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Steven A Moore

Showing results (41-50 of 141) with videos related to

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Brain Research. Molecular Brain Research|April 20, 2004
Human angiotensin II type-2 receptor inhibition of insulin-mediated ERK-2 activity via a G-protein coupled signaling pathwaySteven A Moore, Nancy Huang, Olivia Hinthong, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 21, 2008
Cardiac damage after lesions of the nucleus tractus solitariiAmeya Nayate, Steven A Moore, Robert Weiss, et al.
Pediatric Neurology|May 24, 2024
Expedited Exome Reanalysis Following Deep Phenotyping and Muscle Biopsy in Suspected Mitochondrial DisorderElizabeth Pickup, Steven A Moore, Pim Suwannarat, et al.
Human Molecular Genetics|February 7, 2008
A common disease-associated missense mutation in alpha-sarcoglycan fails to cause muscular dystrophy in miceKazuhiro Kobuke, Federica Piccolo, Keith W Garringer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2008
Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblastJakob S Satz, Rita Barresi, Madeleine Durbeej, et al.
Redox Biology|September 12, 2013
Differential activation of catalase expression and activity by PPAR agonists: implications for astrocyte protection in anti-glioma therapyNicholas K H Khoo, Sachin Hebbar, Weiling Zhao, et al.
Human Molecular Genetics|September 27, 2021
Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophySarah J Smith, Lacramioara Fabian, Adeel Sheikh, et al.
Muscle & Nerve|February 4, 2014
Late adult-onset of X-linked myopathy with excessive autophagyCameron D Crockett, Alessandra Ruggieri, Meena Gujrati, et al.
Case Reports in Neurology|July 27, 2023
Thirty-Year Follow-Up of Early Onset Amyotrophic Lateral Sclerosis with a Pathogenic Variant in SPTLC1Aparna Ajjarapu, Shawna M E Feely, Michael E Shy, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Regenerative Index reveals declining muscle regeneration in paediatric patients with Duchenne muscular dystrophyJohnathan K Smid, Charis A McPherson, Jacob G Monast, et al.
Pageof 15

Showing results (41-50 of 141) with videos related to

Sort By:
Pageof 15
Brain Research. Molecular Brain Research|April 20, 2004
Human angiotensin II type-2 receptor inhibition of insulin-mediated ERK-2 activity via a G-protein coupled signaling pathwaySteven A Moore, Nancy Huang, Olivia Hinthong, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 21, 2008
Cardiac damage after lesions of the nucleus tractus solitariiAmeya Nayate, Steven A Moore, Robert Weiss, et al.
Pediatric Neurology|May 24, 2024
Expedited Exome Reanalysis Following Deep Phenotyping and Muscle Biopsy in Suspected Mitochondrial DisorderElizabeth Pickup, Steven A Moore, Pim Suwannarat, et al.
Human Molecular Genetics|February 7, 2008
A common disease-associated missense mutation in alpha-sarcoglycan fails to cause muscular dystrophy in miceKazuhiro Kobuke, Federica Piccolo, Keith W Garringer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2008
Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblastJakob S Satz, Rita Barresi, Madeleine Durbeej, et al.
Redox Biology|September 12, 2013
Differential activation of catalase expression and activity by PPAR agonists: implications for astrocyte protection in anti-glioma therapyNicholas K H Khoo, Sachin Hebbar, Weiling Zhao, et al.
Human Molecular Genetics|September 27, 2021
Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophySarah J Smith, Lacramioara Fabian, Adeel Sheikh, et al.
Muscle & Nerve|February 4, 2014
Late adult-onset of X-linked myopathy with excessive autophagyCameron D Crockett, Alessandra Ruggieri, Meena Gujrati, et al.
Case Reports in Neurology|July 27, 2023
Thirty-Year Follow-Up of Early Onset Amyotrophic Lateral Sclerosis with a Pathogenic Variant in SPTLC1Aparna Ajjarapu, Shawna M E Feely, Michael E Shy, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Regenerative Index reveals declining muscle regeneration in paediatric patients with Duchenne muscular dystrophyJohnathan K Smid, Charis A McPherson, Jacob G Monast, et al.
Pageof 15