Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Dominique, Eladari"'
Autor:
Frank Bienaimé, Mordi Muorah, Marie Metzger, Melanie Broeuilh, Pascal Houiller, Martin Flamant, Jean-Philippe Haymann, Jacky Vonderscher, Jacques Mizrahi, Gérard Friedlander, Bénédicte Stengel, Fabiola Terzi, François Vrtovsnik, Eric Daugas, Emmanuelle Vidal-Petiot, Christian Jacquot, Alexandre Karras, Stéphane Roueff, Eric Thervet, Pascal Houillier, Marie Courbebaisse, Dominique Eladari et Gérard Maruani, Pablo Urena-Torres, Jean-Jacques Boffa, Pierre Ronco, H. Fessi, Eric Rondeau, Emmanuel Letavernier, Nahid Tabibzadeh
Publikováno v:
EBioMedicine, Vol 93, Iss , Pp 104635- (2023)
Summary: Background: Urinary biomarkers may improve the prediction of chronic kidney disease (CKD) progression. Yet, data reporting the applicability of most commercial biomarker assays to the detection of their target analyte in urine together with
Externí odkaz:
https://doaj.org/article/7817ac03d9a2498697a600d278abdb45
Autor:
Jean-Philippe Bertocchio, Sandrine Genetet, Lydie Da Costa, Stephen B. Walsh, Bertrand Knebelmann, Julie Galimand, Lucie Bessenay, Corinne Guitton, Renaud De Lafaille, Rosa Vargas-Poussou, Dominique Eladari, Isabelle Mouro-Chanteloup
Publikováno v:
Kidney International Reports, Vol 5, Iss 3, Pp 348-357 (2020)
Introduction: Anion exchanger 1 (AE1) (SLC4A1 gene product) is a membrane protein expressed in both kidney and red blood cells (RBCs): it exchanges extracellular bicarbonate (HCO3–) for intracellular chloride (Cl–) and participates in acid−base
Externí odkaz:
https://doaj.org/article/79ff7ef222314bfb9509f28ea7aa4c2c
Autor:
Maxime Louet, Sara Bitam, Naziha Bakouh, Yohan Bignon, Gabrielle Planelles, David Lagorce, Maria A. Miteva, Dominique Eladari, Jacques Teulon, Bruno O. Villoutreix
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract The human ClC-Kb channel plays a key role in exporting chloride ions from the cytosol and is known to be involved in Bartter syndrome type 3 when its permeation capacity is decreased. The ClC-Kb channel has been recently proposed as a potent
Externí odkaz:
https://doaj.org/article/4dc1bd937e734475b48e1b0e7b1ec36e
Autor:
Nicolas Cornière, R Brent Thomson, Stéphanie Thauvin, Bruno O Villoutreix, Sophie Karp, Diane W Dynia, Sarah Burlein, Lennart Brinkmann, Alaa Badreddine, Aurélie Dechaume, Mehdi Derhourhi, Emmanuelle Durand, Emmanuel Vaillant, Philippe Froguel, Régine Chambrey, Peter S Aronson, Amélie Bonnefond, Dominique Eladari
Publikováno v:
Journal of Medical Genetics. 59:1035-1043
BackgroundNephrolithiasis (NL) is a complex multifactorial disease affecting up to 10%–20% of the human population and causing a significant burden on public health systems worldwide. It results from a combination of environmental and genetic facto
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:
Régine Chambrey, Dominique Eladari
Publikováno v:
American Journal of Physiology-Renal Physiology. 324:F431-F432
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:
Nicolas Cornière, Dominique Eladari
Publikováno v:
Kidney Int
Distal renal tubular acidosis is a rare renal tubular disorder characterized by hyperchloremic metabolic acidosis and impaired urinary acidification. Mutations in three genes (ATP6V0A4, ATP6V1B1 and SLC4A1) constitute a monogenic causation in 58–70
Autor:
J. Christopher Hennings, Nicolas Picard, Antje K. Huebner, Tobias Stauber, Hannes Maier, Dennis Brown, Thomas J. Jentsch, Rosa Vargas‐Poussou, Dominique Eladari, Christian A. Hübner
Publikováno v:
EMBO Molecular Medicine, Vol 4, Iss 10, Pp 1057-1071 (2012)
Abstract The V‐ATPase is a multisubunit complex that transports protons across membranes. Mutations of its B1 or a4 subunit are associated with distal renal tubular acidosis and deafness. In the kidney, the a4 subunit is expressed in intercalated c
Externí odkaz:
https://doaj.org/article/6264d470c0c14d32bb944a94935ba5d0
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