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Benjamin A Salisbury

Showing results (1-10 of 29) with videos related to

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Cladistics : the International Journal of the Willi Hennig Society|December 14, 2021
Strongest Evidence: Maximum Apparent Phylogenetic Signal as a New Cladistic Optimality CriterionBenjamin A Salisbury
Cladistics : the International Journal of the Willi Hennig Society|December 14, 2021
Strongest Evidence RevisitedBenjamin A Salisbury
Pharmacogenomics|December 20, 2003
Genetic variability and evolution of two pharmacologically important classes of genesManish S Pungliya, Benjamin A Salisbury, Krishnan Nandabalan, et al.
Molecular Diagnosis & Therapy|June 15, 2006
Pharmacogenetic issues in thorough QT trialsRichard S Judson, Benjamin A Salisbury, Carol R Reed, et al.
American Journal of Human Genetics|November 14, 2007
The structure of common genetic variation in United States populationsStephen L Guthery, Benjamin A Salisbury, Manish S Pungliya, et al.
Mutation Research|April 26, 2003
SNP and haplotype variation in the human genomeBenjamin A Salisbury, Manish Pungliya, Julie Y Choi, et al.
Heart Rhythm|May 3, 2008
Prevalence of early-onset atrial fibrillation in congenital long QT syndromeJonathan N Johnson, David J Tester, James Perry, et al.
Journal of the American College of Cardiology|October 17, 2009
The SLCO1B1*5 genetic variant is associated with statin-induced side effectsDeepak Voora, Svati H Shah, Ivan Spasojevic, et al.
Journal of Cardiovascular Translational Research|February 11, 2014
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, J Martijn Bos, et al.
Mechanisms of Ageing and Development|March 6, 2003
DNA variability of human genesJulie A Schneider, Manish S Pungliya, Julie Y Choi, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Cladistics : the International Journal of the Willi Hennig Society|December 14, 2021
Strongest Evidence: Maximum Apparent Phylogenetic Signal as a New Cladistic Optimality CriterionBenjamin A Salisbury
Cladistics : the International Journal of the Willi Hennig Society|December 14, 2021
Strongest Evidence RevisitedBenjamin A Salisbury
Pharmacogenomics|December 20, 2003
Genetic variability and evolution of two pharmacologically important classes of genesManish S Pungliya, Benjamin A Salisbury, Krishnan Nandabalan, et al.
Molecular Diagnosis & Therapy|June 15, 2006
Pharmacogenetic issues in thorough QT trialsRichard S Judson, Benjamin A Salisbury, Carol R Reed, et al.
American Journal of Human Genetics|November 14, 2007
The structure of common genetic variation in United States populationsStephen L Guthery, Benjamin A Salisbury, Manish S Pungliya, et al.
Mutation Research|April 26, 2003
SNP and haplotype variation in the human genomeBenjamin A Salisbury, Manish Pungliya, Julie Y Choi, et al.
Heart Rhythm|May 3, 2008
Prevalence of early-onset atrial fibrillation in congenital long QT syndromeJonathan N Johnson, David J Tester, James Perry, et al.
Journal of the American College of Cardiology|October 17, 2009
The SLCO1B1*5 genetic variant is associated with statin-induced side effectsDeepak Voora, Svati H Shah, Ivan Spasojevic, et al.
Journal of Cardiovascular Translational Research|February 11, 2014
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, J Martijn Bos, et al.
Mechanisms of Ageing and Development|March 6, 2003
DNA variability of human genesJulie A Schneider, Manish S Pungliya, Julie Y Choi, et al.
Pageof 3