Molecular mechanisms underlying hereditary nonpolyposis colorectal carcinoma.
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[1] K Sankaranarayanan,et al. Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. III. Effects of incomplete penetrance and dose-dependent radiosensitivity on cancer risks in populations. , 1997, Radiation research.
[2] K. Kinzler,et al. Genomic organization of the human PMS2 gene family. , 1995, Genomics.
[3] T. Petes,et al. Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[4] E. Seeberg,et al. The base excision repair pathway. , 1995, Trends in biochemical sciences.
[5] R. Kolodner. Mismatch repair: mechanisms and relationship to cancer susceptibility. , 1995, Trends in biochemical sciences.
[6] M. Hawn,et al. Evidence for a connection between the mismatch repair system and the G2 cell cycle checkpoint. , 1995, Cancer research.
[7] Asad Umar,et al. A hPMS2 Mutant Cell Line Is Defective in Strand-specific Mismatch Repair (*) , 1995, The Journal of Biological Chemistry.
[8] C. Boland,et al. Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives. , 1995, Journal of the National Cancer Institute.
[9] K Sankaranarayanan,et al. Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. I. Background. , 1995, Radiation research.
[10] M. Radman,et al. Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer , 1995, Cell.
[11] Jian Yu,et al. Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis , 1995, Cell.
[12] K. Kinzler,et al. Mutations of GTBP in genetically unstable cells. , 1995, Science.
[13] P. Modrich,et al. Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells. , 1995, Science.
[14] J. Jiricny,et al. GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells. , 1995, Science.
[15] K. Kinzler,et al. Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability. , 1995, Science.
[16] K. Kinzler,et al. Mismatch repair deficiency in phenotypically normal human cells , 1995, Science.
[17] S. Tornaletti,et al. Complete and tissue-independent methylation of CpG sites in the p53 gene: implications for mutations in human cancers. , 1995, Oncogene.
[18] P. Modrich,et al. Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[19] L. New,et al. Mismatch correction acts as a barrier to homeologous recombination in Saccharomyces cerevisiae. , 1995, Genetics.
[20] J. A. Halliday,et al. Editing DNA replication and recombination by mismatch repair: from bacterial genetics to mechanisms of predisposition to cancer in humans. , 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[21] R. Kolodner,et al. The Saccharomyces cerevisiae Msh2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions. , 1995, Genes & development.
[22] Y. Nakamura,et al. Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes. , 1994, Biochemical and biophysical research communications.
[23] T. Kunkel,et al. DNA loop repair by human cell extracts. , 1994, Science.
[24] G. Aquilina,et al. A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[25] R. Fleischmann,et al. Mutations of two P/WS homologues in hereditary nonpolyposis colon cancer , 1994, Nature.
[26] T. Prolla,et al. MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast. , 1994, Science.
[27] Sajeev P. Cherian,et al. Human chromosome 3 corrects mismatch repair deficiency and microsatellite instability and reduces N-methyl-N'-nitro-N-nitrosoguanidine tolerance in colon tumor cells with homozygous hMLH1 mutation. , 1994, Cancer research.
[28] M. Meuth,et al. Mutator phenotypes in human colorectal carcinoma cell lines. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[29] Y. Kow,et al. Base Excision Repair in E. Coli—an Overview a , 1994, Annals of the New York Academy of Sciences.
[30] A. McCullough,et al. Nucleotide Excision Repair in E. Coli a , 1994, Annals of the New York Academy of Sciences.
[31] J. Weissenbach,et al. Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[32] P. Jones,et al. Ubiquitous and tenacious methylation of the CpG site in codon 248 of the p53 gene may explain its frequent appearance as a mutational hot spot in human cancer , 1994, Molecular and cellular biology.
[33] J. Hoeijmakers,et al. The molecular basis of nucleotide excision repair syndromes. , 1994, Mutation research.
[34] R. Reenan,et al. Interaction between mismatch repair and genetic recombination in Saccharomyces cerevisiae. , 1994, Genetics.
[35] M. Radman,et al. Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[36] R. Fleischmann,et al. Mutation of a mutL homolog in hereditary colon cancer. , 1994, Science.
[37] D. Ward,et al. Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer , 1994, Nature.
[38] J. Jiricny,et al. Mismatch repair and cancer , 1994, Nature.
[39] S. West. The processing of recombination intermediates: Mechanistic insights from studies of bacterial proteins , 1994, Cell.
[40] Bert Vogelstein,et al. Hypermutability and mismatch repair deficiency in RER+ tumor cells , 1993, Cell.
[41] Robin J. Leach,et al. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer , 1993, Cell.
[42] L. Aaltonen,et al. Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history. , 1993, Cancer research.
[43] N. Copeland,et al. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer , 1993, Cell.
[44] A. Lindblom,et al. Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer , 1993, Nature Genetics.
[45] Tomas A. Prolla,et al. Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair , 1993, Nature.
[46] Darryl Shibata,et al. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis , 1993, Nature.
[47] J. Griffith,et al. Bidirectional excision in methyl-directed mismatch repair. , 1993, The Journal of biological chemistry.
[48] P. Modrich,et al. Methyl-directed mismatch repair is bidirectional. , 1993, The Journal of biological chemistry.
[49] W. Fang,et al. Human strand-specific mismatch repair occurs by a bidirectional mechanism similar to that of the bacterial reaction. , 1993, The Journal of biological chemistry.
[50] K. Kinzler,et al. Clues to the pathogenesis of familial colorectal cancer. , 1993, Science.
[51] J. Weber,et al. Genetic mapping of a locus predisposing to human colorectal cancer. , 1993, Science.
[52] S N Thibodeau,et al. Microsatellite instability in cancer of the proximal colon. , 1993, Science.
[53] C. Boland,et al. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review. , 1993, Gastroenterology.
[54] G. Aquilina,et al. Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage , 1993, Nature.
[55] R. Reenan,et al. Characterization of insertion mutations in the Saccharomyces cerevisiae MSH1 and MSH2 genes: evidence for separate mitochondrial and nuclear functions. , 1992, Genetics.
[56] R. Reenan,et al. Isolation and characterization of two Saccharomyces cerevisiae genes encoding homologs of the bacterial HexA and MutS mismatch repair proteins. , 1992, Genetics.
[57] P. Modrich,et al. Initiation of methyl-directed mismatch repair. , 1992, The Journal of biological chemistry.
[58] J. Haber. Exploring the pathways of homologous recombination , 1992, Current Biology.
[59] M. Sporn,et al. Inhibition of growth by transforming growth factor-beta following fusion of two nonresponsive human carcinoma cell lines. Implication of the type II receptor in growth inhibitory responses. , 1992, The Journal of biological chemistry.
[60] M. Radman,et al. Control of large chromosomal duplications in Escherichia coli by the mismatch repair system. , 1991, Genetics.
[61] L. Loeb,et al. Mutator phenotype may be required for multistage carcinogenesis. , 1991, Cancer research.
[62] J. Massagué,et al. Responsiveness to transforming growth factor-beta (TGF-beta) restored by genetic complementation between cells defective in TGF-beta receptors I and II. , 1991, The Journal of biological chemistry.
[63] T. Kunkel,et al. Heteroduplex repair in extracts of human HeLa cells. , 1991, The Journal of biological chemistry.
[64] J. Massagué,et al. Concomitant loss of transforming growth factor (TGF)-beta receptor types I and II in TGF-beta-resistant cell mutants implicates both receptor types in signal transduction. , 1990, The Journal of biological chemistry.
[65] M. Radman,et al. DNA mismatch repair in Xenopus egg extracts: repair efficiency and DNA repair synthesis for all single base-pair mismatches. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[66] G. Coetzee,et al. 5-Methylcytosine as an endogenous mutagen in the human LDL receptor and p53 genes. , 1990, Science.
[67] P. Modrich,et al. Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[68] M. Ehrlich,et al. Spontaneous deamination of cytosine and 5-methylcytosine residues in DNA and replacement of 5-methylcytosine residues with cytosine residues. , 1990, Mutation research.
[69] M. Radman,et al. The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants , 1989, Nature.
[70] L. Loeb,et al. Endogenous carcinogenesis: molecular oncology into the twenty-first century--presidential address. , 1989, Cancer research.
[71] S. Fogel,et al. Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB , 1989, Journal of bacteriology.
[72] S. Fogel,et al. Heteroduplex DNA correction in Saccharomyces cerevisiae is mismatch specific and requires functional PMS genes , 1989, Molecular and cellular biology.
[73] P. Modrich,et al. DNA mismatch correction in a defined system. , 1989, Science.
[74] J. Andersen,et al. Specificity of mismatch repair following transformation of Saccharomyces cerevisiae with heteroduplex plasmid DNA. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[75] P. Modrich,et al. Methyl-directed DNA mismatch correction. , 1989, The Journal of biological chemistry.
[76] J. Massagué,et al. Transforming growth factor-beta inhibition of epithelial cell proliferation linked to the expression of a 53-kDa membrane receptor. , 1989, The Journal of biological chemistry.
[77] P. Modrich,et al. Isolation and characterization of the Escherichia coli mutL gene product. , 1989, The Journal of biological chemistry.
[78] J. Jiricny,et al. Different base/base mispairs are corrected with different efficiencies and specificities in monkey kidney cells , 1988, Cell.
[79] P. Modrich,et al. Mispair specificity of methyl-directed DNA mismatch correction in vitro. , 1988, The Journal of biological chemistry.
[80] P. Modrich,et al. Isolation and characterization of the Escherichia coli mutH gene product. , 1987, The Journal of biological chemistry.
[81] M. Lieb,et al. Bacterial genes mutL, mutS, and dcm participate in repair of mismatches at 5-methylcytosine sites , 1987, Journal of bacteriology.
[82] R. Kolodner,et al. The role of heteroduplex correction in gene conversion in Saccharomyces cerevisiae , 1987, Nature.
[83] R. Zell,et al. DNA mismatch‐repair in Escherichia coli counteracting the hydrolytic deamination of 5‐methyl‐cytosine residues. , 1987, The EMBO journal.
[84] P. Glazer,et al. DNA mismatch repair detected in human cell extracts , 1987, Molecular and cellular biology.
[85] P. Modrich,et al. Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[86] S. Lacks,et al. Heteroduplex deoxyribonucleic acid base mismatch repair in bacteria , 1986, Microbiological reviews.
[87] S. Feinstein,et al. Hyper-recombining recipient strains in bacterial conjugation. , 1986, Genetics.
[88] Henry Huang,et al. Homologous recombination in Escherichia coli: dependence on substrate length and homology. , 1986, Genetics.
[89] J. H. Taylor,et al. One role for DNA methylation in vertebrate cells is strand discrimination in mismatch repair. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[90] J. Game,et al. Meiotic gene conversion mutants in Saccharomyces cerevisiae. I. Isolation and characterization of pms1-1 and pms1-2. , 1985, Genetics.
[91] M. Marinus,et al. Mismatch repair of cis-diamminedichloroplatinum(II)-induced DNA damage. , 1985, Molecular pharmacology.
[92] P. Schendel,et al. Kinetics of methylation in Escherichia coli K-12 , 1984, Journal of bacteriology.
[93] F. Troncale,et al. Familial colonic cancer without antecedent polyposis. , 1984, Annals of internal medicine.
[94] M. Sekiguchi,et al. Identification of the uvrD gene product of Escherichia coli as DNA helicase II and its induction by DNA-damaging agents. , 1984, The Journal of biological chemistry.
[95] R. Scheuermann,et al. Identification of the epsilon-subunit of Escherichia coli DNA polymerase III holoenzyme as the dnaQ gene product: a fidelity subunit for DNA replication. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[96] P. Modrich,et al. Methyl-directed repair of DNA base-pair mismatches in vitro. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[97] S. R. Kushner,et al. DNA repair in Escherichia coli: identification of the uvrD gene product. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[98] M. Marinus,et al. Mismatch correction at O6-methylguanine residues in E. coli DNA , 1982, Nature.
[99] A. Fersht,et al. DNA polymerase accuracy and spontaneous mutation rates: frequencies of purine.purine, purine.pyrimidine, and pyrimidine.pyrimidine mismatches during DNA replication. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[100] S. Fogel,et al. Mitotic recombination in yeast: isolation and characterization of mutants with enhanced spontaneous mitotic gene conversion rates. , 1980, Genetics.
[101] B W Glickman,et al. Escherichia coli mutator mutants deficient in methylation-instructed DNA mismatch correction. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[102] Philip J. Farabaugh,et al. Molecular basis of base substitution hotspots in Escherichia coli , 1978, Nature.
[103] M. Meselson,et al. Repair tracts in mismatched DNA heteroduplexes. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[104] M. D. Topal,et al. Complementary base pairing and the origin of substitution mutations , 1976, Nature.
[105] M. Fox,et al. Marker discrimination in transformation and mutation of pneumococcus. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[106] S. Lacks. Mutants of Diplococcus pneumoniae that Lack Deoxyribonucleases and Other Activities Possibly Pertinent to Genetic Transformation , 1970, Journal of bacteriology.
[107] Ernest,et al. Enzymatic synthesis of deoxyribonucleic acid. , 1969, Harvey lectures.
[108] J. Drake,et al. Spontaneous Mutation: Comparative Rates of Spontaneous Mutation , 1969, Nature.
[109] H. Ephrussi-Taylor,et al. Genetic Studies of Recombining DNA in Pneumococcal Transformation , 1966, The Journal of general physiology.
[110] P. Modrich,et al. Mismatch repair in replication fidelity, genetic recombination, and cancer biology. , 1996, Annual review of biochemistry.
[111] W. Thilly,et al. Mismatch repair and genetic stability in human cells. , 1993, Cold Spring Harbor symposia on quantitative biology.
[112] J. Massagué,et al. TGF beta signals through a heteromeric protein kinase receptor complex. , 1992, Cell.
[113] H. Echols,et al. Fidelity mechanisms in DNA replication. , 1991, Annual review of biochemistry.
[114] P. Modrich,et al. Mechanisms and biological effects of mismatch repair. , 1991, Annual review of genetics.
[115] J. Griffith,et al. Gap formation is associated with methyl-directed mismatch correction under conditions of restricted DNA synthesis. , 1989, Genome.
[116] R. Elston,et al. Segregation analysis of hereditary nonpolyposis colorectal cancer , 1986, Genetic epidemiology.
[117] P. Modrich,et al. Repair of DNA base-pair mismatches in extracts of Escherichia coli. , 1984, Cold Spring Harbor symposia on quantitative biology.
[118] T. Kunkel,et al. Fidelity of DNA synthesis. , 1982, Annual review of biochemistry.
[119] E. Cox. Bacterial mutator genes and the control of spontaneous mutation. , 1976, Annual review of genetics.
[120] H. Spatz,et al. Escherichia coli mutants uvr D and uvr E deficient in gene conversion of lambda-heteroduplexes. , 1975, Molecular & general genetics : MGG.
[121] A. Kornberg,et al. Enzymatic synthesis of deoxyribonucleic acid. 36. A proofreading function for the 3' leads to 5' exonuclease activity in deoxyribonucleic acid polymerases. , 1972, The Journal of biological chemistry.
[122] J. Drake. Comparative rates of spontaneous mutation. , 1969, Nature.