About: An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer

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About: An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 1997

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1997 (uk) article scientifique publié en 1997 (fr) im Oktober 1997 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 1997 (ast) scientific article published on 01 October 1997 (en)
publication date	wds:Q74202107-4B22A9C4-9C41-4F7D-AF77-6F7B410D9D00
publication date	1997-10-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q74202107-191C36D8-134F-490B-97D2-AC014B94C3D8 wds:Q74202107-24264613-6D2A-4AFC-8824-E5AFE7945F50 wds:Q74202107-3673D98F-0F6D-427D-BC34-A71E7DF80CFE wds:Q74202107-3F5E26AD-BDFE-4654-9350-B1222147ADCF wds:Q74202107-43D859B9-C946-4100-94A9-05DFBAD9139C wds:Q74202107-51221704-383C-434B-8E4F-C2A2EC0CA025 wds:Q74202107-5934661A-37B3-4F87-B39E-8FC731DABBC4 wds:Q74202107-5A714AA9-28FB-4F87-A2F2-45526A551FB6 wds:Q74202107-67077526-5DD1-4BD2-80BB-DBB38CDCE228 wds:Q74202107-6F91D3AF-806B-4B7F-8C4A-31A797993A23 wds:Q74202107-73CD220D-30E8-47B1-A8A7-4001D44ED29B wds:Q74202107-829CCCEB-24B9-473B-8FD1-FD1F17595C1E wds:Q74202107-84E19489-E908-4340-B65E-4DB0B3DFA36B wds:Q74202107-8D3AD130-5E99-44A5-809A-CD5D9FFF01A7 wds:Q74202107-92DDDDA2-C0C2-4B68-8434-CF4DF97FCF17 wds:Q74202107-95FFCF14-71F9-4121-9517-8015878CDB7B wds:Q74202107-9F3DE5A3-92AA-4958-98A3-67E35B3935B7 wds:Q74202107-A7B3A42B-5099-4D5A-AEF4-830CC4BC82CC wds:Q74202107-A9E9B683-6067-4890-BA19-AA9E7B4C187B wds:Q74202107-BB15C70F-54BA-4F71-9C22-95F49A9C289B wds:Q74202107-BBE020A8-C605-4D0F-9615-A661928D36FA wds:Q74202107-C10CE9B4-315B-4C8E-A827-83B40DC2FA17 wds:Q74202107-D555865A-D47C-4F1F-A347-9664C37AC559 wds:Q74202107-D8F917E3-69AE-4226-AA62-66917F7720CF wds:Q74202107-E0FB253B-1671-4DFA-B656-B2E751031DEA wds:Q74202107-EF77DC23-EA91-4C47-A9AD-069BFEDBB339 wds:Q74202107-F7D0133C-25F2-4C4C-BBA2-BCD24CF08BC9
cites work	The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review Hypermutability and mismatch repair deficiency in RER+ tumor cells Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability Mutations of GTBP in genetically unstable cells Microsatellite instability in cancer of the proximal colon Clues to the pathogenesis of familial colorectal cancer Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers Microsatellite instability in colorectal cancer: improved assessment using fluorescent polymerase chain reaction. Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients Identification and characterization of genes that are required for the accelerated degradation of mRNAs containing a premature translational termination codon An association between the risk of cancer and mutations in the HRAS1 minisatellite locus. Diet, acetylator phenotype, and risk of colorectal neoplasia Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis Somatic mutations at CA-repeat loci MSH2 sequence variations and inherited colorectal cancer susceptibility Blood money: blood donors' attitudes to changes in the New Zealand blood transfusion service Mismatch repair function and neoplasia in ulcerative colitis The use of gene tests to detect hereditary predisposition to cancer: economic considerations. Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2 How Many Colon Cancer Genes?
author name string	wds:Q74202107-038A0460-21AB-49D7-9989-AD9C39B68E98 wds:Q74202107-235AA2C0-BEC1-4248-BECB-AAC95646BDE8 wds:Q74202107-26FEA135-4929-4E3A-9FDD-CCFF4E59615C wds:Q74202107-5DAB62C1-E94C-43D1-9E08-4FE0C3812DC8 wds:Q74202107-687FC419-356D-420D-B556-12C531129F50 wds:Q74202107-6F02BC3F-66E5-4777-B9AB-F65937113774 wds:Q74202107-801523C2-1CC4-4E98-96EC-9C5B9C542268 wds:Q74202107-C877FD8F-5CFE-41BA-8EA6-0204531B8EAC wds:Q74202107-CB04F8D2-9683-44F4-8126-537065B5D78B wds:Q74202107-F720AA46-1AA9-4EBC-9829-5AAB5C71DE49
author name string	H D Saeger H K Schackert R Koch M Hahn S Frank J Plaschke M Hampl C Goessl H Görgens S Pistorius
rdfs:label	An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (en) An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (nl)
skos:prefLabel	An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (en) An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (nl)
name	An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (en) An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (nl)
title	wds:Q74202107-64BB8B75-6F5D-44FE-8CBA-03E0F4B54F51
title	An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer (en)
page(s)	wds:Q74202107-BF2A9229-AD69-4395-8102-9F8A077328FB
page(s)	1869-1874
instance of	wds:Q74202107-0E81340E-DDBF-434A-85CC-EC6A71A2E254
instance of	scholarly article
main subject	wds:Q74202107-4FFCF0D1-FC9A-4839-8A04-68B42B8FC47B wds:Q74202107-535B8CFA-960B-4629-964A-44ACCA3121A6 wds:Q74202107-7929F58E-FCA2-4EF5-9061-956097E8B01D
main subject	Lynch syndrome colorectal cancer

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