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

M Vance

Showing results (251-260 of 428) with videos related to

Pageof 43
Sort By:
Nature Genetics|February 26, 2005
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseStephan Züchner, Maher Noureddine, Marina Kennerson, et al.
Elife|August 26, 2025
Chronic hyperactivation of midbrain dopamine neurons causes preferential dopamine neuron degenerationKaterina Rademacher, Zak Doric, Dominik Haddad, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic reviewShiying Liu, William S Bush, Rufus Olusola Akinyemi, et al.
Annals of Human Genetics|October 19, 2006
Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5qS H Shah, W E Kraus, D C Crossman, et al.
American Journal of Human Genetics|February 12, 2002
Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosisSilke Schmidt, Lisa F Barcellos, Karen DeSombre, et al.
Plos One|October 18, 2011
Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's diseaseMadalena Martins, Alexandra Rosa, Leonor C Guedes, et al.
Experimental Gerontology|December 13, 2000
Identification of novel genes in late-onset Alzheimer's diseaseM A Pericak-Vance, J Grubber, L R Bailey, et al.
Neuroscience Letters|July 24, 2003
The Q7R Saitohin gene polymorphism is not associated with Alzheimer diseaseSofia A Oliveira, Eden R Martin, William K Scott, et al.
Science (New York, N.Y.)|May 10, 2005
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosisMichelle P Winn, Peter J Conlon, Kelvin L Lynn, et al.
Annals of Human Genetics|July 13, 2013
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson diseaseKaren Nuytemans, Güney Bademci, Martin M Kohli, et al.
Pageof 43

Showing results (251-260 of 428) with videos related to

Sort By:
Pageof 43
Nature Genetics|February 26, 2005
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseStephan Züchner, Maher Noureddine, Marina Kennerson, et al.
Elife|August 26, 2025
Chronic hyperactivation of midbrain dopamine neurons causes preferential dopamine neuron degenerationKaterina Rademacher, Zak Doric, Dominik Haddad, et al.
Medrxiv : the Preprint Server for Health Sciences|May 9, 2025
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic reviewShiying Liu, William S Bush, Rufus Olusola Akinyemi, et al.
Annals of Human Genetics|October 19, 2006
Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5qS H Shah, W E Kraus, D C Crossman, et al.
American Journal of Human Genetics|February 12, 2002
Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosisSilke Schmidt, Lisa F Barcellos, Karen DeSombre, et al.
Plos One|October 18, 2011
Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's diseaseMadalena Martins, Alexandra Rosa, Leonor C Guedes, et al.
Experimental Gerontology|December 13, 2000
Identification of novel genes in late-onset Alzheimer's diseaseM A Pericak-Vance, J Grubber, L R Bailey, et al.
Neuroscience Letters|July 24, 2003
The Q7R Saitohin gene polymorphism is not associated with Alzheimer diseaseSofia A Oliveira, Eden R Martin, William K Scott, et al.
Science (New York, N.Y.)|May 10, 2005
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosisMichelle P Winn, Peter J Conlon, Kelvin L Lynn, et al.
Annals of Human Genetics|July 13, 2013
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson diseaseKaren Nuytemans, Güney Bademci, Martin M Kohli, et al.
Pageof 43