Cavβ4

1

Subramanian M et al. Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent.
Case Rep Neurol Med, 2015 , 2015 (906049).

2

Etemad S et al. The juvenile myoclonic epilepsy mutant of the calcium channel β(4) subunit displays normal nuclear targeting in nerve and muscle cells.
Channels (Austin), 2014 , 8 (334-43).

3

Ronjat M et al. Nuclear life of the voltage-gated Cacnb4 subunit and its role in gene transcription regulation.
Channels (Austin), 2013 Mar-Apr , 7 (119-25).

4

Chung S et al. A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.
Breast Cancer Res., 2013 , 15 (R81).

5

Tadmouri A et al. Cacnb4 directly couples electrical activity to gene expression, a process defective in juvenile epilepsy.
EMBO J., 2012 Sep 12 , 31 (3730-44).

6

Kotagal V Acetazolamide-responsive ataxia.
Semin Neurol, 2012 Nov , 32 (533-7).

7

Wang Y et al. Probing the structural basis for differential KCNQ1 modulation by KCNE1 and KCNE2.
J. Gen. Physiol., 2012 Dec , 140 (653-69).

8

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

9

Srikanth S et al. A novel EF-hand protein, CRACR2A, is a cytosolic Ca2+ sensor that stabilizes CRAC channels in T cells.
Nat. Cell Biol., 2010 May , 12 (436-46).

10

Layouni S et al. Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family.
Epilepsy Res., 2010 Jun , 90 (33-8).

11

Mantuano E et al. Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.
J. Neurol. Sci., 2010 Apr 15 , 291 (30-6).

12

Damak M et al. Late onset hereditary episodic ataxia.
J. Neurol. Neurosurg. Psychiatr., 2009 May , 80 (566-8).

13

Graves TD et al. Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity.
J. Neurol., 2008 Jul , 255 (1097-9).

14

Ebert AM et al. Ca2+ channel-independent requirement for MAGUK family CACNB4 genes in initiation of zebrafish epiboly.
Proc. Natl. Acad. Sci. U.S.A., 2008 Jan 8 , 105 (198-203).

15

Ohmori I et al. A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy.
Neurobiol. Dis., 2008 Dec , 32 (349-54).

16

Zhou W et al. Identification and expression of voltage-gated calcium channel beta subunits in Zebrafish.
Dev. Dyn., 2008 Dec , 237 (3842-52).

17

Genini S et al. Analysis and mapping of CACNB4, CHRNA1, KCNJ3, SCN2A and SPG4, physiological candidate genes for porcine congenital progressive ataxia and spastic paresis.
J. Anim. Breed. Genet., 2007 Oct , 124 (269-76).

18

von Brevern M et al. Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.
Headache, 2006 Jul-Aug , 46 (1136-41).

19

Popa RV et al. The N-butylcarbamate derivative of galantamine acts as an allosteric potentiating ligand on alpha7 nicotinic receptors in hippocampal neurons: clinical implications for treatment of Alzheimer's disease.
J. Mol. Neurosci., 2006 , 30 (227-32).

20

Herrmann A et al. [Episodic ataxias]
Tidsskr. Nor. Laegeforen., 2005 Aug 11 , 125 (2005-7).

21

Sáez-Hernández L et al. Characterization of a 6p21 translocation breakpoint in a family with idiopathic generalized epilepsy.
Epilepsy Res., 2003 Oct , 56 (155-63).

22

Taske NL et al. Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14.
Epilepsy Res., 2002 Apr , 49 (157-72).

23

Jin K et al. Microarray analysis of hippocampal gene expression in global cerebral ischemia.
Ann. Neurol., 2001 Jul , 50 (93-103).

24

Escayg A et al. Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
Am. J. Hum. Genet., 2000 May , 66 (1531-9).

25

Burgess DL et al. Single gene defects in mice: the role of voltage-dependent calcium channels in absence models.
Epilepsy Res., 1999 Sep , 36 (111-22).

26

Caddick SJ et al. Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami.
J. Neurophysiol., 1999 May , 81 (2066-74).

27

Lin F et al. Decreased (45)Ca(2)(+) uptake in P/Q-type calcium channels in homozygous lethargic (Cacnb4lh) mice is associated with increased beta3 and decreased beta4 calcium channel subunit mRNA expression.
Brain Res. Mol. Brain Res., 1999 Jul 23 , 71 (1-10).

28

Lin FH et al. Glutamate decarboxylase isoforms in thalamic nuclei in lethargic mouse model of absence seizures.
Brain Res. Mol. Brain Res., 1999 Jul 23 , 71 (127-30).

29

Lin F et al. Age-related relationship between mRNA expression of GABA(B) receptors and calcium channel beta4 subunits in cacnb4lh mice.
Brain Res. Mol. Brain Res., 1999 Jul 23 , 71 (131-5).

30

Escayg A et al. Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic.
Genomics, 1998 May 15 , 50 (14-22).

31

Kaupmann K et al. Human gamma-aminobutyric acid type B receptors are differentially expressed and regulate inwardly rectifying K+ channels.
Proc. Natl. Acad. Sci. U.S.A., 1998 Dec 8 , 95 (14991-6).

32

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).

33

Sander T et al. Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies.
Neurology, 1995 Sep , 45 (1713-20).

34

Phillips HA et al. Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2.
Nat. Genet., 1995 May , 10 (117-8).