| P50 | author | David Jonah Grunwald | Q91557845 |
| P2093 | author name string | Kazuyuki Hoshijima | |
| | Dana Klatt Shaw | |
| | Alexis A Chagovetz | |
| | Erin Ritchie | |
| P2860 | cites work | Ensembl 2011 | Q24614810 |
| | Malignant hyperthermia: a review | Q26799652 |
| | Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigm | Q26823743 |
| | Stages of embryonic development of the zebrafish | Q27860947 |
| | Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle | Q28117333 |
| | An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line | Q28586418 |
| | Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene | Q28587644 |
| | Finite element modelling predicts changes in joint shape and cell behaviour due to loss of muscle strain in jaw development | Q28606529 |
| | Calcium signalling: dynamics, homeostasis and remodelling | Q29547635 |
| | The zebrafish reference genome sequence and its relationship to the human genome | Q29616593 |
| | Type 3 ryanodine receptors of skeletal muscle are segregated in a parajunctional position | Q30803286 |
| | Locomotor repertoire of the larval zebrafish: swimming, turning and prey capture | Q30898586 |
| | Gene regulation by patterned electrical activity during neural and skeletal muscle development | Q33540114 |
| | Need-based up-regulation of protein levels in response to deletion of their duplicate genes | Q33548755 |
| | Frameshift indels introduced by genome editing can lead to in-frame exon skipping. | Q33751947 |
| | Ryanodine receptors: structure, expression, molecular details, and function in calcium release. | Q34024377 |
| | Somite development in zebrafish | Q34077484 |
| | Ryanodine receptors, a family of intracellular calcium ion channels, are expressed throughout early vertebrate development | Q34101037 |
| | Control of apoptosis by IP(3) and ryanodine receptor driven calcium signals | Q34104059 |
| | Isoform-dependent formation of heteromeric Ca2+ release channels (ryanodine receptors). | Q34147927 |
| | Sarcomere length operating range of vertebrate muscles during movement | Q34214909 |
| | Molecular cloning and characterization of the ryanodine receptor/junctional channel complex cDNA from skeletal muscle sarcoplasmic reticulum | Q34318323 |
| | Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome | Q34390580 |
| | SEPN1: associated with congenital fiber-type disproportion and insulin resistance | Q34478122 |
| | Structural interaction between RYRs and DHPRs in calcium release units of cardiac and skeletal muscle cells | Q34542127 |
| | Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA. | Q34560693 |
| | Pharmacologic and functional characterization of malignant hyperthermia in the R163C RyR1 knock-in mouse | Q34583987 |
| | Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor. | Q34677465 |
| | Mutations in TPM3 are a common cause of congenital fiber type disproportion | Q34755501 |
| | Ryanodine receptor calcium release channels | Q34882627 |
| | Nonsense-mediated mRNA decay: molecular insights and mechanistic variations across species | Q36131531 |
| | Presynaptic calcium stores and synaptic transmission | Q36140951 |
| | Myocardial NF-κB activation is essential for zebrafish heart regeneration. | Q36238400 |
| | Severe congenital RYR1-associated myopathy: the expanding clinicopathologic and genetic spectrum | Q36870145 |
| | Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm | Q37099504 |
| | Genotype-phenotype correlations in recessive RYR1-related myopathies | Q37114746 |
| | Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum | Q37813850 |
| | Fiber types in mammalian skeletal muscles | Q37947567 |
| | Core myopathies | Q37968743 |
| | The role of intracellular calcium stores in synaptic plasticity and memory consolidation | Q38103722 |
| | Ryanodine receptors: allosteric ion channel giants. | Q38241007 |
| | Control of acetylcholine receptors in skeletal muscle | Q38503504 |
| | Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives. | Q38840808 |
| | RYR1-related myopathies: a wide spectrum of phenotypes throughout life | Q39008908 |
| | Genetic compensation induced by deleterious mutations but not gene knockdowns. | Q40744194 |
| | CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion | Q42176221 |
| | Transcription control reprogramming in genetic backup circuits | Q42648483 |
| | RYR1 mutations are a common cause of congenital myopathies with central nuclei | Q42908171 |
| | Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion | Q43003614 |
| | RyR1 S-nitrosylation underlies environmental heat stroke and sudden death in Y522S RyR1 knockin mice | Q43204679 |
| | RyR3 amplifies RyR1-mediated Ca(2+)-induced Ca(2+) release in neonatal mammalian skeletal muscle. | Q43704273 |
| | Requirement of functional ryanodine receptor type 3 for astrocyte migration. | Q43800078 |
| | Multiple muscle cell identities induced by distinct levels and timing of hedgehog activity in the zebrafish embryo | Q44515860 |
| | Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis. | Q45982130 |
| | King-denborough syndrome caused by a novel mutation in the ryanodine receptor gene. | Q46395272 |
| | Presynaptic ryanodine receptors are required for normal quantal size at the Caenorhabditis elegans neuromuscular junction. | Q46610671 |
| | Acetylcholine and calcium signalling regulates muscle fibre formation in the zebrafish embryo | Q46774490 |
| | Heat- and anesthesia-induced malignant hyperthermia in an RyR1 knock-in mouse. | Q46801191 |
| | Unraveling RYR1 mutations and muscle biopsies | Q46818945 |
| | Muscle contraction controls skeletal morphogenesis through regulation of chondrocyte convergent extension | Q47073931 |
| | Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease. | Q47074166 |
| | RYR1 causing distal myopathy | Q47117914 |
| | mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay | Q47150815 |
| | Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients. | Q48603346 |
| | Mental retardation in congenital nonprogressive myopathy with uniform type 1 fibers | Q48628885 |
| | Primary structure and functional expression from cDNA of the cardiac ryanodine receptor/calcium release channel | Q48887625 |
| | Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction | Q49388884 |
| | A two-color acid-free cartilage and bone stain for zebrafish larvae. | Q50468807 |
| | OpenSPIM: an open-access light-sheet microscopy platform. | Q53106278 |
| | 182nd ENMC International Workshop: RYR1-related myopathies, 15-17th April 2011, Naarden, The Netherlands. | Q53137877 |
| | The development and behavioral characteristics of the startle response in the zebra fish. | Q54275725 |
| | Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation | Q56906866 |
| | King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene | Q57053868 |
| | Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies | Q57334263 |
| | Congenital myopathies | Q60173420 |
| | Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene | Q61794284 |
| | Identification and localization of two triad junctional foot protein isoforms in mature avian fast twitch skeletal muscle | Q68890419 |
| | Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation | Q71849941 |
| | Vertebrate genome evolution and the zebrafish gene map | Q74428368 |
| | Ryanodinopathies: RyR-Linked Muscle Diseases | Q83483025 |
| | Challenging zebrafish escape responses by increasing water viscosity | Q84100273 |
| | Intracellular Calcium Mobilization Is Required for Sonic Hedgehog Signaling | Q88653253 |
| | Ryanodine receptor dysfunction in human disorders | Q90443719 |
| | Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength | Q91680644 |
| | Mouse model of severe recessive RYR1-related myopathy | Q92157539 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 2 | |
| P577 | publication date | 2019-09-18 | |
| P1433 | published in | Disease Models & Mechanisms | Q1524006 |
| P1476 | title | Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function | |
| P478 | volume | 13 | |