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

Magalie S Leduc

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
Journal of Lipid Research|June 22, 2010
Untangling HDL quantitative trait loci on mouse chromosome 5 and identifying Scarb1 and Acads as the underlying genesZhiguang Su, Magalie S Leduc, Ron Korstanje, et al.
Genetics|January 19, 2011
A Bayesian framework for inference of the genotype-phenotype map for segregating populationsRachael S Hageman, Magalie S Leduc, Ron Korstanje, et al.
Journal of the American Society of Nephrology : JASN|October 30, 2010
Uncovering genes and regulatory pathways related to urinary albumin excretionRachael S Hageman, Magalie S Leduc, Christina R Caputo, et al.
Journal of Lipid Research|August 5, 2008
Comprehensive evaluation of apolipoprotein H gene (APOH) variation identifies novel associations with measures of lipid metabolism in GENOAMagalie S Leduc, Lawrence C Shimmin, Kathy L E Klos, et al.
Molecular Genetics and Genomics : MGG|September 27, 2012
A major X-linked locus affects kidney function in miceMagalie S Leduc, Holly S Savage, Timothy M Stearns, et al.
Journal of Lipid Research|April 14, 2012
Using bioinformatics and systems genetics to dissect HDL-cholesterol genetics in an MRL/MpJ x SM/J intercrossMagalie S Leduc, Rachael Hageman Blair, Ricardo A Verdugo, et al.
Journal of Lipid Research|May 31, 2011
Integration of QTL and bioinformatic tools to identify candidate genes for triglycerides in miceMagalie S Leduc, Rachael S Hageman, Ricardo A Verdugo, et al.
Journal of Human Genetics|September 17, 2008
An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to diseaseDong-Chuan Guo, Prateek Gupta, Van Tran-Fadulu, et al.
Aging Cell|August 26, 2010
Identification of genetic determinants of IGF-1 levels and longevity among mouse inbred strainsMagalie S Leduc, Rachael S Hageman, Qingying Meng, et al.
Human Genetics|March 21, 2018
De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalitiesMagalie S Leduc, Marianne Mcguire, Suneeta Madan-Khetarpal, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Journal of Lipid Research|June 22, 2010
Untangling HDL quantitative trait loci on mouse chromosome 5 and identifying Scarb1 and Acads as the underlying genesZhiguang Su, Magalie S Leduc, Ron Korstanje, et al.
Genetics|January 19, 2011
A Bayesian framework for inference of the genotype-phenotype map for segregating populationsRachael S Hageman, Magalie S Leduc, Ron Korstanje, et al.
Journal of the American Society of Nephrology : JASN|October 30, 2010
Uncovering genes and regulatory pathways related to urinary albumin excretionRachael S Hageman, Magalie S Leduc, Christina R Caputo, et al.
Journal of Lipid Research|August 5, 2008
Comprehensive evaluation of apolipoprotein H gene (APOH) variation identifies novel associations with measures of lipid metabolism in GENOAMagalie S Leduc, Lawrence C Shimmin, Kathy L E Klos, et al.
Molecular Genetics and Genomics : MGG|September 27, 2012
A major X-linked locus affects kidney function in miceMagalie S Leduc, Holly S Savage, Timothy M Stearns, et al.
Journal of Lipid Research|April 14, 2012
Using bioinformatics and systems genetics to dissect HDL-cholesterol genetics in an MRL/MpJ x SM/J intercrossMagalie S Leduc, Rachael Hageman Blair, Ricardo A Verdugo, et al.
Journal of Lipid Research|May 31, 2011
Integration of QTL and bioinformatic tools to identify candidate genes for triglycerides in miceMagalie S Leduc, Rachael S Hageman, Ricardo A Verdugo, et al.
Journal of Human Genetics|September 17, 2008
An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to diseaseDong-Chuan Guo, Prateek Gupta, Van Tran-Fadulu, et al.
Aging Cell|August 26, 2010
Identification of genetic determinants of IGF-1 levels and longevity among mouse inbred strainsMagalie S Leduc, Rachael S Hageman, Qingying Meng, et al.
Human Genetics|March 21, 2018
De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalitiesMagalie S Leduc, Marianne Mcguire, Suneeta Madan-Khetarpal, et al.
Pageof 3