Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Clarisse Fuster"'
Autor:
Romane Idoux, Pierre Charnet, Manfred Grabner, Clarisse Fuster, Anamika Dayal, Vincent Jacquemond, Bruno Allard
Publikováno v:
Cell Calcium
Cell Calcium, Elsevier, 2020
Cell Calcium, Elsevier, 2020
In response to excitation of skeletal muscle fibers, trains of action potentials induce changes in the configuration of the dihydropyridine receptor (DHPR) anchored in the tubular membrane which opens the Ca2+ release channel in the sarcoplasmic reti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77df887f2d227c112cd945418c877ec1
https://hal.archives-ouvertes.fr/hal-03001292
https://hal.archives-ouvertes.fr/hal-03001292
Autor:
Romane, Idoux, Clarisse, Fuster, Vincent, Jacquemond, Anamika, Dayal, Manfred, Grabner, Pierre, Charnet, Bruno, Allard
Publikováno v:
Cell calcium. 91
In response to excitation of skeletal muscle fibers, trains of action potentials induce changes in the configuration of the dihydropyridine receptor (DHPR) anchored in the tubular membrane which opens the Ca
Publikováno v:
American Journal of Physiology-Cell Physiology. 315:C776-C779
High metabolic activity and existence of a large transmembrane inward electrochemical gradient for H+ at rest promote intracellular acidification of skeletal muscle. Exchangers and cotransports efficiently contend against accumulation of intracellula
Autor:
Clarisse Fuster, Bruno Allard
Publikováno v:
The Journal of Physiology. 596:2019-2027
Patients suffering from type 1 hypokalaemic periodic paralysis (HypoPP1) experience attacks of muscle paralysis associated with hypokalaemia. The disease arises from missense mutations in the gene encoding the α1 subunit of the dihydropyridine recep
Publikováno v:
The Journal of Physiology. 595:6417-6428
Key points Missense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage-gated Ca2+ channel induce type 1 hypokalaemic periodic paralysis, a poorly understood neuromuscular disease characterized by episodic attacks of paralys
Na leak with gating pore properties in hypokalemic periodic paralysis V876E mutant muscle Ca channel
Autor:
Pierre Charnet, Vincent Jacquemond, Bruno Allard, Christine Berthier, Jimmy Perrot, Clarisse Fuster
Publikováno v:
The Journal of General Physiology
The V876E mutation in the muscle voltage-gated Ca2+ channel induces hypokalemic periodic paralysis. Fuster et al. show that the mutation generates strong resting inward leak Na+ currents even though it is not located in the voltage sensor segments.
Publikováno v:
Les Cahiers de Myologie. :63-65
La Paralysie Periodique Hypokaliemique de type 1 (HypoPPl) est une maladie neuromusculaire caracterisee par des crises de paralysies musculaires transitoires pouvant durer de quelques heures a quelques jours et associees a une hypokaliemie. Ces paral
Publikováno v:
American journal of physiology. Cell physiology. 315(5)
High metabolic activity and existence of a large transmembrane inward electrochemical gradient for H
Publikováno v:
The Journal of General Physiology
Missense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage-gated CaMissense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage-gated Ca
Autor:
François Seghers, Clarisse Fuster, Yuko Iwata, Olivier Schakman, Bruno Allard, Marie de Clippele, Inès Dufour, Nicolas Tajeddine, Nadège Zanou, Philippe Gailly, Thomas Voets, Ludivine Mondin, Shigeo Wakabayashi
Increased plasma osmolarity induces intracellular water depletion and cell shrinkage (CS) followed by activation of a regulatory volume increase (RVI). In skeletal muscle, the hyperosmotic shock-induced CS is accompanied by a small membrane depolariz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69b7a7af390ea763c6f564b9d1d6f707
https://europepmc.org/articles/PMC4575573/
https://europepmc.org/articles/PMC4575573/