Zobrazeno 1 - 10
of 187
pro vyhledávání: '"S C, Froehner"'
Autor:
Wang, Yifan1,2 (AUTHOR), Yang, Hui1,2 (AUTHOR), Li, Na1,2 (AUTHOR), Wang, Lili1,2 (AUTHOR), Guo, Chang1,2 (AUTHOR), Ma, Weining3 (AUTHOR), Liu, Shiqi1,2 (AUTHOR), Peng, Chao1,2 (AUTHOR), Chen, Jiexin1,2 (AUTHOR), Song, Huifang1,2 (AUTHOR), Chen, Hedan1,2 (AUTHOR), Ma, Xinyue1,2 (AUTHOR), Yi, Jingyun1,2 (AUTHOR), Lian, Jingjing1,2 (AUTHOR), Kong, Weikaixin1,2 (AUTHOR), Dong, Jie1,2 (AUTHOR), Tu, Xinyu1,2 (AUTHOR), Shah, Mala4 (AUTHOR), Tian, Xin5 (AUTHOR) xintian@cqmu.edu.cn, Huang, Zhuo1,2 (AUTHOR) huangz@hsc.pku.edu.cn
Publikováno v:
Advanced Science. 8/7/2024, Vol. 11 Issue 29, p1-20. 20p.
Autor:
De Masi, Alessia1 (AUTHOR), Zanou, Nadège2 (AUTHOR), Strotjohann, Keno1 (AUTHOR), Lee, Dohyun3 (AUTHOR), Lima, Tanes I.1 (AUTHOR), Li, Xiaoxu1 (AUTHOR), Jeon, Jongsu3 (AUTHOR), Place, Nicolas2 (AUTHOR), Jung, Hoe‐Yune3,4 (AUTHOR) elijah98@postech.ac.kr, Auwerx, Johan1 (AUTHOR) admin.auwerx@epfl.ch
Publikováno v:
Advanced Science. 7/24/2024, Vol. 11 Issue 28, p1-14. 14p.
Autor:
Enrico Stefani, Juan Codina, L. Toro, F M Strickland, A M Spiegel, Atsuko Yatani, T Sawada, S C Froehner, Susan L. Hamilton, M. J. Hawkes
Publikováno v:
Journal of Biological Chemistry. 266:19528-19535
The alpha subunits of heterotrimeric GTP-binding (G) proteins act upon ion channels through both cytoplasmic and membrane-delimited pathways (Brown, A. M., and Birnbaumer, L. (1990) Annu. Rev. Physiol. 52, 197-213). The membrane pathway may involve e
Publikováno v:
American journal of medical genetics. 92(2)
The autosomal dominant hereditary spastic paraplegias (AD-HSP) are a heterogeneous group of degenerative disorders of the central motor system, characterized by progressive spasticity of the lower limbs. Five loci for pure AD-HSP have been identified
Publikováno v:
The Journal of biological chemistry. 272(50)
Dystrophin, the protein disrupted in Duchenne muscular dystrophy, is one of several related proteins that are key components of the submembrane cytoskeleton. Three dystrophin-related proteins (utrophin, dystrophin-related protein-2 (DRP2), and dystro
Publikováno v:
Society of General Physiologists series. 52
Publikováno v:
Neuroreport. 5(13)
The syntrophins are a multigene family of proteins which bind C-terminal domains of dystrophin, utrophin and homologs thereof. We report here that antibodies specific for one isoform, beta 2-syntrophin, labeled only the neuromuscular junction (NMJ) i
Publikováno v:
The Journal of biological chemistry. 269(4)
Electric tissue syntrophin, originally described as an M(r) 58,000 postsynaptic protein having homologs in mammalian muscle, was previously shown to associate with dystrophin in Triton extracts of Torpedo postsynaptic membranes. It also associates wi
Publikováno v:
The Journal of biological chemistry. 267(9)
Dystrophin was purified by immunoaffinity chromatography from detergent-solubilized Torpedo electric organ postsynaptic membranes using monoclonal antibodies. A major doublet of proteins at Mr 58,000 and minor proteins at Mr 87,000, Mr 45,000, and Mr
Autor:
S L, Hamilton, J, Codina, M J, Hawkes, A, Yatani, T, Sawada, F M, Strickland, S C, Froehner, A M, Spiegel, L, Toro, E, Stefani
Publikováno v:
The Journal of biological chemistry. 266(29)
The alpha subunits of heterotrimeric GTP-binding (G) proteins act upon ion channels through both cytoplasmic and membrane-delimited pathways (Brown, A. M., and Birnbaumer, L. (1990) Annu. Rev. Physiol. 52, 197-213). The membrane pathway may involve e