Channelpedia

Cav2.1 Channel

737 automatically matched literature references

1

Berecki G et al. Mechanism of direct Cav2.2 channel block by the κ-opioid receptor agonist U50488H.
Neuropharmacology, 2016 May 28 , 109 (49-58).

7

Kim TY et al. Absence-like seizures and their pharmacological profile in tottering-6j mice.
Biochem. Biophys. Res. Commun., 2015 Jul 17-24 , 463 (148-53).

8

Chang CY et al. Apigenin, a natural flavonoid, inhibits glutamate release in the rat hippocampus.
Eur. J. Pharmacol., 2015 Sep 5 , 762 (72-81).

15

18

Murakami M et al. Modified autonomic regulation in mice mutated in the β4 subunit of the lh/lh calcium channel.
Biochem. Biophys. Res. Commun., 2015 May 29 , 461 (200-5).

20

21

Blumkin L et al. Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A.
Eur. J. Paediatr. Neurol., 2015 May , 19 (292-7).

28

Kros L et al. Cerebellar output controls generalized spike-and-wave discharge occurrence.
Ann. Neurol., 2015 Jun , 77 (1027-49).

30

Langlhofer G et al. Length of the TM3-4 loop of the glycine receptor modulates receptor desensitization.
Neurosci. Lett., 2015 Jul 23 , 600 (176-81).

37

Baur D et al. Developmental tightening of cerebellar cortical synaptic influx-release coupling.
J. Neurosci., 2015 Feb 4 , 35 (1858-71).

39

Dileköz E et al. Migraine mutations impair hippocampal learning despite enhanced long-term potentiation.
J. Neurosci., 2015 Feb 25 , 35 (3397-402).

40

Spillane J et al. Lambert-Eaton syndrome IgG inhibits transmitter release via P/Q Ca2+ channels.
Neurology, 2015 Feb 10 , 84 (575-9).

41

Molina-Campos E et al. Age-dependent contribution of P/Q- and R-type Ca2+ channels to neuromuscular transmission in lethargic mice.
J. Pharmacol. Exp. Ther., 2015 Feb , 352 (395-404).

43

Zhou MH et al. Molecular Basis of Regulating High Voltage-Activated Calcium Channels by S-Nitrosylation.
J. Biol. Chem., 2015 Dec 18 , 290 (30616-23).

49

Charlesworth G et al. Mutations in HPCA cause autosomal-recessive primary isolated dystonia.
Am. J. Hum. Genet., 2015 Apr 2 , 96 (657-65).

52

53

Serikawa T et al. Advances on genetic rat models of epilepsy.
Exp. Anim., 2015 , 64 (1-7).

56

57

Fernández-Morales JC et al. Hypoxia-elicited catecholamine release is controlled by L-type as well as N/PQ types of calcium channels in rat embryo chromaffin cells.
Am. J. Physiol., Cell Physiol., 2014 Sep 1 , 307 (C455-65).

59

Kim TY et al. Age-dependent kainate sensitivity in heterozygous rolling Nagoya Cav2.1 channel mutant mice.
Pharmacol. Biochem. Behav., 2014 Sep , 124 (250-9).

60

van Gaalen J et al. Language impairment in cerebellar ataxia.
Mov. Disord., 2014 Sep , 29 (1307-12).

64

García-Baró-Huarte M et al. Phenotypic variability in a four generation family with a p.Thr666Met CACNA1A gene mutation.
Pediatr. Neurol., 2014 Oct , 51 (557-9).

66

Carattino MD et al. Prostasin interacts with the epithelial Na+ channel and facilitates cleavage of the γ-subunit by a second protease.
Am. J. Physiol. Renal Physiol., 2014 Nov 1 , 307 (F1080-7).

67

Rose SJ et al. The first knockin mouse model of episodic ataxia type 2.
Exp. Neurol., 2014 Nov , 261 (553-62).

72

Perissinotti PP et al. Down-regulation of endogenous KLHL1 decreases voltage-gated calcium current density.
Cell Calcium, 2014 May , 55 (269-80).

74

Vila-Pueyo M et al. A loss-of-function CACNA1A mutation causing benign paroxysmal torticollis of infancy.
Eur. J. Paediatr. Neurol., 2014 May , 18 (430-3).

78

79

Ricoy UM et al. Distinct roles for Cav2.1-2.3 in activity-dependent synaptic dynamics.
J. Neurophysiol., 2014 Jun 15 , 111 (2404-13).

81

84

Kline CF et al. Ankyrin-B regulates Cav2.1 and Cav2.2 Expression and Targeting.
J. Biol. Chem., 2014 Jan 6 , ().

87

Bashir A et al. Association of single nucleotide polymorphisms of CACNA1A gene in migraine.
Indian J Hum Genet, 2014 Jan , 20 (59-63).

88

Niimi K et al. Blockade of Cav2.1-mediated NMDA receptor signaling disrupts conditioned fear extinction.
Behav. Brain Res., 2014 Feb 1 , 259 (45-9).

89

Rochester L et al. Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.
Mov. Disord., 2014 Feb , 29 (252-5).

90

Cox DH Modeling a Ca(2+) channel/BKCa channel complex at the single-complex level.
Biophys. J., 2014 Dec 16 , 107 (2797-814).

91

Schubert M et al. Paraneoplastic CDR2 and CDR2L antibodies affect Purkinje cell calcium homeostasis.
Acta Neuropathol., 2014 Dec , 128 (835-52).

92

Wang T et al. Endostatin is a trans-synaptic signal for homeostatic synaptic plasticity.
Neuron, 2014 Aug 6 , 83 (616-29).

94

Yoshimoto T et al. Rolling Nagoya mouse strain (PROD-rol/rol) with classic piebald mutation.
J. Vet. Med. Sci., 2014 Aug , 76 (1093-8).

104

Gambardella A et al. The role of calcium channel mutations in human epilepsy.
Prog. Brain Res., 2014 , 213 (87-96).

107

et al. De novo mutations in epileptic encephalopathies.
Nature, 2013 Sep 12 , 501 (217-21).

110

Ramachandra R et al. Identification of CaV channel types expressed in muscle afferent neurons.
J. Neurophysiol., 2013 Oct , 110 (1535-43).

113

Campiglio M et al. Stable incorporation versus dynamic exchange of β subunits in a native Ca2+ channel complex.
J. Cell. Sci., 2013 May 1 , 126 (2092-101).

114

Ducros A [Genetics of migraine].
Rev. Neurol. (Paris), 2013 May , 169 (360-71).

116

Nimmakayalu M et al. Apparent germline mosaicism for a novel 19p13.13 deletion disrupting NFIX and CACNA1A.
Am. J. Med. Genet. A, 2013 May , 161A (1105-9).

120

Lohmann K et al. Genetics of dystonia: what's known? What's new? What's next?
Mov. Disord., 2013 Jun 15 , 28 (899-905).

121

Molloy A et al. A novel CACNA1A mutation associated with adult-onset, paroxysmal head tremor.
Mov. Disord., 2013 Jun , 28 (842-3).

124

Pietrobon D Calcium channels and migraine.
Biochim. Biophys. Acta, 2013 Jul , 1828 (1655-65).

126

130

Ohmori I et al. CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.
Neurobiol. Dis., 2013 Feb , 50 (209-17).

131

Girach F et al. RIM1α SUMOylation is required for fast synaptic vesicle exocytosis.
Cell Rep, 2013 Dec 12 , 5 (1294-301).

133

Kipfer S et al. Novel CACNA1A mutation(s) associated with slow saccade velocities.
J. Neurol., 2013 Dec , 260 (3010-4).

136

Tian X et al. Analysis of ischemic neuronal injury in Cav2.1 channel α1 subunit mutant mice.
Biochem. Biophys. Res. Commun., 2013 Apr 26 , 434 (60-4).

142

Eikermann-Haerter K et al. Spreading depression and the clinical correlates of migraine.
Rev Neurosci, 2013 , 24 (353-63).

145

Wagner-Britz L et al. Protein kinase Cα and P-type Ca channel CaV2.1 in red blood cell calcium signalling.
Cell. Physiol. Biochem., 2013 , 31 (883-91).

146

Mallmann RT et al. Tetraspanin-13 modulates voltage-gated CaV2.2 Ca2+ channels.
Sci Rep, 2013 , 3 (1777).

150

Gandini MA Channeling headache: novel findings in the study of Ca(2+)-channels and FHM-1.
Channels (Austin), 2012 Nov-Dec , 6 (414-5).

151

Domitrz I et al. A single-fibre electromyography study of neuromuscular transmission in patients with cluster headache.
Neurol. Neurochir. Pol., 2012 Mar-Apr , 46 (140-4).

154

Ohmura K et al. Sporadic hemiplegic migraine presenting as acute encephalopathy.
Brain Dev., 2012 Sep , 34 (691-5).

156

Aranda-Sicilia MN et al. Arabidopsis KEA2, a homolog of bacterial KefC, encodes a K(+)/H(+) antiporter with a chloroplast transit peptide.
Biochim. Biophys. Acta, 2012 Sep , 1818 (2362-71).

158

Lafrenière RG et al. Identification of novel genes involved in migraine.
Headache, 2012 Oct , 52 Suppl 2 (107-10).

160

Fujioka S et al. A novel de novo pathogenic mutation in the CACNA1A gene.
Mov. Disord., 2012 Oct , 27 (1578-9).

163

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

167

170

Di Cristofori A et al. R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update.
J Headache Pain, 2012 Jul , 13 (419-23).

171

Low SE et al. Touch responsiveness in zebrafish requires voltage-gated calcium channel 2.1b.
J. Neurophysiol., 2012 Jul , 108 (148-59).

172

Billings SE et al. ELKS1 and Ca(2+) channel subunit β4 interact and colocalize at cerebellar synapses.
Neuroreport, 2012 Jan 4 , 23 (49-54).

174

Nanou E et al. Molecular determinants of modulation of CaV2.1 channels by visinin-like protein 2.
J. Biol. Chem., 2012 Jan 2 , 287 (504-13).

176

Eikermann-Haerter K et al. Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizations.
Circulation, 2012 Jan 17 , 125 (335-45).

179

Stuart S et al. Detection of a novel mutation in the CACNA1A gene.
Twin Res Hum Genet, 2012 Feb , 15 (120-5).

182

Patel AB et al. Tissue kallikrein activation of the epithelial Na channel.
Am. J. Physiol. Renal Physiol., 2012 Aug 15 , 303 (F540-50).

185

Baloh RW Episodic ataxias 1 and 2.
Handb Clin Neurol, 2012 , 103 (595-602).

186

Solodkin A et al. Spinocerebellar ataxia type 6.
Handb Clin Neurol, 2012 , 103 (461-73).

189

Carreño O et al. Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation.
Headache, 2011 Nov-Dec , 51 (1542-6).

191

Yamazaki S et al. Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutation.
Pediatr. Neurol., 2011 Sep , 45 (193-6).

192

Hansen JM et al. Trigger factors for familial hemiplegic migraine.
Cephalalgia, 2011 Sep , 31 (1274-81).

193

Geerlings RP et al. Head tremor related to CACNA1A mutations.
Cephalalgia, 2011 Sep , 31 (1315-9).

199

Naik S et al. Early-onset cerebellar atrophy associated with mutation in the CACNA1A gene.
Pediatr. Neurol., 2011 Nov , 45 (328-30).

200

Bhatia KP Paroxysmal dyskinesias.
Mov. Disord., 2011 May , 26 (1157-65).

204

Nikaido K et al. New mutation of CACNA1A gene in episodic ataxia type 2.
Pediatr Int, 2011 Jun , 53 (415-6).

205

Strupp M et al. A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
Neurology, 2011 Jul 19 , 77 (269-75).

209

Stam AH et al. A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.
Cephalalgia, 2011 Jan , 31 (199-205).

212

Few AP et al. Molecular determinants of CaV2.1 channel regulation by calcium-binding protein-1.
J. Biol. Chem., 2011 Dec 9 , 286 (41917-23).

216

217

Currie KP G protein modulation of CaV2 voltage-gated calcium channels.
Channels (Austin), 2010 Nov-Dec , 4 (497-509).

219

Sułek-Piatkowska A et al. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
Neurol. Neurochir. Pol., 2010 May-Jun , 44 (238-45).

220

Cohen-Kutner M et al. CaV2.1 (P/Q channel) interaction with synaptic proteins is essential for depolarization-evoked release.
Channels (Austin), 2010 Jul-Aug , 4 (266-77).

223

Hansen JM Familial hemiplegic migraine.
Dan Med Bull, 2010 Sep , 57 (B4183).

224

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

228

Rajakulendran S et al. PAW31 Clinical and genetic spectrum of the episodic ataxias: the UK perspective.
J. Neurol. Neurosurg. Psychiatr., 2010 Nov , 81 (e32).

229

Watase K et al. [SCA6: From gene identification to recent progress on pathogenesis].
Rinsho Shinkeigaku, 2010 Nov , 50 (858-60).

230

Alviña K et al. KCa channels as therapeutic targets in episodic ataxia type-2.
J. Neurosci., 2010 May 26 , 30 (7249-57).

231

Kim JM et al. The wide clinical spectrum and nigrostriatal dopaminergic damage in spinocerebellar ataxia type 6.
J. Neurol. Neurosurg. Psychiatr., 2010 May , 81 (529-32).

232

Takahashi E et al. Neonatal motor functions in Cacna1a-mutant rolling Nagoya mice.
Behav. Brain Res., 2010 Mar 5 , 207 (273-9).

233

Russell MB Management of sporadic and familial hemiplegic migraine.
Expert Rev Neurother, 2010 Mar , 10 (381-7).

236

Rajakulendran S et al. Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
J. Physiol. (Lond.), 2010 Jun 1 , 588 (1905-13).

237

Wang X et al. A neuropathological study at autopsy of early onset spinocerebellar ataxia 6.
J Clin Neurosci, 2010 Jun , 17 (751-5).

239

Pietrobon D CaV2.1 channelopathies.
Pflugers Arch., 2010 Jul , 460 (375-93).

241

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Zangaladze A et al. Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.
Epilepsy Behav, 2010 Feb , 17 (293-5).

255

Pietrobon D Biological science of headache channels.
, 2010 , 97C (73-83).

257

264

Stam AH et al. Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
J. Neurol. Neurosurg. Psychiatr., 2009 Oct , 80 (1125-9).

265

Selmer KK et al. Parental SCN1A mutation mosaicism in familial Dravet syndrome.
Clin. Genet., 2009 Oct , 76 (398-403).

266

Tomlinson SE et al. Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.
Clin Neurophysiol, 2009 Oct , 120 (1768-76).

267

Eikermann-Haerter K et al. Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice.
Ann. Neurol., 2009 Oct , 66 (564-8).

268

Bertholon P et al. Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood.
J. Neurol. Neurosurg. Psychiatr., 2009 Nov , 80 (1289-92).

273

Ishikawa K et al. [Molecular genetic approach to spinocerebellar ataxias]
Rinsho Shinkeigaku, 2009 Nov , 49 (907-9).

274

275

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

276

Iwanaka Y et al. [Case of sporadic hemiplegic migraine with cerebellar ataxia]
Rinsho Shinkeigaku, 2009 May , 49 (267-70).

277

Jen JC et al. Familial episodic ataxia: a model for migrainous vertigo.
Ann. N. Y. Acad. Sci., 2009 May , 1164 (252-6).

279

Ohba T et al. Modified autonomic regulation in mice with a P/Q-type calcium channel mutation.
Biochem. Biophys. Res. Commun., 2009 Mar 27 , 381 (27-32).

284

Takahashi E et al. Motor coordination impairment in aged heterozygous rolling Nagoya, Cav2.1 mutant mice.
Brain Res., 2009 Jul 7 , 1279 (50-7).

285

287

Horak S et al. Use-dependent block of voltage-gated Cav2.1 Ca2+ channels by petasins and eudesmol isomers.
J. Pharmacol. Exp. Ther., 2009 Jul , 330 (220-6).

288

de Vries B et al. Molecular genetics of migraine.
Hum. Genet., 2009 Jul , 126 (115-32).

293

Yu-Wai-Man P et al. Vertigo and vestibular abnormalities in spinocerebellar ataxia type 6.
J. Neurol., 2009 Jan , 256 (78-82).

295

Takano T et al. Deciphering migraine.
J. Clin. Invest., 2009 Jan , 119 (16-9).

298

Wiwanitkit V FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2.
J. Neurol. Sci., 2009 Feb 15 , 277 (76-9).

301

Wang Z et al. [Implanting the conducting electrode in rat and investigating its effect on the rat's penicillin-induced seizure]
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi, 2009 Feb , 26 (63-6).

303

Zamponi GW et al. Role of voltage-gated calcium channels in epilepsy.
, 2009 Dec 20 , ().

305

Takahashi E et al. Age-related spatial and nonspatial short-term memory in Cav2.1alpha1 mutant mice, Rolling Nagoya.
Behav. Brain Res., 2009 Dec 1 , 204 (241-5).

308

Iturralde-Torres P et al. [Genetic in long QT syndromes]
Arch Cardiol Mex, 2009 Dec , 79 Suppl 2 (26-30).

312

315

Kapur J Is epilepsy a disease of synaptic transmission?
, 2008 Sep-Oct , 8 (139-41).

317

Thomsen LL et al. Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients.
Cephalalgia, 2008 Sep , 28 (914-21).

319

Haan J et al. Migraine and epilepsy: genetically linked?
, 2008 Sep , 8 (1307-11).

320

van Oosterhout F et al. Enhanced circadian phase resetting in R192Q Cav2.1 calcium channel migraine mice.
Ann. Neurol., 2008 Sep , 64 (315-24).

321

Teive HA et al. Spinocerebellar ataxia type 6 in Brazil.
Arq Neuropsiquiatr, 2008 Sep , 66 (691-4).

326

Globas C et al. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.
Mov. Disord., 2008 Nov 15 , 23 (2232-8).

327

329

Stam AH et al. CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
Clin. Genet., 2008 Nov , 74 (481-5).

331

Guerin AA et al. Stepwise developmental regression associated with novel CACNA1A mutation.
Pediatr. Neurol., 2008 Nov , 39 (363-4).

333

Krishnan AV et al. Axonal function in a family with episodic ataxia type 2 due to a novel mutation.
J. Neurol., 2008 May , 255 (750-5).

335

Su X et al. Role of spinal Cav2.2 and Cav2.1 ion channels in bladder nociception.
J. Urol., 2008 Jun , 179 (2464-9).

336

Stam AH et al. Genetics of migraine: an update with special attention to genetic comorbidity.
Curr. Opin. Neurol., 2008 Jun , 21 (288-93).

337

Riant F et al. Large CACNA1A deletion in a family with episodic ataxia type 2.
Arch. Neurol., 2008 Jun , 65 (817-20).

338

340

Kahlig KM et al. Divergent sodium channel defects in familial hemiplegic migraine.
Proc. Natl. Acad. Sci. U.S.A., 2008 Jul 15 , 105 (9799-804).

342

Jiang X et al. Modulation of CaV2.1 channels by Ca2+/calmodulin-dependent protein kinase II bound to the C-terminal domain.
Proc. Natl. Acad. Sci. U.S.A., 2008 Jan 8 , 105 (341-6).

344

Fernandez DM et al. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Headache, 2008 Jan , 48 (101-8).

345

Lee H et al. [Familial hemiplegic migraine resulting in recurrent coma]
, 2008 Feb 16 , 152 (393-6).

347

Jen JC Recent advances in the genetics of recurrent vertigo and vestibulopathy.
Curr. Opin. Neurol., 2008 Feb , 21 (3-7).

348

Tsunemi T et al. Cell-type-specific alternative splicing in spinocerebellar ataxia type 6.
Neurosci. Lett., 2008 Dec 5 , 447 (78-81).

350

Berkefeld H et al. Repolarizing responses of BKCa-Cav complexes are distinctly shaped by their Cav subunits.
J. Neurosci., 2008 Aug 13 , 28 (8238-45).

354

de Vries B et al. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.
Cephalalgia, 2008 Aug , 28 (887-91).

358

Christova P et al. Impaired eye movements in presymptomatic spinocerebellar ataxia type 6.
Arch. Neurol., 2008 Apr , 65 (530-6).

359

Johnson J et al. Clinical and genetic analysis of spinocerebellar ataxia type 11.
Cerebellum, 2008 , 7 (159-64).

361

Jones HM et al. An NH2-terminal multi-basic RKR motif is required for the ATP-dependent regulation of hIK1.
Channels (Austin), 2007 Mar-Apr , 1 (80-91).

362

Jordan BD Genetic influences on outcome following traumatic brain injury.
Neurochem. Res., 2007 Apr-May , 32 (905-15).

363

Tanaka K et al. Increased Ca2+ channel currents in cerebellar Purkinje cells of the ataxic groggy rat.
Neurosci. Lett., 2007 Oct 16 , 426 (75-80).

364

365

Jen JC et al. Primary episodic ataxias: diagnosis, pathogenesis and treatment.
Brain, 2007 Oct , 130 (2484-93).

366

Llinás RR et al. Gamma-band deficiency and abnormal thalamocortical activity in P/Q-type channel mutant mice.
Proc. Natl. Acad. Sci. U.S.A., 2007 Nov 6 , 104 (17819-24).

368

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).

371

372

Van De Ven RC et al. Genetic models of migraine.
Arch. Neurol., 2007 May , 64 (643-6).

373

Montagna P Recent advances in the pharmacogenomics of pain and headache.
Neurol. Sci., 2007 May , 28 Suppl 2 (S208-12).

374

Chaudhuri D et al. Elementary mechanisms producing facilitation of Cav2.1 (P/Q-type) channels.
J. Gen. Physiol., 2007 May , 129 (385-401).

376

377

Mao X et al. Dual regulation of the ATP-sensitive potassium channel by caffeine.
Am. J. Physiol., Cell Physiol., 2007 Jun , 292 (C2239-58).

378

Van Den Maagdenberg AM et al. Migraine: gene mutations and functional consequences.
Curr. Opin. Neurol., 2007 Jun , 20 (299-305).

379

Vincent M et al. The cerebellum and migraine.
Headache, 2007 Jun , 47 (820-33).

383

Weiss N et al. [Role of P/Q calcium channel in familial hemiplegic migraine]
Med Sci (Paris), 2007 Jan , 23 (53-63).

387

Colson NJ et al. The search for migraine genes: an overview of current knowledge.
Cell. Mol. Life Sci., 2007 Feb , 64 (331-44).

389

390

391

Mantuano E et al. Early onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
J. Neurol. Sci., 2007 Dec 15 , 263 (226; author reply 226-7).

394

Glasscock E et al. Masking epilepsy by combining two epilepsy genes.
Nat. Neurosci., 2007 Dec , 10 (1554-8).

395

399

Strupp M et al. Episodic ataxia type 2.
, 2007 Apr , 4 (267-73).

400

Pietrobon D Familial hemiplegic migraine.
, 2007 Apr , 4 (274-84).

401

Kordasiewicz HB et al. Molecular pathogenesis of spinocerebellar ataxia type 6.
, 2007 Apr , 4 (285-94).

406

408

409

Berkefeld H et al. BKCa-Cav channel complexes mediate rapid and localized Ca2+-activated K+ signaling.
Science, 2006 Oct 27 , 314 (615-20).

412

Freilinger T et al. [Genetics of migraine]
, 2006 Oct , 77 (1186, 1188-95).

416

Kirchmann M et al. Basilar-type migraine: clinical, epidemiologic, and genetic features.
Neurology, 2006 Mar 28 , 66 (880-6).

418

Stahl JS et al. Eye movements of the murine P/Q calcium channel mutant tottering, and the impact of aging.
J. Neurophysiol., 2006 Mar , 95 (1588-607).

423

Estevez M Invertebrate modeling of a migraine channelopathy.
Headache, 2006 Jun , 46 Suppl 1 (S25-31).

424

Halling DB et al. Regulation of voltage-gated Ca2+ channels by calmodulin.
Sci. STKE, 2006 Jan 17 , 2006 (er1).

427

Jackson SN et al. Phosphate stabilization of intermolecular interactions.
J. Proteome Res., 2006 Jan , 5 (122-6).

429

433

Todorov B et al. Conditional inactivation of the Cacna1a gene in transgenic mice.
Genesis, 2006 Dec , 44 (589-94).

436

437

Kirchmann M et al. The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura.
Am. J. Med. Genet. B Neuropsychiatr. Genet., 2006 Apr 5 , 141B (250-6).

439

Jeng CJ et al. Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.
Am. J. Physiol., Cell Physiol., 2006 Apr , 290 (C1209-20).

443

444

445

Imbrici P et al. Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.
Neurology, 2005 Sep 27 , 65 (944-6).

449

Shikano S et al. Genetic isolation of transport signals directing cell surface expression.
Nat. Cell Biol., 2005 Oct , 7 (985-92).

451

Takeshima T et al. [Genetic analysis of migraine headache: a review]
Nippon Rinsho, 2005 Oct , 63 (1727-32).

458

Yu GY et al. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
Ann. Neurol., 2005 Mar , 57 (349-54).

460

Barrett CF et al. Gating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channel.
J. Biol. Chem., 2005 Jun 24 , 280 (24064-71).

461

Haan J et al. Migraine genetics: an update.
, 2005 Jun , 9 (213-20).

462

463

Lautermilch NJ et al. Modulation of CaV2.1 channels by the neuronal calcium-binding protein visinin-like protein-2.
J. Neurosci., 2005 Jul 27 , 25 (7062-70).

465

Eunson LH et al. New calcium channel mutations predict aberrant RNA splicing in episodic ataxia.
Neurology, 2005 Jul 26 , 65 (308-10).

466

Kaunisto MA et al. Chromosome 19p13 loci in Finnish migraine with aura families.
Am. J. Med. Genet. B Neuropsychiatr. Genet., 2005 Jan 5 , 132B (85-9).

467

Richman RW et al. RGS12 interacts with the SNARE-binding region of the Cav2.2 calcium channel.
J. Biol. Chem., 2005 Jan 14 , 280 (1521-8).

468

Yang SN et al. Beta-cell CaV channel regulation in physiology and pathophysiology.
Am. J. Physiol. Endocrinol. Metab., 2005 Jan , 288 (E16-28).

469

Wan J et al. Nonconsensus intronic mutations cause episodic ataxia.
Ann. Neurol., 2005 Jan , 57 (131-5).

470

Harno H et al. Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study.
Neurology, 2005 Feb 8 , 64 (542-4).

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