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List of works by Mathilde Keck

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

scientific article published on 24 December 2019

Brain renin-angiotensin system blockade with orally active aminopeptidase A inhibitor prevents cardiac dysfunction after myocardial infarction in mice

scientific article published on 30 December 2018

CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca2+ dependence of ClC-Kb channels

scientific article published on 24 November 2013

Cardiac inflammatory CD11b/c cells exert a protective role in hypertrophied cardiomyocyte by promoting TNFR- and Orai3- dependent signaling

scientific article published on 15 April 2019

Characterization of the mouse ClC-K1/Barttin chloride channel.

scientific article published on 18 June 2013

ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.

scientific article published on 25 March 2015

Clinical and Genetic Spectrum of Bartter Syndrome Type 3.

scientific article published on 5 April 2017

Emergence of Orai3 activity during cardiac hypertrophy.

scientific article published on 11 September 2014

From a Cone Snail Toxin to a Competitive MC4R Antagonist

scientific article published in 2022

Heterogeneity in the processing of CLCN5 mutants related to Dent disease.

scientific article published in April 2011

Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell development

scientific article published on 28 August 2013

NI956/QGC006, a Potent Orally Active, Brain-Penetrating Aminopeptidase A Inhibitor for Treating Hypertension

scientific article published on 01 June 2019

Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression.

scientific article published on 12 June 2013

Orally Active Aminopeptidase A Inhibitor Prodrugs: Current State and Future Directions

scientific article published on 21 May 2019

Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome.

scientific article

The ClC-K2 Chloride Channel Is Critical for Salt Handling in the Distal Nephron.

scientific article published on 22 June 2016