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Mark Lathrop

Showing results (101-110 of 443) with videos related to

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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 13, 2005
Genomic approach of AIDS pathogenesis: exhaustive genotyping of the TNFR1 gene in a French AIDS cohortGora Diop, Jean-Louis Spadoni, Hervé Do, et al.
JAMA Cardiology|November 13, 2017
Association of LPA Variants With Aortic Stenosis: A Large-Scale Study Using Diagnostic and Procedural Codes From Electronic Health RecordsHao Yu Chen, Line Dufresne, Hannah Burr, et al.
Blood|October 24, 2002
A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibilityJosé Manuel Soria, Laura Almasy, Joan Carles Souto, et al.
BMC Medical Genetics|March 21, 2013
A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosisNicolas Greliche, Marine Germain, Jean-Charles Lambert, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2016
Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 DeficiencyLaurence Salle-Teyssières, Martine Auclair, Faraj Terro, et al.
Biological Psychiatry|April 13, 2011
Sex-specific role for adenylyl cyclase type 7 in alcohol dependenceSylvane Desrivières, Sergey P Pronko, Anbarasu Lourdusamy, et al.
Human Molecular Genetics|April 21, 2011
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese populationChikashi Terao, Ryo Yamada, Koichiro Ohmura, et al.
Human Molecular Genetics|September 24, 2004
L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1Meral Topçu, Florence Jobard, Sophie Halliez, et al.
The Journal of Investigative Dermatology|December 2, 2006
Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13Fabienne Lesueur, Bakar Bouadjar, Caroline Lefèvre, et al.
European Journal of Human Genetics : EJHG|September 13, 2018
Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traitsAndréanne Morin, Anne-Marie Madore, Tony Kwan, et al.
Pageof 45

Showing results (101-110 of 443) with videos related to

Sort By:
Pageof 45
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 13, 2005
Genomic approach of AIDS pathogenesis: exhaustive genotyping of the TNFR1 gene in a French AIDS cohortGora Diop, Jean-Louis Spadoni, Hervé Do, et al.
JAMA Cardiology|November 13, 2017
Association of LPA Variants With Aortic Stenosis: A Large-Scale Study Using Diagnostic and Procedural Codes From Electronic Health RecordsHao Yu Chen, Line Dufresne, Hannah Burr, et al.
Blood|October 24, 2002
A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibilityJosé Manuel Soria, Laura Almasy, Joan Carles Souto, et al.
BMC Medical Genetics|March 21, 2013
A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosisNicolas Greliche, Marine Germain, Jean-Charles Lambert, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2016
Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 DeficiencyLaurence Salle-Teyssières, Martine Auclair, Faraj Terro, et al.
Biological Psychiatry|April 13, 2011
Sex-specific role for adenylyl cyclase type 7 in alcohol dependenceSylvane Desrivières, Sergey P Pronko, Anbarasu Lourdusamy, et al.
Human Molecular Genetics|April 21, 2011
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese populationChikashi Terao, Ryo Yamada, Koichiro Ohmura, et al.
Human Molecular Genetics|September 24, 2004
L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1Meral Topçu, Florence Jobard, Sophie Halliez, et al.
The Journal of Investigative Dermatology|December 2, 2006
Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13Fabienne Lesueur, Bakar Bouadjar, Caroline Lefèvre, et al.
European Journal of Human Genetics : EJHG|September 13, 2018
Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traitsAndréanne Morin, Anne-Marie Madore, Tony Kwan, et al.
Pageof 45