Robin N. Stringer

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 12 publications

Pathophysiology of homocysteine: insights into ion channel dysfunction.

Pathophysiology of homocysteine: insights into ion channel dysfunction.

Journal: Pflugers Archiv : European journal of physiology
Published: February 06, 2026

Electrophysiological characterization of sourced human iPSC-derived motor neurons.

Electrophysiological characterization of sourced human iPSC-derived motor neurons.

Journal: Channels (Austin, Tex.)
Published: March 25, 2025

Homocysteine enhances the excitability of cultured hippocampal neurons without altering the gene expression of voltage-gated ion channels.

Homocysteine enhances the excitability of cultured hippocampal neurons without altering the gene expression of voltage-gated ion channels.

Journal: Molecular brain
Published: March 14, 2025

Functional characterization of a novel de novo CACNA1C pathogenic variant in a patient with neurodevelopmental disorder.

Functional characterization of a novel de novo CACNA1C pathogenic variant in a patient with neurodevelopmental disorder.

Journal: Molecular brain
Published: February 06, 2025

Pathophysiology of ion channels in amyotrophic lateral sclerosis.

Pathophysiology of ion channels in amyotrophic lateral sclerosis.

Journal: Molecular brain
Published: August 22, 2023

Electrophysiological characterization of a Cav3.2 calcium channel missense variant associated with epilepsy and hearing loss.

Electrophysiological characterization of a Cav3.2 calcium channel missense variant associated with epilepsy and hearing loss.

Journal: Molecular brain
Published: August 14, 2023

Electrophysiological and computational analysis of Cav3.2 channel variants associated with familial trigeminal neuralgia.

Electrophysiological and computational analysis of Cav3.2 channel variants associated with familial trigeminal neuralgia.

Journal: Molecular brain
Published: October 12, 2022

Secretory carrier-associated membrane protein 2 (SCAMP2) regulates cell surface expression of T-type calcium channels.

Secretory carrier-associated membrane protein 2 (SCAMP2) regulates cell surface expression of T-type calcium channels.

Journal: Molecular brain
Published: December 02, 2021

De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.

De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.

Journal: Molecular brain
Published: June 29, 2021

Functional identification of potential non-canonical N-glycosylation sites within Cav3.2 T-type calcium channels.

Functional identification of potential non-canonical N-glycosylation sites within Cav3.2 T-type calcium channels.

Journal: Molecular brain
Published: August 27, 2020

Transcriptomic analysis of glycan-processing genes in the dorsal root ganglia of diabetic mice and functional characterization on Cav3.2 channels.

Transcriptomic analysis of glycan-processing genes in the dorsal root ganglia of diabetic mice and functional characterization on Cav3.2 channels.

Journal: Channels (Austin, Tex.)
Published: April 03, 2020

A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.

A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.

Journal: Molecular brain
Published: November 25, 2019
Showing 1-12 of 12

Last Updated: 09/26/2026