Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes

scientific article

Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/J.1469-7793.2001.00343.X
P8608Fatcat IDrelease_3dky4cixnvg4lplcirrl7oejxu
P932PMC publication ID2278716
P698PubMed publication ID11454955
P5875ResearchGate publication ID25937181

P2093author name stringB Constantin
C Cognard
C Vandebrouck
G Raymond
A A Hassoni
M J Cullen
G Duport
N Imbert
P2860cites workGating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528HQ22008539
Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patchesQ22337395
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 muscleQ24676753
A new generation of Ca2+ indicators with greatly improved fluorescence propertiesQ27860793
A calcium channel mutation causing hypokalemic periodic paralysisQ28242375
Dihydropyridine receptor mutations cause hypokalemic periodic paralysisQ28243593
Dystrophin: the protein product of the Duchenne muscular dystrophy locusQ29618077
Changes in cytosolic resting ionized calcium level and in calcium transients during in vitro development of normal and Duchenne muscular dystrophy cultured skeletal muscle measured by laser cytofluorimetry using indo-1.Q36773101
Abnormal calcium homeostasis in Duchenne muscular dystrophy myotubes contracting in vitroQ36787204
Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsiesQ39486051
Cationic channels in normal and dystrophic human myotubesQ42641718
A third type of calcium current in cultured human skeletal muscle cellsQ43477626
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surfaceQ44350613
Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: importance of dorsal root ganglia for achieving successful functional innervationQ46104282
Comparison of the muscle fiber diameter and satellite cell frequency in human muscle biopsiesQ48207385
Kinetics of inactivation and restoration from inactivation of the L-type calcium current in human myotubes.Q52222555
Appearance and evolution of calcium currents and contraction during the early post-fusional stages of rat skeletal muscle cells developing in primary culture.Q52226680
Ca2+ current and charge movement in adult single human skeletal muscle fibresQ54265713
Calcium currents in normal and dystrophic human skeletal muscle cells in cultureQ68640904
Human myotube differentiation in vitro in different culture conditionsQ70014686
Hypoosmotic shocks induce elevation of resting calcium level in Duchenne muscular dystrophy myotubes contracting in vitroQ71822775
Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubesQ71998269
Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibresQ72111438
L-type calcium current activation in cultured human myotubesQ73388759
The effect of methylprednisolone on intracellular calcium of normal and dystrophic human skeletal muscle cellsQ78076761
P433issuePt. 2
P407language of work or nameEnglishQ1860
P921main subjectDuchenne muscular dystrophyQ1648484
P304page(s)343-55
P577publication date2001-07-15
P1433published inJournal of PhysiologyQ7743612
P1476titleCalcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes
P478volume534

Reverse relations

cites work (P2860)
Q36221574Expression analysis in multiple muscle groups and serum reveals complexity in the microRNA transcriptome of the mdx mouse with implications for therapy
Q36530917Functional classification of skeletal muscle networks. II. Applications to pathophysiology
Q77959497Hypotonic medium increases calcium permeant channels activity in human normal and dystrophic myotubes
Q40542404Improvement of calcium handling and changes in calcium-release properties after mini- or full-length dystrophin forced expression in cultured skeletal myotubes
Q27438151Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression
Q41882302Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers
Q33339391L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle
Q35682302Low-voltage-activated ("T-Type") calcium channels in review
Q24679517Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes
Q33647871Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle
Q36295558Mini-dystrophin expression down-regulates overactivation of G protein-mediated IP3 signaling pathway in dystrophin-deficient muscle cells.
Q44640506Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice.
Q44122960Na(+)/Ca(2+) exchange in human myotubes: intracellular calcium rises in response to external sodium depletion are enhanced in DMD.
Q36560597New insights in the regulation of calcium transfers by muscle dystrophin-based cytoskeleton: implications in DMD.
Q35069506Nifedipine treatment reduces resting calcium concentration, oxidative and apoptotic gene expression, and improves muscle function in dystrophic mdx mice
Q34755164Partial block by riluzole of muscle sodium channels in myotubes from amyotrophic lateral sclerosis patients.
Q34807169Pre-clinical trials in Duchenne dystrophy: what animal models can tell us about potential drug effectiveness
Q39790252Regulation of TRPC1 and TRPC4 cation channels requires an alpha1-syntrophin-dependent complex in skeletal mouse myotubes.
Q39982403Role for stress fiber contraction in surface tension development and stretch-activated channel regulation in C2C12 myoblasts.
Q37930824The role of in vivo Ca²⁺ signals acting on Ca²⁺-calmodulin-dependent proteins for skeletal muscle plasticity

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