Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Stanley C, Froehner"'
Autor:
Shirin Katoozi, Shreyas B. Rao, Nadia Skauli, Stanley C. Froehner, Ole Petter Ottersen, Marvin E. Adams, Mahmood Amiry-Moghaddam
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-13 (2020)
Abstract Retinal Müller cells are highly polarized macroglial cells with accumulation of the aquaporin-4 (AQP4) water channel and the inwardly rectifying potassium channel Kir4.1 at specialized endfoot membrane domains abutting microvessels and corp
Externí odkaz:
https://doaj.org/article/d9f1a63c5dd84b42957d3cff9c71c266
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)
Autor:
Ole Petter Ottersen, Mahmood Amiry-Moghaddam, Nadia Skauli, Shreyas B. Rao, Stanley C. Froehner, Shirin Katoozi, Marvin E. Adams
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-13 (2020)
Molecular Brain
Molecular Brain
Retinal Müller cells are highly polarized macroglial cells with accumulation of the aquaporin-4 (AQP4) water channel and the inwardly rectifying potassium channel Kir4.1 at specialized endfoot membrane domains abutting microvessels and corpus vitreu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d03cecea3bb357820d06b3bd30116e2b
https://zenodo.org/record/3723974
https://zenodo.org/record/3723974
Autor:
Heike Fuhrmann-Stroissnigg, Rainer Noiges, Luise Descovich, Irmgard Fischer, Douglas E Albrecht, Fatiha Nothias, Stanley C Froehner, Friedrich Propst
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49722 (2012)
Microtubule-associated proteins of the MAP1 family (MAP1A, MAP1B, and MAP1S) share, among other features, a highly conserved COOH-terminal domain approximately 125 amino acids in length. We conducted a yeast 2-hybrid screen to search for proteins int
Externí odkaz:
https://doaj.org/article/860395f0e13040099dc163ca57a38d9e
Autor:
Eric K Johnson, Liwen Zhang, Marvin E Adams, Alistair Phillips, Michael A Freitas, Stanley C Froehner, Kari B Green-Church, Federica Montanaro
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43515 (2012)
Mutations affecting the expression of dystrophin result in progressive loss of skeletal muscle function and cardiomyopathy leading to early mortality. Interestingly, clinical studies revealed no correlation in disease severity or age of onset between
Externí odkaz:
https://doaj.org/article/3c5decfd48fe4009b024f1b4aa48a87d
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e15355 (2010)
α-Syntrophin is a scaffolding protein linking signaling proteins to the sarcolemmal dystrophin complex in mature muscle. However, α-syntrophin is also expressed in differentiating myoblasts during the early stages of muscle differentiation. In this
Externí odkaz:
https://doaj.org/article/93feecfac6b64156bceec0898bed0056
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e15354 (2010)
Recent studies have shown that oxidative stress contributes to the pathogenesis of muscle damage in dystrophic (mdx) mice. In this study we have investigated the role of NADPH oxidase as a source of the oxidative stress in these mice. The NADPH oxida
Externí odkaz:
https://doaj.org/article/826629b012794c32807243f67805b67e
Autor:
Sandra Schubert, Klaus-Peter Knoch, Joke Ouwendijk, Shabaz Mohammed, Yury Bodrov, Melanie Jäger, Anke Altkrüger, Carolin Wegbrod, Marvin E Adams, Yong Kim, Stanley C Froehner, Ole N Jensen, Yannis Kalaidzidis, Michele Solimena
Publikováno v:
PLoS ONE, Vol 5, Iss 9, p e12929 (2010)
The molecular basis for the interaction of insulin granules with the cortical cytoskeleton of pancreatic β-cells remains unknown. We have proposed that binding of the granule protein ICA512 to the PDZ domain of β2-syntrophin anchors granules to act
Externí odkaz:
https://doaj.org/article/5d0da52b8e9b4c528ee12740e508caba
Autor:
Justin M Percival, Kendra N E Anderson, Paul Gregorevic, Jeffrey S Chamberlain, Stanley C Froehner
Publikováno v:
PLoS ONE, Vol 3, Iss 10, p e3387 (2008)
Skeletal muscle nNOSmu (neuronal nitric oxide synthase mu) localizes to the sarcolemma through interaction with the dystrophin-associated glycoprotein (DAG) complex, where it synthesizes nitric oxide (NO). Disruption of the DAG complex occurs in dyst
Externí odkaz:
https://doaj.org/article/4c4336dd73f24520a706edc1eafa68ad