When calcium goes wrong: genetic alterations of a ubiquitous signaling route (Q35140775)

6 August 2017

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title

When calcium goes wrong: genetic alterations of a ubiquitous signaling route (English)

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6 August 2017

Rosario Rizzuto

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Tullio Pozzan

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6 August 2017

language of work or name

English

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publication date

1 June 2003

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6 August 2017

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

135-141

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The versatility and universality of calcium signalling

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Molecular and cellular physiology of intracellular calcium stores

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7 January 2021

Sorting out MIC, TRP, and CRAC ion channels.

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7 January 2021

The Golgi apparatus is an inositol 1,4,5-trisphosphate-sensitive Ca2+ store, with functional properties distinct from those of the endoplasmic reticulum

1 reference

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7 January 2021

A new phospholipase-C-calcium signalling pathway mediated by cyclic AMP and a Rap GTPase

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7 January 2021

Presenilin-mediated modulation of capacitative calcium entry

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7 January 2021

Capacitative calcium entry deficits and elevated luminal calcium content in mutant presenilin-1 knockin mice

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7 January 2021

Reduced loading of intracellular Ca(2+) stores and downregulation of capacitative Ca(2+) influx in Bcl-2-overexpressing cells.

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7 January 2021

Close contacts with the endoplasmic reticulum as determinants of mitochondrial Ca2+ responses

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7 January 2021

Regulation of mitochondrial ATP synthesis by calcium: evidence for a long-term metabolic priming

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7 January 2021

The Ca2+ concentration of the endoplasmic reticulum is a key determinant of ceramide-induced apoptosis: significance for the molecular mechanism of Bcl-2 action

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7 January 2021

Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines.

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7 January 2021

A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency

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7 January 2021

The role of Ca2+ ions in excitation-contraction coupling of skeletal muscle fibres

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7 January 2021

Ryanodine receptors of striated muscles: a complex channel capable of multiple interactions

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7 January 2021

Malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

A mutation in the human ryanodine receptor gene associated with central core disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Detection of a novel mutation at amino acid position 614 in the ryanodine receptor in malignant hyperthermia.

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Identification of a Mutation in Porcine Ryanodine Receptor Associated with Malignant Hyperthermia

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Malignant hyperthermia: excitation-contraction coupling, Ca2+ release channel, and cell Ca2+ regulation defects

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Malignant hyperthermia and central core disease: disorders of Ca2+ release channels

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Altered ryanodine receptor function in central core disease: leaky or uncoupled Ca(2+) release channels?

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7 January 2021

Ca2+ signalling and muscle disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Alteration in calcium handling at the subcellular level in mdx myotubes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptor

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Hypokalemic periodic paralysis associated with malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Muscle contracture induced by exercise. A syndrome attributable to decreased relaxing factor

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Myopathy caused by a deficiency of Ca2+-adenosine triphosphatase in sarcoplasmic reticulum (Brody's disease)

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Differential nociceptive responses in mice lacking the alpha(1B) subunit of N-type Ca(2+) channels

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Calcium channels and channelopathies of the central nervous system

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Structure and regulation of voltage-gated Ca2+ channels

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

The spinocerebellar ataxias: order emerges from chaos

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6.

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Ca(2+)-ATPase function is required for intracellular trafficking of the Notch receptor in Drosophila

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Calcium-pump inhibitors induce functional surface expression of Delta F508-CFTR protein in cystic fibrosis epithelial cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Calreticulin is essential for cardiac development

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Signals transduced by Ca(2+)/calcineurin and NFATc3/c4 pattern the developing vasculature

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Polycystin-2 is an intracellular calcium release channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Facilitation of NMDAR-independent LTP and spatial learning in mutant mice lacking ryanodine receptor type 3.

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning

1 reference

https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Nomenclature of voltage-gated calcium channels

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https://api.crossref.org/works/10.1038%2FNG0603-135

7 January 2021

Identifiers

DOI

10.1038/NG0603-135

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6 August 2017

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