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

M Bard

Showing results (281-290 of 289) with videos related to

Pageof 29
Sort By:
You have reached the last page of results.This site can display upto 289 results.
Molecular Cell|November 25, 2025
Transcriptome-wide mRNP condensation precedes stress granule formation and excludes new mRNAsHendrik Glauninger, Jared A M Bard, Caitlin J Wong Hickernell, et al.
Pilot and Feasibility Studies|December 4, 2018
Correction to: The help for people with money, employment or housing problems (HOPE) intervention: pilot randomised trial with mixed methods feasibility researchM C Barnes, A M Haase, L J Scott, et al.
Pilot and Feasibility Studies|November 22, 2018
The help for people with money, employment or housing problems (HOPE) intervention: pilot randomised trial with mixed methods feasibility researchM C Barnes, A M Haase, L J Scott, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
AAV-mediated interneuron-specific gene replacement for Dravet syndromeJohn K Mich, Jiyun Ryu, Aguan D Wei, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome SequencingAngela M Bard, Lindsay V Clark, Erdal Cosgun, et al.
American Journal of Medical Genetics. Part A|June 19, 2024
Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencingAngela M Bard, Lindsay V Clark, Erdal Cosgun, et al.
Science Translational Medicine|March 19, 2025
Interneuron-specific dual-AAV <i>SCN1A</i> gene replacement corrects epileptic phenotypes in mouse models of Dravet syndromeJohn K Mich, Jiyun Ryu, Aguan D Wei, et al.
Cell|August 10, 2000
Functional discovery via a compendium of expression profilesT R Hughes, M J Marton, A R Jones, et al.
Journal of Neurophysiology|May 18, 2022
Human <i>KCNQ5</i> de novo mutations underlie epilepsy and intellectual disabilityAguan D Wei, Paul Wakenight, Theresa A Zwingman, et al.
Pageof 29

Showing results (281-290 of 289) with videos related to

Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 289 results.
Molecular Cell|November 25, 2025
Transcriptome-wide mRNP condensation precedes stress granule formation and excludes new mRNAsHendrik Glauninger, Jared A M Bard, Caitlin J Wong Hickernell, et al.
Pilot and Feasibility Studies|December 4, 2018
Correction to: The help for people with money, employment or housing problems (HOPE) intervention: pilot randomised trial with mixed methods feasibility researchM C Barnes, A M Haase, L J Scott, et al.
Pilot and Feasibility Studies|November 22, 2018
The help for people with money, employment or housing problems (HOPE) intervention: pilot randomised trial with mixed methods feasibility researchM C Barnes, A M Haase, L J Scott, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
AAV-mediated interneuron-specific gene replacement for Dravet syndromeJohn K Mich, Jiyun Ryu, Aguan D Wei, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome SequencingAngela M Bard, Lindsay V Clark, Erdal Cosgun, et al.
American Journal of Medical Genetics. Part A|June 19, 2024
Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencingAngela M Bard, Lindsay V Clark, Erdal Cosgun, et al.
Science Translational Medicine|March 19, 2025
Interneuron-specific dual-AAV <i>SCN1A</i> gene replacement corrects epileptic phenotypes in mouse models of Dravet syndromeJohn K Mich, Jiyun Ryu, Aguan D Wei, et al.
Cell|August 10, 2000
Functional discovery via a compendium of expression profilesT R Hughes, M J Marton, A R Jones, et al.
Journal of Neurophysiology|May 18, 2022
Human <i>KCNQ5</i> de novo mutations underlie epilepsy and intellectual disabilityAguan D Wei, Paul Wakenight, Theresa A Zwingman, et al.
Pageof 29