-
2
-
-
0026355962
-
Mechanisms and biological effects of mismatch repair
-
Modrich P. Mechanisms and biological effects of mismatch repair. Annu Rev Genet. 25:1991;229-253.
-
(1991)
Annu Rev Genet
, vol.25
, pp. 229-253
-
-
Modrich, P.1
-
3
-
-
0000083876
-
Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs
-
Su S-S, Modrich P. Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs. Proc Natl Acad Sci USA. 83:1986;5057-5061.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 5057-5061
-
-
Su, S.-S.1
Modrich, P.2
-
4
-
-
0024396565
-
DNA mismatch correction in a defined system
-
Lahue RS, Au KG, Modrich P. DNA mismatch correction in a defined system. Science. 245:1989;160-164.
-
(1989)
Science
, vol.245
, pp. 160-164
-
-
Lahue, R.S.1
Au, K.G.2
Modrich, P.3
-
5
-
-
0014106075
-
Mutator gene of Escherichia coli B
-
Siegel EC, Bryson V. Mutator gene of Escherichia coli B. J Bacteriol. 94:1967;38-47.
-
(1967)
J Bacteriol
, vol.94
, pp. 38-47
-
-
Siegel, E.C.1
Bryson, V.2
-
6
-
-
0024469392
-
The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants
-
Rayssiguier C, Thaler DS, Radman M. The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants. Nature. 342:1989;396-401.
-
(1989)
Nature
, vol.342
, pp. 396-401
-
-
Rayssiguier, C.1
Thaler, D.S.2
Radman, M.3
-
7
-
-
0020332947
-
6-methylguanine residues in E. coli DNA
-
6-methylguanine residues in E. coli DNA. Nature. 296:1982;868-869.
-
(1982)
Nature
, vol.296
, pp. 868-869
-
-
Karran, P.1
Marinus, M.G.2
-
8
-
-
0030034077
-
Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide excision repair of the lactose operon in Escherichia coli
-
of special interest. By demonstrating that mutations in MutS and MutL selectively abolish rapid repair in the transcribed strand of DNA, this study was the first to show an association between mismatch correction and nucleotide excision repair and implicated components of the DNA mismatch repair system in transcription-coupled repair.
-
Mellon I, Champe GN. Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide excision repair of the lactose operon in Escherichia coli. of special interest Proc Natl Acad Sci USA. 93:1995;1292-1297 By demonstrating that mutations in MutS and MutL selectively abolish rapid repair in the transcribed strand of DNA, this study was the first to show an association between mismatch correction and nucleotide excision repair and implicated components of the DNA mismatch repair system in transcription-coupled repair.
-
(1995)
Proc Natl Acad Sci USA
, vol.93
, pp. 1292-1297
-
-
Mellon, I.1
Champe, G.N.2
-
9
-
-
0029042130
-
Identification of mismatch repair genes and their role in the development of cancer
-
Fishel R, Kolodner RD. Identification of mismatch repair genes and their role in the development of cancer. Curr Opin Genet Dev. 5:1995;382-395.
-
(1995)
Curr Opin Genet Dev
, vol.5
, pp. 382-395
-
-
Fishel, R.1
Kolodner, R.D.2
-
10
-
-
0026446241
-
Isolation and characterization of two Saccharomyces cerevisiae genes encoding homologs of the bacterial HexA and MutS mismatch repair proteins
-
Reenan RAG, Kolodner RD. Isolation and characterization of two Saccharomyces cerevisiae genes encoding homologs of the bacterial HexA and MutS mismatch repair proteins. Genetics. 132:1992;963-973.
-
(1992)
Genetics
, vol.132
, pp. 963-973
-
-
Reenan, R.A.G.1
Kolodner, R.D.2
-
11
-
-
0027245585
-
The yeast gene MSH3 defines a new class of eukaryotic MutS homologues
-
New L, Liu K, Crouse GF. The yeast gene MSH3 defines a new class of eukaryotic MutS homologues. Mol Gen Genet. 239:1993;97-108.
-
(1993)
Mol Gen Genet
, vol.239
, pp. 97-108
-
-
New, L.1
Liu, K.2
Crouse, G.F.3
-
12
-
-
0028215472
-
Large-scale analysis of gene expression, protein localization and gene disruption in Saccharomyces cerevisiae
-
Burns N, Grimwade B, Ross-Macdonald PB, Choi E, Finberg K, Roeder GS, Snyder MS. Large-scale analysis of gene expression, protein localization and gene disruption in Saccharomyces cerevisiae. Genes Dev. 8:1994;1087-1105.
-
(1994)
Genes Dev
, vol.8
, pp. 1087-1105
-
-
Burns, N.1
Grimwade, B.2
Ross-Macdonald, P.B.3
Choi, E.4
Finberg, K.5
Roeder, G.S.6
Snyder, M.S.7
-
13
-
-
0029145505
-
MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair
-
Hollingsworth NM, Ponte L, Halsey C. MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair. Genes Dev. 9:1995;1728-1739.
-
(1995)
Genes Dev
, vol.9
, pp. 1728-1739
-
-
Hollingsworth, N.M.1
Ponte, L.2
Halsey, C.3
-
14
-
-
0026445628
-
Characterization of insertion mutations in the Saccharomyces cerevisiae MSH1 and MSH2 genes: Evidence for separate mitochondrial and nuclear functions
-
Reenan RAG, Kolodner RD. Characterization of insertion mutations in the Saccharomyces cerevisiae MSH1 and MSH2 genes: evidence for separate mitochondrial and nuclear functions. Genetics. 132:1992;975-985.
-
(1992)
Genetics
, vol.132
, pp. 975-985
-
-
Reenan, R.A.G.1
Kolodner, R.D.2
-
15
-
-
0029868110
-
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair
-
of outstanding interest. In a comprehensive genetic analysis, the properties of MSH2, MSh3, and MSh6 were studied. The results indicated that S. cerevisiae has two pathways of MSH2-dependent mismatch repair: one that recognized simple mispairs and requires MSH2 and MSH6 and a second that recognizes small insertion/deletion mispairs and requires a combination of either MSH2 and MSH6 or MSH2 and MSH3.
-
Marsischky GT, Filosi N, Kane MF, Kolodner R. Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair. of outstanding interest Genes Dev. 10:1996;407-420 In a comprehensive genetic analysis, the properties of MSH2, MSh3, and MSh6 were studied. The results indicated that S. cerevisiae has two pathways of MSH2-dependent mismatch repair: one that recognized simple mispairs and requires MSH2 and MSH6 and a second that recognizes small insertion/deletion mispairs and requires a combination of either MSH2 and MSH6 or MSH2 and MSH3.
-
(1996)
Genes Dev
, vol.10
, pp. 407-420
-
-
Marsischky, G.T.1
Filosi, N.2
Kane, M.F.3
Kolodner, R.4
-
16
-
-
0029870366
-
Requirement of the yeast Msh3 and Msh6 genes for MSH2-dependent genomic stability
-
of outstanding interest. of special interest. See annotation [15].
-
of outstanding interest Johnson RE, Kovvali GK, Prakash L, Prakash S. Requirement of the yeast Msh3 and Msh6 genes for MSH2-dependent genomic stability. of special interest Biol Chem. 271:1996;7285-7288 See annotation [15].
-
(1996)
Biol Chem
, vol.271
, pp. 7285-7288
-
-
Johnson, R.E.1
Kovvali, G.K.2
Prakash, L.3
Prakash, S.4
-
17
-
-
0028560427
-
Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction
-
Ross-Macdonald P, Roeder GS. Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction. Cell. 79:1994;1069-1080.
-
(1994)
Cell
, vol.79
, pp. 1069-1080
-
-
Ross-Macdonald, P.1
Roeder, G.S.2
-
18
-
-
0030250603
-
Binding of insertion/deletion DNA mismatches by the heterodimer of yeast mismatch repair proteins MSH2 and MSH3
-
Habraken Y, Sung P, Prakash L, Prakash S. Binding of insertion/deletion DNA mismatches by the heterodimer of yeast mismatch repair proteins MSH2 and MSH3. Curr Biol. 6:1996;1186-1187.
-
(1996)
Curr Biol
, vol.6
, pp. 1186-1187
-
-
Habraken, Y.1
Sung, P.2
Prakash, L.3
Prakash, S.4
-
19
-
-
0030113449
-
Msh6, a Saccharomyces cerevisiae protein that binds to mismatches as a heterodimer with MSH2
-
Iaccarino I, Palombo F, Drummond J, Totty NF, Hsuan JJ, Modrich P, Jiricny J. Msh6, a Saccharomyces cerevisiae protein that binds to mismatches as a heterodimer with MSH2. Curr Biol. 6:1996;484-486.
-
(1996)
Curr Biol
, vol.6
, pp. 484-486
-
-
Iaccarino, I.1
Palombo, F.2
Drummond, J.3
Totty, N.F.4
Hsuan, J.J.5
Modrich, P.6
Jiricny, J.7
-
20
-
-
0028981276
-
The Saccharomyces cerevisiae MSH2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions
-
of special interest. By using purified yeast MSH2 protein, it was demonstrated that MSH2 could bind selectively to duplex oligonucleotide substrates containing a G/T mismatch, 1-14-nucleotide insertion mismatches, and palindromic (12-14-nucleotide) insertion mismatches.
-
Alani E, Chi NW, Kolodner R. The Saccharomyces cerevisiae MSH2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions. of special interest Genes Dev. 9:1995;234-247 By using purified yeast MSH2 protein, it was demonstrated that MSH2 could bind selectively to duplex oligonucleotide substrates containing a G/T mismatch, 1-14-nucleotide insertion mismatches, and palindromic (12-14-nucleotide) insertion mismatches.
-
(1995)
Genes Dev
, vol.9
, pp. 234-247
-
-
Alani, E.1
Chi, N.W.2
Kolodner, R.3
-
21
-
-
0028053411
-
Purified human MSH2 protein binds to DNA containing mismatched nucleotides
-
Fishel R, Ewel A, Lescoe MK. Purified human MSH2 protein binds to DNA containing mismatched nucleotides. Cancer Res. 54:1994;5539-5542.
-
(1994)
Cancer Res
, vol.54
, pp. 5539-5542
-
-
Fishel, R.1
Ewel, A.2
Lescoe, M.K.3
-
22
-
-
0028595722
-
Binding of mismatched microsatellite DNA sequences by the human MSH2 protein
-
Fishel R, Ewel A, Lee S, Lescoe MK, Griffith J. Binding of mismatched microsatellite DNA sequences by the human MSH2 protein. Science. 266:1994;1403-1405.
-
(1994)
Science
, vol.266
, pp. 1403-1405
-
-
Fishel, R.1
Ewel, A.2
Lee, S.3
Lescoe, M.K.4
Griffith, J.5
-
23
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
Fishel RA, Lescoe MK, Rao MRS, Copland N, Jenkins N, Garber J, Kane M, Kolodner R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell. 75:1993;1027-1038.
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.A.1
Lescoe, M.K.2
Rao, M.R.S.3
Copland, N.4
Jenkins, N.5
Garber, J.6
Kane, M.7
Kolodner, R.8
-
24
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, Peltomaki P, Sistonen P, Aaltonen LA, Nystrom-Lahti M, et al. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell. 75:1993;1215-1225.
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
Peltomaki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nystrom-Lahti, M.10
-
25
-
-
0025773554
-
Mutator phenotype may be required for multistage carcinogenesis
-
Loeb LA. Mutator phenotype may be required for multistage carcinogenesis. Cancer Res. 51:1991;3075-3079.
-
(1991)
Cancer Res
, vol.51
, pp. 3075-3079
-
-
Loeb, L.A.1
-
26
-
-
36949071802
-
Multiple mutation theory of carcinogenesis
-
Fisher JC. Multiple mutation theory of carcinogenesis. Nature. 181:1958;651-652.
-
(1958)
Nature
, vol.181
, pp. 651-652
-
-
Fisher, J.C.1
-
27
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon ER, Vogelstein B. A genetic model for colorectal tumorigenesis. Cell. 61:1990;759-767.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
28
-
-
0028221943
-
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary nonpolyposis colon cancer
-
Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A, et al. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary nonpolyposis colon cancer. Nature. 368:1994;258-261.
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
Baker, S.M.2
Morrison, P.T.3
Warren, G.4
Smith, L.G.5
Lescoe, M.K.6
Kane, M.7
Earabino, C.8
Lipford, J.9
Lindblom, A.10
-
29
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos N, Nicolaides NC, Wei Y-F, Ruben SM, Carter KC, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, Adams MD, et al. Mutation of a mutL homolog in hereditary colon cancer. Science. 263:1994;1625-1629.
-
(1994)
Science
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Wei, Y.-F.3
Ruben, S.M.4
Carter, K.C.5
Rosen, C.A.6
Haseltine, W.A.7
Fleischmann, R.D.8
Fraser, C.M.9
Adams, M.D.10
-
30
-
-
0027933070
-
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
-
Nicolaides NC, Papadopoulos N, Liu B, Wei Y-F, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, et al. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature. 371:1994;75-80.
-
(1994)
Nature
, vol.371
, pp. 75-80
-
-
Nicolaides, N.C.1
Papadopoulos, N.2
Liu, B.3
Wei, Y.-F.4
Carter, K.C.5
Ruben, S.M.6
Rosen, C.A.7
Haseltine, W.A.8
Fleischmann, R.D.9
Fraser, C.M.10
-
31
-
-
0024385605
-
Dual bidirectional promoters at the mouse dhfr locus: Cloning and characterization of two mRNA classes of the divergently transcribed Rep-1 gene
-
Linton JP, Yen JY, Selby E, Chen Z, Chinsky JM, Liu K, Kellems RE, Crouse GF. Dual bidirectional promoters at the mouse dhfr locus: cloning and characterization of two mRNA classes of the divergently transcribed Rep-1 gene. Mol Cell Biol. 9:1989;3058-3072.
-
(1989)
Mol Cell Biol
, vol.9
, pp. 3058-3072
-
-
Linton, J.P.1
Yen, J.Y.2
Selby, E.3
Chen, Z.4
Chinsky, J.M.5
Liu, K.6
Kellems, R.E.7
Crouse, G.F.8
-
32
-
-
0024994313
-
Analysis of the mouse Dhfr/Rep-3 major promoter region by using linker-scanning and internal deletion mutations and DNase I footprinting
-
Smith ML, Mitchell PJ, Crouse GF. Analysis of the mouse Dhfr/Rep-3 major promoter region by using linker-scanning and internal deletion mutations and DNase I footprinting. Mol Cell Biol. 10:1990;6003-6012.
-
(1990)
Mol Cell Biol
, vol.10
, pp. 6003-6012
-
-
Smith, M.L.1
Mitchell, P.J.2
Crouse, G.F.3
-
33
-
-
0024328152
-
Isolation and characterization of cDNA clones derived from the divergently transcribed gene in the region upstream from the human dihydrofolate reductase gene
-
Fujii H, Shimada T. Isolation and characterization of cDNA clones derived from the divergently transcribed gene in the region upstream from the human dihydrofolate reductase gene. J Biol Chem. 264:1989;10057-10064.
-
(1989)
J Biol Chem
, vol.264
, pp. 10057-10064
-
-
Fujii, H.1
Shimada, T.2
-
34
-
-
0029008683
-
GTBP, a 160 kilodalton protein essential for mismatch binding activity in human cells
-
Palombo F, Gallinari P, Iaccarino I, Lettieri T, Hughes M, D'Arrigo A, Truong O, Hsuan JJ, Jiricny J. GTBP, a 160 kilodalton protein essential for mismatch binding activity in human cells. Science. 268:1995;1912-1914.
-
(1995)
Science
, vol.268
, pp. 1912-1914
-
-
Palombo, F.1
Gallinari, P.2
Iaccarino, I.3
Lettieri, T.4
Hughes, M.5
D'Arrigo, A.6
Truong, O.7
Hsuan, J.J.8
Jiricny, J.9
-
35
-
-
0028596385
-
Cloning and expression of the Xenopus and mouse MSH2 DNA mismatch repair genes
-
Varlet I, Pallard C, Radman M, Moreau J, De Wind N. Cloning and expression of the Xenopus and mouse MSH2 DNA mismatch repair genes. Nucleic Acids Res. 22:1994;5723-5728.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 5723-5728
-
-
Varlet, I.1
Pallard, C.2
Radman, M.3
Moreau, J.4
De Wind, N.5
-
36
-
-
0025734115
-
Altering the conserved nucleotide binding motif in the Salmonella typhimurium MutS mismatch repair protein affects both its ATPase and mismatch binding activities
-
Haber LT, Walker GC. Altering the conserved nucleotide binding motif in the Salmonella typhimurium MutS mismatch repair protein affects both its ATPase and mismatch binding activities. EMBO J. 10:1991;2707-2715.
-
(1991)
EMBO J
, vol.10
, pp. 2707-2715
-
-
Haber, L.T.1
Walker, G.C.2
-
37
-
-
0028157956
-
A requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the baterial mutL gene
-
Prolla TA, Christie D-M, Liskay RM. A requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the baterial mutL gene. Mol Cell Biol. 14:1994;407-415.
-
(1994)
Mol Cell Biol
, vol.14
, pp. 407-415
-
-
Prolla, T.A.1
Christie, D.-M.2
Liskay, R.M.3
-
38
-
-
0024209144
-
A human 200kDa protein binds selectively to DNA fragments containing GT mismatches
-
Jiricny J, Hughes M, Corman N, Rudkin BB. A human 200kDa protein binds selectively to DNA fragments containing GT mismatches. Proc Natl Acad Sci USA. 85:1988;8860-8864.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 8860-8864
-
-
Jiricny, J.1
Hughes, M.2
Corman, N.3
Rudkin, B.B.4
-
39
-
-
23444439521
-
Mismatch repair and cancer
-
Palombo F, Hughes M, Jiricny J, Truong O, Hsuan J. Mismatch repair and cancer. Nature. 367:1994;417.
-
(1994)
Nature
, vol.367
, pp. 417
-
-
Palombo, F.1
Hughes, M.2
Jiricny, J.3
Truong, O.4
Hsuan, J.5
-
40
-
-
0027095976
-
The purification of a human mismatch binding protein and identification of its associated ATPase and helicase activities
-
Hughes MJ, Jiricny J. The purification of a human mismatch binding protein and identification of its associated ATPase and helicase activities. J Biol Chem. 267:1992;23876-23882.
-
(1992)
J Biol Chem
, vol.267
, pp. 23876-23882
-
-
Hughes, M.J.1
Jiricny, J.2
-
41
-
-
0029070143
-
Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells
-
of outstanding interest. First publication to demonstrate that hMSH2 and hMSH6 (GTBP/p160) acted as a heterodimer in mismatch recognition/binding in vitro.
-
Drummond JT, Li G-M, Longley MJ, Modrich P. Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells. of outstanding interest Science. 268:1995;1909-1912 First publication to demonstrate that hMSH2 and hMSH6 (GTBP/p160) acted as a heterodimer in mismatch recognition/binding in vitro.
-
(1995)
Science
, vol.268
, pp. 1909-1912
-
-
Drummond, J.T.1
Li, G.-M.2
Longley, M.J.3
Modrich, P.4
-
42
-
-
0030465237
-
HMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6
-
of outstanding interest. Demonstration that hMSH2 forms specific heterodimeric protein complexes with both hMSH3 and hMSH6. The hMSH2-hMSH3 and hMSH2-hMSH6 complexes have overlapping and redundant mispair recognition properties which explains the low prevalence of hmsh3 and hmsh6 in HNPCC.
-
Acharya S, Wilson T, Gradia S, Kane MF, Guerrette S, Marsischky GT, Kolodner R, Fishel R. hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6. of outstanding interest Proc Natl Acad Sci USA. 93:1996;13629-13634 Demonstration that hMSH2 forms specific heterodimeric protein complexes with both hMSH3 and hMSH6. The hMSH2-hMSH3 and hMSH2-hMSH6 complexes have overlapping and redundant mispair recognition properties which explains the low prevalence of hmsh3 and hmsh6 in HNPCC.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13629-13634
-
-
Acharya, S.1
Wilson, T.2
Gradia, S.3
Kane, M.F.4
Guerrette, S.5
Marsischky, G.T.6
Kolodner, R.7
Fishel, R.8
-
43
-
-
0029659046
-
HMutSb, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA
-
Palombo F, Iccarino I, Nakajima E, Ikejima M, Shimada T, Jiricny J. hMutSb, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA. Curr Biol. 6:1996;1181-1184.
-
(1996)
Curr Biol
, vol.6
, pp. 1181-1184
-
-
Palombo, F.1
Iccarino, I.2
Nakajima, E.3
Ikejima, M.4
Shimada, T.5
Jiricny, J.6
-
44
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov Y, Peinado MA, Malkbosyan S, Shibata D, Perucho M. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature. 363:1993;558-561.
-
(1993)
Nature
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkbosyan, S.3
Shibata, D.4
Perucho, M.5
-
45
-
-
0027314411
-
Microsatellite instability in cancer of the proximal colon
-
Thibodeau SN, Bren G, Schaid D. Microsatellite instability in cancer of the proximal colon. Science. 260:1993;816-819.
-
(1993)
Science
, vol.260
, pp. 816-819
-
-
Thibodeau, S.N.1
Bren, G.2
Schaid, D.3
-
46
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
Aaltonen LA, Peltomaki P, Leach F, Sistonen P, Pylkkanen SM, Mecklin J-P, Jarvinen H, Powell S, Jen J, Hamilton SR, et al. Clues to the pathogenesis of familial colorectal cancer. Science. 260:1993;812-816.
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomaki, P.2
Leach, F.3
Sistonen, P.4
Pylkkanen, S.M.5
Mecklin, J.-P.6
Jarvinen, H.7
Powell, S.8
Jen, J.9
Hamilton, S.R.10
-
47
-
-
0023649836
-
High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12
-
Levinson G, Gutman GA. High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. Nucleic Acids Res. 15:1987;5313-5338.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 5313-5338
-
-
Levinson, G.1
Gutman, G.A.2
-
48
-
-
0027306173
-
Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair
-
Strand M, Prolla TA, Liskay RM, Petes TD. Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair. Nature. 365:1993;274-276.
-
(1993)
Nature
, vol.365
, pp. 274-276
-
-
Strand, M.1
Prolla, T.A.2
Liskay, R.M.3
Petes, T.D.4
-
49
-
-
0028862897
-
Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae
-
of special interest. A genetic study in yeast which suggests that MSH3 encodes a protein with different substrate specificities than the other mismatch repair proteins. Mutations in this gene were shown to result in microsatellite instability and indicated that the human MSH3 homolog, MRP1, might be mutated in some tumors with microsatellite instability.
-
Strand M, Earley MC, Crouse GF, Petes TD. Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae. of special interest Proc Natl Acad Sci USA. 92:1995;10418-10421 A genetic study in yeast which suggests that MSH3 encodes a protein with different substrate specificities than the other mismatch repair proteins. Mutations in this gene were shown to result in microsatellite instability and indicated that the human MSH3 homolog, MRP1, might be mutated in some tumors with microsatellite instability.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 10418-10421
-
-
Strand, M.1
Earley, M.C.2
Crouse, G.F.3
Petes, T.D.4
-
50
-
-
0027137935
-
Hypermutability and mismatch repair deficiency in RER+ tumor cells
-
Parsons R, Li G-M, Longley MJ, Fang W-H, Papadopoulos N, Jen J, De la Chapelle A, Kinzler KW, Vogelstein B, Modrich P. Hypermutability and mismatch repair deficiency in RER+ tumor cells. Cell. 75:1993;1227-1236.
-
(1993)
Cell
, vol.75
, pp. 1227-1236
-
-
Parsons, R.1
Li, G.-M.2
Longley, M.J.3
Fang, W.-H.4
Papadopoulos, N.5
Jen, J.6
De La Chapelle, A.7
Kinzler, K.W.8
Vogelstein, B.9
Modrich, P.10
-
51
-
-
0000215505
-
Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability
-
Umar A, Boyer JC, Thomas DC, Nguyen DC, Risinger JI, Boyd J, Ionov Y, Perucho M, Kunkel TA. Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability. J Biol Chem. 259:1994;1-4.
-
(1994)
J Biol Chem
, vol.259
, pp. 1-4
-
-
Umar, A.1
Boyer, J.C.2
Thomas, D.C.3
Nguyen, D.C.4
Risinger, J.I.5
Boyd, J.6
Ionov, Y.7
Perucho, M.8
Kunkel, T.A.9
-
52
-
-
0028784167
-
Microsatellite instability, mismatch repair deficiency, and genetic defects in human cancer cell lines
-
Boyer JC, Umar A, Risinger JI, Lipford JR, Kane M, Yin S, Barrett JC, Kolodner RD, Kunkel TA. Microsatellite instability, mismatch repair deficiency, and genetic defects in human cancer cell lines. Cancer Res. 55:1995;6063-6070.
-
(1995)
Cancer Res
, vol.55
, pp. 6063-6070
-
-
Boyer, J.C.1
Umar, A.2
Risinger, J.I.3
Lipford, J.R.4
Kane, M.5
Yin, S.6
Barrett, J.C.7
Kolodner, R.D.8
Kunkel, T.A.9
-
53
-
-
0028224645
-
Mutator phenotype in human colorectal carcinoma cell lines
-
Bhattacharyya NP, Skandalis A, Ganesh A, Groden J, Meuth M. Mutator phenotype in human colorectal carcinoma cell lines. Proc Natl Acad Sci USA. 91:1994;6319-6323.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6319-6323
-
-
Bhattacharyya, N.P.1
Skandalis, A.2
Ganesh, A.3
Groden, J.4
Meuth, M.5
-
54
-
-
0015729624
-
Marker discrimination in transformation and mutation of pneumococcus
-
Tiraby J-G, Fox MS. Marker discrimination in transformation and mutation of pneumococcus. Proc Natl Acad Sci USA. 70:1973;3541-3545.
-
(1973)
Proc Natl Acad Sci USA
, vol.70
, pp. 3541-3545
-
-
Tiraby, J.-G.1
Fox, M.S.2
-
55
-
-
0016748011
-
Escherichia coli mutants uvrD uvrE deficient in gene conversion of lambda heteroduplexes
-
Nevers P, Spatz H. Escherichia coli mutants uvrD uvrE deficient in gene conversion of lambda heteroduplexes. Mol Gen Genet. 139:1975;233-243.
-
(1975)
Mol Gen Genet
, vol.139
, pp. 233-243
-
-
Nevers, P.1
Spatz, H.2
-
56
-
-
0028845722
-
Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas
-
Borresen AL, Lothe RA, Meling GI, Lystad S, Morrison P, Lipford J, Kane MF, Rognum TO, Kolodner RD. Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas. Hum Mol Genet. 4:1995;2065-2072.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2065-2072
-
-
Borresen, A.L.1
Lothe, R.A.2
Meling, G.I.3
Lystad, S.4
Morrison, P.5
Lipford, J.6
Kane, M.F.7
Rognum, T.O.8
Kolodner, R.D.9
-
57
-
-
0028859671
-
Mismatch repair gene defects in sporatic colorectal cancers with microsatellite instability
-
Liu B, Nicolaides MC, Markowitz S, Wilson JKV, Parsons RE, Jen J, Papadopolous N, Peltomaki P, De la Chapelle A, Hamilton SR, et al. Mismatch repair gene defects in sporatic colorectal cancers with microsatellite instability. Nat Genet. 9:1995;48-55.
-
(1995)
Nat Genet
, vol.9
, pp. 48-55
-
-
Liu, B.1
Nicolaides, M.C.2
Markowitz, S.3
Wilson, J.K.V.4
Parsons, R.E.5
Jen, J.6
Papadopolous, N.7
Peltomaki, P.8
De La Chapelle, A.9
Hamilton, S.R.10
-
58
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons R, Papadopoulos N, Nicolaides NC, Lynch HT, Watson P, Jass JR, Dunlop M, Wyllie A, Peltomaki P, et al. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med. 2:1996;169-174.
-
(1996)
Nat Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
Nicolaides, N.C.4
Lynch, H.T.5
Watson, P.6
Jass, J.R.7
Dunlop, M.8
Wyllie, A.9
Peltomaki, P.10
-
59
-
-
10144250305
-
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer
-
of outstanding interest. Mutational analysis of hMSH2 and hMLH1 suggests that >90% of HNPCC families, and a large fraction of sporadic microsatellite unstable tumors, have an alteration of one of these genes.
-
Moslein G, Tester DJ, Lindor NM, Honchel R, Cunningham JM, French AJ, Halling KC, Schwab M, Goretzki P, Thibodeau SN. Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. of outstanding interest Hum Mol Genet. 5:1996;1245-1252 Mutational analysis of hMSH2 and hMLH1 suggests that >90% of HNPCC families, and a large fraction of sporadic microsatellite unstable tumors, have an alteration of one of these genes.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1245-1252
-
-
Moslein, G.1
Tester, D.J.2
Lindor, N.M.3
Honchel, R.4
Cunningham, J.M.5
French, A.J.6
Halling, K.C.7
Schwab, M.8
Goretzki, P.9
Thibodeau, S.N.10
-
60
-
-
0029887819
-
Transcription-coupled repair deficiency and mutations in human mismatch repair genes
-
Mellon I, Deepak KR, Koi MC, Boland RC, Champe GN. Transcription-coupled repair deficiency and mutations in human mismatch repair genes. Science. 272:1996;557-560.
-
(1996)
Science
, vol.272
, pp. 557-560
-
-
Mellon, I.1
Deepak, K.R.2
Koi, M.C.3
Boland, R.C.4
Champe, G.N.5
-
61
-
-
0028606403
-
Mechanisms of DNA excision repair
-
Sancar A. Mechanisms of DNA excision repair. Science. 266:1994;954-956.
-
(1994)
Science
, vol.266
, pp. 954-956
-
-
Sancar, A.1
-
62
-
-
0027502938
-
Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage
-
Branch P, Aquilina G, Bignami M, Karran P. Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage. Nature. 362:1993;652-654.
-
(1993)
Nature
, vol.362
, pp. 652-654
-
-
Branch, P.1
Aquilina, G.2
Bignami, M.3
Karran, P.4
-
63
-
-
0027292234
-
An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair
-
Kat A, Thilly WG, Fang W-H, Longley MJ, Li G-M, Modrich P. An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. Proc Natl Acad Sci USA. 90:1993;6424-6428.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 6424-6428
-
-
Kat, A.1
Thilly, W.G.2
Fang, W.-H.3
Longley, M.J.4
Li, G.-M.5
Modrich, P.6
-
64
-
-
0029007870
-
DNA mismatch binding defects, DNA damage tolorance, and mutator phenotypes in human colorectal carcinoma cell lines
-
Branch P, Hampson R, Karran P. DNA mismatch binding defects, DNA damage tolorance, and mutator phenotypes in human colorectal carcinoma cell lines. Cancer Res. 55:1995;2304-2309.
-
(1995)
Cancer Res
, vol.55
, pp. 2304-2309
-
-
Branch, P.1
Hampson, R.2
Karran, P.3
-
65
-
-
0021888203
-
Mismatch repair and cis-diamminedichloroplatinum (II)-induced DNA damage
-
Fram RJ, Cusick PS, Wilson JM, Marinus MG. Mismatch repair and cis-diamminedichloroplatinum (II)-induced DNA damage. Mol Pharmacol. 28:1985;51-55.
-
(1985)
Mol Pharmacol
, vol.28
, pp. 51-55
-
-
Fram, R.J.1
Cusick, P.S.2
Wilson, J.M.3
Marinus, M.G.4
-
66
-
-
8944230189
-
Loss of mismatch repair in acquired resistance to cisplatin
-
of outstanding interest. A human ovarian tumor cell line was selected for resistance to cisplatin and subsequently found to have acquired a mutation in a human mismatch repair gene. Furthermore, cell lines with known mismatch repair mutations were also resistant to cisplatin.
-
Aebi S, Kurdi-Haidar B, Gordon R, Cenni B, Zheng H, Fink D, Christen RD, Boland CR, Koi M, Fishel R, et al. Loss of mismatch repair in acquired resistance to cisplatin. of outstanding interest Cancer Res. 56:1996;3087-3090 A human ovarian tumor cell line was selected for resistance to cisplatin and subsequently found to have acquired a mutation in a human mismatch repair gene. Furthermore, cell lines with known mismatch repair mutations were also resistant to cisplatin.
-
(1996)
Cancer Res
, vol.56
, pp. 3087-3090
-
-
Aebi, S.1
Kurdi-Haidar, B.2
Gordon, R.3
Cenni, B.4
Zheng, H.5
Fink, D.6
Christen, R.D.7
Boland, C.R.8
Koi, M.9
Fishel, R.10
-
67
-
-
0029812676
-
Cisplatin and adriamycin resistance are associated with MutLα and mismatch repair deficiency in ovarian tumor cell line
-
Drummond JT, Anthoney A, Brown R, Modrich P. Cisplatin and adriamycin resistance are associated with MutLα and mismatch repair deficiency in ovarian tumor cell line. J Biol Chem. 271:1996;19645-19648.
-
(1996)
J Biol Chem
, vol.271
, pp. 19645-19648
-
-
Drummond, J.T.1
Anthoney, A.2
Brown, R.3
Modrich, P.4
-
68
-
-
0030198880
-
The mismatch-repair protein hMSH2 binds selectively to DNA adducts of the anticancer drug cisplatin
-
of outstanding interest. The specific binding of purified hMSH2 protein to cisplatin-modified DNA suggested a role for hMSH2 in the mediation of cisplatin toxicity. The hMSH2 binding was also found to be specific for therapeutically active chemical isomers of platinum. Additionally, hMSH2 was found to be overexpressed in testicular and ovarian tissue; tumors in these tissues are treated most effectively by cisplatin.
-
Mello JA, Acharya S, Fishel R, Essigmann JM. The mismatch-repair protein hMSH2 binds selectively to DNA adducts of the anticancer drug cisplatin. of outstanding interest Chem Biol. 3:1996;579-589 The specific binding of purified hMSH2 protein to cisplatin-modified DNA suggested a role for hMSH2 in the mediation of cisplatin toxicity. The hMSH2 binding was also found to be specific for therapeutically active chemical isomers of platinum. Additionally, hMSH2 was found to be overexpressed in testicular and ovarian tissue; tumors in these tissues are treated most effectively by cisplatin.
-
(1996)
Chem Biol
, vol.3
, pp. 579-589
-
-
Mello, J.A.1
Acharya, S.2
Fishel, R.3
Essigmann, J.M.4
-
69
-
-
0029665878
-
Human MutSα recognizes damaged DNA base pairs containing O-6-methylguanine, O-4-methylthymine, or the cisplatin-D (GpG) adduct
-
of special interest. These studies suggest a direct involvement of the MutSα (hMSH2-hMSH6) complex in the cytotoxic effects and recognition of DNA-methylating agents as well as the cytotoxic effects and recognition of 1,2-intrastrand cis-diamminedichloroplatinum(II) adducts.
-
Duckett DR, Drummond JT, Murchie AIH, Reardon JT, Sancar A, Lilley DM, Modrich P. Human MutSα recognizes damaged DNA base pairs containing O-6-methylguanine, O-4-methylthymine, or the cisplatin-D (GpG) adduct. of special interest Proc Natl Acad Sci USA. 93:1996;6443-6447 These studies suggest a direct involvement of the MutSα (hMSH2-hMSH6) complex in the cytotoxic effects and recognition of DNA-methylating agents as well as the cytotoxic effects and recognition of 1,2-intrastrand cis-diamminedichloroplatinum(II) adducts.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 6443-6447
-
-
Duckett, D.R.1
Drummond, J.T.2
Murchie, A.I.H.3
Reardon, J.T.4
Sancar, A.5
Lilley, D.M.6
Modrich, P.7
-
70
-
-
0026750738
-
Self-distruction and tolerance in resistance of mammalian cells to alkylation damage
-
Karran P, Bignami M. Self-distruction and tolerance in resistance of mammalian cells to alkylation damage. Nucleic Acids Res. 20:1992;2933-2940.
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 2933-2940
-
-
Karran, P.1
Bignami, M.2
-
72
-
-
0030015770
-
Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N-nitro-N'-nitrosoguanitdine
-
Carethers JM, Hawn MT, Chauhan DP, Luce MC, Mara G, Koi M, Boland CR. Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N-nitro-N'-nitrosoguanitdine. J Clin Invest. 98:1996;199-206.
-
(1996)
J Clin Invest
, vol.98
, pp. 199-206
-
-
Carethers, J.M.1
Hawn, M.T.2
Chauhan, D.P.3
Luce, M.C.4
Mara, G.5
Koi, M.6
Boland, C.R.7
-
73
-
-
0028844574
-
Differential cellular expression of the human MSH2 repair protein in small and large intestine
-
Wilson TM, Ewel A, Duguid JR, Eble JN, Lescoe MK, Fishel R, Kelley MR. Differential cellular expression of the human MSH2 repair protein in small and large intestine. Cancer Res. 55:1995;5146-5150.
-
(1995)
Cancer Res
, vol.55
, pp. 5146-5150
-
-
Wilson, T.M.1
Ewel, A.2
Duguid, J.R.3
Eble, J.N.4
Lescoe, M.K.5
Fishel, R.6
Kelley, M.R.7
-
74
-
-
9044245700
-
Expression of the human mismatch repair gene hMSH2 in normal and neoplastic tissues
-
Leach FS, Polyak K, Burrell M, Johnson KA, Hill D, Dunlop MG, Wyllie AH, Peltomaki P, De la Chapelle A, Hamilton SR, et al. Expression of the human mismatch repair gene hMSH2 in normal and neoplastic tissues. Cancer Res. 56:1996;235-240.
-
(1996)
Cancer Res
, vol.56
, pp. 235-240
-
-
Leach, F.S.1
Polyak, K.2
Burrell, M.3
Johnson, K.A.4
Hill, D.5
Dunlop, M.G.6
Wyllie, A.H.7
Peltomaki, P.8
De La Chapelle, A.9
Hamilton, S.R.10
-
76
-
-
0028141683
-
Hereditary nonpolyposis colorectal cancer: Morphologies, genes, and mutations
-
Jass JR, Stewart SM, Stewart J, Lane MR. Hereditary nonpolyposis colorectal cancer: morphologies, genes, and mutations. Mutat Res. 310:1994;125-133.
-
(1994)
Mutat Res
, vol.310
, pp. 125-133
-
-
Jass, J.R.1
Stewart, S.M.2
Stewart, J.3
Lane, M.R.4
-
77
-
-
15444355644
-
Cell-cycle regulation of the human mismatch repair genes hMSH2, hMLH1 and hPMS2
-
in press
-
Meyers M, Theodosiou M, Acharya S, Odegaard EJ, Wilson T, Lewis JE, Davis TW, Wilson-Van Patten C, Fishel R, Boothman DA. Cell-cycle regulation of the human mismatch repair genes hMSH2, hMLH1 and hPMS2. Cancer Res. 1997;. in press.
-
(1997)
Cancer Res
-
-
Meyers, M.1
Theodosiou, M.2
Acharya, S.3
Odegaard, E.J.4
Wilson, T.5
Lewis, J.E.6
Davis, T.W.7
Wilson-Van Patten, C.8
Fishel, R.9
Boothman, D.A.10
-
78
-
-
0029783835
-
Mutation of MSH3 is endometrial cancer and evidence for its functional role in heteroduplex repair
-
Risinger JI, Umar A, Boyd J, Berchuck A, Kunkel TA, Barrett JC. Mutation of MSH3 is endometrial cancer and evidence for its functional role in heteroduplex repair. Nat Genet. 14:1996;102-105.
-
(1996)
Nat Genet
, vol.14
, pp. 102-105
-
-
Risinger, J.I.1
Umar, A.2
Boyd, J.3
Berchuck, A.4
Kunkel, T.A.5
Barrett, J.C.6
-
79
-
-
0029101616
-
Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination and predisposition to cancer
-
De Wind N, Dekker M, Berns A, Radman M, Te Riele H. Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination and predisposition to cancer. Cell. 82:1995;321-330.
-
(1995)
Cell
, vol.82
, pp. 321-330
-
-
De Wind, N.1
Dekker, M.2
Berns, A.3
Radman, M.4
Te Riele, H.5
-
80
-
-
0029111463
-
MSH2 deficient mice are viable and susceptible to lymphoid tumours
-
Reitmair AH, Scmits R, Ewel A, Bapat B, Redston M, Mitri A, Waterhouse P, Mittrucker H-W, Wakeman A, Liu B, et al. MSH2 deficient mice are viable and susceptible to lymphoid tumours. Nat Genet. 11:1995;64-70.
-
(1995)
Nat Genet
, vol.11
, pp. 64-70
-
-
Reitmair, A.H.1
Scmits, R.2
Ewel, A.3
Bapat, B.4
Redston, M.5
Mitri, A.6
Waterhouse, P.7
Mittrucker, H.-W.8
Wakeman, A.9
Liu, B.10
-
81
-
-
9444271133
-
Spontaneous intestinal carcinomas and skin neoplasms in MSH2-deficient mice
-
Reitmair AH, Redston M, Cai JC, Chuang TYC, Bjerknes M, Cheng H, Hay K, Gallinger S, Bapat B, Mak TW. Spontaneous intestinal carcinomas and skin neoplasms in MSH2-deficient mice. Cancer Res. 56:1996;3842-3849.
-
(1996)
Cancer Res
, vol.56
, pp. 3842-3849
-
-
Reitmair, A.H.1
Redston, M.2
Cai, J.C.3
Chuang, T.Y.C.4
Bjerknes, M.5
Cheng, H.6
Hay, K.7
Gallinger, S.8
Bapat, B.9
Mak, T.W.10
-
82
-
-
0022120826
-
Identification and characterization of the mutL and mutS gene products of Salmonella typhimurium LT2
-
Pang PP, Lundberg AS, Walker GC. Identification and characterization of the mutL and mutS gene products of Salmonella typhimurium LT2. J Bacteriol. 163:1985;1007-1015.
-
(1985)
J Bacteriol
, vol.163
, pp. 1007-1015
-
-
Pang, P.P.1
Lundberg, A.S.2
Walker, G.C.3
-
83
-
-
0024430850
-
Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: Homology of PMS1 to procaryotic MutL and HesB
-
Kramer W, Dramer B, Williamson MS, Fogel S. Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HesB. J Bacteriol. 171:1989;5339-5346.
-
(1989)
J Bacteriol
, vol.171
, pp. 5339-5346
-
-
Kramer, W.1
Dramer, B.2
Williamson, M.S.3
Fogel, S.4
-
84
-
-
0028080973
-
Cloning and characterization and chromosomal assignment of the human homologues to yeast PMS1, a member of mismatch repair genes
-
Horii A, Han H-J, Sasaki S, Shimada M, Nakamura Y. Cloning and characterization and chromosomal assignment of the human homologues to yeast PMS1, a member of mismatch repair genes. Biochem Biophys Res Comm. 204:1994;1257-1264.
-
(1994)
Biochem Biophys Res Comm
, vol.204
, pp. 1257-1264
-
-
Horii, A.1
Han, H.-J.2
Sasaki, S.3
Shimada, M.4
Nakamura, Y.5
|