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Steven A Moore

Showing results (51-60 of 141) with videos related to

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Skeletal Muscle|July 2, 2026
Regenerative Index: a method to assess muscle regeneration in patients with Duchenne muscular dystrophyJohnathan K Smid, Charis A McPherson, Jacob G Monast, et al.
Science Advances|April 18, 2025
A genetic variant in <i>SMAD7</i> acts as a modifier of <i>LMNA</i>-associated muscular dystrophy, implicating SMAD signaling as a therapeutic targetNathaniel P Mohar, Christopher J Langland, Zachary Darr, et al.
Muscle & Nerve|September 8, 2017
Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21Jennifer M Martinez-Thompson, Zhiyv Niu, Jennifer A Tracy, et al.
Journal of Human Genetics|December 25, 2014
Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27Takeshi Tsuda, Kristi Fitzgerald, Mena Scavena, et al.
Human Molecular Genetics|December 22, 2011
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscleGeorge Dialynas, Kaitlin M Flannery, Luka N Zirbel, et al.
International Journal of Molecular Sciences|May 11, 2024
The Influence of a Genetic Variant in <i>CCDC78</i> on <i>LMNA</i>-Associated Skeletal Muscle DiseaseNathaniel P Mohar, Efrem M Cox, Emily Adelizzi, et al.
Brain Research. Molecular Brain Research|January 18, 2003
Effects of mutations in the highly conserved DRY motif on binding affinity, expression, and G-protein recruitment of the human angiotensin II type-2 receptorSteven A Moore, Anjali S Patel, Nancy Huang, et al.
JACC. Case Reports|February 20, 2026
Dilated Cardiomyopathy and Later Onset Limb-Girdle Muscular Dystrophy Associated With Fukutin and LaminA/C MutationsAlejandra Cardona Perez, Renee Moenning, Cynthia Bodkin, et al.
Nature|October 18, 2013
LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophyMatthew M Goddeeris, Biming Wu, David Venzke, et al.
Acta Neuropathologica Communications|November 21, 2013
Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteinsHuy Nguyen, Adam P Ostendorf, Jakob S Satz, et al.
Pageof 15

Showing results (51-60 of 141) with videos related to

Sort By:
Pageof 15
Skeletal Muscle|July 2, 2026
Regenerative Index: a method to assess muscle regeneration in patients with Duchenne muscular dystrophyJohnathan K Smid, Charis A McPherson, Jacob G Monast, et al.
Science Advances|April 18, 2025
A genetic variant in <i>SMAD7</i> acts as a modifier of <i>LMNA</i>-associated muscular dystrophy, implicating SMAD signaling as a therapeutic targetNathaniel P Mohar, Christopher J Langland, Zachary Darr, et al.
Muscle & Nerve|September 8, 2017
Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21Jennifer M Martinez-Thompson, Zhiyv Niu, Jennifer A Tracy, et al.
Journal of Human Genetics|December 25, 2014
Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27Takeshi Tsuda, Kristi Fitzgerald, Mena Scavena, et al.
Human Molecular Genetics|December 22, 2011
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscleGeorge Dialynas, Kaitlin M Flannery, Luka N Zirbel, et al.
International Journal of Molecular Sciences|May 11, 2024
The Influence of a Genetic Variant in <i>CCDC78</i> on <i>LMNA</i>-Associated Skeletal Muscle DiseaseNathaniel P Mohar, Efrem M Cox, Emily Adelizzi, et al.
Brain Research. Molecular Brain Research|January 18, 2003
Effects of mutations in the highly conserved DRY motif on binding affinity, expression, and G-protein recruitment of the human angiotensin II type-2 receptorSteven A Moore, Anjali S Patel, Nancy Huang, et al.
JACC. Case Reports|February 20, 2026
Dilated Cardiomyopathy and Later Onset Limb-Girdle Muscular Dystrophy Associated With Fukutin and LaminA/C MutationsAlejandra Cardona Perez, Renee Moenning, Cynthia Bodkin, et al.
Nature|October 18, 2013
LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophyMatthew M Goddeeris, Biming Wu, David Venzke, et al.
Acta Neuropathologica Communications|November 21, 2013
Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteinsHuy Nguyen, Adam P Ostendorf, Jakob S Satz, et al.
Pageof 15