Formation of triads without the dihydropyridine receptor alpha subunits in cell lines from dysgenic skeletal muscle
about
Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction couplingTowards a Unified Theory of Calmodulin Regulation (Calmodulation) of Voltage-Gated Calcium and Sodium ChannelsType 3 and type 1 ryanodine receptors are localized in triads of the same mammalian skeletal muscle fibersThe Ca2+ channel alpha2delta-1 subunit determines Ca2+ current kinetics in skeletal muscle but not targeting of alpha1S or excitation-contraction couplingSTAC3 stably interacts through its C1 domain with CaV1.1 in skeletal muscle triadsA carboxyl-terminal region important for the expression and targeting of the skeletal muscle dihydropyridine receptor.Electrical coupling between the human serotonin transporter and voltage-gated Ca(2+) channels.Non-Ca2+-conducting Ca2+ channels in fish skeletal muscle excitation-contraction coupling.Activity and calcium regulate nuclear targeting of the calcium channel beta4b subunit in nerve and muscle cellsRecovery of Ca2+ current, charge movements, and Ca2+ transients in myotubes deficient in dihydropyridine receptor beta 1 subunit transfected with beta 1 cDNA.Cooperation of two-domain Ca(2+) channel fragments in triad targeting and restoration of excitation- contraction coupling in skeletal muscle.IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibersCardiac-type EC-coupling in dysgenic myotubes restored with Ca2+ channel subunit isoforms alpha1C and alpha1D does not correlate with current densityFunctional interaction of CaV channel isoforms with ryanodine receptors studied in dysgenic myotubesThe juvenile myoclonic epilepsy mutant of the calcium channel β(4) subunit displays normal nuclear targeting in nerve and muscle cells.Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavalpha1S-subunit.N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy.T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases.Computer modeling of siRNA knockdown effects indicates an essential role of the Ca2+ channel alpha2delta-1 subunit in cardiac excitation-contraction coupling.Excitation-contraction coupling is unaffected by drastic alteration of the sequence surrounding residues L720-L764 of the alpha 1S II-III loop.Association of calcium channel alpha1S and beta1a subunits is required for the targeting of beta1a but not of alpha1S into skeletal muscle triads.Coordinated incorporation of skeletal muscle dihydropyridine receptors and ryanodine receptors in peripheral couplings of BC3H1 cells.Role of ryanodine receptors in the assembly of calcium release units in skeletal muscleDihydropyridine receptors as voltage sensors for a depolarization-evoked, IP3R-mediated, slow calcium signal in skeletal muscle cellsA CaV1.1 Ca2+ channel splice variant with high conductance and voltage-sensitivity alters EC coupling in developing skeletal muscle.Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit.Differential neuronal targeting of a new and two known calcium channel β4 subunit splice variants correlates with their regulation of gene expressionDifferential contribution of skeletal and cardiac II-III loop sequences to the assembly of dihydropyridine-receptor arrays in skeletal muscle.Mechanobiology of embryonic skeletal development: Insights from animal modelsPhysiological and pharmacological modulation of the embryonic skeletal muscle calcium channel splice variant CaV1.1eDihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.The proximal C-terminus of α(1C) subunits is necessary for junctional membrane targeting of cardiac L-type calcium channels.Voltage-activated calcium signals in myotubes loaded with high concentrations of EGTA.Slow calcium signals after tetanic electrical stimulation in skeletal myotubes.Voltage-controlled Ca2+ release and entry flux in isolated adult muscle fibres of the mouse.Structural requirements of the dihydropyridine receptor alpha1S II-III loop for skeletal-type excitation-contraction coupling.Insertion of the full-length calcium channel alpha(1S) subunit into triads of skeletal muscle in vitro.Calcium currents and transients of native and heterologously expressed mutant skeletal muscle DHP receptor alpha1 subunits (R528H)The mammalian skeletal muscle DHPR has larger Ca2+ conductance and is phylogenetically ancient to the early ray-finned fish sterlet (Acipenser ruthenus).The triad targeting signal of the skeletal muscle calcium channel is localized in the COOH terminus of the alpha(1S) subunit
P2860
Q24680364-DDD95258-902D-425B-9B59-D1748C71D0C1Q27002550-3EDAD74C-B2D2-49FC-B752-C7D8445EAE68Q28586235-42B8539E-22D6-4ABA-B60F-2E788EBEED8BQ28593153-6BDD0289-95A1-4B01-84FC-09F309495857Q30008782-9E32DE13-F286-4224-AB9A-85C90640239AQ30868788-869BBB95-9985-447D-9D69-A04EA93DFC4FQ33736971-BC551E0E-D8B1-45F6-AA30-8AA7EDF24ADFQ33778038-0DB18ACC-710E-4016-B134-44EF6F20A34EQ33785664-06B70BBF-E621-4B0F-9594-E5E1E02C65A4Q33907194-FDEFB2BA-C330-451B-8335-27E7F244CDB3Q34099532-0B728C03-5BAC-431E-82FE-51C30643D559Q34161447-D0C599AE-FE6B-4009-B910-32CBFAB87811Q34181475-3760F6EA-4A4E-45AC-BA5F-26AF58DD0077Q34189364-2161397A-4C8A-43E0-9B24-92EEBA0FB5FAQ34373916-75251308-902A-47D0-8876-99895AE9FF8EQ34426471-E15B22D2-2772-46E6-BC7C-EC3DFA8BFB2BQ34542692-162FDD1A-340E-46E2-BA76-A9D74B533BD9Q35166273-E2EA3FEA-7FD6-42E0-9BB2-D95ACDCAF6B2Q35864999-6EF79453-F4D0-41AC-B8B7-75622AFE8168Q35901193-21EEDD20-A4D1-44F3-9908-AE65A84155B6Q36063022-D67D6017-03F9-4B6D-B084-BD177AEC2BD7Q36273983-4144913B-864B-43A1-B02C-E2FC1C1C2E81Q36276654-A9158CF0-B6D1-40E1-842C-39F0C51B0755Q36412364-57BDD2AE-BA1C-43F9-96D6-3CB383EC8FEEQ37260318-8E181E50-7C2D-402E-B92D-8E922CF2170AQ37264390-53758FCE-EDCD-416D-B6A7-3C9A27202321Q37502534-EC09731D-190B-45A6-874F-736DF5F165E8Q37657281-8B5A8160-BC54-496F-B4C3-46DF869C2435Q37791099-9F6E5374-82B9-4403-9E4A-2EE2D1E422FDQ38900957-DBA2FD2E-33EE-4559-94CE-0290E6DA51AFQ39067296-4D0CC6A1-016A-48FB-BF26-F7B71FC9063AQ39289429-6EC3C539-CC0C-42EE-BECD-C897762B9749Q40229264-5A6F628A-8C83-424E-AF1A-CEA8CA3B825FQ40281271-45D697ED-1796-4112-BF36-8F8D0A689845Q40470361-307CF2D9-6EA4-440F-9CDC-F64C2AA75AB3Q40615240-F1D8E71D-DE62-4AA6-BB21-1570388CC602Q40877344-3E75BC88-143E-4EB4-81F3-A198A9FA7AE4Q41057145-62C212F6-268D-446A-853C-0FCE19B08EEFQ41199019-F834CA75-8F5B-49E9-AE68-CB0F209C8CA1Q42057968-43BC4CDF-4EF3-4A0E-9672-10788089BC3F
P2860
Formation of triads without the dihydropyridine receptor alpha subunits in cell lines from dysgenic skeletal muscle
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Formation of triads without th ...... from dysgenic skeletal muscle
@ast
Formation of triads without th ...... from dysgenic skeletal muscle
@en
type
label
Formation of triads without th ...... from dysgenic skeletal muscle
@ast
Formation of triads without th ...... from dysgenic skeletal muscle
@en
prefLabel
Formation of triads without th ...... from dysgenic skeletal muscle
@ast
Formation of triads without th ...... from dysgenic skeletal muscle
@en
P2860
P356
P1476
Formation of triads without th ...... from dysgenic skeletal muscle
@en
P2093
J A Powell
L Petherbridge
P2860
P304
P356
10.1083/JCB.134.2.375
P407
P577
1996-07-01T00:00:00Z