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Ronald D Cohn

Showing results (51-60 of 100) with videos related to

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ACS Applied Materials & Interfaces|December 7, 2021
Self-Assembled Oligo-Urethane Nanoparticles: Their Characterization and Use for the Delivery of Active Biomolecules into Mammalian CellsSuja Shrestha, Meghan J McFadden, Allen C T Teng, et al.
Nature|July 26, 2002
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophySteven A Moore, Fumiaki Saito, Jianguo Chen, et al.
Disease Models & Mechanisms|September 29, 2020
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic <i>Dmd</i> deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, et al.
Journal of Genetic Counseling|October 21, 2021
Genome sequencing among children with medical complexity: What constitutes value from parents' perspective?Whiwon Lee, Stephanie Luca, Gregory Costain, et al.
Disease Models & Mechanisms|April 4, 2025
Correction: A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai, Ying Wong, Abdalla Ahmed, et al.
NPJ Genomic Medicine|December 22, 2017
Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort studyIris Cohn, Tara A Paton, Christian R Marshall, et al.
Nature Medicine|June 9, 2004
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophiesRita Barresi, Daniel E Michele, Motoi Kanagawa, et al.
Cell|September 17, 2002
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regenerationRonald D Cohn, Michael D Henry, Daniel E Michele, et al.
Nature|July 26, 2002
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesDaniel E Michele, Rita Barresi, Motoi Kanagawa, et al.
Disease Models & Mechanisms|June 17, 2024
An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndromeEleonora Maino, Ori Scott, Samar Z Rizvi, et al.
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
ACS Applied Materials & Interfaces|December 7, 2021
Self-Assembled Oligo-Urethane Nanoparticles: Their Characterization and Use for the Delivery of Active Biomolecules into Mammalian CellsSuja Shrestha, Meghan J McFadden, Allen C T Teng, et al.
Nature|July 26, 2002
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophySteven A Moore, Fumiaki Saito, Jianguo Chen, et al.
Disease Models & Mechanisms|September 29, 2020
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic <i>Dmd</i> deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, et al.
Journal of Genetic Counseling|October 21, 2021
Genome sequencing among children with medical complexity: What constitutes value from parents' perspective?Whiwon Lee, Stephanie Luca, Gregory Costain, et al.
Disease Models & Mechanisms|April 4, 2025
Correction: A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathyTatianna Wai, Ying Wong, Abdalla Ahmed, et al.
NPJ Genomic Medicine|December 22, 2017
Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort studyIris Cohn, Tara A Paton, Christian R Marshall, et al.
Nature Medicine|June 9, 2004
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophiesRita Barresi, Daniel E Michele, Motoi Kanagawa, et al.
Cell|September 17, 2002
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regenerationRonald D Cohn, Michael D Henry, Daniel E Michele, et al.
Nature|July 26, 2002
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesDaniel E Michele, Rita Barresi, Motoi Kanagawa, et al.
Disease Models & Mechanisms|June 17, 2024
An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndromeEleonora Maino, Ori Scott, Samar Z Rizvi, et al.
Pageof 10