Cavα2δ2

1

Warnier M et al. CACNA2D2 promotes tumorigenesis by stimulating cell proliferation and angiogenesis.
Oncogene, 2015 Oct 16 , 34 (5383-94).

2

Mendus D et al. Increased sensitivity to kindling in mice lacking TSP1.
Neuroscience, 2015 Oct 1 , 305 (302-8).

3

Cromer MK et al. Neomorphic effects of recurrent somatic mutations in Yin Yang 1 in insulin-producing adenomas.
Proc. Natl. Acad. Sci. U.S.A., 2015 Mar 31 , 112 (4062-7).

4

Tian X et al. A voltage-gated calcium channel regulates lysosomal fusion with endosomes and autophagosomes and is required for neuronal homeostasis.
PLoS Biol., 2015 Mar , 13 (e1002103).

5

Li B et al. Effect of β3-adrenergic receptor on atrial L-type Ca(2+) current in rats with chronic heart failure.
Heart Lung Circ, 2014 Apr , 23 (369-77).

6

Cioli C et al. Differences in human cortical gene expression match the temporal properties of large-scale functional networks.
PLoS ONE, 2014 , 9 (e115913).

7

Edvardson S et al. Early infantile epileptic encephalopathy associated with a high voltage gated calcium channelopathy.
J. Med. Genet., 2013 Feb , 50 (118-23).

8

Rhodin A et al. Combined analysis of circulating β-endorphin with gene polymorphisms in OPRM1, CACNAD2 and ABCB1 reveals correlation with pain, opioid sensitivity and opioid-related side effects.
Mol Brain, 2013 , 6 (8).

9

Pippucci T et al. A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
PLoS ONE, 2013 , 8 (e82154).

10

Mitra S et al. Alterations of RASSF1A in premalignant cervical lesions: clinical and prognostic significance.
Mol. Carcinog., 2012 Sep , 51 (723-33).

11

Wisniewska MB et al. Novel β-catenin target genes identified in thalamic neurons encode modulators of neuronal excitability.
BMC Genomics, 2012 , 13 (635).

12

Abouda H et al. Familial form of typical childhood absence epilepsy in a consanguineous context.
Epilepsia, 2010 Sep , 51 (1889-93).

13

Watanabe Y et al. Accumulation of common polymorphisms is associated with development of hypertension: a 12-year follow-up from the Ohasama study.
Hypertens. Res., 2010 Feb , 33 (129-34).

14

Wanajo A et al. Methylation of the calcium channel-related gene, CACNA2D3, is frequent and a poor prognostic factor in gastric cancer.
Gastroenterology, 2008 Aug , 135 (580-90).

15

Knorr C et al. Chromosomal assignment of porcine oncogenic and apoptopic genes CACNA2D2, TUSC4, ATP2A1, COL1A1, TAC1, BAK1 and CASP9.
Anim. Genet., 2006 Oct , 37 (523-5).

16

Donato R et al. The ducky(2J) mutation in Cacna2d2 results in reduced spontaneous Purkinje cell activity and altered gene expression.
J. Neurosci., 2006 Nov 29 , 26 (12576-86).

17

Hatano S et al. Molecular and electrophysiological differences in the L-type Ca2+ channel of the atrium and ventricle of rat hearts.
Circ. J., 2006 May , 70 (610-4).

18

Ivanov SV et al. Cerebellar ataxia, seizures, premature death, and cardiac abnormalities in mice with targeted disruption of the Cacna2d2 gene.
Am. J. Pathol., 2004 Sep , 165 (1007-18).

19

Senchenko VN et al. Discovery of frequent homozygous deletions in chromosome 3p21.3 LUCA and AP20 regions in renal, lung and breast carcinomas.
Oncogene, 2004 Jul 29 , 23 (5719-28).

20

Brill J et al. entla, a novel epileptic and ataxic Cacna2d2 mutant of the mouse.
J. Biol. Chem., 2004 Feb 20 , 279 (7322-30).

21

Carboni GL et al. CACNA2D2-mediated apoptosis in NSCLC cells is associated with alterations of the intracellular calcium signaling and disruption of mitochondria membrane integrity.
Oncogene, 2003 Jan 30 , 22 (615-26).

22

Brodbeck J et al. 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.
J. Biol. Chem., 2002 Mar 8 , 277 (7684-93).

23

Barclay J et al. Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells.
J. Neurosci., 2001 Aug 15 , 21 (6095-104).

24

Angeloni D et al. A G-to-A single nucleotide polymorphism in intron 2 of the human CACNA2D2 gene that maps at 3p21.3.
Mol. Cell. Probes, 2001 Apr , 15 (125-7).

25

Gao B et al. Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2).
J. Biol. Chem., 2000 Apr 21 , 275 (12237-42).