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Stephen W Scherer

Showing results (41-50 of 499) with videos related to

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CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 26, 2021
Genome sequencing as a diagnostic testGregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
Genomics|June 5, 2003
Identification of a novel protein interacting with laforin, the EPM2a progressive myoclonus epilepsy gene productLeonarda Ianzano, Xiao C Zhao, Berge A Minassian, et al.
Bioinformatics (Oxford, England)|June 13, 2003
Genescript: DNA sequence annotation pipelineAlexander K Hudek, Joseph Cheung, Andrew P Boright, et al.
Experimental Cell Research|March 8, 2005
Early BrdU-responsive genes constitute a novel class of senescence-associated genes in human cellsSachi Minagawa, Kazuhiko Nakabayashi, Michihiko Fujii, et al.
Advances in Neurology|December 31, 2005
On the road to tractability: the current biochemical understanding of progressive myoclonus epilepsiesHannes Lohi, Elayne M Chan, Stephen W Scherer, et al.
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
The American Journal of Psychiatry|February 16, 2019
A Third Linear Association Between Olduvai (DUF1220) Copy Number and Severity of the Classic Symptoms of Inherited AutismJonathan M Davis, Ilea Heft, Stephen W Scherer, et al.
Experimental Gerontology|July 9, 2004
Functional and chromosomal clustering of genes responsive to 5-bromodeoxyuridine in human cellsSachi Minagawa, Kazuhiko Nakabayashi, Michihiko Fujii, et al.
Annals of Clinical and Translational Neurology|December 20, 2018
<i>PI4K2A</i> deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndromeReem A Alkhater, Stephen W Scherer, Berge A Minassian, et al.
Genomics|March 28, 2003
Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein familyFelipe A Cisternas, John B Vincent, Stephen W Scherer, et al.
Pageof 50

Showing results (41-50 of 499) with videos related to

Sort By:
Pageof 50
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 26, 2021
Genome sequencing as a diagnostic testGregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
Genomics|June 5, 2003
Identification of a novel protein interacting with laforin, the EPM2a progressive myoclonus epilepsy gene productLeonarda Ianzano, Xiao C Zhao, Berge A Minassian, et al.
Bioinformatics (Oxford, England)|June 13, 2003
Genescript: DNA sequence annotation pipelineAlexander K Hudek, Joseph Cheung, Andrew P Boright, et al.
Experimental Cell Research|March 8, 2005
Early BrdU-responsive genes constitute a novel class of senescence-associated genes in human cellsSachi Minagawa, Kazuhiko Nakabayashi, Michihiko Fujii, et al.
Advances in Neurology|December 31, 2005
On the road to tractability: the current biochemical understanding of progressive myoclonus epilepsiesHannes Lohi, Elayne M Chan, Stephen W Scherer, et al.
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
The American Journal of Psychiatry|February 16, 2019
A Third Linear Association Between Olduvai (DUF1220) Copy Number and Severity of the Classic Symptoms of Inherited AutismJonathan M Davis, Ilea Heft, Stephen W Scherer, et al.
Experimental Gerontology|July 9, 2004
Functional and chromosomal clustering of genes responsive to 5-bromodeoxyuridine in human cellsSachi Minagawa, Kazuhiko Nakabayashi, Michihiko Fujii, et al.
Annals of Clinical and Translational Neurology|December 20, 2018
<i>PI4K2A</i> deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndromeReem A Alkhater, Stephen W Scherer, Berge A Minassian, et al.
Genomics|March 28, 2003
Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein familyFelipe A Cisternas, John B Vincent, Stephen W Scherer, et al.
Pageof 50