Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum.

doi:10.1016/j.bbamcr.2010.11.009

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum.

Biochimica et biophysica acta - 1 May 2011

Maclennan David H, Zvaritch Elena

Abstract excerpt

This review focuses on muscle disorders and diseases caused by defects in the Ca(2+) release channels of the sarcoplasmic reticulum, the ryanodine receptors, and in the luminal, low affinity, high capacity Ca(2+)-binding proteins, calsequestrins. It provides a time line over the past half century of the highlights of research on malignant hyperthermia (MH), central core disease (CCD) and catecholaminergic...

Topics

Animals
Calcium Signaling
Humans
Models, Biological
Muscular Diseases
Mutation
Penetrance
Sarcoplasmic Reticulum

Source

Open in PubMed

Identifiers

PMID: 21118704
DOI: 10.1016/j.bbamcr.2010.11.009

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics