Literature DB >> 7885145

A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome.

N J Froggatt, J A Joyce, R Davies, D Gareth, R Evans, B A Ponder, D E Barton, E R Maher.   

Abstract

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Year:  1995        PMID： 7885145     DOI： 10.1016/s0140-6736(95)90900-1

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  18 in total

1.  The genetics of inherited colon cancer.

Authors:  Y Wallis; F Macdonald
Journal:  Clin Mol Pathol       Date:  1996-04

2.  Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.

Authors:  A L Moisio; P Sistonen; J Weissenbach; A de la Chapelle; P Peltomäki
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

3.  Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients.

Authors:  M Spaepen; B Vankeirsbilck; S Van Opstal; S Tejpar; E Van Cutsem; K Geboes; E Legius; G Matthijs
Journal:  Fam Cancer       Date:  2006       Impact factor: 2.375

4.  Reduction in hMSH2 mRNA levels by premature translation termination: implications for mutation screening in hereditary nonpolyposis colorectal cancer.

Authors:  X Lin; J H Choi; P Lynch; L Xi; E Wu; M L Frazier
Journal:  Dig Dis Sci       Date:  1999-03       Impact factor: 3.199

5.  A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.

Authors:  N J Froggatt; J Green; C Brassett; D G Evans; D T Bishop; R Kolodner; E R Maher
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

6.  Recurrent germline mutation in MSH2 arises frequently de novo.

Authors:  D C Desai; J C Lockman; R B Chadwick; X Gao; A Percesepe; D G Evans; M Miyaki; S T Yuen; P Radice; E R Maher; F A Wright; A de La Chapelle
Journal:  J Med Genet       Date:  2000-09       Impact factor: 6.318

7.  The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome.

Authors:  Susan Stuckless; Patrick S Parfrey; Michael O Woods; Janet Cox; G William Fitzgerald; Jane S Green; Roger C Green
Journal:  Fam Cancer       Date:  2007       Impact factor: 2.375

8.  First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome.

Authors:  H Ziada-Bouchaar; K Sifi; T Filali; T Hammada; D Satta; N Abadi
Journal:  Fam Cancer       Date:  2017-01       Impact factor: 2.375

9.  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.

Authors:  M Miyaki; M Konishi; M Muraoka; R Kikuchi-Yanoshita; K Tanaka; T Iwama; T Mori; M Koike; K Ushio; M Chiba
Journal:  J Mol Med (Berl)       Date:  1995-10       Impact factor: 4.599

10.  Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

Authors:  J Wijnen; P M Khan; H Vasen; F Menko; H van der Klift; M van den Broek; I van Leeuwen-Cornelisse; F Nagengast; E J Meijers-Heijboer; D Lindhout; G Griffioen; A Cats; J Kleibeuker; L Varesco; L Bertario; M L Bisgaard; J Mohr; R Kolodner; R Fodde
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025
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