Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marie-Laure Niepon"'
Autor:
Charlotte Duwat, Pauline Léal, Audrey Vautheny, Gwennaëlle Aurégan, Charlène Joséphine, Marie-Claude Gaillard, Anne-Sophie Hérard, Caroline Jan, Pauline Gipchtein, Julien Mitja, Stéphane Fouquet, Marie-Laure Niepon, Philippe Hantraye, Emmanuel Brouillet, Gilles Bonvento, Karine Cambon, Alexis-Pierre Bemelmans
Publikováno v:
Neurobiology of Disease, Vol 181, Iss , Pp 106116- (2023)
Tauopathy is a typical feature of Alzheimer's disease of major importance because it strongly correlates with the severity of cognitive deficits experienced by patients. During the pathology, it follows a characteristic spatiotemporal course which ta
Externí odkaz:
https://doaj.org/article/6df829acc824451a93ba913807abbb2e
Autor:
Sophie Lambard, Sacha Reichman, Cynthia Berlinicke, Marie-Laure Niepon, Olivier Goureau, José-Alain Sahel, Thierry Léveillard, Donald J Zack
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13075 (2010)
RdCVF and RdCVF2, encoded by the nucleoredoxin-like genes NXNL1 and NXNL2, are trophic factors with therapeutic potential that are involved in cone photoreceptor survival. Studying how their expression is regulated in the retina has implications for
Externí odkaz:
https://doaj.org/article/9479dc390cb64115aafd29069b661187
Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity
Autor:
Aurélie Mouret, Therese Cronin, Thierry Leveillard, José-Alain Sahel, Bernd Kinzel, Marie-Laure Niepon, Olivier Poch, Najate Aït-Ali, Céline Jaillard, Ying Yang, Géraldine Millet-Puel, Alain Trembleau, Wolfgang Raffelsberger, Tina Sedmak, Jean Bennett, Pierre-Marie Lledo, Emmanuelle Clérin, Uwe Wolfrum, Irene Lee-Rivera
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (10), pp.2298-311. ⟨10.1093/hmg/dds050⟩
Human Molecular Genetics, 2012, 21 (10), pp.2298-311. ⟨10.1093/hmg/dds050⟩
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (10), pp.2298-311. ⟨10.1093/hmg/dds050⟩
Human Molecular Genetics, 2012, 21 (10), pp.2298-311. ⟨10.1093/hmg/dds050⟩
International audience; The rod-derived cone viability factors, RdCVF and RdCVF2, have potential therapeutical interests for the treatment of inherited photoreceptor degenerations. In the mouse lacking Nxnl2, the gene encoding RdCVF2, the progressive
Autor:
Marie Laure Niepon, Donald J. Zack, Sophie Lambard, Olivier Goureau, Cynthia A. Berlinicke, Thierry Léveillard, José-Alain Sahel, Sacha Reichman
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13075 (2010)
PLoS ONE
PLoS ONE, Public Library of Science, 2010, 5 (10), pii: e13075. ⟨10.1371/journal.pone.0013075⟩
PLoS ONE, 2010, 5 (10), pii: e13075. ⟨10.1371/journal.pone.0013075⟩
PLoS ONE
PLoS ONE, Public Library of Science, 2010, 5 (10), pii: e13075. ⟨10.1371/journal.pone.0013075⟩
PLoS ONE, 2010, 5 (10), pii: e13075. ⟨10.1371/journal.pone.0013075⟩
International audience; BACKGROUND: RdCVF and RdCVF2, encoded by the nucleoredoxin-like genes NXNL1 and NXNL2, are trophic factors with therapeutic potential that are involved in cone photoreceptor survival. Studying how their expression is regulated
Autor:
Marie-Laure Niepon, Serge Picaud, Andranik Petrosian, Céline Jaillard, Thierry Léveillard, Emmanuelle Clérin, Olivier Poch, Irene Lee-Rivera, Wolfgang Raffelsberger, Bernd Kinzel, Therese Cronin, José-Alain Sahel
Publikováno v:
Cell Death and Differentiation
Cell Death and Differentiation, Nature Publishing Group, 2010, 17 (7), pp.1199-1210. ⟨10.1038/cdd.2010.2⟩
Cell Death and Differentiation, 2010, 17 (7), pp.1199-210. ⟨10.1038/cdd.2010.2⟩
Cell Death and Differentiation, Nature Publishing Group, 2010, 17 (7), pp.1199-210. ⟨10.1038/cdd.2010.2⟩
Cell Death and Differentiation, Nature Publishing Group, 2010, 17 (7), pp.1199-1210. ⟨10.1038/cdd.2010.2⟩
Cell Death and Differentiation, 2010, 17 (7), pp.1199-210. ⟨10.1038/cdd.2010.2⟩
Cell Death and Differentiation, Nature Publishing Group, 2010, 17 (7), pp.1199-210. ⟨10.1038/cdd.2010.2⟩
International audience; Rod-derived cone viability factor (RdCVF) is a thioredoxin-like protein, which has therapeutic potential for rod-cone dystrophies such as retinitis pigmentosa (RP). Cone loss in rodent models of RP is effectively reduced by Rd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::971f1d6282772da3b75b9ac31b362ee6
https://www.hal.inserm.fr/inserm-02894155/file/cdd20102.pdf
https://www.hal.inserm.fr/inserm-02894155/file/cdd20102.pdf
Autor:
François Delalande, Olivier Poch, Therese Cronin, Géraldine Millet-Puel, Ram Fridlich, Alain Van Dorsselaer, Arne Holmgren, Céline Jaillard, Jun Lu, Ludivine Perrocheau, Thierry Léveillard, José-Alain Sahel, Marie-Laure Niepon, Laetitia Poidevin
Publikováno v:
Molecular and Cellular Proteomics
Molecular and Cellular Proteomics, 2009, 8 (6), pp.1206-18. ⟨10.1074/mcp.M800406-MCP200⟩
Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2009, 8 (6), pp.1206-18. ⟨10.1074/mcp.M800406-MCP200⟩
Molecular and Cellular Proteomics, 2009, 8 (6), pp.1206-18. ⟨10.1074/mcp.M800406-MCP200⟩
Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2009, 8 (6), pp.1206-18. ⟨10.1074/mcp.M800406-MCP200⟩
International audience; Rod-derived cone viability factor (RdCVF) is produced by the Nxnl1 gene that codes for a second polypeptide, RdCVFL, by alternative splicing. Although the role of RdCVF in promoting cone survival has been described, the implic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ec6fc1e71ce997627dd15c7d4e651e
https://www.hal.inserm.fr/inserm-00420386
https://www.hal.inserm.fr/inserm-00420386