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 Goldman

Showing results (201-210 of 488) with videos related to

Pageof 49
Sort By:
Addiction Biology|September 18, 2003
Investigation of DUSP8 and CALCA in alcohol dependenceRaquel L Hink, John E Hokanson, Imran Shah, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 6, 2009
More aroused, less fatigued: fatty acid amide hydrolase gene polymorphisms influence acute response to amphetamineAndrea M Dlugos, Ajna Hamidovic, Colin A Hodgkinson, et al.
Research Square|July 28, 2023
Early Life Stress and Body-Mass Index Modulate Brain Connectivity in Alcohol Use DisorderKhushbu Agarwal, Paule Joseph, Rui Zhang, et al.
Frontiers in Psychiatry|August 14, 2023
Preliminary evidence for changes in frontoparietal network connectivity in the early abstinence period in alcohol use disorder: a longitudinal resting-state functional magnetic resonance imaging studyJasper van Oort, Nancy Diazgranados, David T George, et al.
The Journal of Biological Chemistry|September 7, 2020
A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformationHe-Qin Zhan, Mitra Najmi, Kai Lin, et al.
The Journal of Biological Chemistry|April 25, 2009
The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1Ersin Selcuk Unal, Rongbao Zhao, Min-Hwang Chang, et al.
The Journal of Pediatrics|August 23, 2008
The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorptionSang Hee Min, Sun Young Oh, George I Karp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 31, 2008
Monoamine oxidase A genotype predicts human serotonin 1A receptor availability in vivoBrian J Mickey, Francesca Ducci, Colin A Hodgkinson, et al.
Cell|February 5, 2013
Genomes on the edge: programmed genome instability in ciliatesJohn R Bracht, Wenwen Fang, Aaron David Goldman, et al.
Archives of General Psychiatry|January 4, 2012
Interaction between FKBP5 and childhood trauma and risk of aggressive behaviorLaura Bevilacqua, Vladimir Carli, Marco Sarchiapone, et al.
Pageof 49

Showing results (201-210 of 488) with videos related to

Sort By:
Pageof 49
Addiction Biology|September 18, 2003
Investigation of DUSP8 and CALCA in alcohol dependenceRaquel L Hink, John E Hokanson, Imran Shah, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 6, 2009
More aroused, less fatigued: fatty acid amide hydrolase gene polymorphisms influence acute response to amphetamineAndrea M Dlugos, Ajna Hamidovic, Colin A Hodgkinson, et al.
Research Square|July 28, 2023
Early Life Stress and Body-Mass Index Modulate Brain Connectivity in Alcohol Use DisorderKhushbu Agarwal, Paule Joseph, Rui Zhang, et al.
Frontiers in Psychiatry|August 14, 2023
Preliminary evidence for changes in frontoparietal network connectivity in the early abstinence period in alcohol use disorder: a longitudinal resting-state functional magnetic resonance imaging studyJasper van Oort, Nancy Diazgranados, David T George, et al.
The Journal of Biological Chemistry|September 7, 2020
A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformationHe-Qin Zhan, Mitra Najmi, Kai Lin, et al.
The Journal of Biological Chemistry|April 25, 2009
The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1Ersin Selcuk Unal, Rongbao Zhao, Min-Hwang Chang, et al.
The Journal of Pediatrics|August 23, 2008
The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorptionSang Hee Min, Sun Young Oh, George I Karp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 31, 2008
Monoamine oxidase A genotype predicts human serotonin 1A receptor availability in vivoBrian J Mickey, Francesca Ducci, Colin A Hodgkinson, et al.
Cell|February 5, 2013
Genomes on the edge: programmed genome instability in ciliatesJohn R Bracht, Wenwen Fang, Aaron David Goldman, et al.
Archives of General Psychiatry|January 4, 2012
Interaction between FKBP5 and childhood trauma and risk of aggressive behaviorLaura Bevilacqua, Vladimir Carli, Marco Sarchiapone, et al.
Pageof 49