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http://purl.uniprot.org/citations/32899693http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/32899693http://www.w3.org/2000/01/rdf-schema#comment"Cardiac arrhythmias are serious, life-threatening diseases associated with the dysregulation of Ca2+ influx into the cytoplasm of cardiomyocytes. This dysregulation often arises from dysfunction of ryanodine receptor 2 (RyR2), the principal Ca2+ release channel. Dysfunction of RyR1, the skeletal muscle isoform, also results in less severe, but also potentially life-threatening syndromes. The RYR2 and RYR1 genes have been found to harbor three main mutation "hot spots", where mutations change the channel structure, its interdomain interface properties, its interactions with its binding partners, or its dynamics. In all cases, the result is a defective release of Ca2+ ions from the sarcoplasmic reticulum into the myocyte cytoplasm. Here, we provide an overview of the most frequent diseases resulting from mutations to RyR1 and RyR2, briefly review some of the recent experimental structural work on these two molecules, detail some of the computational work describing their dynamics, and summarize the known changes to the structure and function of these receptors with particular emphasis on their N-terminal, central, and channel domains."xsd:string
http://purl.uniprot.org/citations/32899693http://purl.org/dc/terms/identifier"doi:10.3390/molecules25184040"xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/author"Bauer J.A."xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/author"Bauerova-Hlinkova V."xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/author"Hajduchova D."xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/name"Molecules"xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/pages"E4040"xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/title"Structure and Function of the Human Ryanodine Receptors and Their Association with Myopathies-Present State, Challenges, and Perspectives."xsd:string
http://purl.uniprot.org/citations/32899693http://purl.uniprot.org/core/volume"25"xsd:string
http://purl.uniprot.org/citations/32899693http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/32899693
http://purl.uniprot.org/citations/32899693http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/32899693
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http://purl.uniprot.org/uniprot/#_G9I486-mappedCitation-32899693http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/32899693
http://purl.uniprot.org/uniprot/#_G9I593-mappedCitation-32899693http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/32899693
http://purl.uniprot.org/uniprot/#_L8E9F3-mappedCitation-32899693http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/32899693
http://purl.uniprot.org/uniprot/#_L8E9M2-mappedCitation-32899693http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/32899693