Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes (Q28344004)

2

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G Duport

3

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G Raymond

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A A Hassoni

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B Constantin

6

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M J Cullen

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C Cognard

Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H

8

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language of work or name

English

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publication date

15 July 2001

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published in

Journal of Physiology

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volume

534

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issue

Pt. 2

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page(s)

343-55

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cites work

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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 muscle

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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

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A calcium channel mutation causing hypokalemic periodic paralysis

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A new generation of Ca2+ indicators with greatly improved fluorescence properties

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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Abnormal calcium homeostasis in Duchenne muscular dystrophy myotubes contracting in vitro

7 April 2017

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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.

29 September 2017

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Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsies

29 September 2017

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Kinetics of inactivation and restoration from inactivation of the L-type calcium current in human myotubes.

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Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: importance of dorsal root ganglia for achieving successful functional innervation

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Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface

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Ca2+ current and charge movement in adult single human skeletal muscle fibres

2 June 2018

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Comparison of the muscle fiber diameter and satellite cell frequency in human muscle biopsies.

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https://api.crossref.org/works/10.1111%2FJ.1469-7793.2001.00343.X

Cationic channels in normal and dystrophic human myotubes

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Appearance and evolution of calcium currents and contraction during the early post-fusional stages of rat skeletal muscle cells developing in primary culture.

21 January 2018

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The effect of methylprednisolone on intracellular calcium of normal and dystrophic human skeletal muscle cells

27 November 2018

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12 December 2020

Human myotube differentiation in vitro in different culture conditions

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12 December 2020

Calcium currents in normal and dystrophic human skeletal muscle cells in culture

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12 December 2020

Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres

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12 December 2020

Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubes

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12 December 2020

Hypoosmotic shocks induce elevation of resting calcium level in Duchenne muscular dystrophy myotubes contracting in vitro

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12 December 2020

L-type calcium current activation in cultured human myotubes

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12 December 2020