FAQ

CACNA2D1 gene

Known as: CALCIUM CHANNEL, L TYPE, ALPHA-2 POLYPEPTIDE, CALCIUM CHANNEL, ALPHA-2/DELTA SUBUNIT, calcium voltage-gated channel auxiliary subunit alpha2delta 1 
 

Topic mentions per year

Topic mentions per year

1994-2018
02419942018

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Related topics

1 relation
CACNA2D3 gene

Related mentions per year

Related mentions per year

1994-2018
1990200020102020
CACNA2D1 gene
CACNA2D3 gene

Papers overview

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2016
2016
Pregabalin can prevent, but not treat, cognitive dysfunction following abdominal surgery in aged rats.
AIMS The present study aimed to explore the preventive or therapeutic effect of peri-operative pregabalin treatment on the memory… (More)
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2016
2016
Prognostic and clinicopathological significance of Cacna2d1 expression in epithelial ovarian cancers: a retrospective study.
Ovarian cancer is the most lethal gynecologic malignancy, in which cancer stem cells (CSC) have been reported to be the driving… (More)
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2015
2015
Genomic analysis identifies candidate pathogenic variants in 9 of 18 patients with unexplained West syndrome
West syndrome, which is narrowly defined as infantile spasms that occur in clusters and hypsarrhythmia on EEG, is the most common… (More)
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2015
2015
Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2
OBJECTIVES To evaluate the association between a KCNQ1 mutation, R259H, and short QT syndrome (SQTS) and to explore the… (More)
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2014
2014
Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic male.
It is widely accepted that the incidence of chromosomal aberration is 10-15.2% in the azoospermic male; however, the exact… (More)
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2010
2010
Single nucleotide polymorphism of CACNA2D1 gene and its association with milk somatic cell score in cattle
The objective of the present study was to identify polymorphisms of the CACNA2D1 gene, and to analyze associations between these… (More)
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Highly Cited
2010
Highly Cited
2010
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
BACKGROUND L-type calcium channel (LTCC) mutations have been associated with Brugada syndrome (BrS), short QT (SQT) syndrome, and… (More)
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Highly Cited
2007
Highly Cited
2007
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.
BACKGROUND Cardiac ion channelopathies are responsible for an ever-increasing number and diversity of familial cardiac arrhythmia… (More)
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1996
1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved
We present the case of a patient affected with Williams syndrome (WS), who developed a suspected malignant hyperthermia (MH… (More)
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1994
1994
Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant…
Malignant hyperthermia susceptibility (MHS) is an autosomal dominant disorder of skeletal muscle which manifests as a potentially… (More)
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