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

D Cohn

Showing results (341-350 of 379) with videos related to

Pageof 38
Sort By:
Nature Medicine|January 24, 2007
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic statesRonald D Cohn, Christel van Erp, Jennifer P Habashi, et al.
Nature Medicine|July 18, 2017
Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanismDwi U Kemaladewi, Eleonora Maino, Elzbieta Hyatt, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 9, 2009
Helicobacter pylori promotes hepatic fibrosis in the animal modelMoon-Jung Goo, Mi-Ran Ki, Hye-Rim Lee, et al.
Science (New York, N.Y.)|April 16, 2011
Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome miceTammy M Holm, Jennifer P Habashi, Jefferson J Doyle, et al.
European Journal of Human Genetics : EJHG|November 22, 2017
Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarrayRobin Z Hayeems, Jasmin Bhawra, Kate Tsiplova, et al.
American Journal of Human Genetics|May 4, 2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian DiseaseHernan D Gonorazky, Sergey Naumenko, Arun K Ramani, et al.
American Journal of Human Genetics|March 5, 2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian DiseaseHernan D Gonorazky, Sergey Naumenko, Arun K Ramani, et al.
Neuron|June 12, 2003
Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilizationFumiaki Saito, Steven A Moore, Rita Barresi, et al.
Pageof 38

Showing results (341-350 of 379) with videos related to

Sort By:
Pageof 38
Nature Medicine|January 24, 2007
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic statesRonald D Cohn, Christel van Erp, Jennifer P Habashi, et al.
Nature Medicine|July 18, 2017
Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanismDwi U Kemaladewi, Eleonora Maino, Elzbieta Hyatt, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 9, 2009
Helicobacter pylori promotes hepatic fibrosis in the animal modelMoon-Jung Goo, Mi-Ran Ki, Hye-Rim Lee, et al.
Science (New York, N.Y.)|April 16, 2011
Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome miceTammy M Holm, Jennifer P Habashi, Jefferson J Doyle, et al.
European Journal of Human Genetics : EJHG|November 22, 2017
Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarrayRobin Z Hayeems, Jasmin Bhawra, Kate Tsiplova, et al.
American Journal of Human Genetics|May 4, 2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian DiseaseHernan D Gonorazky, Sergey Naumenko, Arun K Ramani, et al.
American Journal of Human Genetics|March 5, 2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian DiseaseHernan D Gonorazky, Sergey Naumenko, Arun K Ramani, et al.
Neuron|June 12, 2003
Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilizationFumiaki Saito, Steven A Moore, Rita Barresi, et al.
Pageof 38