Nadia Frachon
Paris, France
Last Updated: 09/26/2026
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Found 11 publications
Empagliflozin does not prevent progression of Dent's disease type 1 in a mouse model.
Journal: Experimental physiology
Published: March 09, 2025
The apical 70-pS potassium K channel in the thick ascending limb of Henle's loop is a large-conductance Na+-and Cl--activated, KNa1.1-like, channel.
Journal: American journal of physiology. Renal physiology
Published: January 25, 2024
AUP1 Regulates the Endoplasmic Reticulum-Associated Degradation and Polyubiquitination of NKCC2.
Journal: Cells
Published: January 01, 2024
Diacidic Motifs in the Carboxyl Terminus Are Required for ER Exit and Translocation to the Plasma Membrane of NKCC2.
Journal: International journal of molecular sciences
Published: October 07, 2022
New insights into the role of endoplasmic reticulum-associated degradation in Bartter Syndrome Type 1.
Journal: Human mutation
Published: November 10, 2020
Diversity of functional alterations of the ClC-5 exchanger in the region of the proton glutamate in patients with Dent disease 1.
Journal: Human mutation
Published: September 25, 2020
Analysis of CLCNKB mutations at dimer-interface, calcium-binding site, and pore reveals a variety of functional alterations in ClC-Kb channel leading to Bartter syndrome.
Journal: Human mutation
Published: June 24, 2019
Defective bicarbonate reabsorption in Kir4.2 potassium channel deficient mice impairs acid-base balance and ammonia excretion.
Journal: Kidney international
Published: October 23, 2018
A novel CLCN5 pathogenic mutation supports Dent disease with normal endosomal acidification.
Journal: Human mutation
Published: January 23, 2018
Showing 1-11 of 11
Last Updated: 09/26/2026