Cavβ2
56 literature references associated to Cavβ2
1
Wu ZJ
et al.
Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2.
J Geriatr Cardiol,
2015
Jul
, 12 (394-401).
2
Katiyar R
et al.
Influence of the β2-Subunit of L-Type Voltage-Gated Cav Channels on the Structural and Functional Development of Photoreceptor Ribbon Synapses.
Invest. Ophthalmol. Vis. Sci.,
2015
Apr
, 56 (2312-24).
3
Allegue C
et al.
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
PLoS ONE,
2015
, 10 (e0133037).
4
Lu Y
et al.
Expression profile analysis of circulating microRNAs and their effects on ion channels in Chinese atrial fibrillation patients.
Int J Clin Exp Med,
2015
, 8 (845-53).
5
Barana A
et al.
Chronic atrial fibrillation increases microRNA-21 in human atrial myocytes decreasing L-type calcium current.
Circ Arrhythm Electrophysiol,
2014
Oct
, 7 (861-8).
6
Jan WC
et al.
Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder.
J Affect Disord,
2014
Mar
, 157 (80-6).
7
Juraeva D
et al.
Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia.
PLoS Genet.,
2014
Jun
, 10 (e1004345).
8
Dixson L
et al.
Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain.
Proc. Natl. Acad. Sci. U.S.A.,
2014
Jul
1
, 111 (9657-62).
9
Petkeviciene J
et al.
Physical, behavioural and genetic predictors of adult hypertension: the findings of the Kaunas Cardiovascular Risk Cohort study.
PLoS ONE,
2014
, 9 (e109974).
10
Breitenkamp AF
et al.
Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function.
PLoS ONE,
2014
, 9 (e95579).
11
Yu CC
et al.
Apamin does not inhibit human cardiac Na+ current, L-type Ca2+ current or other major K+ currents.
PLoS ONE,
2014
, 9 (e96691).
12
Sugimoto M
et al.
Genetic variants related to gap junctions and hormone secretion influence conception rates in cows.
Proc. Natl. Acad. Sci. U.S.A.,
2013
Nov
26
, 110 (19495-500).
13
Risgaard B
et al.
High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.
Clin. Genet.,
2013
Nov
, 84 (489-95).
14
Sun Q
et al.
[Association between CACNB2 gene polymorphisms and essential hypertension].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi,
2013
Jun
, 30 (340-4).
15
Salem KA
et al.
Effects of exercise training on excitation-contraction coupling and related mRNA expression in hearts of Goto-Kakizaki type 2 diabetic rats.
Mol. Cell. Biochem.,
2013
Aug
, 380 (83-96).
16
et al.
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Lancet,
2013
Apr
20
, 381 (1371-9).
17
Hong GL
et al.
Genetic variations in MOV10 and CACNB2 are associated with hypertension in a Chinese Han population.
Genet. Mol. Res.,
2013
, 12 (6220-7).
18
Fukuyama M
et al.
L-type calcium channel mutations in Japanese patients with inherited arrhythmias.
Circ. J.,
2013
, 77 (1799-806).
19
Molina-Navarro MM
et al.
Differential gene expression of cardiac ion channels in human dilated cardiomyopathy.
PLoS ONE,
2013
, 8 (e79792).
20
Brandmayr J
et al.
Deletion of the C-terminal phosphorylation sites in the cardiac β-subunit does not affect the basic β-adrenergic response of the heart and the Ca(v)1.2 channel.
J. Biol. Chem.,
2012
Jun
29
, 287 (22584-92).
21
Johnson JA
Advancing management of hypertension through pharmacogenomics.
Ann. Med.,
2012
Jun
, 44 Suppl 1 (S17-22).
22
Wu Y
et al.
[Effects of microRNA-1 on negatively regulating L-type calcium channel beta2 subunit gene expression during cardiac hypertrophy].
Zhongguo Ying Yong Sheng Li Xue Za Zhi,
2012
Jul
, 28 (304-8).
23
Kanter RJ
et al.
Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.
Circulation,
2012
Jan
3
, 125 (14-22).
24
Barajas-Martinez H
et al.
Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8.
Heart Rhythm,
2012
Apr
, 9 (548-55).
25
Chernyavskaya Y
et al.
Voltage-gated calcium channel CACNB2 (β2.1) protein is required in the heart for control of cell proliferation and heart tube integrity.
Dev. Dyn.,
2012
Apr
, 241 (648-62).
26
Lippi G
et al.
Genetic and clinical aspects of Brugada syndrome: an update.
Adv Clin Chem,
2012
, 56 (197-208).
27
Nakajima T
et al.
KCNE3 T4A as the genetic basis of Brugada-pattern electrocardiogram.
Circ. J.,
2012
, 76 (2763-72).
28
Chockalingam P
et al.
Loss-of-Function Sodium Channel Mutations in Infancy: A Pattern Unfolds.
,
2011
Nov
16
, ().
29
Meissner M
et al.
Moderate calcium channel dysfunction in adult mice with inducible cardiomyocyte-specific excision of the cacnb2 gene.
J. Biol. Chem.,
2011
May
6
, 286 (15875-82).
30
Lee MT
et al.
Genome-wide association study of bipolar I disorder in the Han Chinese population.
Mol. Psychiatry,
2011
May
, 16 (548-56).
31
Chambers KF
et al.
Stromal upregulation of lateral epithelial adhesions: Gene expression analysis of signalling pathways in prostate epithelium.
,
2011
Jun
22
, 18 (45).
32
Lin Y
et al.
Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in She ethnic minority of China.
Atherosclerosis,
2011
Dec
, 219 (709-14).
33
Howarth FC
et al.
Structural lesions and changing pattern of expression of genes encoding cardiac muscle proteins are associated with ventricular myocyte dysfunction in type 2 diabetic Goto-Kakizaki rats fed a high-fat diet.
Exp. Physiol.,
2011
Aug
, 96 (765-77).
34
Hu D
et al.
Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.
Pacing Clin Electrophysiol,
2010
Mar
, 33 (274-85).
35
Niu Y
et al.
Genetic variation in the beta2 subunit of the voltage-gated calcium channel and pharmacogenetic association with adverse cardiovascular outcomes in the INternational VErapamil SR-Trandolapril STudy GENEtic Substudy (INVEST-GENES).
Circ Cardiovasc Genet,
2010
Dec
1
, 3 (548-55).
36
Burashnikov E
et al.
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
Heart Rhythm,
2010
Dec
, 7 (1872-82).
37
Tang M
et al.
Enhanced basal contractility but reduced excitation-contraction coupling efficiency and beta-adrenergic reserve of hearts with increased Cav1.2 activity.
Am. J. Physiol. Heart Circ. Physiol.,
2010
Aug
, 299 (H519-28).
38
Nof E
et al.
A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.
Circ Cardiovasc Genet,
2010
Apr
, 3 (199-206).
39
Thomsen MB
et al.
Transcriptional and electrophysiological consequences of KChIP2-mediated regulation of CaV1.2.
Channels (Austin),
2009 Sep-Oct
, 3 (308-10).
40
Link S
et al.
Diversity and developmental expression of L-type calcium channel beta2 proteins and their influence on calcium current in murine heart.
J. Biol. Chem.,
2009
Oct
30
, 284 (30129-37).
41
Mitra-Ganguli T
et al.
Orientation of palmitoylated CaVbeta2a relative to CaV2.2 is critical for slow pathway modulation of N-type Ca2+ current by tachykinin receptor activation.
J. Gen. Physiol.,
2009
Nov
, 134 (385-96).
42
Cordeiro JM
et al.
Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome.
J. Mol. Cell. Cardiol.,
2009
May
, 46 (695-703).
43
Hedley PL
et al.
The genetic basis of Brugada syndrome: A mutation update.
Hum. Mutat.,
2009
Jun
16
, ().
44
Nyholt DR
et al.
A high-density association screen of 155 ion transport genes for involvement with common migraine.
Hum. Mol. Genet.,
2008
Nov
1
, 17 (3318-31).
45
Schimpf R
et al.
Clinical and molecular genetics of the short QT syndrome.
Curr. Opin. Cardiol.,
2008
May
, 23 (192-8).
46
Lao QZ
et al.
New Determinant for the CaVbeta2 subunit modulation of the CaV1.2 calcium channel.
J. Biol. Chem.,
2008
Jun
6
, 283 (15577-88).
47
Ebert AM
et al.
The calcium channel beta2 (CACNB2) subunit repertoire in teleosts.
BMC Mol. Biol.,
2008
, 9 (38).
48
Richards KS
et al.
Novel CaV2.1 clone replicates many properties of Purkinje cell CaV2.1 current.
Eur. J. Neurosci.,
2007
Nov
, 26 (2950-61).
49
Xie M
et al.
Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca2+ channel Cavbeta4 versus Cavbeta2 subunits to synaptic terminals.
J. Cell Biol.,
2007
Jul
30
, 178 (489-502).
50
Antzelevitch C
et al.
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.
Circulation,
2007
Jan
30
, 115 (442-9).
51
52
Harry JB
et al.
New short splice variants of the human cardiac Cavbeta2 subunit: redefining the major functional motifs implemented in modulation of the Cav1.2 channel.
J. Biol. Chem.,
2004
Nov
5
, 279 (46367-72).
53
Dafi O
et al.
Negatively charged residues in the N-terminal of the AID helix confer slow voltage dependent inactivation gating to CaV1.2.
Biophys. J.,
2004
Nov
, 87 (3181-92).
54
Maselli RA
et al.
Effect of inherited abnormalities of calcium regulation on human neuromuscular transmission.
Ann. N. Y. Acad. Sci.,
2003
Sep
, 998 (18-28).
55
Valle C
et al.
Sequence and level of endogenous expression of calcium channel beta subunits in Schistosoma mansoni displaying different susceptibilities to praziquantel.
Mol. Biochem. Parasitol.,
2003
Aug
31
, 130 (111-5).
56
Taviaux S
et al.
Assignment of human genes for beta 2 and beta 4 subunits of voltage-dependent Ca2+ channels to chromosomes 10p12 and 2q22-q23.
Hum. Genet.,
1997
Aug
, 100 (151-4).