Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Frédéric Brau"'
Autor:
Sylvain Bonnefond, Antoine Reynaud, Julie Cazareth, Sophie Abélanet, Massimo Vassalli, Frédéric Brau, Gian Luca Lippi
Publikováno v:
Nanomaterials, Vol 13, Iss 21, p 2875 (2023)
Weak fluorescence signals, which are important in research and applications, are often masked by the background. Different amplification techniques are actively investigated. Here, a broadband, geometry-independent and flexible feedback scheme based
Externí odkaz:
https://doaj.org/article/97436fb909d645caa17d4a122cc2cf50
Autor:
Rémi Valarcher, Rayan Zoghlami, Manon Carvalho, Maxence Delannoy, Pierre Pouchin, Marc Mongy, Clémence Belle, Frédéric Brau, Sophie Desset
Publikováno v:
F1000Research, Vol 11 (2022)
The Open Microscopy Environment Remote Objects (OMERO) is an open-source image manager used by many biologists to store, organize, view, and share microscopy images, while the open-source software ImageJ/Fiji is a very popular program used to analyse
Externí odkaz:
https://doaj.org/article/3336e3fc105e457a9648d944c83d350c
Autor:
Marta Prieto, Alessandra Folci, Gwénola Poupon, Sara Schiavi, Valeria Buzzelli, Marie Pronot, Urielle François, Paula Pousinha, Norma Lattuada, Sophie Abelanet, Sara Castagnola, Magda Chafai, Anouar Khayachi, Carole Gwizdek, Frédéric Brau, Emmanuel Deval, Maura Francolini, Barbara Bardoni, Yann Humeau, Viviana Trezza, Stéphane Martin
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
The R138Q mutation in the Fragile X Mental Retardation 1 (FMR1) gene has been associated with Fragile X syndrome (FXS). Here, the authors present a Fmr1 R138Q Knock-In mouse model and show that R138Q mutation results in impaired long-term potentiatio
Externí odkaz:
https://doaj.org/article/1f547051b6104cb2ae2a8dd5047148af
Publikováno v:
Cell Reports, Vol 39, Iss 5, Pp 110765- (2022)
Summary: Cocaine use is a major comorbidity of HIV-associated neurocognitive disorder (HAND). In this study, we show that cocaine exposure worsens the learning and memory of doxycycline-inducible and brain-specific HIV Tat transgenic mice (iTat) and
Externí odkaz:
https://doaj.org/article/0b889cbc07224fa094403df685bb30b5
Autor:
Rémi Valarcher, Rayan Zoghlami, Manon Carvalho, Maxence Delannoy, Pierre Pouchin, Marc Mongy, Clémence Belle, Frédéric Brau, Sophie Desset
Publikováno v:
F1000Research, Vol 11 (2022)
The Open Microscopy Environment Remote Objects (OMERO) is an open source image manager used by many biologists to store, organize, view and share microscopy images, while the open source software ImageJ/Fiji is a very popular program used to analyse
Externí odkaz:
https://doaj.org/article/25a16de6e00e41a492cd5a8b1ee6c28b
Autor:
Malgorzata Drozd, Sébastien Delhaye, Thomas Maurin, Sara Castagnola, Mauro Grossi, Frédéric Brau, Marielle Jarjat, Rob Willemsen, Maria Capovilla, Renate K. Hukema, Enzo Lalli, Barbara Bardoni
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 18, Iss , Pp 546-553 (2019)
Fragile X-associated tremor ataxia syndrome (FXTAS) is a rare disorder associated to the presence of the fragile X premutation, a 55–200 CGG repeat expansion in the 5′ UTR of the FMR1 gene. Two main neurological phenotypes have been described in
Externí odkaz:
https://doaj.org/article/12547d51214040b2ad0ebfb52e3a2f10
Autor:
Anouar Khayachi, Carole Gwizdek, Gwénola Poupon, Damien Alcor, Magda Chafai, Frédéric Cassé, Thomas Maurin, Marta Prieto, Alessandra Folci, Fabienne De Graeve, Sara Castagnola, Romain Gautier, Lenka Schorova, Céline Loriol, Marie Pronot, Florence Besse, Frédéric Brau, Emmanuel Deval, Barbara Bardoni, Stéphane Martin
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
Fragile X syndrome patients display intellectual disability and autism, caused by mutations in the RNA-binding protein fragile X mental retardation protein (FMRP). Here, the authors show that FMRP sumoylation is required for regulating spine density
Externí odkaz:
https://doaj.org/article/57e3d66daa9b4a92b4183ee79455e739
Autor:
Sara Castagnola, Sébastien Delhaye, Alessandra Folci, Agnès Paquet, Frédéric Brau, Fabrice Duprat, Marielle Jarjat, Mauro Grossi, Méline Béal, Stéphane Martin, Massimo Mantegazza, Barbara Bardoni, Thomas Maurin
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Fragile X syndrome (FXS), the most common form of inherited intellectual disability (ID) and a leading cause of autism, results from the loss of expression of the Fmr1 gene which encodes the RNA-binding protein Fragile X Mental Retardation Protein (F
Externí odkaz:
https://doaj.org/article/0058b1e755374ea09c5b1a77cba6af5c
Autor:
Nina Milosavljevic, Michaël Monet, Isabelle Léna, Frédéric Brau, Sandra Lacas-Gervais, Sylvain Feliciangeli, Laurent Counillon, Mallorie Poët
Publikováno v:
Cell Reports, Vol 7, Iss 3, Pp 689-696 (2014)
Vesicular H+-ATPases and ClC-chloride transporters are described to acidify intracellular compartments, which also express the highly conserved Na+/H+ exchangers NHE6, NHE7, and NHE9. Mutations of these exchangers cause autism-spectrum disorders and
Externí odkaz:
https://doaj.org/article/5ed5e3d9e4a14ff6887a40dbb4eb51a3
Publikováno v:
PLoS ONE, Vol 5, Iss 7, p e11524 (2010)
Memory CD8(+) T cells represent an important effector arm of the immune response in maintaining long-lived protective immunity against viruses and some intracellular bacteria such as Listeria monocytogenes (L.m). Memory CD8(+) T cells are endowed wit
Externí odkaz:
https://doaj.org/article/e15a3edda47a4a1c842d68584219256c