Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maxime R. F. Gosselin"'
Autor:
Maxime R. F. Gosselin, Virginie Mournetas, Malgorzata Borczyk, Suraj Verma, Annalisa Occhipinti, Justyna Róg, Lukasz Bozycki, Michal Korostynski, Samuel C. Robson, Claudio Angione, Christian Pinset, Dariusz C. Górecki
Background Duchenne muscular dystrophy (DMD) is the most common inherited muscle disease that leads to severe disability and death in young men. DMD is caused by out-of-frame mutations in the largest known gene, which encodes dystrophin. The loss of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e367bcfcfd595eaa64d2b421433ca45
https://doi.org/10.1101/2021.08.24.457331
https://doi.org/10.1101/2021.08.24.457331
Autor:
Maxime R. F. Gosselin, Natalia Nowak, Wojciech Brutkowski, Dorota Dymkowska, Dariusz C. Górecki, Justyna Róg, Krzysztof Zabłocki, Aleksandra Oksiejuk, Samuel Robson
Publikováno v:
Róg, J, Oksiejuk, A, Gosselin, M R F, Brutkowski, W, Dymkowska, D, Nowak, N, Robson, S, Górecki, D C & Zabłocki, K 2019, ' Dystrophic mdx mouse myoblasts exhibit elevated ATP/UTP-evoked metabotropic purinergic responses and alterations in calcium signalling ', Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease . https://doi.org/10.1016/j.bbadis.2019.01.002
Pathophysiology of Duchenne Muscular Dystrophy (DMD) is still elusive. Although progressive wasting of muscle fibres is a cause of muscle deterioration, there is a growing body of evidence that the triggering effects of DMD mutation are present at th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae3ffeffd69cd820b96f53623a63201e
https://doi.org/10.1016/j.bbadis.2019.01.002
https://doi.org/10.1016/j.bbadis.2019.01.002
Autor:
Maxime R. F. Gosselin, Etienne Kornobis, Jean-Baptiste Dupont, Spiros D. Garbis, Christian Pinset, Alan R L Dorval, Antigoni Manousopoulou, Virginie Mournetas, Margot Jarrige, Dariusz C. Górecki, Hélène Polvèche, Emmanuelle Massouridès
Publikováno v:
Mournetas, V, Massouridès, E, Dupont, JB, Kornobis, E, Polvèche, H, Jarrige, M, Dorval, A R L, Gosselin, M R F, Manousopoulou, A, Garbis, S D, Górecki, D C & Pinset, C 2021, ' Myogenesis modelled by human pluripotent stem cells: a multi-omic study of Duchenne myopathy early onset ', Journal of Cachexia, Sarcopenia and Muscle, vol. 12, no. 1, pp. 209-232 . https://doi.org/10.1002/jcsm.12665
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle, 2021, 12 (1), pp.209-232. ⟨10.1002/jcsm.12665⟩
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 1, Pp 209-232 (2021)
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle, 2021, 12 (1), pp.209-232. ⟨10.1002/jcsm.12665⟩
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 1, Pp 209-232 (2021)
Background: Duchenne muscular dystrophy (DMD) causes severe disability of children and death of young men, with an incidence of approximately 1/5000 male births. Symptoms appear in early childhood, with a diagnosis made mostly around 4 years old, a t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e690e39a8f6eafa14f5f09df8d5f1d3
https://researchportal.port.ac.uk/ws/files/27071227/Myogenesis_modelled_by_human_pluripotent_stem_cells.pdf
https://researchportal.port.ac.uk/ws/files/27071227/Myogenesis_modelled_by_human_pluripotent_stem_cells.pdf
Autor:
Antigoni Manousopoulou, Virginie Mournetas, Christian Pinset, Margot Jarrige, Spiros D. Garbis, Maxime R. F. Gosselin, Etienne Kornobis, Hélène Polvèche, Dariusz C. Górecki, Emmanuelle Massouridès, Jean-Baptiste Dupont
Duchenne muscular dystrophy (DMD) causes severe disability of children and death of young men, with an incidence of approximately 1/5,000 male births. Symptoms appear in early childhood, with a diagnosis made around 4 years old, a time where the amou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3733cc8390b80854863ffe2a1687b8aa
Autor:
J. Dunlop, Darek Gorecki, Aleksandra Oksiejuk, Maxime R. F. Gosselin, Kacper Łukasiewicz, Natalia Chira, Paweł Matryba, Robin M. H. Rumney, Alexander P. Kao, Christopher N. J. Young, Samuel Robson, Krzysztof Zabłocki, Lukasz Bozycki
Publikováno v:
Young, C, Gosselin, M R F, Rumney, R M H, Oksiejuk, A, Chira, N, Bozycki, L, Matryba, P, Łukasiewicz, K, Kao, A, Dunlop, J N, Robson, S, Zabłocki, K & Gorecki, D 2020, ' Total absence of dystrophin expression exacerbates ectopic myofiber calcification and fibrosis and alters macrophage infiltration patterns ', American Journal of Pathology, vol. 190, no. 1, pp. 190-205 . https://doi.org/10.1016/j.ajpath.2019.09.021
The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link. Duchenne muscular dystrophy (DMD) causes severe disability and death of young men due to progressive m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2421c92eb4330bb99f188781cca4375
https://pubmed.ncbi.nlm.nih.gov/31726040
https://pubmed.ncbi.nlm.nih.gov/31726040