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

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

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

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

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

5 he transformation of membrane potential into intracellular calcium concentration.

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

7 ential and corresponding oscillations of the intracellular calcium concentration.

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

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

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

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

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

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

14 ellular calcium concentration with increased intracellular calcium concentration.

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

16 thymocyte exhibited persistent elevations in intracellular calcium concentration.

17 f depolarization were mediated by increasing intracellular calcium concentration.

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

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

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

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

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

23 signalling networks responsive to changes in intracellular calcium concentration.

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

25 activate phospholipase C beta2 and increase intracellular calcium concentration.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 2 gene expression was dependent on a rise in intracellular calcium concentration derived from extrace

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

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

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

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

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

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

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

173 1990s that astrocytes undergo elevations in intracellular calcium concentration following activation

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

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

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

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

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

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

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

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

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

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

184 Basal intracellular calcium concentration in single DCT cells

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

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

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

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

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

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

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

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

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

194 The intracellular calcium concentration increased significan

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

196 Subsequent to elevations in intracellular calcium concentrations induced by ionomyci

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

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

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

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

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

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

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

204 Furthermore, the intracellular calcium concentration of isolated neuroepi

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

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

207 Intracellular calcium concentrations regulate diverse ce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

226 Intracellular calcium concentration was measured by micr

227 Changes of intracellular calcium concentration were involved not on

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

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

230 Changes in intracellular calcium concentration were quantitated by

231 Parasite intracellular calcium concentrations were altered by cha

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

233 Intracellular calcium concentrations were measured in is

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

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

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

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

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

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

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

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

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