ライフサイエンスコーパス: calcium-activated

1 ne a signaling pathway from chloride channel calcium-activated 1 (CLCA1) to MAPK13 that is responsibl

2 ctrometry identified murine chloride channel calcium-activated 1 (mCLCA1) as the 10.1.1 Ag, a 90-kDa

3 s, Western blot analysis of chloride channel calcium activated 3 (CLCA3) expression in lung homogenat

4 Lowering the activity of Gelsolin, a known calcium-activated actin filament-severing protein, also

5 chment), which regulates voltage-independent calcium-activated action potentials at the neuronal syna

6 w that the functional expression of the slow calcium-activated afterhyperpolarizing current in pyrami

7 ensor proteins in the activation of the slow calcium-activated afterhyperpolarizing current.

8 Both calcium-activated and stretch-activated tensions increas

9 significantly from caspases because they are calcium-activated, arginine-specific peptidases that do

10 tress axis-regulated exon (STREX)-containing calcium-activated big potassium (BKCa) channel splice va

11 Calcium-activated binding of S100A4 to CD16A, promoted b

12 an-neurexin deletion reduced the function of calcium-activated BK potassium channels, whose activatio

13 Large conductance calcium-activated (BK) channels are broadly expressed in

14 This increase in cytosolic calcium activated by postsynaptic Gs-coupled CRF recepto

15 emonstrated that the increase in cytoplasmic calcium activated Ca(2+) dependent potassium currents an

16 amine receptor (amitraz metabolite), and the calcium-activated calcium channel (diamides).

17 shots of ryanodine receptor type 1 (RyR1), a calcium-activated calcium channel engaged in the binding

18 ha-mediated Ser648 phosphorylation abrogated calcium-activated calmodulin (CaM) binding to the regula

19 cing it into a peptide that is recognized by calcium-activated calmodulin.

20 Proteolytic processing of PKCalpha by calcium-activated calpain activates pathological cardiac

21 Moreover, these findings identify calcium-activated calpains as powerful modulators of cel

22 norganic phosphate [Pi] were investigated in calcium-activated cardiac myofibrils.

23 One candidate subpopulation expresses the calcium activated cation channel TRPM5 (transient recept

24 Calcium-activated CCTalpha nuclear import is mediated by

25 mily of membrane proteins, which encompasses calcium-activated channels for ions and lipids.

26 ial cells (PDECs) have been shown to express calcium activated chloride channels (CaCCs) and there is

27 TMEM16A (ANO1) is a calcium-activated chloride channel (CaCC) expressed in s

28 eins with unknown function 16 (TMEM16A) is a calcium-activated chloride channel (CaCC) important for

29 ver, the molecular identity of the olfactory calcium-activated chloride channel (CaCC) is unknown.

30 Here, we show that the recently identified calcium-activated chloride channel (CaCC) TMEM16A is exp

31 The calcium-activated chloride channel (CaCC) TMEM16A plays

32 te that TMEM16A, an evolutionarily conserved calcium-activated chloride channel (CaCC), regulates cyt

33 inhibit self-cleavage prevent activation of calcium-activated chloride channel (CaCC)-mediated chlor

34 TMEM16A (ANO1) functions as a calcium-activated chloride channel (CaCC).

35 ugmentation in iPSC-RPE fully restored BEST1 calcium-activated chloride channel activity and improved

36 BEST1 is presumed to assemble into a calcium-activated chloride channel and be involved in ch

37 The calcium-activated chloride channel ANO1 regulates multip

38 To date, only five mutations in the proposed calcium-activated chloride channel ANO5/TMEM16E gene hav

39 sought to investigate the involvement of the calcium-activated chloride channel anoctamin 1 (ANO1) in

40 The calcium-activated chloride channel anoctamin 1 (ANO1) is

41 s in the ANO5 gene, which encodes a putative calcium-activated chloride channel belonging to the Anoc

42 EM16A), also called anoctamin 1 (ANO1), is a calcium-activated chloride channel expressed widely mamm

43 Human bestrophin-1 (hBest1) is a calcium-activated chloride channel from the retinal pigm

44 16A is the major constituent of the vascular calcium-activated chloride channel in rat pulmonary arte

45 characterized the expression of the TMEM16B calcium-activated chloride channel in the LS and showed

46 inhibited the expression of Gob5, a putative calcium-activated chloride channel involved in the regul

47 Calcium-activated chloride channel regulator 1 (CLCA1) a

48 Calcium-activated chloride channel regulator 1 (CLCA1) i

49 nes, including IL13, IL5, periostin (POSTN), calcium-activated chloride channel regulator 1 (CLCA1),

50 ), which revealed an increased expression of calcium-activated chloride channel regulator 1 (CLCA1).

51 ANO1 is a calcium-activated chloride channel that is frequently ov

52 Human Bestrophin 1 (hBest1) is a calcium-activated chloride channel that regulates neuron

53 Inducible expression of either CFTR or the calcium-activated chloride channel TMEM16A attenuated th

54 Here, we report that the calcium-activated chloride channel TMEM16A is a biomarke

55 The calcium-activated chloride channel TMEM16A is a member o

56 The calcium-activated chloride channel TMEM16A is overexpres

57 KEY POINTS: The calcium-activated chloride channel TMEM16A provides a pa

58 Targeted disruption of the calcium-activated chloride channel TMEM16A, also known a

59 A selective inhibitor of the calcium-activated chloride channel TMEM16A, N-((4-methox

60 produced by a nanomolar-potency inhibitor of calcium-activated chloride channel TMEM16A.

61 igated the physiological contribution of the calcium-activated chloride channel to LS neuronal signal

62 terstitial cells of Cajal, which express the calcium-activated chloride channel transmembrane member

63 ANO1, a calcium-activated chloride channel, is highly expressed

64 we determined the expression pattern of the calcium-activated chloride channel, TMEM16B, in the LS o

65 propose that ANO2 constitutes the olfactory calcium-activated chloride channel.

66 y was performed to detect ANO4 activity as a calcium-activated chloride channel.

67 Calcium-activated chloride channels (CaCC) with similar

68 Calcium-activated chloride channels (CaCCs) are key play

69 Calcium-activated chloride channels (CaCCs) are major re

70 Calcium-activated chloride channels (CaCCs) encoded by T

71 Calcium-activated chloride channels (CaCCs) play importa

72 r components of the physiologically relevant calcium-activated chloride channels (CaCCs) present in m

73 Bestrophin calcium-activated chloride channels (CaCCs) regulate the

74 TMEM16A forms calcium-activated chloride channels (CaCCs) that regulat

75 TMEM16A and TMEM16B are calcium-activated chloride channels (CaCCs) with importa

76 enuated inward currents carried by TRPC2 and calcium-activated chloride channels (CACCs).

77 hippocampal neuronal signaling that involves calcium-activated chloride channels (CaCCs).

78 n absence of expression/activity of reported calcium-activated chloride channels (TMEM16A, Bestrophin

79 an intrinsic property observed in endogenous calcium-activated chloride channels and could be relevan

80 ng pathway in the VNO and the requirement of calcium-activated chloride channels currents to mediate

81 Recently, calcium-activated chloride channels have been shown to c

82 Evidence is provided for a role for calcium-activated chloride channels such as TMEM16a in G

83 r the analyses of physiological functions of calcium-activated chloride channels that contain TMEM16A

84 Calcium-activated chloride channels TMEM16A and TMEM16B

85 In contrast to its paralogs, the TMEM16A/B calcium-activated chloride channels, mouse TMEM16F has b

86 gative effect through interaction with other calcium-activated chloride channels, such as hBest2, 3,

87 ffects of calcium signaling on CFTR or other calcium-activated chloride channels; here, we investigat

88 The calcium-activated chloride conductance anoctamin-1 (Ano1

89 vertebrate olfactory signal transduction, a calcium-activated chloride conductance serves as a major

90 ide secretion, which consists, in part, of a calcium-activated chloride conductance.

91 re, our analysis suggests that activation of calcium-activated chloride conductances by intracellular

92 ient for HIF-1alpha almost completely lacked calcium-activated chloride secretion.

93 rowth, primarily due to HIF-1alpha-dependent calcium-activated chloride secretion.

94 TMEM16A was found recently to be a calcium-activated Cl(-) channel (CaCC).

95 lso found to strongly inhibit the intestinal calcium-activated Cl(-) channel TMEM16A by a voltage-ind

96 ost two decades, it has been postulated that calcium-activated Cl(-) channels (CaCCs) play a role in

97 The chloride channel calcium-activated (CLCA) family are secreted proteins th

98 Although a weaker activator than zinc, calcium activated CPE in vitro.

99 a potential feed-forward mechanism in which calcium-activated CPK32 activates CNGC18, further promot

100 the mean intracellular activity of calpains, calcium-activated cysteine proteases that are known to c

101 Calpains, calcium-activated cysteine proteases, have been shown to

102 The neuronal signal is transmitted through calcium-activated dense core vesicle neurosecretion.

103 A new study reveals that a calcium-activated endoribonuclease of the EndoU protein

104 force of diaphragm strips, absolute maximal calcium activated force, and maximal specific calcium-ac

105 Compared with control, maximal calcium-activated force and calcium sensitivity declined

106 alcium activated force, and maximal specific calcium-activated force of permeabilized diaphragm fiber

107 ss spectrometric analysis of the products of calcium-activated hydrolysis of endogenous mitochondrial

108 , as a result of the excessive activation of calcium-activated hyperpolarizing conductances.

109 ium influx accompanying such signaling opens calcium-activated ion channels for feedback regulation.

110 By aligning distantly related calcium-activated ion channels in the TMEM16 family and

111 The calcium activated K(+) channel KCa3.1 plays an important

112 est in the pharmacology of large conductance calcium-activated K (BK) channels.

113 ses of ion channels, including examples from calcium-activated K(+) (BK(Ca)), voltage-activated K(+)

114 idal neurons revealed that large-conductance calcium-activated K(+) (BK) channel open probability was

115 Large conductance, calcium-activated K(+) (BK) channels are important regul

116 Large-conductance voltage- and calcium-activated K(+) (BK) channels are key physiologic

117 ons, FMRP interaction with large-conductance calcium-activated K(+) (BK) channels, specifically their

118 Large-conductance calcium-activated K(+) (BK-type) channels, abundantly di

119 Voltage-dependent and calcium-activated K(+) (MaxiK, BK) channels are widely e

120 The calcium-activated K(+) channel KCa3.1 plays an important

121 tigated two candidate ethanol effectors, the calcium-activated K(+) channel SLO-1 and gap junctions,

122 excitotoxicity: anti-apoptotic Bcl-2, and a calcium-activated K(+) channel, SK2.

123 1-2.3) and intermediate-conductance (KCa3.1) calcium-activated K(+) channels are critically involved

124 ctance (KCa3.1) and small-conductance (KCa2) calcium-activated K(+) channels are gated by calcium bin

125 (KCa2) and intermediate-conductance (KCa3.1) calcium-activated K(+) channels are voltage-independent

126 mediated by activation of small conductance calcium-activated K(+) channels in PDGFRalpha(+) cells,

127 Purkinje-cell-specific knockout (KO) of the calcium-activated K+ channel SK2 (L7-SK2) show intact ve

128 assium efflux through voltage gated (Kv) and calcium activated (K(Ca)) potassium channels.

129 goal of this study was to determine whether calcium-activated kinases such as calcium/calmodulin-dep

130 l increase in phosphorylation likely tied to calcium-activated kinases.

131 n synaptic transmission properties, LTD, and calcium-activated membrane channels of hippocampal CA1 p

132 id, an antagonist of a previously identified calcium activated non-selective cation channel (I(CAN)).

133 while flufenamic acid, an antagonist for the calcium-activated non-selective cation conductance (ICAN

134 ity, while flufenamic acid, a blocker of the calcium-activated non-selective cation conductance, abol

135 ion further excites the cell by recruiting a calcium-activated non-selective cation current (ICAN) ca

136 t sodium current ([Formula: see text]) and a calcium-activated non-selective cationic current ([Formu

137 Calcium-activated non-specific cation (CAN) channels con

138 d synaptic efficacy, and a small-conductance calcium-activated nonselective cation channel, TMEM16F,

139 carinic afterdepolarization is mediated by a calcium-activated nonselective cation current, suggestin

140 ained responses were found to be mediated by calcium-activated nonselective cationic current induced

141 Here we show that calcium activated NOX-independent NETosis is fast and me

142 tinguished DBQD type 1 and identified CANT1 (calcium activated nucleotidase 1) mutations as responsib

143 Human soluble calcium-activated nucleotidase 1 (hSCAN-1) represents a

144 sponses to herbivory can be separated into a calcium-activated oxidative response and a K(+) -depende

145 ignaling through the small GTPase Rho and by calcium-activated pathways.

146 ibits AT1R phosphorylation by activating the calcium-activated phosphatase calcineurin in a Ca(2+)/ca

147 cium channels but not on the activity of the calcium-activated phosphatase calcineurin, and was oppos

148 The calcium pathway involved the calcium-activated phosphatase calcineurin, which stabili

149 TRPM4 is a calcium-activated, phosphatidylinositol-4,5-bisphosphate

150 Calcium-activated phospholipid scramblase mediates the e

151 tructure-function relationship of this novel calcium-activated phosphoryl transfer enzyme.

152 rylation was phenocopied only by deletion of calcium-activated PKC-2.

153 ulting from a reduction in large-conductance calcium-activated potassium (BK) and subthreshold-activa

154 lcium channel CaV1.3 and the big conductance calcium-activated potassium (BK) channel are preferentia

155 The large-conductance calcium-activated potassium (BK) channel lacks a classic

156 The large conductance, voltage and calcium-activated potassium (BK) channel negatively regu

157 ract with the auxiliary beta4 subunit of the calcium-activated potassium (BK) channel; this interacti

158 ction in the expression of large-conductance calcium-activated potassium (BK) channels and Kv3.3 volt

159 ncreases in cytoplasmic Ca(2+), voltage- and calcium-activated potassium (BK) channels and their modu

160 Large conductance voltage- and calcium-activated potassium (BK) channels are highly exp

161 The large-conductance, calcium-activated potassium (BK) channels help eliminate

162 xon domain of large conductance voltage- and calcium-activated potassium (BK) channels inhibiting cha

163 MRP's interaction with the large-conductance calcium-activated potassium (BK) channels that modulate

164 h nonmammals and mammals, large-conductance, calcium-activated potassium (BK) channels underlie a pri

165 spines act by suppressing large-conductance calcium-activated potassium (BK) channels, and this effe

166 of ion channels, including large conductance calcium-activated potassium (BK) channels.

167 The appearance of large-conductance, calcium-activated potassium (BK) current is a hallmark o

168 Large-conductance, voltage- and calcium-activated potassium (BK, or K(Ca)1.1) channels a

169 ABSTRACT: Large conductance, calcium-activated potassium (BKCa ) channels have numero

170 larization potential, a voltage signature of calcium-activated potassium (Kca) channel activity.

171 ting through nitric oxide synthase (NOS) and calcium-activated potassium (KCa) channels in young adul

172 ctivation of nitric oxide synthase (NOS) and calcium-activated potassium (KCa) channels.

173 firing through their close association with calcium-activated potassium (KCa) channels.

174 Small-conductance calcium-activated potassium (KCa2) channels have also be

175 High-conductance calcium-activated potassium (Maxi-K) channels are presen

176 Large conductance calcium-activated potassium (MaxiK) channels play a pivo

177 are occluded by apamin, a small-conductance calcium-activated potassium (SK(Ca)) channel blocker.

178 vivo, and were mediated by small-conductance calcium-activated potassium (SK) channel and CB1 cannabi

179 Small conductance calcium-activated potassium (SK) channels are required f

180 um conductance mediated by small-conductance calcium-activated potassium (SK) channels in rat MNTB pr

181 +) conductance mediated by small-conductance calcium-activated potassium (SK) channels in the MNTB ne

182 Pharmacological inhibition of calcium-activated potassium (SK) channels increases the

183 Small-conductance calcium-activated potassium (SK) channels mediate a pota

184 Small-conductance calcium-activated potassium (SK) channels mediate medium

185 Small-conductance calcium-activated potassium (SK) channels play an import

186 Small-conductance calcium-activated potassium (SK) channels regulate actio

187 nucleotide-gated (HCN) and small conductance calcium-activated potassium (SK) channels.

188 increased contribution of small-conductance calcium-activated potassium (SK) channels.

189 t that voltage-independent small conductance calcium-activated potassium (SK)-channel dysfunction cau

190 Small conductance calcium-activated potassium (SK2/K(Ca)2.2) channels are

191 Large-conductance calcium-activated potassium BK channels are widely expre

192 ET-cGMP-S (50 muM), and the high-conductance calcium-activated potassium channel (BK(Ca) channel) inh

193 The Drosophila large-conductance calcium-activated potassium channel (dSlo) binds to and

194 e gene encoding the intermediate conductance calcium-activated potassium channel (IKCa) was termed SK

195 Large-conductance calcium-activated potassium channel (KCa1.1; BK, Slo1, M

196 is associated with reduced small-conductance calcium-activated potassium channel (SK) currents and de

197 Three small conductance calcium-activated potassium channel (SK) subunits have b

198 KCNN2 encodes the small conductance calcium-activated potassium channel 2 (SK2).

199 inding and also normalized large-conductance calcium-activated potassium channel activity.

200 ized protein levels of the large conductance calcium-activated potassium channel and the water channe

201 fication of a role for the large conductance calcium-activated potassium channel brings new thinking

202 nergic neuron burst firing by decreasing the calcium-activated potassium channel current (SK), as wel

203 dent activation of MthK, a two transmembrane calcium-activated potassium channel from thermophilic ar

204 rther demonstrate that the activation of the calcium-activated potassium channel is sufficient to ind

205 The intermediate conductance calcium-activated potassium channel KCa3.1 contributes t

206 The calcium-activated potassium channel KCa3.1 controls diff

207 The calcium-activated potassium channel KCa3.1 is critically

208 The intermediate-conductance calcium-activated potassium channel KCa3.1 is expressed

209 Among the altered genes, an increase of the calcium-activated potassium channel Kcnn2 in the motor c

210 staining to determine small conductance (SK) calcium-activated potassium channel protein levels.

211 members of the small-intermediate family of calcium-activated potassium channel proteins.

212 We found that the calcium-activated potassium channel SK3 and the G protei

213 eterminant of its anthelmintic effect is the calcium-activated potassium channel SLO-1.

214 e found that Magi-1 bound to sequence like a calcium-activated potassium channel sodium-activated (Sl

215 ing peptide (GRP) and the small conductance, calcium-activated potassium channel, SK2.

216 releasing peptide and the small conductance, calcium-activated potassium channel, SK2.

217 g protein) modulates the Drosophila SLOWPOKE calcium-activated potassium channel.

218 um efflux from RBCs is the Gardos channel, a calcium-activated potassium channel.

219 These findings identify calcium-activated potassium channelopathy as a cause of

220 he presence of functional large-conductance, calcium-activated potassium channels (BK channels) on th

221 RATIONALE: Large-conductance calcium-activated potassium channels (BK) are composed o

222 Voltage- and calcium-activated potassium channels (BK) are important

223 Large-conductance calcium-activated potassium channels (BK) are potent neg

224 Mammalian large-conductance, voltage- and calcium-activated potassium channels (BK, K(Ca)1.1) are

225 howed several significant results, including calcium-activated potassium channels (GO:0016286; P=2.30

226 ctifier channels (I(KV)) and noninactivating calcium-activated potassium channels (I(BK,steady)), and

227 co-localization of intermediate-conductance calcium-activated potassium channels (IKCa) and IP3 rece

228 e colocalization of intermediate-conductance calcium-activated potassium channels (IKCa) and TRPV4 ch

229 voltage-gated potassium channels (K(v)) and calcium-activated potassium channels (K(Ca)).

230 Large conductance voltage- and calcium-activated potassium channels (MaxiK, BK(Ca)) are

231 Small conductance calcium-activated potassium channels (SK channels) are p

232 investigate the impact of small conductance calcium-activated potassium channels (SK channels) on de

233 d after acute dissociation, we found that BK calcium-activated potassium channels and Kv2 channels bo

234 This work shows that BK calcium-activated potassium channels and Kv2 voltage-act

235 o identify the molecular gating mechanism in calcium-activated potassium channels by obtaining struct

236 f N-type voltage-gated calcium channels with calcium-activated potassium channels in DCN neurons.

237 f calcium-calmodulin-dependent kinase II and calcium-activated potassium channels in mediating these

238 d is abolished by blocking small conductance calcium-activated potassium channels with apamin.

239 ent is reduced by blocking large conductance calcium-activated potassium channels with iberiotoxin, a

240 For large-conductance calcium-activated potassium channels, data are satisfact

241 Administration of an activator of calcium-activated potassium channels, SKA-31, partially

242 ropic acetylcholine receptors and associated calcium-activated potassium channels.

243 enced by the activation of small-conductance calcium-activated potassium channels.

244 ue to an increase in the open probability of calcium-activated potassium channels.

245 ation of small- and intermediate-conductance calcium-activated potassium channels.

246 cellular calcium that gated surface-membrane calcium-activated potassium channels.

247 ncreases the expression of small-conductance calcium-activated potassium channels.

248 ated by calcium-dependent processes, such as calcium-activated potassium channels.

249 I(AHP) was occluded by previous blockade of calcium-activated potassium channels.

250 d by a nonselective cation conductance and a calcium-activated potassium conductance (SK), respective

251 , we show that the excessive activation of a calcium-activated potassium conductance disrupts the ace

252 The slow afterhyperpolarization (sAHP) is a calcium-activated potassium conductance with critical ro

253 Elevation of [K(+) ](c) occurs through a calcium-activated potassium conductance, G(BK) , and a l

254 to calcium influx and activation of a large calcium-activated potassium conductance, G(BK) , that ca

255 endritic activation of the small conductance calcium-activated potassium current, SK.

256 hyperpolarization that is mediated by a slow calcium-activated potassium current.

257 perpolarizations that are mediated by a slow calcium-activated potassium current.

258 -clamp) that changes in the leak, sodium and calcium-activated potassium currents are central to thes

259 plasticity mediated by reductions in BK-type calcium-activated potassium currents in spontaneously fi

260 and a reduction in the fast-inactivating and calcium-activated potassium currents.

261 c outward currents through small-conductance calcium-activated potassium SK2 channels.

262 he contribution of the SK (small-conductance calcium-activated potassium) channel to neuronal functio

263 r firing range, and of SK (small-conductance calcium-activated potassium) currents, which were essent

264 ovary cells' plasma membrane gave rise to a calcium-activated, potassium-selective activity in patch

265 Length-tension relationships in maximally calcium activated preparations are relatively shallow an

266 tic cleavage of p35 to a p25 fragment by the calcium-activated protease calpain or by phosphorylation

267 y calpeptin and MDL-28170, inhibitors of the calcium-activated protease calpain.

268 ins220 was found to occur through calpain, a calcium-activated protease.

269 We report that calpastatin, an inhibitor of calcium-activated proteases of the calpain family, funct

270 animal models, the dysregulated activity of calcium-activated proteases, calpains, contributes direc

271 could cleave filamin A through activation of calcium-activated proteases, such as calpains.

272 The calcium activated protein, calcium/calmodulin-dependent

273 ction of the carboxypeptidase EGL-21 and the calcium-activated protein for secretion (CAPS) UNC-31, s

274 Additionally, the synaptic protein UNC-31 [calcium-activated protein for secretion (CAPS)] acts thr

275 s and SLO BK potassium channels to repress a calcium-activated protein kinase pathway.

276 Finally, we show that the calcium-activated protein phosphatase calcineurin dephos

277 We investigated the role of the calcium-activated protein phosphatase calcineurin in sev

278 cataracts, and opacification may result from calcium-activated proteolysis.

279 suggest CXCL12 regulates restitution through calcium-activated Pyk2 localized to active focal adhesio

280 Together, these results demonstrate that calcium-activated removal of RNA from membranes by Xendo

281 we identified type 5 NADPH oxidase (NOX5), a calcium-activated, ROS-forming enzyme, as the missing li

282 The signaling axis comprising the calcium-activated Ser/Thr phosphatase calcineurin (CN),

283 Calcineurin (Cn) is a calcium-activated serine/threonine protein phosphatase t

284 entify a unique mechanism of virus-mediated, calcium-activated signaling that initiates autophagy and

285 blocked by apamin, a selective antagonist of calcium-activated SK channels.

286 yed rectifier, A-type, and small-conductance calcium-activated (SK) potassium and HCN) and two recept

287 ntaining ionotropic receptors and associated calcium-activated (SK2) potassium channels, providing th

288 ce was mediated via intermediate conductance calcium-activated (SK4) potassium channels.

289 eartbeat, cardiac contractility results from calcium-activated sliding of actin thin filaments toward

290 The calcium-activated slow afterhyperpolarization (sAHP) is

291 t KCNQ channels might partially underlie the calcium-activated slow afterhyperpolarization (sAHP), a

292 We focus on calcium-activated small conductance (SK) potassium chann

293 ndependent NETosis is fast and mediated by a calcium-activated small conductance potassium (SK) chann

294 The calcium-activated small conductance potassium channel SK

295 holinergic receptors functionally coupled to calcium-activated, small conductance (SK2) potassium cha

296 nge likely used during flight), stretch- and calcium-activated tension contributed 80% and 20%, respe

297 V domain-caged protease cleavage site, and a calcium-activated TEV protease that we designed through

298 We found that EGF and extracellular calcium activated the C-terminus of ERalpha and the acti

299 Muscle cell preparations were calcium activated to yield 50% maximal force, after whic

300 Our study links calpain and dysferlin in the calcium-activated vesicle fusion of membrane repair, pla