Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Gérard Duport"'
Publikováno v:
Neuromuscular Disorders. 11:72-79
Human skeletal muscle cells obtained from normal and Duchenne muscular dystrophy patients were cocultured with explants of rat dorsal root ganglions. Single-channel recordings were performed with the cell-attached configuration of the patch-clamp tec
Autor:
Guy Raymond, Gérard Duport, Clarissre Vandebrouck, Nathalie Imbert, Christian Cognard, C Guillou, Bruno Constantin
Publikováno v:
Neuromuscular Disorders. 6:351-360
In Duchenne muscular dystrophy (DMD) muscle cells which lack dystrophin, contraction seems to be a dominant factor contributing to the abnormal elevated intracellular calcium level. Human normal and DMD contracting myotubes cocultured with nervous ce
Autor:
Capucine Thirault, Pierre Pries, John R. Bach, Nicolas Fons, Yves Rideau, Alice Renardel-Irani, Gérard Duport, Etienne Gayet
Publikováno v:
Seminars in Neurology. 15:29-37
Publikováno v:
Cell Calcium. 11:507-514
Human muscle cells obtained from biopsy specimens were grown in a primary culture system and electrophysiologically studied. Whole cell patch-clamp recordings revealed the presence of two types of calcium currents: (i) a low-threshold (-60 mV) one (I
Publikováno v:
Neuroscience letters. 323(3)
Duchenne muscular dystrophy (DMD) is characterized by the absence of dystrophin and an elevated intracellular calcium level. Single-channel recordings were performed with the cell-attached configuration of the patch-clamp technique. The present study
Autor:
Nathalie Imbert, Guy Raymond, Bruno Constantin, Christian Cognard, Clarisse Vandebrouck, Gérard Duport
Publikováno v:
Neuromuscular Disorders
Neuromuscular Disorders, Elsevier, 2002, 12 (3), pp.266-272. ⟨10.1016/s0960-8966(01)00279-6⟩
Neuromuscular Disorders, Elsevier, 2002, 12 (3), pp.266-272. ⟨10.1016/s0960-8966(01)00279-6⟩
International audience; The aim of this study was to provide a set of data on mechanisms involved in the calcium homeostasis of facioscapulohumeral muscular dystrophy (FSHD) co-cultured myotubes. In fact, abnormal regulation of calcium have been show
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::026736edfa309a573f197ad4687e90ca
https://hal.archives-ouvertes.fr/hal-02881537
https://hal.archives-ouvertes.fr/hal-02881537
Autor:
Nathalie Imbert, Christian Cognard, Bruno Constantin, Clarisse Vandebrouck, Guy Raymond, Michael J. Cullen, Gérard Duport, Abdul A. Hassoni
Publikováno v:
The Journal of Physiology
The Journal of Physiology, Wiley, 2001, 534 (2), pp.343-355. ⟨10.1111/j.1469-7793.2001.00343.x⟩
The Journal of Physiology, Wiley, 2001, 534 (2), pp.343-355. ⟨10.1111/j.1469-7793.2001.00343.x⟩
International audience; 1. The goal of the present study was to investigate differences in calcium movements between normal and Duchenne muscular dystrophy (DMD) human contracting myotubes co-cultured with explants of rat spinal cord with attached do
Publikováno v:
Neuroscience letters. 269(2)
Clinical trials have shown that a glucocorticoid, the methyiprednisolone (PDN), has a beneficial effect on muscle strength and function in Duchenne muscular dystrophy (DMD) patients. The aim of this study was to test if the effect of PDN could be med
Publikováno v:
Seminars in neurology. 15(1)
Publikováno v:
Scopus-Elsevier
Intracellular calcium activity was recorded during in vitro myogenesis of human normal and DMD muscle, using the calcium probe Indo-1 under laser illumination, at rest and during different kinds of stimulation (acetylcholine, high K+, caffeine). In m