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Showing results (731-740 of 809) with videos related to

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Cell Reports|June 13, 2019
Poly(ADP-Ribose) Links the DNA Damage Response and BiomineralizationKarin H Müller, Robert Hayward, Rakesh Rajan, et al.
Nature|August 10, 2000
Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and leanJ C Clapham, J R Arch, H Chapman, et al.
The New England Journal of Medicine|March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseFrederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Journal of Medicinal Chemistry|October 14, 2005
Structure-based design and discovery of protein tyrosine phosphatase inhibitors incorporating novel isothiazolidinone heterocyclic phosphotyrosine mimeticsAndrew P Combs, Eddy W Yue, Michael Bower, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyBelinda K Cornes, Jennifer A Brody, Naghmeh Nikpoor, et al.
Nature Genetics|August 9, 2023
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosisSirui Zhou, Olukayode A Sosina, Jonas Bovijn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
BMC Genomics|April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genomeAdam C English, William J Salerno, Oliver A Hampton, et al.
Science (New York, N.Y.)|December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care systemNoura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Nature Genetics|June 29, 2021
Advancing human genetics research and drug discovery through exome sequencing of the UK BiobankJoseph D Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, et al.
Pageof 81

Showing results (731-740 of 809) with videos related to

Sort By:
Pageof 81
Cell Reports|June 13, 2019
Poly(ADP-Ribose) Links the DNA Damage Response and BiomineralizationKarin H Müller, Robert Hayward, Rakesh Rajan, et al.
Nature|August 10, 2000
Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and leanJ C Clapham, J R Arch, H Chapman, et al.
The New England Journal of Medicine|March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseFrederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Journal of Medicinal Chemistry|October 14, 2005
Structure-based design and discovery of protein tyrosine phosphatase inhibitors incorporating novel isothiazolidinone heterocyclic phosphotyrosine mimeticsAndrew P Combs, Eddy W Yue, Michael Bower, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyBelinda K Cornes, Jennifer A Brody, Naghmeh Nikpoor, et al.
Nature Genetics|August 9, 2023
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosisSirui Zhou, Olukayode A Sosina, Jonas Bovijn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
BMC Genomics|April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genomeAdam C English, William J Salerno, Oliver A Hampton, et al.
Science (New York, N.Y.)|December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care systemNoura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Nature Genetics|June 29, 2021
Advancing human genetics research and drug discovery through exome sequencing of the UK BiobankJoseph D Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, et al.
Pageof 81