Laurent Schild

Lausanne, VD, Switzerland

Last Updated: 09/26/2026

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Found 10 publications

A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene.

A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene.

Journal: American journal of physiology. Endocrinology and metabolism
Published: May 03, 2023

Imatinib Uptake into Cells is Not Mediated by Organic Cation Transporters OCT1, OCT2, or OCT3, But is Influenced by Extracellular pH.

Imatinib Uptake into Cells is Not Mediated by Organic Cation Transporters OCT1, OCT2, or OCT3, But is Influenced by Extracellular pH.

Journal: Drug metabolism letters
Published: October 04, 2018

Human Mutations in SLC2A9 (Glut9) Affect Transport Capacity for Urate.

Human Mutations in SLC2A9 (Glut9) Affect Transport Capacity for Urate.

Journal: Frontiers in physiology
Published: January 09, 2018

A Missense Mutation in the Extracellular Domain of αENaC Causes Liddle Syndrome.

A Missense Mutation in the Extracellular Domain of αENaC Causes Liddle Syndrome.

Journal: Journal of the American Society of Nephrology : JASN
Published: November 02, 2016

Proton and non-proton activation of ASIC channels.

Proton and non-proton activation of ASIC channels.

Journal: PloS one
Published: September 02, 2016

Renal Fanconi Syndrome and Hypophosphatemic Rickets in the Absence of Xenotropic and Polytropic Retroviral Receptor in the Nephron.

Renal Fanconi Syndrome and Hypophosphatemic Rickets in the Absence of Xenotropic and Polytropic Retroviral Receptor in the Nephron.

Journal: Journal of the American Society of Nephrology : JASN
Published: July 06, 2016

The Human Acid-Sensing Ion Channel ASIC1a: Evidence for a Homotetrameric Assembly State at the Cell Surface.

The Human Acid-Sensing Ion Channel ASIC1a: Evidence for a Homotetrameric Assembly State at the Cell Surface.

Journal: PloS one
Published: May 01, 2015

International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel.

International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel.

Journal: Pharmacological reviews
Published: October 08, 2014

Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.

Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.

Journal: Journal of the neurological sciences
Published: December 09, 2013

Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea.

Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea.

Journal: PloS one
Published: October 23, 2013
Showing 1-10 of 10

Last Updated: 09/26/2026