scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1469-7793.2001.00343.X |
P8608 | Fatcat ID | release_3dky4cixnvg4lplcirrl7oejxu |
P932 | PMC publication ID | 2278716 |
P698 | PubMed publication ID | 11454955 |
P5875 | ResearchGate publication ID | 25937181 |
P2093 | author name string | B Constantin | |
C Cognard | |||
C Vandebrouck | |||
G Raymond | |||
A A Hassoni | |||
M J Cullen | |||
G Duport | |||
N Imbert | |||
P2860 | cites work | Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H | Q22008539 |
Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches | Q22337395 | ||
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 | Q24676753 | ||
A new generation of Ca2+ indicators with greatly improved fluorescence properties | Q27860793 | ||
A calcium channel mutation causing hypokalemic periodic paralysis | Q28242375 | ||
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis | Q28243593 | ||
Dystrophin: the protein product of the Duchenne muscular dystrophy locus | Q29618077 | ||
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 vitro | Q36787204 | ||
Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsies | Q39486051 | ||
Cationic channels in normal and dystrophic human myotubes | Q42641718 | ||
A third type of calcium current in cultured human skeletal muscle cells | Q43477626 | ||
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface | Q44350613 | ||
Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: importance of dorsal root ganglia for achieving successful functional innervation | Q46104282 | ||
Comparison of the muscle fiber diameter and satellite cell frequency in human muscle biopsies | Q48207385 | ||
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 fibres | Q54265713 | ||
Calcium currents in normal and dystrophic human skeletal muscle cells in culture | Q68640904 | ||
Human myotube differentiation in vitro in different culture conditions | Q70014686 | ||
Hypoosmotic shocks induce elevation of resting calcium level in Duchenne muscular dystrophy myotubes contracting in vitro | Q71822775 | ||
Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubes | Q71998269 | ||
Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres | Q72111438 | ||
L-type calcium current activation in cultured human myotubes | Q73388759 | ||
The effect of methylprednisolone on intracellular calcium of normal and dystrophic human skeletal muscle cells | Q78076761 | ||
P433 | issue | Pt. 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Duchenne muscular dystrophy | Q1648484 |
P304 | page(s) | 343-55 | |
P577 | publication date | 2001-07-15 | |
P1433 | published in | Journal of Physiology | Q7743612 |
P1476 | title | Calcium currents and transients in co-cultured contracting normal and Duchenne muscular dystrophy human myotubes | |
P478 | volume | 534 |
Q36221574 | Expression analysis in multiple muscle groups and serum reveals complexity in the microRNA transcriptome of the mdx mouse with implications for therapy |
Q36530917 | Functional classification of skeletal muscle networks. II. Applications to pathophysiology |
Q77959497 | Hypotonic medium increases calcium permeant channels activity in human normal and dystrophic myotubes |
Q40542404 | Improvement of calcium handling and changes in calcium-release properties after mini- or full-length dystrophin forced expression in cultured skeletal myotubes |
Q27438151 | Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression |
Q41882302 | Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers |
Q33339391 | L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle |
Q35682302 | Low-voltage-activated ("T-Type") calcium channels in review |
Q24679517 | Mechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubes |
Q33647871 | Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle |
Q36295558 | Mini-dystrophin expression down-regulates overactivation of G protein-mediated IP3 signaling pathway in dystrophin-deficient muscle cells. |
Q44640506 | Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice. |
Q44122960 | Na(+)/Ca(2+) exchange in human myotubes: intracellular calcium rises in response to external sodium depletion are enhanced in DMD. |
Q36560597 | New insights in the regulation of calcium transfers by muscle dystrophin-based cytoskeleton: implications in DMD. |
Q35069506 | Nifedipine treatment reduces resting calcium concentration, oxidative and apoptotic gene expression, and improves muscle function in dystrophic mdx mice |
Q34755164 | Partial block by riluzole of muscle sodium channels in myotubes from amyotrophic lateral sclerosis patients. |
Q34807169 | Pre-clinical trials in Duchenne dystrophy: what animal models can tell us about potential drug effectiveness |
Q39790252 | Regulation of TRPC1 and TRPC4 cation channels requires an alpha1-syntrophin-dependent complex in skeletal mouse myotubes. |
Q39982403 | Role for stress fiber contraction in surface tension development and stretch-activated channel regulation in C2C12 myoblasts. |
Q37930824 | The role of in vivo Ca²⁺ signals acting on Ca²⁺-calmodulin-dependent proteins for skeletal muscle plasticity |
Search more.