ライフサイエンスコーパス: intracellular calcium concentration

1 NPE cells was used to record changes in the intracellular calcium concentration.

2 letely antagonized E2-induced attenuation of intracellular calcium concentration.

3 type switching in response to alterations in intracellular calcium concentration.

4 ed the excitotoxic glutamate-induced rise in intracellular calcium concentration.

5 ential and corresponding oscillations of the intracellular calcium concentration.

6 inase (PI3K) or MAPK signaling or increasing intracellular calcium concentration.

7 termined by the magnitude of the increase in intracellular calcium concentration.

8 calcineurin, which are both dependent on the intracellular calcium concentration.

9 ertussis toxin-sensitive pathway to increase intracellular calcium concentration.

10 se in both inositol phosphate production and intracellular calcium concentration.

11 isomer, NPS S-467, was not active in raising intracellular calcium concentration.

12 sed F-actin content, and increased the basal intracellular calcium concentration.

13 ellular calcium concentration with increased intracellular calcium concentration.

14 he transformation of membrane potential into intracellular calcium concentration.

15 -activated calcium channels and increase the intracellular calcium concentration.

16 f depolarization were mediated by increasing intracellular calcium concentration.

17 phospholipids and is regulated by changes in intracellular calcium concentration.

18 ed rises in inositol-1,4,5-trisphosphate and intracellular calcium concentration.

19 of OHCs which has been reported to depend on intracellular calcium concentration.

20 g thin filaments triggered by an increase in intracellular calcium concentration.

21 calcium retention with Delta160E may affect intracellular calcium concentration.

22 thymocyte exhibited persistent elevations in intracellular calcium concentration.

23 e, there was a 65% increase in the mean free intracellular calcium concentration.

24 nogenesis is regulated in part by an optimal intracellular calcium concentration.

25 signalling networks responsive to changes in intracellular calcium concentration.

26 ctivation of T cells, and Akt, and increased intracellular calcium concentration.

27 activate phospholipase C beta2 and increase intracellular calcium concentration.

28 , in parallel with their ability to increase intracellular calcium concentration.

29 to monitor the effect of CB(1) activation on intracellular calcium concentration.

30 gargin treatment, which results in increased intracellular calcium concentrations.

31 t CNP attenuates AVP-dependent elevations in intracellular calcium concentrations.

32 tained, but moderate, elevations of the free intracellular calcium concentrations.

33 operoxides that coincided wih an increase in intracellular calcium concentrations.

34 bitors and is not mediated by an increase in intracellular calcium concentrations.

35 that are activated in response to increased intracellular calcium concentrations.

36 C terminus on 1) UTP-stimulated increases in intracellular calcium concentration, 2) homologous desen

37 cant and concentration-dependent increase in intracellular calcium concentration, an effect that was

38 om or less in diameter caused rapid rises in intracellular calcium concentration, an effect that was

39 Similarly, SP-induced increases in intracellular calcium concentration and actomyosin stres

40 t the level of transcription by increases in intracellular calcium concentration and by the calcium-a

41 study was performed to determine the role of intracellular calcium concentration and calpain activity

42 beta occur immediately, including changes in intracellular calcium concentration and changes in membr

43 blocked spontaneous correlated increases in intracellular calcium concentration and compound postsyn

44 t that fails to bind Raf, potently increases intracellular calcium concentration and cytokine product

45 that the sigmoidal relationship between the intracellular calcium concentration and force production

46 of extracellular calcium with an increase of intracellular calcium concentration and inositol trispho

47 ted that hemichannel activity depends on the intracellular calcium concentration and is associated wi

48 the myofilament and reducing the affinity to intracellular calcium concentration and overall prolongi

49 h recombinant core and NS3 protein increased intracellular calcium concentration and reactive oxygen

50 olene and BAPTA-AM prevented the increase in intracellular calcium concentration and reduced cell rou

51 TCR engagement led to an increase in intracellular calcium concentration and the dissociation

52 iting concentrations of glucose increase the intracellular calcium concentration and the frequency of

53 the absence of GTP, the relationship between intracellular calcium concentration and the maximum rate

54 e data support the hypothesis that increased intracellular calcium concentrations and a diminished ca

55 ond to mechanical stimulation with increased intracellular calcium concentrations and increased inwar

56 by thapsigargin and ionomycin (that elevate intracellular calcium concentrations) and mutations in P

57 ed with activation of Vav-1, increase of the intracellular calcium concentration, and nuclear translo

58 yte fractional shortening without increasing intracellular calcium concentrations, and the biological

59 In most cell types, changes in intracellular calcium concentrations are sensed by calmo

60 f interest--spike trains and/or time varying intracellular calcium concentrations--are hidden.

61 ling to 0 degrees C evoked a 40% increase in intracellular calcium concentration as determined by liv

62 osphorylation of TCRzeta, ZAP70, and LAT and intracellular calcium concentration, as well as IL-2 gen

63 mechanotransduction is often an increase in intracellular calcium concentration associated with intr

64 uscle cell membrane, a transient increase of intracellular calcium concentration, binding of calcium

65 Naive thymocytes were highly motile at low intracellular calcium concentrations, but during positiv

66 filament, but inhibits contractility at high intracellular calcium concentration by disrupting the ac

67 This suggests that the increase in intracellular calcium concentration by these agents is d

68 rocess was partially reversed by raising the intracellular calcium concentration by use of the ionoph

69 fluorescent spectroscopic determinations of intracellular calcium concentrations (Ca(i)) and the rat

70 sue suggest that membrane voltage (V(m)) and intracellular calcium concentrations (Ca) become dissoci

71 POINTS: For the heart to function as a pump, intracellular calcium concentration ([Ca(2+) ]i ) must i

72 of AE that directly evaluate alterations in intracellular calcium concentration ([Ca(2+)](i)) and Ca

73 The relationship between increased intracellular calcium concentration ([Ca(2+)](i)) and ch

74 ulmonary arterial smooth muscle cell (PASMC) intracellular calcium concentration ([Ca(2+)](i)) and pH

75 c Ca(2+) confirmed the transient rise in the intracellular calcium concentration ([Ca(2+)](i)) during

76 ng this activation results in an increase in intracellular calcium concentration ([Ca(2+)](i)) follow

77 The intracellular calcium concentration ([Ca(2+)](i)) has be

78 hat in rodents, neuronal activity raised the intracellular calcium concentration ([Ca(2+)](i)) in ast

79 nvestigated the role of a Ca(2+) channel and intracellular calcium concentration ([Ca(2+)](i)) in osm

80 neuron axon we found that activity-dependent intracellular calcium concentration ([Ca(2+)](i)) in the

81 ates from cytosol to membrane in response to intracellular calcium concentration ([Ca(2+)](i)) increa

82 trocytes display excitability in the form of intracellular calcium concentration ([Ca(2+)](i)) increa

83 Intracellular calcium concentration ([Ca(2+)](i)) is a k

84 ases, which were synchronized with a rise in intracellular calcium concentration ([Ca(2+)](i)) near t

85 changes in ciliary beat frequency (CBF) and intracellular calcium concentration ([Ca(2+)](i)) of rab

86 PC6-5 cascade causes a prolonged increase in intracellular calcium concentration ([Ca(2+)](i)) that i

87 po) stimulates a significant increase in the intracellular calcium concentration ([Ca(2+)](i)) throug

88 trophysiological methods and measurements of intracellular calcium concentration ([Ca(2+)](i)) to sho

89 Intracellular calcium concentration ([Ca(2+)](i)) was ex

90 Intracellular calcium concentration ([Ca(2+)](i)) was me

91 Intracellular calcium concentration ([Ca(2+)](i)) was me

92 ellular-dependent early increase (30 min) in intracellular calcium concentration ([Ca(2+)](i)), follo

93 Small increases in the intracellular calcium concentration ([Ca(2+)](i)), incre

94 s trigger an early and transient increase of intracellular calcium concentration ([Ca(2+)](i)), requi

95 em is associated with stereotypic changes in intracellular calcium concentration ([Ca(2+)](i)), yet t

96 ive oxygen species (ROS)-evoked and pericyte intracellular calcium concentration ([Ca(2+)](i))-mediat

97 with TNF induces an abnormal increase in the intracellular calcium concentration ([Ca(2+)](i)).

98 ypes, these parameters are controlled by the intracellular calcium concentration ([Ca(2+)](i)).

99 FSS rapidly increases the intracellular calcium concentration ([Ca(2+)]) and nitri

100 tes to skeletal muscle atrophy by increasing intracellular calcium concentration ([Ca(2+)]i) and enha

101 n above 0.03 mM leads to a rapid increase in intracellular calcium concentration ([Ca(2+)]i) and inos

102 Transient elevations in intracellular calcium concentration ([Ca(2+)]i) and migr

103 Sustained increases in intracellular calcium concentration ([Ca(2+)]i) are pres

104 , a specific alpha7 nAChR agonist, increases intracellular calcium concentration ([Ca(2+)]i) mainly r

105 ated influences of transmembrane voltage and intracellular calcium concentration ([Ca(2+)]i) that gat

106 In resistance arteries, coupling a rise of intracellular calcium concentration ([Ca(2+)]i) to endot

107 ing combined with indo-1 measurement of free intracellular calcium concentration ([Ca(2+)]i) was used

108 his was followed by a sustained elevation of intracellular calcium concentration ([Ca(2+)]i) which co

109 blasts were used for microinjection and free intracellular calcium concentration ([Ca(i)]) was measur

110 This study investigated the role of intracellular calcium concentration ([Ca]i) as a possibl

111 tes, as indicated by increases in astrocytic intracellular calcium concentrations ([Ca(2)(+)](i)).

112 ating is dictated by membrane voltage (Vm ), intracellular calcium concentrations ([Ca(2+) ]i ) and e

113 tamate receptors induced a rapid increase in intracellular calcium concentrations ([Ca(2+)](i)) and a

114 analyze spontaneous dynamic fluctuations in intracellular calcium concentrations ([Ca(2+)](i)) in sm

115 es the cell membrane and blunts increases in intracellular calcium concentrations ([Ca(2+)](i)) simil

116 n neurons enabled simultaneous monitoring of intracellular calcium concentrations ([Ca(2+)]i) in mult

117 in filaments are activated by an increase in intracellular calcium concentration [Ca(2+)](i) and by m

118 TARC, MDC, and SDF-1 increased intracellular calcium concentrations [Ca(2+)](i) when co

119 lowed, within 205+/-34 seconds, by increased intracellular calcium concentration, [Ca(2+)](i).

120 High intracellular calcium concentration, [Ca]i, lowered prop

121 implicated its activity in the regulation of intracellular calcium concentration ([Ca2+](i)) and secr

122 n analog iloprost alone had no effect on the intracellular calcium concentration ([Ca2+](i)), it did

123 ngs showed that BDNF elicited an increase in intracellular calcium concentration ([Ca2+]c).

124 n of Ca2+-signaling pathways, the effects on intracellular calcium concentration ([Ca2+]i) after expo

125 current, which is induced by an increase in intracellular calcium concentration ([Ca2+]i) and is its

126 Intracellular calcium concentration ([Ca2+]i) and Na(+)-

127 showed spontaneous rhythmic oscillations in intracellular calcium concentration ([Ca2+]i) and sponta

128 Tyrosine kinases indirectly raise intracellular calcium concentration ([Ca2+]i) by activat

129 Elevation of intracellular calcium concentration ([Ca2+]i) by applica

130 was measured using micropuncture techniques, intracellular calcium concentration ([Ca2+]i) by fura-2

131 toring the effects of NGF on the increase in intracellular calcium concentration ([Ca2+]i) following

132 ed the relations between isometric force and intracellular calcium concentration ([Ca2+]i) in fibrobl

133 The relationship between tension and intracellular calcium concentration ([Ca2+]i) in intact

134 record changes in the membrane potential and intracellular calcium concentration ([Ca2+]i) in SCN neu

135 The effect of albumin on intracellular calcium concentration ([Ca2+]i) in single

136 In response to an intracellular calcium concentration ([Ca2+]i) increase,

137 Intracellular calcium concentration ([Ca2+]i) measuremen

138 The intracellular calcium concentration ([Ca2+]i) of growth

139 changes in ciliary beat frequency (CBF) and intracellular calcium concentration ([Ca2+]i) of rabbit

140 microg/ml) dramatically enhanced BCR-induced intracellular calcium concentration ([Ca2+]i) responses

141 e expressed in brain endothelium and mediate intracellular calcium concentration ([Ca2+]i) signaling,

142 sed to determine the sources for the rise in intracellular calcium concentration ([Ca2+]i) that occur

143 T lymphocytes results in a rapid increase in intracellular calcium concentration ([Ca2+]i) that paral

144 We measured intracellular calcium concentration ([Ca2+]i) transients

145 troprusside (SNP) on intracellular pH (pHi), intracellular calcium concentration ([Ca2+]i) transients

146 contractility is mediated by a reduction in intracellular calcium concentration ([Ca2+]i) via inhibi

147 activate any membrane current in cells where intracellular calcium concentration ([Ca2+]i) was buffer

148 Intracellular calcium concentration ([Ca2+]i) was determ

149 The intracellular calcium concentration ([Ca2+]i) was measur

150 After addition of lipopolysaccharide (LPS), intracellular calcium concentration ([Ca2+]i) was measur

151 The intracellular calcium concentration ([Ca2+]i) was monito

152 Intracellular calcium concentration ([Ca2+]i) was monito

153 Decay in intracellular calcium concentration ([Ca2+]i) was record

154 rane repolarisation, even though the average intracellular calcium concentration ([Ca2+]i) was still

155 ing combined with indo-l measurement of free intracellular calcium concentration ([Ca2+]i) was used t

156 (PLCgamma1) and corresponding elevations in intracellular calcium concentration ([Ca2+]i) were intac

157 ssing of bursts during up-states, changes in intracellular calcium concentration ([Ca2+]i) were measu

158 of nontransgenic recipients, and changes in intracellular calcium concentration ([Ca2+]i) were monit

159 Our results indicate that the rise in intracellular calcium concentration ([Ca2+]i) which acco

160 f ECs inhibited agonist-induced increases in intracellular calcium concentration ([Ca2+]i), in both E

161 e inhibition of oxidative phosphorylation on intracellular calcium concentration ([Ca2+]i), phosphory

162 chanical stimuli with transient increases in intracellular calcium concentration ([Ca2+]i).

163 could result from a progressive elevation of intracellular calcium concentration ([Ca2+]i).

164 Quantitation of free intracellular calcium concentrations ([Ca2+]i) after mit

165 The minimum intracellular calcium concentrations ([Ca2+]i) for trigg

166 - current (I(Cl(Ca))) evoked by adding fixed intracellular calcium concentrations ([Ca2+]i) to the pi

167 High intracellular calcium concentrations ([Ca2+]i; 10-1000 m

168 the fluorescent dye fluo-3 AM and changes in intracellular calcium concentration [Ca2+]i were analyze

169 a2+ exchanger, I(NaCa), which depends on the intracellular calcium concentration [Ca2+]i.

170 The relationship between intracellular calcium concentration, [Ca2+]i, and fixed-

171 Changes in intracellular calcium concentration, [Ca2+]i, modulate t

172 virus for cell fusion induced an increase in intracellular calcium concentration, causing premature o

173 vents in eosinophils, including increases in intracellular calcium concentration, cell surface expres

174 determine that a large biphasic increase in intracellular calcium concentration, characterized by re

175 dary to reduced ROS levels and reduced basal intracellular calcium concentration compared with mock c

176 Changes in intracellular calcium concentration (DeltaCa(i)2+) induc

177 2 gene expression was dependent on a rise in intracellular calcium concentration derived from extrace

178 e propensity to produce a global rise in the intracellular calcium concentration differed among the v

179 lasma membrane in response to DAG at a basal intracellular calcium concentration due to the inaccessi

180 shing the SR calcium store, the evolution of intracellular calcium concentration during a train of lo

181 changes in caldesmon phosphorylation and/or intracellular calcium concentrations during signal trans

182 and are instrumental in generating sustained intracellular calcium concentration elevations that are

183 ccur with essentially equal magnitude at all intracellular calcium concentrations examined (range, 0-

184 Cold preservation caused an increase in intracellular calcium concentration first detected at 1

185 s that exhibit activity-related increases in intracellular calcium concentration (FLiCRE).

186 1990s that astrocytes undergo elevations in intracellular calcium concentration following activation

187 mmature B cells display greater increases in intracellular calcium concentrations following Ag stimul

188 was reduced dose dependently by increases in intracellular calcium concentration from 0.1 to 0.5 micr

189 echanical flow stimulation by changing their intracellular calcium concentration in a manner similar

190 ke activity which leads to a greater rise in intracellular calcium concentration in aging than that i

191 the hyperpolarization-activated current and intracellular calcium concentration in both normal contr

192 fura-2 fluorescence revealed an increase of intracellular calcium concentration in cells when challe

193 Both SPC and LPC induce increases in intracellular calcium concentration in GPR4-, but not ve

194 S1P (10 microM) also stimulated increases in intracellular calcium concentration in HTM cells.

195 strated that as in eukaryotic organisms, the intracellular calcium concentration in prokaryotes is ti

196 Eosinophils showed an increased intracellular calcium concentration in response to Alter

197 Basal intracellular calcium concentration in single DCT cells

198 since it failed to stimulate an increase in intracellular calcium concentration in the CCR5 transfec

199 thick filament stress but are independent of intracellular calcium concentration in the physiological

200 phin, contributing to abnormal regulation of intracellular calcium concentrations in dystrophic muscl

201 Fluorescence imaging of intracellular calcium concentrations in live RA FLS stim

202 ted in a 0.56 micromol/L shift toward higher intracellular calcium concentrations in nonfailing myoca

203 h glutamate, NMDA, or kainate (KA) increased intracellular calcium concentrations in RA FLS, demonstr

204 ined the role of nucleus isthmi in enhancing intracellular calcium concentrations in retinotectal fib

205 integrin receptors initiates an increase in intracellular calcium concentrations in T cells, potenti

206 al slices showed increased baseline and peak intracellular calcium concentrations in the zona glomeru

207 dicators Fura-2 and Fluo-3 we show that root intracellular calcium concentrations increase in respons

208 The intracellular calcium concentration increased significan

209 SEC to cold results sequentially in elevated intracellular calcium concentration, increased calpain a

210 Subsequent to elevations in intracellular calcium concentrations induced by ionomyci

211 Activation of G2A by LPC increased intracellular calcium concentration, induced receptor in

212 The subsequent increase in intracellular calcium concentration induces proteolytic

213 lcium sensors that transduce fluctuations in intracellular calcium concentrations into changes in mem

214 n is mediated by PKA and that an increase in intracellular calcium concentration is required for maxi

215 bit aberrant T cell expansion by maintaining intracellular calcium concentration levels low enough to

216 r-alpha, changes in osmolarity, elevation in intracellular calcium concentration, lysophosphatidic ac

217 cardial mechanisms: calcitropes, which alter intracellular calcium concentrations; myotropes, which a

218 ing large, transient, localized increases in intracellular calcium concentration near the calcium-con

219 ever, hVPLA2 induced neither the increase in intracellular calcium concentration nor cPLA2 phosphoryl

220 arginine deiminase activity depends on high intracellular calcium concentrations occurring in dying

221 Furthermore, the intracellular calcium concentration of isolated neuroepi

222 chemia was insensitive to maneuvers altering intracellular calcium concentration or myofilament calci

223 n of mitochondrial complex I, an increase in intracellular calcium concentration, or formation of rea

224 SignificanceOscillations in intracellular calcium concentration play an essential ro

225 nium, quinine and dextromethorphan increased intracellular calcium concentration preferentially in is

226 channels in the plasma membrane, and if the intracellular calcium concentration reaches a threshold,

227 Intracellular calcium concentrations regulate diverse ce

228 PIP2 and, in response to local increases in intracellular calcium concentration, release it to inter

229 forms of protein kinase C (PKC) and elevate intracellular calcium concentrations, respectively.

230 nce of 0.03 mM Ca2+, NPS R-467 increased the intracellular calcium concentration response in a concen

231 nor endothelin-1, both of which elevated the intracellular calcium concentration, restored insulin-st

232 ells in reduced calcium medium, and lowering intracellular calcium concentration, results in the loss

233 In some cells, the intracellular calcium concentration rise produced by 50

234 nnel) underlies the sustained or oscillatory intracellular calcium concentration signal required for

235 DMS also inhibited the increase in intracellular calcium concentration stimulated by platel

236 ide to L929 cells caused rapid elevations in intracellular calcium concentration that were independen

237 Apoptotic stimuli augment intracellular calcium concentration through inositol 1,4

238 NMDA receptor is modulated by changes in the intracellular calcium concentration, through activation

239 lex is a molecular switch that ties shifting intracellular calcium concentration to association and d

240 alcium channels, and ultimately elevates the intracellular calcium concentration to increase the rele

241 ts that neurons monitor their activity using intracellular calcium concentrations to regulate their i

242 AChRs), and our data suggest that changes in intracellular calcium concentrations triggered by nAChR

243 Notably, the rise of intracellular calcium concentration upon immunoglobulin

244 embrane proteins is to measure the change in intracellular calcium concentration upon receptor stimul

245 ure for histamine release and for changes in intracellular calcium concentration using video imaging.

246 lular calcium release because no increase in intracellular calcium concentration was detected in resp

247 Also, the lysoPC-induced increase in intracellular calcium concentration was inhibited in ECs

248 Intracellular calcium concentration was measured by micr

249 Changes of intracellular calcium concentration were involved not on

250 These receptor-mediated increases in intracellular calcium concentration were measured by bot

251 e to 4-CMC or caffeine, similar increases in intracellular calcium concentration were observed in Sta

252 Changes in intracellular calcium concentration were quantitated by

253 Parasite intracellular calcium concentrations were altered by cha

254 was not affected but systolic and diastolic intracellular calcium concentrations were decreased and

255 In the present study, free intracellular calcium concentrations were examined in re

256 Intracellular calcium concentrations were measured in is

257 such as tyrosine protein phosphorylation and intracellular calcium concentrations, were found to be i

258 andamide acting on CB(1) receptors increases intracellular calcium concentration when administered in

259 predicts that hyperexcited states cause high intracellular calcium concentrations, which could trigge

260 ory about reading neuronal information using intracellular calcium concentrations, which includes the

261 MIP-1beta induced a significant increase in intracellular calcium concentrations, which was blocked

262 n enhanced IL-6 secretion and an increase in intracellular calcium concentrations, which were depende

263 tin filaments with latrunculin A or reducing intracellular calcium concentration with BAPTA-AM.

264 ucagon-mediated increases in cAMP levels and intracellular calcium concentrations, with EC50 values n

265 al signals are transduced through changes in intracellular calcium concentrations, yet only a few cal