Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lydie Fasquelle"'
Knock down of heat shock protein 27 (HspB1) induces degradation of several putative client proteins.
Autor:
Benjamin Gibert, Bénédicte Eckel, Lydie Fasquelle, Maryline Moulin, Frantz Bouhallier, Vincent Gonin, Gregory Mellier, Stéphanie Simon, Carole Kretz-Remy, André-Patrick Arrigo, Chantal Diaz-Latoud
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e29719 (2012)
Hsp27 belongs to the heat shock protein family and displays chaperone properties in stress conditions by holding unfolded polypeptides, hence avoiding their inclination to aggregate. Hsp27 is often referenced as an anti-cancer therapeutic target, but
Externí odkaz:
https://doaj.org/article/c51afa4923024b758fc69a3d4b5dfe06
Autor:
Jean-Luc Puel, Laurence Molina, Benjamin Delprat, Régis Nouvian, Franck Molina, Hamish S. Scott, Lydie Fasquelle, Nicolas Salvetat, Michel Guipponi
Publikováno v:
Human Molecular Genetics. 22:1289-1299
usc Before acquiring their mature state, cochlear hair cells undergo a series of changes in expression of ion channels. How this complex mechanism is achieved is not fully understood. Tmprss3, a type II serine protease expressed in hair cells, is req
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::589439e27706c2a235687bab9b16e2e9
https://doi.org/10.1093/hmg/dds532
https://doi.org/10.1093/hmg/dds532
Autor:
Stylianos E. Antonarakis, Benjamin Delprat, Florence François, Lydie Fasquelle, Jean-Luc Puel, Michel Guipponi, Christian Chabbert, Elizabeth Neidhart, Sophie Gaboyard, Marc Lenoir, Guy Rebillard, Stéphanie Ventéo, Anne-Laure Mausset-Bonnefont, Hamish S. Scott, Jing Wang
Publikováno v:
Journal of Biological Chemistry, Vol. 286, No 19 (2011) pp. 17383-97
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2011, ⟨10.1074/jbc.M110.190652⟩
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2011, ⟨10.1074/jbc.M110.190652⟩
International audience; Mutations in the type II transmembrane serine protease 3 (TMPRSS3) gene cause non-syndromic autosomal recessive deafness (DFNB8/10), characterized by congenital or childhood onset bilateral profound hearing loss. In order to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ab4eda59ab3febb748e31e16b4b6e9
https://doi.org/10.1074/jbc.m110.190652
https://doi.org/10.1074/jbc.m110.190652
Autor:
Maryline Moulin, Carole Kretz-Remy, Vincent Gonin, André-Patrick Arrigo, Frantz Bouhallier, Benjamin Gibert, Stéphanie Simon, Lydie Fasquelle, Benedicte Eckel, Chantal Diaz-Latoud, Gregory Mellier
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2012, 7 (1), pp.e29719. ⟨10.1371/journal.pone.0029719⟩
Plos One 1 (7), . (2012)
PLoS ONE, 2012, 7 (1), pp.e29719. ⟨10.1371/journal.pone.0029719⟩
PLoS ONE, Vol 7, Iss 1, p e29719 (2012)
PLoS ONE, Public Library of Science, 2012, 7 (1), pp.e29719. ⟨10.1371/journal.pone.0029719⟩
Plos One 1 (7), . (2012)
PLoS ONE, 2012, 7 (1), pp.e29719. ⟨10.1371/journal.pone.0029719⟩
PLoS ONE, Vol 7, Iss 1, p e29719 (2012)
International audience; Hsp27 belongs to the heat shock protein family and displays chaperone properties in stress conditions by holding unfolded polypeptides, hence avoiding their inclination to aggregate. Hsp27 is often referenced as an anti-cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f142d13f59355bd5df5fe8b533570560
http://europepmc.org/articles/PMC3251601
http://europepmc.org/articles/PMC3251601