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

Sean Ennis

Showing results (41-50 of 58) with videos related to

Pageof 6
Sort By:
Molecular Autism|January 2, 2020
Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup></sup> neurons derived from ASD induced pluripotent stem cellsSahar Avazzadeh, Katya McDonagh, Jamie Reilly, et al.
European Journal of Human Genetics : EJHG|April 30, 2015
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility lociCiara Coleman, Emma M Quinn, Anthony W Ryan, et al.
Frontiers in Medicine|September 13, 2021
Rapid and Laboratory SARS-CoV-2 Antibody Testing in High-Risk Hospital Associated Cohorts of Unknown COVID-19 Exposure, a Validation and Epidemiological Study After the First Wave of the PandemicBrendan O'Kelly, Ronan McLaughlin, Roseann O'Doherty, et al.
Nature Genetics|March 25, 2014
TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural functionFernando Gómez-Herreros, Janneke H M Schuurs-Hoeijmakers, Mark McCormack, et al.
BMC Neuroscience|September 16, 2021
NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neuronsSahar Avazzadeh, Leo R Quinlan, Jamie Reilly, et al.
Journal of Medical Genetics|January 24, 2018
Catalogue of inherited disorders found among the Irish Traveller populationSally Ann Lynch, Ellen Crushell, Deborah M Lambert, et al.
Translational Psychiatry|June 24, 2020
The role of rare compound heterozygous events in autism spectrum disorderBochao Danae Lin, Fabrice Colas, Isaac J Nijman, et al.
Frontiers in Genetics|July 29, 2015
Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the worldMargaux A Morrison, Tiago R Magalhaes, Jacqueline Ramke, et al.
Cell Systems|May 3, 2016
Modern Methods for Delineating Metagenomic ComplexityEbrahim Afshinnekoo, Cem Meydan, Shanin Chowdhury, et al.
Cell Systems|May 3, 2016
Geospatial Resolution of Human and Bacterial Diversity with City-Scale MetagenomicsEbrahim Afshinnekoo, Cem Meydan, Shanin Chowdhury, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Molecular Autism|January 2, 2020
Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup></sup> neurons derived from ASD induced pluripotent stem cellsSahar Avazzadeh, Katya McDonagh, Jamie Reilly, et al.
European Journal of Human Genetics : EJHG|April 30, 2015
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility lociCiara Coleman, Emma M Quinn, Anthony W Ryan, et al.
Frontiers in Medicine|September 13, 2021
Rapid and Laboratory SARS-CoV-2 Antibody Testing in High-Risk Hospital Associated Cohorts of Unknown COVID-19 Exposure, a Validation and Epidemiological Study After the First Wave of the PandemicBrendan O'Kelly, Ronan McLaughlin, Roseann O'Doherty, et al.
Nature Genetics|March 25, 2014
TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural functionFernando Gómez-Herreros, Janneke H M Schuurs-Hoeijmakers, Mark McCormack, et al.
BMC Neuroscience|September 16, 2021
NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neuronsSahar Avazzadeh, Leo R Quinlan, Jamie Reilly, et al.
Journal of Medical Genetics|January 24, 2018
Catalogue of inherited disorders found among the Irish Traveller populationSally Ann Lynch, Ellen Crushell, Deborah M Lambert, et al.
Translational Psychiatry|June 24, 2020
The role of rare compound heterozygous events in autism spectrum disorderBochao Danae Lin, Fabrice Colas, Isaac J Nijman, et al.
Frontiers in Genetics|July 29, 2015
Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the worldMargaux A Morrison, Tiago R Magalhaes, Jacqueline Ramke, et al.
Cell Systems|May 3, 2016
Modern Methods for Delineating Metagenomic ComplexityEbrahim Afshinnekoo, Cem Meydan, Shanin Chowdhury, et al.
Cell Systems|May 3, 2016
Geospatial Resolution of Human and Bacterial Diversity with City-Scale MetagenomicsEbrahim Afshinnekoo, Cem Meydan, Shanin Chowdhury, et al.
Pageof 6