نتایج جستجو برای: hmsh2

تعداد نتایج: 448  

Journal: :Cancer research 2001
T Liu H Yan S Kuismanen A Percesepe M L Bisgaard M Pedroni P Benatti K W Kinzler B Vogelstein M Ponz de Leon P Peltomäki A Lindblom

Hereditary nonpolyposis colorectal cancer (HNPCC) is attributable to a deficiency of mismatch repair. Inactivation of DNA mismatch repair underlies the genesis of microsatellite instability in colorectal cancer. Germline mutations in three DNA mismatch repair genes, hMSH2, hMLH1, and hMSH6, have been found to segregate in HNPCC and HNPCC-like families. The two DNA mismatch repair genes hPMS1 an...

Journal: :Nihon rinsho. Japanese journal of clinical medicine 1994
Seiichi Takenoshita Kenichi Takita

Hereditary non-polyposis colorectal cancer (HNPCC) is a type of hereditary colorectal cancer with autosomal dominant traits. Its causal genes are mismatch repair genes such as the hMSH2 and hMLH1 genes. Owing to its frequency, juvenile onset, and the outbreaks of multiple colorectal cancers and cancers occurring over multiple organs, it is recognized as a very important disease for the purpose ...

2000
Henry D Janowitz

Microsatellite instability in colitis associated colorectal cancer As molecular pathways of colon carcinogenesis continue to be defined for high risk hereditary colon cancer syndromes and for average risk sporadic colon cancers, it seems that colon carcinogenesis in the setting of chronic idiopathic inflammatory bowel disease (IBD) may be unique. 1 Although to some extent this notion seems intu...

Journal: :Gut 2000
H Iino L Simms J Young J Arnold I M Winship S I Webb K L Furlong B Leggett J R Jass

BACKGROUND AND AIM Hereditary non-polyposis colorectal cancer (HNPCC), as its name implies, is associated with few adenomas, and the early evolution of colorectal neoplasia is poorly understood. In this study our aim was to clarify the genetic profiles of benign polyps in subjects with HNPCC using a combined molecular and immunohistochemical approach. METHODS Thirty adenomas and 17 hyperplast...

Journal: :Cancer research 1996
S Aebi B Kurdi-Haidar R Gordon B Cenni H Zheng D Fink R D Christen C R Boland M Koi R Fishel S B Howell

Selection of cells for resistance to cisplatin, a well-recognized mutagen, could result in mutations in genes involved in DNA mismatch repair and thereby to resistance to DNA-alkylating agents. Parental cells of the human ovarian adenocarcinoma cell line 2008 expressed hMLH1 when analyzed with immunoblot. One subline selected for resistance to cisplatin (2008/A) expressed no hMLH1, whereas anot...

Journal: :The Journal of biological chemistry 2000
P Dufner G Marra M Räschle J Jiricny

The most abundant mismatch binding factor in human cells, hMutSalpha, is a heterodimer of hMSH2 and hMSH6, two homologues of the bacterial MutS protein. The C-terminal portions of all MutS homologues contain an ATP binding motif and are highly conserved throughout evolution. Although the N termini are generally divergent, they too contain short conserved sequence elements. A phenylalanine --> a...

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