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Search Results to Kurt G Beam Jr.

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Beam, Kurt

One or more keywords matched the following items that are connected to Beam, Kurt

Item Type	Name
Academic Article	Role of S4 segments and the leucine heptad motif in the activation of an L-type calcium channel.
Academic Article	Critical roles of the S3 segment and S3-S4 linker of repeat I in activation of L-type calcium channels.
Academic Article	Calcium channelopathies.
Academic Article	Potentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms.
Academic Article	Insertion of alpha1S II-III loop and C terminal sequences into alpha1H fails to restore excitation-contraction coupling in dysgenic myotubes.
Academic Article	A malignant hyperthermia-inducing mutation in RYR1 (R163C): consequent alterations in the functional properties of DHPR channels.
Academic Article	A malignant hyperthermia-inducing mutation in RYR1 (R163C): alterations in Ca2+ entry, release, and retrograde signaling to the DHPR.
Academic Article	Properties of Na+ currents conducted by a skeletal muscle L-type Ca2+ channel pore mutant (SkEIIIK).
Academic Article	The muscular dysgenesis mutation in mice leads to arrest of the genetic program for muscle differentiation.
Academic Article	Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA.
Academic Article	Impaired gating of an L-Type Ca(2+) channel carrying a mutation linked to malignant hyperthermia.
Academic Article	Ryanodine receptor type 1 (RyR1) mutations C4958S and C4961S reveal excitation-coupled calcium entry (ECCE) is independent of sarcoplasmic reticulum store depletion.
Academic Article	Disease causing mutations of calcium channels.
Academic Article	A lethal mutation in mice eliminates the slow calcium current in skeletal muscle cells.
Academic Article	Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis.
Academic Article	Structure, function, and regulation of the skeletal muscle dihydropyridine receptor.
Academic Article	Malignant hyperthermia susceptibility arising from altered resting coupling between the skeletal muscle L-type Ca2+ channel and the type 1 ryanodine receptor.
Concept	Mutation
Concept	Point Mutation
Concept	Mutation, Missense
Academic Article	Distinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1.
Academic Article	Stac3 has a direct role in skeletal muscle-type excitation-contraction coupling that is disrupted by a myopathy-causing mutation.
Grant	2009 GRC Muscle: Excitation/Contraction Coupling
Grant	Regulation of Membrane Excitability
Grant	ONTOGENY OF NEURONAL ION CHANNELS
Grant	PHYSIOLOGICAL CONTROL OF CELLULAR EXCITABILITY
Grant	Regulation of Membrane Excitability
Academic Article	Putative malignant hyperthermia mutation CaV1.1-R174W is insufficient to trigger a fulminant response to halothane or confer heat stress intolerance.

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