Literature DB >> 7881445

DGGE polymorphism in intron 10 of MSH2, the HNPCC gene.

J Wijnen1, R Fodde, P M Khan.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 7881445     DOI： 10.1093/hmg/3.12.2268-a

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


× No keyword cloud information.
  3 in total

1.  Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.

Authors:  J Wijnen; H Vasen; P M Khan; F H Menko; H van der Klift; C van Leeuwen; M van den Broek; I van Leeuwen-Cornelisse; F Nagengast; A Meijers-Heijboer
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

2.  Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.

Authors:  Anja Wagner; Alicia Barrows; Juul Th Wijnen; Heleen van der Klift; Patrick F Franken; Paul Verkuijlen; Hidewaki Nakagawa; Marjan Geugien; Shantie Jaghmohan-Changur; Cor Breukel; Hanne Meijers-Heijboer; Hans Morreau; Marjo van Puijenbroek; John Burn; Stephany Coronel; Yulia Kinarski; Ross Okimoto; Patrice Watson; Jane F Lynch; Albert de la Chapelle; Henry T Lynch; Riccardo Fodde
Journal:  Am J Hum Genet       Date:  2003-03-25       Impact factor: 11.025

3.  Microsatellite instability and mismatch repair gene inactivation in sporadic pancreatic and colon tumours.

Authors:  C Ghimenti; P Tannergård; S Wahlberg; T Liu; P G Giulianotti; F Mosca; G Fornaciari; G Bevilacqua; A Lindblom; M A Caligo
Journal:  Br J Cancer       Date:  1999-04       Impact factor: 7.640
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.