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

C Tai

Showing results (561-570 of 579) with videos related to

Pageof 58
Sort By:
Nature Genetics|October 25, 2022
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pDaniel J Weiner, Emi Ling, Serkan Erdin, et al.
Biological Psychiatry|December 29, 2022
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived NeuronsEuan Parnell, Lorenza Culotta, Marc P Forrest, et al.
American Journal of Human Genetics|October 25, 2022
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal modelsKiana Mohajeri, Rachita Yadav, Eva D'haene, et al.
Nature Communications|November 25, 2017
Whole blood stabilization for the microfluidic isolation and molecular characterization of circulating tumor cellsKeith H K Wong, Shannon N Tessier, David T Miyamoto, et al.
American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Diseases (Basel, Switzerland)|April 24, 2023
Association between Multiple Myeloma and Ulcerative Colitis: A Cross-Sectional AnalysisAyrton Bangolo, Sowmya Sagireddy, Paul Desrochers, et al.
American Journal of Human Genetics|March 8, 2024
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
Analytical Chemistry|April 5, 2017
Development of an Improved Standard Reference Material for Vitamin D Metabolites in Human SerumKaren W Phinney, Susan S-C Tai, Mary Bedner, et al.
Genome Medicine|May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart diseaseAlexander Hsieh, Sarah U Morton, Jon A L Willcox, et al.
American Journal of Human Genetics|September 24, 2022
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
Pageof 58

Showing results (561-570 of 579) with videos related to

Sort By:
Pageof 58
Nature Genetics|October 25, 2022
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pDaniel J Weiner, Emi Ling, Serkan Erdin, et al.
Biological Psychiatry|December 29, 2022
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived NeuronsEuan Parnell, Lorenza Culotta, Marc P Forrest, et al.
American Journal of Human Genetics|October 25, 2022
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal modelsKiana Mohajeri, Rachita Yadav, Eva D'haene, et al.
Nature Communications|November 25, 2017
Whole blood stabilization for the microfluidic isolation and molecular characterization of circulating tumor cellsKeith H K Wong, Shannon N Tessier, David T Miyamoto, et al.
American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Diseases (Basel, Switzerland)|April 24, 2023
Association between Multiple Myeloma and Ulcerative Colitis: A Cross-Sectional AnalysisAyrton Bangolo, Sowmya Sagireddy, Paul Desrochers, et al.
American Journal of Human Genetics|March 8, 2024
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
Analytical Chemistry|April 5, 2017
Development of an Improved Standard Reference Material for Vitamin D Metabolites in Human SerumKaren W Phinney, Susan S-C Tai, Mary Bedner, et al.
Genome Medicine|May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart diseaseAlexander Hsieh, Sarah U Morton, Jon A L Willcox, et al.
American Journal of Human Genetics|September 24, 2022
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
Pageof 58