(Q39988648)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18434528%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

title

A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels (English)

1 reference

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6 January 2020

2

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6 January 2020

Katrin Watschinger

3

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6 January 2020

Christian Barrere

5

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6 January 2020

Emmanuel Bourinet

6

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6 January 2020

Joel Nargeot

7

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6 January 2020

Joerg Striessnig

8

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6 January 2020

Philippe Lory

9

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6 January 2020

author name string

Alexandre Mezghrani

1

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6 January 2020

Martina J Sinnegger-Brauns

4

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6 January 2020

language of work or name

English

0 references

publication date

1 April 2008

1 reference

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6 January 2020

published in

Journal of Neuroscience

1 reference

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6 January 2020

volume

28

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6 January 2020

issue

17

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6 January 2020

page(s)

4501-4511

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describes a project that uses

6 January 2020

ImageQuant

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC6670939/fullTextXML

inferred from PubMed Central ID database lookup

cites work

The ubiquitin-proteasome pathway and pathogenesis of human diseases

1 reference

12 December 2020

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

1 reference

12 December 2020

The I-II loop of the Ca2+ channel alpha1 subunit contains an endoplasmic reticulum retention signal antagonized by the beta subunit.

1 reference

12 December 2020

The dominant negative LQT2 mutation A561V reduces wild-type HERG expression

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12 December 2020

Familial Episodic Ataxias and Related Ion Channel Disorders

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12 December 2020

Pharmacological chaperones: a new twist on receptor folding.

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12 December 2020

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

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12 December 2020

Analysis of endoplasmic reticulum trafficking signals by combinatorial screening in mammalian cells

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12 December 2020

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

1 reference

12 December 2020

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

1 reference

12 December 2020

Dominant-negative synthesis suppression of voltage-gated calcium channel Cav2.2 induced by truncated constructs

1 reference

12 December 2020

Manipulation of oxidative protein folding and PDI redox state in mammalian cells

1 reference

12 December 2020

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

1 reference

12 December 2020

XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor

1 reference

12 December 2020

Calcium channels and channelopathies of the central nervous system

1 reference

12 December 2020

Transcriptional and translational control in the Mammalian unfolded protein response

1 reference

12 December 2020

Neuronal T-type alpha 1H calcium channels induce neuritogenesis and expression of high-voltage-activated calcium channels in the NG108-15 cell line.

1 reference

12 December 2020

Translational control in the endoplasmic reticulum stress response

1 reference

12 December 2020

Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel alpha(1)2.1 subunit

1 reference

12 December 2020

Molecular physiology of low-voltage-activated t-type calcium channels

1 reference

12 December 2020

Altered properties of quantal neurotransmitter release at endplates of mice lacking P/Q-type Ca2+ channels

1 reference

12 December 2020

For whom the bell tolls: protein quality control of the endoplasmic reticulum and the ubiquitin-proteasome connection

1 reference

12 December 2020

Cystic fibrosis: premature degradation of mutant proteins as a molecular disease mechanism

1 reference

12 December 2020

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

12 December 2020

Mutual functional destruction of HIV-1 Vpu and host TASK-1 channel

1 reference

12 December 2020

Plasma membrane expression of T-type calcium channel alpha(1) subunits is modulated by high voltage-activated auxiliary subunits.

1 reference

12 December 2020

Dominant-negative calcium channel suppression by truncated constructs involves a kinase implicated in the unfolded protein response.

1 reference

12 December 2020

Biology of cardiac arrhythmias: ion channel protein trafficking

1 reference

12 December 2020

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy

1 reference

12 December 2020

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

1 reference

12 December 2020

Pharmacologic rescue of conformationally-defective proteins: implications for the treatment of human disease

1 reference

12 December 2020

A synthetic chaperone corrects the trafficking defect and disease phenotype in a protein misfolding disorder

1 reference

12 December 2020

Function and dysfunction of synaptic calcium channels: insights from mouse models

1 reference

12 December 2020

CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics

1 reference

12 December 2020

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.

1 reference

12 December 2020

Divergent roles of IRE1alpha and PERK in the unfolded protein response

1 reference

12 December 2020

Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia

1 reference

12 December 2020

The ducky(2J) mutation in Cacna2d2 results in reduced spontaneous Purkinje cell activity and altered gene expression

1 reference

12 December 2020

Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits

1 reference

12 December 2020

The I-II loop controls plasma membrane expression and gating of Ca(v)3.2 T-type Ca2+ channels: a paradigm for childhood absence epilepsy mutations

1 reference

12 December 2020

Dominant-negative effects of episodic ataxia type 2 mutations involve disruption of membrane trafficking of human P/Q-type Ca2+ channels.

1 reference

12 December 2020

Auxiliary subunits of voltage-gated ion channels

1 reference

12 December 2020

Oligomerization and phosphorylation of the Ire1p kinase during intracellular signaling from the endoplasmic reticulum to the nucleus

1 reference

12 December 2020

Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits

1 reference

12 December 2020

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

12 December 2020

Transmembrane auxiliary subunits of voltage-dependent ion channels

1 reference

12 December 2020

Progressive ataxia due to a missense mutation in a calcium-channel gene

1 reference

12 December 2020

Endocrinopathies in the family of endoplasmic reticulum (ER) storage diseases: disorders of protein trafficking and the role of ER molecular chaperones

1 reference

12 December 2020

Diversity and properties of calcium channel types in NG108-15 hybrid cells

1 reference

12 December 2020

Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase

1 reference

12 December 2020

10.1523/JNEUROSCI.2844-07.2008

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18434528%20AND%20SRC:MED&resulttype=core&format=json

release_7ftrxdu32zdavka5mdfvw2d3re

6 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7ftrxdu32zdavka5mdfvw2d3re

24 November 2022

mapped directly with Wikidata item

1 reference

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6 January 2020

PubMed publication ID

18434528

1 reference