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Alan R Shuldiner

Showing results (121-130 of 406) with videos related to

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Trials|January 9, 2019
Polyherbal dietary supplementation for prediabetic adults: study protocol for a randomized controlled trialTermeh Feinberg, L Susan Wieland, Larry E Miller, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|November 3, 2015
Development of a physiology-directed population pharmacokinetic and pharmacodynamic model for characterizing the impact of genetic and demographic factors on clopidogrel response in healthy adultsXi-Ling Jiang, Snehal Samant, Joshua P Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
The role of phenotype-based search approaches using public online databases in diagnostics of Mendelian disordersAvi Fellner, Noa Ruhrman-Shahar, Naama Orenstein, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|January 13, 2004
Beta2- and beta3-adrenergic receptor polymorphisms and exercise hemodynamics in postmenopausal womenSteve D McCole, Alan R Shuldiner, Michael D Brown, et al.
The American Journal of Clinical Nutrition|May 31, 2002
Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysisNanette I Steinle, Wen-Chi Hsueh, Soren Snitker, et al.
Nutrients|February 11, 2016
A Common Variant in the SETD7 Gene Predicts Serum Lycopene ConcentrationsChristopher R D'Adamo, Antonietta D'Urso, Kathleen A Ryan, et al.
Diabetes|October 1, 2015
American Diabetes Association and JDRF Research Symposium: Diabetes and the MicrobiomeClay F Semenkovich, Jayne Danska, Tamara Darsow, et al.
Nature Aging|May 18, 2023
SuperAger Initiative: unlocking the genetic potential of exceptional longevitySofiya Milman, Nir Barzilai, Kara A Wilson, et al.
Clinical Genetics|January 25, 2021
Two intronic cis-acting variants in both alleles of the POLR3A gene cause progressive spastic ataxia with hypodontiaAvi Fellner, Alexander Lossos, Elena Kogan, et al.
Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.
Pageof 41

Showing results (121-130 of 406) with videos related to

Sort By:
Pageof 41
Trials|January 9, 2019
Polyherbal dietary supplementation for prediabetic adults: study protocol for a randomized controlled trialTermeh Feinberg, L Susan Wieland, Larry E Miller, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|November 3, 2015
Development of a physiology-directed population pharmacokinetic and pharmacodynamic model for characterizing the impact of genetic and demographic factors on clopidogrel response in healthy adultsXi-Ling Jiang, Snehal Samant, Joshua P Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
The role of phenotype-based search approaches using public online databases in diagnostics of Mendelian disordersAvi Fellner, Noa Ruhrman-Shahar, Naama Orenstein, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|January 13, 2004
Beta2- and beta3-adrenergic receptor polymorphisms and exercise hemodynamics in postmenopausal womenSteve D McCole, Alan R Shuldiner, Michael D Brown, et al.
The American Journal of Clinical Nutrition|May 31, 2002
Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysisNanette I Steinle, Wen-Chi Hsueh, Soren Snitker, et al.
Nutrients|February 11, 2016
A Common Variant in the SETD7 Gene Predicts Serum Lycopene ConcentrationsChristopher R D'Adamo, Antonietta D'Urso, Kathleen A Ryan, et al.
Diabetes|October 1, 2015
American Diabetes Association and JDRF Research Symposium: Diabetes and the MicrobiomeClay F Semenkovich, Jayne Danska, Tamara Darsow, et al.
Nature Aging|May 18, 2023
SuperAger Initiative: unlocking the genetic potential of exceptional longevitySofiya Milman, Nir Barzilai, Kara A Wilson, et al.
Clinical Genetics|January 25, 2021
Two intronic cis-acting variants in both alleles of the POLR3A gene cause progressive spastic ataxia with hypodontiaAvi Fellner, Alexander Lossos, Elena Kogan, et al.
Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.
Pageof 41