Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kenneth L. Bible"'
Autor:
Min J. Kim, Kenneth L. Bible, Michael Regnier, Marvin E. Adams, Stanley C. Froehner, Nicholas P. Whitehead
Publikováno v:
Physiological Reports, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Duchenne muscular dystrophy (DMD), caused by absence of the protein dystrophin, is a common, degenerative muscle disease affecting 1:5000 males worldwide. With recent advances in respiratory care, cardiac dysfunction now accounts for 50% of
Externí odkaz:
https://doaj.org/article/b8d2d59258424c0ba76b891fe24df002
Publikováno v:
Journal of neuromuscular diseases. 8(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d07f5cc6a6ff192dffdeb81d299f4a98
https://pubmed.ncbi.nlm.nih.gov/34542081
https://pubmed.ncbi.nlm.nih.gov/34542081
Autor:
Min Jeong Kim, Kenneth L. Bible, Stanley C. Froehner, Nicholas P. Whitehead, Guy L. Odom, Marvin E. Adams
Publikováno v:
The Journal of Physiology. 594:7215-7227
Key points Duchenne muscular dystrophy (DMD) is a severe, degenerative muscle disease that is commonly studied using the mdx mouse. The mdx diaphragm muscle closely mimics the pathophysiological changes in DMD muscles. mdx diaphragm force is commonly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a9da766b7c3f3feaf7d75d7f022f84e
https://doi.org/10.1113/jp272707
https://doi.org/10.1113/jp272707
Publikováno v:
Human molecular genetics. 28(3)
Syntrophins are a family of modular adaptor proteins that are part of the dystrophin protein complex, where they recruit and anchor a variety of signaling proteins. Previously we generated mice lacking α- and/or β2-syntrophin but showed that in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc57848ad863306ebde67eab5688170f
https://pubmed.ncbi.nlm.nih.gov/30256963
https://pubmed.ncbi.nlm.nih.gov/30256963
Autor:
Kenneth L. Bible, Stanley C. Froehner, Michael Regnier, Marvin E. Adams, Nicholas P. Whitehead, Min J. Kim
Publikováno v:
Physiological Reports, Vol 7, Iss 6, Pp n/a-n/a (2019)
Physiological Reports
Physiological Reports
Duchenne muscular dystrophy (DMD), caused by absence of the protein dystrophin, is a common, degenerative muscle disease affecting 1:5000 males worldwide. With recent advances in respiratory care, cardiac dysfunction now accounts for 50% of mortality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc4bb1a20c28216ec3a66bc9b5379bfa
https://doi.org/10.14814/phy2.14018
https://doi.org/10.14814/phy2.14018
Autor:
Nicholas P, Whitehead, Kenneth L, Bible, Min Jeong, Kim, Guy L, Odom, Marvin E, Adams, Stanley C, Froehner
Publikováno v:
The Journal of physiology. 594(24)
Duchenne muscular dystrophy (DMD) is a severe, degenerative muscle disease that is commonly studied using the mdx mouse. The mdx diaphragm muscle closely mimics the pathophysiological changes in DMD muscles. mdx diaphragm force is commonly assessed e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4d0cea466c18fbbd8b244d1b5189ab73
https://pubmed.ncbi.nlm.nih.gov/27976400
https://pubmed.ncbi.nlm.nih.gov/27976400
Publikováno v:
Rare Diseases
Duchenne muscular dystrophy (DMD) is the most common and severe inherited neuromuscular disorder. DMD is caused by mutations in the gene encoding the dystrophin protein in muscle fibers. Dystrophin was originally proposed to be a structural protein t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4074277b3dbc9caba74db4ca56014fda
http://europepmc.org/articles/PMC4838314
http://europepmc.org/articles/PMC4838314
Duchenne muscular dystrophy (DMD) is a lethal, degenerative muscle disease with no effective treatment. DMD muscle pathogenesis is characterized by chronic inflammation, oxidative stress, and fibrosis. Statins, cholesterol-lowering drugs, inhibit the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cbea4942b472a5f9c5c3edc3d52a6b9
https://europepmc.org/articles/PMC4611601/
https://europepmc.org/articles/PMC4611601/
Autor:
Jeffrey S. Chamberlain, Marvin E. Adams, Guy L. Odom, Kenneth L. Bible, Stanley C. Froehner, Glen B. Banks
Publikováno v:
Molecular Therapy. 23:S242-S243
The dystrophin-glycoprotein complex (DGC) primarily functions as a structural element enabling a linkage between the cytoskeleton and the extracellular matrix. Alpha-dystrobrevin (α-Db), a dystrophin subfamily member, is a component of the DGC withi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e835b6988d62f4994fd174707cab3a0
https://doi.org/10.1016/s1525-0016(16)34220-4
https://doi.org/10.1016/s1525-0016(16)34220-4
Publikováno v:
BMC Research Notes, Vol 3, Iss 1, p 307 (2010)
BMC Research Notes
BMC Research Notes
Background PKA is a ubiquitous, multi-subunit cellular kinase that regulates a number of different physiological responses in response to cAMP, including metabolism, cell division, and cardiac function. Numerous studies have implicated altered PKA si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::385cf11d9c2774d6abfcdcc1feb25252
http://www.biomedcentral.com/1756-0500/3/307
http://www.biomedcentral.com/1756-0500/3/307