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

B Goldstein

Showing results (1291-1300 of 1,434) with videos related to

Pageof 144
Sort By:
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.
American Journal of Community Psychology|September 13, 2006
Depressive symptomatology among HIV-positive women in the era of HAART: a stress and coping modelRobert H Remien, Theresa Exner, Robert M Kertzner, 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.
Cell Reports|October 28, 2020
Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood EpilepsyAmy N Shore, Sophie Colombo, William F Tobin, et al.
Oncotarget|November 21, 2017
Outcomes of phase I clinical trials for patients with advanced pancreatic cancer: update of the MD Anderson Cancer Center experienceJennifer B Goldstein, Chad Tang, Kenneth R Hess, et al.
Nature Genetics|June 2, 2009
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillinAnn K Daly, Peter T Donaldson, Pallav Bhatnagar, et al.
The Journal of Investigative Dermatology|June 7, 2024
SASH1 S519N Variant Links Skin Hyperpigmentation and Premature Hair Graying to Dysfunction of Melanocyte LineageKaroline A Lambert, Christopher M Clements, Nabanita Mukherjee, et al.
American Journal of Human Genetics|November 27, 2012
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.
Journal of Alzheimer'S Disease : JAD|November 8, 2018
Distinct White Matter Changes Associated with Cerebrospinal Fluid Amyloid-β1-42 and HypertensionOmar M Al-Janabi, Christopher A Brown, Ahmed A Bahrani, et al.
Pageof 144

Showing results (1291-1300 of 1,434) with videos related to

Sort By:
Pageof 144
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.
American Journal of Community Psychology|September 13, 2006
Depressive symptomatology among HIV-positive women in the era of HAART: a stress and coping modelRobert H Remien, Theresa Exner, Robert M Kertzner, 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.
Cell Reports|October 28, 2020
Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood EpilepsyAmy N Shore, Sophie Colombo, William F Tobin, et al.
Oncotarget|November 21, 2017
Outcomes of phase I clinical trials for patients with advanced pancreatic cancer: update of the MD Anderson Cancer Center experienceJennifer B Goldstein, Chad Tang, Kenneth R Hess, et al.
Nature Genetics|June 2, 2009
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillinAnn K Daly, Peter T Donaldson, Pallav Bhatnagar, et al.
The Journal of Investigative Dermatology|June 7, 2024
SASH1 S519N Variant Links Skin Hyperpigmentation and Premature Hair Graying to Dysfunction of Melanocyte LineageKaroline A Lambert, Christopher M Clements, Nabanita Mukherjee, et al.
American Journal of Human Genetics|November 27, 2012
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.
Journal of Alzheimer'S Disease : JAD|November 8, 2018
Distinct White Matter Changes Associated with Cerebrospinal Fluid Amyloid-β1-42 and HypertensionOmar M Al-Janabi, Christopher A Brown, Ahmed A Bahrani, et al.
Pageof 144