Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Regine Chambrey"'
Autor:
Valérie Olivier, Ali Sassi, Gregoire Arnoux, Regine Chambrey, Isabelle Roth, Alexandra Chassot, Khalil Udwan, Eva Dizin, Joseph M. Rutkowski, Lydie Cheval, Gilles Crambert, Carsten A. Wagner, Alain Doucet, Dominique Eladari, Solange Moll, Eric Feraille, Suresh K Ramakrishnan
BackgroundNephrotic syndrome (NS) is characterized by massive sodium chloride retention. Along the kidney tubule, sodium and chloride reabsorption are coupled via a combination of transcellular and paracellular transport pathways. The mechanism of so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d09d3106dc666448d4929d98b858ddd
https://doi.org/10.1101/2022.06.01.494142
https://doi.org/10.1101/2022.06.01.494142
Autor:
Masayoshi, Nanami, Truyen D, Pham, Young Hee, Kim, Baoli, Yang, Roy L, Sutliff, Olivier, Staub, Janet D, Klein, Karen I, Lopez-Cayuqueo, Regine, Chambrey, Annie Y, Park, Xiaonan, Wang, Vladimir, Pech, Jill W, Verlander, Susan M, Wall
Publikováno v:
Journal of the American Society of Nephrology : JASN. 29(6)
Background Nedd4–2 is an E3 ubiquitin-protein ligase that associates with transport proteins, causing their ubiquitylation, and then internalization and degradation. Previous research has suggested a correlation between Nedd4–2 and BP. In this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb19e0d0ea30d9eebb3c355fb326be6d
https://pubmed.ncbi.nlm.nih.gov/29773687
https://pubmed.ncbi.nlm.nih.gov/29773687
Autor:
Dominique, Eladari, Regine, Chambrey
Publikováno v:
Journal of nephrology. 20(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed9af0a050a920495aca516c520c5d7f
https://pubmed.ncbi.nlm.nih.gov/17557258
https://pubmed.ncbi.nlm.nih.gov/17557258
Autor:
Isabel Cornejo, Sandra Villanueva, Johanna Burgos, Karen I. López-Cayuqueo, Régine Chambrey, Francisca Julio-Kalajzić, Neudo Buelvas, María I. Niemeyer, Dulce Figueiras-Fierro, Peter D. Brown, Francisco V. Sepúlveda, L. P. Cid
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
Kir7.1 encoded by the Kcnj13 gene in the mouse is an inwardly rectifying K+ channel present in epithelia where it shares membrane localization with the Na+/K+-pump. Further investigations of the localisation and function of Kir7.1 would benefit from
Externí odkaz:
https://doaj.org/article/6db18327ca47476fadae929679c78f84
Autor:
Devishree Krishnan, Wanling Pan, Megan R. Beggs, Francesco Trepiccione, Régine Chambrey, Dominique Eladari, Emmanuelle Cordat, Henrik Dimke, R. Todd Alexander
Publikováno v:
Frontiers in Physiology, Vol 8 (2018)
Carbonic anhydrase II (CAII) is expressed along the nephron where it interacts with a number of transport proteins augmenting their activity. Aquaporin-1 (AQP1) interacts with CAII to increase water flux through the water channel. Both CAII and aquap
Externí odkaz:
https://doaj.org/article/4962294ff82340fc8a597ac5390d9bb1
Autor:
Xiangming Li, Joel D Sanneman, Donald G Harbidge, Fei Zhou, Taku Ito, Raoul Nelson, Nicolas Picard, Régine Chambrey, Dominique Eladari, Tracy Miesner, Andrew J Griffith, Daniel C Marcus, Philine Wangemann
Publikováno v:
PLoS Genetics, Vol 9, Iss 7, p e1003641 (2013)
Mutations of SLC26A4 are a common cause of human hearing loss associated with enlargement of the vestibular aqueduct. SLC26A4 encodes pendrin, an anion exchanger expressed in a variety of epithelial cells in the cochlea, the vestibular labyrinth and
Externí odkaz:
https://doaj.org/article/a86719aa2c854770b010a3f7775fd156