Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Timothy J Aitman

Showing results (61-70 of 103) with videos related to

Pageof 11
Sort By:
Journal of Immunology (Baltimore, Md. : 1950)|April 5, 2015
Macrophage epoxygenase determines a profibrotic transcriptome signatureJacques Behmoaras, Ana Garcia Diaz, Lara Venda, et al.
Molecular Metabolism|April 16, 2018
Epoxygenase inactivation exacerbates diet and aging-associated metabolic dysfunction resulting from impaired adipogenesisAntoni Olona, Ximena Terra, Jeong-Hun Ko, et al.
American Journal of Human Genetics|August 4, 2018
A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian CancerD Gareth R Evans, Elke M van Veen, Helen J Byers, et al.
BMC Medical Genetics|June 25, 2014
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based studyPenny J Norsworthy, Jana Vandrovcova, Ellen R A Thomas, et al.
Scientific Reports|July 31, 2019
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohortShona M Kerr, Lucija Klaric, Mihail Halachev, et al.
Hypertension (Dallas, Tex. : 1979)|July 23, 2019
Camk2n1 Is a Negative Regulator of Blood Pressure, Left Ventricular Mass, Insulin Sensitivity, and Promotes AdiposityNeza Alfazema, Marjorie Barrier, Sophie Marion de Procé, et al.
Neurobiology of Aging|January 17, 2017
Genetic epidemiology of motor neuron disease-associated variants in the Scottish populationHolly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Neurobiology of Aging|June 14, 2017
Corrigendum to "Genetic epidemiology of motor neuron disease-associated variants in the Scottish population." [Neurobiol. Aging 51 (2017) 178.e11-178.e20]Holly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Obesity (Silver Spring, Md.)|July 16, 2011
Association of sirtuin 1 (SIRT1) gene SNPs and transcript expression levels with severe obesityStephen J Clark, Mario Falchi, Bob Olsson, et al.
Plos Genetics|November 26, 2019
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regionsMihail Halachev, Alison Meynert, Martin S Taylor, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Journal of Immunology (Baltimore, Md. : 1950)|April 5, 2015
Macrophage epoxygenase determines a profibrotic transcriptome signatureJacques Behmoaras, Ana Garcia Diaz, Lara Venda, et al.
Molecular Metabolism|April 16, 2018
Epoxygenase inactivation exacerbates diet and aging-associated metabolic dysfunction resulting from impaired adipogenesisAntoni Olona, Ximena Terra, Jeong-Hun Ko, et al.
American Journal of Human Genetics|August 4, 2018
A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian CancerD Gareth R Evans, Elke M van Veen, Helen J Byers, et al.
BMC Medical Genetics|June 25, 2014
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based studyPenny J Norsworthy, Jana Vandrovcova, Ellen R A Thomas, et al.
Scientific Reports|July 31, 2019
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohortShona M Kerr, Lucija Klaric, Mihail Halachev, et al.
Hypertension (Dallas, Tex. : 1979)|July 23, 2019
Camk2n1 Is a Negative Regulator of Blood Pressure, Left Ventricular Mass, Insulin Sensitivity, and Promotes AdiposityNeza Alfazema, Marjorie Barrier, Sophie Marion de Procé, et al.
Neurobiology of Aging|January 17, 2017
Genetic epidemiology of motor neuron disease-associated variants in the Scottish populationHolly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Neurobiology of Aging|June 14, 2017
Corrigendum to "Genetic epidemiology of motor neuron disease-associated variants in the Scottish population." [Neurobiol. Aging 51 (2017) 178.e11-178.e20]Holly A Black, Danielle J Leighton, Elaine M Cleary, et al.
Obesity (Silver Spring, Md.)|July 16, 2011
Association of sirtuin 1 (SIRT1) gene SNPs and transcript expression levels with severe obesityStephen J Clark, Mario Falchi, Bob Olsson, et al.
Plos Genetics|November 26, 2019
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regionsMihail Halachev, Alison Meynert, Martin S Taylor, et al.
Pageof 11