mutation Research 41(2-3): 391-394
Mills, B.J.; Holloway, B.W. 1976: Mutants of Pseudomonas aeruginosa that show specific hypersensitivity to aminoglycosides. Antimicrobial Agents and ChemoTherapy 10(3): 411-416
Jones, M.R.; Fowler, G.J.; Gibson, L.C.; Grief, G.G.; Olsen, J.D.; Crielaard, W.; Hunter, C.N. 1992: Mutants of Rhodobacter sphaeroides lacking one or more pigment-protein complexes and complementation with reaction-centre, LH1, and LH2 genes. Molecular Microbiology 6(9): 1173-1184
Martin, G.S.; Radke, K.; Hughes, S.; Quintrell, N.; Bishop, J.M.; Varmus, H.E. 1979: Mutants of Rous sarcoma virus with extensive deletions of the viral genome. Virology 96(2): 530-546
Sleigh, M.J.; Topp, W.C.; Hanich, R.; Sambrook, J.F. 1978: Mutants of SV40 with an altered small t protein are reduced in their ability to transform cells. Cell 14(1): 79-88
Ivanov, E.L.; Koval'tsova, S.V.; Korolev, V.G. 1987: Mutants of Saccharomyces cerevisiae characterized by increased level of induced mutagenesis. I. Isolation and preliminary characterization of mutants. Genetika 23(5): 784-792
Hjelmstad, R.H.; Bell, R.M. 1987: Mutants of Saccharomyces cerevisiae defective in sn-1,2-diacylglycerol cholinephosphotransferase. Isolation, characterization, and cloning of the CPT1 gene. Journal of Biological Chemistry 262(8): 3909-3917
Tillman, T.S.; Bell, R.M. 1986: Mutants of Saccharomyces cerevisiae defective in sn-glycerol-3-phosphate acyltransferase. Simultaneous loss of dihydroxyacetone phosphate acyltransferase indicates a common gene. Journal of Biological Chemistry 261(20): 9144-9149
Sahota, A.; Ranjekar, P.K.; Alfonzo, J.; Lewin, A.S.; Taylor, M.W. 1987: Mutants of Saccharomyces cerevisiae deficient in adenine phosphoribosyltransferase. Mutation Research 180(1): 81-87
Cooper, T.G. 1978: Mutants of Saccharomyces cerevisiae possessing fully induced levels of urea amido-lyase in the absence of added inducer. Biochemical and Biophysical Research Communications 82(4): 1258-1263
Zimmermann, F.K.; Scheel, I. 1977: Mutants of Saccharomyces cerevisiae resistant to carbon catabolite repression. Molecular and General Genetics: Mgg 154(1): 75-82
Pavlov, I.I. 1986: Mutants of Saccharomyces cerevisiae supersensitive to the mutagenic effect of 6-N-hydroxylaminopurine. Genetika 22(9): 2235-2243
Wickner, R.B. 1975: Mutants of Saccharomyces cerevisiae that incorporate deoxythymidine 5'-monophosphate into DNA in vivo. Methods in Cell Biology 11: 295-302
MacPhee, D.G.; Beazer, M.R. 1975: Mutants of Salmonella typhimurium deficient in DNA polymerase I: further characterization and genetic analysis. Australian Journal of Biological Sciences 28(5-6): 559-565
Miller, C.G.; Heiman, C.; Yen, C. 1976: Mutants of Salmonella typhimurium deficient in an endoprotease. Journal of Bacteriology 127(1): 490-497
Fields, P.I.; Swanson, R.V.; Haidaris, C.G.; Heffron, F. 1986: Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent. Proceedings of the National Academy of Sciences of the United States of America 83(14): 5189-5193
Winkler, U.; Scholle, H.; Bohne, L. 1975: Mutants of Serratia marcescens lacking cyclic nucleotide phosphodiesterase activity and requiring cyclic 3',5'-AMP for the utilization of various carbohydrates. Archives of Microbiology 104(2): 189-196
Strauss, E.G. 1978: Mutants of Sindbis virus. III. Host polypeptides present in purified HR and ts103 virus particles. Journal of Virology 28(2): 466-474
Goering, R.V. 1979: Mutants of Staphylococcus aureus deficient in recombinational repair. Improved isolation by selecting for mutants exhibiting concurrent sensitivity to ultraviolet radiation and N-methyl-N'-nitro-N-nitrosoguanidine. Mutation Research 60(3): 279-289
Haisman, R.J.; Jenkinson, H.F. 1991: Mutants of Streptococcus gordonii Challis over-producing glucosyltransferase. Journal of General Microbiology 137(3): 483-489
García, P.; García, E.; Ronda, C.; Lopez, R.; Jiang, R.Z.; Tomasz, A. 1986: Mutants of Streptococcus pneumoniae that contain a temperature-sensitive autolysin. Journal of General Microbiology 132(5): 1401-1405
Pao, C.C.; Speyer, J.F. 1975: Mutants of T7 bacteriophage inhibited by lambda prophage. Proceedings of the National Academy of Sciences of the United States of America 72(9): 3642-3646
Droin, A. 1991: Mutants of Xenopus laevis. Methods in Cell Biology 36: 671-673
Breuning, A.; Müller, K.; Scholtissek, C. 1987: Mutants of an influenza a reassortant which are cold-sensitive (cs) as well as temperature-sensitive (ts): on the role of the neuraminidase activity for influenza virus infection. Virology 156(1): 101-106
Sirtori, C.R.; Lovati, M.R. 1986: Mutants of apolipoproteins a and C. Verhandlungen der Deutschen Gesellschaft für Innere Medizin 92: 403-412
Snustad, D.P.; Bursch, C.J.; Parson, K.A.; Hefeneider, S.H. 1976: Mutants of bacteriophage T4 deficient in the ability to induce nuclear disruption: shutoff of host DNA and protein synthesis gene dosage experiments, identification of a restrictive host, and possible biological significance. Journal of Virology 18(1): 268-288
Pees, E.; de Groot, B. 1975: Mutants of bacteriophage T4 unable to exclude T2 from the progeny of crosses. Virology 67(1): 94-106
Molineux, I.J.; Schmitt, C.K.; Condreay, J.P. 1989: Mutants of bacteriophage T7 that escape F restriction. Journal of Molecular Biology 207(3): 563-574
Mathias, P.; Carrillo, C.J.; Zepf, N.E.; Cooper, N.R.; Ogata, R.T. 1992: Mutants of complement component C3 cleaved by the C4-specific C1-s protease. Proceedings of the National Academy of Sciences of the United States of America 89(17): 8125-8129
Nakano, E. 1992: Mutants of firefly luciferase which produce different colors of light. Tanpakushitsu Kakusan Koso. Protein Nucleic Acid Enzyme 37(3 Suppl): 205-207
McKenzie, K.Q.; Jones, E.W. 1977: Mutants of formyltetrahydrofolate interconversion pathway of Saccharomyces cerevisiae. Genetics 86(1): 85-102
Hay, J.; Subak-Sharpe, J.H. 1976: Mutants of herpes simplex virus types 1 and 2 that are resistant to phosphonoacetic acid induce altered DNA polymerase activities in infected cells. Journal of General Virology 31(1): 145-148
Cascieri, M.A.; Chicchi, G.G.; Applebaum, J.; Hayes, N.S.; Green, B.G.; Bayne, M.L. 1988: Mutants of human insulin-like growth factor i with reduced affinity for the type 1 insulin-like growth factor receptor. Biochemistry 27(9): 3229-3233
Lüthi, C.; Roth, B.V.; Humbel, R.E. 1992: Mutants of human insulin-like growth factor Ii (IGF II). Expression and characterization of truncated IGF Ii and of two naturally occurring variants. European Journal of Biochemistry 205(2): 483-490
Roth, B.V.; Bürgisser, D.M.; Lüthi, C.; Humbel, R.E. 1991: Mutants of human insulin-like growth factor II: expression and characterization of analogs with a substitution of TYR27 and/or a deletion of residues 62-67. Biochemical and Biophysical Research Communications 181(2): 907-914
Varshney, U.; Lee, C.P.; Seong, B.L.; RajBhandary, U.L. 1991: Mutants of initiator tRNA that function both as initiators and elongators. Journal of Biological Chemistry 266(27): 18018-18024
Pouysségur, J.; Pastan, I. 1977: Mutants of mouse fibroblasts altered in the synthesis of cell surface glycoproteins. Preliminary evidence for a defect in the acetylation of glucosamine 6-phosphate. Journal of Biological Chemistry 252(5): 1639-1646
Chalupová, V.; Lenhart, K.; Kunert, J.; Lýsek, H. 1987: Mutants of ovicidal fungus Verticillium chlamydosporium with changed chitinolytic activity. Acta Universitatis Palackianae Olomucensis Facultatis Medicae 116: 71-79
Pages, D.; Buckingham, R.H. 1990: Mutants of pheV in Escherichia coli affecting control by attenuation of the pheS, T and pheA operons. two distinct mechanisms for de-attenuation. Journal of Molecular Biology 216(1): 17-24
Boronin, A.M.; Borisoglebskaia, A.N.; Starovoĭtov, I.I. 1977: Mutants of plasmid NPL-1, controlling the oxidation of naphthalene. Doklady Akademii Nauk SSSR 235(2): 494-496
Markland, W.; Smith, A.E. 1987: Mutants of polyomavirus middle-T antigen. Biochimica et Biophysica Acta 907(3): 299-321
Shortle, D.; Nathans, D. 1979: Mutants of simian virus 40 with base substitutions at the origin of DNA replication. Cold Spring Harbor Symposia on Quantitative Biology 43 Pt 2: 663-668
Ankenbauer, R.G.; Best, E.A.; Palanca, C.A.; Nester, E.W. 1991: Mutants of the Agrobacterium tumefaciens virA gene exhibiting acetosyringone-independent expression of the vir regulon. Molecular Plant-Microbe Interactions: Mpmi 4(4): 400-406
Andreoli, P.M.; Nijkamp, H.J. 1976: Mutants of the Clo DF13 plasmid in Escherichia coli with a decreased bacteriocinogenic activity. Molecular and General Genetics: Mgg 144(2): 159-170
Heitman, J.; Model, P. 1990: Mutants of the EcoRI endonuclease with promiscuous substrate specificity implicate residues involved in substrate recognition. EMBO Journal 9(10): 3369-3378
Payne, D.J.; Marriott, M.S.; Amyes, S.G. 1989: Mutants of the TEM-1 beta-lactamase conferring resistance to ceftazidime. Journal of Antimicrobial ChemoTherapy 24(2): 103-110
Irwin, N.; Ptashne, M. 1987: Mutants of the catabolite activator protein of Escherichia coli that are specifically deficient in the gene-activation function. Proceedings of the National Academy of Sciences of the United States of America 84(23): 8315-8319
Vijgenboom, E.; Vink, T.; Kraal, B.; Bosch, L. 1985: Mutants of the elongation factor EF-Tu, a new class of nonsense suppressors. EMBO Journal 4(4): 1049-1052
Ashton-Rickardt, P.G.; Murray, K. 1989: Mutants of the hepatitis B virus surface antigen that define some antigenically essential residues in the immunodominant a region. Journal of Medical Virology 29(3): 196-203
Wickner, R.B. 1976: Mutants of the killer plasmid of Saccharomyces cerevisiae dependent on chromosomal diploidy for expression and maintenance. Genetics 82(2): 273-285
Cutler, D.F.; Garoff, H. 1986: Mutants of the membrane-binding region of Semliki Forest virus E2 protein. I. Cell surface transport and fusogenic activity. Journal of Cell Biology 102(3): 889-901
Cutler, D.F.; Melancon, P.; Garoff, H. 1986: Mutants of the membrane-binding region of Semliki Forest virus E2 protein. II. Topology and membrane binding. Journal of Cell Biology 102(3): 902-910
Eichenlaub, R. 1979: Mutants of the mini-F plasmid pML31 thermosensitive in replication. Journal of Bacteriology 138(2): 559-566
Rodina, N.E.; Karbysheva, E.A.; Kameneva, S.V. 1988: Mutants of the phototrophic bacteria Rhodobacter sphaeroides sensitive to the mutagenic action of long-wave ultraviolet light. Nauchnye Doklady Vysshei Shkoly. Biologicheskie Nauki 5: 83-88
Temiralieva, G.A. 1977: Mutants of the plaque microbe defective in the dark repair system. Genetika 13(3): 518-523
Kulakova, A.N.; Boronin, A.M. 1989: Mutants of the plasmid for biodegradation of naphthalene, determining catechol oxidation via the meta-pathway. Mikrobiologiia 58(2): 298-304
Ivanov, E.L.; Koval'tsova, S.V.; Korolev, V.G. 1987: Mutants of the yeast Saccharomyces cerevisiae characterized by enhanced induced mutagenesis. III. Effect of the him mutation on the effectiveness and specificity of UF-induced mutagenesis. Genetika 23(9): 1555-1563
Robertson, D.E.; Daldal, F.; Dutton, P.L. 1990: Mutants of ubiquinol-cytochrome c2 oxidoreductase resistant to Qo site inhibitors: consequences for ubiquinone and ubiquinol affinity and catalysis. Biochemistry 29(51): 11249-11260
Johnston, L.H.; Game, J.C. 1978: Mutants of yeast with depressed DNA synthesis. Molecular and General Genetics: Mgg 161(2): 205-214
Smith, J.D. 1975: Mutants which allows accumulation of tRNATyr precursor molecules. Brookhaven Symposia in Biology 26: 1-11
Rottmann, N.; Kleuvers, B.; Atmadja, J.; Wagner, R. 1988: Mutants with base changes at the 3'-end of the 16S RNA from Escherichia coli. Construction, expression and functional analysis. European Journal of Biochemistry 177(1): 81-90
Kimura, K.; Tanimura, T. 1992: Mutants with delayed cell death of the ptilinal head muscles in Drosophila. Journal of Neurogenetics 8(2): 57-69
Cueto, P.H.; Giulietti, A.M.; dos Santos, C.; Méndez, B.S. 1990: Mutants with high butanol production from a strain of solventogenic Clostridium isolated from olive black-water. Revista Argentina de Microbiologia 22(2): 57-61
Kuchel, P.W.; Bulliman, B.T.; Chapman, B.E. 1988: Mutarotase equilibrium exchange kinetics studied by 13C-NMR. Biophysical Chemistry 32(1): 89-95
Okuda, J.; Taguchi, T.; Tomimura, A. 1987: Mutarotation of D-glucose in body fluids and perfused rat liver. Chemical and Pharmaceutical Bulletin 35(10): 4332-4337
Paine, T.M.; Fontanini, G.; Basolo, F.; Geronimo, I.; Elliott, J.W.; Russo, J. 1992: Mutated c-Ha-ras oncogene alters cytokeratin expression in the human breast epithelial cell line MCF-10A. American Journal of Pathology 140(6): 1483-1488
McKenzie, A.N.; Ely, B.; Sanderson, C.J. 1991: Mutated interleukin-5 monomers are biologically inactive. Molecular Immunology 28(1-2): 155-158
Broxmeyer, H.E.; Cooper, S.; Levi, S.; Arosio, P. 1991: Mutated recombinant human heavy-chain ferritins and myelosuppression in vitro and in vivo: a link between ferritin ferroxidase activity and biological function. Proceedings of the National Academy of Sciences of the United States of America 88(3): 770-774
Jupp, R.A.; Phylip, L.H.; Mills, J.S.; Le Grice, S.F.; Kay, J. 1991: Mutating P2 and P1 residues at cleavage junctions in the HIV-1 pol polyprotein. Effects on hydrolysis by HIV-1 proteinase. Febs Letters 283(2): 180-184
Shabb, J.B.; Buzzeo, B.D.; Ng, L.; Corbin, J.D. 1991: Mutating protein kinase cAMP-binding sites into cGMP-binding sites. Mechanism of cGMP selectivity. Journal of Biological Chemistry 266(36): 24320-24326
Zhang, J.; Liu, Z.P.; Jones, T.A.; Gierasch, L.M.; Sambrook, J.F. 1992: Mutating the charged residues in the binding pocket of cellular retinoic acid-binding protein simultaneously reduces its binding affinity to retinoic acid and increases its thermostability. Proteins 13(2): 87-99
Crotty, P.L.; Braun, S.E.; Anderson, R.A.; Whitley, C.B. 1992: Mutation R468W of the iduronate-2-sulfatase gene in mild Hunter syndrome (mucopolysaccharidosis type II) confirmed by in vitro mutagenesis and expression. Human Molecular Genetics 1(9): 755-757
Anonymous 1990: Mutation Research. Annual cumulative index. Vol. 228-245 (1990). Mutation research 1990: 1-49
Jackson, J.H.; Henderson, E.K. 1975: Mutation affecting regulation of synthesis of acetohydroxy acid synthetase in Escherichia coli K-12. Journal of Bacteriology 121(2): 504-510
Hrebenda, J.; Heleszko, H.; Brzostek, K.; Bielecki, J. 1985: Mutation affecting resistance of Escherichia coli K12 to nalidixic acid. Journal of General Microbiology 131(9): 2285-2292
Ramos, F.; Wiame, J.M. 1985: Mutation affecting the specific regulatory control of lysine biosynthetic enzymes in Saccharomyces cerevisiae. Molecular and General Genetics: Mgg 200(2): 291-294
Gross, C.; Hoffman, J.; Ward, C.; Hager, D.; Burdick, G.; Berger, H.; Burgess, R. 1978: Mutation affecting thermostability of sigma subunit of Escherichia coli RNA polymerase lies near the dnaG locus at about 66 min on the E. coli genetic map. Proceedings of the National Academy of Sciences of the United States of America 75(1): 427-431
Marcus, S.; Steen, A.M.; Andersson, B.; Lambert, B.; Kristoffersson, U.; Francke, U. 1992: Mutation analysis and prenatal diagnosis in a Lesch-Nyhan family showing non-random X-inactivation interfering with carrier detection tests. Human Genetics 89(4): 395-400
Harris, A.; Beards, F.; Mathew, C. 1990: Mutation analysis at the cystic fibrosis locus in the British population. Human Genetics 85(4): 408-409
Beaudet, A.L.; Feldman, G.L.; Kobayashi, K.; Lemna, W.K.; Fernbach, S.D.; Knowles, M.R.; Boucher, R.C.; O'Brien, W.E. 1991: Mutation analysis for cystic fibrosis in a North American population. Advances in Experimental Medicine and Biology 290: 53-54
Dahl, N.; Wadelius, C.; Annerén, G.; Gustavson, K.H. 1992: Mutation analysis for prenatal diagnosis and heterozygote detection of Gaucher disease type IIi (Norrbottnian type). Prenatal Diagnosis 12(7): 603-608
Beutler, E.; Gelbart, T. 1992: Mutation analysis in Gaucher disease. American Journal of Medical Genetics 44(3): 389-390
Eigel, A.; Schnee, J.; Oehme, R.; Horst, J. 1989: Mutation analysis of beta-thalassemia genes in a German family reveals a rare transversion in the first intron. Human Genetics 81(4): 371-372
Lázaro, C.; Estivill, X. 1992: Mutation analysis of genetic diseases by asymmetric-PCR SSCP and ethidium bromide staining: application to neurofibromatosis and cystic fibrosis. Molecular and Cellular Probes 6(5): 357-359
Beutler, E.; Kuhl, W.; Sáenz, G.F.; Rodríguez, W. 1991: Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica. Human Genetics 87(4): 462-464
Pérez, B.; Desviat, L.R.; Die, M.; Ugarte, M. 1992: Mutation analysis of phenylketonuria in Spain: prevalence of two Mediterranean mutations. Human Genetics 89(3): 341-342
Senn, H.P.; Trân-Thang, C.; Wodnar-Filipowicz, A.; Jiricny, J.; Fopp, M.; Gratwohl, A.; Signer, E.; Weber, W.; Moroni, C. 1988: Mutation analysis of the N-ras proto-oncogene in active and remission phase of human acute leukemias. International Journal of Cancer 41(1): 59-64
Smarda, J.; Sevcíková, I. 1988: Mutation analysis of the receptor for colicins E1-E7. a pilot study. Folia Microbiologica 33(1): 59-67
Jiménez-Sánchez, A.; Cerdá-Olmedo, E. 1975: Mutation and DNA replication in Escherichia coli treated with low concentrations of N-methyl-N'-nitro-N-nitrosoguanidine. Mutation Research 28(3): 337-345
Kondo, S. 1988: Mutation and cancer in relation to the atomic-bomb radiation effects. Japanese Journal of Cancer Research: Gann 79(7): 785-799
Knudson, A.G.; Hethcote, H.W.; Brown, B.W. 1975: Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma. Proceedings of the National Academy of Sciences of the United States of America 72(12): 5116-5120
Paulus, T.J.; Tuan, J.S.; Luebke, V.E.; Maine, G.T.; DeWitt, J.P.; Katz, L. 1990: Mutation and cloning of eryG, the structural gene for erythromycin O-methyltransferase from Saccharopolyspora erythraea, and expression of eryG in Escherichia coli. Journal of Bacteriology 172(5): 2541-2546
Cox, R.; Masson, W.K. 1979: Mutation and inactivation of cultured mammalian cells exposed to beams of accelerated heavy ions. III. Human diploid fibroblasts. International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine 36(2): 149-160
Abbondandolo, A. 1975: Mutation and nuclear stage in Schizosaccharomyces pombe. I. An experimental approach to the role of recombination in mutation induction. Mutation Research 27(2): 225-233
Crow, T.J. 1987: Mutation and psychosis: a suggested explanation of seasonality of birth. Psychological Medicine 17(4): 821-828
Rada, C.; Gupta, S.K.; Gherardi, E.; Milstein, C. 1991: Mutation and selection during the secondary response to 2-phenyloxazolone. Proceedings of the National Academy of Sciences of the United States of America 88(13): 5508-5512
Thilly, W.G.; DeLuca, J.G.; Hoppe, H.; Liber, H.L.; Penman, B.W. 1977: Mutation assay in diploid human lymphoblasts: methodological aspects. Journal of Environmental Pathology and Toxicology 1(2): 91-99
O'Donovan, M.R. 1990: Mutation assays of ethyl methanesulphonate, benzidine and benzo[a]pyrene using Chinese hamster V79 cells. Mutagenesis 5 Suppl: 9-13
Christadoss, P.; Lindstrom, J.M.; Melvold, R.W.; Talal, N. 1985: Mutation at I-A beta chain prevents experimental autoimmune myasthenia gravis. Immunogenetics 21(1): 33-38
Rubocki, R.J.; Connolly, J.M.; Hansen, T.H.; Melvold, R.W.; Kim, B.S.; Hildebrand, W.H.; Martinko, J. 1991: Mutation at amino acid position 133 of H-2Dd prevents beta 2m association and immune recognition but not surface expression. Journal of Immunology 146(7): 2352-2357
Tapprich, W.E.; Goss, D.J.; Dahlberg, A.E. 1989: Mutation at position 791 in Escherichia coli 16S ribosomal RNA affects processes involved in the initiation of protein synthesis. Proceedings of the National Academy of Sciences of the United States of America 86(13): 4927-4931
Burgess, J.A.; Stevens, C.W.; Fahl, W.E. 1985: Mutation at separate gene loci in Salmonella typhimurium TA100 related to DNA nucleotide modification by stereoisomeric benzo(a)pyrene 7,8-diol-9,10-epoxides. Cancer Research 45(9): 4257-4262
McKenna, P.G.; Ward, P.E. 1987: Mutation at the APRT locus in Friend erythroleukaemia cells. 1. Mutation rates and properties of mutants. Mutation Research 180(2): 267-271
Kuchka, M.R.; Goldschmidt-Clermont, M.; van Dillewijn, J.; Rochaix, J.D. 1989: Mutation at the Chlamydomonas nuclear NAC2 locus specifically affects stability of the chloroplast psbD transcript encoding polypeptide D2 of PS Ii. Cell 58(5): 869-876
Liber, H.L.; Yandell, D.W.; Little, J.B. 1989: A comparison of mutation induction at the tk and hprt loci in human lymphoblastoid cells; quantitative differences are due to an additional class of mutations at the autosomal tk locus. Mutation Research 216(1): 9-17
Zuber, P.; Healy, J.; Carter, H.L.; Cutting, S.; Moran, C.P.; Losick, R. 1989: Mutation changing the specificity of an RNA polymerase sigma factor. Journal of Molecular Biology 206(4): 605-614
Nørby, S.; Lestienne, P.; Nelson, I.; Rosenberg, T. 1991: Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming. Biochemical and Biophysical Research Communications 175(2): 631-636
Anvret, M.; Lee, J.S.; Lundin, G. 1991: Mutation diagnosis is a possibility for the half of the families with acute intermittent porphyria. Lakartidningen 88(30-31): 2513-2514
Guo, X.C.; Cleaver, J.E. 1986: Mutation frequencies from X-rays, ultraviolet light, and methyl methanesulfonate in Chinese hamster ovary cells incubated with 3-aminobenzamide. Mutagenesis 1(4): 237-239
Lawrence, C.W.; Borden, A.; Banerjee, S.K.; LeClerc, J.E. 1990: Mutation frequency and spectrum resulting from a single abasic site in a single-stranded vector. Nucleic Acids Research 18(8): 2153-2157
Clarke, C.H.; Hill, R.F. 1976: Mutation frequency decline and the Clarke-Hill effect for UV-induced streptomycin-resistant mutations in an incision-defective E. coli strain. Mutation Research 41(2-3): 387-390
Bockrath, R.; Barlow, A.; Engstrom, J. 1987: Mutation frequency decline in Escherichia coli B/r after mutagenesis with ethyl methanesulfonate. Mutation Research 183(3): 241-247
Juutilainen, J.; Liimatainen, A. 1986: Mutation frequency in Salmonella exposed to weak 100-Hz magnetic fields. Hereditas 104(1): 145-147
Oyaide, K.; Sono, A.; Kobayashi, Y.; Yamamoto, H. 1986: Mutation frequency test for isepamicin (HAPA-B). Japanese Journal of Antibiotics 39(12): 3349-3352
Bol'shakova, T.N.; Erlagaeva, R.S.; Dobrynina, O.I.; Gershanovich, V.N. 1988: Mutation fruB in the fructose regulon affecting beta-galactosidase synthesis and adenylate cyclase activity of E. coli K12. Molekuliarnaia Genetika Mikrobiologiia i Virusologiia 3: 33-39
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Ohno, K.; Suzuki, K. 1988: Mutation in GM2-gangliosidosis B1 variant. Journal of Neurochemistry 50(1): 316-318
Lehrman, M.A.; Schneider, W.J.; Südhof, T.C.; Brown, M.S.; Goldstein, J.L.; Russell, D.W. 1985: Mutation in LDL receptor: Alu-Alu recombination deletes exons encoding transmembrane and cytoplasmic domains. Science 227(4683): 140-146
Essani, K.; Goorha, R.; Granoff, A. 1987: Mutation in a DNA-binding protein reveals an association between DNA-methyltransferase activity and a 26,000-Da polypeptide in frog virus 3-infected cells. Virology 161(1): 211-217
Holden, D.W.; Kronstad, J.W.; Leong, S.A. 1989: Mutation in a heat-regulated hsp70 gene of Ustilago maydis. EMBO Journal 8(7): 1927-1934
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Shinners, E.N.; Catlin, B.W. 1988: Mutation in a locus linked to penB-nmp causes suppression of the Mtr phenotype of Neisseria gonorrhoeae. Antimicrobial Agents and ChemoTherapy 32(7): 971-977
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Goldfarb, L.G.; Korczyn, A.D.; Brown, P.; Chapman, J.; Gajdusek, D.C. 1990: Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin. Lancet 336(8715): 637-638
Goldfarb, L.G.; Mitrová, E.; Brown, P.; Toh, B.K.; Gajdusek, D.C. 1990: Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia. Lancet 336(8713): 514-515
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Palsdottir, A.; Abrahamson, M.; Thorsteinsson, L.; Arnason, A.; Olafsson, I.; Grubb, A.; Jensson, O. 1988: Mutation in cystatin C gene causes hereditary brain haemorrhage. Lancet 2(8611): 603-604
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Ajlani, G.; Meyer, I.; Vernotte, C.; Astier, C. 1989: Mutation in phenol-type herbicide resistance maps within the psbA gene in Synechocystis 6714. Febs Letters 246(1-2): 207-210
Marshall, C.J. 1989: Mutation in ras proto-oncogenes and malignancy. Journal of Uoeh 11(Suppl): 398-405
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Amor, M.; Parker, K.L.; Globerman, H.; New, M.I.; White, P.C. 1988: Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. Proceedings of the National Academy of Sciences of the United States of America 85(5): 1600-1604
Lindler, L.E.; Anders, J.C.; Herman, W.E. 1991: Mutation in the Escherichia coli htpR locus results in stabilization of recombinant expression products that are susceptible to proteolytic degradation. Protein Expression and Purification 2(5-6): 321-329
Han, E.S.; Moyer, M.P.; Naylor, S.; Sakaguchi, A.Y. 1991: Mutation in the TP53 gene in colorectal carcinoma detected by polymerase chain reaction. Genes Chromosomes and Cancer 3(4): 313-317
Kanda, T.; Furuno, A.; Yoshiike, K. 1986: Mutation in the VP-1 gene is responsible for the extended host range of a monkey B-lymphotropic papovavirus mutant capable of growing in T-lymphoblastoid cells. Journal of Virology 59(2): 531-534
Zhou, J.; Hertz, J.M.; Tryggvason, K. 1992: Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: detection by denaturing gradient gel electrophoresis of a PCR product. American Journal of Human Genetics 50(6): 1291-1300
Palsdottir, A.; Abrahamson, M.; Thorsteinsson, L.; Arnason, A.; Olafsson, I.; Grubb, A.; Jensson, O. 1989: Mutation in the cystatin C gene causes hereditary brain hemorrhage. Progress in Clinical and Biological Research 317: 241-246
Miller, J.L.; Cunningham, D.; Lyle, V.A.; Finch, C.N. 1991: Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease. Proceedings of the National Academy of Sciences of the United States of America 88(11): 4761-4765
Asselin, C.; Vass-Marengo, J.; Bastin, M. 1986: Mutation in the polyomavirus genome that activates the properties of large T associated with neoplastic transformation. Journal of Virology 57(1): 165-172
Gu, C.H. 1992: Mutation in the pre-C gene of hepatitis B virus and anti-HBE positive chronic hepatitis B. Zhonghua Nei Ke Za Zhi 31(5): 306-309
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Mitra, S.N. 1989: Mutation induced by vibriophage PS166 infection changes biotype and phage type of Vibrio cholerae. Journal of Medical Microbiology 30(2): 137-141
Sahm, J.; Turkington, E.; LaPointe, D.; Strauss, B. 1989: Mutation induced in vitro on a C-8 guanine aminofluorene containing template by a modified T7 DNA polymerase. Biochemistry 28(7): 2836-2843
Heflich, R.H.; Fifer, E.K.; Djurić, Z.; Beland, F.A. 1986: Mutation induction and DNA adduct formation by 1,8-dinitropyrene in Chinese hamster ovary cells. Progress in Clinical and Biological Research 209a: 265-273
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Hei, T.K.; Hall, E.J.; Waldren, C.A. 1988: Mutation induction and relative biological effectiveness of neutrons in mammalian cells. Experimental observations. Radiation Research 115(2): 281-291
Whaley, J.M.; Kassis, A.I.; Kinsey, B.M.; Adelstein, S.J.; Little, J.B. 1990: Mutation induction by 125iodoacetylproflavine, a DNA-intercalating agent, in human cells. International Journal of Radiation Biology 57(6): 1087-1103
Aebersold, P.M. 1979: Mutation induction by 5-fluorodeoxyuridine in synchronous Chinese hamster cells. Cancer Research 39(3): 808-810
Boling, M.E.; Kimball, R.F. 1976: Mutation induction by MNNG in a bacteriophage of Haemophilus influenzae. Mutation Research 37(1): 1-10
Furuno-Fukushi, I.; Matsudaira, H. 1989: Mutation induction by different dose rates of gamma rays in radiation-sensitive mutants of mouse leukemia cells. Radiation Research 120(2): 370-374
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Aonuma, S.; Ushijima, T.; Nakayasu, M.; Shima, H.; Sugimura, T.; Nagao, M. 1991: Mutation induction by okadaic acid, a protein phosphatase inhibitor, in CHL cells, but not in S. typhimurium. Mutation Research 250(1-2): 375-381
Ong, T.M.; Callen, D.F.; Huang, S.L.; Batzinger, R.P.; Bueding, E. 1977: Mutation induction by the antischistosomal drug F30066 in various test systems. Mutation Research 48(1): 37-42
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Mennigmann, H.D.; Pons, F.W. 1979: Mutation induction by thymidine deprivation in Escherichia coli B/r. I. Influence of caffeine. Mutation Research 60(1): 13-23
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Huberman, E.; Bartsch, H.; Sachs, L. 1975: Mutation induction in Chinese hamster V79 cells by two vinyl chloride metabolites, chloroethylene oxide and 2-chloroacetaldehyde. International Journal of Cancer 16(4): 639-644
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Yoneda, Y.; Maruo, B. 1975: Mutation of Bacillus subtilis causing hyperproduction of alpha-amylase and protease, and its synergistic effect. Journal of Bacteriology 124(1): 48-54
Ito, M.; Huq, A.H.; Naito, E.; Saijo, T.; Takeda, E.; Kuroda, Y. 1992: Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein. Journal of Inherited Metabolic Disease 15(6): 848-856
Murayama, S.Y.; Yamamoto, T.; Suzuki, I.; Sawai, T. 1986: Mutation of Escherichia coli capable of expressing gene(s) for beta-lactamase production of Citrobacter freundii. Antimicrobial Agents and ChemoTherapy 29(4): 707-709
Maruyama, K.; Usami, M.; Yamao-Harigaya, W.; Tagawa, K.; Ishiura, S. 1991: Mutation of Glu693 to Gln or Val717 to Ile has no effect on the processing of Alzheimer amyloid precursor protein expressed in COS-1 cells by cDNA transfection. Neuroscience Letters 132(1): 97-100
Lyons, J.; Janssen, J.W.; Bartram, C.; Layton, M.; Mufti, G.J. 1988: Mutation of Ki-ras and N-ras oncogenes in myelodysplastic syndromes. Blood 71(6): 1707-1712
Kamps, M.P.; Buss, J.E.; Sefton, B.M. 1985: Mutation of NH2-terminal glycine of p60src prevents both myristoylation and morphological transformation. Proceedings of the National Academy of Sciences of the United States of America 82(14): 4625-4628
Bell, S.M.; Pham, J.N.; Lanzarone, J.Y. 1985: Mutation of Pseudomonas aeruginosa to piperacillin resistance mediated by beta-lactamase production. Journal of Antimicrobial ChemoTherapy 15(6): 665-670
Tanaka, K.; Takechi, M.; Kamada, N. 1991: Mutation of RAS oncogene in atomic bomb radiation-exposed leukemia. Journal of Radiation Research 32(4): 378-388
Kato, M.; Ishizaki, K.; Sasaki, M.S. 1990: Mutation of RB gene in retinoblastoma. Nihon Rinsho. Japanese Journal of Clinical Medicine 48(8): 204-212
Gutmann, L.; Billot-Klein, D.; Williamson, R.; Goldstein, F.W.; Mounier, J.; Acar, J.F.; Collatz, E. 1988: Mutation of Salmonella paratyphi a conferring cross-resistance to several groups of antibiotics by decreased permeability and loss of invasiveness. Antimicrobial Agents and ChemoTherapy 32(2): 195-201
Chejanovsky, N.; Carter, B.J. 1990: Mutation of a consensus purine nucleotide binding site in the adeno-associated virus rep gene generates a dominant negative phenotype for DNA replication. Journal of Virology 64(4): 1764-1770
Canessa, C.M.; Horisberger, J.D.; Louvard, D.; Rossier, B.C. 1992: Mutation of a cysteine in the first transmembrane segment of Na,K-ATPase alpha subunit confers ouabain resistance. EMBO Journal 11(5): 1681-1687
Decker, S.J.; Dorai, B.; Russell, S. 1988: Mutation of a protein kinase C phosphorylation site in the erbB protein of avian erythroblastosis virus. Journal of Virology 62(10): 3649-3654
Amrein, K.E.; Sefton, B.M. 1988: Mutation of a site of tyrosine phosphorylation in the lymphocyte-specific tyrosine protein kinase, p56lck, reveals its oncogenic potential in fibroblasts. Proceedings of the National Academy of Sciences of the United States of America 85(12): 4247-4251
Kosugi, S.; Okajima, F.; Ban, T.; Hidaka, A.; Shenker, A.; Kohn, L.D. 1992: Mutation of alanine 623 in the third cytoplasmic loop of the rat thyrotropin (TSH) receptor results in a loss in the phosphoinositide but not cAMP signal induced by TSH and receptor autoantibodies. Journal of Biological Chemistry 267(34): 24153-24156
De Souza, M.; Lindeman, R.; Volpato, F.; Trent, R.J.; Kamath, R. 1990: Mutation of aldolase B genes in hereditary fructose intolerance. Lancet 335(8693): 856
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Stenberg, G.; Board, P.G.; Mannervik, B. 1991: Mutation of an evolutionarily conserved tyrosine residue in the active site of a human class Alpha glutathione transferase. Febs Letters 293(1-2): 153-155
Chène, P.; Day, A.G.; Fersht, A.R. 1992: Mutation of asparagine 111 of rubisco from Rhodospirillum rubrum alters the carboxylase/oxygenase specificity. Journal of Molecular Biology 225(3): 891-896
Maruyama, K.; MacLennan, D.H. 1988: Mutation of aspartic acid-351, lysine-352, and lysine-515 alters the Ca2+ transport activity of the Ca2+-ATPase expressed in COS-1 cells. Proceedings of the National Academy of Sciences of the United States of America 85(10): 3314-3318
Buianovskaia, E.A.; Gordeev, V.K. 1977: Mutation of bacteriophage T4 restoring phage supressor psul+ activity in bacterial strain Escherichia coli BN. Genetika 13(2): 286-291
Tranchant, C.; Doh-Ura, K.; Steinmetz, G.; Chevalier, Y.; Kitamoto, T.; Tateishi, J.; Warter, J.M. 1991: Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease. Revue Neurologique (Paris) 147(4): 274-278
Dirckx, L.; Lindemann, D.; Ette, R.; Manzoni, C.; Moritz, D.; Mous, J. 1990: Mutation of conserved N-glycosylation sites around the CD4-binding site of human immunodeficiency virus type 1 GP120 affects viral infectivity. Virus Research 18(1): 9-20
Sung, P.; Prakash, S.; Prakash, L. 1990: Mutation of cysteine-88 in the Saccharomyces cerevisiae RAD6 protein abolishes its ubiquitin-conjugating activity and its various biological functions. Proceedings of the National Academy of Sciences of the United States of America 87(7): 2695-2699
Donald, R.G.; Cashmore, A.R. 1990: Mutation of either G box or I box sequences profoundly affects expression from the Arabidopsis rbcS-1A promoter. EMBO Journal 9(6): 1717-1726
Enoch, T.; Nurse, P. 1990: Mutation of fission yeast cell cycle control genes abolishes dependence of mitosis on DNA replication. Cell 60(4): 665-673
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Daya, M.; Wong, F.; Cervin, M.; Evans, G.; Vennema, H.; Spaan, W.; Anderson, R. 1989: Mutation of host cell determinants which discriminate between lytic and persistent mouse hepatitis virus infection results in a fusion-resistant phenotype. Journal of General Virology 70: 3335-3346
Dai, L.C.; West, K.; Littaua, R.; Takahashi, K.; Ennis, F.A. 1992: Mutation of human immunodeficiency virus type 1 at amino acid 585 on gp41 results in loss of killing by CD8+ A24-restricted cytotoxic T lymphocytes. Journal of Virology 66(5): 3151-3154
Thilly, W.G.; DeLuca, J.G.; Hoppe, H.; Penman, B.W. 1976: Mutation of human lymphoblasts by methylnitrosourea. Chemico-Biological Interactions 15(1): 33-50
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Miller, J.L.; Lyle, V.A.; Cunningham, D. 1992: Mutation of leucine-57 to phenylalanine in a platelet glycoprotein Ib alpha leucine tandem repeat occurring in patients with an autosomal dominant variant of Bernard-Soulier disease. Blood 79(2): 439-446
Li, X.; Rhode, S.L. 1990: Mutation of lysine 405 to serine in the parvovirus H-1 NS1 abolishes its functions for viral DNA replication, late promoter trans activation, and cytotoxicity. Journal of Virology 64(10): 4654-4660
Sung, P.; Higgins, D.; Prakash, L.; Prakash, S. 1988: Mutation of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to bind ATP. EMBO Journal 7(10): 3263-3269
Tsushita, K.; Hotta, T.; Ichikawa, A.; Saito, H. 1992: Mutation of p53 gene does not play a critical role in myelodysplastic syndrome and its transformation to acute leukaemia. British Journal of Haematology 81(3): 456-457
Akman, S.A.; Forrest, G.P.; Doroshow, J.H.; Dizdaroglu, M. 1991: Mutation of potassium permanganate- and hydrogen peroxide-treated plasmid pZ189 replicating in CV-1 monkey kidney cells. Mutation Research 261(2): 123-130
Nielander, H.B.; Schrama, L.H.; van Rozen, A.J.; Kasperaitis, M.; Oestreicher, A.B.; Gispen, W.H.; Schotman, P. 1990: Mutation of serine 41 in the neuron-specific protein B-50 (GAP-43) prohibits phosphorylation by protein kinase C. Journal of Neurochemistry 55(4): 1442-1445
Jacobs, C.; Dubus, A.; Monnaie, D.; Normark, S.; Frère, J.M. 1992: Mutation of serine residue 318 in the class C beta-lactamase of Enterobacter cloacae 908R. Fems Microbiology Letters 71(1): 95-100
Manak, J.R.; Prywes, R. 1991: Mutation of serum response factor phosphorylation sites and the mechanism by which its DNA-binding activity is increased by casein kinase Ii. Molecular and Cellular Biology 11(7): 3652-3659
Chia, W.; Savakis, C.; Karp, R.; Pelham, H.; Ashburner, M. 1985: Mutation of the Adh gene of Drosophila melanogaster containing an internal tandem duplication. Journal of Molecular Biology 186(4): 679-688
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Bakker, E.; Pearson, P.L. 1986: Mutation of the Duchenne muscular dystrophy gene associated with meiotic recombination. Clinical Genetics 30(4): 347-349
Kitano, A.; Endo, F.; Matsuda, I.; Miyabayashi, S.; Dahl, H.H. 1989: Mutation of the E1 alpha subunit of the pyruvate dehydrogenase complex, in relation to heterogeneity. Journal of Inherited Metabolic Disease 12(2): 97-107
Osawa, S.; Heasley, L.E.; Dhanasekaran, N.; Gupta, S.K.; Woon, C.W.; Berlot, C.; Johnson, G.L. 1990: Mutation of the Gs protein alpha subunit NH2 terminus relieves an attenuator function, resulting in constitutive adenylyl cyclase stimulation. Molecular and Cellular Biology 10(6): 2931-2940
Itoh, M.; Wang, X.L.; Suzuki, Y.; Homma, M. 1992: Mutation of the HANA protein of Sendai virus by passage in eggs. Virology 190(1): 356-364
Giebel, L.B.; Spritz, R.A. 1991: Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism. Proceedings of the National Academy of Sciences of the United States of America 88(19): 8696-8699
Pfäffle, R.W.; DiMattia, G.E.; Parks, J.S.; Brown, M.R.; Wit, J.M.; Jansen, M.; Van der Nat, H.; Van den Brande, J.L.; Rosenfeld, M.G.; Ingraham, H.A. 1992: Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Science 257(5073): 1118-1121
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Rafaeloff, R.; Patel, R.; Yip, C.; Goldfine, I.D.; Hawley, D.M. 1989: Mutation of the high cysteine region of the human insulin receptor alpha-subunit increases insulin receptor binding affinity and transmembrane signaling. Journal of Biological Chemistry 264(27): 15900-15904
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Stueland, C.S.; Ikeda, T.P.; LaPorte, D.C. 1989: Mutation of the predicted ATP binding site inactivates both activities of isocitrate dehydrogenase kinase/phosphatase. Journal of Biological Chemistry 264(23): 13775-13779
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Arnold, A.; Horst, S.A.; Gardella, T.J.; Baba, H.; Levine, M.A.; Kronenberg, H.M. 1990: Mutation of the signal peptide-encoding region of the preproparathyroid hormone gene in familial isolated hypoparathyroidism. Journal of Clinical Investigation 86(4): 1084-1087
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Picologlou, S.; Brown, N.; Liebman, S.W. 1990: Mutations in RAD6, a yeast gene encoding a ubiquitin-conjugating enzyme, stimulate retrotransposition. Molecular and Cellular Biology 10(3): 1017-1022
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Méric, C.; Gouilloud, E.; Spahr, P.F. 1988: Mutations in Rous sarcoma virus nucleocapsid protein p12 (NC): deletions of Cys-His boxes. Journal of Virology 62(9): 3328-3333
Malone, E.A.; Clark, C.D.; Chiang, A.; Winston, F. 1991: Mutations in SPT16/CDC68 suppress cis- and trans-acting mutations that affect promoter function in Saccharomyces cerevisiae. Molecular and Cellular Biology 11(11): 5710-5717
Iwamoto, A.; Omote, H.; Hanada, H.; Tomioka, N.; Itai, A.; Maeda, M.; Futai, M. 1991: Mutations in Ser174 and the glycine-rich sequence (Gly149, Gly150, and Thr156) in the beta subunit of Escherichia coli H(+)-ATPase. Journal of Biological Chemistry 266(25): 16350-16355
Jensen, R.E.; Schmidt, S.; Mark, R.J. 1992: Mutations in a 19-amino-acid hydrophobic region of the yeast cytochrome c1 presequence prevent sorting to the mitochondrial intermembrane space. Molecular and Cellular Biology 12(10): 4677-4686
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Brissette, R.E.; Tsung, K.; Inouye, M. 1992: Mutations in a central highly conserved non-DNA-binding region of OmpR, an Escherichia coli transcriptional activator, influence its DNA-binding ability. Journal of Bacteriology 174(15): 4907-4912
Hernandez, T.R.; Dutch, R.E.; Lehman, I.R.; Gustafsson, C.; Elias, P. 1991: Mutations in a herpes simplex virus type 1 origin that inhibit interaction with origin-binding protein also inhibit DNA replication. Journal of Virology 65(3): 1649-1652
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Young, B.; Herschlag, D.; Cech, T.R. 1991: Mutations in a nonconserved sequence of the Tetrahymena ribozyme increase activity and specificity. Cell 67(5): 1007-1019
Uchino, S.; Sakimura, K.; Nagahari, K.; Mishina, M. 1992: Mutations in a putative agonist binding region of the AMPA-selective glutamate receptor channel. Febs Letters 308(3): 253-257
Restifo, L.L.; White, K. 1991: Mutations in a steroid hormone-regulated gene disrupt the metamorphosis of the central nervous system in Drosophila. Developmental Biology 148(1): 174-194
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McMahon, G.; Huber, L.J.; Moore, M.J.; Stegeman, J.J.; Wogan, G.N. 1990: Mutations in c-Ki-ras oncogenes in diseased livers of winter flounder from Boston Harbor. Proceedings of the National Academy of Sciences of the United States of America 87(2): 841-845
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Sandbaken, M.G.; Culbertson, M.R. 1988: Mutations in elongation factor EF-1 alpha affect the frequency of frameshifting and amino acid misincorporation in Saccharomyces cerevisiae. Genetics 120(4): 923-934
Nickell, C.; Lloyd, R.S. 1991: Mutations in endonuclease V that affect both protein-protein association and target site location. Biochemistry 30(35): 8638-8648
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Melville, S.B.; Gunsalus, R.P. 1990: Mutations in fnr that alter anaerobic regulation of electron transport-associated genes in Escherichia coli. Journal of Biological Chemistry 265(31): 18733-18736
Merrick, M.J.; Coppard, J.R. 1989: Mutations in genes downstream of the rpoN gene (encoding sigma 54) of Klebsiella pneumoniae affect expression from sigma 54-dependent promoters. Molecular Microbiology 3(12): 1765-1775
Groner, B.; Hynes, N.E. 1990: Mutations in human breast cancer cells: dominantly-acting oncogenes and tumor suppressor genes suggest strategies for targeted interference. International Journal of Cancer. Supplement 5: 40-46
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Phillips, M.D.; Shearn, A. 1990: Mutations in polycombeotic, a Drosophila polycomb-group gene, cause a wide range of maternal and zygotic phenotypes. Genetics 125(1): 91-101
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Furie, B. 1992: Mutations in protein C: molecular pathology of thrombosis. Journal of Laboratory and Clinical Medicine 119(6): 592-593
Solioz, M.; Schatz, G. 1979: Mutations in putative intervening sequences of the mitochondrial cytochrome b gene of yeast produce abnormal cytochrome b polypeptides. Journal of Biological Chemistry 254(19): 9331-9334
Bilgin, N.; Kirsebom, L.A.; Ehrenberg, M.; Kurland, C.G. 1988: Mutations in ribosomal proteins L7/L12 perturb EF-G and EF-Tu functions. Biochimie 70(5): 611-618
Allen, P.N.; Noller, H.F. 1989: Mutations in ribosomal proteins S4 and S12 influence the higher order structure of 16 S ribosomal RNA. Journal of Molecular Biology 208(3): 457-468
Hu, J.C.; Gross, C.A. 1988: Mutations in rpoD that increase expression of genes in the mal regulon of Escherichia coli K-12. Journal of Molecular Biology 203(1): 15-27
Siegele, D.A.; Hu, J.C.; Gross, C.A. 1988: Mutations in rpoD, the gene encoding the sigma 70 subunit of Escherichia coli RNA polymerase, that increase expression of the lac operon in the absence of CAP-cAMP. Journal of Molecular Biology 203(1): 29-37
Wiren, K.M.; Ivashkiv, L.; Ma, P.; Freeman, M.W.; Potts, J.T.; Kronenberg, H.M. 1989: Mutations in signal sequence cleavage domain of preproparathyroid hormone alter protein translocation, signal sequence cleavage, and membrane-binding properties. Molecular Endocrinology 3(2): 240-250
Sassone-Corsi, P.; Borrelli, E. 1992: Mutations in signal transduction pathways and inherited diseases. Current Opinion in Genetics and Development 2(3): 455-458
Hirai, H.; Varmus, H.E. 1990: Mutations in src homology regions 2 and 3 of activated chicken c-src that result in preferential transformation of mouse or chicken cells. Proceedings of the National Academy of Sciences of the United States of America 87(21): 8592-8596
Chipens, G.I. 1991: Mutations in structures of homologous proteins confirm the existence of an amino acid interaction code. Bioorganicheskaia Khimiia 17(9): 1284-1288
Manson, M.D.; Kossmann, M. 1986: Mutations in tar suppress defects in maltose chemotaxis caused by specific malE mutations. Journal of Bacteriology 165(1): 34-40
Loktionov, A.S. 1991: Mutations in the 61st codon of the c-Ki-ras oncogene during transplacental lung tumor induction in mice and their difference in spontaneous and induced tumors. Molekuliarnaia Biologiia 25(6): 1517-1525
Ottolenghi, S.; Giglioni, B.; Comi, P.; Mantovani, R.; Malgaretti, N.; Nicolis, S.; Longinotti, M.; Sciarratta, G.V.; Pirastu, M.; Camaschella, C. 1987: Mutations in the a gamma-globin promoter in hereditary persistence of fetal hemoglobin and delta beta zero-thalassemia. Progress in Clinical and Biological Research 251: 373-382
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Yudkin, M.D.; Millonig, J.H.; Appleby, L. 1989: Mutations that alter the helix-turn-helix region of the spollAC protein: a Bacillus subtilis sporulation-specific sigma factor. Molecular Microbiology 3(2): 257-259
Benson, S.A.; Occi, J.L.; Sampson, B.A. 1988: Mutations that alter the pore function of the OmpF porin of Escherichia coli K12. Journal of Molecular Biology 203(4): 961-970
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Ashton-Rickardt, P.G.; Murray, K. 1989: Mutations that change the immunological subtype of hepatitis B virus surface antigen and distinguish between antigenic and immunogenic determination. Journal of Medical Virology 29(3): 204-214
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Voronova, A.; Baltimore, D. 1990: Mutations that disrupt DNA binding and dimer formation in the E47 helix-loop-helix protein map to distinct domains. Proceedings of the National Academy of Sciences of the United States of America 87(12): 4722-4726
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Mahoney, M.E.; Wulff, D.L. 1987: Mutations that improve the pRE promoter of coliphage lambda. Genetics 115(4): 591-595
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Kearsey, S.E.; Edwards, J. 1987: Mutations that increase the mitotic stability of minichromosomes in yeast: characterization of RAR1. Molecular and General Genetics: Mgg 210(3): 509-517
Parker-Thornburg, J.; Bonner, J.J. 1987: Mutations that induce the heat shock response of Drosophila. Cell 51(5): 763-772
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Bingham, A.H.; Ponnambalam, S.; Chan, B.; Busby, S. 1986: Mutations that reduce expression from the P2 promoter of the Escherichia coli galactose operon. Gene 41(1): 67-74
Strader, C.D.; Dixon, R.A.; Cheung, A.H.; Candelore, M.R.; Blake, A.D.; Sigal, I.S. 1987: Mutations that uncouple the beta-adrenergic receptor from Gs and increase agonist affinity. Journal of Biological Chemistry 262(34): 16439-16443
Maher, V.M.; Wessel, J.E. 1975: Mutations to azaguanine resistance induced in cultured diploid human fibroblasts by the carcinogen, N-acetoxy-2-acetylaminofluorene. Mutation Research 28(2): 227-284
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