EurekaMag PDF full texts Chapter 40,760

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

Marx, J. 1991: Mutation identified as a possible cause of Alzheimer's disease. Science 251(4996): 876-877

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

Eissenberg, J.C.; James, T.C.; Foster-Hartnett, D.M.; Hartnett, T.; Ngan, V.; Elgin, S.C. 1990: Mutation in a heterochromatin-specific chromosomal protein is associated with suppression of position-effect variegation in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the United States of America 87(24): 9923-9927

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

Miyazaki, J.I.; Ryo, Y.; Fujisawa, H.; Minagawa, T. 1978: Mutation in bacteriophage T3 affecting host cell lysis. Virology 89(1): 327-329

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

McAthey, P.; Kilbey, B.J. 1977: Mutation in continuous cultures of Schizosaccharomyces pombe. I. Dependence of the kinetics of mutation accumulation upon the growth-limiting nutrilite. Mutation Research 44(2): 227-234

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

Crow, J.F.; Denniston, C. 1985: Mutation in human populations. Advances in Human Genetics 14: 59-123

Brookes, P.; Ellis, M.V.; Pataki, J.; Harvey, R.G. 1986: Mutation in mammalian cells by isomers of 5-methylchrysene diolepoxide. Carcinogenesis 7(3): 463-466

Puck, T.T.; Waldren, C.A. 1987: Mutation in mammalian cells: theory and implications. Somatic Cell and Molecular Genetics 13(4): 405-409

Longmore, G.D.; Pharr, P.; Lodish, H.F. 1992: Mutation in murine erythropoietin receptor induces erythropoietin-independent erythroid proliferation in vitro, polycythemia in vivo. Leukemia 6(Suppl 3): 130s-134s

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

Liber, H.L.; Danheiser, S.L.; Thilly, W.G. 1985: Mutation in single-cell systems induced by low-level mutagen exposure. Basic Life Sciences 33: 169-204

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

Schnabel, D.; Schröder, M.; Sandhoff, K. 1991: Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease. Febs Letters 284(1): 57-59

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

Delclos, K.B.; Heflich, R.H. 1992: Mutation induction and DNA adduct formation in Chinese hamster ovary cells treated with 6-nitrochrysene, 6-aminochrysene and their metabolites. Mutation Research 279(3): 153-164

Belli, M.; Cera, F.; Cherubini, R.; Ianzini, F.; Moschini, G.; Sapora, O.; Simone, G.; Tabocchini, M.A.; Tiveron, P. 1991: Mutation induction and RBE-LET relationship of low-energy protons in V79 cells. International Journal of Radiation Biology 59(2): 459-465

Bridges, B.A.; Mottershead, R.P.; Knowles, A. 1979: Mutation induction and killing of Escherichia coli by DNA adducts and crosslinks: a photobiological study with 8-methoxypsoralen. Chemico-Biological Interactions 27(2-3): 221-233

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

Ong, T.M.; Serres, F.J. 1975: Mutation induction by difunctional alkylating agents in Neurospora crassa. Genetics 3: 475-482

Brendel, M. 1985: Mutation induction by excess deoxyribonucleotides in Saccharomyces cerevisiae. Basic Life Sciences 31: 425-434

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

Felkner, I.C. 1977: Mutation induction by the direct treatment of Bacillus subtilis deoxyribonucleic acid. Mutation Research 42(2): 175-180

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

Pons, F.W.; Mennigmann, H.D. 1979: Mutation induction by thymine deprivation in Escherichia coli B/R. II. Mutation in the repressed and derepressed tryptophan operon. Mutation Research 60(3): 271-278

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

Canonero, R.; Martelli, A.; Marinari, U.M.; Brambilla, G. 1990: Mutation induction in Chinese hamster lung V79 cells by five alk-2-enals produced by lipid peroxidation. Mutation Research 244(2): 153-156

Redpath, J.L.; Thaden, J.J.; Fong, R.L. 1986: Mutation induction in Escherichia coli WP2 uvrA by Cerenkov emission associated with 137Cs gamma irradiation. Radiation Research 105(1): 8-17

Akasaka, S.; Yonei, S. 1985: Mutation induction in Escherichia coli incubated in the reaction mixture of NADPH-dependent lipid peroxidation of rat-liver microsomes. Mutation Research 149(3): 321-326

Kranert, T.; Schneider, E.; Kiefer, J. 1990: Mutation induction in V79 Chinese hamster cells by very heavy ions. International Journal of Radiation Biology 58(6): 975-987

Schenk, K.; Zölzer, F.; Kiefer, J. 1989: Mutation induction in haploid yeast after split-dose radiation-exposure. I. Fractionated UV-irradiation. Radiation and Environmental Biophysics 28(2): 101-111

Tanooka, H.; Munakata, N.; Kitahara, S. 1978: Mutation induction with UV- and X-radiations in spores and vegetative cells of Bacillus subtilis. Mutation Research 49(2): 179-186

Sampedro, J.; Galceran, J.; Izquierdo, M. 1989: Mutation mapping of the 2B5 ecdysone locus in Drosophila melanogaster reveals a long-distance controlling element. Molecular and Cellular Biology 9(8): 3588-3591

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

Yaciuk, P.; Choi, J.K.; Shalloway, D. 1989: Mutation of amino acids in pp60c-src that are phosphorylated by protein kinases C and A. Molecular and Cellular Biology 9(6): 2453-2463

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

Woon, C.W.; Heasley, L.; Osawa, S.; Johnson, G.L. 1989: Mutation of glycine 49 to valine in the alpha subunit of GS results in the constitutive elevation of cyclic AMP synthesis. Biochemistry 28(11): 4547-4551

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

Smith, B.J. 1976: Mutation of lambda during prophage induction by nitrosamides. Molecular and General Genetics: Mgg 145(2): 219-222

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

Levy, E.; Carman, M.D.; Fernandez-Madrid, I.J.; Power, M.D.; Lieberburg, I.; van Duinen, S.G.; Bots, G.T.; Luyendijk, W.; Frangione, B. 1990: Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. Science 248(4959): 1124-1126

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

Greenberg, M.E.; Siegfried, Z.; Ziff, E.B. 1987: Mutation of the c-fos gene dyad symmetry element inhibits serum inducibility of transcription in vivo and the nuclear regulatory factor binding in vitro. Molecular and Cellular Biology 7(3): 1217-1225

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

Tobal, K.; Pagliuca, A.; Bhatt, B.; Bailey, N.; Layton, D.M.; Mufti, G.J. 1990: Mutation of the human FMS gene (M-CSF receptor) in myelodysplastic syndromes and acute myeloid leukemia. Leukemia 4(7): 486-489

Van Leeuwen, F.; van de Vijver, M.J.; Lomans, J.; van Deemter, L.; Jenster, G.; Akiyama, T.; Yamamoto, T.; Nusse, R. 1990: Mutation of the human neu protein facilitates down-modulation by monoclonal antibodies. Oncogene 5(4): 497-503

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

Hsiao, K.; Meiner, Z.; Kahana, E.; Cass, C.; Kahana, I.; Avrahami, D.; Scarlato, G.; Abramsky, O.; Prusiner, S.B.; Gabizon, R. 1991: Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. New England Journal of Medicine 324(16): 1091-1097

Salles, B.; Weinstock, G.M. 1989: Mutation of the promoter and LexA binding sites of cea, the gene encoding colicin E1. Molecular and General Genetics: Mgg 215(3): 483-489

Johansson, C.; Brodin, P.; Grundström, T.; Forsén, S.; Drakenberg, T. 1991: Mutation of the pseudo-EF-hand of calbindin D9k into a normal EF-hand. Biophysical studies. European Journal of Biochemistry 202(3): 1283-1290

Meek, D.W.; Eckhart, W. 1990: Mutation of the serine 312 phosphorylation site does not alter the ability of mouse p53 to inhibit simian virus 40 DNA replication in vivo. Journal of Virology 64(4): 1734-1744

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

Takata, Y.; Webster, N.J.; Olefsky, J.M. 1991: Mutation of the two carboxyl-terminal tyrosines results in an insulin receptor with normal metabolic signaling but enhanced mitogenic signaling properties. Journal of Biological Chemistry 266(14): 9135-9139

Drinkwater, C.C.; Suter, U.; Angst, C.; Shooter, E.M. 1991: Mutation of tryptophan-21 in mouse nerve growth factor (NGF) affects binding to the fast NGF receptor but not induction of neurites on PC12 cells. Proceedings. Biological Sciences 246(1317): 307-313

Kondo, F.; Ogata, M. 1975: Mutation of type D strain of Clostridium perfringens treated with acriflavine. Nihon Saikingaku Zasshi. Japanese Journal of Bacteriology 30(2): 315-325

Nakajima, K.; Nakajima, S. 1992: Mutation of virus genome. Tanpakushitsu Kakusan Koso. Protein Nucleic Acid Enzyme 37(14 Suppl): 2884-2894

Carman, W.F.; Jacyna, M.R.; Hadziyannis, S.; Karayiannis, P.; McGarvey, M.J.; Makris, A.; Thomas, H.C. 1989: Mutation preventing formation of hepatitis B e antigen in patients with chronic hepatitis B infection. Lancet 2(8663): 588-591

Bockrath, R.; Mosbaugh, P. 1986: Mutation probe of gene structure in E. coli: suppressor mutations in the seven-tRNA operon. Molecular and General Genetics: Mgg 204(3): 457-462

Lukash, L.L. 1986: Mutation process and malignant transformation induced by adenoviruses in mammalian cells. Tsitologiia i Genetika 20(1): 55-58; 72

Bochkov, N.P. 1976: Mutation process in man. Vestnik Akademii Meditsinskikh Nauk SSSR 7: 47-53

Person, S.; Snipes, W.; Krasin, F. 1976: Mutation production from tritium decay: a local effect for (3H)a-adenosine and (3H)6-thymidine decays. Mutation Research 34(2): 327-332

Bale, S.J.; Tucker, M.A. 1990: Mutation rate estimate in hereditary cutaneous malignant melanoma/dysplastic nevi. American Journal of Medical Genetics 35(2): 293-294

Chakraborty, R.; Roychoudhury, A.K. 1978: Mutation rates from rare variants of proteins in Indian tribes. Human Genetics 43(2): 179-183

Smith, J.T. 1990: Mutation rates to 4-quinolone resistance. Arzneimittel-Forschung 40(1): 65-68

Köberle, B.; Haupter, S.; Just, W.; Speit, G. 1991: Mutation screening of bleomycin-induced V79 Chinese hamster hprt mutants using multiplex polymerase chain reaction. Mutagenesis 6(6): 527-531

Horsfall, M.J.; Glickman, B.W. 1988: Mutation site specificity of N-nitroso-N-methyl-N-alpha-acetoxybenzylamine: a model derivative of an esophageal carcinogen. Carcinogenesis 9(9): 1529-1532

Richardson, K.K.; Crosby, R.M.; Skopek, T.R. 1988: Mutation spectra of N-ethyl-N'-nitro-N-nitrosoguanidine and 1-(2-hydroxyethyl)-1-nitrosourea in Escherichia coli. Molecular and General Genetics: Mgg 214(3): 460-466

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Lowman, H.B.; Cunningham, B.C.; Wells, J.A. 1991: Mutational analysis and protein engineering of receptor-binding determinants in human placental lactogen. Journal of Biological Chemistry 266(17): 10982-10988

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Mason, J.O.; Kitajewski, J.; Varmus, H.E. 1992: Mutational analysis of mouse Wnt-1 identifies two temperature-sensitive alleles and attributes of Wnt-1 protein essential for transformation of a mammary cell line. Molecular Biology of the Cell 3(5): 521-533

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Wetzel, R.; Perry, L.J.; Veilleux, C.; Chang, G. 1990: Mutational analysis of the C-terminus of human interferon-gamma. Protein Engineering 3(7): 611-623

Kanaan, M.N.; Marzluf, G.A. 1991: Mutational analysis of the DNA-binding domain of the CYS3 regulatory protein of Neurospora crassa. Molecular and Cellular Biology 11(9): 4356-4362

Tsang, S.Y.; Nakanishi, M.; Peterlin, B.M. 1990: Mutational analysis of the DRA promoter: cis-acting sequences and trans-acting factors. Molecular and Cellular Biology 10(2): 711-719

Newby, L.M.; White, L.; DiBartolomeis, S.M.; Walker, B.J.; Dowse, H.B.; Ringo, J.M.; Khuda, N.; Jackson, F.R. 1991: Mutational analysis of the Drosophila miniature-dusky (m-dy) locus: effects on cell size and circadian rhythms. Genetics 128(3): 571-582

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Romanelli, M.G.; Mavromara-Nazos, P.; Spector, D.; Roizman, B. 1992: Mutational analysis of the ICP4 binding sites in the 5' transcribed noncoding domains of the herpes simplex virus 1 UL 49.5 gamma 2 gene. Journal of Virology 66(8): 4855-4863

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Felkner, R.H.; Roth, M.J. 1992: Mutational analysis of the N-linked glycosylation sites of the SU envelope protein of Moloney murine leukemia virus. Journal of Virology 66(7): 4258-4264

Brierley, I.; Rolley, N.J.; Jenner, A.J.; Inglis, S.C. 1991: Mutational analysis of the RNA pseudoknot component of a coronavirus ribosomal frameshifting signal. Journal of Molecular Biology 220(4): 889-902

Celenza, J.L.; Carlson, M. 1989: Mutational analysis of the Saccharomyces cerevisiae SNF1 protein kinase and evidence for functional interaction with the SNF4 protein. Molecular and Cellular Biology 9(11): 5034-5044

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Roitsch, T.; Wang, H.; Jin, S.G.; Nester, E.W. 1990: Mutational analysis of the VirG protein, a transcriptional activator of Agrobacterium tumefaciens virulence genes. Journal of Bacteriology 172(10): 6054-6060

Yang, Q.; Kadam, A.; Trempe, J.P. 1992: Mutational analysis of the adeno-associated virus rep gene. Journal of Virology 66(10): 6058-6069

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Reitman, M.; Felsenfeld, G. 1988: Mutational analysis of the chicken beta-globin enhancer reveals two positive-acting domains. Proceedings of the National Academy of Sciences of the United States of America 85(17): 6267-6271

Thomas, P.J.; Garboczi, D.N.; Pedersen, P.L. 1992: Mutational analysis of the consensus nucleotide binding sequences in the rat liver mitochondrial ATP synthase beta-subunit. Journal of Biological Chemistry 267(28): 20331-20338

Rice, A.P.; Carlotti, F. 1990: Mutational analysis of the conserved cysteine-rich region of the human immunodeficiency virus type 1 Tat protein. Journal of Virology 64(4): 1864-1868

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Baldick, C.J.; Keck, J.G.; Moss, B. 1992: Mutational analysis of the core, spacer, and initiator regions of vaccinia virus intermediate-class promoters. Journal of Virology 66(8): 4710-4719

Hasemann, C.A.; Capra, J.D. 1991: Mutational analysis of the cross-reactive idiotype of the a strain mouse. Journal of Immunology 147(9): 3170-3179

Gironès, N.; Alverez, E.; Seth, A.; Lin, I.M.; Latour, D.A.; Davis, R.J. 1991: Mutational analysis of the cytoplasmic tail of the human transferrin receptor. Identification of a sub-domain that is required for rapid endocytosis. Journal of Biological Chemistry 266(28): 19006-19012

Zeng, G.Q.; De Reuse, H.; Danchin, A. 1992: Mutational analysis of the enzyme IIIGlc of the phosphoenolpyruvate phosphotransferase system in Escherichia coli. Research in Microbiology 143(3): 251-261

Schlessinger, J. 1990: Mutational analysis of the epidermal growth factor-receptor kinase. Biochemical Society Symposium 56: 13-19

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Howitt, S.M.; Lightowlers, R.N.; Gibson, F.; Cox, G.B. 1990: Mutational analysis of the function of the a-subunit of the F0F1-APPase of Escherichia coli. Biochimica et Biophysica Acta 1015(2): 264-268

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Norris, U.; Karp, P.E.; Fimmel, A.L. 1992: Mutational analysis of the glycine-rich region of the c subunit of the Escherichia coli F0F1 ATPase. Journal of Bacteriology 174(13): 4496-4499

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Shibata, R.; Miura, T.; Hayami, M.; Ogawa, K.; Sakai, H.; Kiyomasu, T.; Ishimoto, A.; Adachi, A. 1990: Mutational analysis of the human immunodeficiency virus type 2 (HIV-2) genome in relation to HIV-1 and simian immunodeficiency virus SIV (AGM). Journal of Virology 64(2): 742-747

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Fleury, S.; Lamarre, D.; Meloche, S.; Ryu, S.E.; Cantin, C.; Hendrickson, W.A.; Sekaly, R.P. 1991: Mutational analysis of the interaction between CD4 and class Ii MHC: class Ii antigens contact CD4 on a surface opposite the gp120-binding site. Cell 66(5): 1037-1049

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Deresiewicz, R.L.; Calderwood, S.B.; Robertus, J.D.; Collier, R.J. 1992: Mutations affecting the activity of the Shiga-like toxin i A-chain. Biochemistry 31(12): 3272-3280

Davidow, L.S.; Dumais, D.R.; Smyth, A.P.; Greer, J.; Moir, D.T. 1991: Mutations affecting the activity of urokinase-type plasminogen activator. Protein Engineering 4(8): 923-928

Brown, M.S.; Anderson, R.G.; Goldstein, J.L. 1977: Mutations affecting the binding, internalization, and lysosomal hydrolysis of low density lipoprotein in cultured human fibroblasts, lymphocytes, and aortic smooth muscle cells. Journal of Supramolecular Structure 6(1): 85-94

Lim, H.M.; Pène, J.J. 1989: Mutations affecting the catalytic activity of Bacillus cereus 5/B/6 beta-lactamase Ii. Journal of Biological Chemistry 264(20): 11682-11687

Ramos, F.; el Guezzar, M.; Grenson, M.; Wiame, J.M. 1985: Mutations affecting the enzymes involved in the utilization of 4-aminobutyric acid as nitrogen source by the yeast Saccharomyces cerevisiae. European Journal of Biochemistry 149(2): 401-404

Smith, J.M.; Smith, F.J.; Umbarger, H.E. 1979: Mutations affecting the formation of acetohydroxy acid synthase Ii in Escherichia coli K-12. Molecular and General Genetics: Mgg 169(3): 299-314

Young, I.G.; Wallace, B.J. 1976: Mutations affecting the reduced nicotinamide adenine dinucleotide dehydrogenase complex of Escherichia coli. Biochimica et Biophysica Acta 449(3): 376-385

Urbanowski, M.L.; Plamann, L.S.; Stauffer, G.V. 1987: Mutations affecting the regulation of the metB gene of Salmonella typhimurium LT2. Journal of Bacteriology 169(1): 126-130

Hankinson, O.; Andersen, R.D.; Birren, B.W.; Sander, F.; Negishi, M.; Nebert, D.W. 1985: Mutations affecting the regulation of transcription of the cytochrome P1-450 gene in the mouse Hepa-1 cell line. Journal of Biological Chemistry 260(3): 1790-1795

Hrebenda, J.; Heleszko, H. 1985: Mutations affecting the resistance of Escherichia coli K-12 to beta-lactam antibiotics. Journal of Antimicrobial ChemoTherapy 16(2): 149-156

Isono, S.; Isono, K. 1978: Mutations affecting the structural genes and the genes coding for modifying enzymes for ribosomal proteins in Escherichia coli. Molecular and General Genetics: Mgg 165(1): 15-20

Joannou, C.L.; Brown, P.R.; Tata, R. 1988: Mutations affecting the synthesis of NADP-dependent glutamate dehydrogenase in Pseudomonas aeruginosa. Journal of General Microbiology 134(2): 441-452

Shinedling, S.; Gayle, M.; Pribnow, D.; Gold, L. 1987: Mutations affecting translation of the bacteriophage T4 rIIB gene cloned in Escherichia coli. Molecular and General Genetics: Mgg 207(2-3): 224-232

Lengeler, J. 1975: Mutations affecting transport of the hexitols D-mannitol, D-glucitol, and galactitol in Escherichia coli K-12: isolation and mapping. Journal of Bacteriology 124(1): 26-38

Falconi, M.; McGovern, V.; Gualerzi, C.; Hillyard, D.; Higgins, N.P. 1991: Mutations altering chromosomal protein H-NS induce mini-Mu transposition. New Biologist 3(6): 615-625

Hamlett, N.V.; Berger, H. 1975: Mutations altering genetic recombination and repair of DNA in bacteriophage T4. Virology 63(2): 539-567

Kelley, M.R.; Kidd, S.; Deutsch, W.A.; Young, M.W. 1987: Mutations altering the structure of epidermal growth factor-like coding sequences at the Drosophila Notch locus. Cell 51(4): 539-548

Bautz, E.K. 1975: Mutations and DNA replication. Mutation Research 29(2): 189-193

Sarasin, A. 1989: Mutations and cancer. Journal de Toxicologie Clinique et Experimentale 9(2 Part 2): 5-13

Gleba, D.M.; Gleba, I.I. 1978: Mutations and epigenetic changes in cultures of cells and protoplasts of higher plants. Tsitologiia i Genetika 12(5): 458-469

Maher, V.M.; Patton, J.D.; Yang, J.L.; Wang, Y.Y.; Yang, L.L.; Aust, A.E.; Bhattacharyya, N.; McCormick, J.J. 1987: Mutations and homologous recombination induced in mammalian cells by metabolites of benzo[a]pyrene and 1-nitropyrene. Environmental Health Perspectives 76: 33-39

Dahl, H.H.; Brown, G.K.; Brown, R.M.; Hansen, L.L.; Kerr, D.S.; Wexler, I.D.; Patel, M.S.; De Meirleir, L.; Lissens, W.; Chun, K. 1992: Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene. Human Mutation 1(2): 97-102

Cheng, S.H.; Markland, W.; Markham, A.F.; Smith, A.E. 1986: Mutations around the NG59 lesion indicate an active association of polyoma virus middle-T antigen with pp60c-src is required for cell transformation. EMBO Journal 5(2): 325-334

LaRoe, D.J.; Vik, S.B. 1992: Mutations at Glu-32 and His-39 in the epsilon subunit of the Escherichia coli F1F0 ATP synthase affect its inhibitory properties. Journal of Bacteriology 174(2): 633-637

Donahue, T.F.; Cigan, A.M.; Pabich, E.K.; Valavicius, B.C. 1988: Mutations at a Zn(II) finger motif in the yeast eIF-2 beta gene alter ribosomal start-site selection during the scanning process. Cell 54(5): 621-632

Buchmann, A.; Mahr, J.; Bauer-Hofmann, R.; Schwarz, M. 1989: Mutations at codon 61 of the Ha-ras proto-oncogene in precancerous liver lesions of the B6C3F1 mouse. Molecular Carcinogenesis 2(3): 121-125

Kumar, S. 1992: Mutations at codon 717 of the beta-amyloid precursor protein gene are a cause of Alzheimer's disease. Indian Journal of Experimental Biology 30(2): 156

Smith, P.D.; Dusenbery, R.L. 1989: Mutations at six additional loci of Drosophila melanogaster cause alkylation hypermutability. Mutation Research 218(1): 21-24

Reich, C.I.; VanHoy, R.W.; Porter, G.L.; Wise, J.A. 1992: Mutations at the 3' splice site can be suppressed by compensatory base changes in U1 snRNA in fission yeast. Cell 69(7): 1159-1169

Shoelson, S.E.; Lu, Z.X.; Parlautan, L.; Lynch, C.S.; Weiss, M.A. 1992: Mutations at the dimer, hexamer, and receptor-binding surfaces of insulin independently affect insulin-insulin and insulin-receptor interactions. Biochemistry 31(6): 1757-1767

Furuya, H.; Shimizu, T.; Hatano, M.; Fujii-Kuriyama, Y. 1989: Mutations at the distal and proximal sites of cytochrome P-450d changed regio-specificity of acetanilide hydroxylations. Biochemical and Biophysical Research Communications 160(2): 669-676

Bryant, P.J.; Huettner, B.; Held, L.I.; Ryerse, J.; Szidonya, J. 1988: Mutations at the fat locus interfere with cell proliferation control and epithelial morphogenesis in Drosophila. Developmental Biology 129(2): 541-554

Galakatos, N.G.; Walsh, C.T. 1989: Mutations at the interdomain hinge region of the DadB alanine racemase: effects of length and conformational constraint of the linker sequence on catalytic efficiency. Biochemistry 28(20): 8167-8174

van der Veen, R.; Kwakman, J.H.; Grivell, L.A. 1987: Mutations at the lariat acceptor site allow self-splicing of a group II intron without lariat formation. EMBO Journal 6(12): 3827-3831

Dusenbery, R.L. 1987: Mutations at the mei-41, mus(1)101, mus(1)103, mus(2)205 and mus(3)310 loci of Drosophila exhibit differential UDS responses with different DNA-damaging agents. Mutation Research 183(1): 45-52

Parkhurst, S.M.; Corces, V.G. 1986: Mutations at the suppressor of forked locus increase the accumulation of gypsy-encoded transcripts in Drosophila melanogaster. Molecular and Cellular Biology 6(6): 2271-2274

Clark, S.E.; Abad, M.S.; Lamppa, G.K. 1989: Mutations at the transit peptide-mature protein junction separate two cleavage events during chloroplast import of the chlorophyll a/b-binding protein. Journal of Biological Chemistry 264(29): 17544-17550

Leroux, C.; Mazure, N.; Martin, P. 1992: Mutations away from splice site recognition sequences might cis-modulate alternative splicing of goat alpha s1-casein transcripts. Structural organization of the relevant gene. Journal of Biological Chemistry 267(9): 6147-6157

Hoerter, J.; Eisenstark, A.; Touati, D. 1989: Mutations by near-ultraviolet radiation in Escherichia coli strains lacking superoxide dismutase. Mutation Research 215(2): 161-165

Rapoport, I.A. 1975: Mutations caused by diazomethane derivatives in the gas phase. Doklady Akademii Nauk SSSR 221(3): 729-731

Steinberg, R.A.; O'Farrell, P.H.; Friedrich, U.; Coffino, P. 1977: Mutations causing charge alterations in regulatory subunits of the cAMP-dependent protein kinase of cultured S49 lymphoma cells. Cell 10(3): 381-391

Koeberl, D.D.; Bottema, C.D.; Ketterling, R.P.; Bridge, P.J.; Lillicrap, D.P.; Sommer, S.S. 1990: Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene. American Journal of Human Genetics 47(2): 202-217

Wanders, R.J.; van Roermund, C.W.; Denis, S.; Schutgens, R.B.; Ijlst, L.; Tager, J.M. 1992: Molecular analysis of disorders of peroxisomal beta-oxidation. Progress in Clinical and Biological Research 375: 507-519

Kessin, R.H. 1977: Mutations causing rapid development of Dictyostelium discoideum. Cell 10(4): 703-708

Fortin, Y.; Phoenix, P.; Drapeau, G.R. 1990: Mutations conferring resistance to azide in Escherichia coli occur primarily in the secA gene. Journal of Bacteriology 172(11): 6607-6610

Blondel, B.; Crainic, R.; Fichot, O.; Dufraisse, G.; Candrea, A.; Diamond, D.; Girard, M.; Horaud, F. 1986: Mutations conferring resistance to neutralization with monoclonal antibodies in type 1 poliovirus can be located outside or inside the antibody-binding site. Journal of Virology 57(1): 81-90

Daldal, F.; Tokito, M.K.; Davidson, E.; Faham, M. 1989: Mutations conferring resistance to quinol oxidation (Qz) inhibitors of the cyt bc1 complex of Rhodobacter capsulatus. EMBO Journal 8(13): 3951-3961

Thorbjarnardóttir, S.H.; Magnúsdóttir, R.A.; Eggertsson, G. 1978: Mutations determining generalized resistance to aminoglycoside antibiotics in Escherichia coli. Molecular and General Genetics: Mgg 161(1): 89-98

Mason, P.J.; Elkington, J.A.; Lloyd, M.M.; Jones, M.B.; Williams, J.G. 1986: Mutations downstream of the polyadenylation site of a Xenopus beta-globin mRNA affect the position but not the efficiency of 3' processing. Cell 46(2): 263-270

Beliaeva, E.S.; Knizhnikova, N.V.; Pasiukova, E.G. 1990: Mutations evoked by retrotransposons with high frequency revert in the genome of a low-fitness Drosophila melanogaster strain. Doklady Akademii Nauk SSSR 315(5): 1249-1251

Jemiolo, D.K.; Taurence, J.S.; Giese, S. 1991: Mutations in 16S rRNA in Escherichia coli at methyl-modified sites: G966, C967, and G1207. Nucleic Acids Research 19(15): 4259-4265

De Stasio, E.A.; Moazed, D.; Noller, H.F.; Dahlberg, A.E. 1989: Mutations in 16S ribosomal RNA disrupt antibiotic--RNA interactions. EMBO Journal 8(4): 1213-1216

Urabe, K. 1990: Mutations in 21-hydroxylase gene caused by gene conversion-like events. Fukuoka Igaku Zasshi 81(2): 77-87

Hirano, A.; Wong, T.C. 1989: Mutations in 3'-untranslated region of avian sarcoma virus mutant LA46 genome confer the cis-acting temperature-sensitive replication defect. Virology 172(2): 651-654

You, Q.M.; Veldhoen, N.; Baudin, F.; Romaniuk, P.J. 1991: Mutations in 5S DNA and 5S RNA have different effects on the binding of Xenopus transcription factor IIIA. Biochemistry 30(9): 2495-2500

Song, J.M.; Liebman, S.W. 1989: Mutations in ADE3 reduce the efficiency of the omnipotent suppressor sup45-2. Current Genetics 16(5-6): 315-321

Strich, R.; Woontner, M.; Scott, J.F. 1986: Mutations in ARS1 increase the rate of simple loss of plasmids in Saccharomyces cerevisiae. Yeast 2(3): 169-178

Sanders, S.K.; Fox, R.O.; Kavathas, P. 1991: Mutations in CD8 that affect interactions with HLA class i and monoclonal anti-CD8 antibodies. Journal of Experimental Medicine 174(2): 371-379

Hachinski, V. 1988: Mutations in Duchenne muscular dystrophy. Archives of Neurology 45(1): 87

Prescott, C.D.; Kornau, H.C. 1992: Mutations in E.coli 16s rRNA that enhance and decrease the activity of a suppressor tRNA. Nucleic Acids Research 20(7): 1567-1571

Kirtikar, D.M.; Cathcart, G.R.; White, J.G.; Ukstins, I.; Goldthwait, D.A. 1977: Mutations in Escherichia coli altering an apurinic endonuclease, endonuclease II, and exonuclease IIi and their effect on in vivo sensitivity to methylmethanesulfonate. Biochemistry 16(25): 5625-5631

Kliachko, E.V.; Lysenko, E.S.; Eremashvili, M.R.; Kozlov, I.I.; Strongin, A.I. 1988: Mutations in Escherichia coli pmp and htpR genes stabilize the products of foreign gene expression. Molekuliarnaia Biologiia 22(3): 760-766

Ward, D.F.; Yudkin, M.D. 1976: Mutations in Escherichia coli that relieve catabolite repression of tryptophanase synthesis. Tryptophanase promoter-like mutations. Journal of General Microbiology 92(1): 133-137

Aleshkin, G.I.; Komissarova, L.V.; Savel'eva, R.A.; Zakharenko, V.I.; Loginskiĭ, P.I.; Skavronskaia, A.G. 1992: Mutations in Francisella tularensis, decreasing the virulence of these bacteria and leading to a change in the immune response upon infection of experimental animals with them. Molekuliarnaia Genetika Mikrobiologiia i Virusologiia 1992(1-2): 23-29

Sidransky, E.; Maysak, K.; Ginns, E.I. 1990: Mutations in Gaucher's disease detected by Mspi. Lancet 336(8715): 628-629

Freissmuth, M. 1991: Mutations in Gs alpha that alter the kinetics of guanine nucleotide binding and hydrolysis. Biochemical Society Transactions 19(2): 437-441

Bos, J.L.; Verlaan-de Vries, M.; van der Eb, A.J.; Janssen, J.W.; Delwel, R.; Löwenberg, B.; Colly, L.P. 1987: Mutations in N-ras predominate in acute myeloid leukemia. Blood 69(4): 1237-1241

Wolfinbarger, L. 1976: Mutations in Neurospora crassa which affect multiple amino acid transport systems. Biochimica et Biophysica Acta 436(4): 774-788

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

Allison, L.A.; Ingles, C.J. 1989: Mutations in RNA polymerase Ii enhance or suppress mutations in GAL4. Proceedings of the National Academy of Sciences of the United States of America 86(8): 2794-2798

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

Irie, K.; Araki, H.; Oshima, Y. 1991: Mutations in a Saccharomyces cerevisiae host showing increased holding stability of the heterologous plasmid pSR1. Molecular and General Genetics: Mgg 225(2): 257-265

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

Lopilato, J.; Bortner, S.; Beckwith, J. 1986: Mutations in a new chromosomal gene of Escherichia coli K-12, pcnB, reduce plasmid copy number of pBR322 and its derivatives. Molecular and General Genetics: Mgg 205(2): 285-290

Boswell, R.E.; Prout, M.E.; Steichen, J.C. 1991: Mutations in a newly identified Drosophila melanogaster gene, mago nashi, disrupt germ cell formation and result in the formation of mirror-image symmetrical double abdomen embryos. Development 113(1): 373-384

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

Fouser, L.A.; Friesen, J.D. 1986: Mutations in a yeast intron demonstrate the importance of specific conserved nucleotides for the two stages of nuclear mRNA splicing. Cell 45(1): 81-93

Pagan, J.; Senior, A.E. 1990: Mutations in alpha-subunit of Escherichia coli F1-ATPase obtained by hydroxylamine-mutagenesis of plasmids carrying the uncA gene. Archives of Biochemistry and Biophysics 277(2): 283-289

Brown, J. 1991: Mutations in amyloid precursor protein gene and disease. Lancet 337(8746): 923-924

Ptácek, L.J.; George, A.L.; Barchi, R.L.; Griggs, R.C.; Riggs, J.E.; Robertson, M.; Leppert, M.F. 1992: Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita. Neuron 8(5): 891-897

Thompson, J.F.; Waechter-Brulla, D.; Gumport, R.I.; Gardner, J.F.; Moitoso de Vargas, L.; Landy, A. 1986: Mutations in an integration host factor-binding site: effect on lambda site-specific recombination and regulatory implications. Journal of Bacteriology 168(3): 1343-1351

Gimble, F.S.; Sauer, R.T. 1985: Mutations in bacteriophage lambda repressor that prevent RecA-mediated cleavage. Journal of Bacteriology 162(1): 147-154

Fuerst, C.R. 1986: Mutations in bacteriophage lambda that alter phage dependence on the htpR gene product of Escherichia coli. Virology 149(1): 128-131

Bertin, P.; Lejeune, P.; Colson, C.; Danchin, A. 1992: Mutations in bglY, the structural gene for the DNA-binding protein H1 of Escherichia coli, increase the expression of the kanamycin resistance gene carried by plasmid pGR71. Molecular and General Genetics: Mgg 233(1-2): 184-192

Bertin, P.; Lejeune, P.; Laurent-Winter, C.; Danchin, A. 1990: Mutations in bglY, the structural gene for the DNA-binding protein H1, affect expression of several Escherichia coli genes. Biochimie 72(12): 889-891

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

Väisänen-Rhen, V.; Saarela, S.; Rhen, M. 1988: Mutations in cloned Escherichia coli P fimbriae genes that makes fimbriae-production resistant to suppression by trimethoprim. Microbial Pathogenesis 4(5): 369-377

Craig, E.A.; Jacobsen, K. 1985: Mutations in cognate genes of Saccharomyces cerevisiae hsp70 result in reduced growth rates at low temperatures. Molecular and Cellular Biology 5(12): 3517-3524

Prockop, D.J. 1991: Mutations in collagen genes as a cause of rare and perhaps common diseases of connective tissue. Acta Paediatrica Scandinavica. Suppl 379: 55-57; Discussion 58

Qadri, I.; Gimeno, C.; Navarro, D.; Pereira, L. 1991: Mutations in conformation-dependent domains of herpes simplex virus 1 glycoprotein B affect the antigenic properties, dimerization, and transport of the molecule. Virology 180(1): 135-152

Rae, P.A.; Gutmann, N.S.; Tsao, J.; Schimmer, B.P. 1979: Mutations in cyclic AMP-dependent protein kinase and corticotropin (ACTH)-sensitive adenylate cyclase affect adrenal steroidogenesis. Proceedings of the National Academy of Sciences of the United States of America 76(4): 1896-1900

Youle, R.J. 1991: Mutations in diphtheria toxin to improve immunotoxin selectivity and understand toxin entry into cells. Seminars in Cell Biology 2(1): 39-45

McEachern, M.J.; Filutowicz, M.; Helinski, D.R. 1985: Mutations in direct repeat sequences and in a conserved sequence adjacent to the repeats result in a defective replication origin in plasmid R6K. Proceedings of the National Academy of Sciences of the United States of America 82(5): 1480-1484

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

Goldgaber, D.; Goldfarb, L.G.; Brown, P.; Asher, D.M.; Brown, W.T.; Lin, S.; Teener, J.W.; Feinstone, S.M.; Rubenstein, R.; Kascsak, R.J. 1989: Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome. Experimental Neurology 106(2): 204-206

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

Taylor, S.I.; Kadowaki, T.; Kadowaki, H.; Accili, D.; Cama, A.; McKeon, C. 1990: Mutations in insulin-receptor gene in insulin-resistant patients. Diabetes Care 13(3): 257-279

Porcellini, A.; Cocozza, S.; Monticelli, A.; Pianese, L.; Riccardi, G.; Ferrara, A.; Varrone, S. 1992: Mutations in insulin-receptor gene. Val996 allele in white NIDDM patients. Diabetes Care 15(4): 591-592

Mann, V.M.; Cooper, J.M.; Javoy-Agid, F.; Agid, Y.; Jenner, P.; Schapira, A.H. 1990: Mitochondrial function and parental sex effect in Huntington's disease. Lancet 336(8717): 749

Lauber, J.; Marsac, C.; Kadenbach, B.; Seibel, P. 1991: Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases. Nucleic Acids Research 19(7): 1393-1397

Van den Ouweland, J.M.; Bruining, G.J.; Lindhout, D.; Wit, J.M.; Veldhuyzen, B.F.; Maassen, J.A. 1992: Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia. Nucleic Acids Research 20(4): 679-682

Prockop, D.J.; Chu, M.L.; de Wet, W.; Myers, J.C.; Pihlajaniemi, T.; Ramirez, F.; Sippola, M. 1985: Mutations in osteogenesis imperfecta leading to the synthesis of abnormal type i procollagens. Annals of the new York Academy of Sciences 460: 289-297

Green, T.L.; Hart, R.P. 1988: Mutations in poly(A) site downstream elements affect in vitro cleavage activity. Molecular and Cellular Biology 8(4): 1839-1841

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

Larose, A.; St-Onge, L.; Bastin, M. 1990: Mutations in polyomavirus large T affecting immortalization of primary rat embryo fibroblasts. Virology 176(1): 98-105

Gelinas, C.; Schaffhausen, B.; Bockus, B.; Ratiarson, A.; Bastin, M. 1989: Mutations in polyomavirus middle T antigen affecting tumorigenesis. Virology 170(1): 193-200

Cohen, S.; Sweeney, H.M.; Basu, S.K. 1977: Mutations in prophage phi11 that impair the transducibility of their Staphylococcus aureus lysogens for methicillin resistance. Journal of Bacteriology 129(1): 237-245

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

Dombroski, A.J.; Platt, T. 1990: Mutations in the ATP-binding domain of Escherichia coli rho factor affect transcription termination in vivo. Journal of Bacteriology 172(5): 2477-2484

Brinkman, A.; Kortleve, D.J.; Zwarthoff, E.C.; Drop, S.L. 1991: Mutations in the C-terminal part of insulin-like growth factor (IGF)-binding protein-1 result in dimer formation and loss of IGF binding capacity. Molecular Endocrinology 5(7): 987-994

Cleves, A.E.; McGee, T.P.; Whitters, E.A.; Champion, K.M.; Aitken, J.R.; Dowhan, W.; Goebl, M.; Bankaitis, V.A. 1991: Mutations in the CDP-choline pathway for phospholipid biosynthesis bypass the requirement for an essential phospholipid transfer protein. Cell 64(4): 789-800

Chory, J.; Peto, C.A. 1990: Mutations in the DET1 gene affect cell-type-specific expression of light-regulated genes and chloroplast development in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America 87(22): 8776-8780

Barnes, D.E.; Tomkinson, A.E.; Lehmann, A.R.; Webster, A.D.; Lindahl, T. 1992: Mutations in the DNA ligase i gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents. Cell 69(3): 495-503

Babiss, L.E.; Liaw, W.S.; Zimmer, S.G.; Godman, G.C.; Ginsberg, H.S.; Fisher, P.B. 1986: Mutations in the E1a gene of adenovirus type 5 alter the tumorigenic properties of transformed cloned rat embryo fibroblast cells. Proceedings of the National Academy of Sciences of the United States of America 83(7): 2167-2171

Ogryz'ko, E.P.; Nikiforov, V.G. 1988: Mutations in the Escherichia coli RNA-polymerase beta-subunit gene cloned in a multicopy plasmid. Genetika 24(10): 1894-1896

Seeley, T.W.; Grossman, L. 1989: Mutations in the Escherichia coli UvrB ATPase motif compromise excision repair capacity. Proceedings of the National Academy of Sciences of the United States of America 86(17): 6577-6581

Grompe, M.; Versalovic, J.; Koeuth, T.; Lupski, J.R. 1991: Mutations in the Escherichia coli dnaG gene suggest coupling between DNA replication and chromosome partitioning. Journal of Bacteriology 173(3): 1268-1278

Ehling, U.H. 1991: Mutations in the F1 generation of mice. Progress in Clinical and Biological Research 372: 481-496

De Hoop, M.; Asgeirsdottir, S.; Blaauw, M.; Veenhuis, M.; Cregg, J.; Gleeson, M.; Geert, A.B. 1991: Mutations in the FAD-binding fold of alcohol oxidase from Hansenula polymorpha. Protein Engineering 4(7): 821-829

Masters, S.B.; Miller, R.T.; Chi, M.H.; Chang, F.H.; Beiderman, B.; Lopez, N.G.; Bourne, H.R. 1989: Mutations in the GTP-binding site of GS alpha alter stimulation of adenylyl cyclase. Journal of Biological Chemistry 264(26): 15467-15474

Jacoby, R.F.; Llor, X.; Teng, B.B.; Davidson, N.O.; Brasitus, T.A. 1991: Mutations in the K-ras oncogene induced by 1,2-dimethylhydrazine in preneoplastic and neoplastic rat colonic mucosa. Journal of Clinical Investigation 87(2): 624-630

Burmer, G.C.; Loeb, L.A. 1989: Mutations in the KRAS2 oncogene during progressive stages of human colon carcinoma. Proceedings of the National Academy of Sciences of the United States of America 86(7): 2403-2407

Motojima, K.; Urano, T.; Nagata, Y.; Shiku, H.; Tsunoda, T.; Kanematsu, T. 1991: Mutations in the Kirsten-ras oncogene are common but lack correlation with prognosis and tumor stage in human pancreatic carcinoma. American Journal of Gastroenterology 86(12): 1784-1788

Gonzalez, I.L.; Sheppard, D.E. 1977: Mutations in the L-arabinose operon of Escherichia coli B/r with reduced initiator function. Journal of Bacteriology 130(2): 684-691

Blair, D.F.; Berg, H.C. 1991: Mutations in the MotA protein of Escherichia coli reveal domains critical for proton conduction. Journal of Molecular Biology 221(4): 1433-1442

Kondo, K.; Umemoto, A.; Akimoto, S.; Uyama, T.; Hayashi, K.; Ohnishi, Y.; Monden, Y. 1992: Mutations in the P53 tumour suppressor gene in primary lung cancer in Japan. Biochemical and Biophysical Research Communications 183(3): 1139-1146

Buck, M.; Cannon, W. 1989: Mutations in the RNA polymerase recognition sequence of the Klebsiella pneumoniae nifH promoter permitting transcriptional activation in the absence of NifA binding to upstream activator sequences. Nucleic Acids Research 17(7): 2597-2612

Lee, H.S.; Ulrich, P.P.; Vyas, G.N. 1991: Mutations in the S-gene affecting the immunologic determinants of the envelope protein of hepatitis B virus. Journal of Hepatology 13(Suppl 4): S97-101

McGraw, P.; Henry, S.A. 1989: Mutations in the Saccharomyces cerevisiae opi3 gene: effects on phospholipid methylation, growth and cross-pathway regulation of inositol synthesis. Genetics 122(2): 317-330

Smith, L.D.; Bertrand, K.P. 1988: Mutations in the Tn10 tet repressor that interfere with induction. Location of the tetracycline-binding domain. Journal of Molecular Biology 203(4): 949-959

Yoshimura, A.; Zimmers, T.; Neumann, D.; Longmore, G.; Yoshimura, Y.; Lodish, H.F. 1992: Mutations in the Trp-Ser-X-Trp-Ser motif of the erythropoietin receptor abolish processing, ligand binding, and activation of the receptor. Journal of Biological Chemistry 267(16): 11619-11625

Hogan, K.T.; Shimojo, N.; Walk, S.F.; Engelhard, V.H.; Maloy, W.L.; Coligan, J.E.; Biddison, W.E. 1988: Mutations in the alpha 2 helix of HLA-A2 affect presentation but do not inhibit binding of influenza virus matrix peptide. Journal of Experimental Medicine 168(2): 725-736

Spada, A.; Arosio, M.; Bassetti, M.; Vallar, L.; Clementi, E.; Bazzoni, N. 1991: Mutations in the alpha subunit of the stimulatory regulatory protein of adenylyl cyclase (Gs) in human GH-secreting pituitary adenomas. Biochemical, clinical, and morphological aspects. Pathology Research and Practice 187(5): 567-570

Smirnova, N.A.; Sorokin, A.V.; Iomantas, I.V.; Abalakina, E.G.; Kozlov, I.I. 1988: Mutations in the alpha-amylase gene of Bacillus amyloliquefaciens, leading to a decrease in the temperature of protein inactivation. Molekuliarnaia Biologiia 22(5): 1257-1264

Mathison, L.; Winey, M.; Soref, C.; Culbertson, M.R.; Knapp, G. 1989: Mutations in the anticodon stem affect removal of introns from pre-tRNA in Saccharomyces cerevisiae. Molecular and Cellular Biology 9(10): 4220-4228

Blázquez, J.; Davies, J.; Moreno, F. 1991: Mutations in the aphA-2 gene of transposon Tn5 mapping within the regions highly conserved in aminoglycoside-phosphotransferases strongly reduce aminoglycoside resistance. Molecular Microbiology 5(6): 1511-1518

Chan, L. 1989: Mutations in the apolipoprotein B-100 gene: an important underlying cause of familially transmitted hypercholesterolemia and premature arteriosclerosis?. American Journal of Cardiology 63(11): 740-742

Clarke, P.; Lee, J.H.; Burke, K.; Wilcox, G. 1992: Mutations in the araC gene of Salmonella typhimurium LT2 which affect both activator and auto-regulatory functions of the AraC protein. Gene 117(1): 31-37

Cass, L.G.; Wilcox, G. 1986: Mutations in the araC regulatory gene of Escherichia coli B/r that affect repressor and activator functions of AraC protein. Journal of Bacteriology 166(3): 892-900

Shozu, M.; Akasofu, K.; Harada, N. 1992: Mutations in the aromatase gene and their effect. Fertility and Sterility 58(5): 1084-1085

Tzamarias, D.; Pu, W.T.; Struhl, K. 1992: Mutations in the bZIP domain of yeast GCN4 that alter DNA-binding specificity. Proceedings of the National Academy of Sciences of the United States of America 89(6): 2007-2011

Chen, J.H.; Porter, R.D. 1990: Mutations in the bacteriophage lambda pL/oL region that spontaneously occur in plasmid pRPZ126. Mutation Research 228(1): 81-87

Lejeune, P.; Danchin, A. 1990: Mutations in the bglY gene increase the frequency of spontaneous deletions in Escherichia coli K-12. Proceedings of the National Academy of Sciences of the United States of America 87(1): 360-363

Cali, J.J.; Hsieh, C.L.; Francke, U.; Russell, D.W. 1991: Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie cerebrotendinous xanthomatosis. Journal of Biological Chemistry 266(12): 7779-7783

Peters, K.; McDowall, J.; Rose, A.M. 1991: Mutations in the bli-4 (I) locus of Caenorhabditis elegans disrupt both adult cuticle and early larval development. Genetics 129(1): 95-102

Willems, L.; Grimonpont, C.; Heremans, H.; Rebeyrotte, N.; Chen, G.; Portetelle, D.; Burny, A.; Kettmann, R. 1992: Mutations in the bovine leukemia virus Tax protein can abrogate the long terminal repeat-directed transactivating activity without concomitant loss of transforming potential. Proceedings of the National Academy of Sciences of the United States of America 89(9): 3957-3961

Orellana, S.A.; McKnight, G.S. 1992: Mutations in the catalytic subunit of cAMP-dependent protein kinase result in unregulated biological activity. Proceedings of the National Academy of Sciences of the United States of America 89(10): 4726-4730

Hungnes, O.; Tjøtta, E.; Grinde, B. 1992: Mutations in the central polypurine tract of HIV-1 result in delayed replication. Virology 190(1): 440-442

Prywes, R.; Livneh, E.; Ullrich, A.; Schlessinger, J. 1986: Mutations in the cytoplasmic domain of EGF receptor affect EGF binding and receptor internalization. EMBO Journal 5(9): 2179-2190

Lobel, P.; Fujimoto, K.; Ye, R.D.; Griffiths, G.; Kornfeld, S. 1989: Mutations in the cytoplasmic domain of the 275 kd mannose 6-phosphate receptor differentially alter lysosomal enzyme sorting and endocytosis. Cell 57(5): 787-796

Liang, J.H.; Nielsen, G.M.; Lies, D.P.; Burris, R.H.; Roberts, G.P.; Ludden, P.W. 1991: Mutations in the draT and draG genes of Rhodospirillum rubrum result in loss of regulation of nitrogenase by reversible ADP-ribosylation. Journal of Bacteriology 173(21): 6903-6909

Majumdar, M.K.; Cho, C.L.; Fox, M.T.; Eckner, K.L.; Kozak, S.; Kabat, D.; Geib, R.W. 1992: Mutations in the env gene of friend spleen focus-forming virus overcome Fv-2r-mediated resistance to Friend virus-induced erythroleukemia. Journal of Virology 66(6): 3652-3660

Plate, C.A. 1986: Mutations in the eup locus of Escherichia coli, energy uncoupled phenotype. Methods in Enzymology 125: 187-190

Cesarman, E.; Dalla-Favera, R.; Bentley, D.; Groudine, M. 1987: Mutations in the first exon are associated with altered transcription of c-myc in Burkitt lymphoma. Science 238(4831): 1272-1275

Brown, S. 1987: Mutations in the gene for EF-G reduce the requirement for 4.5S RNA in the growth of E. coli. Cell 49(6): 825-833

Fujii, J.; Otsu, K. 1992: Mutations in the gene responsible for malignant hyperthermia. Seikagaku. Journal of Japanese Biochemical Society 64(9): 1129-1133

Medvedeva, T.E.; Kudriavtseva, V.K.; Zhikhareva, I.V.; Romashkina, V.V.; Aleksandrova, G.I.; Klimov, A.I. 1991: Mutations in the genes coding for hemagglutinin and neuraminidase in cold-adapted variants of the influenza virus A/Leningrad/134/57 (H2N2). Voprosy Virusologii 36(2): 96-100

Lisowsky, T.; Michaelis, G. 1989: Mutations in the genes for mitochondrial RNA polymerase and a second mitochondrial transcription factor of Saccharomyces cerevisiae. Molecular and General Genetics: Mgg 219(1-2): 125-128

Kurjan, J.; Hirsch, J.P.; Dietzel, C. 1991: Mutations in the guanine nucleotide-binding domains of a yeast G alpha protein confer a constitutive or uninducible state to the pheromone response pathway. Genes and Development 5(3): 475-483

Ostroff, R.M.; Wretlind, B.; Vasil, M.L. 1989: Mutations in the hemolytic-phospholipase C operon result in decreased virulence of Pseudomonas aeruginosa PAO1 grown under phosphate-limiting conditions. Infection and Immunity 57(5): 1369-1373

Heath, W.F.; Cantrell, A.S.; Mayne, N.G.; Jaskunas, S.R. 1991: Mutations in the heparin-binding domains of human basic fibroblast growth factor alter its biological activity. Biochemistry 30(22): 5608-5615

Chiou, H.C.; Weller, S.K.; Coen, D.M. 1985: Mutations in the herpes simplex virus major DNA-binding protein gene leading to altered sensitivity to DNA polymerase inhibitors. Virology 145(2): 213-226

Akeson, A.L.; Wiginton, D.A.; States, J.C.; Perme, C.M.; Dusing, M.R.; Hutton, J.J. 1987: Mutations in the human adenosine deaminase gene that affect protein structure and RNA splicing. Proceedings of the National Academy of Sciences of the United States of America 84(16): 5947-5951

Longo, N.; Langley, S.D.; Griffin, L.D.; Elsas, L.J. 1992: Mutations in the insulin receptor and their effect on glucose transport. Transactions of the Association of American Physicians 105: 204-213

Kadowaki, T.; Kasuga, M. 1991: Mutations in the insulin receptor gene in patients with genetic forms of insulin resistance. Nihon Rinsho. Japanese Journal of Clinical Medicine 49 Suppl: 721-730

Nissley, D.V.; Lindh, F.; Fennewald, M.A. 1991: Mutations in the inverted repeats of Tn3 affect binding of transposase and transposition immunity. Journal of Molecular Biology 218(2): 335-347

Kapeller, R.; Chen, K.S.; Yoakim, M.; Schaffhausen, B.S.; Backer, J.; White, M.F.; Cantley, L.C.; Ruderman, N.B. 1991: Mutations in the juxtamembrane region of the insulin receptor impair activation of phosphatidylinositol 3-kinase by insulin. Molecular Endocrinology 5(6): 769-777

Parsons, G.D.; Donly, B.C.; Mackie, G.A. 1988: Mutations in the leader sequence and initiation codon of the gene for ribosomal protein S20 (rpsT) affect both translational efficiency and autoregulation. Journal of Bacteriology 170(6): 2485-2492

Braun, C.J.; Siedow, J.N.; Williams, M.E.; Levings, C.S. 1989: Mutations in the maize mitochondrial T-urf13 gene eliminate sensitivity to a fungal pathotoxin. Proceedings of the National Academy of Sciences of the United States of America 86(12): 4435-4439

Jacobs, H.; Von Boehmer, H.; Melief, C.J.; Berns, A. 1990: Mutations in the major histocompatibility complex class I antigen-presenting groove affect both negative and positive selection of T cells. European Journal of Immunology 20(10): 2333-2337

Willson, T.A.; Ooi, B.G.; Lukins, H.B.; Linnane, A.W.; Nagley, P. 1986: Mutations in the mitochondrial oli1 gene of Saccharomyces cerevisiae affecting subunit 9 of the mitochondrial ATPase complex. Nucleic Acids Research 14(20): 8228

Macklin, W.B.; Gardinier, M.V.; Obeso, Z.O.; King, K.D.; Wight, P.A. 1991: Mutations in the myelin proteolipid protein gene alter oligodendrocyte gene expression in jimpy and jimpymsd mice. Journal of Neurochemistry 56(1): 163-171

Krylov, V.N.; Yankovsky, N.K. 1975: Mutations in the new gene stIIi of bacteriophage T4B suppressing the lysis defect of gene stIi and a gene e mutant. Journal of Virology 15(1): 22-26

Reinstein, J.; Brune, M.; Wittinghofer, A. 1988: Mutations in the nucleotide binding loop of adenylate kinase of Escherichia coli. Biochemistry 27(13): 4712-4720

Chiba, I.; Takahashi, T.; Nau, M.M.; D'Amico, D.; Curiel, D.T.; Mitsudomi, T.; Buchhagen, D.L.; Carbone, D.; Piantadosi, S.; Koga, H. 1990: Mutations in the p53 gene are frequent in primary, resected non-small cell lung cancer. Lung Cancer Study Group. Oncogene 5(10): 1603-1610

Schiopu, U. 1989: Mutations in the personality nucleus at puberty and adolescence. Revista Medico-Chirurgicala a Societatii de Medici Si Naturalisti Din Iasi 93(4): 677-682

Plesner, P.; Ullrey, D.B.; Kalckar, H.M. 1985: Mutations in the phosphoglucose isomerase gene can lead to marked alterations in cellular ATP levels in cultured fibroblasts exposed to simple nutrient shifts. Proceedings of the National Academy of Sciences of the United States of America 82(9): 2761-2763

Schneider, J.; Fanning, E. 1988: Mutations in the phosphorylation sites of simian virus 40 (SV40) T antigen alter its origin DNA-binding specificity for sites i or Ii and affect SV40 DNA replication activity. Journal of Virology 62(5): 1598-1605

Brunner, A.; Wolf, R.; Pflugfelder, G.O.; Poeck, B.; Heisenberg, M. 1992: Mutations in the proximal region of the optomotor-blind locus of Drosophila melanogaster reveal a gradient of neuroanatomical and behavioral phenotypes. Journal of Neurogenetics 8(1): 43-55

Seelke, R.; Kline, B.; Aleff, R.; Porter, R.D.; Shields, M.S. 1987: Mutations in the recD gene of Escherichia coli that raise the copy number of certain plasmids. Journal of Bacteriology 169(10): 4841-4844

Morrison, L.E.; Boehmelt, G.; Enrietto, P.J. 1992: Mutations in the rel-homology domain alter the biochemical properties of v-rel and render it transformation defective in chicken embryo fibroblasts. Oncogene 7(6): 1137-1147

Hegemann, J.H.; Pridmore, R.D.; Schneider, R.; Philippsen, P. 1986: Mutations in the right boundary of Saccharomyces cerevisiae centromere 6 lead to nonfunctional or partially functional centromeres. Molecular and General Genetics: Mgg 205(2): 305-311

Grossman, A.D.; Zhou, Y.N.; Gross, C.; Heilig, J.; Christie, G.E.; Calendar, R. 1985: Mutations in the rpoH (htpR) gene of Escherichia coli K-12 phenotypically suppress a temperature-sensitive mutant defective in the sigma 70 subunit of RNA polymerase. Journal of Bacteriology 161(3): 939-943

Hu, J.C.; Gross, C.A. 1985: Mutations in the sigma subunit of E. coli RNA polymerase which affect positive control of transcription. Molecular and General Genetics: Mgg 199(1): 7-13

Allison, D.S.; Young, E.T. 1989: Mutations in the signal sequence of prepro-alpha-factor inhibit both translocation into the endoplasmic reticulum and processing by signal peptidase in yeast cells. Molecular and Cellular Biology 9(11): 4977-4985

Lee, B.; Berka, R.M.; Tabita, F.R. 1991: Mutations in the small subunit of cyanobacterial ribulose-bisphosphate carboxylase/oxygenase that modulate interactions with large subunits. Journal of Biological Chemistry 266(12): 7417-7422

Rudd, K.E.; Bochner, B.R.; Cashel, M.; Roth, J.R. 1985: Mutations in the spoT gene of Salmonella typhimurium: effects on his operon expression. Journal of Bacteriology 163(2): 534-542

Ashman, C.R. 1978: Mutations in the structural genes of CHO cell histidyl-, valyl-, and leucyl-tRNA synthetases. Somatic Cell Genetics 4(3): 299-312

Chen, W.Y.; Wight, D.C.; Chen, N.Y.; Coleman, T.A.; Wagner, T.E.; Kopchick, J.J. 1991: Mutations in the third alpha-helix of bovine growth hormone dramatically affect its intracellular distribution in vitro and growth enhancement in transgenic mice. Journal of Biological Chemistry 266(4): 2252-2258

Olson, R.R.; De Magistris, M.T.; Di Tommaso, A.; Karr, R.W. 1992: Mutations in the third, but not the first or second, hypervariable regions of DR(beta 1*0101) eliminate DR1-restricted recognition of a pertussis toxin peptide. Journal of Immunology 148(9): 2703-2708

Kauffman, M.G.; Rose, P.A.; Kelly, T.J. 1991: Mutations in the thymidine kinase gene that allow expression of the enzyme in quiescent (G0) cells. Oncogene 6(8): 1427-1435

Durland, R.H.; Toukdarian, A.; Fang, F.; Helinski, D.R. 1990: Mutations in the trfA replication gene of the broad-host-range plasmid RK2 result in elevated plasmid copy numbers. Journal of Bacteriology 172(7): 3859-3867

Bohman, K.; Isaksson, L.A. 1978: Mutations in the tryptophanyl-transfer ribonucleic acid ligase of E. coli causing temperature-sensitivity for growth. Molecular and General Genetics: Mgg 161(3): 285-289

Minvielle-Sebastia, L.; Winsor, B.; Bonneaud, N.; Lacroute, F. 1991: Mutations in the yeast RNA14 and RNA15 genes result in an abnormal mRNA decay rate; sequence analysis reveals an RNA-binding domain in the RNA15 protein. Molecular and Cellular Biology 11(6): 3075-3087

Segard-Maurel, I.; Jibard, N.; Schweizer-Groyer, G.; Cadepond, F.; Baulieu, E.E. 1992: Mutations in the "zinc fingers" or in the N-terminal region of the DNA binding domain of the human glucocorticosteroid receptor facilitate its salt-induced transformation, but do not modify hormone binding. Journal of Steroid Biochemistry and Molecular Biology 41(3-8): 727-732

Smith, C.M.; Arany, Z.; Orrego, C.; Eisenstadt, E. 1992: Mutations in topA interfere with the inducible expression of DNA damage response loci in Salmonella typhimurium. Environmental and Molecular Mutagenesis 19(3): 185-194

Schlensog, V.; Birkmann, A.; Böck, A. 1989: Mutations in trans which affect the anaerobic expression of a formate dehydrogenase (fdhF) structural gene. Archives of Microbiology 152(1): 83-89

Kamitani, H.; Mariyama, M.; Hori, T.; Nishimura, S. 1992: Mutations in transmembrane domain of c-erbB-2 gene in human malignant tumours of the central nervous system. Neurological Research 14(3): 236-240

Joung, I.; Engler, J.A. 1992: Mutations in two cysteine-histidine-rich clusters in adenovirus type 2 DNA polymerase affect DNA binding. Journal of Virology 66(10): 5788-5796

Ossanna, N.; Mount, D.W. 1989: Mutations in uvrD induce the SOS response in Escherichia coli. Journal of Bacteriology 171(1): 303-307

Introna, M.; Golay, J.; Frampton, J.; Nakano, T.; Ness, S.A.; Graf, T. 1990: Mutations in v-myb alter the differentiation of myelomonocytic cells transformed by the oncogene. Cell 63(6): 1289-1297

Mattano, S.S.; Palella, T.D.; Mitchell, B.S. 1990: Mutations induced at the hypoxanthine-guanine phosphoribosyltransferase locus of human T-lymphoblasts by perturbations of purine deoxyribonucleoside triphosphate pools. Cancer Research 50(15): 4566-4571

Pastink, A.; Vreeken, C.; Vogel, E.W.; Eeken, J.C. 1990: Mutations induced at the white and vermilion loci in Drosophila melanogaster. Mutation Research 231(1): 63-71

Hoebee, B.; vd Ende, M.A.; Brouwer, J.; vd Putte, P.; Loman, H.; Retèl, J. 1989: Mutations induced by 60Co gamma-irradiation in double-stranded M13 bacteriophage DNA in nitrous-oxide saturated solutions are characterized by a high specificity. International Journal of Radiation Biology 56(4): 401-411

Kamiya, H.; Miura, H.; Suzuki, M.; Murata, N.; Ishikawa, H.; Shimizu, M.; Komatsu, Y.; Murata, T.; Sasaki, T.; Inoue, H. 1992: Mutations induced by DNA lesions in hot spots of the c-Ha-ras gene. Nucleic Acids Symposium Series 27: 179-180

Reckmann, B.; Krauss, G. 1986: Mutations induced by DNA polymerase alpha upon in vitro replication of M13mp8(+) DNA. Nucleic Acids Research 14(5): 2365-2380

Vrieling, H.; Simons, J.W.; Arwert, F.; Natarajan, A.T.; van Zeeland, A.A. 1985: Mutations induced by X-rays at the HPRT locus in cultured Chinese hamster cells are mostly large deletions. Mutation Research 144(4): 281-286

Mah, M.C.; Maher, V.M.; Thomas, H.; Reid, T.M.; King, C.M.; McCormick, J.J. 1989: Mutations induced by aminofluorene-DNA adducts during replication in human cells. Carcinogenesis 10(12): 2321-2328

Andersson, B.; Lambert, B. 1990: Mutations induced by benzo[a]pyrene diolepoxide at the hprt locus in human T-lymphocytes in vitro. Mutation Research 245(2): 75-82

Jaberaboansari, A.; Dunn, W.C.; Preston, R.J.; Mitra, S.; Waters, L.C. 1991: Mutations induced by ionizing radiation in a plasmid replicated in human cells. II. Sequence analysis of alpha-particle-induced point mutations. Radiation Research 127(2): 202-210

McBride, T.J.; Schneider, J.E.; Floyd, R.A.; Loeb, L.A. 1992: Mutations induced by methylene blue plus light in single-stranded M13mp2. Proceedings of the National Academy of Sciences of the United States of America 89(15): 6866-6870

Pique, C.; Tursz, T.; Dokhelar, M.C. 1990: Mutations introduced along the HTLV-I envelope gene result in a non-functional protein: a basis for envelope conservation?. EMBO Journal 9(13): 4243-4248

Kassir, Y.; Simchen, G. 1985: Mutations leading to expression of the cryptic HMRa locus in the yeast Saccharomyces cerevisiae. Genetics 109(3): 481-492

Wallis, G.; Beighton, P.; Boyd, C.; Mathew, C.G. 1986: Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type i. Journal of Medical Genetics 23(5): 411-416

McDermit, M.; Pierce, M.; Staley, D.; Shimaji, M.; Shaw, R.; Wulff, D.L. 1976: Mutations masking the lambda cin-1 mutation. Genetics 82(3): 417-422

Pipas, J.M. 1985: Mutations near the carboxyl terminus of the simian virus 40 large tumor antigen alter viral host range. Journal of Virology 54(2): 569-575

Claverie, J.M.; de Souza, A.C.; Thirion, J.P. 1979: Mutations of Chinese hamster somatic cells from 2-deoxygalactose sensitivity to resistance. Genetics 92(2): 563-572

Freissmuth, M.; Gilman, A.G. 1989: Mutations of GS alpha designed to alter the reactivity of the protein with bacterial toxins. Substitutions at ARG187 result in loss of GTPase activity. Journal of Biological Chemistry 264(36): 21907-21914

Mistou, M.Y.; Jacquet, E.; Poullet, P.; Rensland, H.; Gideon, P.; Schlichting, I.; Wittinghofer, A.; Parmeggiani, A. 1992: Mutations of Ha-ras p21 that define important regions for the molecular mechanism of the SDC25 C-domain, a guanine nucleotide dissociation stimulator. EMBO Journal 11(7): 2391-2397

Mano, H.; Ishikawa, F.; Hirai, H.; Takaku, F. 1989: Mutations of N-ras oncogene in myelodysplastic syndromes and leukemias detected by polymerase chain reaction. Japanese Journal of Cancer Research: Gann 80(2): 102-106

Wu, D.A.; Chung, B.C. 1991: Mutations of P450c21 (steroid 21-hydroxylase) at Cys428, Val281, and Ser268 result in complete, partial, or no loss of enzymatic activity, respectively. Journal of Clinical Investigation 88(2): 519-523

Naruse, S.; Tsuji, S.; Miyatake, T. 1992: Mutations of amyloid precursor protein in early-onset familial Alzheimer's disease. Nihon Rinsho. Japanese Journal of Clinical Medicine 50(9): 2270-2277

Dunn, J.J.; Buzash-Pollert, E.; Studier, F.W. 1978: Mutations of bacteriophage T7 that affect initiation of synthesis of the gene 0.3 protein. Proceedings of the National Academy of Sciences of the United States of America 75(6): 2741-2745

Montañez, C.; Bueno, J.; Schmeissner, U.; Court, D.L.; Guarneros, G. 1986: Mutations of bacteriophage lambda that define independent but overlapping RNA processing and transcription termination sites. Journal of Molecular Biology 191(1): 29-37

Conti, C.J. 1992: Mutations of genes of the ras family in human and experimental tumors. Progress in Clinical and Biological Research 376: 357-378

Duronio, R.J.; Reed, S.I.; Gordon, J.I. 1992: Mutations of human myristoyl-CoA:protein N-myristoyltransferase cause temperature-sensitive myristic acid auxotrophy in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences of the United States of America 89(9): 4129-4133

Wunderlich, V. 1990: Mutations of mitochondrial DNA and their relation to neuromuscular diseases. Zentralblatt für Allgemeine Pathologie U. Pathologische Anatomie 136(4): 305-316

Krek, W.; Nigg, E.A. 1991: Mutations of p34cdc2 phosphorylation sites induce premature mitotic events in HeLa cells: evidence for a double block to p34cdc2 kinase activation in vertebrates. EMBO Journal 10(11): 3331-3341

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Ichikawa, A.; Hotta, T.; Takagi, N.; Tsushita, K.; Kinoshita, T.; Nagai, H.; Murakami, Y.; Hayashi, K.; Saito, H. 1992: Mutations of p53 gene and their relation to disease progression in B-cell lymphoma. Blood 79(10): 2701-2707

Heald, R.; McKeon, F. 1990: Mutations of phosphorylation sites in lamin A that prevent nuclear lamina disassembly in mitosis. Cell 61(4): 579-589

Kosheleva, I.A.; Tsoĭ, T.V.; Ivashina, T.V.; Selifonov, S.A.; Starovoĭtov, I.I. 1988: Mutations of plasmid pBS286 blocking the initial stages of naphthalene oxidation induced by Tn5. Genetika 24(3): 396-404

Myers, R.S.; Maloy, S.R. 1988: Mutations of putP that alter the lithium sensitivity of Salmonella typhimurium. Molecular Microbiology 2(6): 749-755

Mitsudomi, T.; Oyama, T.; Gazdar, A.F.; Minna, J.D.; Okabayashi, K.; Shirakusa, T. 1992: Mutations of ras and p53 genes in human non-small cell lung cancer cell lines and their clinical significance. Nihon Geka Gakkai Zasshi 93(9): 944-947

Mitsudomi, T.; Viallet, J.; Mulshine, J.L.; Linnoila, R.I.; Minna, J.D.; Gazdar, A.F. 1991: Mutations of ras genes distinguish a subset of non-small-cell lung cancer cell lines from small-cell lung cancer cell lines. Oncogene 6(8): 1353-1362

Kocharian, S.M.; Chukanova, T.I.; Sukhodolets, V.V. 1977: Mutations of resistance to 2,6-diaminopurine and 6-methylpurine that affect adenine phosphoribosyltransferase in Escherichia coli K-12. Genetika 13(10): 1821-1830

Elisova, T.V.; Feoktistova, T.P.; Stavrakova, N.M. 1988: Mutations of resistance to 6-thioguanine following roentgen irradiation and subsequent treatment with cytosine arabinoside combined with hydroxyurea in Chinese hamster cells in the G1 phase. Radiobiologiia 28(5): 617-622

Nakamura, Y.; Nishisho, I.; Kinzler, K.W.; Vogelstein, B.; Miyoshi, Y.; Miki, Y.; Ando, H.; Horii, A. 1992: Mutations of the APC (adenomatous polyposis coli) gene in FAP (familial polyposis coli) patients and in sporadic colorectal tumors. Tohoku Journal of Experimental Medicine 168(2): 141-147

Henkin, T.M.; Sonenshein, A.L. 1987: Mutations of the Escherichia coli lacUV5 promoter resulting in increased expression in Bacillus subtilis. Molecular and General Genetics: Mgg 209(3): 467-474

Weinstein, L.S.; Gejman, P.V.; Friedman, E.; Kadowaki, T.; Collins, R.M.; Gershon, E.S.; Spiegel, A.M. 1990: Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis. Proceedings of the National Academy of Sciences of the United States of America 87(21): 8287-8290

Ignar-Trowbridge, D.; Risinger, J.I.; Dent, G.A.; Kohler, M.; Berchuck, A.; McLachlan, J.A.; Boyd, J. 1992: Mutations of the Ki-ras oncogene in endometrial carcinoma. American Journal of Obstetrics and Gynecology 167(1): 227-232

Fenaux, P.; Preudhomme, C.; Quiquandon, I.; Jonveaux, P.; Laï, J.L.; Vanrumbeke, M.; Loucheux-Lefebvre, M.H.; Bauters, F.; Berger, R.; Kerckaert, J.P. 1992: Mutations of the P53 gene in acute myeloid leukaemia. British Journal of Haematology 80(2): 178-183

Ishioka, C.; Sato, T.; Gamoh, M.; Suzuki, T.; Shibata, H.; Kanamaru, R.; Wakui, A.; Yamazaki, T. 1991: Mutations of the P53 gene, including an intronic point mutation, in colorectal tumors. Biochemical and Biophysical Research Communications 177(3): 901-906

Nakamura, Y.; Nishisho, I.; Kinzler, K.W.; Vogelstein, B.; Miyoshi, Y.; Miki, Y.; Ando, H.; Horii, A.; Nagase, H. 1991: Mutations of the adenomatous polyposis coli gene in familial polyposis coli patients and sporadic colorectal tumors. Princess Takamatsu Symposia 22: 285-292

Hofmann, K.J.; Schultz, L.D. 1991: Mutations of the alpha-galactosidase signal peptide which greatly enhance secretion of heterologous proteins by yeast. Gene 101(1): 105-111

Malashenko, A.M. 1975: Mutations of the brachyury type in mice of the PT line. Genetika 11(1): 146-147

Super, M.; Schwarz, M.J. 1992: Mutations of the cystic fibrosis gene locus within the population of the Northwest of England. European Journal of Pediatrics 151(2): 108-111

Buianova, N.I.; Shipkov, V.P.; Pekhov, A.P. 1991: Mutations of the genetic region Fin of the F-like plasmid pAP18-1. Biulleten' Eksperimental'noi Biologii i Meditsiny 112(11): 532-534

Campbell, P.T.; Hnatowich, M.; O'Dowd, B.F.; Caron, M.G.; Lefkowitz, R.J.; Hausdorff, W.P. 1991: Mutations of the human beta 2-adrenergic receptor that impair coupling to Gs interfere with receptor down-regulation but not sequestration. Molecular Pharmacology 39(2): 192-198

Lash, R.W.; Desai, R.K.; Zimmerman, C.A.; Flack, M.R.; Yoshida, T.; Wondisford, F.E.; Weintraub, B.D. 1992: Mutations of the human thyrotropin-beta subunit glycosylation site reduce thyrotropin synthesis independent of changes in glycosylation status. Journal of Endocrinological Investigation 15(4): 255-263

Funahashi, T.; Miyake, Y.; Yamamoto, A.; Matsuzawa, Y.; Kishino, B. 1988: Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemia. Human Genetics 79(2): 103-108

Yamamoto, A. 1988: Mutations of the low density lipoprotein receptor in familial hypercholesterolemia--analysis of 21 homozygotes. Japanese Journal of Medicine 27(2): 225-228

Spithill, T.W.; Trembath, M.K.; Lukins, H.B.; Linnane, A.W. 1978: Mutations of the mitochondrial DNA of Saccharomyces cerevisiae which affect the interaction between mitochondrial ribosomes and the inner mitochondrial membrane. Molecular and General Genetics: Mgg 164(2): 155-162

Fenaux, P.; Preudhomme, C.; Laï, J.L.; Quiquandon, I.; Jonveaux, P.; Vanrumbeke, M.; Sartiaux, C.; Morel, P.; Loucheux-Lefebvre, M.H.; Bauters, F. 1992: Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis. Leukemia 6(4): 246-250

Fenaux, P.; Jonveaux, P.; Quiquandon, I.; Preudhomme, C.; Lai, J.L.; Vanrumbeke, M.; Loucheux-Lefebvre, M.H.; Bauters, F.; Berger, R.; Kerckaert, J.P. 1992: Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases. Leukemia 6(1): 42-46

Sakashita, A.; Hattori, T.; Miller, C.W.; Suzushima, H.; Asou, N.; Takatsuki, K.; Koeffler, H.P. 1992: Mutations of the p53 gene in adult T-cell leukemia. Blood 79(2): 477-480

Ratziu, V. 1992: Mutations of the p53 gene in hepatocellular carcinomas. Gastroenterologie Clinique et Biologique 16(10): 824-826

Baron, J.; Weisberg, R.A. 1992: Mutations of the phage lambda nutL region that prevent the action of Nun, a site-specific transcription termination factor. Journal of Bacteriology 174(6): 1983-1989

Fantl, W.J.; Escobedo, J.A.; Williams, L.T. 1989: Mutations of the platelet-derived growth factor receptor that cause a loss of ligand-induced conformational change, subtle changes in kinase activity, and impaired ability to stimulate DNA synthesis. Molecular and Cellular Biology 9(10): 4473-4478

Clanton, D.J.; Hattori, S.; Shih, T.Y. 1986: Mutations of the ras gene product p21 that abolish guanine nucleotide binding. Proceedings of the National Academy of Sciences of the United States of America 83(14): 5076-5080

Neubauer, A.; Shannon, K.; Liu, E. 1991: Mutations of the ras proto-oncogenes in childhood monosomy 7. Blood 77(3): 594-598

Cogswell, P.C.; Morgan, R.; Dunn, M.; Neubauer, A.; Nelson, P.; Poland-Johnston, N.K.; Sandberg, A.A.; Liu, E. 1989: Mutations of the ras protooncogenes in chronic myelogenous leukemia: a high frequency of ras mutations in bcr/abl rearrangement-negative chronic myelogenous leukemia. Blood 74(8): 2629-2633

Baker, N.E.; Moses, K.; Nakahara, D.; Ellis, M.C.; Carthew, R.W.; Rubin, G.M. 1992: Mutations on the second chromosome affecting the Drosophila eye. Journal of Neurogenetics 8(2): 85-100

Pearson, D.; Willis, I.; Hottinger, H.; Bell, J.; Kumar, A.; Leupold, U.; Söll, D. 1985: Mutations preventing expression of sup3 tRNASer nonsense suppressors of Schizosaccharomyces pombe. Molecular and Cellular Biology 5(4): 808-815

Bourne, H.R.; Masters, S.B.; Miller, R.T.; Sullivan, K.A.; Heideman, W. 1988: Mutations probe structure and function of G-protein alpha chains. Cold Spring Harbor Symposia on Quantitative Biology 53 Pt 1: 221-228

Carraway, M.; Rewinski, C.; Marinus, M.G. 1990: Mutations produced by DNA polymerase IIi holoenzyme of Escherichia coli after in vitro synthesis in the absence of single-strand binding protein. Molecular Microbiology 4(10): 1645-1652

Mozola, M.A.; Friedman, D.I.; Crawford, C.L.; Wulff, D.L.; Shimatake, H.; Rosenberg, M. 1979: Mutations reducing the activity of c17, a promoter of phage lambda formed by a tandem duplication. Proceedings of the National Academy of Sciences of the United States of America 76(3): 1122-1125

Chen, J.W.; Harms, E.; Umbarger, H.E. 1991: Mutations replacing the leucine codons or altering the length of the amino acid-coding portion of the ilvGMEDA leader region of Escherichia coli. Journal of Bacteriology 173(7): 2341-2353

Kirilovsky, D.L.; Ajlani, G.; Picaud, M.; Etienne, A.L. 1989: Mutations responsible for high light sensitivity in an atrazine-resistant mutant of Synechocystis 6714. Plant Molecular Biology 13(4): 355-363

Lee, J.H.; Burke, K.; Wilcox, G. 1986: Mutations resulting in promoter-like sequences which enhance the expression of araC in Salmonella typhimurium. Gene 46(1): 113-121

Yajko, D.M.; Weiss, B. 1975: Mutations simultaneously affecting endonuclease Ii and exonuclease IIi in Escherichia coli. Proceedings of the National Academy of Sciences of the United States of America 72(2): 688-692

Aguilera, A. 1987: Mutations suppressing the effects of a deletion of the phosphoglucose isomerase gene PGI1 in Saccharomyces cerevisiae. Current Genetics 11(6-7): 429-434

Stewart, R.C.; Roth, A.F.; Dahlquist, F.W. 1990: Mutations that affect control of the methylesterase activity of CheB, a component of the chemotaxis adaptation system in Escherichia coli. Journal of Bacteriology 172(6): 3388-3399

Morin, N.; Delsert, C.; Klessig, D.F. 1989: Mutations that affect phosphorylation of the adenovirus DNA-binding protein alter its ability to enhance its own synthesis. Journal of Virology 63(12): 5228-5237

Anderson, L.K.; Rayner, M.C.; Eiserling, F.A. 1987: Mutations that affect structure and assembly of light-harvesting proteins in the cyanobacterium Synechocystis sp. strain 6701. Journal of Bacteriology 169(1): 102-109

Teschke, C.M.; Kim, J.; Song, T.; Park, S.; Park, C.; Randall, L.L. 1991: Mutations that affect the folding of ribose-binding protein selected as suppressors of a defect in export in Escherichia coli. Journal of Biological Chemistry 266(18): 11789-11796

Lin, C.K.; Goldfarb, D.S.; Doi, R.H.; Rodriguez, R.L. 1985: Mutations that affect the translation efficiency of Tn9-derived cat gene in Bacillus subtilis. Proceedings of the National Academy of Sciences of the United States of America 82(1): 173-177

Fandl, J.P.; Thorner, L.K.; Artz, S.W. 1990: Mutations that affect transcription and cyclic AMP-CRP regulation of the adenylate cyclase gene (cya) of Salmonella typhimurium. Genetics 125(4): 719-727

Ray, C.; Hay, R.E.; Carter, H.L.; Moran, C.P. 1985: Mutations that affect utilization of a promoter in stationary-phase Bacillus subtilis. Journal of Bacteriology 163(2): 610-614

Aiba, H.; Nakamura, T.; Mitani, H.; Mori, H. 1985: Mutations that alter the allosteric nature of cAMP receptor protein of Escherichia coli. EMBO Journal 4(12): 3329-3332

Steinberg, R.A.; Gorman, K.B.; Ogreid, D.; Døskeland, S.O.; Weber, I.T. 1991: Mutations that alter the charge of type i regulatory subunit and modify activation properties of cyclic AMP-dependent protein kinase from S49 mouse lymphoma cells. Journal of Biological Chemistry 266(6): 3547-3553

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

Dombrowski, K.E.; Vogel, B.E.; Prockop, D.J. 1989: Mutations that alter the primary structure of type i procollagen have long-range effects on its cleavage by procollagen N-proteinase. Biochemistry 28(17): 7107-7112

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

Scheidel, L.M.; Stollar, V. 1991: Mutations that confer resistance to mycophenolic acid and ribavirin on Sindbis virus map to the nonstructural protein nsP1. Virology 181(2): 490-499

Reitzer, L.J.; Bueno, R.; Cheng, W.D.; Abrams, S.A.; Rothstein, D.M.; Hunt, T.P.; Tyler, B.; Magasanik, B. 1987: Mutations that create new promoters suppress the sigma 54 dependence of glnA transcription in Escherichia coli. Journal of Bacteriology 169(9): 4279-4284

Sellers, J.W.; Vincent, A.C.; Struhl, K. 1990: Mutations that define the optimal half-site for binding yeast GCN4 activator protein and identify an ATF/CREB-like repressor that recognizes similar DNA sites. Molecular and Cellular Biology 10(10): 5077-5086

Taylor, R.K.; Garrett, S.; Sodergren, E.; Silhavy, T.J. 1985: Mutations that define the promoter of ompF, a gene specifying a major outer membrane porin protein. Journal of Bacteriology 162(3): 1054-1060

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

DeMars, R.; Rudersdorf, R.; Chang, C.; Petersen, J.; Strandtmann, J.; Korn, N.; Sidwell, B.; Orr, H.T. 1985: Mutations that impair a posttranscriptional step in expression of HLA-A and -B antigens. Proceedings of the National Academy of Sciences of the United States of America 82(23): 8183-8187

Mahoney, M.E.; Wulff, D.L. 1987: Mutations that improve the pRE promoter of coliphage lambda. Genetics 115(4): 591-595

Johnston, M.; Dover, J. 1987: Mutations that inactivate a yeast transcriptional regulatory protein cluster in an evolutionarily conserved DNA binding domain. Proceedings of the National Academy of Sciences of the United States of America 84(8): 2401-2405

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

Ogreid, D.; Døskeland, S.O.; Gorman, K.B.; Steinberg, R.A. 1988: Mutations that prevent cyclic nucleotide binding to binding sites A or B of type I cyclic AMP-dependent protein kinase. Journal of Biological Chemistry 263(33): 17397-17404

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

Coleman, J.; Inouye, M.; Nakamura, K. 1985: Mutations upstream of the ribosome-binding site affect translational efficiency. Journal of Molecular Biology 181(1): 139-143

Steingrimsdottir, H.; Rowley, G.; Dorado, G.; Cole, J.; Lehmann, A.R. 1992: Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene. Nucleic Acids Research 20(6): 1201-1208

Lemm, J.A.; Durbin, R.K.; Stollar, V.; Rice, C.M. 1990: Mutations which alter the level or structure of nsP4 can affect the efficiency of Sindbis virus replication in a host-dependent manner. Journal of Virology 64(6): 3001-3011

Skinner, R.H.; Stark, M.J.; Dahlberg, A.E. 1985: Mutations within the 23S rRNA coding sequence of E. coli which block ribosome assembly. EMBO Journal 4(6): 1605-1608