Voltage-dependent L-type calcium channel subunit alpha-1S
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P129
P688
Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction couplingM-calpain levels increase during fusion of myoblasts in the mutant muscular dysgenesis (mdg) mouseElectrical properties of normal and dysgenic mouse skeletal muscle in cultureMuscle and nerve in muscular dysgenesis in the mouse at birth: sprouting and multiple innervationModification of mitochondrial metabolism in fibroblasts from mice with a skeletal muscle mutation (muscular dysgenesis). Evidence of embryonic communication between myoblasts and fibroblastsRegulation of myogenesis in paralyzed muscles in the mouse mutants peroneal muscular atrophy and muscular dysgenesisRestoration of normal ultrastructure after expression of the alpha 1 subunit of the L-type Ca2+ channel in dysgenic myotubesFine structure of mutant (muscular dysgenesis) embryonic mouse muscleDEVELOPMENTAL GENETICS OF A LETHAL MUTATION, MUSCULAR DYSGENESIS (MDG), IN THE MOUSE. II. DEVELOPMENTAL ANALYSISElimination by necrosis, not apoptosis, of embryonic extraocular muscles in the muscular dysgenesis mutant of the mouseTissue culture study of murine muscular dysgenesis: role of spontaneous action potential generation in the regulation of muscle maturationExtensive nerve overgrowth and paucity of the tailed asymmetric form (16 S) of acetylcholinesterase in the developing skeletal neuromuscular system of the dysgenic (mdg/mdg) mouseCa2+ sparks in embryonic mouse skeletal muscle selectively deficient in dihydropyridine receptor alpha1S or beta1a subunits.DEVELOPMENTAL GENETICS OF A LETHAL MUTATION, MUSCULAR DYSGENESIS (MDG), IN THE MOUSE. I. GENETIC ANALYSIS AND GROSS MORPHOLOGYType 3 and type 1 ryanodine receptors are localized in triads of the same mammalian skeletal muscle fibersA lethal mutation in mice eliminates the slow calcium current in skeletal muscle cellsCa2+ influx through alpha1S DHPR may play a role in regulating Ca2+ release from RyR1 in skeletal muscleEndogenous cardiac Ca2+ channels do not overcome the E-C coupling defect in immortalized dysgenic muscle cells: evidence for a missing linkNeurons induce contractions in myotubes containing only muscular dysgenic nucleiDisease expression in +-/+- ----mdg/mdg mouse chimeras: evidence for an extramuscular component in the pathogenesis of both dysgenic abnormal diaphragm innervation and skeletal muscle 16 S acetylcholinesterase deficiencyDistribution and quantification of ACh receptors and innervation in diaphragm muscle of normal and mdg mouse embryosBarium currents in developing skeletal muscle cells of normal and mutant mice foetuses with 'muscular dysgenesis'The Ca2+ channel alpha2delta-1 subunit determines Ca2+ current kinetics in skeletal muscle but not targeting of alpha1S or excitation-contraction couplingEffects of the muscular dysgenesis gene on developmental stability in the mouse mandibleRelationship of genotype and in vitro contractility in mdg/mdg in equilibrium +/+ "mosaic" myotubesA single nucleotide deletion in the skeletal muscle-specific calcium channel transcript of muscular dysgenesis (mdg) miceA novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle.
P921
Q24680364-6F13A802-98C0-49FE-ADC5-CFFFAE13CE77Q28507733-58B52B32-5AA6-420D-BF76-2BC3C69C79C8Q28508591-008005D1-7FA8-488D-8707-066218B4D590Q28512350-6A1A3F7B-7BBB-4608-90D4-EF0C6F5EF1EEQ28513413-C21978D6-C4A8-4BA1-8847-3EFAE97046AFQ28513639-52AA4961-6519-488C-A2F7-2D4599FE055CQ28513694-DCD378CB-122E-4939-8D3F-BCF18DBA1561Q28513981-2A40998C-712F-421C-AF3B-9746413EC194Q28584771-1DDB2CD1-4028-4CD1-9788-223028620F41Q28584791-5E82C335-C112-45A2-BAF6-B753490817C8Q28584920-818ACE27-3C72-40EE-B08F-956BD4D850CEQ28585298-5311FDD4-0DF5-47EC-B408-EA6409414393Q28585470-B5E6DD99-2E88-4F49-9372-18CB4F2236D7Q28585851-C5399A34-6A71-4F9F-8E24-710F8375F0B8Q28586235-C719B0BE-5EE5-4115-A79E-ADFD6635F70EQ28586651-CCFFB01C-E0AD-4474-930C-A7A705CE9A89Q28588006-854C503B-2BD0-45D2-B7C5-95F2C1D5CF12Q28588243-C6B8502A-EC36-436A-9B8E-AB9BCF18EA5EQ28589518-B5589E95-864C-4CDC-A95E-FDE54F8FAB27Q28590428-819CBF0B-A4D6-4D3D-8511-FA7887F81D70Q28591990-F30CE9F8-CE1C-4CEE-A1A4-202713C5E7E3Q28592184-D8DAD803-9F39-4C84-A8D3-5FC6A889813BQ28593153-2E4F2BFF-CDA6-45C7-ABE0-1718E19A3038Q28593869-579D5B08-72B9-4719-AD88-AAED6E22E66BQ28594389-6A028BAF-C3AC-4D3B-B2EB-50639C8264C6Q28594476-A0F4CF90-1C33-47C3-AC1B-8B1BEAEEE685Q35951670-6EE6A48A-F7D0-4FF5-88B5-147FC96AC65D
P921
Voltage-dependent L-type calcium channel subunit alpha-1S
description
mouse protein (annotated by UniProtKB/Swiss-Prot Q02789)
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proteinë
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proteïne
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بروتين في فأر المنازل
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name
Voltage-dependent L-type calcium channel subunit alpha-1S
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type
label
Voltage-dependent L-type calcium channel subunit alpha-1S
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altLabel
Calcium channel, L type, alpha-1 polypeptide, isoform 3, skeletal muscle
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Voltage-gated calcium channel subunit alpha Cav1.1
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prefLabel
Voltage-dependent L-type calcium channel subunit alpha-1S
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