| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1005841189 |
| P356 | DOI | 10.1038/352800A0 |
| P698 | PubMed publication ID | 1652692 |
| P5875 | ResearchGate publication ID | 21502428 |
| P2093 | author name string | Tanabe T | |
| Adams BA | |||
| Beam KG | |||
| Numa S | |||
| P2860 | cites work | A quantitative description of membrane current and its application to conduction and excitation in nerve | Q22337072 |
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| Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel | Q34661325 | ||
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| Pursuing the structure and function of voltage-gated channels | Q36581941 | ||
| Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs | Q41200795 | ||
| Mutant potassium channels with altered binding of charybdotoxin, a pore-blocking peptide inhibitor | Q43473554 | ||
| Alteration of ionic selectivity of a K+ channel by mutation of the H5 region | Q44911109 | ||
| Exchange of conduction pathways between two related K+ channels | Q48793795 | ||
| Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling. | Q51728761 | ||
| A single point mutation confers tetrodotoxin and saxitoxin insensitivity on the sodium channel II. | Q51744647 | ||
| Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel. | Q52448076 | ||
| Structural parts involved in activation and inactivation of the sodium channel | Q59072056 | ||
| Cardiac-type excitation-contraction coupling in dysgenic skeletal muscle injected with cardiac dihydropyridine receptor cDNA | Q59095343 | ||
| Kinetic analysis of the sodium gating current in the squid giant axon | Q68092686 | ||
| Mutations affecting TEA blockade and ion permeation in voltage-activated K+ channels | Q68568921 | ||
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| P433 | issue | 6338 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 800-803 | |
| P577 | publication date | 1991-08-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics. | |
| P478 | volume | 352 |
| Q40493220 | 2 Regulation of calcium channels in the heart |
| Q48943512 | A mutation affecting dihydropyridine-sensitive current levels and activation kinetics in Drosophila muscle and mammalian heart calcium channels. |
| Q24642407 | Activation of Shaker potassium channels. III. An activation gating model for wild-type and V2 mutant channels |
| Q49080719 | Alteration of channel characteristics by exchange of pore-forming regions between two structurally related Ca2+ channels |
| Q35234567 | Apparent lack of physical or functional interaction between CaV1.1 and its distal C terminus |
| Q40761724 | Application of patch clamp methods to the study of calcium currents and calcium channels |
| Q36435629 | Bay K 8644 reveals two components of L-type Ca2+ channel current in clonal rat pituitary cells |
| Q35103866 | Biochemical evidence for a complex involving dihydropyridine receptor and ryanodine receptor in triad junctions of skeletal muscle |
| Q34040093 | Ca2+ current activation rate correlates with alpha 1 subunit density |
| Q81359824 | Ca2+/CaM-dependent inactivation of the skeletal muscle L-type Ca2+ channel (Cav1.1) |
| Q71513508 | Calcium current reactivation after flash photolysis of nifedipine in skeletal muscle fibres of the frog |
| Q31879451 | Calcium currents and arrhythmias: insights from molecular biology |
| Q34088670 | Charge movement and SR calcium release in frog skeletal muscle can be related by a Hodgkin-Huxley model with four gating particles |
| Q49048781 | Chimeric L-type Ca2+ channels expressed in Xenopus laevis oocytes reveal role of repeats III and IV in activation gating |
| Q52205572 | Co-expression in CHO cells of two muscle proteins involved in excitation-contraction coupling. |
| Q34180598 | Control of ion conduction in L-type Ca2+ channels by the concerted action of S5-6 regions. |
| Q37558500 | Critical roles of the S3 segment and S3-S4 linker of repeat I in activation of L-type calcium channels |
| Q34170119 | Differential regulation of skeletal muscle L-type Ca2+ current and excitation-contraction coupling by the dihydropyridine receptor beta subunit |
| Q44101904 | Dissociation of charge movement from calcium release and calcium current in skeletal myotubes by gabapentin |
| Q42128833 | Divergent biophysical properties, gating mechanisms, and possible functions of the two skeletal muscle Ca(V)1.1 calcium channel splice variants |
| Q35902607 | Domain III regulates N-type (CaV2.2) calcium channel closing kinetics |
| Q48907500 | Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes |
| Q52519047 | Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor. |
| Q45009232 | External Ca(2+)-dependent excitation--contraction coupling in a population of ageing mouse skeletal muscle fibres. |
| Q36237030 | Formation of triads without the dihydropyridine receptor alpha subunits in cell lines from dysgenic skeletal muscle |
| Q59054369 | Function of a truncated dihydropyridine receptor as both voltage sensor and calcium channel |
| Q33801924 | Functional expression of transgenic 1sDHPR channels in adult mammalian skeletal muscle fibres |
| Q36444962 | Functional impact of the ryanodine receptor on the skeletal muscle L-type Ca(2+) channel |
| Q22008539 | Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H |
| Q35228568 | Heterologous expression of calcium channels |
| Q36824454 | Impaired gating of an L-Type Ca(2+) channel carrying a mutation linked to malignant hyperthermia |
| Q34171879 | Involvement of the carboxy-terminus region of the dihydropyridine receptor beta1a subunit in excitation-contraction coupling of skeletal muscle |
| Q36415673 | Isolation of myocardial L-type calcium channel gating currents with the spider toxin omega-Aga-IIIA. |
| Q41464028 | Kinetic properties of skeletal-muscle-like high-threshold calcium currents in a non-fusing muscle cell line |
| Q52222555 | Kinetics of inactivation and restoration from inactivation of the L-type calcium current in human myotubes. |
| Q46844233 | L-type Ca2+ channel function and expression in neonatal rabbit ventricular myocytes |
| Q36435633 | L-type Ca2+ channels access multiple open states to produce two components of Bay K 8644-dependent current in GH3 cells |
| Q38175138 | L-type CaV1.2 calcium channels: from in vitro findings to in vivo function. |
| Q73388759 | L-type calcium current activation in cultured human myotubes |
| Q34285881 | Malignant hyperthermia and excitation-contraction coupling |
| Q71755457 | Modulation of Ca2+ channels, charge movement and Ca2+ transients by heparin in frog skeletal muscle fibres |
| Q67510158 | Modulation of calcium current gating in frog skeletal muscle by conditioning depolarization |
| Q40124922 | Molecular Interactions in the Voltage Sensor Controlling Gating Properties of CaV Calcium Channels |
| Q34089132 | Molecular analysis of voltage dependence of heterotypic gap junctions formed by connexins 26 and 32 |
| Q40950178 | Molecular biology of calcium channels |
| Q48022935 | Molecular cloning and functional expression of a skeletal muscle dihydropyridine receptor from Rana catesbeiana |
| Q40532102 | Molecular determinants of Ca2+ channel function and drug action |
| Q30311272 | Molecular dissection of functional domains of the E1E2-ATPase using sodium and calcium pump chimeric molecules |
| Q34168362 | Molecular origin of the L-type Ca2+ current of skeletal muscle myotubes selectively deficient in dihydropyridine receptor beta1a subunit |
| Q34350397 | Multiple loops of the dihydropyridine receptor pore subunit are required for full-scale excitation-contraction coupling in skeletal muscle |
| Q71437930 | Periodic paralysis and voltage-gated ion channels |
| Q35388651 | Pore stability and gating in voltage-activated calcium channels |
| Q36445185 | Potentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms |
| Q73300474 | Prolonged depolarization promotes fast gating kinetics of L-type Ca2+ channels in mouse skeletal myotubes |
| Q71513406 | Properties and roles of an intramembranous charge mobilized at high voltages in frog skeletal muscle |
| Q37945102 | Reciprocal dihydropyridine and ryanodine receptor interactions in skeletal muscle activation |
| Q42976855 | Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors |
| Q48879089 | Role of Repeat I in the fast inactivation kinetics of the Ca(V)2.3 channel |
| Q33915557 | Role of S4 segments and the leucine heptad motif in the activation of an L-type calcium channel |
| Q36436215 | Role of calcium permeation in dihydropyridine receptor function. Insights into channel gating and excitation-contraction coupling |
| Q36411941 | Role of the S4 in cooperativity of voltage-dependent potassium channel activation |
| Q42635265 | Serine residue in the IIIS5-S6 linker of the L-type Ca2+ channel alpha 1C subunit is the critical determinant of the action of dihydropyridine Ca2+ channel agonists |
| Q36411441 | Shaker potassium channel gating. III: Evaluation of kinetic models for activation |
| Q36411629 | Single calcium channel behavior in native skeletal muscle |
| Q41524977 | Stable and functional expression of the calcium channel alpha 1 subunit from smooth muscle in somatic cell lines |
| Q44400229 | Store operated Ca2+ influx by selective depletion of ryanodine sensitive Ca2+ pools in primary human skeletal muscle cells |
| Q41710008 | Structural and functional modularity of voltage-gated potassium channels |
| Q38660530 | Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorder |
| Q30433407 | Structural determinants of the high affinity extracellular zinc binding site on Cav3.2 T-type calcium channels |
| Q24537292 | Structural elements in domain IV that influence biophysical and pharmacological properties of human alpha1A-containing high-voltage-activated calcium channels |
| Q41460054 | Structure and function of voltage-dependent calcium channels from muscle |
| Q33907400 | The S5-S6 linker of repeat I is a critical determinant of L-type Ca2+ channel conductance |
| Q34179200 | The structure of Ca(2+) release units in arthropod body muscle indicates an indirect mechanism for excitation-contraction coupling |
| Q70901399 | Transfer of 1,4-dihydropyridine sensitivity from L-type to class A (BI) calcium channels |
| Q24290849 | Triad proteins and intracellular Ca2+ transients during development of human skeletal muscle cells in aneural and innervated cultures |
| Q36416036 | Unitary behavior of skeletal, cardiac, and chimeric L-type Ca2+ channels expressed in dysgenic myotubes |
| Q49064887 | Voltage-dependent inactivation in a cardiac-skeletal chimeric calcium channel |
| Q59530617 | Voltage-gated calcium channels, calcium signaling, and channelopathies |
| Q35224872 | Voltage-sensitive Ca2+ channels |
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