Calsequestrin Is an Inhibitor of Skeletal Muscle Ryanodine Receptor Calcium Release Channels
- 1 January 2002
- journal article
- Published by Elsevier in Biophysical Journal
- Vol. 82 (1) , 310-320
- https://doi.org/10.1016/s0006-3495(02)75396-4
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Coordination between Ca2+ Release and Subsequent Re-Uptake in the Sarcoplasmic ReticulumBiochemistry, 1999
- Dual Regulation of the Skeletal Muscle Ryanodine Receptor by Triadin and CalsequestrinBiochemistry, 1998
- Sarcoplasmic reticulum lumenal Ca2+ has access to cytosolic activation and inactivation sites of skeletal muscle Ca2+ release channelBiophysical Journal, 1996
- Calsequestrin is essential for the Ca2+release induced by myotoxin α in skeletal muscle sarcoplasmic reticulumCanadian Journal of Physiology and Pharmacology, 1995
- The role of Ca2+ ions in excitation-contraction coupling of skeletal muscle fibresBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1995
- Single channel activity of the ryanodine receptor calcium release channel is modulated by FK‐506FEBS Letters, 1994
- Regulation of Calcium Channel in Sarcoplasmic Reticulum by CalsequestrinBiochemical and Biophysical Research Communications, 1994
- Characterization of the junctional face membrane from terminal cisternae of sarcoplasmic reticulum.The Journal of cell biology, 1986
- Autocatalytic phosphorylation of calsequestrinFEBS Letters, 1980
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970