Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Fabrice Glibert"'
Autor:
Serguei, Nabirotchkin, Jan, Bouaziz, Fabrice, Glibert, Jonas, Mandel, Julie, Foucquier, Rodolphe, Hajj, Noëlle, Callizot, Nathalie, Cholet, Mickaël, Guedj, Daniel, Cohen
Publikováno v:
Journal of Alzheimer's Disease. 88:1585-1603
Background: Human diseases are multi-factorial biological phenomena resulting from perturbations of numerous functional networks. The complex nature of human diseases explains frequently observed marginal or transitory efficacy of mono-therapeutic in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3689c941909510a2251ed0bd5d8421b6
https://doi.org/10.3233/jad-220120
https://doi.org/10.3233/jad-220120
Autor:
Yannick Pereira, Julien Laffaire, Gwenaël Primas, Emmanuel Vial, Jonas Mandel, Serguei Nabirotchkin, Aude Milet, Esther Graudens, Mickaël Guedj, Fabrice Glibert, Ilya Chumakov, Julie Foucquier, Michael W. Sereda, Daniel Cohen, Nathalie Cholet, Klaus-Armin Nave, Aurélie Boucard, Rodolphe Hajj, Viviane Bertrand
Publikováno v:
Orphanet Journal of Rare Diseases
Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited sensory and motor peripheral neuropathy. It is caused by PMP22 overexpression which leads to defects of peripheral myelination, loss of long axons, and progressive impairment th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93103b85734e265012438f4aaacfa7ed
http://europepmc.org/articles/PMC4279797
http://europepmc.org/articles/PMC4279797
Autor:
Laurent Susini, Stuart Pook, Bruno Lacroix, Isabelle Georges, Denis Le Paslier, Jennifer Lu-Kuo, David C. Ward, Isabelle Gros, Thomas Ried, Sandrine Beaufils, Christine Bellanné-Chantelot, Georges Lucotte, Alain Billault, Philippe Gesnouin, Ilya Chumakov, Daniel Cohen, Emmanuel Barillot, Fabrice Glibert, Guy Vaysseix, Stéphane Bertrand, Pierre Ougen, Jean-Jacques Codani
Publikováno v:
Cell. 70:1059-1068
Physical mapping of the human genome has until now been envisioned through single chromosome strategies. We demonstrate that by using large insert yeast artificial chromosomes (YACs) a whole genome approach becomes feasible. YACs (22,000) of 810 kb m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc37a9ecbcba6f2157ebbd2e8c887aa3
https://doi.org/10.1016/0092-8674(92)90254-a
https://doi.org/10.1016/0092-8674(92)90254-a
Autor:
Fabrice Glibert, Dung Le Nguyen, Odile Durieu-Trautmann, Pierre-Olivier Couraud, A. Donny Strosberg, Philippe Marin
Publikováno v:
European Journal of Pharmacology: Molecular Pharmacology. 206:191-198
Rat astrocytoma C6 cells have been recently identified as target cells for ET-1, which stimulates inositol lipid turnover in these cells. It is shown here that binding of ET-1 to high-affinity receptors on C6 cells leads to 40-45% inhibition of isopr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f816009c7155ce3eb2bfbcb41271c5
https://doi.org/10.1016/s0922-4106(05)80018-5
https://doi.org/10.1016/s0922-4106(05)80018-5
Autor:
Nabirotchkin, Serguei, Bouaziz, Jan, Glibert, Fabrice, Mandel, Jonas, Foucquier, Julie, Hajj, Rodolphe, Callizot, Noëlle, Cholet, Nathalie, Guedj, Mickaël, Cohen, Daniel
Publikováno v:
Journal of Alzheimer's Disease; 2022, Vol. 88 Issue 4, p1585-1603, 19p
Autor:
Chumakov, Ilya1 ichumakov@pharnext.com, Milet, Aude1 amilet@pharnext.com, Cholet, Nathalie1 ncholet@pharnext.com, Primas, Gwenaël1 gprimas@pharnext.com, Boucard, Aurélie1 aboucard@pharnext.com, Pereira, Yannick1 ypereira@pharnext.com, Graudens, Esther1 egraudens@pharnext.com, Mandel, Jonas1 jmandel@pharnext.com, Laffaire, Julien1 jlaffaire@pharnext.com, Foucquier, Julie1 jfoucquier@pharnext.com, Glibert, Fabrice1 fglibert@pharnext.com, Bertrand, Viviane1 vbertrand@pharnext.com, Nave, Klaus-Armin2 nave@em.mpg.de, Sereda, Michael W.2,3 sereda@em.mpg.de, Vial, Emmanuel1 evg.vial@gmail.com, Guedj, Mickaël1 mguedj@pharnext.com, Hajj, Rodolphe1 rhajj@pharnext.com, Nabirotchkin, Serguei1 snabirotchkin@pharnext.com, Cohen, Daniel1 dcohen@pharnext.com
Publikováno v:
Orphanet Journal of Rare Diseases. 2014, Vol. 9 Issue 1, p282-311. 30p.
Autor:
Bouaziz, Matthieu1,2 matthieu.x.bouaziz@gmail.com, Paccard, Caroline1, Guedj, Mickael1, Ambroise, Christophe2
Publikováno v:
PLoS ONE. Oct2012, Vol. 7 Issue 10, Special section p1-17. 17p.
Since the beginning of the genome project, the necessary involvement of scientists of widely divergent backgrounds has been evident. The proper handling, analysis, dissemination of information, and the control and data gathering of automated process
