ライフサイエンスコーパス: cytosolic calcium

1 osphorylation in response to oscillations in cytosolic calcium.

2 actomyosin contractility through increasing cytosolic calcium.

3 boxyl termini, as detected by changes in the cytosolic calcium.

4 ons relies on antigen-dependent increases in cytosolic calcium.

5 sm as thapsigargin (TG), involving increased cytosolic calcium.

6 in the context of HBV replication, elevates cytosolic calcium.

7 espite inducing a significant rise in global cytosolic calcium.

8 e proposed HBx function is the regulation of cytosolic calcium.

9 flow shear stress with the typical change in cytosolic calcium.

10 lead to cell depolarization and increases in cytosolic calcium.

11 (FGP phage), elicits a transient increase in cytosolic calcium.

12 een shown to exhibit circadian variations in cytosolic calcium.

13 APK by E2 is preceded by a rapid increase in cytosolic calcium.

14 ydroxy tryptamine (5-HT), and an increase in cytosolic calcium.

15 riched for genes related to the elevation of cytosolic calcium.

16 ir depends on the injury-induced increase in cytosolic calcium.

17 y to stress responses involving elevation of cytosolic calcium.

18 increases in mitochondrial-derived H2O2 and cytosolic calcium.

19 ch can be substantially rescued by restoring cytosolic calcium.

20 viours in response to transient increases in cytosolic calcium.

21 ms, it is unknown what initiates the rise of cytosolic calcium across the wound field.

22 This increase in cytosolic calcium activated by postsynaptic Gs-coupled C

23 proteolysis in HepG2 liver cells mediated by cytosolic calcium-activated neutral protease (calpains).

24 In the absence of nuclear calcium signaling, cytosolic calcium activating nuclear factor of activated

25 is is typically triggered by an elevation in cytosolic calcium activity.

26 a pertussis toxin-sensitive increase in PMN cytosolic calcium analogous to that observed with Galpha

27 olipase C pathway, leading to an increase in cytosolic calcium and activation of PKC.

28 hich together induce death through a rise in cytosolic calcium and activation of toll-like receptor-4

29 frequency spiking, irreversible increases in cytosolic calcium and cell death.

30 responsible for the slower sequestration of cytosolic calcium and consequent prolonged muscle relaxa

31 de receptor2/lipoxin A4 receptor, suppresses cytosolic calcium and decreases activation of the calciu

32 ls, such as glycolysis inhibition, increased cytosolic calcium and endoplasmic reticulum stress.

33 FLARE senses the coincidence of elevated cytosolic calcium and externally applied blue light, whi

34 ation of S-type anion currents downstream of cytosolic calcium and extracellular calcium-induced stom

35 g the notion that ERA1 functions upstream of cytosolic calcium and indicating the genetic interaction

36 tic load placed on neurons by increased free cytosolic calcium and may help explain the neuroprotecti

37 Both the VEGF165-mediated rise in cytosolic calcium and membrane depolarization are elimin

38 Cytosolic calcium and membrane potential were monitored

39 Cytosolic calcium and nitric oxide recordings further sh

40 Beyond transient elevation of cytosolic calcium and perturbation of Na+/K+ homeostasis

41 loading them with Fluo-4/Fura Red to measure cytosolic calcium and positioning them in direct contact

42 cancer cells by 2 mechanisms: attenuation of cytosolic calcium and stabilization of lysosomes.

43 and promote increased SOCE to sustain higher cytosolic calcium and stimulate HBV replication.

44 ations (0.1 microM), increases of guard cell cytosolic calcium and stomatal closure were activated to

45 tinely contribute to the regulation of basal cytosolic calcium and that their relative role correlate

46 the effects of activators and inhibitors of cytosolic calcium and tyrosine kinase signaling pathways

47 ed increases in tyrosine phosphorylation and cytosolic calcium, and are likely to contribute to TCR-p

48 urse measurements of inositol trisphosphate, cytosolic calcium, and diacylglycerol, focuses particula

49 2-induced increases in oxidative metabolism, cytosolic calcium, and ductal smooth muscle cells prolif

50 ilization (LMP), a sustained accumulation of cytosolic calcium, and eventually cell death in pancreat

51 preserved mitochondrial morphology, reduced cytosolic calcium, and prevented cell death.

52 SP rapidly increases cytosolic calcium, and so does IL-33 to a smaller extent

53 nt oscillations in the concentration of free cytosolic calcium are a vital mechanism for the control

54 nt oscillations in the concentration of free cytosolic calcium are a vital mechanism for the control

55 Changes in cytosolic calcium are crucial for numerous processes inc

56 2 family members and subsequent elevation of cytosolic calcium are important for HBV viral replicatio

57 rent evidence suggests an important role for cytosolic calcium as a second messenger.

58 m, and AAL(R) treatment resulted in elevated cytosolic calcium, Bax redistribution from cytosol to mi

59 4) and its heterodimeric partner, MRP-8, are cytosolic calcium-binding proteins, highly expressed in

60 n reports the neuronal distribution of three cytosolic calcium-binding proteins: calbindin-D28k (CB),

61 Studies indicate that an increase in cytosolic calcium boosts the generation of H(2)O(2).

62 y response, driven most significantly by the cytosolic calcium buffering system and changes in diasto

63 y the activation of the cAMP-sensor Epac1 or cytosolic calcium but are unaffected by protein kinase C

64 This study investigates the regulation of cytosolic calcium by corticotropin-releasing factor (CRF

65 annel activity by sensitizing the channel to cytosolic calcium (Ca(2)+).

66 ) and disrupt membrane integrity, leading to cytosolic calcium (Ca(2+)) elevation.

67 ng concentrations found in patients, induced cytosolic calcium (Ca(2+)) oscillations in a human neuro

68 ,4,5)-trisphosphate receptors (InsP(3)R1) by cytosolic calcium (Ca(2+)) plays an essential role in th

69 r stimulation evokes increases in astrocytic cytosolic calcium (Ca(2+)) within the barrel cortex of a

70 Furthermore, tip cytosolic calcium ([Ca(2)(+)](cyt) ) oscillations were d

71 cerk1 plants had an irregular increase of cytosolic calcium ([Ca(2+) ]cyt ) after NaCl treatment.

72 athways including phosphoinositide-dependent cytosolic calcium ([Ca(2+) ]i ) increases, which can adv

73 f the pathophysiology of KATPHI, we examined cytosolic calcium ([Ca(2+)] i ), insulin secretion, oxyg

74 With the increase of caffeine dose (0-50 mM) cytosolic calcium ([Ca(2+)](c)) increased from 85+/-15 n

75 ecystokinin (CCK) results in an elevation of cytosolic calcium ([Ca(2+)](c)) through activation of in

76 uced elevations in the concentration of free cytosolic calcium ([Ca(2+)](cyt)) and stomatal closure i

77 as well as the hypoxia-induced increases in cytosolic calcium ([Ca(2+)](i)), assessed by the Ca(2+)-

78 AM was used to measure the concentrations of cytosolic calcium ([Ca(2+)]c).

79 ncer-like phenotype is promoted by increased cytosolic calcium ([Ca(2+)]cyto), aerobic glycolysis, an

80 ndria act as significant, dynamic buffers of cytosolic calcium ([Ca(2+)]i) in heart.

81 zation, voltage gated K(+) channel activity, cytosolic calcium [Ca(2+) ](cyt) and reactive oxygen spe

82 itochondrial axonal transport in response to cytosolic calcium (Ca2+) levels ([Ca2+]c) and mitochondr

83 In vitro changes in cytosolic calcium ([Ca2+]c) and chemosensory discharge w

84 tical during fertilization and triggers free cytosolic calcium ([Ca2+]cyto) as a key signal for egg a

85 erlying such insensitivity to transitions in cytosolic calcium ([Ca2+]i) in microvascular endothelial

86 Cytosolic calcium ([Ca2+]i) responses to MIP-2/PAF were

87 Acute transitions in cytosolic calcium ([Ca2+]i) through store-operated calci

88 er calcium increases, we measured changes in cytosolic calcium ([Ca2+]i) using fura 2-AM (fluorescenc

89 Because basal cytosolic calcium ([Ca2+]i), a second messenger, may be

90 zation, voltage gated K(+) channel activity, cytosolic calcium [Ca2+]cyt and reactive oxygen species

91 gonist anti-Tim-1 mAb elicits a rise in free cytosolic calcium, calcineurin-dependent nuclear translo

92 asmic reticulum stress in a manner requiring cytosolic calcium, calcium/calmodulin-dependent protein

93 The increase in cytosolic calcium caused by activation of Gq-coupled AT1

94 AMPK was induced by elevated cytosolic calcium caused by impaired sarco/endoplasmic r

95 Interestingly, the cytosolic calcium chelator BAPTA-AM and K-201 protected

96 the effect of 4-aminopyridine (4-AP) on free cytosolic calcium concentration ([Ca(2+)](i)) in basal c

97 The consequent lowering of the cytosolic calcium concentration ([Ca(2+)](i)), if protra

98 hat generated high-amplitude fluctuations in cytosolic calcium concentration ([Ca(2+)](i)).

99 Oscillations in cytosolic calcium concentration ([Ca2+]cyt) are central

100 reveals that: calcium signals in the form of cytosolic calcium concentration elevations are nonlinear

101 lin-1 produces a dose-dependent elevation in cytosolic calcium concentration in ET(B)-transfected cel

102 Here we show that a chronic increase of the cytosolic calcium concentration in hepatocytes during ob

103 exin II, V, or VI inhibited the increases in cytosolic calcium concentration in RA-treated chondrocyt

104 Robust elevation of the cytosolic calcium concentration is a crucial early step

105 A dramatic rise in free cytosolic calcium concentration is thought to be a centr

106 The resulting increased cytosolic calcium concentration leads to a further up-re

107 Glucagon increased cytosolic calcium concentration through the PKA-mediated

108 h RA and EDTA revealed that increases in the cytosolic calcium concentration were due to influx of ex

109 the mitochondria and an increase in the free cytosolic calcium concentration were observed.

110 nucleus correlate with transient changes in cytosolic calcium concentration within these progenitor

111 s not appear to be in response to changes in cytosolic calcium concentration, [Ca(2+)](i).

112 ineralization of these cultures: increase in cytosolic calcium concentration, followed by up-regulati

113 ve detrimental consequences for the numerous cytosolic calcium concentration-dependent pathways.

114 ctin polymers in response to fluctuations in cytosolic calcium concentration.

115 calcium storage, and it regulates the local cytosolic calcium concentration.

116 itochondrial membrane potential and elevated cytosolic calcium concentration.

117 hways and displaying an acute effect on free cytosolic calcium concentration.

118 oforms respond to the signal of an increased cytosolic calcium concentration.

119 Measurement of cytosolic calcium concentrations ([Ca(2+)](i)) in tubule

120 healis cells were loaded with fura 2-AM, and cytosolic calcium concentrations ([Ca2+]i) were measured

121 The calculated cytosolic calcium concentrations are 368 +/- 68 nM and 6

122 Cytosolic calcium concentrations were assessed under the

123 n transmembrane potential and an increase in cytosolic calcium concentrations, are inhibited by low l

124 ondrial biogenesis in response to increasing cytosolic calcium concentrations.

125 vated currents, or NMDA-induced increases in cytosolic calcium concentrations.

126 ased calcium permeability and elevated basal cytosolic calcium concentrations.

127 membrane inward K+ conductance (IK,in) in a cytosolic calcium-dependent manner.

128 ontribute equally to circadian variations in cytosolic calcium, different promoters eliciting differe

129 ion of inositol trisphosphate production and cytosolic calcium distribution, substrates for many acut

130 ry complex is not disrupted by elevations of cytosolic calcium during cardiac contraction (systole).

131 RCA2a), the pump responsible for reuptake of cytosolic calcium during diastole, plays a central role

132 Using the kinetic model for cytosolic calcium dynamics in RAW 264.7 cells developed

133 ent HBx binding to Bcl-2 and Bcl-xL abrogate cytosolic calcium elevation and cell death induced by HB

134 sponsive genes and diminished chitin-induced cytosolic calcium elevation as well as enhanced suscepti

135 treatment resulted in a marked and sustained cytosolic calcium elevation during the C5a-induced respo

136 oteins through its BH3-like motif to promote cytosolic calcium elevation, cell death, and viral repli

137 ential canonical (TRPCs) channels to control cytosolic calcium equilibria and consequent cell behavio

138 ysregulated integrin alphaIIbbeta3-dependent cytosolic calcium flux and phosphatidylinositol(3,4)P2 a

139 Total cytosolic calcium flux during the transient was inferred

140 atory reserve, independent of alterations in cytosolic calcium flux.

141 this activation may occur in the absence of cytosolic calcium fluxes.

142 of VEGF165 to cells elicits a rapid rise in cytosolic calcium followed by a slower decline toward co

143 kely in response to an observed elevation in cytosolic calcium following diazoxide treatment.

144 le effect on OCR despite a large increase in cytosolic calcium, further supporting the notion that in

145 asmic reticulum calcium pumps, but buffering cytosolic calcium had no effect.

146 Raising cytosolic calcium has been shown to activate calcium/cal

147 rice and barley aleurone because changes in cytosolic calcium have been implicated in the response o

148 As a pharmacological approach to restore cytosolic calcium homeostasis in vivo, we administered t

149 d with Fluo-4/AM revealed that ATP mobilized cytosolic calcium in astrocytic end feet, whereas electr

150 d PAR1-AP (10 microM) induced an increase in cytosolic calcium in both anterior and equatorial lens c

151 n (from -51+/-2 to -44+/-1 mV) and increased cytosolic calcium in both rat and human PASMCs.

152 Enhanced cytosolic calcium in CBE-N2a cells was blocked by either

153 By imaging patterns of free cytosolic calcium in Drosophila embryos, we found that s

154 te store-operated calcium entry and increase cytosolic calcium in endothelium.

155 ABA triggers an increase in cytosolic calcium in guard cells ([Ca2+]cyt) that has be

156 Second, NAADP increased cytosolic calcium in isolated cells when microinjected a

157 d induce a pertussis toxin-sensitive rise in cytosolic calcium in monocytes as well as in neutrophils

158 Previous studies have shown that raising cytosolic calcium in myotubes induces increases in perox

159 DREADD activation increased cytosolic calcium in primary astrocytes, facilitated res

160 on exists between intracellular H(2)O(2) and cytosolic calcium in response to biotic and abiotic stre

161 This finding suggests that the increases in cytosolic calcium in skeletal muscle during exercise may

162 Measurements of cytosolic calcium in spontaneously beating cells showed

163 orting the positioning of era1-2 upstream of cytosolic calcium in the guard cell ABA signaling cascad

164 neuropeptide FF, evoked a rapid increase in cytosolic calcium in the MrgC11 expressing cells but not

165 a substance(s) that stimulated increases in cytosolic calcium in the MrgC11 expressing cells that fa

166 e, enabling determination of the dynamics of cytosolic calcium in the perfused mouse heart.

167 P3-mediated calcium release and elevation of cytosolic calcium in WEHI7.2 T cells.

168 The increased cytosolic calcium, in turn, led to the phosphorylation o

169 re a higher level of shear stress to evoke a cytosolic calcium increase than do mouse renal epithelia

170 Cytosolic calcium increased with incubation time in both

171 type in wild-type plants both in ABA-induced cytosolic calcium increases and in seed germination, and

172 Interestingly, ABA-hypersensitive cytosolic calcium increases in abh1 guard cells demonstr

173 n of seed germination, stomatal closing, and cytosolic calcium increases in guard cells.

174 es show a reduced sensitivity of ABA-induced cytosolic calcium increases in rcn1, whereas mechanisms

175 rinergic membrane responses are triggered by cytosolic calcium increases or G protein activation.

176 es in rcn1, whereas mechanisms downstream of cytosolic calcium increases show wild-type responses, su

177 ithin the mitochondrial matrix regulates the cytosolic calcium increases that drive GSIS remains a my

178 Cytosolic calcium increases were analyzed in guard cells

179 ceptor-dependent manner, Rac1 activation and cytosolic calcium increases.

180 Evidence that group VIA cytosolic calcium-independent phospholipase A(2) (iPLA(2

181 o discriminate between the varying levels of cytosolic calcium induced by different stimuli.

182 Cytosolic calcium influx activates signaling pathways kn

183 inhibition of cAMP synthesis, stimulation of cytosolic calcium influx, and chemotaxis.

184 denylate cyclase and MCP-1- and MCP-3-driven cytosolic calcium influx; the compounds are not agonists

185 hat agonist-stimulated increases in platelet cytosolic calcium initiate actin filament turnover.

186 lopment and plasticity in which increases in cytosolic calcium ion concentration ([Ca(2+)](cyto) coup

187 arious signaling pathways rely on changes in cytosolic calcium ion concentration ([Ca2+]i).

188 A surge in cytosolic calcium ion concentration by entry of extracel

189 e receptor 5 (mGluR5)-dependent increases in cytosolic calcium ions (Ca(2+)) in response to glutamate

190 These data suggest that elevated cytosolic calcium is a common critical process for all r

191 fission is disabled, AC-induced increase in cytosolic calcium is blunted owing to mitochondrial calc

192 Cytosolic calcium is involved in the regulation of many

193 the notion that influx of calcium, not bulk cytosolic calcium, is associated with the increase in AT

194 manifested as intercellular waves of rising cytosolic calcium, is, in many cell types, the result of

195 in a signaling pathway by which increases in cytosolic calcium lead to increases in peroxisome prolif

196 evis egg extract, we found that increases in cytosolic calcium lead to the activation of an endogenou

197 ontaneous calcium elevations as a measure of cytosolic calcium leak.

198 However, an increase in cytosolic calcium led to exocytosis of only the lysosome

199 unted in Ussing chambers for measurements of cytosolic calcium levels ([Ca(2+)](i)), membrane voltage

200 ular signaling pathway resulting in elevated cytosolic calcium levels ([Ca(2+)](i)).

201 GTPase-1 (Miro1) which acts as a sensor for cytosolic calcium levels ([Ca(2+)]c); elevated [Ca(2+)]c

202 It is now evident that elevation of cytosolic calcium levels ([Ca2+]i) can compromise the BB

203 inc finger 1 (IKZF1), resulting in increased cytosolic calcium levels and activation of a calcium-dep

204 ) inhibited isoflurane-induced elevations in cytosolic calcium levels and attenuated isoflurane-induc

205 TG neurons showed decreased basal cytosolic calcium levels and decreased Ca(2+) cytosolic

206 hibit impaired rate-dependent enhancement of cytosolic calcium levels and fractional shortening.

207 Resveratrol increased cytosolic calcium levels and promoted AMPK activation by

208 required for the Wnt-5a-mediated increase in cytosolic calcium levels and spinogenesis.

209 atment of cells with compounds that increase cytosolic calcium levels by a variety of mechanisms resc

210 brane calcium-ATPase (PMCA) helps to control cytosolic calcium levels by pumping out excess Ca2+.

211 Real time measurements of cytosolic calcium levels during heating in Arabidopsis d

212 umin, suggesting that transient increases in cytosolic calcium levels function to mobilize intracellu

213 o induce EMT produce a transient increase in cytosolic calcium levels in human breast cancer cells.

214 Expression of wolframin also increased cytosolic calcium levels in oocytes.

215 ular calcium, in a manner that followed peak cytosolic calcium levels in the aggregate.

216 anisms in taste cells that functions to keep cytosolic calcium levels in the appropriate range for ce

217 -adaptor that translates a transient rise in cytosolic calcium levels into more persistent SEC31 ubiq

218 ectly suppresses the electrical activity and cytosolic calcium levels of orexin cells.

219 Studies in many organisms have shown that cytosolic calcium levels rise within a field of cells ar

220 discharge (AD) causes prolonged elevation in cytosolic calcium levels that is associated with prolong

221 s are more toxic to neurons due to increased cytosolic calcium levels throughout their action on NMDA

222 ly41 to the early secretory pathway elevates cytosolic calcium levels to suppress vesicle-tethering m

223 hich may contribute to observed increases in cytosolic calcium levels under conditions of oxidative s

224 and when stimulated by amino acids, whereas cytosolic calcium levels were not affected.

225 of RVB and RVC NSP4s significantly elevated cytosolic calcium levels, demonstrating that despite str

226 reticulum (ER) stores as manifested by lower cytosolic calcium levels, higher expression of the ER pr

227 se activation and apoptosis are dependent on cytosolic calcium levels, should facilitate the provisio

228 ich include periodic, transient increases in cytosolic calcium levels, termed calcium spiking.

229 Sly41 overexpression significantly increases cytosolic calcium levels.

230 EA also caused a sustained increase in cytosolic calcium levels.

231 IM-3/Gal-9 signaling involving modulation of cytosolic calcium levels.

232 rotransmitters, and decreased the total free cytosolic calcium load.

233 de within T lymphocytes, including a rise in cytosolic calcium, lymphokine production, and cell divis

234 also triggered integrin-dependent changes in cytosolic calcium, measured by single cell imaging.

235 Triple combined recordings of cytosolic calcium, mitochondrial calcium and NADH reveal

236 ations to FAEEs induced a larger increase in cytosolic calcium, mitochondrial depolarization, and nec

237 n species through a mechanism dependent upon cytosolic-calcium mobilization and a significant decline

238 eukemia cells (U937) manifested by immediate cytosolic-calcium mobilization, GADD153 and GADD34 prote

239 teoblasts failed to elicit the increments in cytosolic calcium observed in wild-type controls.

240 rimarily probe cell-based variables, such as cytosolic calcium or membrane potential, but not cell-to

241 support without arrhythmogenic increases in cytosolic calcium or side effects of more traditional ag

242 The role of cytosolic calcium oscillation has long been recognized i

243 Cytosolic calcium oscillations control signaling in anim

244 ng studies revealed that PHE caused dramatic cytosolic calcium oscillations in NST neurones.

245 During the transient cytosolic calcium oscillations induced by intermediate d

246 stress, cold, and external calcium elicited cytosolic calcium oscillations of differing amplitudes a

247 These oscillations may be in phase with cytosolic calcium oscillations or out of phase.

248 also corrected by vesnarinone; however, the cytosolic calcium overload characteristic of LPS hearts

249 especially those related to the elevation of cytosolic calcium (P = 2 x 10-4).

250 arathyroid and other cell types, and include cytosolic calcium, phospholipases C, A2, and D, protein

251 o chilling cause blood platelets to increase cytosolic calcium, polymerize actin, and change shape.

252 The elevation in cytosolic calcium potentiated calcium-sensitive potassiu

253 ntracellular signaling via second messengers-cytosolic calcium, reactive oxygen species, and nitric o

254 as been variously attributed to increases in cytosolic calcium, reactive oxygen species, and phosphor

255 ocytes, suggesting a diminished capacity for cytosolic calcium removal not associated with a change i

256 Furthermore, the IgE-mediated cytosolic calcium response ([Ca(++)](i)) was also dimini

257 ange while the EC50s for phospho-Erk and the cytosolic calcium response did shift 100-fold.

258 L-3 induced little change in the C5a-induced cytosolic calcium response, while 24 h of treatment resu

259 ing results from a qualitative change in the cytosolic calcium response.

260 ility of IL-3 to alter secretagogue-mediated cytosolic calcium responses following 18-h cultures, 18-

261 In the present study raising cytosolic calcium resulted in increases in phosphorylati

262 stress-induced apoptosis, we have shown that cytosolic calcium resulting from ER stress induces expre

263 yocytes had delayed sarcomere relaxation and cytosolic calcium reuptake kinetics, indicating diastoli

264 Measurement of cytosolic calcium showed normal basal levels and abnorma

265 Experimental increases of cytosolic calcium showed that the activation of S-type a

266 This results in inhibition of cytosolic calcium signaling and down-regulation of HGF-i

267 nked HBx regulation of cell proliferation to cytosolic calcium signaling and HBx stimulation of HBV r

268 cyclosporine H, and SDZ NIM811, which block cytosolic calcium signaling and specifically the mitocho

269 nt, amplitude of field action potential, and cytosolic calcium signaling of cardiomyocytes.

270 Parotid acinar cells exhibit rapid cytosolic calcium signals ([Ca2+]i) that initiate in the

271 l cells (ECs), we discovered that repetitive cytosolic calcium signals (oscillations) chronically loa

272 otential, sequestration of hormonally evoked cytosolic calcium signals and timing of permeability tra

273 Exactly how HBx elevates cytosolic calcium signals is not clear.

274 Cytosolic calcium signals were studied using Fura Red or

275 lcium (CRAC) channel and generates sustained cytosolic calcium signals when triggered by depletion of

276 One fundamental HBx function is elevation of cytosolic calcium signals; this HBx activity has been li

277 or, we show that XA triggers a rapid rise in cytosolic calcium specifically in gametocytes that is es

278 te (ADP) receptor, or regulate platelet free cytosolic calcium, such as direct nitric oxide donors, m

279 channel activation, leading to increases in cytosolic calcium that activate the AMPK upstream kinase

280 nly, sigma antagonists evoke a rapid rise in cytosolic calcium that is inhibited by sigma-1 agonists.

281 ericycle displayed prolonged oscillations in cytosolic calcium that were distinct from the responses

282 K(ATP) conductance is increased by rises in cytosolic calcium through indirect effects on metabolism

283 with a concentration of caffeine that raises cytosolic calcium to a concentration too low to cause co

284 We linked this elevation of cytosolic calcium to the association of HBx with the mit

285 raction, action potential (AP) morphology or cytosolic calcium transient (CaT) amplitude--is a high r

286 nd attenuates the metabolic coupling between cytosolic calcium transients and activation of matrix de

287 ology by stimulating ATP production, shaping cytosolic calcium transients and regulating cell death.

288 Optical mapping of cytosolic calcium transients in intact mammalian hearts

289 This led to abnormally high cytosolic calcium transients in presynaptic terminals an

290 RII constructs showed significant effects on cytosolic calcium transients.

291 nction plays an essential role in activating cytosolic calcium transitions through the membrane I(SOC

292 Since elevation of cytosolic calcium triggered by avirulent P. syringae was

293 opment of individual signals: an increase in cytosolic calcium was accompanied by a slower mitochondr

294 Total cytosolic calcium was calculated from the latter part of

295 Recovery of cytosolic calcium was faster than recovery of mitochondr

296 play a major role in the rapid buffering of cytosolic calcium, we hypothesized that altered mitochon

297 GluR1alpha maintains its ability to increase cytosolic calcium while it no longer activates the neuro

298 In addition, chelating cytosolic calcium with 1,2-bis(2-aminophenoxy)ethane-N,N

299 Increasing cytosolic calcium with adrenergic stimulation, calcium i

300 or therapeutic intervention, as elevation of cytosolic calcium with curcumin normalized NPC1 disease