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

Neurogenetics

Showing results (721-730 of 949) with videos related to

Pageof 95
Sort By:
Neurogenetics|April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Neurogenetics|February 29, 2012
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicoresSteven E Boyden, Lane J Mahoney, Genri Kawahara, et al.
Neurogenetics|March 14, 2012
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patientsMascha C Schmied, Sonja Zehetmayer, Markus Reindl, et al.
Neurogenetics|September 16, 2008
Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disordersStormy J Chamberlain, Xue-Jun Li, Marc Lalande
Neurogenetics|August 22, 2008
The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese populationChin-Song Lu, Yah-Huei Wu-Chou, Marina van Doeselaar, et al.
Neurogenetics|July 30, 2008
Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's diseaseDana B Hancock, Eden R Martin, Jeffery M Vance, et al.
Neurogenetics|March 30, 2012
Regulation of estrogen receptor alpha gene expression in the mouse prefrontal cortex during early postnatal developmentJenne M Westberry, Melinda E Wilson
Neurogenetics|February 2, 2022
Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case seriesAnthony Cheung, Catherine Argyriou, Christine Yergeau, et al.
Neurogenetics|March 24, 2022
Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohortNasna Nassir, Isra Sati, Shaiban Al Shaibani, et al.
Neurogenetics|February 11, 2022
An intronic GNAO1 variant leading to in-frame insertion cause movement disorder controlled by deep brain stimulationSachiko Miyamoto, Mitsuko Nakashima, Shinobu Fukumura, et al.
Pageof 95

Showing results (721-730 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Neurogenetics|February 29, 2012
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicoresSteven E Boyden, Lane J Mahoney, Genri Kawahara, et al.
Neurogenetics|March 14, 2012
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patientsMascha C Schmied, Sonja Zehetmayer, Markus Reindl, et al.
Neurogenetics|September 16, 2008
Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disordersStormy J Chamberlain, Xue-Jun Li, Marc Lalande
Neurogenetics|August 22, 2008
The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese populationChin-Song Lu, Yah-Huei Wu-Chou, Marina van Doeselaar, et al.
Neurogenetics|July 30, 2008
Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's diseaseDana B Hancock, Eden R Martin, Jeffery M Vance, et al.
Neurogenetics|March 30, 2012
Regulation of estrogen receptor alpha gene expression in the mouse prefrontal cortex during early postnatal developmentJenne M Westberry, Melinda E Wilson
Neurogenetics|February 2, 2022
Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case seriesAnthony Cheung, Catherine Argyriou, Christine Yergeau, et al.
Neurogenetics|March 24, 2022
Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohortNasna Nassir, Isra Sati, Shaiban Al Shaibani, et al.
Neurogenetics|February 11, 2022
An intronic GNAO1 variant leading to in-frame insertion cause movement disorder controlled by deep brain stimulationSachiko Miyamoto, Mitsuko Nakashima, Shinobu Fukumura, et al.
Pageof 95