STAC3 stably interacts through its C1 domain with CaV1.1 in skeletal muscle triads
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep41003.pdf
Reference27 articles.
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2. Schredelseker, J. et al. The beta 1a subunit is essential for the assembly of dihydropyridine-receptor arrays in skeletal muscle. Proceedings of the National Academy of Sciences of the United States of America 102, 17219–17224, doi: 10.1073/pnas.0508710102 (2005).
3. Takeshima, H. et al. Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene. Nature 369, 556–559, doi: 10.1038/369556a0 (1994).
4. Nelson, B. R. et al. Skeletal muscle-specific T-tubule protein STAC3 mediates voltage-induced Ca2+ release and contractility. Proceedings of the National Academy of Sciences of the United States of America 110, 11881–11886, doi: 10.1073/pnas.1310571110 (2013).
5. Horstick, E. J. et al. Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy. Nature communications 4, 1952, doi: 10.1038/ncomms2952 (2013).
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