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

Mark Lathrop

Showing results (121-130 of 443) with videos related to

Pageof 45
Sort By:
European Heart Journal|July 24, 2020
Independent risk factors for simvastatin-related myopathy and relevance to different types of muscle symptomJemma C Hopewell, Alison Offer, Richard Haynes, et al.
Genetics|August 28, 2007
Genetic and haplotypic structure in 14 European and African cattle breedsMathieu Gautier, Thomas Faraut, Katayoun Moazami-Goudarzi, et al.
Plos Medicine|May 10, 2017
Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization studyDespoina Manousaki, Lavinia Paternoster, Marie Standl, et al.
The Journal of Infectious Diseases|November 4, 2006
Exhaustive genotyping of the interleukin-1 family genes and associations with AIDS progression in a French cohortHerve Do, Alexandre Vasilescu, Wassila Carpentier, et al.
Nature Communications|May 9, 2015
eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissuesJinyan Huang, Jun Chen, Jorge Esparza, et al.
Human Molecular Genetics|August 14, 2003
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2Caroline Lefévre, Stéphanie Audebert, Florence Jobard, et al.
Scientific Reports|May 9, 2025
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene lociXiaojian Shao, Sophie Le Fur, Warren Cheung, et al.
Plos Genetics|June 12, 2013
Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humansFranz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, et al.
The Journal of Allergy and Clinical Immunology|February 25, 2014
The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotypeMarie-Hélène Dizier, Patricia Margaritte-Jeannin, Anne-Marie Madore, et al.
Hypertension (Dallas, Tex. : 1979)|January 5, 2006
Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension StudySandosh Padmanabhan, Chris Wallace, Patricia B Munroe, et al.
Pageof 45

Showing results (121-130 of 443) with videos related to

Sort By:
Pageof 45
European Heart Journal|July 24, 2020
Independent risk factors for simvastatin-related myopathy and relevance to different types of muscle symptomJemma C Hopewell, Alison Offer, Richard Haynes, et al.
Genetics|August 28, 2007
Genetic and haplotypic structure in 14 European and African cattle breedsMathieu Gautier, Thomas Faraut, Katayoun Moazami-Goudarzi, et al.
Plos Medicine|May 10, 2017
Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization studyDespoina Manousaki, Lavinia Paternoster, Marie Standl, et al.
The Journal of Infectious Diseases|November 4, 2006
Exhaustive genotyping of the interleukin-1 family genes and associations with AIDS progression in a French cohortHerve Do, Alexandre Vasilescu, Wassila Carpentier, et al.
Nature Communications|May 9, 2015
eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissuesJinyan Huang, Jun Chen, Jorge Esparza, et al.
Human Molecular Genetics|August 14, 2003
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2Caroline Lefévre, Stéphanie Audebert, Florence Jobard, et al.
Scientific Reports|May 9, 2025
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene lociXiaojian Shao, Sophie Le Fur, Warren Cheung, et al.
Plos Genetics|June 12, 2013
Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humansFranz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, et al.
The Journal of Allergy and Clinical Immunology|February 25, 2014
The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotypeMarie-Hélène Dizier, Patricia Margaritte-Jeannin, Anne-Marie Madore, et al.
Hypertension (Dallas, Tex. : 1979)|January 5, 2006
Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension StudySandosh Padmanabhan, Chris Wallace, Patricia B Munroe, et al.
Pageof 45