Emmanuelle Cordat

Edmonton, AB, Canada

Last Updated: 09/26/2026

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Found 35 publications

A-intercalated cell dysfunction disrupts renal epithelial-immune balance and impairs host defense during UTI.

A-intercalated cell dysfunction disrupts renal epithelial-immune balance and impairs host defense during UTI.

Journal: American journal of physiology. Renal physiology
Published: June 15, 2026

SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy.

SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy.

Journal: eLife
Published: March 04, 2026

Molecular mechanisms of acute inflammation: systemic responses and kidney-specific pathophysiology.

Molecular mechanisms of acute inflammation: systemic responses and kidney-specific pathophysiology.

Journal: Function (Oxford, England)
Published: December 16, 2025

Urinary sodium wasting and disrupted collecting duct function in mice with distal renal tubular acidosis mutations.

Urinary sodium wasting and disrupted collecting duct function in mice with distal renal tubular acidosis mutations.

Journal: Disease models & mechanisms
Published: October 04, 2024

Unraveling the molecular landscape of kAE1: a narrative review.

Unraveling the molecular landscape of kAE1: a narrative review.

Journal: Canadian journal of physiology and pharmacology
Published: April 26, 2024

Expression of the kidney anion exchanger 1 affects WNK4 and SPAK phosphorylation and results in claudin-4 phosphorylation.

Expression of the kidney anion exchanger 1 affects WNK4 and SPAK phosphorylation and results in claudin-4 phosphorylation.

Journal: Heliyon
Published: May 24, 2023

Urinary Tract Infections: Renal Intercalated Cells Protect against Pathogens.

Urinary Tract Infections: Renal Intercalated Cells Protect against Pathogens.

Journal: Journal of the American Society of Nephrology : JASN
Published: January 19, 2023

Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome.

Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome.

Journal: Human molecular genetics
Published: November 15, 2022

Claudin-2 and claudin-12 form independent, complementary pores required to maintain calcium homeostasis.

Claudin-2 and claudin-12 form independent, complementary pores required to maintain calcium homeostasis.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 18, 2021

Boosting endoplasmic reticulum folding capacity reduces unfolded protein response activation and intracellular accumulation of human kidney anion exchanger 1 in Saccharomyces cerevisiae.

Boosting endoplasmic reticulum folding capacity reduces unfolded protein response activation and intracellular accumulation of human kidney anion exchanger 1 in Saccharomyces cerevisiae.

Journal: Yeast (Chichester, England)
Published: March 08, 2021

Characterization of five novel vasopressin V2 receptor mutants causing nephrogenic diabetes insipidus reveals a role of tolvaptan for M272R-V2R mutation.

Characterization of five novel vasopressin V2 receptor mutants causing nephrogenic diabetes insipidus reveals a role of tolvaptan for M272R-V2R mutation.

Journal: Scientific reports
Published: April 20, 2020

Human red blood cell uptake and sequestration of arsenite and selenite: Evidence of seleno-bis(S-glutathionyl) arsinium ion formation in human cells.

Human red blood cell uptake and sequestration of arsenite and selenite: Evidence of seleno-bis(S-glutathionyl) arsinium ion formation in human cells.

Journal: Biochemical pharmacology
Published: March 31, 2020
Showing 1-12 of 35

Last Updated: 09/26/2026