Channelpedia

Cav1.1

260 literature references associated to Cav1.1

used / unused
Pubmed id

2

364783

Kim H et al. Protein Network Interacting with BK Channels.
Int. Rev. Neurobiol., 2016 , 128 (127-61).

5

366206

Yu L et al. Unoprostone activation of BK (KCa1.1) channel splice variants.
Biochim. Biophys. Acta, 2015 Nov , 1848 (2859-67).

6

362344

Golder FJ et al. Identification and Characterization of GAL-021 as a Novel Breathing Control Modulator.
Anesthesiology, 2015 Nov , 123 (1093-104).

7

358198

12

358520

13

367847

15

358514

Polster A et al. Stac adaptor proteins regulate trafficking and function of muscle and neuronal L-type Ca2+ channels.
Proc. Natl. Acad. Sci. U.S.A., 2015 Jan 13 , 112 (602-6).

20

361738

Wu J et al. Structure of the voltage-gated calcium channel Cav1.1 complex.
Science, 2015 Dec 18 , 350 (aad2395).

22

363207

Ohrtman JD et al. Apparent lack of physical or functional interaction between CaV1.1 and its distal C terminus.
J. Gen. Physiol., 2015 Apr , 145 (303-14).

23

357760

Cannon SC Channelopathies of skeletal muscle excitability.
Compr Physiol, 2015 Apr , 5 (761-90).

26

361479

28

363068

29

357726

32

351155

Petkov GV Central role of the BK channel in urinary bladder smooth muscle physiology and pathophysiology.
Am. J. Physiol. Regul. Integr. Comp. Physiol., 2014 Sep 15 , 307 (R571-84).

33

344657

Bartok A et al. Margatoxin is a non-selective inhibitor of human Kv1.3 K(+) channels.
Toxicon, 2014 Sep , 87 (6-16).

34

350739

Stunnenberg BC et al. Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?
Muscle Nerve, 2014 Sep , 50 (327-32).

35

351277

36

359900

37

350988

38

351797

39

354573

Toro L et al. MaxiK channel and cell signalling.
Pflugers Arch., 2014 May , 466 (875-86).

40

351634

Climent B et al. Effects of obesity on vascular potassium channels.
Curr Vasc Pharmacol, 2014 May , 12 (438-52).

41

360752

Na SJ et al. Whole-genome analysis in Korean patients with autoimmune myasthenia gravis.
Yonsei Med. J., 2014 May , 55 (660-8).

42

345755

43

345711

Tummala SR et al. Localization of Cacna1s to ON bipolar dendritic tips requires mGluR6-related cascade elements.
Invest. Ophthalmol. Vis. Sci., 2014 Mar , 55 (1483-92).

45

351327

47

351997

Li HJ et al. Chlorpromazine confers neuroprotection against brain ischemia by activating BKCa channel.
Eur. J. Pharmacol., 2014 Jul 15 , 735 (38-43).

48

360526

49

341400

Turner RW et al. T-type channels buddy up.
Pflugers Arch., 2014 Jan 11 , ().

51

345901

Sheng J et al. Electrophysiology of human cardiac atrial and ventricular telocytes.
J. Cell. Mol. Med., 2014 Feb , 18 (355-62).

52

352661

53

345947

Stowell KM DNA testing for malignant hyperthermia: the reality and the dream.
Anesth. Analg., 2014 Feb , 118 (397-406).

56

351875

Kunert-Keil CH et al. Differential expression of genes involved in the calcium homeostasis in masticatory muscles of MDX mice.
J. Physiol. Pharmacol., 2014 Apr , 65 (317-24).

57

346116

58

349244

Takacs Z et al. Interaction of the BKCa channel gating ring with dendrotoxins.
Channels (Austin), 2014 , 8 (421-32).

63

341708

Guerrero-Hernández A et al. Ryanodine receptors as leak channels.
Eur. J. Pharmacol., 2013 Nov 28 , ().

65

341904

Gonsalves SG et al. Using exome data to identify malignant hyperthermia susceptibility mutations.
Anesthesiology, 2013 Nov , 119 (1043-53).

66

354622

67

343011

68

343530

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).

69

336321

Stoneking CJ et al. Voltage dependence of the Ca(2+)-activated K(+) channel K(Ca)3.1 in human erythroleukemia cells.
Am. J. Physiol., Cell Physiol., 2013 May 1 , 304 (C858-72).

72

343740

Jorquera G et al. Cav1.1 controls frequency-dependent events regulating adult skeletal muscle plasticity.
J. Cell. Sci., 2013 Mar 1 , 126 (1189-98).

76

339870

Engbers JD et al. Modeling interactions between voltage-gated Ca ( 2+) channels and KCa1.1 channels.
Channels (Austin), 2013 Jul 31 , 7 ().

78

336084

79

336953

Suzuki Y et al. Direct molecular interaction of caveolin-3 with KCa1.1 channel in living HEK293 cell expression system.
Biochem. Biophys. Res. Commun., 2013 Jan 18 , 430 (1169-74).

80

331088

82

348106

Wei CJ et al. [Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis].
Zhonghua Er Ke Za Zhi, 2013 Jan , 51 (47-51).

86

353469

Novaković R et al. The effect of resveratrol on contractility of non-pregnant rat uterus: the contribution of K(+) channels.
J. Physiol. Pharmacol., 2013 Dec , 64 (795-805).

87

347762

Lee EJ et al. Transthyretin is a key regulator of myoblast differentiation.
PLoS ONE, 2013 , 8 (e63627).

89

343099

Rehak R et al. Low voltage activation of KCa1.1 current by Cav3-KCa1.1 complexes.
PLoS ONE, 2013 , 8 (e61844).

92

341764

99

334348

George AL Leaky channels make weak muscles.
J. Clin. Invest., 2012 Dec 3 , 122 (4333-6).

100

334352

Wu F et al. A calcium channel mutant mouse model of hypokalemic periodic paralysis.
J. Clin. Invest., 2012 Dec 3 , 122 (4580-91).

101

330708

102

334421

Zhang J et al. Role of the BK channel (KCa1.1) during activation of electrogenic K+ secretion in guinea pig distal colon.
Am. J. Physiol. Gastrointest. Liver Physiol., 2012 Dec 15 , 303 (G1322-34).

103

338334

Song YW et al. Normokalemic periodic paralysis is not a distinct disease.
Muscle Nerve, 2012 Dec , 46 (914-6).

105

333645

106

327122

Sung CC et al. Genotype and phenotype analysis of patients with sporadic periodic paralysis.
Am. J. Med. Sci., 2012 Apr , 343 (281-5).

109

320808

110

329259

111

323360

Banas K et al. The KATP channel Kir6.2 subunit content is higher in glycolytic than oxidative skeletal muscle fibers.
Am. J. Physiol. Regul. Integr. Comp. Physiol., 2011 Oct , 301 (R916-25).

113

323723

114

319283

117

322282

Li BY et al. KCa1.1 channel contributes to cell excitability in unmyelinated but not myelinated rat vagal afferents.
Am. J. Physiol., Cell Physiol., 2011 Jun , 300 (C1393-403).

118

322063

120

317910

He ML et al. Effects of ion channels on proliferation in cultured human cardiac fibroblasts.
J. Mol. Cell. Cardiol., 2011 Aug , 51 (198-206).

121

326518

Stroffekova K The IQ motif is crucial for Cav1.1 function.
J. Biomed. Biotechnol., 2011 , 2011 (504649).

123

141228

Incecik F et al. Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family.
Turk. J. Pediatr., 2010 Jul-Aug , 52 (409-10).

124

141776

Raja Rayan DL et al. Skeletal muscle channelopathies: nondystrophic myotonias and periodic paralysis.
Curr. Opin. Neurol., 2010 Oct , 23 (466-76).

126

136224

128

139201

Li J et al. Skeletal phenotype of mice with a null mutation in Cav 1.3 L-type calcium channel.
J Musculoskelet Neuronal Interact, 2010 Jun , 10 (180-7).

129

139632

130

124441

131

124467

Sorensen MV et al. Colonic potassium handling.
, 2010 Feb 10 , ().

137

123652

141

131839

Matthews E et al. Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.
Neurology, 2009 May 5 , 72 (1544-7).

142

123007

Harron SA et al. Volume regulation in the human airway epithelial cell line Calu-3.
Can. J. Physiol. Pharmacol., 2009 May , 87 (337-46).

143

1535

146

123773

Maffè S et al. Atypical arrhythmic complications in familial hypokalemic periodic paralysis.
J Cardiovasc Med (Hagerstown), 2009 Jan , 10 (68-71).

147

3380

Poulsen AN et al. Differential expression of BK channel isoforms and beta-subunits in rat neuro-vascular tissues.
Biochim. Biophys. Acta, 2009 Feb , 1788 (380-9).

148

9913

Hu H et al. Characterization of ion channels in human preadipocytes.
J. Cell. Physiol., 2009 Feb , 218 (427-35).

151

124014

Takacs Z et al. A designer ligand specific for Kv1.3 channels from a scorpion neurotoxin-based library.
Proc. Natl. Acad. Sci. U.S.A., 2009 Dec 29 , 106 (22211-6).

152

7337

Levano S et al. Increasing the number of diagnostic mutations in malignant hyperthermia.
Hum. Mutat., 2009 Apr , 30 (590-8).

153

123647

Carpenter D et al. The role of CACNA1S in predisposition to malignant hyperthermia.
BMC Med. Genet., 2009 , 10 (104).

154

1233

Sørensen MV et al. Aldosterone increases KCa1.1 (BK) channel-mediated colonic K+ secretion.
J. Physiol. (Lond.), 2008 Sep 1 , 586 (4251-64).

157

9604

158

4494

159

6889

Nakamoto T et al. Apical maxi-K (KCa1.1) channels mediate K+ secretion by the mouse submandibular exocrine gland.
Am. J. Physiol., Cell Physiol., 2008 Mar , 294 (C810-9).

161

13754

162

19513

Tricarico D et al. Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted rats.
Neuromuscul. Disord., 2008 Jan , 18 (74-80).

163

132292

164

13476

Stroffekova K Ca2+/CaM-dependent inactivation of the skeletal muscle L-type Ca2+ channel (Cav1.1).
Pflugers Arch., 2008 Feb , 455 (873-84).

167

17538

168

15940

Sandoval A et al. gamma1-dependent down-regulation of recombinant voltage-gated Ca2+ channels.
Cell. Mol. Neurobiol., 2007 Nov , 27 (901-8).

169

12295

Houinato D et al. Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family.
Neuromuscul. Disord., 2007 May , 17 (419-22).

171

17174

Kuzmenkin A et al. Gating of the HypoPP-1 mutations: I. Mutant-specific effects and cooperativity.
Pflugers Arch., 2007 Jun , 454 (495-505).

172

12951

Kuzmenkin A et al. Gating of the HypoPP-1 mutations: II. Effects of a calcium-channel agonist BayK 8644.
Pflugers Arch., 2007 Jul , 454 (605-14).

173

15934

175

7052

177

14676

Carle T et al. Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysis.
Biochem. Biophys. Res. Commun., 2006 Sep 22 , 348 (653-61).

178

12097

Deng XL et al. Properties of ion channels in rabbit mesenchymal stem cells from bone marrow.
Biochem. Biophys. Res. Commun., 2006 Sep 15 , 348 (301-9).

181

26802

182

28682

183

25668

184

26044

Ke Q et al. [R1239H mutation of CACNA1S gene in a Chinese family with hypokalaemic periodic paralysis]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2006 Jun , 23 (272-4).

186

25854

Venance SL et al. The primary periodic paralyses: diagnosis, pathogenesis and treatment.
Brain, 2006 Jan , 129 (8-17).

189

21051

Fang XM et al. Mapping CACNA1S to chromosome 10 in swine using radiation hybrid mapping.
Anim. Genet., 2005 Oct , 36 (437).

190

28261

Vicart S et al. Human skeletal muscle sodium channelopathies.
Neurol. Sci., 2005 Oct , 26 (194-202).

195

31301

200

133711

Miller TM et al. Correlating phenotype and genotype in the periodic paralyses.
Neurology, 2004 Nov 9 , 63 (1647-55).

202

38989

203

33509

Links TP et al. [From gene to diseases; hypokalemic periodic paralysis]
, 2004 May 22 , 148 (1035-8).

204

36939

Lunardi J et al. [Genetic of diseases by abnormal functioning of the skeletal muscle-calcium releasing complex]
Rev. Neurol. (Paris), 2004 May , 160 (S70-7).

206

39636

209

38626

Vicart S et al. New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.
Neurology, 2004 Dec 14 , 63 (2120-7).

211

49012

Carsana A et al. Identification of new polymorphisms in the CACNA1S gene.
Clin. Chem. Lab. Med., 2003 Jan , 41 (20-2).

212

33545

Muniz VP et al. Screening for mutations in the RYR1 gene in families with malignant hyperthermia.
J. Mol. Neurosci., 2003 , 21 (35-42).

215

45980

Lehmann-Horn F et al. Periodic paralysis: understanding channelopathies.
, 2002 Jan , 2 (61-9).

216

41320

219

57953

220

23825

Ikeda Y et al. [Familial hypokalemic periodic paralysis]
, 2001 Nov , 11 (1464-7).

221

59877

229

134960

231

61128

232

65403

Bulman DE et al. A novel sodium channel mutation in a family with hypokalemic periodic paralysis.
Neurology, 1999 Dec 10 , 53 (1932-6).

234

69851

Lory P et al. [Physiopathology of calcium channels: identification of calcium channelopathies]
C. R. Seances Soc. Biol. Fil., 1998 , 192 (137-47).

236

79210

240

77860

243

82535

245

83860

246

82748

Iaizzo PA et al. Differential diagnosis of periodic paralysis aided by in vitro myography.
Neuromuscul. Disord., 1995 Mar , 5 (115-24).

249

84699

250

87099

Plassart E et al. Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP).
Hum. Genet., 1994 Nov , 94 (551-6).

255

86371

Jurkat-Rott K et al. A calcium channel mutation causing hypokalemic periodic paralysis.
Hum. Mol. Genet., 1994 Aug , 3 (1415-9).

259

97680