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

Shapour Jalilzadeh

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Biotechniques|September 12, 2024
When is an SNP not an SNP?Shapour Jalilzadeh, Valerie Walker, Gary P Leggatt, et al.
Frontiers in Neurology|August 5, 2025
Genetics of progressive multifocal leukoencephalopathy: update on case reports with an inborn error of immunity and risk variants found in drug-linked casesPeggy S Eis, Edward B Smith, Shapour Jalilzadeh, et al.
Circulation Research|July 4, 2009
Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiencySteven Marston, O'Neal Copeland, Adam Jacques, et al.
European Heart Journal|January 18, 2007
The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA studyMahmut Akyol, Shapour Jalilzadeh, Moritz F Sinner, et al.
Journal of Molecular and Cellular Cardiology|July 10, 2010
Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathyAnita C Hoskins, Adam Jacques, Sonya C Bardswell, et al.
Circulation Research|March 5, 2005
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA studyArne Pfeufer, Shapour Jalilzadeh, Siegfried Perz, et al.
Cardiovascular Research|April 16, 2008
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathyAdam M Jacques, Natalia Briceno, Andrew E Messer, et al.
Circulation|April 30, 2013
Interactions between vascular wall and perivascular adipose tissue reveal novel roles for adiponectin in the regulation of endothelial nitric oxide synthase function in human vesselsMarios Margaritis, Alexios S Antonopoulos, Janet Digby, et al.
Nature Genetics|July 20, 2007
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regionsJuliane Winkelmann, Barbara Schormair, Peter Lichtner, et al.
Nature Genetics|May 2, 2006
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarizationDan E Arking, Arne Pfeufer, Wendy Post, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Biotechniques|September 12, 2024
When is an SNP not an SNP?Shapour Jalilzadeh, Valerie Walker, Gary P Leggatt, et al.
Frontiers in Neurology|August 5, 2025
Genetics of progressive multifocal leukoencephalopathy: update on case reports with an inborn error of immunity and risk variants found in drug-linked casesPeggy S Eis, Edward B Smith, Shapour Jalilzadeh, et al.
Circulation Research|July 4, 2009
Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiencySteven Marston, O'Neal Copeland, Adam Jacques, et al.
European Heart Journal|January 18, 2007
The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA studyMahmut Akyol, Shapour Jalilzadeh, Moritz F Sinner, et al.
Journal of Molecular and Cellular Cardiology|July 10, 2010
Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathyAnita C Hoskins, Adam Jacques, Sonya C Bardswell, et al.
Circulation Research|March 5, 2005
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA studyArne Pfeufer, Shapour Jalilzadeh, Siegfried Perz, et al.
Cardiovascular Research|April 16, 2008
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathyAdam M Jacques, Natalia Briceno, Andrew E Messer, et al.
Circulation|April 30, 2013
Interactions between vascular wall and perivascular adipose tissue reveal novel roles for adiponectin in the regulation of endothelial nitric oxide synthase function in human vesselsMarios Margaritis, Alexios S Antonopoulos, Janet Digby, et al.
Nature Genetics|July 20, 2007
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regionsJuliane Winkelmann, Barbara Schormair, Peter Lichtner, et al.
Nature Genetics|May 2, 2006
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarizationDan E Arking, Arne Pfeufer, Wendy Post, et al.
Pageof 2