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

Steven A Moore

Showing results (81-90 of 141) with videos related to

Pageof 15
Sort By:
Human Molecular Genetics|September 22, 2018
Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signalingSahaana Chandran, Jennifer A Suggs, Bingyan J Wang, et al.
Neuromuscular Disorders : NMD|February 5, 2014
A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutationsStephanie E Wallace, Jessie H Conta, Thomas L Winder, et al.
Molecular Genetics and Metabolism|July 17, 2013
Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophyAmy C Yang, Bobby G Ng, Steven A Moore, et al.
Case Reports in Genetics|April 17, 2015
Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP MutationNivedita U Jerath, Cameron D Crockett, Steven A Moore, et al.
American Journal of Physiology. Heart and Circulatory Physiology|June 20, 2006
20-Hydroxyeicosatetraenoic acid is a potent dilator of mouse basilar artery: role of cyclooxygenaseXiang Fang, Frank M Faraci, Terry L Kaduce, et al.
Journal of Neuropathology and Experimental Neurology|November 14, 2012
Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortexTimothy D Myshrall, Steven A Moore, Adam P Ostendorf, et al.
Journal of Neuropathology and Experimental Neurology|August 23, 2020
Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)Himali Jayakody, Sanam Zarei, Huy Nguyen, et al.
Journal of Neuropathology and Experimental Neurology|January 30, 2016
Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species ComparisonsMichael W Lawlor, Alan H Beggs, Ana Buj-Bello, et al.
Human Mutation|August 28, 2015
GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype CorrelationBraden S Jensen, Tobias Willer, Dimah N Saade, et al.
Journal of Child Neurology|June 9, 2018
Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and ArthrogryposisAlexander Conant, Julian Curiel, Amy Pizzino, et al.
Pageof 15

Showing results (81-90 of 141) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|September 22, 2018
Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signalingSahaana Chandran, Jennifer A Suggs, Bingyan J Wang, et al.
Neuromuscular Disorders : NMD|February 5, 2014
A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutationsStephanie E Wallace, Jessie H Conta, Thomas L Winder, et al.
Molecular Genetics and Metabolism|July 17, 2013
Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophyAmy C Yang, Bobby G Ng, Steven A Moore, et al.
Case Reports in Genetics|April 17, 2015
Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP MutationNivedita U Jerath, Cameron D Crockett, Steven A Moore, et al.
American Journal of Physiology. Heart and Circulatory Physiology|June 20, 2006
20-Hydroxyeicosatetraenoic acid is a potent dilator of mouse basilar artery: role of cyclooxygenaseXiang Fang, Frank M Faraci, Terry L Kaduce, et al.
Journal of Neuropathology and Experimental Neurology|November 14, 2012
Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortexTimothy D Myshrall, Steven A Moore, Adam P Ostendorf, et al.
Journal of Neuropathology and Experimental Neurology|August 23, 2020
Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)Himali Jayakody, Sanam Zarei, Huy Nguyen, et al.
Journal of Neuropathology and Experimental Neurology|January 30, 2016
Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species ComparisonsMichael W Lawlor, Alan H Beggs, Ana Buj-Bello, et al.
Human Mutation|August 28, 2015
GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype CorrelationBraden S Jensen, Tobias Willer, Dimah N Saade, et al.
Journal of Child Neurology|June 9, 2018
Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and ArthrogryposisAlexander Conant, Julian Curiel, Amy Pizzino, et al.
Pageof 15