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Stephanie J Valberg

Showing results (71-80 of 89) with videos related to

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Journal of Veterinary Internal Medicine|December 26, 2006
Idiopathic hemorrhagic pericardial effusion in cowsAnna M Firshman, Abby M Sage, Stephanie J Valberg, et al.
Equine Veterinary Journal|September 8, 2020
Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosisStephanie J Valberg, Carrie J Finno, Marisa L Henry, et al.
Plos One|January 29, 2026
Aberrant skeletal muscle morphogenesis and myofiber differentiation characterize equine myotonic dystrophyStephanie J Valberg, Zoë J Williams, Elizabeth G Ames, et al.
Equine Veterinary Journal|September 14, 2022
Type 2 polysaccharide storage myopathy in Quarter Horses is a novel glycogen storage disease causing exertional rhabdomyolysisStephanie J Valberg, Zoë J Williams, Carrie J Finno, et al.
The Journal of Heredity|November 12, 2013
Evidence of positive selection for a glycogen synthase (GYS1) mutation in domestic horse populationsAnnette M McCoy, Robert Schaefer, Jessica L Petersen, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|July 3, 2026
Thoroughbred horses susceptible to Recurrent Exertional Rhabdomyolysis have elevated skeletal muscle mitochondrial capacitiesLauren T Wesolowski, Jessica L Artman, Pier L Semanchik, et al.
Journal of Veterinary Internal Medicine|February 6, 2019
Coding sequences of sarcoplasmic reticulum calcium ATPase regulatory peptides and expression of calcium regulatory genes in recurrent exertional rhabdomyolysisStephanie J Valberg, Kaitlin Soave, Zoë J Williams, et al.
Free Radical Biology & Medicine|November 5, 2016
Transcriptome profiling of equine vitamin E deficient neuroaxonal dystrophy identifies upregulation of liver X receptor target genesCarrie J Finno, Matthew H Bordbari, Stephanie J Valberg, et al.
Skeletal Muscle|March 8, 2018
A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter HorsesCarrie J Finno, Giuliana Gianino, Sudeep Perumbakkam, et al.
Journal of Veterinary Internal Medicine|October 30, 2019
Impact of alpha-tocopherol deficiency and supplementation on sacrocaudalis and gluteal muscle fiber histopathology and morphology in horsesLauren Bookbinder, Carrie J Finno, Anna M Firshman, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Journal of Veterinary Internal Medicine|December 26, 2006
Idiopathic hemorrhagic pericardial effusion in cowsAnna M Firshman, Abby M Sage, Stephanie J Valberg, et al.
Equine Veterinary Journal|September 8, 2020
Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosisStephanie J Valberg, Carrie J Finno, Marisa L Henry, et al.
Plos One|January 29, 2026
Aberrant skeletal muscle morphogenesis and myofiber differentiation characterize equine myotonic dystrophyStephanie J Valberg, Zoë J Williams, Elizabeth G Ames, et al.
Equine Veterinary Journal|September 14, 2022
Type 2 polysaccharide storage myopathy in Quarter Horses is a novel glycogen storage disease causing exertional rhabdomyolysisStephanie J Valberg, Zoë J Williams, Carrie J Finno, et al.
The Journal of Heredity|November 12, 2013
Evidence of positive selection for a glycogen synthase (GYS1) mutation in domestic horse populationsAnnette M McCoy, Robert Schaefer, Jessica L Petersen, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|July 3, 2026
Thoroughbred horses susceptible to Recurrent Exertional Rhabdomyolysis have elevated skeletal muscle mitochondrial capacitiesLauren T Wesolowski, Jessica L Artman, Pier L Semanchik, et al.
Journal of Veterinary Internal Medicine|February 6, 2019
Coding sequences of sarcoplasmic reticulum calcium ATPase regulatory peptides and expression of calcium regulatory genes in recurrent exertional rhabdomyolysisStephanie J Valberg, Kaitlin Soave, Zoë J Williams, et al.
Free Radical Biology & Medicine|November 5, 2016
Transcriptome profiling of equine vitamin E deficient neuroaxonal dystrophy identifies upregulation of liver X receptor target genesCarrie J Finno, Matthew H Bordbari, Stephanie J Valberg, et al.
Skeletal Muscle|March 8, 2018
A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter HorsesCarrie J Finno, Giuliana Gianino, Sudeep Perumbakkam, et al.
Journal of Veterinary Internal Medicine|October 30, 2019
Impact of alpha-tocopherol deficiency and supplementation on sacrocaudalis and gluteal muscle fiber histopathology and morphology in horsesLauren Bookbinder, Carrie J Finno, Anna M Firshman, et al.
Pageof 9