(Q24294413)

GOA release 2020-03-11

protein polymerization

1 reference

GOA release 2020-03-11

5

Hendrik Milting

Hendrik

Milting

1 reference

26 October 2023

7

ChulHee Kang

ChulHee

Kang

1 reference

26 October 2023

2

Buhyun Youn

Buhyun

Youn

1 reference

26 October 2023

Eunjung Kim

1

Eunjung

Kim

1 reference

26 October 2023

Lenord Kemper

series ordinal

3

author given names

Lenord

author last names

Kemper

1 reference

26 October 2023

Cait Campbell

series ordinal

4

author given names

Cait

author last names

Campbell

1 reference

26 October 2023

Magdolna Varsanyi

series ordinal

6

author given names

Magdolna

author last names

Varsanyi

1 reference

Journal of Molecular Biology

26 October 2023

language of work or name

English

0 references

publication date

2 November 2007

0 references

published in

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volume

373

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issue

4

0 references

page(s)

1047-57

0 references

cites work

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Apparent cooperativity of Ca2+ binding associated with crystallization of Ca2+-binding protein from sarcoplasmic reticulum

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Calsequestrin mutant D307H exhibits depressed binding to its protein targets and a depressed response to calcium

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Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insights

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Polymorphic ventricular tachyarrhythmias in the absence of organic heart disease: classification, differential diagnosis, and implications for therapy

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Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.

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Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

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A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

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7 January 2021

Intravesicular calcium transient during calcium release from sarcoplasmic reticulum

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Localization and partial characterization of the oligomeric disulfide-linked molecular weight 95,000 protein (triadin) which binds the ryanodine and dihydropyridine receptors in skeletal muscle triadic vesicles

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Characterization of cardiac calsequestrin

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Crystal structure of calsequestrin from rabbit skeletal muscle sarcoplasmic reticulum

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Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms

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Role of ryanodine receptor mutations in cardiac pathology: more questions than answers?

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RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR)

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Depletion "skraps" and dynamic buffering inside the cellular calcium store.

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Calsequestrin determines the functional size and stability of cardiac intracellular calcium stores: Mechanism for hereditary arrhythmia

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Isolation of a calcium-sequestering protein from sarcoplasmic reticulum

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Purification and crystallization of the calcium binding protein of sarcoplasmic reticulum from skeletal muscle

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Purification, primary structure, and immunological characterization of the 26-kDa calsequestrin binding protein (junctin) from cardiac junctional sarcoplasmic reticulum

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Complex formation between junctin, triadin, calsequestrin, and the ryanodine receptor. Proteins of the cardiac junctional sarcoplasmic reticulum membrane

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Localization and characterization of the calsequestrin-binding domain of triadin 1. Evidence for a charged beta-strand in mediating the protein-protein interaction

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Polymerization of calsequestrin. Implications for Ca2+ regulation

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Comparing skeletal and cardiac calsequestrin structures and their calcium binding: a proposed mechanism for coupled calcium binding and protein polymerization

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7 January 2021

A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

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7 January 2021

The structure of calsequestrin in triads of vertebrate skeletal muscle: a deep-etch study

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Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle

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A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

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Changes in left ventricular repolarization and ion channel currents following a transient rate increase superimposed on bradycardia in anesthetized dogs

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7 January 2021

Interaction between cardiac calsequestrin and drugs with known cardiotoxicity

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7 January 2021

Effects of drugs with muscle-related side effects and affinity for calsequestrin on the calcium regulatory function of sarcoplasmic reticulum microsomes.

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7 January 2021

Exercise-induced ventricular arrhythmias in patients with no structural cardiac disease

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7 January 2021

Rate-dependent [K+](o) accumulation in canine right atria in vivo: electrophysiological consequences

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7 January 2021

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

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7 January 2021

Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

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7 January 2021

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia

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7 January 2021

Abnormal calcium signaling and sudden cardiac death associated with mutation of calsequestrin

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7 January 2021

Abnormal interactions of calsequestrin with the ryanodine receptor calcium release channel complex linked to exercise-induced sudden cardiac death

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7 January 2021

Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia

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7 January 2021

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

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7 January 2021

Modulation of sarcoplasmic reticulum calcium release by calsequestrin in cardiac myocytes

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7 January 2021