FKBP12.6 Activates RyR1: Investigating the Amino Acid Residues Critical for Channel Modulation
Author:
Publisher
Elsevier BV
Subject
Biophysics
Reference65 articles.
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1. A novel, patient-derived RyR1 mutation impairs muscle function and calcium homeostasis in mice;Journal of General Physiology;2024-03-04
2. FKBP12 binds to the cardiac ryanodine receptor with negative cooperativity: implications for heart muscle physiology in health and disease;Philosophical Transactions of the Royal Society B: Biological Sciences;2023-05
3. Mutation in RyR2-FKBP Binding site alters Ca2+ signaling modestly but increases “arrhythmogenesis” in human stem cells derived cardiomyocytes;Cell Calcium;2022-01
4. Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength;Human Molecular Genetics;2019-05-02
5. FKBP Ligands—Where We Are and Where to Go?;Frontiers in Pharmacology;2018-12-05
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