Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Benoit Schneider"'
Autor:
Chloé Bizingre, Clara Bianchi, Anne Baudry, Aurélie Alleaume-Butaux, Benoit Schneider, Mathéa Pietri
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 17 (2024)
More than 650 reversible and irreversible post-translational modifications (PTMs) of proteins have been listed so far. Canonical PTMs of proteins consist of the covalent addition of functional or chemical groups on target backbone amino-acids or the
Externí odkaz:
https://doaj.org/article/02a3acd0f74d42b093cca5d951abc113
Autor:
Nassima Bekaddour, Nikaïa Smith, Benoit Beitz, Alba Llibre, Tom Dott, Anne Baudry, Anne-Sophie Korganow, Sébastien Nisole, Richard Mouy, Sylvain Breton, Brigitte Bader-Meunier, Darragh Duffy, Benjamin Terrier, Benoit Schneider, Pierre Quartier, Mathieu P. Rodero, Jean-Philippe Herbeuval
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionAmong immune cells, activated monocytes play a detrimental role in chronic and viral-induced inflammatory pathologies, particularly in Juvenile Idiopathic Arthritis (JIA), a childhood rheumatoid arthritis (RA) disease. The uncontrolled ac
Externí odkaz:
https://doaj.org/article/211367eb2e744db5b42f0c81bd117414
Autor:
Luiz W. Ribeiro, Mathéa Pietri, Hector Ardila-Osorio, Anne Baudry, François Boudet-Devaud, Chloé Bizingre, Zaira E. Arellano-Anaya, Anne-Marie Haeberlé, Nicolas Gadot, Sonja Boland, Stéphanie Devineau, Yannick Bailly, Odile Kellermann, Anna Bencsik, Benoit Schneider
Publikováno v:
Particle and Fibre Toxicology, Vol 19, Iss 1, Pp 1-22 (2022)
Abstract Background Epidemiological emerging evidence shows that human exposure to some nanosized materials present in the environment would contribute to the onset and/or progression of Alzheimer’s disease (AD). The cellular and molecular mechanis
Externí odkaz:
https://doaj.org/article/39138cafd6da479a9d8511efe7d61aa2
Autor:
Hélène Arnould, Vincent Baudouin, Anne Baudry, Luiz W Ribeiro, Hector Ardila-Osorio, Mathéa Pietri, Cédric Caradeuc, Cynthia Soultawi, Declan Williams, Marjorie Alvarez, Carole Crozet, Fatima Djouadi, Mireille Laforge, Gildas Bertho, Odile Kellermann, Jean-Marie Launay, Gerold Schmitt-Ulms, Benoit Schneider
Publikováno v:
PLoS Pathogens, Vol 17, Iss 10, p e1009991 (2021)
Corruption of cellular prion protein (PrPC) function(s) at the plasma membrane of neurons is at the root of prion diseases, such as Creutzfeldt-Jakob disease and its variant in humans, and Bovine Spongiform Encephalopathies, better known as mad cow d
Externí odkaz:
https://doaj.org/article/e0f84de0ab084344b839c7190a6a9010
Autor:
Benoit Schneider, Anne Baudry, Mathéa Pietri, Aurélie Alleaume-Butaux, Chloé Bizingre, Pierre Nioche, Odile Kellermann, Jean-Marie Launay
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Amyloid-based neurodegenerative diseases such as prion, Alzheimer's, and Parkinson's diseases have distinct etiologies and clinical manifestations, but they share common pathological events. These diseases are caused by abnormally folded proteins (pa
Externí odkaz:
https://doaj.org/article/b12abf07f59a4a9a925fce07329b3a9c
Autor:
Juliette Ezpeleta, Vincent Baudouin, Zaira E. Arellano-Anaya, François Boudet-Devaud, Mathéa Pietri, Anne Baudry, Anne-Marie Haeberlé, Yannick Bailly, Odile Kellermann, Jean-Marie Launay, Benoit Schneider
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
Aβ plaques have been detected in brains of patients with prion diseases. Here, using mice, the authors show that prion infection enhances Aβ production via a PDK1-TACE mechanism and that brain deposition of Aβ induced by Aβ seeds co-transmitted w
Externí odkaz:
https://doaj.org/article/1e4e707388e247a5aac2217f5c04838e
Autor:
Juliette Ezpeleta, François Boudet-Devaud, Mathéa Pietri, Anne Baudry, Vincent Baudouin, Aurélie Alleaume-Butaux, Nathalie Dagoneau, Odile Kellermann, Jean-Marie Launay, Benoit Schneider
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Abstract Although cellular prion protein PrPC is well known for its implication in Transmissible Spongiform Encephalopathies, its functions remain elusive. Combining in vitro and in vivo approaches, we here show that PrPC displays the intrinsic capac
Externí odkaz:
https://doaj.org/article/98b23f663c354ca58b1295e144d129b8
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Serotonin transporter, SERT (SLC64A for solute carrier family 6, member A4), is a twelve transmembrane domain (TMDs) protein that assumes the uptake of serotonin (5-HT) through dissipation of the Na+ gradient established by the electrogenic pump Na/K
Externí odkaz:
https://doaj.org/article/e40116cf5a6648ba8d04b223891d6f73
Autor:
Mohadeseh Mehrabian, Dylan Brethour, Declan Williams, Hansen Wang, Hélène Arnould, Benoit Schneider, Gerold Schmitt-Ulms
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0156779 (2016)
A popular method for studying the function of a given protein is to generate and characterize a suitable model deficient for its expression. For the prion protein (PrP), best known for its role in several invariably fatal neurodegenerative diseases,
Externí odkaz:
https://doaj.org/article/81a139e5572b41e8bc3b8e57dd0d406c
Autor:
Aurélie Alleaume-Butaux, Simon Nicot, Mathéa Pietri, Anne Baudry, Caroline Dakowski, Philippe Tixador, Hector Ardila-Osorio, Anne-Marie Haeberlé, Yannick Bailly, Jean-Michel Peyrin, Jean-Marie Launay, Odile Kellermann, Benoit Schneider
Publikováno v:
PLoS Pathogens, Vol 11, Iss 8, p e1005073 (2015)
In prion diseases, synapse dysfunction, axon retraction and loss of neuronal polarity precede neuronal death. The mechanisms driving such polarization defects, however, remain unclear. Here, we examined the contribution of RhoA-associated coiled-coil
Externí odkaz:
https://doaj.org/article/f1c7ab37f8994140b4f83ce0e621baa2