Kurt G. Beam

La Aurora, CES, Colombia

Last Updated: 09/26/2026

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Found 22 publications

Interaction between CaV2.1 and Junctophilin3/4 depends on the II-III loop of CaV2.1 and on the α-helical region of Junctophilin3/4.

Interaction between CaV2.1 and Junctophilin3/4 depends on the II-III loop of CaV2.1 and on the α-helical region of Junctophilin3/4.

Journal: The Journal of biological chemistry

Published: September 16, 2024

Putative malignant hyperthermia mutation CaV1.1-R174W is insufficient to trigger a fulminant response to halothane or confer heat stress intolerance.

Putative malignant hyperthermia mutation CaV1.1-R174W is insufficient to trigger a fulminant response to halothane or confer heat stress intolerance.

Journal: The Journal of biological chemistry

Published: April 04, 2023

The funny current If is essential for the fight-or-flight response in cardiac pacemaker cells.

The funny current If is essential for the fight-or-flight response in cardiac pacemaker cells.

Journal: The Journal of general physiology

Published: May 12, 2022

The distal C terminus of the dihydropyridine receptor β1a subunit is essential for tetrad formation in skeletal muscle.

The distal C terminus of the dihydropyridine receptor β1a subunit is essential for tetrad formation in skeletal muscle.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 04, 2022

Junctophilins 1, 2, and 3 all support voltage-induced Ca2+ release despite considerable divergence.

Junctophilins 1, 2, and 3 all support voltage-induced Ca2+ release despite considerable divergence.

Journal: The Journal of general physiology

Published: September 08, 2021

Neuronal junctophilins recruit specific CaV and RyR isoforms to ER-PM junctions and functionally alter CaV2.1 and CaV2.2.

Neuronal junctophilins recruit specific CaV and RyR isoforms to ER-PM junctions and functionally alter CaV2.1 and CaV2.2.

Journal: eLife

Published: October 22, 2020

Stac Proteins Suppress Ca2+-Dependent Inactivation of Neuronal l-type Ca2+ Channels.

Stac Proteins Suppress Ca2+-Dependent Inactivation of Neuronal l-type Ca2+ Channels.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: March 15, 2018

De novo reconstitution reveals the proteins required for skeletal muscle voltage-induced Ca2+ release.

De novo reconstitution reveals the proteins required for skeletal muscle voltage-induced Ca2+ release.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: December 13, 2017

Stac proteins associate with the critical domain for excitation-contraction coupling in the II-III loop of CaV1.1.

Stac proteins associate with the critical domain for excitation-contraction coupling in the II-III loop of CaV1.1.

Journal: The Journal of general physiology

Published: October 02, 2017

Junctional trafficking and restoration of retrograde signaling by the cytoplasmic RyR1 domain.

Junctional trafficking and restoration of retrograde signaling by the cytoplasmic RyR1 domain.

Journal: The Journal of general physiology

Published: August 10, 2017

Stac3 has a direct role in skeletal muscle-type excitation-contraction coupling that is disrupted by a myopathy-causing mutation.

Stac3 has a direct role in skeletal muscle-type excitation-contraction coupling that is disrupted by a myopathy-causing mutation.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 14, 2016

Distinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1.

Distinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1.

Journal: Biophysical journal

Published: November 16, 2015

Showing 1-12 of 22

Last Updated: 09/26/2026