Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Camille Januel"'
Autor:
Domenico D'Amico, Olivier Biondi, Camille Januel, Cynthia Bezier, Delphine Sapaly, Zoé Clerc, Mirella El Khoury, Venkat Krishnan Sundaram, Léo Houdebine, Thibaut Josse, Bruno Della Gaspera, Cécile Martinat, Charbel Massaad, Laure Weill, Frédéric Charbonnier
Publikováno v:
Neuropathology and applied neurobiologyREFERENCES. 48(5)
Spinal muscular atrophy (SMA) is a neuromuscular disease caused by survival of motor neuron (SMN) deficiency that induces motor neuron (MN) degeneration and severe muscular atrophy. Gene therapies that increase SMN have proven their efficacy but not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e70612a800f55254aa961bd4feb989dc
https://pubmed.ncbi.nlm.nih.gov/35338505
https://pubmed.ncbi.nlm.nih.gov/35338505
Autor:
Camille Januel, Giovanna Menduti, Kamel Mamchaoui, Cecile Martinat, Ruben Artero, Piotr Konieczny, Marina Boido
Publikováno v:
Cellular and Molecular Life Sciences
Cellular and Molecular Life Sciences, 2022, 79 (8), pp.441. ⟨10.1007/s00018-022-04450-8⟩
Cellular and Molecular Life Sciences, 2022, 79 (8), pp.441. ⟨10.1007/s00018-022-04450-8⟩
Spinal muscular atrophy (SMA) is a genetic disease resulting in the loss of α-motoneurons followed by muscle atrophy. It is caused by knock-out mutations in the survival of motor neuron 1 (SMN1) gene, which has an unaffected, but due to preferential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53a992eee717f55b39ba0b36e0d1c561
https://pubmed.ncbi.nlm.nih.gov/35864358
https://pubmed.ncbi.nlm.nih.gov/35864358
Publikováno v:
Les Cahiers de Myologie. :42-43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3f166a751704a42dafec102a2741eb2
https://doi.org/10.1051/myolog/201919017
https://doi.org/10.1051/myolog/201919017