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

David B Goldstein

Showing results (221-230 of 338) with videos related to

Pageof 34
Sort By:
Plos Computational Biology|October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arraysSahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Nature|February 23, 2010
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis CJacques Fellay, Alexander J Thompson, Dongliang Ge, et al.
Annals of Neurology|May 21, 2013
Mutations in TNK2 in severe autosomal recessive infantile onset epilepsyYuki Hitomi, Erin L Heinzen, Simona Donatello, et al.
Epilepsia|March 26, 2018
A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsyTalia A Atkin, Chani M Maher, Aaron C Gerlach, et al.
Annals of Neurology|March 3, 2004
A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's diseaseDaniel G Healy, Patrick M Abou-Sleiman, Tetsutaro Ozawa, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 22, 2008
Failure to replicate effect of Kibra on human memory in two large cohorts of European originAnna C Need, Deborah K Attix, Jill M McEvoy, et al.
Annals of Neurology|March 5, 2014
KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidineCarol J Milligan, Melody Li, Elena V Gazina, et al.
Plos Genetics|June 26, 2010
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease geneNara L M Sobreira, Elizabeth T Cirulli, Dimitrios Avramopoulos, et al.
Human Molecular Genetics|September 8, 2009
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABAnna C Need, Deborah K Attix, Jill M McEvoy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.
Pageof 34

Showing results (221-230 of 338) with videos related to

Sort By:
Pageof 34
Plos Computational Biology|October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arraysSahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Nature|February 23, 2010
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis CJacques Fellay, Alexander J Thompson, Dongliang Ge, et al.
Annals of Neurology|May 21, 2013
Mutations in TNK2 in severe autosomal recessive infantile onset epilepsyYuki Hitomi, Erin L Heinzen, Simona Donatello, et al.
Epilepsia|March 26, 2018
A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsyTalia A Atkin, Chani M Maher, Aaron C Gerlach, et al.
Annals of Neurology|March 3, 2004
A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's diseaseDaniel G Healy, Patrick M Abou-Sleiman, Tetsutaro Ozawa, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 22, 2008
Failure to replicate effect of Kibra on human memory in two large cohorts of European originAnna C Need, Deborah K Attix, Jill M McEvoy, et al.
Annals of Neurology|March 5, 2014
KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidineCarol J Milligan, Melody Li, Elena V Gazina, et al.
Plos Genetics|June 26, 2010
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease geneNara L M Sobreira, Elizabeth T Cirulli, Dimitrios Avramopoulos, et al.
Human Molecular Genetics|September 8, 2009
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABAnna C Need, Deborah K Attix, Jill M McEvoy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.
Pageof 34