-
1
-
-
0023753017
-
Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers
-
Cannon-Albright LA, Skolnick MH, Bishop DT, Lee RG, Burt RW. Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers. N Engl J Med 1988;319:533-7.
-
(1988)
N Engl J Med
, vol.319
, pp. 533-537
-
-
Cannon-Albright, L.A.1
Skolnick, M.H.2
Bishop, D.T.3
Lee, R.G.4
Burt, R.W.5
-
3
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland
-
Lichtenstein P, Holm NV, Verkasalo PK, et al. Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000;343: 78-85.
-
(2000)
N Engl J Med
, vol.343
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
-
4
-
-
0034955851
-
AGA technical review on hereditary colorectal cancer and genetic testing
-
Giardiello FM, Brensinger JD, Petersen GM. AGA technical review on hereditary colorectal cancer and genetic testing. Gastroenterology 2001;121:198-213.
-
(2001)
Gastroenterology
, vol.121
, pp. 198-213
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Petersen, G.M.3
-
5
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen LA, Salovaara R, Kristo P, et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med 1998;338:1481-7.
-
(1998)
N Engl J Med
, vol.338
, pp. 1481-1487
-
-
Aaltonen, L.A.1
Salovaara, R.2
Kristo, P.3
-
6
-
-
0033039409
-
Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis
-
discussion 715-6
-
Park JG, Vasen HF, Park KJ, et al. Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis. Dis Colon Rectum 1999;42: 710-5; discussion 715-6.
-
(1999)
Dis Colon Rectum
, vol.42
, pp. 710-715
-
-
Park, J.G.1
Vasen, H.F.2
Park, K.J.3
-
7
-
-
0033564464
-
Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer
-
Heinimann K, Scott RJ, Buerstedde JM, et al. Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer. Cancer 1999;85:2512-8.
-
(1999)
Cancer
, vol.85
, pp. 2512-2518
-
-
Heinimann, K.1
Scott, R.J.2
Buerstedde, J.M.3
-
8
-
-
0041411163
-
Low mutation rate of hMSH2 and hMLH1 in Taiwanese hereditary non-polyposis colorectal cancer
-
Wei SC, Yu CY, Tsai-Wu JJ, et al. Low mutation rate of hMSH2 and hMLH1 in Taiwanese hereditary non-polyposis colorectal cancer. Clin Genet 2003;64: 243-51.
-
(2003)
Clin Genet
, vol.64
, pp. 243-251
-
-
Wei, S.C.1
Yu, C.Y.2
Tsai-Wu, J.J.3
-
9
-
-
0025848680
-
-
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
-
Vasen HF, Mecklin JP, Khan PM, Lynch HT. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 1991;34:424-5.
-
(1991)
Dis Colon Rectum
, vol.34
, pp. 424-425
-
-
Vasen, H.F.1
Mecklin, J.P.2
Khan, P.M.3
Lynch, H.T.4
-
10
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
-
Vasen HF, Watson P, Mecklin JP, Lynch HT New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 1999;116:1453-6.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.1
Watson, P.2
Mecklin, J.P.3
Lynch, H.T.4
-
11
-
-
0027248156
-
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: An updated review
-
Lynch HT, Smyrk TC, Watson P, et al. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review. Gastroenterology 1993;104:1535-49.
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.C.2
Watson, P.3
-
12
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara R, Loukola A, Kristo P, et al. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol 2000;18:2193-200.
-
(2000)
J Clin Oncol
, vol.18
, pp. 2193-2200
-
-
Salovaara, R.1
Loukola, A.2
Kristo, P.3
-
13
-
-
0034799747
-
The colon cancer burden of genetically defined hereditary non-polyposis colon cancer
-
Samowitz WS, Curtin K, Lin HH, et al. The colon cancer burden of genetically defined hereditary non-polyposis colon cancer. Gastroenterology 2001;121: 830-8.
-
(2001)
Gastroenterology
, vol.121
, pp. 830-838
-
-
Samowitz, W.S.1
Curtin, K.2
Lin, H.H.3
-
14
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach FS, Nicolaides NC, Papadopoulos N, et al. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell 1993;75:1215-25.
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
-
15
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
Fishel R, Lescoe MK, Rao MR, et al. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell 1993;75: 1027-38.
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.3
-
16
-
-
0028221943
-
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
-
Bronner CE, Baker SM, Morrison PT, et al. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature 1994;368:258-61.
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
Baker, S.M.2
Morrison, P.T.3
-
17
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos N, Nicolaides NC, Wei YF, et al. Mutation of a mutL homolog in hereditary colon cancer. Science 1994;263:1625-9.
-
(1994)
Science
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Wei, Y.F.3
-
18
-
-
0030870631
-
Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred
-
Akiyama Y, Sato H, Yamada T, et al. Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred. Cancer Res 1997;57:3920-3.
-
(1997)
Cancer Res
, vol.57
, pp. 3920-3923
-
-
Akiyama, Y.1
Sato, H.2
Yamada, T.3
-
19
-
-
0027933070
-
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
-
Nicolaides NC, Papadopoulos N, Liu B, et al. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature 1994;371:75-80.
-
(1994)
Nature
, vol.371
, pp. 75-80
-
-
Nicolaides, N.C.1
Papadopoulos, N.2
Liu, B.3
-
20
-
-
0035503698
-
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer
-
Liu T Yan H, Kuismanen S, et al. The role of hPMS1 and hPMS2 in predisposing to colorectal cancer. Cancer Res 2001;61:7798-802.
-
(2001)
Cancer Res
, vol.61
, pp. 7798-7802
-
-
Liu, T.1
Yan, H.2
Kuismanen, S.3
-
21
-
-
0001510499
-
Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene
-
De Rosa M, Fasano C, Panariello L, et al. Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene. Oncogene 2000;19:1719-23.
-
(2000)
Oncogene
, vol.19
, pp. 1719-1723
-
-
De Rosa, M.1
Fasano, C.2
Panariello, L.3
-
22
-
-
3142748325
-
Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation
-
Nakagawa H, Lockman JC, Frankel WL, et al. Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation. Cancer Res 2004;64:4721-7.
-
(2004)
Cancer Res
, vol.64
, pp. 4721-4727
-
-
Nakagawa, H.1
Lockman, J.C.2
Frankel, W.L.3
-
23
-
-
0037447157
-
The role of hMLH3 in familial colorectal cancer
-
Liu HX, Zhou XL, Liu T, et al. The role of hMLH3 in familial colorectal cancer. Cancer Res 2003;63: 1894-9.
-
(2003)
Cancer Res
, vol.63
, pp. 1894-1899
-
-
Liu, H.X.1
Zhou, X.L.2
Liu, T.3
-
24
-
-
0038493613
-
Little evidence for involvement of MLH3 in colorectal cancer predisposition
-
Hienonen T, Laiho P, Salovaara R, et al. Little evidence for involvement of MLH3 in colorectal cancer predisposition, Int J Cancer 2003;106:292-6.
-
(2003)
Int J Cancer
, vol.106
, pp. 292-296
-
-
Hienonen, T.1
Laiho, P.2
Salovaara, R.3
-
25
-
-
2942556714
-
No association between two MLH3 variants (S845G and P844L) and colorectal cancer risk
-
de Jong MM, Hofstra RM, Kooi KA, et al. No association between two MLH3 variants (S845G and P844L) and colorectal cancer risk. Cancer Genet Cytogenet 2004;152:70-1.
-
(2004)
Cancer Genet Cytogenet
, vol.152
, pp. 70-71
-
-
De Jong, M.M.1
Hofstra, R.M.2
Kooi, K.A.3
-
26
-
-
0034480735
-
The population structure of ten Newfoundland outports
-
Martin LJ, Crawford MH, Koertvelyessy T, Keeping D, Collins M, Huntsman R. The population structure of ten Newfoundland outports. Hum Biol 2000;72: 997-1016.
-
(2000)
Hum Biol
, vol.72
, pp. 997-1016
-
-
Martin, L.J.1
Crawford, M.H.2
Koertvelyessy, T.3
Keeping, D.4
Collins, M.5
Huntsman, R.6
-
27
-
-
0036098875
-
Clinical and genetic epidemiology of inherited renal disease in Newfoundland
-
Parfrey PS, Davidson WS, Green JS. Clinical and genetic epidemiology of inherited renal disease in Newfoundland. Kidney Int 2002;61:1925-34.
-
(2002)
Kidney Int
, vol.61
, pp. 1925-1934
-
-
Parfrey, P.S.1
Davidson, W.S.2
Green, J.S.3
-
28
-
-
0023640668
-
Persistent genetic isolation in outport Newfoundland
-
Bear JC, Nemec TF, Kennedy JC, et al. Persistent genetic isolation in outport Newfoundland. Am J Med Genet 1987;27:807-30.
-
(1987)
Am J Med Genet
, vol.27
, pp. 807-830
-
-
Bear, J.C.1
Nemec, T.F.2
Kennedy, J.C.3
-
29
-
-
0036732650
-
Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation
-
Green J, O'Driscoll M, Barnes A, et al. Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation. Dis Colon Rectum 2002;45:1223-32.
-
(2002)
Dis Colon Rectum
, vol.45
, pp. 1223-1232
-
-
Green, J.1
O'Driscoll, M.2
Barnes, A.3
-
30
-
-
0032534069
-
A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
-
Boland CR, Thibodeau SN, Hamilton SR, et al. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998;58:5248-57.
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
Thibodeau, S.N.2
Hamilton, S.R.3
-
31
-
-
0032522658
-
Microsatellite instability in colorectal cancer: Different mutator phenotypes and the principal involvement of hMLH1
-
Thibodeau SN, French AJ, Cunningham JM, et al. Microsatellite instability in colorectal cancer: different mutator phenotypes and the principal involvement of hMLH1. Cancer Res 1998;58:1713-8.
-
(1998)
Cancer Res
, vol.58
, pp. 1713-1718
-
-
Thibodeau, S.N.1
French, A.J.2
Cunningham, J.M.3
-
32
-
-
0032974189
-
Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer
-
Bapat BV, Madlensky L, Temple LK, et al. Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer. Hum Genet 1999;104:167-76.
-
(1999)
Hum Genet
, vol.104
, pp. 167-176
-
-
Bapat, B.V.1
Madlensky, L.2
Temple, L.K.3
-
33
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
34
-
-
3543023204
-
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
-
Schouten JP, McElgunn CJ, Waaijer R, Zwijnenburg D, Diepvens F, Pals G. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. Nucleic Acids Res 2002;30:e57.
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Schouten, J.P.1
McElgunn, C.J.2
Waaijer, R.3
Zwijnenburg, D.4
Diepvens, F.5
Pals, G.6
-
35
-
-
0033135049
-
Methylation of CpG in a small region of the hMLH1 promoter invariably correlates with the absence of gene expression
-
Deng G, Chen A, Hong J, Chae HS, Kim YS. Methylation of CpG in a small region of the hMLH1 promoter invariably correlates with the absence of gene expression. Cancer Res 1999;59:2029-33.
-
(1999)
Cancer Res
, vol.59
, pp. 2029-2033
-
-
Deng, G.1
Chen, A.2
Hong, J.3
Chae, H.S.4
Kim, Y.S.5
-
36
-
-
13144266670
-
Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma
-
Herman JG, Umar A, Polyak K, et al. Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma. Proc Natl Acad Sci USA 1998;95:6870-5.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 6870-6875
-
-
Herman, J.G.1
Umar, A.2
Polyak, K.3
-
37
-
-
10744233937
-
Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, et al. Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer lnst 2004;96:261-8.
-
(2004)
J Natl Cancer Lnst
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
-
38
-
-
0031017268
-
Methylation of the h MLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines
-
Kane MF, Loda M, Gaida GM, et al. Methylation of the h MLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines. Cancer Res 1997;57:808-11.
-
(1997)
Cancer Res
, vol.57
, pp. 808-811
-
-
Kane, M.F.1
Loda, M.2
Gaida, G.M.3
-
39
-
-
13144307115
-
Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers
-
Veigl ML, Kasturi L, Olechnowicz J, et al. Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. Proc Natl Acad Sci U S A 1998;95:8698-702.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 8698-8702
-
-
Veigl, M.L.1
Kasturi, L.2
Olechnowicz, J.3
-
40
-
-
0035866348
-
MSH6 and MSH3 are rarely involved in genetic predisposition to non-polypoticcolon cancer
-
Huang J, Kuismanen SA, Liu T, et al. MSH6 and MSH3 are rarely involved in genetic predisposition to non-polypoticcolon cancer. Cancer Res 2001;61:1619-23.
-
(2001)
Cancer Res
, vol.61
, pp. 1619-1623
-
-
Huang, J.1
Kuismanen, S.A.2
Liu, T.3
-
41
-
-
10744226607
-
Germline truncating mutations in both MSH2 and BRCA2 in a single kindred
-
Thiffault I, Hamel N, Pal T, et al. Germline truncating mutations in both MSH2 and BRCA2 in a single kindred. Br J Cancer 2004;90:483-91.
-
(2004)
Br J Cancer
, vol.90
, pp. 483-491
-
-
Thiffault, I.1
Hamel, N.2
Pal, T.3
-
42
-
-
0037455807
-
Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes
-
Wang Y, Friedl W, Lamberti C, et al. Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes, Int J Cancer 2003;103:636-41.
-
(2003)
Int J Cancer
, vol.103
, pp. 636-641
-
-
Wang, Y.1
Friedl, W.2
Lamberti, C.3
-
43
-
-
0036119504
-
Accounting for human polymorphisms predicted to affect protein function
-
Ng PC, Henikoff S. Accounting for human polymorphisms predicted to affect protein function. Genome Res 2002;12:436-46.
-
(2002)
Genome Res
, vol.12
, pp. 436-446
-
-
Ng, P.C.1
Henikoff, S.2
-
44
-
-
10144250305
-
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer
-
Moslein G, Tester DJ, Lindor NM, et al. Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. Hum Mol Genet 1996;5:1245-52.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1245-1252
-
-
Moslein, G.1
Tester, D.J.2
Lindor, N.M.3
-
45
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons R, Papadopoulos N, et al. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med 1996;2:169-74.
-
(1996)
Nat Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
-
46
-
-
0028845722
-
Somatic mutations in the HMSH2 gene in microsatellite unstable colorectal carcinomas
-
Borresen AL, Lothe RA, Meling GI, et al. Somatic mutations in the HMSH2 gene in microsatellite unstable colorectal carcinomas. Hum Mol Genet 1995;4: 2065-72.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2065-2072
-
-
Borresen, A.L.1
Lothe, R.A.2
Meling, G.I.3
-
47
-
-
0031023545
-
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer
-
Viel A, Genuardi M, Capozzi E, et al. Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. Genes Chromosomes Cancer 1997;18:8-18.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 8-18
-
-
Viel, A.1
Genuardi, M.2
Capozzi, E.3
-
48
-
-
0031784272
-
Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair
-
Studamire B, Quach T, Alani E. Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair. Mol Cell Biol 1998;18:7590-601.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 7590-7601
-
-
Studamire, B.1
Quach, T.2
Alani, E.3
-
49
-
-
0033361894
-
Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations
-
Wu Y, Berends MJ, Mensink RG, et al. Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. Am J Hum Genet 1999: 65:1291-8.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1291-1298
-
-
Wu, Y.1
Berends, M.J.2
Mensink, R.G.3
-
50
-
-
0032749569
-
Germline msh6 mutations in colorectal cancer families
-
Kolodner RD, Tytell JD, Schmeits JL, et al. Germline msh6 mutations in colorectal cancer families. Cancer Res 1999;59:5068-74.
-
(1999)
Cancer Res
, vol.59
, pp. 5068-5074
-
-
Kolodner, R.D.1
Tytell, J.D.2
Schmeits, J.L.3
-
51
-
-
18244380349
-
Molecular and clinical characteristics of MSH6 variants: An analysis of 25 index carriers of a germline variant
-
Berends MJ, Wu Y, Sijmons RH, et al. Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant. Am J Hum Genet 2002:70:26-37.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 26-37
-
-
Berends, M.J.1
Wu, Y.2
Sijmons, R.H.3
-
52
-
-
6044244954
-
Human MutL homolog (MLH1) function in DNA mismatch repair: A prospective screen for missense mutations in the ATPase domain
-
Ellison AR, LofingJ , Bitter GA. Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain. Nucleic Acids Res 2004;32:5321-38.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 5321-5338
-
-
Ellison, A.R.1
Lofing, J.2
Bitter, G.A.3
-
53
-
-
0345050350
-
DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer
-
Nystrom-Lahti M, Wu Y, Moisio AL, et al. DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. Hum Mol Genet 1996;5:763-9.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 763-769
-
-
Nystrom-Lahti, M.1
Wu, Y.2
Moisio, A.L.3
-
54
-
-
15444355648
-
Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees
-
Weber TK, Conlon W, Petrelli NJ, et al. Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees. Cancer Res 1997;57: 3798-803.
-
(1997)
Cancer Res
, vol.57
, pp. 3798-3803
-
-
Weber, T.K.1
Conlon, W.2
Petrelli, N.J.3
-
55
-
-
7944225535
-
Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk
-
Croitoru ME, Cleary SP, Di Nicola N, et al. Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk. J Natl Cancer Inst 2004;96:1631-4.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 1631-1634
-
-
Croitoru, M.E.1
Cleary, S.P.2
Di Nicola, N.3
-
56
-
-
0033916373
-
Giant fundic polyp complicating attenuated familial adenomatous polyposis
-
McGarrity TJ, Ruggiero FM, Chey WY, Bajaj R, Kelly JE, Kauffman GL, Jr. Giant fundic polyp complicating attenuated familial adenomatous polyposis. Am J Gastroenterol 2000;95:1824-8.
-
(2000)
Am J Gastroenterol
, vol.95
, pp. 1824-1828
-
-
McGarrity, T.J.1
Ruggiero, F.M.2
Chey, W.Y.3
Bajaj, R.4
Kelly, J.E.5
Kauffman Jr., G.L.6
-
57
-
-
0035162347
-
Hereditary nonpolyposis colorectal cancer in 95 families: Differences and similarities between mutation-positive and mutation-negative kindreds
-
Scott RJ, McPhillips M, Meldrum CJ, et al. Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds. Am J Hum Genet 2001;68:118-27.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 118-127
-
-
Scott, R.J.1
McPhillips, M.2
Meldrum, C.J.3
-
58
-
-
20244386256
-
Lower cancer incidence in Amsterdam-l criteria families without mismatch repair deficiency: Familial colorectal cancer type X
-
Lindor NM, Rabe K, Petersen G, et al. Lower cancer incidence in Amsterdam-l criteria families without mismatch repair deficiency: familial colorectal cancer type X. JAMA 2005;293:1979-85.
-
(2005)
JAMA
, vol.293
, pp. 1979-1985
-
-
Lindor, N.M.1
Rabe, K.2
Petersen, G.3
-
59
-
-
17944368971
-
Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes
-
Chan TL, Curtis LC, Leung SY, et al. Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes. Oncogene 2001;20: 4871-6.
-
(2001)
Oncogene
, vol.20
, pp. 4871-4876
-
-
Chan, T.L.1
Curtis, L.C.2
Leung, S.Y.3
-
60
-
-
14944362453
-
Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations
-
Abdel-Rahman WM, Ollikainen M, Kariola R, et al. Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations. Oncogene 2005;24:1542-51.
-
(2005)
Oncogene
, vol.24
, pp. 1542-1551
-
-
Abdel-Rahman, W.M.1
Ollikainen, M.2
Kariola, R.3
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