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David N Cooper

Showing results (31-40 of 398) with videos related to

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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 Cooper
Journal 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 Cooper
Transfusion|June 11, 2011
Local DNA sequence determinants of FUT2 copy number variationJian-Min Chen, David N Cooper, Claude Férec
Genetic Testing and Molecular Biomarkers|July 21, 2010
Chromosomal distribution of disease genes in the human genomeDavid N Cooper, Edward V Ball, Matthew Mort
Human Genomics|December 19, 2012
Local sequence determinants of two in-frame triplet deletion/duplication hotspots in the RHD/RHCE genesJian-Min Chen, David N Cooper, Claude Férec
Genes|April 8, 2014
Mechanisms of base substitution mutagenesis in cancer genomesAlbino Bacolla, David N Cooper, Karen M Vasquez
Genome Medicine|June 26, 2013
DNA structure mattersAlbino Bacolla, David N Cooper, Karen M Vasquez
Human Mutation|December 31, 2013
A new and more accurate estimate of the rate of concurrent tandem-base substitution mutations in the human germline: ∼0.4% of the single-nucleotide substitution mutation rateJian-Min Chen, David N Cooper, Claude Férec
Investigative Genetics|November 25, 2010
Is the NIH policy for sharing GWAS data running the risk of being counterproductive?Michael Krawczak, Jürgen W Goebel, David N Cooper
Human Genetics|April 6, 2002
Proposed guidelines for papers describing DNA polymorphism-disease associationsDavid N Cooper, Robert L Nussbaum, Michael Krawczak
Pageof 40

Showing results (31-40 of 398) with videos related to

Sort By:
Pageof 40
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 Cooper
Journal 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 Cooper
Transfusion|June 11, 2011
Local DNA sequence determinants of FUT2 copy number variationJian-Min Chen, David N Cooper, Claude Férec
Genetic Testing and Molecular Biomarkers|July 21, 2010
Chromosomal distribution of disease genes in the human genomeDavid N Cooper, Edward V Ball, Matthew Mort
Human Genomics|December 19, 2012
Local sequence determinants of two in-frame triplet deletion/duplication hotspots in the RHD/RHCE genesJian-Min Chen, David N Cooper, Claude Férec
Genes|April 8, 2014
Mechanisms of base substitution mutagenesis in cancer genomesAlbino Bacolla, David N Cooper, Karen M Vasquez
Genome Medicine|June 26, 2013
DNA structure mattersAlbino Bacolla, David N Cooper, Karen M Vasquez
Human Mutation|December 31, 2013
A new and more accurate estimate of the rate of concurrent tandem-base substitution mutations in the human germline: ∼0.4% of the single-nucleotide substitution mutation rateJian-Min Chen, David N Cooper, Claude Férec
Investigative Genetics|November 25, 2010
Is the NIH policy for sharing GWAS data running the risk of being counterproductive?Michael Krawczak, Jürgen W Goebel, David N Cooper
Human Genetics|April 6, 2002
Proposed guidelines for papers describing DNA polymorphism-disease associationsDavid N Cooper, Robert L Nussbaum, Michael Krawczak
Pageof 40