Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sophie Reibel-Foisset"'
Autor:
Jurate Skerniskyte, Céline Mulet, Antonin C. André, Mark C. Anderson, Louise Injarabian, Achim Buck, Verena M. Prade, Philippe J. Sansonetti, Sophie Reibel-Foisset, Axel K. Walch, Michel Lebel, Jens Lykkesfeldt, Benoit S. Marteyn
Publikováno v:
Gut Microbes, Vol 15, Iss 2 (2023)
ABSTRACTShigella spp. are the causative agents of bacterial dysentery and shigellosis, mainly in children living in developing countries. The study of Shigella entire life cycle in vivo and the evaluation of vaccine candidates’ protective efficacy
Externí odkaz:
https://doaj.org/article/89d9b94eee7e4f86934d999908bc40af
Autor:
Clément Léna, Daniela Popa, Fekrije Selimi, Vanessa Gautheron, Nicolas Guyon, Stéphane Dieudonné, Jean-Christophe Cassel, Frédéric Doussau, Joseph Chaumont, Guillaume P. Dugué, Jean-Luc Dupont, Bernard Poulain, Aline Stephan, Antoine M. Valera, Philippe Isope, Païkan Marcaggi, Michel Barrot, Sophie Reibel-Foisset
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2013, 110 (40), pp.16223-16228. ⟨10.1073/pnas.1302310110⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2013, 110 (40), pp.16223-16228. ⟨10.1073/pnas.1302310110⟩
Climbing fibers, the projections from the inferior olive to the cerebellar cortex, carry sensorimotor error and clock signals that trigger motor learning by controlling cerebellar Purkinje cell synaptic plasticity and discharge. Purkinje cells target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7074f4286299e7e183624ef36822e611
https://doi.org/10.1073/pnas.1302310110
https://doi.org/10.1073/pnas.1302310110
Autor:
Fabrice Riet, Sophie Reibel-Foisset, Noemi Morello, Maurizio Giustetto, Jamel Chelly, Mohammed Selloum, Thierry Bienvenu, Bassem Hiba, Ginevra Zanni, Eleonora Calcagno, Malik Khelfaoui, Yann Humeau, Hamid Meziane, Yann Herault, Pierre Billuart
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (11), pp.2314-2323. ⟨10.1093/hmg/ddw102⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (11), pp.2314-2323. ⟨10.1093/hmg/ddw102⟩
International audience; Loss of function mutations in human Oligophrenin1 (OPHN1) gene are responsible for syndromic intellectual disability (ID) associated with cerebellar hypoplasia and cerebral ventricles enlargement. Functional studies in rodent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::257ae5840a271944c8c1e4574edeee49
http://hdl.handle.net/2318/1620873
http://hdl.handle.net/2318/1620873
Autor:
Pierre Billuart, Marie Kneib, Frédéric Gambino, Marilyn Lepleux, Nicolas Vitale, Philippe Gastrein, Jamel Chelly, Sophie Reibel-Foisset, Bernard Poulain, Bruno Ragazzon, Christian Müller, Andreas Lüthi, Frederic Lanore, Mario Carta, Malik Khelfaoui, Yann Humeau, Xander Houbaert, B.N. Srikumar, Chun-Lei Zhang
Publikováno v:
Phil Trans R Soc B
Philosophical Transactions of the Royal Society B: Biological Sciences
Philosophical Transactions of the Royal Society B: Biological Sciences, 2014, 369 (1633), pp.20130160. ⟨10.1098/rstb.2013.0160⟩
Philosophical Transactions of the Royal Society B: Biological Sciences, Royal Society, The, 2014, 369 (1633), pp.20130160. ⟨10.1098/rstb.2013.0160⟩
Philosophical Transactions of the Royal Society B: Biological Sciences; Vol 369
Philosophical Transactions of the Royal Society B: Biological Sciences
Philosophical Transactions of the Royal Society B: Biological Sciences, 2014, 369 (1633), pp.20130160. ⟨10.1098/rstb.2013.0160⟩
Philosophical Transactions of the Royal Society B: Biological Sciences, Royal Society, The, 2014, 369 (1633), pp.20130160. ⟨10.1098/rstb.2013.0160⟩
Philosophical Transactions of the Royal Society B: Biological Sciences; Vol 369
Loss-of-function mutations in the gene encoding for the RhoGAP protein of oligophrenin-1 (OPHN1) lead to cognitive disabilities (CDs) in humans, yet the underlying mechanisms are not known. Here, we show that in mice constitutive lack ofOphn1is assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3731a09802e93cc261bb07d97346bd93