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Human 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 CooperJournal 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 CooperHuman Mutation|April 23, 2013
Patterns and mutational signatures of tandem base substitutions causing human inherited diseaseJian-Min Chen, Claude Férec, David N CooperHuman Genetics|June 30, 2006
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variantsJian-Min Chen, Claude Férec, David N CooperHuman 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 CooperGenomic Medicine|October 17, 2008
Searching for potential microRNA-binding site mutations amongst known disease-associated 3' UTR variantsNadia Chuzhanova, David N Cooper, Claude Férec, et al.Pageof 56