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 (71-80 of 443) with videos related to

Pageof 45
Sort By:
International Journal of Epidemiology|July 17, 2004
Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease riskBernard Keavney, Alison Palmer, Sarah Parish, et al.
Journal of Human Genetics|July 9, 2024
Genomic variants associated with age at diagnosis of childhood-onset type 1 diabetesPierre Bougnères, Sophie Le Fur, Yoichiro Kamatani, et al.
Human Molecular Genetics|January 5, 2002
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1Florence Jobard, Caroline Lefèvre, Aysen Karaduman, et al.
Human Molecular Genetics|April 2, 2003
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndromeFlorence Jobard, Bakar Bouadjar, Frédéric Caux, et al.
Lancet (London, England)|February 8, 2003
Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E epsilon2/epsilon3/epsilon4 genotypeBernard Keavney, Sarah Parish, Alison Palmer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 21, 2012
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regionsPhilippe Pinel, Fabien Fauchereau, Antonio Moreno, et al.
BMC Medical Genetics|August 4, 2011
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levelsGuillemette Antoni, Tiphaine Oudot-Mellakh, Apostolos Dimitromanolakis, et al.
Scientific Reports|February 22, 2018
Consequences of VHL Loss on Global DNA MethylomeClaire M Robinson, Francois Lefebvre, Betty P Poon, et al.
Cardiovascular Research|March 30, 2002
Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive proteinMark A Vickers, Fiona R Green, Catherine Terry, et al.
American Journal of Human Genetics|June 3, 2017
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in HumansLisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, et al.
Pageof 45

Showing results (71-80 of 443) with videos related to

Sort By:
Pageof 45
International Journal of Epidemiology|July 17, 2004
Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease riskBernard Keavney, Alison Palmer, Sarah Parish, et al.
Journal of Human Genetics|July 9, 2024
Genomic variants associated with age at diagnosis of childhood-onset type 1 diabetesPierre Bougnères, Sophie Le Fur, Yoichiro Kamatani, et al.
Human Molecular Genetics|January 5, 2002
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1Florence Jobard, Caroline Lefèvre, Aysen Karaduman, et al.
Human Molecular Genetics|April 2, 2003
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndromeFlorence Jobard, Bakar Bouadjar, Frédéric Caux, et al.
Lancet (London, England)|February 8, 2003
Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E epsilon2/epsilon3/epsilon4 genotypeBernard Keavney, Sarah Parish, Alison Palmer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 21, 2012
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regionsPhilippe Pinel, Fabien Fauchereau, Antonio Moreno, et al.
BMC Medical Genetics|August 4, 2011
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levelsGuillemette Antoni, Tiphaine Oudot-Mellakh, Apostolos Dimitromanolakis, et al.
Scientific Reports|February 22, 2018
Consequences of VHL Loss on Global DNA MethylomeClaire M Robinson, Francois Lefebvre, Betty P Poon, et al.
Cardiovascular Research|March 30, 2002
Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive proteinMark A Vickers, Fiona R Green, Catherine Terry, et al.
American Journal of Human Genetics|June 3, 2017
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in HumansLisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, et al.
Pageof 45