ライフサイエンスコーパス: calcium-dependent

1 r phospholipids and that this interaction is calcium dependent.

2 ture IL-1beta, was confirmed and shown to be calcium-dependent.

3 ordered arrays, and their adhesion is always calcium-dependent.

4 eraction between EHB1 and plant membranes is calcium-dependent.

5 The glycinocins are a class of calcium-dependent, acidic cyclolipopeptide antibiotics s

6 Importantly, adipocytes induce calcium-dependent activation and autophosphorylation of

7 We further propose a calcium-dependent activation mechanism for Vasohibin pro

8 pO-mediated phosphorylation partially mimics calcium-dependent activation of gelsolin, potentially co

9 Calcium-dependent activation of human TRESK (TWIK-relate

10 intained by an alternative pathway involving calcium-dependent activation of PKCalpha.

11 ium (BK) channel; this interaction increases calcium-dependent activation of the BK channel.

12 al encoding proteins with known roles (CAPS [calcium-dependent activator protein for secretion 1], Mu

13 Genetic loss of CAPS1 (aka calcium-dependent activator protein for secretion, CADPS

14 The calcium-dependent activator proteins for secretion (CAPS

15 cium-binding EF-hand domain, crucial for the calcium-dependent activity of the PC2 channel.

16 hyperadhesive form, but can adopt a weaker, calcium-dependent adhesion during wound healing and earl

17 rons of the supraoptic nucleus (SON) display calcium-dependent afterhyperpolarizations (AHPs) followi

18 oskeleton and AJs during the steady-state or calcium-dependent AJ reassembly.

19 ne quality and osteoporosis, principally via calcium-dependent alteration of bone structure and turno

20 hat led to the discovery of an unprecedented calcium-dependent AmbU1-AmbU4 enzymatic complex for the

21 calization of CAPS-1-EYFP in DKO neurons was calcium dependent and DCV fusion probability correlated

22 Purified SlpB demonstrated calcium-dependent and AprI-inhibited protease activity a

23 model where the profilaggrin N-terminus uses calcium-dependent and calcium-independent protein-protei

24 esmosomes have two distinct adhesive states, calcium-dependent and hyperadhesive, which balance tissu

25 ng with a number of binding partners in both calcium-dependent and independent manners, and acting in

26 moves hydroxylamine, which severely inhibits calcium-dependent, and as we show here, lanthanide-depen

27 Malacidin A is a new member of the calcium-dependent antibiotic (CDAs) family with activity

28 rodigiosin, and diminished production of the calcium-dependent antibiotic, in comparison with the par

29 Calcium-dependent antibiotics are a small family of stru

30 at is distinct from previously characterized calcium-dependent antibiotics in terms of both overall s

31 The three natural products exhibited calcium-dependent antimicrobial activity against Staphyl

32 reactive oxygen species signals can prevent calcium-dependent arrhythmias.

33 gain of inhibitory function as quantified by calcium-dependent ATPase activity.

34 ospholipid membranes with SERCA and measured calcium-dependent ATPase activity.

35 CN) and two receptors (AMPAR and NMDAR) on a calcium-dependent Bienenstock-Cooper-Munro-like plastici

36 racellular Ca(2+) concentrations through its calcium-dependent binding affinities to numerous target

37 Syt1 calcium-dependent binding to SNAP25Delta3 was reduced by

38 Voltage- and calcium-dependent BK channels regulate calcium-dependent

39 usion bears the risk of an acute deleterious calcium-dependent breakdown of the blood-brain barrier.

40 In addition, calcium-dependent, but not calcium-independent exocytoti

41 Polycystin 2 (PC2) is a calcium-dependent calcium channel, and mutations to huma

42 IDR to study the functional significance of calcium-dependent, calmodulin binding on OHC function.

43 d intracellular calcium flux, and activating calcium-dependent calpain proteases.

44 cytosolic calcium levels and activation of a calcium-dependent calpain, CAPN1, which were requisite s

45 otagmins, or in other calcium-independent or calcium-dependent capacities is debated.

46 Cadherins are a superfamily of calcium-dependent cell adhesion molecules that are invol

47 surface transmembrane receptor that mediates calcium-dependent cell-cell adhesion and is a major comp

48 amily of transmembrane proteins that mediate calcium-dependent cell-cell adhesion.

49 - and calcium-dependent BK channels regulate calcium-dependent cellular events such as neurotransmitt

50 control of voltage-gated calcium influx and calcium-dependent cellular functions.

51 f calcium flux genes accompanied by abnormal calcium-dependent cerebellar membrane excitability.

52 This includes a calcium-dependent change in channel selectivity and evid

53 identification of ANO1/TMEM16A as the likely calcium-dependent chloride channel of exocrine glands ha

54 We demonstrate that secreted CLCA1 activates calcium-dependent chloride currents in HEK293T cells in

55 rface expression, which results in increased calcium-dependent chloride currents.

56 loride channel regulator 1 (CLCA1) activates calcium-dependent chloride currents; neither the target,

57 padi2, that results in a loss of detectable calcium-dependent citrullination.

58 st to micrococcal nuclease (MNase) to target calcium-dependent cleavage to specific genomic loci in v

59 The drug pentamidine inhibits calcium-dependent complex formation with p53 ((Ca)S100B.

60 cyte differentiation and collagen synthesis, calcium-dependent control of CUL3(KLHL12) integrates col

61 Daptomycin is a calcium-dependent cyclic lipodepsipeptide derived from t

62 limit cycle solutions can coexist, and that calcium dependent Cyclin D dynamics extend the oscillato

63 desaturase mediates protein degradation by a calcium-dependent cysteine protease in response to unsat

64 endogenous specific inhibitor of calpain, a calcium-dependent cysteine protease.

65 Calpains are a family of intracellular, calcium-dependent cysteine proteases involved in a varie

66 actin-binding protein) and calpain 1 and 2 (calcium-dependent cysteine proteases that control the po

67 Calpains, a group of calcium-dependent cysteine proteases, are important medi

68 imulation of NMDAR is activation of calpains-calcium-dependent cysteine proteases.

69 lar calcium homeostasis led to activation of calcium-dependent cytosolic protease calpain 2 and cleav

70 Previous in vivo cocaine exposure removed calcium-dependent D2 autoreceptor desensitization in wil

71 l that D2S, but not D2L receptors, exhibited calcium-dependent desensitization similar to that exhibi

72 while protein exchange confers plasticity on calcium-dependent desmosomes, thereby providing rapid co

73 We investigated the molecular function of C2 calcium-dependent domain containing 3 (C2cd3), an essent

74 as well as NMDA receptors (NMDAR) and their calcium-dependent downstream effectors, including CaMKII

75 -permeable ion channels are also involved in calcium-dependent EMT induction.

76 Calpain is a family of calcium-dependent endopeptidases, which plays an importa

77 ress-induced activation of the pro-apoptotic calcium-dependent enzyme, calpain, and partly suppress b

78 hanges are correlated with activation of the calcium-dependent enzyme, calpain.

79 Calpains are broadly distributed, calcium-dependent enzymes that induce limited proteolysi

80 tidylarginine deiminases (PADs), a family of calcium-dependent enzymes, catalyze citrullination, a po

81 apalindole-type alkaloids as a new family of calcium-dependent enzymes, where the metal ions are show

82 at underlie both normal cardiac function and calcium-dependent etiologies in heart disease.

83 e host erythrocyte is a highly regulated and calcium-dependent event that is critical for disease pro

84 omain with target cell membranes, which is a calcium-dependent event.

85 etermining BK current and thus regulation of calcium-dependent events.

86 highly conserved domain of Munc13, enhances calcium-dependent exocytosis downstream of vesicle primi

87 either up- or downregulated upon triggering calcium-dependent exocytosis.

88 The precise neurophysiological role of this calcium-dependent facilitation (CDF) remains uncertain,

89 This study identifies a long-duration calcium-dependent facilitation (L-CDF) of CaV1.3 channel

90 not CaV1.2 channels exhibit a long-duration calcium-dependent facilitation (L-CDF) that lasts up to

91 a robust enhancement or sensitization, in a calcium-dependent fashion.

92 stimuli, others obtained data showing only a calcium-dependent fast adaptation response.

93 ER-localized calcium sensor and a source of calcium-dependent feedback for the homeostatic stabiliza

94 nterest in the mechanism behind TMEM16A-CaCC calcium-dependent gating, comprehensive surveys to ident

95 the mammalian brain, including function as a calcium-dependent gliotransmitter mediating communicatio

96 A calcium-dependent glucuronic acid binding site shows dis

97 Here, we report calcium-dependent glutamate release from vGluT3-expressi

98 ecessary for growth cone steering toward the calcium-dependent guidance cue BDNF, with STIM1 function

99 n (CRP), in normal human serum, displaying a calcium-dependent, high-avidity interaction and ability

100 Calcium-dependent HrpZ1 oligomerization targets ATG4b-me

101 trols and patients on hemodialysis using the calcium-dependent IF-1 mAb against fibrinogen for additi

102 the pattern-recognition receptor complex and calcium-dependent immunity programs in the PAMP-triggere

103 Yet, their effects on calcium-dependent inactivation (CDI) have remained uncer

104 Calcium-dependent inactivation (CDI) is a fundamental au

105 he boosting of channel activity and promotes calcium-dependent inactivation (CDI).

106 s of the receptor that may contribute to the calcium-dependent inactivation.

107 classical LTP involves an NMDA-receptor- and calcium-dependent increase in functional synaptic AMPA r

108 e intracellular calcium levels, leading to a calcium-dependent increase in TgMyoA phosphorylation.

109 feedback on phototransduction that includes calcium-dependent inhibition of rhodopsin kinase (GRK1)

110 biological activation of CIPKs relies on the calcium-dependent interaction of a self-inhibitory NAF m

111 nd protocadherin-15 form tip links through a calcium-dependent interaction of their extracellular dom

112 affected transport at least in part through calcium-dependent interactions between apoptosis-linked

113 further assembly, but did reveal reversible, calcium-dependent interactions between the dimerization

114 We show that transient calcium-dependent interactions of PYR/PYL ABA receptors

115 structurally related to the TMEM16 family of calcium-dependent ion channels and lipid scramblases.

116 tiates signaling and transcription through a calcium-dependent isoform of adenylate cyclase, ADCY8, a

117 were tested: inhibition of the autoactivated calcium-dependent kinase (calmodulin kinase II [CaMKII])

118 tion in a manner dependent upon AMPK and the calcium-dependent kinase CAMKII.

119 ivation of phagophore formation requires the calcium-dependent kinase CaMKKbeta and AMPK, which incre

120 tor signaling pathways after engagement with calcium-dependent lectins expressed by tissue macrophage

121 ch revealed that, in addition to a classical calcium-dependent lipid binding C2 domain, a specific CA

122 lts show that CaM directly binds to DR5 in a calcium dependent manner in breast cancer cells.

123 onstrated that hippocalcin oligomerises in a calcium-dependent manner and binds to voltage-gated calc

124 y co-expression of TCF4 plus calmodulin in a calcium-dependent manner and by dampening neuronal excit

125 domains directly interact with betaGRP2 in a calcium-dependent manner and that high-affinity interact

126 pitulates these differentiation defects in a calcium-dependent manner and that in utero Ca(v)1.2 gain

127 sed in a synaptic NMDA receptor- and nuclear calcium-dependent manner in hippocampal neurons within 2

128 imulating the kinase activity of mTORC1 in a calcium-dependent manner in vitro.

129 Calmodulin binds to helix 8 of the A2AR in a calcium-dependent manner that can displace binding of A2

130 MBL bound to CC in a calcium-dependent manner whereas ficolin-2 binding was c

131 ayed in trypsin relative to trypsinogen in a calcium-dependent manner, but for this bond cleavage was

132 through activation of the CDK-5 pathway in a calcium-dependent manner, involving a calpain clp-4.

133 phobic site on the C terminus of KChIP3 in a calcium-dependent manner, with an equilibrium dissociati

134 irments on autophagy flux and apoptosis in a calcium-dependent manner.

135 SP-D bound to Phleum pratense in a dose- and calcium-dependent manner.

136 bound the C-terminal portion of Phl p 7 in a calcium-dependent manner.

137 ING TRANSCRIPTION ACTIVATOR 3 (CAMTA3), in a calcium-dependent manner.

138 totagmin 1 (Syt1) for binding to SNAP25 in a calcium-dependent manner.

139 of proteins that bind to phospholipids in a calcium-dependent manner.

140 mplex that regulates flagellar motility in a calcium-dependent manner.

141 e state and compete with native folding in a calcium-dependent manner.

142 eterocomplexes with rMASP-1 and rMASP-3 in a calcium-dependent manner.

143 d the divergent iamP and iamA promoters in a calcium-dependent manner.

144 tials and modulated by calmodulin (CaM) in a calcium-dependent manner.

145 ath in apoptosis-resistant cancer cells in a calcium-dependent manner.

146 ndii produces a family of seven secreted and calcium-dependent mannuronan C-5 epimerases (AlgE1-7).

147 lanthanide-dependent MDH (XoxF)-type, to the calcium-dependent MDH (MxaF)-type.

148 We noted that FUS is translocated through a calcium-dependent mechanism and that its translocation c

149 ase in cell lysis, which was suppressed by a calcium-dependent mechanism involving a homologue to syn

150 ar mitochondrial particles was mediated by a calcium-dependent mechanism involving CD38 and cyclic AD

151 tic increase in reactive oxygen species by a calcium-dependent mechanism.

152 pression of S1P3 and VEGFR2 is mediated by a calcium-dependent mechanism.

153 wed that the initial probability of release, calcium-dependent mechanisms of recovery, and desensitiz

154 h is regulated by NFIA in astrocytes through calcium-dependent mechanisms.

155 ssion and enhance aldosterone production via calcium-dependent mechanisms.

156 or otoferlin in exocytosis and modulation of calcium-dependent membrane fusion.

157 the previously demonstrated role for I368 in calcium-dependent membrane penetration.

158 ber of the evolutionary conserved eukaryotic calcium-dependent membrane-binding protein family.

159 ined that the P6 protein interacts with a C2 calcium-dependent membrane-targeting protein (designated

160 re that heterologous expression of metazoan, calcium-dependent, membrane-binding proteins of the anne

161 binds apoptotic cells via a higher-affinity calcium-dependent mode that is acidic region dependent.

162 Cell adhesion in sponges is mediated by the calcium-dependent multivalent self-interactions of sulfa

163 es can functionally replace the alternative, calcium-dependent, MxaFI-type methanol dehydrogenases, w

164 ther, we postulate the basis for a conserved calcium-dependent NAF-mediated regulation of CIPKs and a

165 splay decreased sensitivity to extracellular calcium-dependent neurotransmitter release, which leads

166 Calpains are calcium-dependent neutral cysteine proteases that modula

167 flammatory cytokine production, and promoted calcium-dependent neutrophil recruitment.

168 ering maintains lymphoid-biased HSCs through calcium-dependent NFAT signaling, providing molecular in

169 In accordance with this, calpains, which are calcium-dependent nonlysosomal cysteine proteases, were

170 Calcium-dependent nuclear export of histone deacetylase

171 leus, which cells initially counteract via a calcium-dependent nuclear softening driven by loss of H3

172 that calcium nutrient status is critical for calcium-dependent PAMP-triggered immunity in plants.

173 ne in hypertension, and propose the reported calcium-dependent parameters as indexes to predict how t

174 vate heterotrimeric G protein signaling in a calcium-dependent pathway.

175 rough activation of phosphofructokinase by a calcium-dependent pathway.

176 Beside inhibitors of calcium-dependent pathways and antimetabolites, modulato

177 to mitochondrial calcium sequestration, and calcium-dependent phagosome formation around secondarily

178 nase Ypk1, by repressing the activity of the calcium-dependent phosphatase calcineurin and promoting

179 The calcium-dependent phosphatase calcineurin is highly expr

180 e demonstrate that activating calcineurin, a calcium-dependent phosphatase, following the reactivatio

181 extracellular calcium ions and activation of calcium-dependent phosphatases that modify regulators of

182 ransitions of the three calcineurin A genes, calcium-dependent phosphatases that regulate multiple as

183 ng mTORC2-PKCzeta-mediated activation of the calcium-dependent phospholipase A2 (cPLA2).

184 in mitochondria from non-failing hearts was calcium-dependent phospholipase A2zeta (cPLA2zeta) ident

185 xposure through transmembrane protein 16F, a calcium-dependent phospholipid scramblase.

186 Annexin A8 (AnxA8), a calcium-dependent phospholipid-binding protein, and cano

187 tivation in the axonal bouton by PKC-induced calcium-dependent phosphorylation at Ser-41 (pGAP-43).

188 hat are paused in early G2 phase to activate calcium-dependent phosphorylation of ERK1/2, thereby act

189 These data demonstrate that TgMyoA undergoes calcium-dependent phosphorylation, which modulates myosi

190 Here, we evaluated aequorin, a calcium-dependent photoprotein, as a potential biolumine

191 PKC triple knock-out (TKO) mice in which all calcium-dependent PKC isoforms have been eliminated (PKC

192 cted differential actions of closely related calcium-dependent PKC isoforms.

193 h and found that PTP was unaffected when all calcium-dependent PKC isozymes were eliminated.

194 hormone-stimulated PLC activity, indicating calcium-dependent PLCs are not upregulated by alcohol.

195 nction of Ca(2+)-activated small-conductance calcium-dependent potassium (SK) channels; SK channels r

196 m channel (KATP ) inhibitor, an intermediate calcium-dependent potassium channel (KCa ) inhibitor, a

197 ic plasticity and restores small-conductance calcium-dependent potassium channel function, normalizin

198 ed, in part, by tetraethylammonium-sensitive calcium-dependent potassium channels and not by ATP-sens

199 Although this is the case for calcium-dependent potassium channels found at the cell b

200 ls found at the cell body, we show here that calcium-dependent potassium channels in dendrites of cor

201 pic cholinergic receptor with that of nearby calcium-dependent potassium channels to shunt and hyperp

202 ne such process is through the activation of calcium-dependent potassium channels, which usually act

203 bition of hair cells occurs by activation of calcium-dependent potassium channels.

204 fraction of cells, there was a component of calcium-dependent potassium current that showed frequenc

205 rough mechanisms involving small conductance calcium-dependent potassium currents (SK).

206 into pores in the target cell membrane via a calcium-dependent process and facilitate translocation o

207 stable cell-cell contacts, and is an active, calcium-dependent process.

208 m ideal candidates to regulate activity- and calcium-dependent processes in neurodevelopment.

209 high rates of auditory nerve firing, or that calcium-dependent processes involved in release are alte

210 Calcium-dependent processes that degrade the actin cytos

211 um influx they are likely to be modulated by calcium-dependent processes, such as calcium-activated p

212 with calcium influx they can be regulated by calcium-dependent processes.

213 n of AJs was the result of activation of the calcium-dependent protease calpain and degradation of th

214 Calcium dependent protein kinase 1 (CDPK1) is an essenti

215 Calcium dependent protein kinase 1 (CDPK1) is an essenti

216 n mechanisms via which it regulates invasion.Calcium dependent protein kinase 1 (CDPK1) plays an impo

217 Calcium Dependent Protein Kinases are key effectors of c

218 d the proposed consensus motif for the plant calcium-dependent protein kinase (CDPK) and Snf1-related

219 Calcium-dependent protein kinase (CDPK) family members r

220 itogen-activated protein kinase (MAPK) and 1 calcium-dependent protein kinase (CDPK) were upregulated

221 A rice (Oryza sativa) calcium-dependent protein kinase (CDPK), CPK18, was iden

222 ers reveal that mutations in two proteins, a calcium-dependent protein kinase (PfCDPK5) and a P-type

223 e cyclic AMP dependent protein kinase (PKA), calcium-dependent protein kinase (PKC), and immune regul

224 inhibitors (BKIs) of Cryptosporidium parvum calcium-dependent protein kinase 1 (CpCDPK1) are leading

225 ng a homology model of Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) was used to

226 inhibitor (compound 1) of Toxoplasma gondii calcium-dependent protein kinase 1 (TgCDPK1) that posses

227 lation via PKG (protein kinase G) and CDPK1 (calcium-dependent protein kinase 1) and by methylation v

228 to be potent inhibitors of Toxoplasma gondii calcium-dependent protein kinase 1.

229 Calcium-dependent protein kinase 3 (TgCDPK3) was previou

230 KG), and Ca(2+) , mediated by the parasite's calcium-dependent protein kinase 4 (CDPK4).

231 ived from drought-responsible genes encoding calcium-dependent protein kinase and cytokinin oxidase/d

232 plant immune responses, mainly those in the calcium-dependent protein kinase and mitogen-activated p

233 s presynaptic calcium that in turn activates calcium-dependent protein kinase C (PKC) isoforms to pho

234 they demonstrate decreased expression of the calcium-dependent protein kinase C conventional subclass

235 The calcium-dependent protein kinase C isoform, PKCalpha, ha

236 tase interaction with the defense-associated calcium-dependent protein kinase CPK1 and present indica

237 lved in PTI and characterize the Arabidopsis calcium-dependent protein kinase CPK28 as a negative reg

238 This work describes the role played by the CALCIUM-DEPENDENT PROTEIN KINASE CPK28 in balancing phyt

239 Here, we report that the Arabidopsis calcium-dependent protein kinase CPK3 is a key regulator

240 art, through a decrease in the levels of the calcium-dependent protein kinase PKC-betaI after a trans

241 ent of ABA signal transduction in stomata of calcium-dependent protein kinase quadruple mutant plants

242 The evidence presented here indicates that a calcium-dependent protein kinase, CPK32, controls polar

243 This correlates with the finding that the calcium-dependent protein kinase, PfCDPK1, is phosphoryl

244 entify in vivo phosphorylation substrates of CALCIUM-DEPENDENT PROTEIN KINASE1 (CPK1), we analyzed th

245 BUNIT 70A1 (EXO70A1), PEROXIDASE7 (PRX7) and CALCIUM-DEPENDENT PROTEIN KINASE11 (CPK11) are required

246 For Toxoplasma species, calcium-dependent protein kinases (CDPKs) are critical.

247 Calcium-dependent protein kinases (CDPKs) are distinct f

248 Calcium-dependent protein kinases (CDPKs) are expanded i

249 Calcium-dependent protein kinases (CDPKs) comprise the m

250 nase inhibitors (BKIs) specific for parasite calcium-dependent protein kinases (CDPKs) have been show

251 ection of a large gene family encoding novel calcium-dependent protein kinases (CDPKs) that provides

252 Calcium-dependent protein kinases (CPKs) and calcineurin

253 ne is a member of the complex gene family of calcium-dependent protein kinases in rice (Oryza sativa)

254 BIK1 phosphorylates different residues than calcium-dependent protein kinases, and both PAMP-induced

255 The calcium-dependent protein phosphatase, calcineurin (CaN)

256 argeting is likely to be more efficient than calcium-dependent protein targeting.

257 The calcium-dependent proteins involved in this process appe

258 cation and the possible role of the uniquely calcium-dependent reactive oxygen species (ROS)-forming

259 time window and mechanism of excitatory and calcium-dependent refinements during late postnatal deve

260 demonstrate a time window for activity- and calcium-dependent refinements limited to shortly after h

261 We propose a model of tight calcium-dependent regulation of oxidative metabolism and

262 membrane trafficking protein involved in the calcium-dependent regulation of secretory vesicle exocyt

263 d LQLP motifs were required to eliminate the calcium-dependent regulation of the channel.

264 te the induction of ATF4, and calcineurin, a calcium-dependent regulator of NFAT, synergistically sup

265 LTP was calcium dependent, required the activation of both g-pro

266 toward a gradient of metallothionein II was calcium-dependent, required the expression of both LRP1

267 rigger local translation revealed a role for calcium-dependent retrograde netrin-1/DCC receptor signa

268 73B) showed reduced inward rectification and calcium-dependent reversal potential shifts decreased by

269 8-sulfonamide were also linear and showed no calcium-dependent reversal potential shifts.

270 This lytic cycle is delicately regulated by calcium-dependent reversible phosphorylation of the mole

271 on of NFAT requires dephosphorylation by the calcium-dependent serine/threonine phosphatase calcineur

272 2)R activation, and downstream intracellular calcium-dependent signal transduction.

273 wed that CAFs regulate endothelial LPP via a calcium-dependent signaling pathway involving microfibri

274 Calcium-dependent signaling pathways initiated by store-

275 e in calcium mobilization and the subsequent calcium-dependent signaling that is essential for proper

276 ing of extracellular DNA by PRRs, leading to calcium-dependent signaling, although no receptor has be

277 to dilate these arterioles; an additional EC calcium-dependent signalling mechanism is required for v

278 modelling enzyme integrates two antagonistic calcium-dependent signalling pathways that control myoge

279 and depends in part on the downregulation of calcium-dependent SK-type K(+) channels, which contribut

280 idal neurons: transient inhibition driven by calcium-dependent small conductance potassium ('SK') cha

281 idal neurons: transient inhibition driven by calcium-dependent small conductance potassium ('SK') cha

282 mpairs oxidative phosphorylation, triggering calcium-dependent stress signalling and adaptive metabol

283 d the heart is thought to be controlled by a calcium-dependent structural change in the actin-contain

284 are shown to impair its calcium-binding and calcium-dependent structural changes, suggesting a key r

285 ty to bind Gbetagamma while retaining normal calcium-dependent Syt1 binding to soluble N-ethylmaleimi

286 ARGX-117 exhibits pH- and calcium-dependent target binding and is Fc-engineered to

287 These mutations typically alter calcium-dependent tension generation within the sarcomer

288 s mechanisms regulating MDR in HCC cells are calcium dependent through the TRPC6/calcium/STAT3 pathwa

289 ression transforms desmosome adhesion from a calcium-dependent to a calcium-independent and hyperadhe

290 It is primarily known for its calcium-dependent transamidation activity that leads to

291 l studies identify CAMTA3, a MEcPP-activated calcium-dependent transcriptional regulator, as critical

292 This, in turn, initiates calcium-dependent transgene expression.

293 tension in swollen nuclei directly promotes calcium-dependent translocation and activation of enzyme

294 ingosine kinase 1 (SphK1) activation and its calcium-dependent translocation downstream of ERK1/2.

295 of these family members, S100A6, exhibits a calcium-dependent translocation to the plasma membrane.

296 rin phosphatase, which is known to evoke the calcium-dependent TRESK activation.

297 nel subtypes and accounts for all aspects of calcium-dependent TRPA1 regulation, including potentiati

298 e-gated calcium channels have been linked to calcium-dependent vesicular gliotransmitter release.

299 Furthermore, their effects are calcium dependent, which is consistent with in vivo data

300 3 and the hydrophobic N terminus of Kv4.3 is calcium-dependent, with an equilibrium dissociation cons