Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Christine Berthier"'
Probenecid affects muscle Ca2+ homeostasis and contraction independently from pannexin channel block
Autor:
Francisco Jaque-Fernandez, Bruno Allard, Laloé Monteiro, Aude Lafoux, Corinne Huchet, Enrique Jaimovich, Christine Berthier, Vincent Jacquemond
Publikováno v:
Journal of General Physiology. 155
Tight control of skeletal muscle contractile activation is secured by the excitation–contraction (EC) coupling protein complex, a molecular machinery allowing the plasma membrane voltage to control the activity of the ryanodine receptor Ca2+ releas
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:
A. Lafoux, Enrique Jaimovich, Corinne Huchet, Vincent Jacquemond, Bruno Allard, Christine Berthier, Francisco Jaque-Fernandez, Laloe Monteiro
Publikováno v:
Journal of General Physiology. 154
Pannexins are plasma membrane heptameric channels mediating ATP release from the cytosol to the extracellular space. Skeletal muscle activity is associated with Pannexin 1 (Panx1) channels activation, ATP release out to the extracellular space and su
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:
Jennifer Rieusset, Agathe Beaulant, Bruno Allard, Francisco Jaque-Fernandez, Christine Berthier, Mariana Casas, Vincent Jacquemond, Laloe Monteiro
Publikováno v:
Diabetologia
Diabetologia, Springer Verlag, 2020, 63 (11), pp.2471-2481. ⟨10.1007/s00125-020-05256-8⟩
Diabetologia, Springer Verlag, 2020, 63 (11), pp.2471-2481. ⟨10.1007/s00125-020-05256-8⟩
International audience; Aims/hypothesis Disrupted intracellular Ca2+ handling is known to play a role in diabetic cardiomyopathy but it has also been postulated to contribute to obesity- and type 2 diabetes-associated skeletal muscle dysfunction. Sti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cfa0751c5b1ffd4c9f9a4573b93e57f
https://hal.archives-ouvertes.fr/hal-03001299/file/Ms_JAQUE_2020_DIABETOLOGIA_NONEDITED.pdf
https://hal.archives-ouvertes.fr/hal-03001299/file/Ms_JAQUE_2020_DIABETOLOGIA_NONEDITED.pdf
Autor:
Francisco, Jaque-Fernandez, Agathe, Beaulant, Christine, Berthier, Laloé, Monteiro, Bruno, Allard, Mariana, Casas, Jennifer, Rieusset, Vincent, Jacquemond
Publikováno v:
Diabetologia. 63(11)
Disrupted intracellular CaIntact muscle fibres were isolated from mice fed either with a standard chow diet or with a high-fat, high-sucrose diet generating obesity, insulin resistance and glucose intolerance. Properties of muscle fibres were investi
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:
Vincent Jacquemond, Péter Szentesi, Delphine Trochet, Pascale Guicheney, Bruno Allard, Maud Beuvin, Candice Kutchukian, Marc Bitoun, László Csernoch, Yves Tourneur, Christine Berthier
Publikováno v:
The Journal of Physiology. 595:7369-7382
Key points Dynamin 2 is a ubiquitously expressed protein involved in membrane trafficking processes. Mutations in the gene encoding dynamin 2 are responsible for a congenital myopathy associated with centrally located nuclei in the muscle fibres. Usi