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

T Cho

Showing results (291-300 of 375) with videos related to

Pageof 38
Sort By:
Neurogenetics|March 23, 2016
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic featuresHallie Steinfeld, Megan T Cho, Kyle Retterer, et al.
Journal of Medical Genetics|July 9, 2016
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotoniaEsther R Berko, Megan T Cho, Christine Eng, et al.
Neurology|March 7, 2008
New VAPB deletion variant and exclusion of VAPB mutations in familial ALSJ E Landers, A L Leclerc, L Shi, et al.
Cold Spring Harbor Molecular Case Studies|November 23, 2017
De novo variants in <i>EBF3</i> are associated with hypotonia, developmental delay, intellectual disability, and autismAkemi J Tanaka, Megan T Cho, Rebecca Willaert, et al.
Psychological Medicine|August 22, 2025
Prediction of antipsychotic medication inception in antipsychotic-naive youth at clinical high risk for psychosisHesham Mukhtar, Dolores Zhou, Emily A Farina, et al.
Physical Review Letters|March 24, 2005
Observation of the effects of radially sheared electric fields on the suppression of turbulent vortex structures and the associated transverse loss in GAMMA 10T Cho, M Yoshida, J Kohagura, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
De novo truncating variants in the AHDC1 gene encoding the AT-hook DNA-binding motif-containing protein 1 are associated with intellectual disability and developmental delayHui Yang, Ganka Douglas, Kristin G Monaghan, et al.
Journal of Medical Genetics|September 4, 2017
Missense variants in the chromatin remodeler <i>CHD1</i> are associated with neurodevelopmental disabilityGenay O Pilarowski, Hilary J Vernon, Carolyn D Applegate, et al.
Journal of Medical Genetics|June 5, 2015
Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelinationNadirah Damseh, Alexandre Simonin, Chaim Jalas, et al.
Schizophrenia Bulletin|August 23, 2021
Dopamine D1R Receptor Stimulation as a Mechanistic Pro-cognitive Target for SchizophreniaAnissa Abi-Dargham, Jonathan A Javitch, Mark Slifstein, et al.
Pageof 38

Showing results (291-300 of 375) with videos related to

Sort By:
Pageof 38
Neurogenetics|March 23, 2016
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic featuresHallie Steinfeld, Megan T Cho, Kyle Retterer, et al.
Journal of Medical Genetics|July 9, 2016
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotoniaEsther R Berko, Megan T Cho, Christine Eng, et al.
Neurology|March 7, 2008
New VAPB deletion variant and exclusion of VAPB mutations in familial ALSJ E Landers, A L Leclerc, L Shi, et al.
Cold Spring Harbor Molecular Case Studies|November 23, 2017
De novo variants in <i>EBF3</i> are associated with hypotonia, developmental delay, intellectual disability, and autismAkemi J Tanaka, Megan T Cho, Rebecca Willaert, et al.
Psychological Medicine|August 22, 2025
Prediction of antipsychotic medication inception in antipsychotic-naive youth at clinical high risk for psychosisHesham Mukhtar, Dolores Zhou, Emily A Farina, et al.
Physical Review Letters|March 24, 2005
Observation of the effects of radially sheared electric fields on the suppression of turbulent vortex structures and the associated transverse loss in GAMMA 10T Cho, M Yoshida, J Kohagura, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
De novo truncating variants in the AHDC1 gene encoding the AT-hook DNA-binding motif-containing protein 1 are associated with intellectual disability and developmental delayHui Yang, Ganka Douglas, Kristin G Monaghan, et al.
Journal of Medical Genetics|September 4, 2017
Missense variants in the chromatin remodeler <i>CHD1</i> are associated with neurodevelopmental disabilityGenay O Pilarowski, Hilary J Vernon, Carolyn D Applegate, et al.
Journal of Medical Genetics|June 5, 2015
Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelinationNadirah Damseh, Alexandre Simonin, Chaim Jalas, et al.
Schizophrenia Bulletin|August 23, 2021
Dopamine D1R Receptor Stimulation as a Mechanistic Pro-cognitive Target for SchizophreniaAnissa Abi-Dargham, Jonathan A Javitch, Mark Slifstein, et al.
Pageof 38