327 related articles for article (PubMed ID: 10612836)
61. Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain.
Ellison AR; Lofing J; Bitter GA
Nucleic Acids Res; 2004; 32(18):5321-38. PubMed ID: 15475387
[TBL] [Abstract][Full Text] [Related]
62. Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria.
Beck NE; Tomlinson IP; Homfray T; Frayling I; Hodgson SV; Harocopos C; Bodmer WF
Hum Genet; 1997 Feb; 99(2):219-24. PubMed ID: 9048925
[TBL] [Abstract][Full Text] [Related]
63. Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer.
Peltomäki P; Vasen HF
Gastroenterology; 1997 Oct; 113(4):1146-58. PubMed ID: 9322509
[TBL] [Abstract][Full Text] [Related]
64. Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.
Peltomäki P; Vasen H
Dis Markers; 2004; 20(4-5):269-76. PubMed ID: 15528792
[TBL] [Abstract][Full Text] [Related]
65. Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States.
Kurzawski G; Suchy J; Kładny J; Safranow K; Jakubowska A; Elsakov P; Kucinskas V; Gardovski J; Irmejs A; Sibul H; Huzarski T; Byrski T; Debniak T; Cybulski C; Gronwald J; Oszurek O; Clark J; Góźdź S; Niepsuj S; Słomski R; Pławski A; Łacka-Wojciechowska A; Rozmiarek A; Fiszer-Maliszewska Ł; Bebenek M; Sorokin D; Stawicka M; Godlewski D; Richter P; Brozek I; Wysocka B; Jawień A; Banaszkiewicz Z; Kowalczyk J; Czudowska D; Goretzki PE; Moeslein G; Lubiński J
J Med Genet; 2002 Oct; 39(10):E65. PubMed ID: 12362047
[No Abstract] [Full Text] [Related]
66. [Germline mutation analysis in hMLH 1 and hMSH 2 genes in hereditary nonpolyposis colorectal cancer and colorectal cancer patients with familial history].
Wang Y; Friedl W; Propping P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Dec; 15(6):333-6. PubMed ID: 9845760
[TBL] [Abstract][Full Text] [Related]
67. A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer.
Maillet P; Chappuis PO; Vaudan G; Dobbie Z; Müller H; Hutter P; Sappino AP
Int J Cancer; 2000 Dec; 88(6):928-31. PubMed ID: 11093816
[TBL] [Abstract][Full Text] [Related]
68. Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis.
Andermann A; Thiffault I; Wong N; Gordon P; MacNamara E; Chong G; Foulkes W
J Clin Oncol; 2002 Mar; 20(6):1705-7. PubMed ID: 11896123
[No Abstract] [Full Text] [Related]
69. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
Lindor NM; Rabe K; Petersen GM; Haile R; Casey G; Baron J; Gallinger S; Bapat B; Aronson M; Hopper J; Jass J; LeMarchand L; Grove J; Potter J; Newcomb P; Terdiman JP; Conrad P; Moslein G; Goldberg R; Ziogas A; Anton-Culver H; de Andrade M; Siegmund K; Thibodeau SN; Boardman LA; Seminara D
JAMA; 2005 Apr; 293(16):1979-85. PubMed ID: 15855431
[TBL] [Abstract][Full Text] [Related]
70. Histologic comparison of hereditary nonpolyposis colorectal cancer associated with MSH2 and MLH1 and colorectal cancer from the general population.
Shashidharan M; Smyrk T; Lin KM; Ternent CA; Thorson AG; Blatchford GJ; Christensen MA; Lynch HT
Dis Colon Rectum; 1999 Jun; 42(6):722-6. PubMed ID: 10378595
[TBL] [Abstract][Full Text] [Related]
71. Mutational analysis of MLH1 and MSH2 in 25 prospectively-acquired RER+ endometrial cancers.
Kowalski LD; Mutch DG; Herzog TJ; Rader JS; Goodfellow PJ
Genes Chromosomes Cancer; 1997 Mar; 18(3):219-27. PubMed ID: 9071575
[TBL] [Abstract][Full Text] [Related]
72. Investigation of G2-phase chromosomal radiosensitivity in hereditary non-polyposis colorectal cancer cells.
Franchitto A; Pichierri P; Genuardi M; De Santis A; Palitti F
Int J Radiat Biol; 2001 Jul; 77(7):773-80. PubMed ID: 11454277
[TBL] [Abstract][Full Text] [Related]
73. Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC).
Glasl S; Papatheodorou L; Baretton G; Jung C; Gross M
Hum Mutat; 2000 Jul; 16(1):91-2. PubMed ID: 10874318
[TBL] [Abstract][Full Text] [Related]
74. Evaluation of enzymatic mutation detectiontrade mark in hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Kohonen-Corish M
Hum Mutat; 2000; 16(1):61-7. PubMed ID: 10874307
[TBL] [Abstract][Full Text] [Related]
75. Molecular basis of HNPCC: mutations of MMR genes.
Papadopoulos N; Lindblom A
Hum Mutat; 1997; 10(2):89-99. PubMed ID: 9259192
[TBL] [Abstract][Full Text] [Related]
76. Nationwide study of clinical and molecular features of hereditary non-polyposis colorectal cancer (HNPCC) in Latvia.
Irmejs A; Borosenko V; Melbarde-Gorkusa I; Gardovskis A; Bitina M; Kurzawski G; Suchy J; Gorski B; Gardovskis J
Anticancer Res; 2007; 27(1B):653-8. PubMed ID: 17348456
[TBL] [Abstract][Full Text] [Related]
77. Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.
Sarroca C; Peltomäki P; Alfano N; Tedesco G; Della Valle A; Dominguez A; Lynch HT
Cancer Genet Cytogenet; 2003 Apr; 142(1):13-20. PubMed ID: 12660027
[TBL] [Abstract][Full Text] [Related]
78. Novel and recurrent germline alterations in the MLH1 and MSH2 genes identified in hereditary nonpolyposis colorectal cancer patients in Slovakia.
Zavodna K; Bujalkova M; Krivulcik T; Alemayehu A; Skorvaga M; Marra G; Fridrichova I; Jiricny J; Bartosova Z
Neoplasma; 2006; 53(4):269-76. PubMed ID: 16830052
[TBL] [Abstract][Full Text] [Related]
79. Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques.
Nakagawa H; Hampel H; de la Chapelle A
Hum Mutat; 2003 Sep; 22(3):258. PubMed ID: 12938096
[TBL] [Abstract][Full Text] [Related]
80. Microsatellite instability and immunohistochemical analysis of MLH1 and MSH2 in normal endometrium, endometrial hyperplasia and endometrial cancer from a hereditary nonpolyposis colorectal cancer patient.
Ichikawa Y; Tsunoda H; Takano K; Oki A; Yoshikawa H
Jpn J Clin Oncol; 2002 Mar; 32(3):110-2. PubMed ID: 11956307
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
