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

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).

4

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).

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

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).

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

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).

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

Molina-Navarro MM et al. Differential gene expression of cardiac ion channels in human dilated cardiomyopathy.
PLoS ONE, 2013 , 8 (e79792).

18

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).

19

Fukuyama M et al. L-type calcium channel mutations in Japanese patients with inherited arrhythmias.
Circ. J., 2013 , 77 (1799-806).

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

Leroy J et al. Interaction via a key tryptophan in the I-II linker of N-type calcium channels is required for beta1 but not for palmitoylated beta2, implicating an additional binding site in the regulation of channel voltage-dependent properties.
J. Neurosci., 2005 Jul 27 , 25 (6984-96).

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).