42 related articles for article (PubMed ID: 8625301)
1. A truncated hMSH2 transcript occurs as a common variant in the population: implications for genetic diagnosis.
Xia L; Shen W; Ritacca F; Mitri A; Madlensky L; Berk T; Cohen Z; Gallinger S; Bapat B
Cancer Res; 1996 May; 56(10):2289-92. PubMed ID: 8625301
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.
Baudi F; Fersini G; Lavecchia A; Terracciano R; Leone F; Quaresima B; Faniello MC; De Paola L; Doldo P; Cuda G; Costanzo F; Venuta S
Cancer Lett; 2005 Jun; 223(2):285-91. PubMed ID: 15896463
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.
Swensen J; Lewis CM; Cannon-Albright LA
Hum Mutat; 1997; 10(1):80-1. PubMed ID: 9222765
[No Abstract] [Full Text] [Related]
6. [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]
7. Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers.
Okamura S; Koyama K; Miyoshi Y; Monden M; Takami M
J Hum Genet; 1998; 43(2):143-5. PubMed ID: 9621522
[TBL] [Abstract][Full Text] [Related]
8. Aberrant RNA splicing in the hMSH2 gene: molecular identification of three aberrant RNA in Scottish patients with colorectal cancer in the West of Scotland.
Davoodi-Semiromi A; Lanyon GW; Davidson R; Connor MJ
Am J Med Genet; 2000 Nov; 95(1):49-52. PubMed ID: 11074494
[TBL] [Abstract][Full Text] [Related]
9. [Expression and sequence analysis of human MutS homologue 2 during different stages of human bronchial epithelial cells induced by cadmium chloride].
Zhou ZH; Lei YX; Wang CX; Wang M; Wei L; Ji WD
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi; 2008 Mar; 26(3):131-4. PubMed ID: 18761787
[TBL] [Abstract][Full Text] [Related]
10. Isolation and characterization of the human mismatch repair gene hMSH2 promoter region.
Scherer SJ; Seib T; Seitz G; Dooley S; Welter C
Hum Genet; 1996 Jan; 97(1):114-6. PubMed ID: 8557250
[TBL] [Abstract][Full Text] [Related]
11. Overexpression of Rad51C splice variants in colorectal tumors.
Kalvala A; Gao L; Aguila B; Reese T; Otterson GA; Villalona-Calero MA; Duan W
Oncotarget; 2015 Apr; 6(11):8777-87. PubMed ID: 25669972
[TBL] [Abstract][Full Text] [Related]
12. Detection of allelic imbalance in the gene expression of hMSH2 or RB1 in lymphocytes from pedigrees of hereditary, nonpolyposis, colorectal cancer and retinoblastoma by an RNA difference plot.
Murakami Y; Isogai K; Tomita H; Sakurai-Yageta M; Maruyama T; Hidaka A; Nose K; Sugano K; Kaneko A
J Hum Genet; 2004; 49(11):635-641. PubMed ID: 15480874
[TBL] [Abstract][Full Text] [Related]
13. A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome.
Froggatt NJ; Joyce JA; Davies R; Gareth D; Evans R; Ponder BA; Barton DE; Maher ER
Lancet; 1995 Mar; 345(8951):727. PubMed ID: 7885145
[No Abstract] [Full Text] [Related]
14. Genetic testing set for takeoff.
Nowak R
Science; 1994 Jul; 265(5171):464-7. PubMed ID: 8036486
[No Abstract] [Full Text] [Related]
15. Screening for Lynch syndrome in the general population-letter.
Sadeghi S; Barzi A; Kattan MW; Meropol NJ
Cancer Prev Res (Phila); 2011 Mar; 4(3):471; author reply 472. PubMed ID: 21372042
[No Abstract] [Full Text] [Related]
16. Alternative splicing of the NF2 gene and its mutation analysis of breast and colorectal cancers.
Arakawa H; Hayashi N; Nagase H; Ogawa M; Nakamura Y
Hum Mol Genet; 1994 Apr; 3(4):565-8. PubMed ID: 8069299
[TBL] [Abstract][Full Text] [Related]
17. National Cancer Institute Workshop on Genetic Screening for Colorectal Cancer.
Rossi SC; Srivastava S
J Natl Cancer Inst; 1996 Mar; 88(6):331-9. PubMed ID: 8609641
[No Abstract] [Full Text] [Related]
18. Molecular diagnosis of hereditary nonpolyposis colon cancer.
Guillem JG
N Engl J Med; 1998 Sep; 339(13):924-5. PubMed ID: 9750095
[No Abstract] [Full Text] [Related]
19. Loss of hMSH2 gene expression correlates with improved survival in patients with sporadic colorectal cancer.
Langner E; Przybylowska K; Trzcinski R; Mik M; Galbfach P; Smolarz B; Romanowicz-Makowska H; Smigileski J; Kulig A; Dziki A
J Genet; 2010 Apr; 89(1):101-4. PubMed ID: 20505253
[No Abstract] [Full Text] [Related]
20. A brave new world of cancer screening.
Rosenthal MA; Burgess AW
Aust N Z J Med; 1994 Dec; 24(6):677-8. PubMed ID: 7717917
[No Abstract] [Full Text] [Related]
[Next] [New Search]
