ライフサイエンスコーパス: basal condition

1 tions with different diffusion properties in basal condition.

2 normal cardiac structure/function under the basal condition.

3 regulated and maintained at low level under basal condition.

4 ic reticulum prevents their activation under basal conditions.

5 related to the control of motor activity in basal conditions.

6 eNOS-derived nitrogen oxides from RBCs under basal conditions.

7 binds to the Nur77 promoter in neurons under basal conditions.

8 present in the nucleus of CD4 T cells under basal conditions.

9 no messenger RNA or protein detectable under basal conditions.

10 eficiency does not impact GSIS in mice under basal conditions.

11 ity of immunolabel within the PSD core under basal conditions.

12 eased luciferase expression when compared to basal conditions.

13 bitor alone had any substantial effect under basal conditions.

14 transport mechanisms are not saturated under basal conditions.

15 response to infection-like conditions versus basal conditions.

16 that NHE3 is phosphorylated by CaMKII under basal conditions.

17 mildly affected anxiety-like behaviors under basal conditions.

18 that captures PD pathogenic processes under basal conditions.

19 e not in close proximity to each other under basal conditions.

20 sed, ARE activity was found to be high under basal conditions.

21 equired to preserve normal [Ca(2+)](m) under basal conditions.

22 ors are saturated by endogenous ligand under basal conditions.

23 ing and sharp increase in urine output under basal conditions.

24 e, we estimate the size of these pools under basal conditions.

25 and cell lines show elevated autophagy under basal conditions.

26 n the suppression of insulin secretion under basal conditions.

27 ostasis and trafficking to the synapse under basal conditions.

28 eading to suppressed glutamate release under basal conditions.

29 e most abundantly expressed Nox in PVN under basal conditions.

30 increased steady-state levels of CXCR4 under basal conditions.

31 ntal for beta-cell growth and function under basal conditions.

32 cytosis in both the dendrite and spine under basal conditions.

33 small intestine during development and under basal conditions.

34 elatively high levels of phospho-eEF-2 under basal conditions.

35 epithelial apoptosis in sepsis but not under basal conditions.

36 eptor clustering and synaptic strength under basal conditions.

37 cription factor B, in adult myocardium under basal conditions.

38 express 4 x 10(5) [(3)H]AS sites/cell under basal conditions.

39 gy leads to up-regulation of CMA, even under basal conditions.

40 viously been shown to repress activity under basal conditions.

41 and increased Syntaxin 4 accessibility under basal conditions.

42 y (DOPAC/DA ratio) of these DA neurons under basal conditions.

43 ancreas but not the liver when induced under basal conditions.

44 serves to prevent synaptic depression under basal conditions.

45 ietal cortical tissue of diabetic rats under basal conditions.

46 inding to both domains is constitutive under basal conditions.

47 nce disease activity in epilepsy, also under basal conditions.

48 ls, including dopamine and acetylcholine, at basal conditions.

49 reting, shallow-deforming, bed and invariant basal conditions.

50 ase and IkappaB were phosphorylated, even in basal conditions.

51 s the dissociation of AMPARs from GRIP under basal conditions.

52 evels greatly influence ISG expression under basal conditions.

53 S, promoted hyperubiquitination of CLR under basal conditions.

54 GU within and between healthy subjects under basal conditions.

55 stinguishable from wild-type (WT) mice under basal conditions.

56 the ability of CGI-58 to activate ATGL under basal conditions.

57 tic reserve, functioning near capacity under basal conditions.

58 e tuning AMPA receptor synaptic levels under basal conditions.

59 l compared with TbetaRII(endo+/+) mice under basal conditions.

60 f proapoptotic factors, such as B-Myb, under basal conditions.

61 -atrophy signaling axis toward atrophy under basal conditions.

62 ad normal organ function and histology under basal conditions.

63 dividuals with allergy expressed VLDLR under basal conditions.

64 of syntaxin4 held in an inactive state under basal conditions.

65 eration of beta-cells under altered, but not basal, conditions.

66 ve tissues under insulin-stimulated, but not basal, conditions.

67 ctly binds NHE3 at the plasma membrane under basal conditions; 2) NHERF3 reconstitutes [Ca(2+)](i) in

68 ependent biliary cholesterol secretion under basal conditions; (2) biliary cholesterol mass secretion

69 Under basal conditions, ABC-me(+/-) mice had normal heart stru

70 We find that, under basal conditions, about half of release sites have a ver

71 These results indicate that, under basal conditions, adrenal signaling is tonically inhibit

72 Under basal conditions, adult human OLs were less metabolicall

73 Mice were analyzed under basal conditions, after phenylhydrazine-induced hemolysi

74 Previous in vitro studies suggested that in basal conditions all p53 molecules are bound in dimers.

75 pears to use a conformation mechanism: Under basal conditions, an intramolecular interaction of the p

76 Fibrocytes were counted at basal condition and after culture with broncho-alveolar

77 T cell metabolic status was evaluated in the basal condition and after T cell stimulation.

78 tone and cardiac contractility), both under basal conditions and after adrenergic activation, are re

79 t ventricular cardiomyocytes in vitro, under basal conditions and after glucose deprivation.

80 he speed of contraction and relaxation under basal conditions and after Iso stimulation.

81 ith fractalkine and responses measured under basal conditions and after isoproterenol (Iso) stimulati

82 earts into myofibroblasts was examined under basal conditions and after stimulation with interferon-g

83 an increase in Ca(2+) spark frequency under basal conditions and after the addition of endothelin-1

84 the transcription of the trkA promoter under basal conditions and also enhance nerve growth factor (N

85 BI-1 to influence calcium homeostasis under basal conditions and also following challenge with thaps

86 -) mice, Tmem178(-/-) mice are osteopenic in basal conditions and are more susceptible to inflammator

87 hesis that phosphoinositides bind NHE3 under basal conditions and are necessary for its acute regulat

88 uced AMPAR accumulation at synapses, in both basal conditions and conditions that can induce synaptic

89 phenylalanine kinetics were determined under basal conditions and during 4 postprandial hours by intr

90 ubjects matched for age, sex, and BMI during basal conditions and during a hyperglycemic (approximate

91 adiponectin, and NEFA concentrations, under basal conditions and during a hyperinsulinemic-euglycemi

92 le of endogenous cardiac myocyte P2X4R under basal conditions and during HF induced by myocardial inf

93 we examined the role of beta-cell PKD1 under basal conditions and during high-fat feeding.

94 d RanGAP1 in dorsal root ganglia (DRG) under basal conditions and during inflammatory hyperalgesia.

95 ittle or no inhibitory A(1) receptor tone in basal conditions and during trains of stimuli.

96 dysfunction in the MHC-PPARalpha mice under basal conditions and following administration of high-fa

97 kine secretion, and protein expression under basal conditions and following bacterial infection.

98 ole in calcium signalling in the heart under basal conditions and following beta-adrenergic stress.

99 ediated by reduced RhoA activity, both under basal conditions and following HGF treatment.

100 on of sodium and creatinine were measured in basal conditions and following twice-daily subcutaneous

101 obtained with a conductance catheter during basal conditions and handgrip exercise.

102 ted increased stress-related behaviors under basal conditions and impaired retention of spatial memor

103 he alpha(1a)AR is a lipid raft protein under basal conditions and implies agonist-mediated signaling

104 on of superoxide anion by brain tissue under basal conditions and in response to angiotensin II in th

105 All together, under basal conditions and in response to drug stimulation, th

106 piration in intact mouse cortical neurons in basal conditions and in response to increased workload c

107 in (mTOR) signaling, was abnormal both under basal conditions and in response to mGlu1/5 agonist (RS)

108 We show here that under basal conditions and in response to secretin and hypoton

109 C1 increased both LC3II and p62 levels under basal conditions and in response to serum starvation, su

110 rats than in unstressed controls, both under basal conditions and in response to single or repeated i

111 ned beta cell replication in aged mice under basal conditions and in response to specific stimuli inc

112 r myocytes regulate the IKs amplitudes under basal conditions and in response to stress.

113 of MRTF-A null fibroblasts is impaired under basal conditions and in response to TGF-beta1 stimulatio

114 p21(WAF1/CIP1) (p21) promoter activity under basal conditions and in response to various forms of str

115 sistent with this data, we found that, under basal conditions and in response to WNT3A stimulation, N

116 e gingiva and the periodontal ligament under basal conditions and in the presence of an inflammatory

117 tion was suppressed in HeLa cells both under basal conditions and in the presence of Haber-Weiss chem

118 y, SMRT is bound to the c-Fos promoter under basal conditions and is removed upon TCR stimulation.

119 ntified PVCs and parenchymal microglia under basal conditions and is robustly expressed in these and

120 ls exposed to TGF-beta compared with resting basal conditions and markedly reduced in classically act

121 lower kinase-mediated phosphorylation under basal conditions and no copper-dependent phosphorylation

122 These differences were apparent under basal conditions and persisted even following prolonged

123 rythrocyte numbers in multiple species under basal conditions and reduced or prevented anemia in muri

124 NHE3 is phosphorylated under basal conditions and Ser/Thr phosphatase inhibitors stim

125 nt mice are metabolically unremarkable under basal conditions and show normal adaptive thermogenesis,

126 ate that NE is released in the rat LHb under basal conditions and that it activates DA-D4 receptors.

127 that transepithelial conductance (Gt) under basal conditions and the cAMP-stimulated increase in Gt

128 e the level of microglial surveillance under basal conditions and the rate of dynamic behavior in res

129 es and proinflammatory cytokines, both under basal conditions and upon infection.

130 reveal the impact of recycling processes in basal conditions and upon synaptic potentiation or depre

131 equired for dendritic development both under basal conditions and upon the induction of mTOR-dependen

132 in systemic or pulmonary hemodynamics under basal conditions and, notably, did not affect isolated r

133 Zonda displays an even distribution under basal conditions and, soon after starvation, nucleates i

134 n of several pathogen-responsive genes under basal conditions and, surprisingly, enhanced worm surviv

135 ower tidal volume compared to controls under basal conditions and, unlike control mice, an inability

136 ion of Bcl-w and downregulation of Bim under basal conditions, and (2) ER-dependent inhibition of Abe

137 luA2/3s are in a low-conductance state under basal conditions, and although present at synapses they

138 itate cell surface expression of EAAC1 under basal conditions, and control internalization of EAAC1 u

139 g9 traffics between the TGN and endosomes in basal conditions, and newly formed autophagosomes in res

140 that PEDF receptors form homooligomers under basal conditions, and PEDF dissociates the homooligomer

141 a regulated intracellular compartment under basal conditions, and that aldosterone/SGK1-dependent AS

142 the principal sites of palmitoylation under basal conditions, and we demonstrate the importance of t

143 rom diabetics compared to nondiabetics under basal conditions, angiotensin II increased superoxide pr

144 Under basal conditions, ARPP-16 is phosphorylated by MAST3 to

145 In vivo, NHE3 and NHERF3 associate under basal conditions as indicated by co-immunoprecipitation,

146 pled to Orai3 and Orai3/Orai1 channels under basal conditions as shown using Forster resonance energy

147 c mechanisms of constitutive autophagy under basal conditions, as well as in response to stress induc

148 copper stores in living cells and mice under basal conditions, as well as in situations of copper ove

149 e (T(b)) and thermoeffector activities under basal conditions, as well as thermoregulatory responses

150 Under basal conditions at both synapses, GluR1-containing AMPA

151 ariability of neurotransmitter release under basal conditions at small central synapses is accounted

152 Under basal conditions, autophagosomes are continuously genera

153 nd subsequent proteasomal degradation; under basal conditions, AXL co-immunoprecipitated with HSP90.

154 Moreover, CCDs secreted bicarbonate under basal conditions but absorbed bicarbonate in response to

155 NHERF3 and NHE3 colocalized in the BB under basal conditions but after elevation of [Ca(2+)](i) by c

156 largely in an intracellular reservoir under basal conditions but can traffic to the cell surface and

157 enic mice exhibited normal muscle mass under basal conditions but elevated satellite cell activation

158 nsable in adult ventricular myocardium under basal conditions but is critical for myocardial prolifer

159 that D2L and D2S share similar functions in basal conditions but not in response to stimulation of t

160 alpha2(-/-) mice are apparently normal under basal conditions but show significantly reduced exercise

161 COX-2 protein was almost undetectable under basal conditions but significantly elevated after treatm

162 ar synapses typically lack GluR2 label under basal conditions, but approximately 40% of peri-PSD pits

163 ve heart development or heart function under basal conditions, but develop heart failure following bi

164 cerevisiae TUB2 did not affect growth under basal conditions, but did result in increased sensitivit

165 [Ca(2+)](i) was further elevated under basal conditions, but insulin release still suppressed i

166 lcin binds to the SH3 region of PSD-95 under basal conditions, but it translocates to the plasma memb

167 ty, which maintained lipid homeostasis under basal conditions, but led to diet-induced hepatic trigly

168 ux/IAA stability compared to wild type under basal conditions, but not in response to an auxin treatm

169 ICER was not detected under basal conditions, but pulsatile GnRH stimulated ICER to

170 of ezrin also induced actin remodeling under basal conditions, but reduced insulin-stimulated actin r

171 3 alleles appear phenotypically normal under basal conditions, but show marked hyperacetylation of se

172 Atf1 and Fbh1 interact under basal conditions, but this binding is lost upon stress.

173 t Nbea regulates synaptic transmission under basal conditions by targeting neurotransmitter receptors

174 These results indicate that under basal conditions, C/EBPzeta occupies the C/EBP site, an

175 The simulations suggest that, under basal conditions, cAMP/PKA signaling could be significan

176 Under basal conditions, Cav-1 binds eNOS and inhibits nitric o

177 Under basal conditions CD36-KO versus WT mice displayed reduce

178 eak iNOS staining was observed in glia under basal conditions, CGRP treatment greatly increased glial

179 Under basal conditions, CK1delta OE mice exhibited horizontal

180 mation and greater insulin sensitivity under basal conditions compared to littermate controls, which

181 ficantly, lower mean arterial pressure under basal conditions compared to wild-type controls.

182 to act as a basic relay mechanism, but under basal conditions, competing dilatory signals may interac

183 sma [aldo] was elevated in Kcnmb1(-/-) under basal conditions (control diet, 0.6% K) and increased si

184 Moreover, under basal conditions, cotreatment with PF-04957325 plus roli

185 ge labile copper pools in living cells under basal conditions, CS3 opens opportunities for discoverin

186 eration in mitochondrial bioenergetics under basal conditions, culture of patient-derived fibroblasts

187 Here we show that in basal conditions Cx43 forms functional hemichannels in a

188 Under basal conditions, D2, D2 long, and D3 knock-out mice dis

189 DE4 inhibition increased CFTR activity under basal conditions (DeltaISC 7.1 muA/cm(2)) and after isop

190 Unlike AMPARs, synaptic SK2 channels under basal conditions do not rapidly recycle.

191 din levels that are similar to WT mice under basal conditions, double KO mice do not suppress hepcidi

192 role of CD36 in muscle fuel selection under basal conditions, during a metabolic challenge (exercise

193 e measured superoxide anion production under basal conditions, during stimulation with NMDA and kaina

194 Our results demonstrated that under basal conditions, endogenous MR1 transiently visits the

195 uences), quantify their expression levels in basal conditions, examine their homology to miRNAs from

196 Under basal conditions, hemodynamic parameters, cardiac anatom

197 Under basal conditions, HIF-1alpha is constitutively expressed

198 Under basal conditions, HuR mRNA is expressed in two forms: on

199 l RyR2 channels but remains undetected under basal conditions if expressed at relatively low levels.

200 that Tyr-219 of Munc18c remains buried under basal conditions in a conformation that is favorable for

201 n Ser-845 is strongly reduced (by 70%) under basal conditions in AKAP5 KO mice but not at all in D36

202 ation factor 2alpha are phosphorylated under basal conditions in eosinophils and neutrophils.

203 of Akt kinase was significantly higher under basal conditions in freshly isolated islets from Fxyd2(-

204 in and GSH adducts are present in vivo under basal conditions in healthy human red cells.

205 tal muscle glucose uptake was observed under basal conditions in healthy subjects.

206 ase II (CaMKII) inhibits NHE3 activity under basal conditions in intact intestine, acting in the BB,

207 is firing onset delay naturally occurs under basal conditions in old rats and is positively correlate

208 lular recycling system that functions during basal conditions in organelle and protein quality contro

209 y bind and tyrosine phosphorylate JIP1 under basal conditions in several naturally occurring systems

210 stsynaptic density (PSD) and activated under basal conditions in the adult mouse brain.

211 TF-ISWI chromatin-remodeling complex), under basal conditions in the cell.

212 DP-ribosylated Axin, which is degraded under basal conditions, increases immediately following Wnt st

213 In the present study, we show that, under basal conditions, IP6K1 forms a ternary complex with CSN

214 f lipid peroxyl radicals in HeLa cells under basal conditions is 33 nM/h within the cell.

215 How, during basal conditions, is the free concentration of TNF tight

216 f 19S function can have a fitness cost under basal conditions, it provided a powerful survival advant

217 MEM131L did not affect LRP6 expression under basal conditions, it triggered lysosome-dependent degrad

218 s, while PSD-95 exhibited low mobility under basal conditions, its levels could be regulated by chron

219 Under basal conditions, Keap1 recruits Nrf2 into the Cul3-cont

220 Although comparable to wild-type mice in basal conditions, knockout mice exposed to pressure over

221 modulated strongly by respiration even under basal conditions, less is known about whether inhibitory

222 Under basal conditions, loss of VCP activity results in autoph

223 Under basal conditions, LPA increased fluid absorption in an N

224 Under basal conditions, LXRalpha is phosphorylated at S198; ph

225 nction (TJ) transmembrane protein that under basal conditions maintains endothelial cell-cell interac

226 In basal conditions, MSNs are more excitable in parkinsonia

227 Under the basal condition, NFATc1 is phosphorylated.

228 1) Under basal conditions, NHE3 closely associates with NHERF2 in

229 To identify kinases that regulate NHE3 under basal conditions, NHE3 was immunoprecipitated; LC-MS/MS

230 Under basal conditions, NHERF2 and NHE3 exhibited robust FRET

231 These data suggest that, under basal conditions, NKA negatively regulates DAR function

232 In basal conditions, no overt dystonic movements or posture

233 Astrocytes did not express Gal-9 under basal conditions nor did IL-6, IL-10, or IL-13 trigger G

234 Under basal conditions, NRF2 is continuously ubiquitylated by

235 Under basal conditions, Nrf2 is polyubiquitinated by the Keap1

236 Under basal conditions, Nrf2 is ubiquitinated by the Keap1-Cul

237 Compared with the basal condition of maternal rearing (MR), leukocytes fro

238 This disruption represented a basal condition of the chronic epileptic hippocampus tha

239 Under basal conditions, old fch/fch mice had significant alter

240 Under basal conditions, only a small portion of KCNQ1 reaches

241 expressed in primary mouse hepatocytes under basal conditions or after APAP and RIPK3(-/-) mice were

242 s not confer any growth advantage, either in basal conditions or following EGF stimulation.

243 ydrogenase I enzymes of S. Typhimurium under basal conditions or following recovery from oxidative st

244 reas they did not affect these parameters in basal conditions or in cells expressing constitutively a

245 ng the acute phase of anaphylaxis but not at basal conditions or in healthy control subjects.

246 does not colocalize with Orai1 either under basal conditions or in response to thrombin.

247 t show release of (35)S-FXIII-A either under basal conditions or when interleukin 1-beta was released

248 d apoptosis in cultured cardiomyocytes under basal conditions or when stressed by H(2)O(2).

249 milar in wild type and knock-out cells under basal conditions or with ER stress-inducing agents.

250 ecrease in fold increase pAkt/Akt ratio from basal conditions (P < 0.01).

251 Under basal conditions, pERK is upregulated in choline acetylt

252 Under basal conditions, plasma and urine osmolalities and urin

253 These results suggest that, under basal conditions, PLD2 expression and concomitant activi

254 However, too much IKs under basal conditions poses an arrhythmogenic risk.

255 onist-activated D1R phosphorylation (>50% at basal condition), prevents D1R internalization and cAMP

256 e histone methyltransferase GLP, which under basal conditions promoted a repressed chromatin state at

257 cks significant amine oxidase activity under basal conditions (prorenalase) but that a brief surge of

258 use salt wasting or excessive diuresis under basal conditions, raising the possibility that these tra

259 Under basal conditions, receptors and G proteins form activity

260 Under basal conditions, Rem2 was subject to post-translational

261 Under basal conditions, selective inhibition of alpha3 using a

262 Under basal conditions, Sirt1(endo-/-) mice showed impaired en

263 Under basal conditions, Slitrk5 interacts primarily with a tra

264 -155, which is the most abundant miRNA under basal conditions, specifically required CD154 for furthe

265 Under basal conditions, such overexpression of iNOS causes mar

266 ters GlcNAcylation of several proteins under basal conditions, suggesting that MYPT1 regulates OGT su

267 orms a precoupled complex with Galphao under basal conditions that dissociates after Wnt-5a stimulati

268 These results suggest that under basal conditions the level of tonic inhibition in vivo e

269 We found that under basal conditions the relative bound amount of CaMKIIalph

270 Under basal conditions, the common Gly(875) variant of ATP7B i

271 synaptic transmission suggesting that under basal conditions, the concentration of adenosine moving

272 Under basal conditions, the K8 G62C/R341H/R341C variant-expres

273 Under basal conditions, the mitochondrial structure of WT and

274 Under basal conditions, the mutation had no effect on neuronal

275 Under basal conditions, the proteins were mobile but mostly in

276 Under basal conditions there was no effect on the levels of ub

277 Under basal conditions, there were no significant differences

278 sate for loss of function of the other under basal conditions, thereby masking the role that each pla

279 d only a moderate deficiency of PIP(2) under basal conditions, they had a striking deficiency in PIP(

280 Under basal conditions, this phosphorylation is maintained at

281 Under basal conditions, TM(LeD/LeD) mice exhibited excess glom

282 creased apical membrane ENaC and I(sc) under basal conditions to approximately 80% of aldosterone-sti

283 monstrate is necessary and sufficient, under basal conditions, to localize CaMKIIalpha at inhibitory

284 Under basal conditions, TRAF6 is methylated by the methyltrans

285 rimary cerebrocortical neuron cultures under basal conditions, we observe that E2 upregulates express

286 l glucose and lipid kinetic rates during the basal condition were compared in three groups: lean wome

287 lay an important cardioprotective role under basal conditions (when iNOS is not upregulated).

288 18:1-NO2 or metabolites were detected under basal conditions, whereas administered 18:1-NO2 is rapid

289 CIRS1KO hearts were reduced in size under basal conditions, whereas CIRS2KO hearts exhibited hyper

290 mRNA represses Hac1 protein production under basal conditions, whereas cytoplasmic splicing of the in

291 ADFP and LSDP5 bind HSL under basal conditions, whereas phosphorylation of serine resi

292 novel astroglial release pathway at play in basal conditions, which tunes the moment-to-moment gluta

293 as the major cause of lipid oxidation under basal conditions, while a 13-lipoxygenase (LOX2) and fre

294 PKCzeta was found to bind to ERK5 under basal conditions with coimmunoprecipitation and the mamm

295 rolonged in PMCA1(cko) atrial myocytes under basal conditions, with Ca(2+) overload leading to even g

296 In contrast, bHRs had lower D2 mRNA under basal conditions, with greater association of H3K9me3 at

297 ubstrate-specific proteolytic activity under basal conditions, with hyperubiquitination of cardiac pr

298 s at 6 h, followed by a decline, approaching basal conditions within 20 h.

299 lly dilated resistance vessels in vivo under basal conditions without a change in renal function.

300 of the abdominothoracic wall (n = 32) during basal conditions (without abdominal distension) and duri