Zobrazeno 1 - 10
of 197
pro vyhledávání: '"Stéphane Martin"'
Publikováno v:
Cells, Vol 13, Iss 5, p 420 (2024)
Neurotransmission occurs within highly specialized compartments forming the active synapse where the complex organization and dynamics of the interactions are tightly orchestrated both in time and space. Post-translational modifications (PTMs) are ce
Externí odkaz:
https://doaj.org/article/8749907bbc7f4e1897b1797e927ec4d4
Autor:
Félicie Kieffer, Fahd Hilal, Anne-Sophie Gay, Delphine Debayle, Marie Pronot, Gwénola Poupon, Iliona Lacagne, Barbara Bardoni, Stéphane Martin, Carole Gwizdek
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Fragile X-Syndrome (FXS) represents the most common inherited form of intellectual disability and the leading monogenic cause of Autism Spectrum Disorders. In most cases, this disease results from the absence of expression of the protein FMRP encoded
Externí odkaz:
https://doaj.org/article/41567188905949fe92005c17d4060778
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
Autor:
Marie Pronot, Félicie Kieffer, Anne-Sophie Gay, Delphine Debayle, Raphaël Forquet, Gwénola Poupon, Lenka Schorova, Stéphane Martin, Carole Gwizdek
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Synapses are highly specialized structures that interconnect neurons to form functional networks dedicated to neuronal communication. During brain development, synapses undergo activity-dependent rearrangements leading to both structural and function
Externí odkaz:
https://doaj.org/article/12953524713c4626b238a6cd7af1dd80
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:
Karine Heerah, Mathieu Woillez, Ronan Fablet, François Garren, Stéphane Martin, Hélène De Pontual
Publikováno v:
Movement Ecology, Vol 5, Iss 1, Pp 1-15 (2017)
Abstract Background Movement pattern variations are reflective of behavioural switches, likely associated with different life history traits in response to the animals’ abiotic and biotic environment. Detecting these can provide rich information on
Externí odkaz:
https://doaj.org/article/6fecf3d55d3549c9a93115861648ad56
Autor:
Stéphane Martin
Publikováno v:
Pallas, Vol 99, Pp 157-173 (2015)
For the lack of texts on the subject, studies in monetary history necessarily rely on numismatics. However, when it comes to grasping the temporal dimension of monetary phenomena, traditional numismatic methods appear lacking. Drawing mainly on data
Externí odkaz:
https://doaj.org/article/5bdbab453b1a4bec81e34bc80ba5c3db
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:
Kevin A. Wilkinson, Stéphane Martin, Shiva K. Tyagarajan, Ottavio Arancio, Tim J. Craig, Chun Guo, Paul E. Fraser, Steven A. N. Goldstein, Jeremy M. Henley
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
Externí odkaz:
https://doaj.org/article/f00d987146aa4356824ac28d80089e77
Autor:
Stéphane Martin
Publikováno v:
Gallia, Vol 70, Iss 2, Pp 59-89 (2013)
On the basis of recent research on the Upper Rhine (Vindonissa, Oedenburg), this study focuses on dating and characterization of the first Roman establishment at Strasbourg, dated until recently from 12 B.C. From the few well defined layers uncovered
Externí odkaz:
https://doaj.org/article/8e9f98d9097942a196763ff852054b09