المؤلفون: Evan Yamasaki, Scott Earley, Pratish Thakore, Harry A. T. Pritchard, Paulo W. Pires

المصدر: Pritchard, H A T, Pires, P W, Yamasaki, E, Thakore, P & Earley, S 2018, ' Nanoscale remodeling of ryanodine receptor cluster size underlies cerebral microvascular dysfunction in Duchenne muscular dystrophy ', Proceedings of the National Academy of Sciences of the United States of America, vol. 115, no. 41, pp. E9745-E9752 . https://doi.org/10.1073/pnas.1804593115

مصطلحات موضوعية: 0301 basic medicine, Male, mdx mouse, BK channel, Vascular smooth muscle, Calcium/metabolism, Duchenne muscular dystrophy, Muscular Dystrophy, Duchenne/metabolism, Ryanodine receptor 2, 03 medical and health sciences, Mice, Muscle, Smooth, Vascular/metabolism, Sarcoplasmic Reticulum/metabolism, medicine, Animals, Homeostasis, Nanotechnology, Calcium Signaling, Cells, Cultured, Multidisciplinary, biology, Chemistry, Ryanodine receptor, Cerebral Arteries/metabolism, Cardiac muscle, Large-Conductance Calcium-Activated Potassium Channels/metabolism, medicine.disease, musculoskeletal system, Cell biology, 030104 developmental biology, medicine.anatomical_structure, Muscular Dystrophy, Animal/metabolism, Vasoconstriction, biology.protein, cardiovascular system, Mice, Inbred mdx, Dystrophin/physiology, Dystrophin, tissues, Ryanodine Receptor Calcium Release Channel/metabolism, Muscle Contraction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f3615d92676736040988ebe2961b818
https://www.research.manchester.ac.uk/portal/en/publications/nanoscale-remodeling-of-ryanodine-receptor-cluster-size-underlies-cerebral-microvascular-dysfunction-in-duchenne-muscular-dystrophy(bbcdfbf9-4928-44fe-b4ce-cf6ef4ccef5b).html

المؤلفون: Sarah Davis, Kevin P. Campbell, Michael B. A. Oldstone, Lance Wells, Takako Yoshida-Moriguchi, Stephanie H. Stalnaker, Harry Schachter, Michael Madson, Liping Yu, Stefan Kunz

المصدر: Science, vol. 327, no. 5961, pp. 88-92

مصطلحات موضوعية: Glycosylation, Magnetic Resonance Spectroscopy, N-Acetylglucosaminyltransferases, Mass Spectrometry, Muscular Dystrophies, Article, Cell Line, Mice, Laminin, Fukuyama congenital muscular dystrophy, medicine, Carbohydrate Conformation, Animals, Humans, Muscular dystrophy, Phosphorylation, Laminin binding, Dystroglycans, Muscle, Skeletal, Multidisciplinary, Fukutin-related protein, biology, Membrane Proteins, Muscular Dystrophy, Animal, medicine.disease, Fukutin, Recombinant Proteins, Mice, Inbred C57BL, Biochemistry, biology.protein, Congenital muscular dystrophy, Dystroglycans/chemistry, Dystroglycans/metabolism, Laminin/metabolism, Mannose/metabolism, Membrane Proteins/metabolism, Muscle, Skeletal/metabolism, Muscular Dystrophies/metabolism, Muscular Dystrophy, Animal/metabolism, N-Acetylglucosaminyltransferases/genetics, N-Acetylglucosaminyltransferases/metabolism, Protein Binding, Recombinant Proteins/chemistry, Recombinant Proteins/metabolism, Dystrophin, Mannose

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0dc05a960b21870d919e61929b3c23
https://pubmed.ncbi.nlm.nih.gov/20044576