Cav1.1

1

Liu Y et al. Unique Expression of Angiotensin Type-2 Receptor in Sex-Specific Distribution of Myelinated Ah-Type Baroreceptor Neuron Contributing to Sex-Dimorphic Neurocontrol of Circulation.
Hypertension, 2016 Feb 16 , ().

2

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

3

Georgiou DK et al. Ca2+ Binding/Permeation via Calcium Channel, CaV1.1, Regulates the Intracellular Distribution of the Fatty Acid Transport Protein, CD36, and Fatty Acid Metabolism.
J. Biol. Chem., 2015 Sep 25 , 290 (23751-65).

4

Zhang YY et al. KCa1.1 is potential marker for distinguishing Ah-type baroreceptor neurons in NTS and contributes to sex-specific presynaptic neurotransmission in baroreflex afferent pathway.
Neurosci. Lett., 2015 Sep 14 , 604 (1-6).

5

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

6

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

7

Fiszer D et al. Next-generation Sequencing of RYR1 and CACNA1S in Malignant Hyperthermia and Exertional Heat Illness.
Anesthesiology, 2015 May , 122 (1033-46).

8

Benedetti B et al. Physiological and pharmacological modulation of the embryonic skeletal muscle calcium channel splice variant CaV1.1e.
Biophys. J., 2015 Mar 10 , 108 (1072-80).

9

Gillies RL et al. Analysis of the entire ryanodine receptor type 1 and alpha 1 subunit of the dihydropyridine receptor (CACNA1S) coding regions for variants associated with malignant hyperthermia in Australian families.
Anaesth Intensive Care, 2015 Mar , 43 (157-66).

10

Dominguez Rieg JA et al. P2Y₂ receptor activation decreases blood pressure via intermediate conductance potassium channels and connexin 37.
Acta Physiol (Oxf), 2015 Mar , 213 (628-41).

11

Ma Y et al. Epoxyeicosatrienoic acids act through TRPV4-TRPC1-KCa1.1 complex to induce smooth muscle membrane hyperpolarization and relaxation in human internal mammary arteries.
Biochim. Biophys. Acta, 2015 Mar , 1852 (552-9).

12

Jia BX et al. Muscle edema of the lower limb determined by MRI in Asian hypokalaemic periodic paralysis patients.
Neurol. Res., 2015 Mar , 37 (246-52).

13

Grajales L et al. Temporal expression of calcium channel subunits in satellite cells and bone marrow mesenchymal cells.
Stem Cell Rev, 2015 Jun , 11 (408-22).

14

Xu WX et al. KCa1.1 β4-subunits are not responsible for iberiotoxin-resistance in baroreceptor neurons in adult male rats.
Int. J. Cardiol., 2015 Jan 15 , 178 (184-7).

15

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).

16

Tanner MR et al. KCa1.1 inhibition attenuates fibroblast-like synoviocyte invasiveness and ameliorates disease in rat models of rheumatoid arthritis.
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17

Lopez RJ et al. Raptor ablation in skeletal muscle decreases Cav1.1 expression and affects the function of the excitation-contraction coupling supramolecular complex.
Biochem. J., 2015 Feb 15 , 466 (123-35).

18

Oliván-Viguera A et al. A novel pan-negative-gating modulator of KCa2/3 channels, fluoro-di-benzoate, RA-2, inhibits endothelium-derived hyperpolarization-type relaxation in coronary artery and produces bradycardia in vivo.
Mol. Pharmacol., 2015 Feb , 87 (338-48).

19

Turner RW et al. Neuronal expression of the intermediate conductance calcium-activated potassium channel KCa3.1 in the mammalian central nervous system.
Pflugers Arch., 2015 Feb , 467 (311-28).

20

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

21

Liu Y et al. KCa1.1-mediated frequency-dependent central and peripheral neuromodulation via Ah-type baroreceptor neurons located within nodose ganglia and nucleus of solitary tract of female rats.
Int. J. Cardiol., 2015 Apr 15 , 185 (84-7).

22

Berthier C et al. Depression of voltage-activated Ca2+ release in skeletal muscle by activation of a voltage-sensing phosphatase.
J. Gen. Physiol., 2015 Apr , 145 (315-30).

23

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

24

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).

25

Parajuli SP et al. Functional link between muscarinic receptors and large-conductance Ca2+ -activated K+ channels in freshly isolated human detrusor smooth muscle cells.
Pflugers Arch., 2015 Apr , 467 (665-75).

26

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).

27

Hernãndez-Ochoa EO et al. Critical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and Disease.
Front Physiol, 2015 , 6 (420).

28

Antony C et al. Regulation of L-type Voltage Gated Calcium Channel CACNA1S in Macrophages upon Mycobacterium tuberculosis Infection.
PLoS ONE, 2015 , 10 (e0124263).

29

Liu XL et al. Mutations of SCN4A gene cause different diseases: 2 case reports and literature review.
Channels (Austin), 2015 , 9 (82-7).

30

Rabjerg M et al. High expression of KCa3.1 in patients with clear cell renal carcinoma predicts high metastatic risk and poor survival.
PLoS ONE, 2015 , 10 (e0122992).

31

Mahalingam M et al. Structural mapping of divergent regions in the type 1 ryanodine receptor using fluorescence resonance energy transfer.
Structure, 2014 Sep 2 , 22 (1322-32).

32

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

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

34

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

35

Nausch B et al. NS19504: a novel BK channel activator with relaxing effect on bladder smooth muscle spontaneous phasic contractions.
J. Pharmacol. Exp. Ther., 2014 Sep , 350 (520-30).

36

Zhang P et al. Nitric oxide and protein kinase G act on TRPC1 to inhibit 11,12-EET-induced vascular relaxation.
Cardiovasc. Res., 2014 Oct 1 , 104 (138-46).

37

Ge L et al. Big Potassium (BK) ion channels in biology, disease and possible targets for cancer immunotherapy.
Int. Immunopharmacol., 2014 Oct , 22 (427-43).

38

Beqollari D et al. Differential effects of RGK proteins on L-type channel function in adult mouse skeletal muscle.
Biophys. J., 2014 May 6 , 106 (1950-7).

39

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

40

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

41

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

42

Chaube R et al. Regulation of the skeletal muscle ryanodine receptor/Ca2+-release channel RyR1 by S-palmitoylation.
J. Biol. Chem., 2014 Mar 21 , 289 (8612-9).

43

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).

44

Fuller MD et al. Differential regulation of CaV1.2 channels by cAMP-dependent protein kinase bound to A-kinase anchoring proteins 15 and 79/150.
J. Gen. Physiol., 2014 Mar , 143 (315-24).

45

Taylor J et al. The Cavβ1a subunit regulates gene expression and suppresses myogenin in muscle progenitor cells.
J. Cell Biol., 2014 Jun 23 , 205 (829-46).

46

Wu CT et al. Disease and region-related cardiac fibroblast potassium current variations and potential functional significance.
Cardiovasc. Res., 2014 Jun 1 , 102 (487-96).

47

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

48

Ruchala I et al. Electrical coupling between the human serotonin transporter and voltage-gated Ca(2+) channels.
Cell Calcium, 2014 Jul , 56 (25-33).

49

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

50

Hernãndez-Ochoa EO et al. β1a490-508, a 19-residue peptide from C-terminal tail of Cav1.1 β1a subunit, potentiates voltage-dependent calcium release in adult skeletal muscle fibers.
Biophys. J., 2014 Feb 4 , 106 (535-47).

51

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

52

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

53

Wang Y et al. [Ca(2+)-activated K(+) channel switching in smooth muscle participates in atherosclerosis development in diabetic rats].
Nan Fang Yi Ke Da Xue Xue Bao, 2014 Feb , 34 (188-92).

54

Larach MG et al. Malignant hyperthermia deaths related to inadequate temperature monitoring, 2007-2012: a report from the North American malignant hyperthermia registry of the malignant hyperthermia association of the United States.
Anesth. Analg., 2014 Dec , 119 (1359-66).

55

Sánchez-Pastor E et al. Cannabinoid receptor type 1 activation by arachidonylcyclopropylamide in rat aortic rings causes vasorelaxation involving calcium-activated potassium channel subunit alpha-1 and calcium channel, voltage-dependent, L type, alpha 1C subunit.
Eur. J. Pharmacol., 2014 Apr 15 , 729 (100-6).

56

Robert V et al. Protein kinase C-dependent activation of CaV1.2 channels selectively controls human TH2-lymphocyte functions.
J. Allergy Clin. Immunol., 2014 Apr , 133 (1175-83).

57

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).

58

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

59

Zapata M et al. Molecular cloning of ion channels in Felis catus that are related to periodic paralyses in man: a contribution to the understanding of the genetic susceptibility to feline neck ventroflexion and paralysis.
Biol Open, 2014 , 3 (785-93).

60

Yang B et al. A rare case of unilateral adrenal hyperplasia accompanied by hypokalaemic periodic paralysis caused by a novel dominant mutation in CACNA1S: features and prognosis after adrenalectomy.
BMC Urol, 2014 , 14 (96).

61

Lau K et al. Crystal structures of wild type and disease mutant forms of the ryanodine receptor SPRY2 domain.
Nat Commun, 2014 , 5 (5397).

62

Watanabe A et al. In silico identification of the genes for sperm-egg interaction in the internal fertilization of the newt Cynops pyrrhogaster.
Int. J. Dev. Biol., 2014 , 58 (873-9).

63

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

64

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

65

Kim JH et al. Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families.
Anesthesiology, 2013 Nov , 119 (1054-65).

66

Yu ZH et al. Up-regulation of KCa3.1 promotes human airway smooth muscle cell phenotypic modulation.
Pharmacol. Res., 2013 Nov , 77 (30-8).

67

Bannister RA et al. Impaired gating of an L-Type Ca(2+) channel carrying a mutation linked to malignant hyperthermia.
Biophys. J., 2013 May 7 , 104 (1917-22).

68

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).

69

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).

70

Brandom BW et al. Ryanodine receptor type 1 gene variants in the malignant hyperthermia-susceptible population of the United States.
Anesth. Analg., 2013 May , 116 (1078-86).

71

Hanchard NA et al. Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weakness.
Clin. Genet., 2013 May , 83 (457-61).

72

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

73

Eltit JM et al. Nonspecific sarcolemmal cation channels are critical for the pathogenesis of malignant hyperthermia.
FASEB J., 2013 Mar , 27 (991-1000).

74

Takai J et al. Laminar shear stress upregulates endothelial Ca2+-activated K+ channels KCa2.3 and KCa3.1 via a Ca2+/calmodulin-dependent protein kinase kinase/Akt/p300 cascade.
Am. J. Physiol. Heart Circ. Physiol., 2013 Jun 21 , ().

75

Park WS et al. Functional expression of smooth muscle-specific ion channels in TGF-β1-treated human adipose-derived mesenchymal stem cells.
Am. J. Physiol., Cell Physiol., 2013 Jun 12 , ().

76

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

77

Zhang YY et al. BKCa and hEag1 channels regulate cell proliferation and differentiation in human bone marrow-derived mesenchymal stem cells.
J. Cell. Physiol., 2013 Jul 23 , ().

78

Nam TS et al. An algorithm for candidate sequencing in non-dystrophic skeletal muscle channelopathies.
J. Neurol., 2013 Jul , 260 (1770-7).

79

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

Ke Q et al. Gender differences in penetrance and phenotype in hypokalemic periodic paralysis.
Muscle Nerve, 2013 Jan , 47 (41-5).

81

Schiemann AH et al. Sequence capture and massively parallel sequencing to detect mutations associated with malignant hyperthermia.
Br J Anaesth, 2013 Jan , 110 (122-7).

82

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).

83

Fritsch EB et al. Triclosan impairs swimming behavior and alters expression of excitation-contraction coupling proteins in fathead minnow (Pimephales promelas).
Environ. Sci. Technol., 2013 Feb 19 , 47 (2008-17).

84

Yang Y et al. Function of BKCa channels is reduced in human vascular smooth muscle cells from Han Chinese patients with hypertension.
Hypertension, 2013 Feb , 61 (519-25).

85

Wu F et al. Beneficial effects of bumetanide in a CaV1.1-R528H mouse model of hypokalaemic periodic paralysis.
Brain, 2013 Dec , 136 (3766-74).

86

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

Lefebvre R et al. Ca2+ release in muscle fibers expressing R4892W and G4896V type 1 ryanodine receptor disease mutants.
PLoS ONE, 2013 , 8 (e54042).

88

Oliván-Viguera A et al. Novel phenolic inhibitors of small/intermediate-conductance Ca²⁺-activated K⁺ channels, KCa3.1 and KCa2.3.
PLoS ONE, 2013 , 8 (e58614).

89

Wu W et al. Cholesterol down-regulates BK channels stably expressed in HEK 293 cells.
PLoS ONE, 2013 , 8 (e79952).

90

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

91

Taiakina V et al. The calmodulin-binding, short linear motif, NSCaTE is conserved in L-type channel ancestors of vertebrate Cav1.2 and Cav1.3 channels.
PLoS ONE, 2013 , 8 (e61765).

92

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

93

Valladares D et al. Electrical stimuli are anti-apoptotic in skeletal muscle via extracellular ATP. Alteration of this signal in Mdx mice is a likely cause of dystrophy.
PLoS ONE, 2013 , 8 (e75340).

94

Xin W et al. Constitutively active phosphodiesterase activity regulates urinary bladder smooth muscle function: critical role of KCa1.1 channel.
Am. J. Physiol. Renal Physiol., 2012 Nov 1 , 303 (F1300-6).

95

Hu X et al. KCa1.1 potassium channels regulate key proinflammatory and invasive properties of fibroblast-like synoviocytes in rheumatoid arthritis.
J. Biol. Chem., 2012 Feb 3 , 287 (4014-22).

96

Zhang J et al. Regulation of Cell Proliferation of Human Induced Pluripotent Stem Cell-Derived Mesenchymal Stem Cells via Ether a go-go 1 (hEAG1) Potassium Channel.
, 2012 Feb 22 , ().

97

Parker MD et al. HCO3--independent conductance with a mutant Na/HCO3 cotransporter (SLC4A4) in a case of proximal renal tubular acidosis with hypokalemic paralysis.
, 2012 Feb 13 , ().

98

Li FF et al. A novel mutation in CACNA1S gene associated with hypokalemic periodic paralysis which has a gender difference in the penetrance.
J. Mol. Neurosci., 2012 Feb , 46 (378-83).

99

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

100

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

101

Schild JH et al. Differential distribution of voltage-gated channels in myelinated and unmyelinated baroreceptor afferents.
Auton Neurosci, 2012 Dec 24 , 172 (4-12).

102

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

Horrigan FT Perspectives on: Conformational coupling in ion channels: Conformational coupling in BK potassium channels.
J. Gen. Physiol., 2012 Dec , 140 (625-34).

104

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

105

Yamamura H et al. Molecular assembly and dynamics of fluorescent protein-tagged single KCa1.1 channel in expression system and vascular smooth muscle cells.
Am. J. Physiol., Cell Physiol., 2012 Apr 15 , 302 (C1257-68).

106

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

107

Evans AM et al. Ion Channel Regulation by the LKB1-AMPK Signalling Pathway: The Key to Carotid Body Activation by Hypoxia and Metabolic Homeostasis at the Whole Body Level.
Adv. Exp. Med. Biol., 2012 , 758 (81-90).

108

Krasnyĭ AM et al. [The expression of genes encoding the voltage-dependent L-type Ca2+ channels in proliferating and differentiating C2C12 myoblasts of mice].
Izv. Akad. Nauk. Ser. Biol., 2011 May-Jun , (349-53).

109

Wu F et al. A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.
J. Clin. Invest., 2011 Oct 3 , 121 (4082-94).

110

Hirano M et al. A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.
J. Neurol. Sci., 2011 Oct 15 , 309 (9-11).

111

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).

112

Burge JA et al. Novel Insights into the Pathomechanisms of Skeletal Muscle Channelopathies.
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113

Kim H et al. Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations.
Korean J Pediatr, 2011 Nov , 54 (473-6).

114

Francis DG et al. Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia.
Neurology, 2011 May 10 , 76 (1635-41).

115

Tammaro A et al. Novel missense mutations and unexpected multiple changes of RYR1 gene in 75 malignant hyperthermia families.
Clin. Genet., 2011 May , 79 (438-47).

116

Kraeva N et al. Ryanodine receptor type 1 gene mutations found in the Canadian malignant hyperthermia population.
Can J Anaesth, 2011 Jun , 58 (504-13).

117

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

Xiao Z et al. [The relationships between the single nueleotide polymorphisms of CACNA1S gene 11 exon and thyrotoxic hypokalemic periodic paralysis in the people of Han Nationality in Sichuan Province, China].
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi, 2011 Jun , 28 (547-52, 558).

119

Delbono O Expression and regulation of excitation-contraction coupling proteins in aging skeletal muscle.
Curr Aging Sci, 2011 Dec , 4 (248-59).

120

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

Kryshtal' DA et al. [Changes in calcium-dependent potassium channels of isolated smooth muscle cells of the bladder in rats with experimental diabetes].
Fiziol Zh, 2011 , 57 (25-32).

122

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

123

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

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

125

Kil TH et al. Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis.
Eur. J. Paediatr. Neurol., 2010 May , 14 (278-81).

126

Sorensen MV et al. Adrenaline-induced colonic K+ secretion is mediated via KCa1.1 (BK) channel.
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127

Zhou H et al. Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene.
Neuromuscul. Disord., 2010 Mar , 20 (166-73).

128

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

Toppin PJ et al. A report of fulminant malignant hyperthermia in a patient with a novel mutation of the CACNA1S gene.
Can J Anaesth, 2010 Jul , 57 (689-93).

130

Cannon SC Voltage-Sensor Mutations in Channelopathies of Skeletal Muscle.
, 2010 Feb 15 , ().

131

Sorensen MV et al. Colonic potassium handling.
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132

Matthews E et al. Muscle channelopathies: does the predicted channel gating pore offer new treatment options for hypokalaemic periodic paralysis?
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133

Pirone A et al. Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavalpha1S-subunit.
Am. J. Physiol., Cell Physiol., 2010 Dec , 299 (C1345-54).

134

Schicker KW et al. P2Y1 receptors mediate an activation of neuronal calcium-dependent K+ channels.
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135

Chiu YH et al. Dominant-negative regulation of cell surface expression by a pentapeptide motif at the extreme COOH terminus of an Slo1 calcium-activated potassium channel splice variant.
Mol. Pharmacol., 2010 Apr , 77 (497-507).

136

Xu X et al. Long-term fish oil supplementation induces cardiac electrical remodeling by changing channel protein expression in the rabbit model.
PLoS ONE, 2010 , 5 (e10140).

137

Sones WR et al. Inhibition of vascular calcium-gated chloride currents by blockers of KCa1.1, but not by modulators of KCa2.1 or KCa2.3 channels.
Br. J. Pharmacol., 2009 Sep , 158 (521-31).

138

Taylor JR et al. Increased CaVbeta1A expression with aging contributes to skeletal muscle weakness.
Aging Cell, 2009 Sep , 8 (584-94).

139

Bentzen BH et al. Synthesis and characterisation of NS13558: a new important tool for addressing KCa1.1 channel function ex vivo.
, 2009 Oct 2 , ().

140

Ke T et al. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
J. Hum. Genet., 2009 Nov , 54 (660-4).

141

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

142

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

Jurkat-Rott K et al. K+-dependent paradoxical membrane depolarization and Na+ overload, major and reversible contributors to weakness by ion channel leaks.
Proc. Natl. Acad. Sci. U.S.A., 2009 Mar 10 , 106 (4036-41).

144

Kaufmann WA et al. Large-conductance calcium-activated potassium channels in purkinje cell plasma membranes are clustered at sites of hypolemmal microdomains.
J. Comp. Neurol., 2009 Jul 10 , 515 (215-30).

145

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

146

Tuluc P et al. A CaV1.1 Ca2+ channel splice variant with high conductance and voltage-sensitivity alters EC coupling in developing skeletal muscle.
Biophys. J., 2009 Jan , 96 (35-44).

147

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

148

Specht D et al. Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses.
Invest. Ophthalmol. Vis. Sci., 2009 Feb , 50 (505-15).

149

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).

150

Köhler R Single-nucleotide polymorphisms in vascular Ca(2+)-activated K (+)-channel genes and cardiovascular disease.
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151

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

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

153

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

154

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

155

Ohrtman J et al. Sequence differences in the IQ motifs of CaV1.1 and CaV1.2 strongly impact calmodulin binding and calcium-dependent inactivation.
J. Biol. Chem., 2008 Oct 24 , 283 (29301-11).

156

Struyk AF et al. Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis.
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