77 related articles for article (PubMed ID: 8723682)
1. Mutation of the hMSH2 gene in two families with hereditary nonpolyposis colorectal cancer.
Jeon HM; Lynch PM; Howard L; Ajani J; Levin B; Frazier ML
Hum Mutat; 1996; 7(4):327-33. PubMed ID: 8723682
[TBL] [Abstract][Full Text] [Related]
2. [Mutation analysis of hMSH2 and hMLH1 genes in Chinese hereditary nonpolyposis colorectal cancer families].
Cai Q; Sun MH; Fu G; Ding CW; Mo SJ; Cai SJ; Ren SX; Min DL; Xu XL; Zhu WP; Zhang TM; Shi DR
Zhonghua Bing Li Xue Za Zhi; 2003 Aug; 32(4):323-8. PubMed ID: 14514376
[TBL] [Abstract][Full Text] [Related]
3. Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes.
Buerstedde JM; Alday P; Torhorst J; Weber W; Müller H; Scott R
J Med Genet; 1995 Nov; 32(11):909-12. PubMed ID: 8592341
[TBL] [Abstract][Full Text] [Related]
4. Germ line mutations of hMSH2 and hMLH1 genes in Japanese families with hereditary nonpolyposis colorectal cancer (HNPCC): usefulness of DNA analysis for screening and diagnosis of HNPCC patients.
Miyaki M; Konishi M; Muraoka M; Kikuchi-Yanoshita R; Tanaka K; Iwama T; Mori T; Koike M; Ushio K; Chiba M
J Mol Med (Berl); 1995 Oct; 73(10):515-20. PubMed ID: 8581513
[TBL] [Abstract][Full Text] [Related]
5. [Clinical features and hMSH2/hMLH1 germline mutation screening of Chinese hereditary nonpolyposis colorectal cancer patients].
Liu SR; Wang ZJ; Zhao B; Wan YL; Huang YT
Zhonghua Yi Xue Za Zhi; 2004 May; 84(9):714-7. PubMed ID: 15200905
[TBL] [Abstract][Full Text] [Related]
6. Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.
Nakahara M; Yokozaki H; Yasui W; Dohi K; Tahara E
Cancer Epidemiol Biomarkers Prev; 1997 Dec; 6(12):1057-64. PubMed ID: 9419403
[TBL] [Abstract][Full Text] [Related]
7. Novel germline hMSH2 genomic deletion and somatic hMSH2 mutations in a hereditary nonpolyposis colorectal cancer family.
Miyaki M; Iijima T; Yamaguchi T; Shirahama S; Ito T; Yasuno M; Mori T
Mutat Res; 2004 Apr; 548(1-2):19-25. PubMed ID: 15063132
[TBL] [Abstract][Full Text] [Related]
8. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene.
Shin KH; Shin JH; Kim JH; Park JG
Cancer Res; 2002 Jan; 62(1):38-42. PubMed ID: 11782355
[TBL] [Abstract][Full Text] [Related]
9. hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer.
Kim JC; Kim HC; Roh SA; Koo KH; Lee DH; Yu CS; Lee JH; Kim TW; Lee HL; Beck NE; Bodmer WF
Cancer Detect Prev; 2001; 25(6):503-10. PubMed ID: 12132870
[TBL] [Abstract][Full Text] [Related]
10. Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees.
Weber TK; Conlon W; Petrelli NJ; Rodriguez-Bigas M; Keitz B; Pazik J; Farrell C; O'Malley L; Oshalim M; Abdo M; Anderson G; Stoler D; Yandell D
Cancer Res; 1997 Sep; 57(17):3798-803. PubMed ID: 9288790
[TBL] [Abstract][Full Text] [Related]
11. The novel germline mutation of hMSH2 gene in a case of a hereditary non-polyposis colorectal cancer (HNPCC) patient who meets the revised Amsterdam criteria.
Tomita N; Fukunaga M; Ohzato H; Tamura S; Sugimoto K; Aihara T; Miki H; Takatsuka Y; Matsuura N; Iwanaga T; Fukayama N; Sugano K
Jpn J Clin Oncol; 2003 Sep; 33(9):486-9. PubMed ID: 14594944
[TBL] [Abstract][Full Text] [Related]
12. Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation.
Bisgaard ML; Jäger AC; Myrhøj T; Bernstein I; Nielsen FC
Hum Mutat; 2002 Jul; 20(1):20-7. PubMed ID: 12112654
[TBL] [Abstract][Full Text] [Related]
13. [Mutations of hMLH1 and hMSH2 genes in suspected hereditary nonpolyposis colorectal cancer].
Yuan Y; Zheng S
Zhonghua Yi Xue Za Zhi; 1999 May; 79(5):346-8. PubMed ID: 11715474
[TBL] [Abstract][Full Text] [Related]
14. [Detection mutations in the DNA mismatch repair genes of hMLH1 and hMSH2 genes in Colombian families with suspicion of hereditary non-polyposis colorectal carcinoma (Lynch syndrome)].
Gómez A; Salguero G; García H; Aristizábal F; Gutiérrez O; Angel LA; Padrón J; Martínez C; Martínez H; Malaver O; Barvo R; Giraldo A
Biomedica; 2005 Sep; 25(3):315-24. PubMed ID: 16276679
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes.
Pensotti V; Radice P; Presciuttini S; Calistri D; Gazzoli I; Grimalt Perez A; Mondini P; Buonsanti G; Sala P; Rossetti C; Ranzani GN; Bertario L; Pierotti MA
Genes Chromosomes Cancer; 1997 Jul; 19(3):135-42. PubMed ID: 9218993
[TBL] [Abstract][Full Text] [Related]
17. Genotype and phenotype of a new 2-bp deletion of hMSH2 at codon 233.
Müller A; Beyser K; Arps H; Bolander S; Becker H; Rüschhoff J
Virchows Arch; 2001 Aug; 439(2):191-5. PubMed ID: 11561760
[TBL] [Abstract][Full Text] [Related]
18. [Diagnosis by directed mutagenesis of a mutation at the hMSH2 gene associated with hereditary nonpolyposis colorectal cancer].
Roqué M; Pusiol E; Giribet G; Perinetti H; Mayorga LS
Medicina (B Aires); 2000; 60(2):188-94. PubMed ID: 10962807
[TBL] [Abstract][Full Text] [Related]
19. Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.
Wijnen J; Vasen H; Khan PM; Menko FH; van der Klift H; van Leeuwen C; van den Broek M; van Leeuwen-Cornelisse I; Nagengast F; Meijers-Heijboer A
Am J Hum Genet; 1995 May; 56(5):1060-6. PubMed ID: 7726159
[TBL] [Abstract][Full Text] [Related]
20. [The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation].
Czakó L; Tiszlavicz L; Takács R; Baradnay G; Lonovics J; Cserni G; Závodná K; Bartosova Z
Orv Hetil; 2005 May; 146(20):1009-16. PubMed ID: 15945244
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
