Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Marvin E. Adams"'
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)
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:
Eric K. Johnson, Marvin E. Adams, Daniel Brayson, Nalinda B. Wasala, Liwen Zhang, Yongping Yue, Hong Wang, Stan C Froehner, Charlotte S Scott, Federica Montanaro, Kwan-Leong Hau, Dongsheng Duan, Aaron J. Trask, Elena Marrosu
Publikováno v:
Human Molecular Genetics
ΔR4-R23/ΔCT micro-dystrophin (μDys) is a miniaturized version of dystrophin currently evaluated in a Duchenne muscular dystrophy (DMD) gene therapy trial to treat skeletal and cardiac muscle disease. In pre-clinical studies, μDys efficiently resc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::123a02491ec3a47377c510bacc94c7ef
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:
Ole Petter Ottersen, Shirin Katoozi, Stanley C. Froehner, Marvin E. Adams, Nenad Jovanovic, Shreyas B. Rao, Nadia Skauli, Mahmood Amiry-Moghaddam, Antonio Frigeri
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Biomembranes. 1863:183616
Aquaporin-4 (AQP4) water channels and gap junction proteins (connexins) are two classes of astrocytic membrane proteins critically involved in brain water and ion homeostasis. AQP4 channels are anchored by α1-syntrophin to the perivascular astrocyti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9d818d9c5b16aae83b176fb428cdeb9
https://doi.org/10.1016/j.bbamem.2021.183616
https://doi.org/10.1016/j.bbamem.2021.183616
Targeted deletion of β1-syntrophin causes a loss of Kir 4.1 from Müller cell endfeet in mouse retina
Autor:
Ole Petter Ottersen, Mahmood Amiry-Moghaddam, Marvin E. Adams, Shreyas B. Rao, Nadia Skauli, Shirin Katoozi, Stanley C. Froehner
Proper function of the retina depends heavily on a specialized form of retinal glia called Muller cells. These cells carry out important homeostatic functions that are contingent on their polarized nature. Specifically, the Muller cell endfeet that c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986b329ff8cb6d7f0a6ce857b7dfc7e3
http://hdl.handle.net/10852/77780
http://hdl.handle.net/10852/77780
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
Autor:
Shreyas B, Rao, Shirin, Katoozi, Nadia, Skauli, Stanley C, Froehner, Ole Petter, Ottersen, Marvin E, Adams, Mahmood, Amiry-Moghaddam
Publikováno v:
Glia
Proper function of the retina depends heavily on a specialized form of retinal glia called Müller cells. These cells carry out important homeostatic functions that are contingent on their polarized nature. Specifically, the Müller cell endfeet that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a97ae25e037c99e503085de1c9886dc1
https://pubmed.ncbi.nlm.nih.gov/30803043
https://pubmed.ncbi.nlm.nih.gov/30803043
Autor:
Bridget B. Kelly, Marvin E. Adams, Douglas E. Albrecht, Guoping Feng, Stanley C. Froehner, Dongqing Wang
The dystrophin glycoprotein complex (DGC) is critical for muscle stability, and mutations in DGC proteins lead to muscular dystrophy. The DGC also contributes to the maturation and maintenance of the neuromuscular junction (NMJ). The gene encoding th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd09b201230527eb646c42758e5442c
https://europepmc.org/articles/PMC6042018/
https://europepmc.org/articles/PMC6042018/