BMC Genomics

official impact factor 4.21
Search for
Advanced search
BMC Genomics
Tools
Share this article
Open Access

In silico and in vivo splicing analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects

Patrizia Lastella, Nicoletta C Surdo, Nicoletta Resta, Ginevra Guanti and Alessandro Stella*

BMC Genomics 2006, 7:243 doi:10.1186/1471-2164-7-243

Accesses  

  • Last 30 days: 56 accesses
  • Last 365 days: 628 accesses
  • All time: 3637 accesses

Cited by

BioMed Central: 2 citations

Research article   Open Access

Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2 transcripts

Phillip J Whiley, Christopher A Pettigrew, Brooke L Brewster, Logan C Walker, Amanda B Spurdle, Melissa A Brown BMC Medical Genetics 2010, 11:80 (28 May 2010)

Abstract | Full text | PDF | PubMed

Research article   Open Access

The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population

Lise Christensen, Bo E Madsen, Friedrik P Wikman, Carsten Wiuf, Karen Koed, Anne Tjønneland, Anja Olsen, Ann-Christine Syvänen, Claus L Andersen, Torben F Ørntoft BMC Medical Genetics 2008, 9:52 (11 June 2008)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Google Scholar: View citations

ISI Web of Science: View citations

PubMed Central: View citations