Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Celine Loriol"'
Autor:
Martine Avella, Franck Borgese, Celine Loriol, Sandrine Dulong, Nicole Gabillat, Jordi Ehrenfeld, Kim E. Boulukos
Publikováno v:
Cellular Physiology and Biochemistry. 22:015-030
SLC26 family members are anionic transporters involved in Cl- and HCO3- absorption or secretion in epithelia. SLC26A9, preferentially expressed in the lung, is a poorl
Publikováno v:
Journal of Cellular Physiology
Journal of Cellular Physiology, Wiley, 2011, 226 (1), pp.212-223. ⟨10.1002/jcp.22328⟩
Journal of Cellular Physiology, Wiley, 2011, 226 (1), pp.212-223. ⟨10.1002/jcp.22328⟩
International audience; We investigated the possible functional- and physical protein-interactions between two airway Cl(-) channels, SLC26A9 and CFTR. Bronchial CFBE41o-cell lines expressing CFTR(WT) or CFTR(DeltaF508) were transduced with SLC26A9.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7533f6ea6cb82ef7fb3b0c68eb099cb4
https://hal.archives-ouvertes.fr/hal-00506171
https://hal.archives-ouvertes.fr/hal-00506171
Autor:
Celine, Loriol, Sandrine, Dulong, Martine, Avella, Nicole, Gabillat, Kim, Boulukos, Franck, Borgese, Jordi, Ehrenfeld
Publikováno v:
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology. 22(1-4)
SLC26 family members are anionic transporters involved in Cl(-) and HCO(3)(-) absorption or secretion in epithelia. SLC26A9, preferentially expressed in the lung, is a poorly characterized member of this family. In this study, we investigated the tra
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
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e33757 (2012)
Small Ubiquitin-like MOdifier protein (SUMO) is a key regulator of nuclear functions but little is known regarding the role of the post-translational modification sumoylation outside of the nucleus, particularly in the Central Nervous System (CNS).He
Externí odkaz:
https://doaj.org/article/afac2dd216a4419cb295a5621999b607