Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Romane Idoux"'
Autor:
Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Sun Huang, Omid Haji-Ghassemi, Romane Idoux, Anna Liashenko, Ivana A. Souza, Yuriy Rzhepetskyy, Lubica Lacinova, Filip Van Petegem, Gerald W. Zamponi, Roger Pamphlett, Norbert Weiss
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-11 (2020)
Abstract Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of cortical, brain stem and spinal motor neurons that leads to muscle weakness and death. A previous study implicated CACNA1H encoding
Externí odkaz:
https://doaj.org/article/aa77ecf927be4dd78a092c2d4008c1cd
Autor:
Romane Idoux, Sandrine Bretaud, Christine Berthier, Florence Ruggiero, Vincent Jacquemond, Bruno Allard
Publikováno v:
Journal of General Physiology
Journal of General Physiology, 2022, 154 (9), ⟨10.1085/jgp.202213158⟩
Journal of General Physiology, 2022, 154 (9), ⟨10.1085/jgp.202213158⟩
International audience; The zebrafish has emerged as a very relevant animal model for probing the pathophysiology of human skeletal muscle disorders. This vertebrate animal model displays a startle response characterized by high-frequency swimming ac
Autor:
Omid Haji-Ghassemi, Norbert Weiss, Bohumila Jurkovicova-Tarabova, Gerald W. Zamponi, Romane Idoux, Filip Van Petegem, Sun Huang, Anna Liashenko, Yuriy Rzhepetskyy, Roger Pamphlett, Ivana A. Souza, Robin N Stringer, Lubica Lacinova
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-11 (2020)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of cortical, brain stem and spinal motor neurons that leads to muscle weakness and death. A previous study implicated CACNA1H encoding for Cav3.
Publikováno v:
Journal of General Physiology. 154
The zebrafish has emerged as a very relevant animal model to decipher the pathophysiology of human muscle disorders. However, the vast majority of studies on zebrafish skeletal muscle have investigated genetic, histological, and molecular aspects, bu
Autor:
Sandrine Bretaud, Christine Berthier, Bruno Allard, Florence Ruggiero, Romane Idoux, Vincent Jacquemond
Publikováno v:
médecine/sciences. 35:39-42
La myopathie de Bethlem (BM) est une maladie caractérisée par des rétractions et une faiblesse musculaires. Cette pathologie résulte de mutations dans un des gènes codant l’une des trois chaînes α du collagène VI (COLVI), un composant de la
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:
Romane, Idoux, Sandrine, Bretaud, Christine, Berthier, Vincent, Jacquemond, Florence, Ruggiero, Bruno, Allard
Publikováno v:
Medecine sciences : M/S.
Bethlem myopathy (BM) is a neuromuscular disease characterized by joint contractures and muscle weakness. BM is caused by mutations in one of the genes encoding one of the three α-chains of collagen VI (COLVI), a component of the skeletal muscle ext
Autor:
Robin N, Stringer, Bohumila, Jurkovicova-Tarabova, Sun, Huang, Omid, Haji-Ghassemi, Romane, Idoux, Anna, Liashenko, Ivana A, Souza, Yuriy, Rzhepetskyy, Lubica, Lacinova, Filip, Van Petegem, Gerald W, Zamponi, Roger, Pamphlett, Norbert, Weiss
Publikováno v:
Molecular Brain
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of cortical, brain stem and spinal motor neurons that leads to muscle weakness and death. A previous study implicated CACNA1H encoding for Cav3.