The cardiac alpha(1C) subunit can support excitation-triggered Ca2+ entry in dysgenic and dyspedic myotubes

scientific article

The cardiac alpha(1C) subunit can support excitation-triggered Ca2+ entry in dysgenic and dyspedic myotubes is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.4161/CHAN.3.4.9342
P932PMC publication ID2927111
P698PubMed publication ID19625771
P5875ResearchGate publication ID26689220

P2093author name stringKurt G Beam
Roger A Bannister
P2860cites workNitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated stateQ28365692
AKAP79/150 anchoring of calcineurin controls neuronal L-type Ca2+ channel activity and nuclear signalingQ28567111
Tagging with green fluorescent protein reveals a distinct subcellular distribution of L-type and non-L-type Ca2+ channels expressed in dysgenic myotubesQ32123389
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.Q34180386
Cardiac-type EC-coupling in dysgenic myotubes restored with Ca2+ channel subunit isoforms alpha1C and alpha1D does not correlate with current densityQ34181475
The TRP ion channel family.Q34271602
Multiple loops of the dihydropyridine receptor pore subunit are required for full-scale excitation-contraction coupling in skeletal muscleQ34350397
Bidirectional signaling between calcium channels of skeletal muscle requires multiple direct and indirect interactionsQ35544373
Excitation-contraction coupling is unaffected by drastic alteration of the sequence surrounding residues L720-L764 of the alpha 1S II-III loop.Q35901193
Functional nonequality of the cardiac and skeletal ryanodine receptorsQ35967874
Potentiated L-type Ca2+ channels rectifyQ36412434
Unitary behavior of skeletal, cardiac, and chimeric L-type Ca2+ channels expressed in dysgenic myotubesQ36416036
Role of calcium permeation in dihydropyridine receptor function. Insights into channel gating and excitation-contraction couplingQ36436215
Functional impact of the ryanodine receptor on the skeletal muscle L-type Ca(2+) channelQ36444962
Potentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanismsQ36445185
Alpha2delta1 dihydropyridine receptor subunit is a critical element for excitation-coupled calcium entry but not for formation of tetrads in skeletal myotubesQ36510485
The skeletal L-type Ca(2+) current is a major contributor to excitation-coupled Ca(2+) entryQ37023260
Electrically silent divalent cation entries in resting and active voltage-controlled muscle fibersQ37263246
Checking your SOCCs and feet: the molecular mechanisms of Ca2+ entry in skeletal muscleQ37305499
Enhanced excitation-coupled calcium entry in myotubes expressing malignant hyperthermia mutation R163C is attenuated by dantroleneQ37328327
Conformational activation of Ca2+ entry by depolarization of skeletal myotubesQ37595562
Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAsQ41200795
Functional and structural approaches to the study of excitation-contraction couplingQ41649828
Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptorsQ42976855
Ca2+ release through ryanodine receptors regulates skeletal muscle L-type Ca2+ channel expression.Q43559613
Novel mechanism of voltage-dependent gating in L-type calcium channelsQ45090175
Reconstitution of local Ca2+ signaling between cardiac L-type Ca2+ channels and ryanodine receptors: insights into regulation by FKBP12.6.Q46622472
Ryanodine receptor type 1 (RyR1) mutations C4958S and C4961S reveal excitation-coupled calcium entry (ECCE) is independent of sarcoplasmic reticulum store depletionQ46667699
Enhanced excitation-coupled calcium entry in myotubes is associated with expression of RyR1 malignant hyperthermia mutationsQ46945600
Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling.Q51728761
Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor.Q52519047
Cardiac-type excitation-contraction coupling in dysgenic skeletal muscle injected with cardiac dihydropyridine receptor cDNAQ59095343
Two regions of the ryanodine receptor involved in coupling with L-type Ca2+ channelsQ74567340
Localization in the II-III loop of the dihydropyridine receptor of a sequence critical for excitation-contraction couplingQ77300019
The II-III loop of the skeletal muscle dihydropyridine receptor is responsible for the Bi-directional coupling with the ryanodine receptorQ78037940
Differential dependence of store-operated and excitation-coupled Ca2+ entry in skeletal muscle on STIM1 and Orai1Q81931445
P433issue4
P407language of work or nameEnglishQ1860
P304page(s)268-273
P577publication date2009-07-24
P1433published inChannelsQ15764469
P1476titleThe cardiac alpha(1C) subunit can support excitation-triggered Ca2+ entry in dysgenic and dyspedic myotubes
P478volume3

Reverse relations

cites work (P2860)
Q33922807A malignant hyperthermia-inducing mutation in RYR1 (R163C): alterations in Ca2+ entry, release, and retrograde signaling to the DHPR.
Q50078145A skeletal muscle L-type Ca2+ channel with a mutation in the selectivity filter (CaV1.1 E1014K) conducts K.
Q26770573Bridging the myoplasmic gap II: more recent advances in skeletal muscle excitation-contraction coupling
Q26866428Ca(V)1.1: The atypical prototypical voltage-gated Ca²⁺ channel
Q36665389Dantrolene-induced inhibition of skeletal L-type Ca2+ current requires RyR1 expression
Q42128833Divergent biophysical properties, gating mechanisms, and possible functions of the two skeletal muscle Ca(V)1.1 calcium channel splice variants
Q33801924Functional expression of transgenic 1sDHPR channels in adult mammalian skeletal muscle fibres
Q36385967Modification of STIM1 by O-linked N-acetylglucosamine (O-GlcNAc) attenuates store-operated calcium entry in neonatal cardiomyocytes
Q94544834Preclinical model systems of ryanodine receptor 1-related myopathies and malignant hyperthermia: a comprehensive scoping review of works published 1990-2019
Q35577775Properties of Na+ currents conducted by a skeletal muscle L-type Ca2+ channel pore mutant (SkEIIIK).
Q34373988RGK protein-mediated impairment of slow depolarization- dependent Ca2+ entry into developing myotubes
Q37945102Reciprocal dihydropyridine and ryanodine receptor interactions in skeletal muscle activation
Q37822957The role of store-operated calcium influx in skeletal muscle signaling

Search more.