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

Clemer Abad

Showing results (11-20 of 27) with videos related to

Pageof 3
Sort By:
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Biology|May 26, 2018
A Rare De Novo <i>RAI1</i> Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome PresentationClemer Abad, Melissa M Cook, Lei Cao, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Molecular Autism|June 7, 2020
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neuronsCatarina M Seabra, Tatsiana Aneichyk, Serkan Erdin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2019
Dysfunction of <i>GRAP</i>, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing lossChong Li, Guney Bademci, Asli Subasioglu, et al.
Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
JCI Insight|February 1, 2024
ADAMTSL2 mutations determine the phenotypic severity in geleophysic dysplasiaVladimir Camarena, Monique M Williams, Alejo A Morales, et al.
Human Genetics|November 22, 2014
Characterization of ANKRD11 mutations in humans and mice related to KBG syndromeKatherina Walz, Devon Cohen, Paul M Neilsen, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Biology|May 26, 2018
A Rare De Novo <i>RAI1</i> Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome PresentationClemer Abad, Melissa M Cook, Lei Cao, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Molecular Autism|June 7, 2020
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neuronsCatarina M Seabra, Tatsiana Aneichyk, Serkan Erdin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2019
Dysfunction of <i>GRAP</i>, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing lossChong Li, Guney Bademci, Asli Subasioglu, et al.
Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
JCI Insight|February 1, 2024
ADAMTSL2 mutations determine the phenotypic severity in geleophysic dysplasiaVladimir Camarena, Monique M Williams, Alejo A Morales, et al.
Human Genetics|November 22, 2014
Characterization of ANKRD11 mutations in humans and mice related to KBG syndromeKatherina Walz, Devon Cohen, Paul M Neilsen, et al.
Pageof 3