scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1006283661 |
P356 | DOI | 10.1038/380072A0 |
P698 | PubMed publication ID | 8598910 |
P5875 | ResearchGate publication ID | 14601461 |
P2093 | author name string | Allen PD | |
Pessah IN | |||
Beam KG | |||
Nguyen HT | |||
Nakai J | |||
Dirksen RT | |||
P2860 | cites work | Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene | Q28587644 |
Heterogeneity of conductance states in calcium channels of skeletal muscle | Q34260106 | ||
Abnormal junctions between surface membrane and sarcoplasmic reticulum in skeletal muscle with a mutation targeted to the ryanodine receptor | Q34439884 | ||
Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA. | Q34560693 | ||
Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor. | Q34677465 | ||
Voltage-dependent inactivation of T-tubular skeletal calcium channels in planar lipid bilayers | Q36410758 | ||
Single calcium channel behavior in native skeletal muscle | Q36411629 | ||
A novel calcium current in dysgenic skeletal muscle | Q36434416 | ||
Effects of perchlorate on the molecules of excitation-contraction coupling of skeletal and cardiac muscle | Q36435118 | ||
Perchlorate enhances transmission in skeletal muscle excitation-contraction coupling | Q36435131 | ||
Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy | Q36534906 | ||
Transgenesis by means of blastocyst-derived embryonic stem cell lines | Q37409515 | ||
Biochemistry and biophysics of excitation-contraction coupling | Q38648051 | ||
Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs | Q41200795 | ||
Voltage-dependent block by zinc of single calcium channels in mouse myotubes | Q41732380 | ||
Functional expression of the calcium release channel from skeletal muscle ryanodine receptor cDNA. | Q41757957 | ||
Restoration of junctional tetrads in dysgenic myotubes by dihydropyridine receptor cDNA. | Q41761102 | ||
The ryanodine receptor/calcium channel genes are widely and differentially expressed in murine brain and peripheral tissues. | Q42054647 | ||
Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors | Q42976855 | ||
Measurement of calcium transients and slow calcium current in myotubes | Q42976857 | ||
Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics. | Q54075376 | ||
Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscle | Q59051250 | ||
Mitogens and oncogenes can block the induction of specific voltage-gated ion channels | Q68992789 | ||
A possible role of sarcoplasmic Ca2+ release in modulating the slow Ca2+ current of skeletal muscle | Q71604472 | ||
P433 | issue | 6569 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 72-75 | |
P577 | publication date | 1996-03-01 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor. | |
P478 | volume | 380 |
Q34319669 | "Current" advances in mechanically skinned skeletal muscle fibres |
Q54566721 | A carboxy-terminal peptide of the alpha 1-subunit of the dihydropyridine receptor inhibits Ca(2+)-release channels. |
Q30868788 | A carboxyl-terminal region important for the expression and targeting of the skeletal muscle dihydropyridine receptor. |
Q28364309 | A cardiac dihydropyridine receptor II-III loop peptide inhibits resting Ca(2+) sparks in ferret ventricular myocytes |
Q33922807 | A malignant hyperthermia-inducing mutation in RYR1 (R163C): alterations in Ca2+ entry, release, and retrograde signaling to the DHPR. |
Q33922848 | A malignant hyperthermia-inducing mutation in RYR1 (R163C): consequent alterations in the functional properties of DHPR channels |
Q42667282 | A probable role of dihydropyridine receptors in repression of Ca2+ sparks demonstrated in cultured mammalian muscle |
Q73174522 | A region of the ryanodine receptor critical for excitation-contraction coupling in skeletal muscle |
Q37132911 | A retrograde signal from RyR1 alters DHP receptor inactivation and limits window Ca2+ release in muscle fibers of Y522S RyR1 knock-in mice |
Q28586041 | A retrograde signal from calsequestrin for the regulation of store-operated Ca2+ entry in skeletal muscle |
Q85030755 | A shortcut to a skeletal muscle DHPR knock-in? |
Q36276697 | A transgenic myogenic cell line lacking ryanodine receptor protein for homologous expression studies: reconstitution of Ry1R protein and function. |
Q37004813 | A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres. |
Q71762770 | Absence of Ca2+ current facilitation in skeletal muscle of transgenic mice lacking the type 1 ryanodine receptor |
Q24680364 | Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction coupling |
Q36296090 | Accessibility of targeted DHPR sites to streptavidin and functional effects of binding on EC coupling |
Q40504749 | Activation of ryanodine receptors induces calcium influx in a neuroblastoma cell line lacking calcium influx factor activity |
Q34478102 | Allele-specific gene silencing in two mouse models of autosomal dominant skeletal myopathy |
Q36510485 | Alpha2delta1 dihydropyridine receptor subunit is a critical element for excitation-coupled calcium entry but not for formation of tetrads in skeletal myotubes |
Q43087539 | Alterations in triad ultrastructure following repetitive stimulation and intracellular changes associated with exercise in amphibian skeletal muscle. |
Q37346777 | Alternative splicing of RyR1 alters the efficacy of skeletal EC coupling. |
Q34774544 | Amino acid residues 489-503 of dihydropyridine receptor (DHPR) β1a subunit are critical for structural communication between the skeletal muscle DHPR complex and type 1 ryanodine receptor |
Q44538223 | Amino acids 1-1,680 of ryanodine receptor type 1 hold critical determinants of skeletal type for excitation-contraction coupling. Role of divergence domain D2. |
Q35234567 | Apparent lack of physical or functional interaction between CaV1.1 and its distal C terminus |
Q35544373 | Bidirectional signaling between calcium channels of skeletal muscle requires multiple direct and indirect interactions |
Q64094977 | Blocking skeletal muscle DHPRs/Ryr1 prevents neuromuscular synapse loss in mutant mice deficient in type III Neuregulin 1 (CRD-Nrg1) |
Q26770573 | Bridging the myoplasmic gap II: more recent advances in skeletal muscle excitation-contraction coupling |
Q36953390 | Bridging the myoplasmic gap: recent developments in skeletal muscle excitation-contraction coupling |
Q36444707 | COOH-terminal truncated alpha(1S) subunits conduct current better than full-length dihydropyridine receptors |
Q35691137 | Ca(2+) sparks operated by membrane depolarization require isoform 3 ryanodine receptor channels in skeletal muscle. |
Q26866428 | Ca(V)1.1: The atypical prototypical voltage-gated Ca²⁺ channel |
Q92259441 | Ca2+ Channels Mediate Bidirectional Signaling between Sarcolemma and Sarcoplasmic Reticulum in Muscle Cells |
Q39302913 | Ca2+ Release Channels Join the 'Resolution Revolution'. |
Q34177806 | Ca2+ activation of RyR1 is not necessary for the initiation of skeletal-type excitation-contraction coupling |
Q47289368 | Ca2+ channel regulation by transforming growth factor-beta 1 and bone morphogenetic protein-2 in developing mice myotubes |
Q34180386 | Ca2+ current and charge movements in skeletal myotubes promoted by the beta-subunit of the dihydropyridine receptor in the absence of ryanodine receptor type 1. |
Q46222115 | Ca2+ release from internal stores: role in generating depolarizing after-potentials in rat supraoptic neurones |
Q43559613 | Ca2+ release through ryanodine receptors regulates skeletal muscle L-type Ca2+ channel expression. |
Q28585470 | Ca2+ sparks in embryonic mouse skeletal muscle selectively deficient in dihydropyridine receptor alpha1S or beta1a subunits |
Q34183948 | Ca2+-dependent excitation-contraction coupling triggered by the heterologous cardiac/brain DHPR beta2a-subunit in skeletal myotubes |
Q36620710 | Ca2+-independent activation of Ca2+/calmodulin-dependent protein kinase II bound to the C-terminal domain of CaV2.1 calcium channels |
Q36411859 | Ca2+-induced Ca2+ release in Chinese hamster ovary (CHO) cells co-expressing dihydropyridine and ryanodine receptors |
Q37129336 | Ca2+-operated transcriptional networks: molecular mechanisms and in vivo models. |
Q36435999 | Caffeine-induced release of intracellular Ca2+ from Chinese hamster ovary cells expressing skeletal muscle ryanodine receptor. Effects on full-length and carboxyl-terminal portion of Ca2+ release channels |
Q33755195 | Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases |
Q46408652 | Calcium and the role of motoneuronal doublets in skeletal muscle control |
Q34661611 | Calcium release in skeletal muscle: from K+ contractures to Ca2+ sparks |
Q28361649 | Calcium waves induced by hypertonic solutions in intact frog skeletal muscle fibres |
Q53839183 | Calcium-induced release of calcium in muscle: 50 years of work and the emerging consensus. |
Q36436420 | Calmodulin binding to the 3614-3643 region of RyR1 is not essential for excitation-contraction coupling in skeletal myotubes |
Q34502231 | Calmodulin kinase is a molecular switch for cardiac excitation-contraction coupling |
Q37305499 | Checking your SOCCs and feet: the molecular mechanisms of Ca2+ entry in skeletal muscle |
Q33798490 | Comparative ultrastructure of Ca2+ release units in skeletal and cardiac muscle |
Q34172770 | Comparison of Ca(2+) sparks produced independently by two ryanodine receptor isoforms (type 1 or type 3) |
Q47852066 | Complex formation between calsequestrin and the ryanodine receptor in fast- and slow-twitch rabbit skeletal muscle |
Q28369433 | Complex interactions between mGluRs, intracellular Ca2+ stores and ion channels in neurons |
Q41489564 | Conformation state of the ryanodine receptor and functional effects of ryanodine on skeletal muscle |
Q46192991 | Conformation-dependent stability of junctophilin 1 (JP1) and ryanodine receptor type 1 (RyR1) channel complex is mediated by their hyper-reactive thiols. |
Q37595562 | Conformational activation of Ca2+ entry by depolarization of skeletal myotubes |
Q40633850 | Conformational coupling of DHPR and RyR1 in skeletal myotubes is influenced by long-range allosterism: evidence for a negative regulatory module |
Q30008804 | Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3. |
Q52529385 | Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors. |
Q27331094 | Coordinated movement of cytoplasmic and transmembrane domains of RyR1 upon gating |
Q92238728 | Cored in the act: the use of models to understand core myopathies |
Q26770423 | Critical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and Disease |
Q53777541 | Crosstalk via the Sarcoplasmic Gap: The DHPR-RyR Interaction. |
Q41607050 | Crystal structures of wild type and disease mutant forms of the ryanodine receptor SPRY2 domain. |
Q32034614 | Cyclic ADP-ribose as a potential second messenger for neuronal Ca2+ signaling |
Q34386035 | Cyclic ADP-ribose as a second messenger revisited from a new aspect of signal transduction from receptors to ADP-ribosyl cyclase |
Q43923091 | Cyclopiazonic acid and thapsigargin reduce Ca2+ influx in frog skeletal muscle fibres as a result of Ca2+ store depletion |
Q36665389 | Dantrolene-induced inhibition of skeletal L-type Ca2+ current requires RyR1 expression |
Q47304950 | De novo reconstitution reveals the proteins required for skeletal muscle voltage-induced Ca2+ release |
Q33907376 | Deletion of amino acids 1641-2437 from the foot region of skeletal muscle ryanodine receptor alters the conduction properties of the Ca release channel |
Q48508890 | Development of the excitation-contraction coupling machinery and its relation to myofibrillogenesis in human iPSC-derived skeletal myocytes |
Q37657281 | Differential contribution of skeletal and cardiac II-III loop sequences to the assembly of dihydropyridine-receptor arrays in skeletal muscle |
Q46438718 | Differential effects of maurocalcine on Ca2+ release events and depolarization-induced Ca2+ release in rat skeletal muscle. |
Q34170119 | Differential regulation of skeletal muscle L-type Ca2+ current and excitation-contraction coupling by the dihydropyridine receptor beta subunit |
Q52142280 | Dihydropyridine-sensitive ion currents and charge movement in vesicles derived from frog skeletal muscle plasma membranes. |
Q44101904 | Dissociation of charge movement from calcium release and calcium current in skeletal myotubes by gabapentin |
Q36644359 | Distinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1. |
Q34187680 | Distinct effects on Ca2+ handling caused by malignant hyperthermia and central core disease mutations in RyR1. |
Q52726366 | Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5. |
Q42128833 | Divergent biophysical properties, gating mechanisms, and possible functions of the two skeletal muscle Ca(V)1.1 calcium channel splice variants |
Q34174280 | Divergent functional properties of ryanodine receptor types 1 and 3 expressed in a myogenic cell line |
Q73149251 | Do ryanodine receptors regulate transmitter release at the neuromuscular junction of rat? |
Q89294511 | Duplex signaling by CaM and Stac3 enhances CaV1.1 function and provides insights into congenital myopathy |
Q43978759 | Dysfunction of store-operated calcium channel in muscle cells lacking mg29. |
Q36910749 | ER-mitochondria communication. How privileged? |
Q83343962 | Effect of theophylline and aminophylline on transmitter release at the mammalian neuromuscular junction is not mediated by cAMP |
Q34978122 | Effects of conformational peptide probe DP4 on bidirectional signaling between DHPR and RyR1 calcium channels in voltage-clamped skeletal muscle fibers |
Q44046135 | Effects of excitatory modulation on intrinsic properties of turtle motoneurons |
Q37267658 | Effects of inserting fluorescent proteins into the alpha1S II-III loop: insights into excitation-contraction coupling |
Q34179074 | Electron tomography of frozen-hydrated isolated triad junctions |
Q24530200 | Elementary and global aspects of calcium signalling |
Q46202669 | Endoplasmic Reticulum-Plasma Membrane Contacts Regulate Cellular Excitability |
Q40974052 | Enhanced dihydropyridine receptor calcium channel activity restores muscle strength in JP45/CASQ1 double knockout mice |
Q37494384 | Evidence for conformational coupling between two calcium channels |
Q36321062 | Evolution of skeletal type e-c coupling: a novel means of controlling calcium delivery |
Q35060776 | Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptor |
Q33998846 | Excitation-contraction coupling from the 1950s into the new millennium. |
Q53606883 | Excitation-contraction coupling in airway smooth muscle. |
Q92719884 | Excitation-contraction coupling in skeletal muscle: recent progress and unanswered questions |
Q74071470 | Excitation-contraction coupling is not affected by scrambled sequence in residues 681-690 of the dihydropyridine receptor II-III loop |
Q35901193 | Excitation-contraction coupling is unaffected by drastic alteration of the sequence surrounding residues L720-L764 of the alpha 1S II-III loop. |
Q30870690 | Expression of ryanodine receptor RyR3 produces Ca2+ sparks in dyspedic myotubes |
Q52172547 | Facilitation of NMDAR-independent LTP and spatial learning in mutant mice lacking ryanodine receptor type 3. |
Q37463586 | Formation of junctions involved in excitation-contraction coupling in skeletal and cardiac muscle. |
Q34195030 | Functional Defects in Six Ryanodine Receptor Isoform-1 (RyR1) Mutations Associated with Malignant Hyperthermia and Their Impact on Skeletal Excitation-Contraction Coupling |
Q48940555 | Functional coupling between ryanodine receptors and L-type calcium channels in neurons |
Q28591767 | Functional coupling of the metabotropic glutamate receptor, InsP3 receptor and L-type Ca2+ channel in mouse CA1 pyramidal cells |
Q36436381 | Functional effects of central core disease mutations in the cytoplasmic region of the skeletal muscle ryanodine receptor |
Q48630542 | Functional expression and characterization of skeletal muscle dihydropyridine receptors in Xenopus oocytes |
Q34172584 | Functional expression of the L-type calcium channel in mice skeletal muscle during prenatal myogenesis |
Q36444962 | Functional impact of the ryanodine receptor on the skeletal muscle L-type Ca(2+) channel |
Q35967874 | Functional nonequality of the cardiac and skeletal ryanodine receptors |
Q42644584 | Functional properties of the ryanodine receptor type 3 (RyR3) Ca2+ release channel |
Q40855582 | Gating of store-operated channels by conformational coupling to ryanodine receptors |
Q35704843 | Gene dose influences cellular and calcium channel dysregulation in heterozygous and homozygous T4826I-RYR1 malignant hyperthermia-susceptible muscle |
Q82362874 | Genetic dissection of ion currents underlying all-or-none action potentials in C. elegans body-wall muscle cells |
Q37672288 | How and why are calcium currents curtailed in the skeletal muscle voltage-gated calcium channels? |
Q41510537 | Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channel. |
Q43722113 | Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families |
Q28207968 | Identification of a region of RyR1 that participates in allosteric coupling with the alpha(1S) (Ca(V)1.1) II-III loop |
Q34177355 | Imperatoxin a enhances Ca(2+) release in developing skeletal muscle containing ryanodine receptor type 3. |
Q48323563 | Inositol-1,4,5-trisphosphate receptor-mediated Ca mobilization is not required for cerebellar long-term depression in reduced preparations |
Q34244881 | Interaction between the dihydropyridine receptor Ca2+ channel beta-subunit and ryanodine receptor type 1 strengthens excitation-contraction coupling |
Q34843211 | Interactions between dihydropyridine receptors and ryanodine receptors in striated muscle |
Q34181217 | Intracellular calcium dynamics--sparks of insight |
Q34186764 | Involvement of a heptad repeat in the carboxyl terminus of the dihydropyridine receptor beta1a subunit in the mechanism of excitation-contraction coupling in skeletal muscle |
Q34171879 | Involvement of the carboxy-terminus region of the dihydropyridine receptor beta1a subunit in excitation-contraction coupling of skeletal muscle |
Q24297615 | JP-45/JSRP1 variants affect skeletal muscle excitation-contraction coupling by decreasing the sensitivity of the dihydropyridine receptor |
Q24684783 | Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion |
Q47248862 | Junctional trafficking and restoration of retrograde signaling by the cytoplasmic RyR1 domain |
Q44683626 | L-type Ca2+ channel and ryanodine receptor cross-talk in frog skeletal muscle |
Q33602333 | L-type calcium channel modulation. |
Q34395653 | Ligand-gated calcium channels inside and out. |
Q36435930 | Local control model of excitation-contraction coupling in skeletal muscle |
Q40061188 | Localization and mobility of the delayed-rectifer K+ channel Kv2.1 in adult cardiomyocytes. |
Q36289083 | Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45 |
Q34471672 | Malignant hyperthermia and central core disease: disorders of Ca2+ release channels |
Q34285881 | Malignant hyperthermia and excitation-contraction coupling |
Q74097754 | Malignant hyperthermia mutation Arg615Cys in the porcine ryanodine receptor alters voltage dependence of Ca2+ release |
Q34883560 | Malignant hyperthermia: a pharmacogenetic disorder |
Q24676753 | Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle |
Q42018621 | Maurocalcine and domain A of the II-III loop of the dihydropyridine receptor Cav 1.1 subunit share common binding sites on the skeletal ryanodine receptor. |
Q42694789 | Maurocalcine and peptide A stabilize distinct subconductance states of ryanodine receptor type 1, revealing a proportional gating mechanism. |
Q38813873 | Membrane depolarization increases ryanodine sensitivity to Ca2+ release to the cytosol in L6 skeletal muscle cells: Implications for excitation-contraction coupling |
Q39641064 | Metabolic regulation of Ca2+ release in permeabilized mammalian skeletal muscle fibres. |
Q35787753 | Mice expressing T4826I-RYR1 are viable but exhibit sex- and genotype-dependent susceptibility to malignant hyperthermia and muscle damage |
Q28393648 | Minding the calcium store: Ryanodine receptor activation as a convergent mechanism of PCB toxicity |
Q39714323 | Mitochondrial redox state and Ca2+ sparks in permeabilized mammalian skeletal muscle |
Q36423545 | Modulation of CaV2.1 channels by Ca2+/calmodulin-dependent protein kinase II bound to the C-terminal domain |
Q27642326 | Molecular basis of the high-affinity activation of type 1 ryanodine receptors by imperatoxin A |
Q24312032 | Molecular cloning and characterization of a human brain ryanodine receptor |
Q48022935 | Molecular cloning and functional expression of a skeletal muscle dihydropyridine receptor from Rana catesbeiana |
Q34360409 | Molecular genetics of Ca(2+) stores and intracellular Ca(2+) signalling. |
Q35051263 | Molecular genetics of ryanodine receptors Ca2+-release channels |
Q35104636 | Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. |
Q24537576 | Multiple regions of RyR1 mediate functional and structural interactions with alpha(1S)-dihydropyridine receptors in skeletal muscle |
Q36295966 | Muscle chloride channel dysfunction in two mouse models of myotonic dystrophy. |
Q34439584 | Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum |
Q73303126 | Neuromuscular development in the avian paralytic mutant crooked neck dwarf (cn/cn): further evidence for the role of neuromuscular activity in motoneuron survival |
Q39569719 | Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors. |
Q39310048 | New factors contributing to dynamic calcium regulation in the skeletal muscle triad-a crowded place |
Q24309139 | New molecular components supporting ryanodine receptor-mediated Ca(2+) release: roles of junctophilin and TRIC channel in embryonic cardiomyocytes |
Q33778038 | Non-Ca2+-conducting Ca2+ channels in fish skeletal muscle excitation-contraction coupling |
Q36586052 | Novel excitation-contraction uncoupled RYR1 mutations in patients with central core disease |
Q46781517 | Ortho-substituted polychlorinated biphenyls alter microsomal calcium transport by direct interaction with ryanodine receptors of mammalian brain |
Q34880821 | Orthograde dihydropyridine receptor signal regulates ryanodine receptor passive leak |
Q37440586 | Overexpression of ryanodine receptor type 1 enhances mitochondrial fragmentation and Ca2+-induced ATP production in cardiac H9c2 myoblasts |
Q95721598 | Paralytic zebrafish lacking acetylcholine receptors fail to localize rapsyn clusters to the synapse |
Q41886433 | Pharmacological distinction between dantrolene and ryanodine binding sites: evidence from normal and malignant hyperthermia-susceptible porcine skeletal muscle. |
Q88311141 | Physical interaction of junctophilin and the CaV1.1 C terminus is crucial for skeletal muscle contraction |
Q38900957 | Physiological and pharmacological modulation of the embryonic skeletal muscle calcium channel splice variant CaV1.1e |
Q48219682 | Physiology and pathophysiology of excitation-contraction coupling: the functional role of ryanodine receptor |
Q48218606 | Plasticity of calcium channels in dendritic spines |
Q94544834 | Preclinical model systems of ryanodine receptor 1-related myopathies and malignant hyperthermia: a comprehensive scoping review of works published 1990-2019 |
Q73300474 | Prolonged depolarization promotes fast gating kinetics of L-type Ca2+ channels in mouse skeletal myotubes |
Q42992623 | Protein-protein interactions in intracellular Ca2+-release channel function. |
Q45298822 | Quantifying SOCE fluorescence measurements in mammalian muscle fibres. The effects of ryanodine and osmotic shocks |
Q71588437 | Reciprocal control of the conformational state of the sarcoplasmic reticulum calcium channel protein by polarization and depolarization in the transverse tubule |
Q37945102 | Reciprocal dihydropyridine and ryanodine receptor interactions in skeletal muscle activation |
Q46622472 | Reconstitution of local Ca2+ signaling between cardiac L-type Ca2+ channels and ryanodine receptors: insights into regulation by FKBP12.6. |
Q33907194 | Recovery of Ca2+ current, charge movements, and Ca2+ transients in myotubes deficient in dihydropyridine receptor beta 1 subunit transfected with beta 1 cDNA. |
Q34041027 | Reduced Ca2+ current, charge movement, and absence of Ca2+ transients in skeletal muscle deficient in dihydropyridine receptor beta 1 subunit |
Q34642130 | Reduced gain of excitation-contraction coupling in triadin-null myotubes is mediated by the disruption of FKBP12/RyR1 interaction |
Q35878200 | Regions of ryanodine receptors that influence activation by the dihydropyridine receptor β1a subunit |
Q36494790 | Rem inhibits skeletal muscle EC coupling by reducing the number of functional L-type Ca2+ channels |
Q35795789 | Rem uncouples excitation-contraction coupling in adult skeletal muscle fibers. |
Q24532855 | Requirement for the ryanodine receptor type 3 for efficient contraction in neonatal skeletal muscles |
Q38739635 | Retrograde Coupling: Muscle's Orphan Signaling Pathway? |
Q35135466 | Retrograde activation of store-operated calcium channel. |
Q28078420 | Review of RyR1 pathway and associated pathomechanisms |
Q36276654 | Role of ryanodine receptors in the assembly of calcium release units in skeletal muscle |
Q42117082 | Role of the JP45-Calsequestrin Complex on Calcium Entry in Slow Twitch Skeletal Muscles. |
Q40540394 | Role of the sequence surrounding predicted transmembrane helix M4 in membrane association and function of the Ca(2+) release channel of skeletal muscle sarcoplasmic reticulum (ryanodine receptor isoform 1). |
Q52639740 | RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling. |
Q34180930 | RyR1/RyR3 chimeras reveal that multiple domains of RyR1 are involved in skeletal-type E-C coupling |
Q43704273 | RyR3 amplifies RyR1-mediated Ca(2+)-induced Ca(2+) release in neonatal mammalian skeletal muscle. |
Q58600210 | Ryanodine Receptor 1-Related Myopathies: Diagnostic and Therapeutic Approaches |
Q33999814 | Ryanodine modification of RyR1 retrogradely affects L-type Ca(2+) channel gating in skeletal muscle |
Q48916793 | Ryanodine produces a low frequency stimulation-induced NMDA receptor-independent long-term potentiation in the rat dentate gyrus in vitro |
Q34429100 | Ryanodine receptor acts as a sensor for redox stress |
Q33912937 | Ryanodine receptor channelopathies |
Q37705608 | Ryanodine receptor studies using genetically engineered mice |
Q46667699 | Ryanodine receptor type 1 (RyR1) mutations C4958S and C4961S reveal excitation-coupled calcium entry (ECCE) is independent of sarcoplasmic reticulum store depletion |
Q46491319 | Ryanodine receptors in muscarinic receptor-mediated bronchoconstriction |
Q34368458 | Sarcolemmal-restricted localization of functional ClC-1 channels in mouse skeletal muscle |
Q93067806 | Sarcopenia: Aging-Related Loss of Muscle Mass and Function |
Q34789227 | Sarcoplasmic reticulum Ca2+ release channel ryanodine receptor (RyR2) plays a crucial role in aconitine-induced arrhythmias |
Q34189934 | Signal transduction from bradykinin, angiotensin, adrenergic and muscarinic receptors to effector enzymes, including ADP-ribosyl cyclase |
Q37785288 | Signaling complexes of voltage-gated sodium and calcium channels |
Q36746937 | Single-particle electron cryomicroscopy of the ion channels in the excitation-contraction coupling junction |
Q24291735 | Skeletal and cardiac ryanodine receptors bind to the Ca(2+)-sensor region of dihydropyridine receptor alpha(1C) subunit |
Q28588104 | Skeletal muscle-specific T-tubule protein STAC3 mediates voltage-induced Ca2+ release and contractility |
Q24316053 | Sorcin associates with the pore-forming subunit of voltage-dependent L-type Ca2+ channels |
Q31437223 | Spatially segregated control of Ca2+ release in developing skeletal muscle of mice |
Q34985729 | Stac adaptor proteins regulate trafficking and function of muscle and neuronal L-type Ca2+ channels |
Q52691686 | Stac proteins associate with the critical domain for excitation-contraction coupling in the II-III loop of CaV1.1. |
Q30008861 | Stac3 has a direct role in skeletal muscle-type excitation-contraction coupling that is disrupted by a myopathy-causing mutation |
Q24294570 | Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy |
Q27026415 | Store-operated Ca2+ entry in muscle physiology and diseases |
Q30621019 | Structural and functional properties of ryanodine receptor type 3 in zebrafish tail muscle |
Q46130508 | Structural insights into binding of STAC proteins to voltage-gated calcium channels |
Q40615240 | Structural requirements of the dihydropyridine receptor alpha1S II-III loop for skeletal-type excitation-contraction coupling |
Q34171452 | Structure of the skeletal muscle calcium release channel activated with Ca2+ and AMP-PCP. |
Q34074422 | Structure of the voltage-gated L-type Ca2+ channel by electron cryomicroscopy |
Q37380782 | Structure-activity relationship of selected meta- and para-hydroxylated non-dioxin like polychlorinated biphenyls: from single RyR1 channels to muscle dysfunction |
Q41078521 | Subtype specificity of the ryanodine receptor for Ca2+ signal amplification in excitation-contraction coupling |
Q39402365 | Suramin interacts with the calmodulin binding site on the ryanodine receptor, RYR1. |
Q83396116 | Synthetic localized calcium transients directly probe signalling mechanisms in skeletal muscle |
Q37413460 | T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase |
Q34161230 | TRPC3 cation channel plays an important role in proliferation and differentiation of skeletal muscle myoblasts |
Q36105323 | Temperature and RyR1 regulate the activation rate of store-operated Ca²+ entry current in myotubes |
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