Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jérémie Vitte"'
Autor:
Margot Fournier, Jérémie Vitte, Jérôme Garrigue, Dominique Langui, Jean-Philippe Dullin, Françoise Saurini, Naïma Hanoun, Fernando Perez-Diaz, Fabien Cornilleau, Chantal Joubert, Héctor Ardila-Osorio, Sabine Traver, René Duchateau, Cécile Goujet-Zalc, Katerina Paleologou, Hilal A Lashuel, Christian Haass, Charles Duyckaerts, Charles Cohen-Salmon, Philipp J Kahle, Michel Hamon, Alexis Brice, Olga Corti
Publikováno v:
PLoS ONE, Vol 4, Iss 8, p e6629 (2009)
In synucleinopathies, including Parkinson's disease, partially ubiquitylated alpha-synuclein species phosphorylated on serine 129 (P(S129)-alpha-synuclein) accumulate abnormally. Parkin, an ubiquitin-protein ligase that is dysfunctional in autosomal
Externí odkaz:
https://doaj.org/article/3b68bd1a5b804cd19da875320f51d756
Autor:
Brian Na, Blake Haist, Shilp R. Shah, Graeme Sabiston, Steven J. Jonas, Jeremie Vitte, Richard E. Wirz, Marco Giovannini
Publikováno v:
Biomedicines, Vol 12, Iss 9, p 1986 (2024)
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder resulting from mutations in the NF1 gene. Patients harboring these mutations are predisposed to a spectrum of peripheral nerve sheath tumors (PNSTs) originating from Schwann cells, of w
Externí odkaz:
https://doaj.org/article/3f901916f71d4f779f1172116037a70f
Autor:
Christine Chiasson-MacKenzie, Jeremie Vitte, Ching-Hui Liu, Emily A. Wright, Elizabeth A. Flynn, Shannon L. Stott, Marco Giovannini, Andrea I. McClatchey
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-17 (2023)
Schwannomas are mainly caused by NF2 tumour suppressor inactivation, but they display intratumoural heterogeneity. Here the authors show that this heterogeneity is caused by the loss of polarity and acquisition of different programmes of ErbB ligand
Externí odkaz:
https://doaj.org/article/910ca0cc6a5e4813874a61e9dbcdad7c
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
SMARCB1 mutations predispose to rhabdoid tumors and schwannomas but the mechanisms underlying the tumor type specificity are unknown. Here the authors present new mouse models and show that early Smarcb1 loss causes rhabdoid tumors whereas loss at la
Externí odkaz:
https://doaj.org/article/1faf2971b5a4423bb8a856e7f90310eb