(Q39888161)

English

The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition

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scholarly article

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Europe PubMed Central

PubMed publication ID

15 September 2017

The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1 reference

based on heuristic

inferred from title

Noèlia Fernàndez-Castillo

2

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

Miguel A Valverde

5

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

José M Fernández-Fernández

6

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

author name string

Selma A Serra

1

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

Alfons Macaya

3

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

3 February 2009

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

Pfluegers Archiv

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

458

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

489-502

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

https://scigraph.springernature.com/pub.10.1007/s00424-009-0637-3

0 references

Co-operative action a calcium ions in transmitter release at the neuromuscular junction

1 reference

https://api.crossref.org/works/10.1007%2FS00424-009-0637-3

21 January 2018

Gain-of-function mutation in the KCNMB1 potassium channel subunit is associated with low prevalence of diastolic hypertension

1 reference

https://api.crossref.org/works/10.1007%2FS00424-009-0637-3

21 January 2018

G-protein modulation of N-type calcium channel gating current in human embryonic kidney cells (HEK 293).

1 reference

https://api.crossref.org/works/10.1007%2FS00424-009-0637-3

21 January 2018

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary structure and functional expression from complementary DNA of a brain calcium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and regulation of voltage-gated Ca2+ channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two atomic constraints unambiguously position the S4 segment relative to S1 and S2 segments in the closed state of Shaker K channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How does voltage open an ion channel?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ca2+- and voltage-dependent inactivation of Ca2+ channels in nerve terminals of the neurohypophysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vertigo and dizziness related to migraine: a diagnostic challenge

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-hand.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign paroxysmal vertigo of childhood.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variations in onset of action potential broadening: effects on calcium current studied in chick ciliary ganglion neurones

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign paroxysmal torticollis of infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hemiplegic migraine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G protein modulation of voltage-gated calcium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactivation of presynaptic calcium current contributes to synaptic depression at a fast central synapse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presynaptic Ca2+ channels--integration centers for neuronal signaling pathways.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ducky mutation in Cacna2d2 results in altered Purkinje cell morphology and is associated with the expression of a truncated alpha 2 delta-2 protein with abnormal function

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/19189122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00424-009-0637-3

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

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