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Inga Peter

Showing results (71-80 of 171) with videos related to

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Alzheimer Disease and Associated Disorders|October 9, 2009
Depression and plasma amyloid beta peptides in the elderly with and without the apolipoprotein E4 alleleXiaoyan Sun, Chi Chia Chiu, Elizabeth Liebson, et al.
Human Genetics|January 16, 2021
Meta-analysis of sample-level dbGaP data reveals novel shared genetic link between body height and Crohn's diseaseAntonio Di Narzo, Itziar Frades, Heidi M Crane, et al.
Psychosomatic Medicine|October 22, 2015
Genetic Predictors of Depressive Symptoms in the Look AHEAD TrialJeanne M McCaffery, George D Papandonatos, Lucy F Faulconbridge, et al.
Journal of Hypertension|December 4, 2008
The KCNMB1 E65K variant is associated with reduced central pulse pressure in the community-based Framingham Offspring CohortAlyson Kelley-Hedgepeth, Inga Peter, Maria Claudia Montefusco, et al.
Atherosclerosis|July 12, 2005
Estrogen receptor-alpha variants are associated with lipoprotein size distribution and particle levels in women: the Framingham Heart StudySerkalem Demissie, L Adrienne Cupples, Amanda M Shearman, et al.
The American Journal of Clinical Nutrition|April 20, 2012
Obesity susceptibility loci and dietary intake in the Look AHEAD TrialJeanne M McCaffery, George D Papandonatos, Inga Peter, et al.
JACC. Basic to Translational Science|August 9, 2021
Myopathic Cardiac Genotypes Increase Risk for MyocarditisAmy R Kontorovich, Nihir Patel, Arden Moscati, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
Variation in estrogen-related genes associated with cardiovascular phenotypes and circulating estradiol, testosterone, and dehydroepiandrosterone sulfate levelsInga Peter, Alyson Kelley-Hedgepeth, Caroline S Fox, et al.
Bioinformatics (Oxford, England)|November 9, 2002
GeneCards 2002: towards a complete, object-oriented, human gene compendiumMarilyn Safran, Irina Solomon, Orit Shmueli, et al.
BMC Developmental Biology|February 24, 2010
Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) miceYingli Wang, Miao Sun, Victoria L Uhlhorn, et al.
Pageof 18

Showing results (71-80 of 171) with videos related to

Sort By:
Pageof 18
Alzheimer Disease and Associated Disorders|October 9, 2009
Depression and plasma amyloid beta peptides in the elderly with and without the apolipoprotein E4 alleleXiaoyan Sun, Chi Chia Chiu, Elizabeth Liebson, et al.
Human Genetics|January 16, 2021
Meta-analysis of sample-level dbGaP data reveals novel shared genetic link between body height and Crohn's diseaseAntonio Di Narzo, Itziar Frades, Heidi M Crane, et al.
Psychosomatic Medicine|October 22, 2015
Genetic Predictors of Depressive Symptoms in the Look AHEAD TrialJeanne M McCaffery, George D Papandonatos, Lucy F Faulconbridge, et al.
Journal of Hypertension|December 4, 2008
The KCNMB1 E65K variant is associated with reduced central pulse pressure in the community-based Framingham Offspring CohortAlyson Kelley-Hedgepeth, Inga Peter, Maria Claudia Montefusco, et al.
Atherosclerosis|July 12, 2005
Estrogen receptor-alpha variants are associated with lipoprotein size distribution and particle levels in women: the Framingham Heart StudySerkalem Demissie, L Adrienne Cupples, Amanda M Shearman, et al.
The American Journal of Clinical Nutrition|April 20, 2012
Obesity susceptibility loci and dietary intake in the Look AHEAD TrialJeanne M McCaffery, George D Papandonatos, Inga Peter, et al.
JACC. Basic to Translational Science|August 9, 2021
Myopathic Cardiac Genotypes Increase Risk for MyocarditisAmy R Kontorovich, Nihir Patel, Arden Moscati, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
Variation in estrogen-related genes associated with cardiovascular phenotypes and circulating estradiol, testosterone, and dehydroepiandrosterone sulfate levelsInga Peter, Alyson Kelley-Hedgepeth, Caroline S Fox, et al.
Bioinformatics (Oxford, England)|November 9, 2002
GeneCards 2002: towards a complete, object-oriented, human gene compendiumMarilyn Safran, Irina Solomon, Orit Shmueli, et al.
BMC Developmental Biology|February 24, 2010
Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) miceYingli Wang, Miao Sun, Victoria L Uhlhorn, et al.
Pageof 18