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Muscle & Nerve
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September 7, 2017
Genetic modifiers of Duchenne and facioscapulohumeral muscular dystrophies
Rylie M Hightower, Matthew S Alexander
Muscle & Nerve
|
March 2, 2021
hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies
Matthew S Alexander, Rylie M Hightower, Andrea L Reid, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 20, 2019
The SINE Compound KPT-350 Blocks Dystrophic Pathologies in DMD Zebrafish and Mice
Rylie M Hightower, Andrea L Reid, Devin E Gibbs, et al.
Human Molecular Genetics
|
August 9, 2020
DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies
Andrea L Reid, Yimin Wang, Adrienne Samani, et al.
Human Molecular Genetics
|
July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy
Madhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
JCI Insight
|
September 21, 2018
A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies
Peter R Serafini, Michael J Feyder, Rylie M Hightower, et al.
Life Science Alliance
|
May 5, 2022
miR-486 is essential for muscle function and suppresses a dystrophic transcriptome
Adrienne Samani, Rylie M Hightower, Andrea L Reid, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Muscle & Nerve
|
September 7, 2017
Genetic modifiers of Duchenne and facioscapulohumeral muscular dystrophies
Rylie M Hightower, Matthew S Alexander
Muscle & Nerve
|
March 2, 2021
hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies
Matthew S Alexander, Rylie M Hightower, Andrea L Reid, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 20, 2019
The SINE Compound KPT-350 Blocks Dystrophic Pathologies in DMD Zebrafish and Mice
Rylie M Hightower, Andrea L Reid, Devin E Gibbs, et al.
Human Molecular Genetics
|
August 9, 2020
DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies
Andrea L Reid, Yimin Wang, Adrienne Samani, et al.
Human Molecular Genetics
|
July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy
Madhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
JCI Insight
|
September 21, 2018
A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies
Peter R Serafini, Michael J Feyder, Rylie M Hightower, et al.
Life Science Alliance
|
May 5, 2022
miR-486 is essential for muscle function and suppresses a dystrophic transcriptome
Adrienne Samani, Rylie M Hightower, Andrea L Reid, et al.
Page
of 1