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Annual Review of Genomics and Human Genetics|May 21, 2009
Chronic pancreatitis: genetics and pathogenesisJian-Min Chen, Claude FérecClinics and Research in Hepatology and Gastroenterology|July 4, 2012
Genetics and pathogenesis of chronic pancreatitis: the 2012 updateJian-Min Chen, Claude FérecHuman Mutation|August 18, 2009
Closely spaced multiple mutations as potential signatures of transient hypermutability in human genesJian-Min Chen, Claude Férec, David N CooperGenomic Medicine|October 17, 2008
Mechanism of Alu integration into the human genomeJian-Min Chen, Claude Férec, David N CooperHuman Mutation|July 15, 2015
Complex Multiple-Nucleotide Substitution Mutations Causing Human Inherited Disease Reveal Novel Insights into the Action of Translesion Synthesis DNA PolymerasesJian-Min Chen, Claude Férec, David N CooperBiological & Pharmaceutical Bulletin|June 17, 2003
Trypsinogen hL is not a new member of the human trypsinogen family, but a known mouse orthologJian-Min Chen, Claude Férec, Miklós Sahin-TóthJournal of Biomedicine & Biotechnology|August 1, 2006
LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease: mutation detection bias and multiple mechanisms of target gene disruptionJian-Min Chen, Claude Férec, David N CooperMutation Research|November 22, 2011
Transient hypermutability, chromothripsis and replication-based mechanisms in the generation of concurrent clustered mutationsJian-Min Chen, Claude Férec, David N CooperGenes|April 9, 2014
Gene conversion in human genetic diseaseJian-Min Chen, Claude Férec, David N CooperHuman Genetics|April 29, 2006
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes I: general principles and overviewJian-Min Chen, Claude Férec, David N CooperPageof 41