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Cited by 371

The DOI matches its Crossref record; 130 of the 130 references it cites were found in a registry or an index.

Modulation of the Ryanodine Receptor and Intracellular Calcium

Zalk, Ran, Lehnart, Stephan E., Marks, Andrew R.·2007·Annual Review of Biochemistry

Abstract

Ryanodine receptors (RyRs)/Ca 2+ release channels, on the endoplasmic and sarcoplasmic reticulum of most cell types, are required for intracellular Ca 2+ release involved in diverse cellular functions, including muscle contraction and neurotransmitter release. The large cytoplasmic domain of the RyR serves as a scaffold for proteins that bind to and modulate the channel's function and that comprise a macromolecular signaling complex. These proteins include calstabins [FK506-binding proteins (FKBPs)], calmodulin (CaM), phosphodiesterase, kinases, phosphatases, and their cognate targeting proteins. This review focuses on recent progress in the understanding of RyR regulation and disease mechanisms that are associated with channel dysfunction.

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Crossref · 10.1146/annurev.biochem.76.053105.094237

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Metadata

Authors
Zalk, R., Lehnart, S. E., & Marks, A. R.
Venue
Annual Review of Biochemistry
Published
2007-06-07
Volume
76
Issue
1
Pages
367-385
ISSN
  • 0066-4154 (ISSN-L)
  • 1545-4509
OpenAlex
W2139909390
Cited by
371
References
130
FWCI
1.53
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Modulation of the Ryanodine Receptor and Intracellular Calcium. https://app.cochat.ai/papers/10.1146/annurev.biochem.76.053105.094237
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Zalk, R., Lehnart, S. E., & Marks, A. R. (2007). Modulation of the Ryanodine Receptor and Intracellular Calcium. Annual Review of Biochemistry. https://doi.org/10.1146/annurev.biochem.76.053105.094237

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.