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

L Girard

Showing results (211-220 of 235) with videos related to

Pageof 24
Sort By:
Human Molecular Genetics|January 8, 2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levelsLan Xiong, Hélène Catoire, Patrick Dion, et al.
Plos Genetics|April 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon L Girard, Caroline Meloche, et al.
Neurology. Genetics|December 26, 2018
No rare deleterious variants from <i>STK32B</i>, <i>PPARGC1A</i>, and <i>CTNNA3</i> are associated with essential tremorGabrielle Houle, Amirthagowri Ambalavanan, Jean-François Schmouth, et al.
Journal of Molecular Neuroscience : MN|May 2, 2015
Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior DisorderZ Gan-Or, S L Girard, A Noreau, et al.
Oncogene|February 16, 2010
Epidermal growth factor receptor regulates MET levels and invasiveness through hypoxia-inducible factor-1alpha in non-small cell lung cancer cellsL Xu, M B Nilsson, P Saintigny, et al.
Human Molecular Genetics|October 26, 2014
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosisHannah M Kaneb, Andrew W Folkmann, Véronique V Belzil, et al.
Nature Genetics|July 12, 2011
Increased exonic de novo mutation rate in individuals with schizophreniaSimon L Girard, Julie Gauthier, Anne Noreau, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing identifies FUS mutations as a cause of essential tremorNancy D Merner, Simon L Girard, Hélène Catoire, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
Dehydroepiandrosterone (DHEA), DHEA sulfate, and aging: contribution of the DHEAge Study to a sociobiomedical issueE E Baulieu, G Thomas, S Legrain, et al.
Neurobiology of Aging|May 2, 2016
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorderZiv Gan-Or, Noreen Mohsin, Simon L Girard, et al.
Pageof 24

Showing results (211-220 of 235) with videos related to

Sort By:
Pageof 24
Human Molecular Genetics|January 8, 2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levelsLan Xiong, Hélène Catoire, Patrick Dion, et al.
Plos Genetics|April 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon L Girard, Caroline Meloche, et al.
Neurology. Genetics|December 26, 2018
No rare deleterious variants from <i>STK32B</i>, <i>PPARGC1A</i>, and <i>CTNNA3</i> are associated with essential tremorGabrielle Houle, Amirthagowri Ambalavanan, Jean-François Schmouth, et al.
Journal of Molecular Neuroscience : MN|May 2, 2015
Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior DisorderZ Gan-Or, S L Girard, A Noreau, et al.
Oncogene|February 16, 2010
Epidermal growth factor receptor regulates MET levels and invasiveness through hypoxia-inducible factor-1alpha in non-small cell lung cancer cellsL Xu, M B Nilsson, P Saintigny, et al.
Human Molecular Genetics|October 26, 2014
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosisHannah M Kaneb, Andrew W Folkmann, Véronique V Belzil, et al.
Nature Genetics|July 12, 2011
Increased exonic de novo mutation rate in individuals with schizophreniaSimon L Girard, Julie Gauthier, Anne Noreau, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing identifies FUS mutations as a cause of essential tremorNancy D Merner, Simon L Girard, Hélène Catoire, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
Dehydroepiandrosterone (DHEA), DHEA sulfate, and aging: contribution of the DHEAge Study to a sociobiomedical issueE E Baulieu, G Thomas, S Legrain, et al.
Neurobiology of Aging|May 2, 2016
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorderZiv Gan-Or, Noreen Mohsin, Simon L Girard, et al.
Pageof 24