Ryanodine Receptor Open Times Are Determined in the Closed State

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Ryanodine Receptor Open Times Are Determined in the Closed State

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im Oktober 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в жовтні 2018

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Ryanodine Receptor Open Times Are Determined in the Closed State

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Ryanodine Receptor Open Times Are Determined in the Closed State

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Ryanodine Receptor Open Times Are Determined in the Closed State

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Ryanodine Receptor Open Times Are Determined in the Closed State

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Ryanodine Receptor Open Times Are Determined in the Closed State

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Ryanodine Receptor Open Times Are Determined in the Closed State

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P1476

Ryanodine Receptor Open Times Are Determined in the Closed State

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P2093

Dirk Gillespie

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Michael Fill

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P2860

The role of calsequestrin, triadin, and junctin in conferring cardiac ryanodine receptor responsiveness to luminal calcium.

Ca2+ stores regulate ryanodine receptor Ca2+ release channels via luminal and cytosolic Ca2+ sites

Markovian models of low and high activity levels of cardiac ryanodine receptors

Data transformations for improved display and fitting of single-channel dwell time histograms

Flux regulation of cardiac ryanodine receptor channels.

On Brownian Distance Covariance and High Dimensional Data

Gating of the native and purified cardiac SR Ca(2+)-release channel with monovalent cations as permeant species

Streaming potentials reveal a short ryanodine-sensitive selectivity filter in cardiac Ca2+ release channel.

Regulation of cardiac muscle Ca2+ release channel by sarcoplasmic reticulum lumenal Ca2+

Regulation of ryanodine receptors by calsequestrin: effect of high luminal Ca2+ and phosphorylation.

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1160-1165

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scholarly article

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10.1016/J.BPJ.2018.08.025

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English

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P478

115

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P577

2018-10-02T00:00:00Z

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30220413

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P921

Biofiseg

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6170654

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