Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ariana Novati"'
Autor:
Chantal Weber, Nadia Messaddeq, Antoine Hache, Frédéric Doussau, Aurélie Eisenmann, Anna Niewiadomska-Cimicka, Marie-France Champy, Yvon Trottier, Michel Roux, Julien Flament, Erwan Grandgirard, Hamid Meziane, Céline Keime, Binnaz Yalcin, Philippe Isope, Alice Karam, Jean-Baptiste Perot, Hoa Huu Phuc Nguyen, Françoise Piguet, Emmanuel Brouillet, Ariana Novati
Publikováno v:
Journal of Neuroscience
Journal of Neuroscience, 2021, 41 (22), pp.4910-4936. ⟨10.1523/JNEUROSCI.1882-20.2021⟩
The journal of neuroscience
J Neurosci
Journal of Neuroscience, Society for Neuroscience, 2021, 41 (22), pp.4910-4936. ⟨10.1523/JNEUROSCI.1882-20.2021⟩
Journal of Neuroscience, 2021, 41 (22), pp.4910-4936. ⟨10.1523/JNEUROSCI.1882-20.2021⟩
The journal of neuroscience
J Neurosci
Journal of Neuroscience, Society for Neuroscience, 2021, 41 (22), pp.4910-4936. ⟨10.1523/JNEUROSCI.1882-20.2021⟩
Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease mainly characterized by motor incoordination because of progressive cerebellar degeneration. SCA7 is caused by polyglutamine expansion in ATXN7, a subunit of the transcrip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea85b30c6dc1216aedad93c59f1bc02e
https://hal.science/hal-03378998
https://hal.science/hal-03378998
Autor:
Emmanuel Brouillet, Hoa Huu Phuc Nguyen, Ariana Novati, Marie-France Champy, Nadia Messaddeq, Yvon Trottier, Alice Karam, Erwan Grandgirard, Jean-Baptiste Perot, Julien Flament, Aurélie Eisenmann, Philippe Isope, Françoise Piguet, Antoine Hache, Hamid Meziane, Frédéric Doussau, Céline Keime, Binnaz Yalcin, Anna Niewiadomska-Cimicka, Chantal Weber, Michel Roux
Background Background: Spinocerebellar ataxia type 7 (SCA7) is primarily characterized by progressive cerebellar degeneration with major alteration of Purkinje cells (PC) due to polyglutamine expansion in ATXN7, a subunit of SAGA transcriptional co-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17d258ea71db38a726bfe0618f797ce1
https://doi.org/10.21203/rs.3.rs-27474/v1
https://doi.org/10.21203/rs.3.rs-27474/v1