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

Ronald D Cohn

Showing results (61-70 of 100) with videos related to

Pageof 10
Sort By:
Cell Reports|November 14, 2019
Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome EditingBianca Garcia, Jooyoung Lee, Alireza Edraki, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin systemPeter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine|March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expressionEleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature|July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier geneDwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One|November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrelsEva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
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.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
Cell Reports|November 14, 2019
Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome EditingBianca Garcia, Jooyoung Lee, Alireza Edraki, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin systemPeter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine|March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expressionEleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature|July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier geneDwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One|November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrelsEva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
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.
Pageof 10