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 LTD and behavior that were not present under basal conditions.

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

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

7 evels greatly influence ISG expression under basal conditions.

8 GU within and between healthy subjects under basal conditions.

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

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

11 tic reserve, functioning near capacity under basal conditions.

12 n-C (cMyBP-C) is highly phosphorylated under basal conditions.

13 e tuning AMPA receptor synaptic levels under basal conditions.

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

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

16 -atrophy signaling axis toward atrophy under basal conditions.

17 ad normal organ function and histology under basal conditions.

18 s in G2435R-RYR1 knock-in mouse muscle under basal conditions.

19 dividuals with allergy expressed VLDLR under basal conditions.

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

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

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

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

24 no messenger RNA or protein detectable under basal conditions.

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

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

27 VERBalpha does not repress lipogenesis under basal conditions.

28 eased luciferase expression when compared to basal conditions.

29 bitor alone had any substantial effect under basal conditions.

30 transport mechanisms are not saturated under basal conditions.

31 ETs also help regulate gene expression under basal conditions.

32 response to infection-like conditions versus basal conditions.

33 that NHE3 is phosphorylated by CaMKII under basal conditions.

34 mildly affected anxiety-like behaviors under basal conditions.

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

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

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

38 ors are saturated by endogenous ligand under basal conditions.

39 striosomes, which were more excitable under basal conditions.

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

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

42 nemia, and increased ductular reaction under basal conditions.

43 and cell lines show elevated autophagy under basal conditions.

44 n the suppression of insulin secretion under basal conditions.

45 ostasis and trafficking to the synapse under basal conditions.

46 eading to suppressed glutamate release under basal conditions.

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

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

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

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

51 AZ did not impair normal hematopoiesis under basal conditions.

52 ine neuron firing and anxiety behavior under basal conditions.

53 pletion results in pexophagy induction under basal conditions.

54 somes and represses Cav2.3 translation under basal conditions.

55 ere in both mobile and immobile states under basal conditions.

56 ic reticulum prevents their activation under basal conditions.

57 S, promoted hyperubiquitination of CLR under basal conditions.

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

59 that captures PD pathogenic processes under basal conditions.

60 small intestine during development and under basal conditions.

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

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

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

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

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

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

67 cultured and injured under 3 conditions: (1) basal conditions, (2) exposed to S aureus exoproducts, a

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 of heart failure markers, NPPA and NPPB, at basal condition and abolished phenylephrine-induced path

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

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

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

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

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

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

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

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

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

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

87 through a Keap1-independent mechanism under basal conditions and an induced effect through a Keap1-d

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

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

90 pendent increase in Tr-OxPL production under basal conditions and augmented Tr-OxPL generation upon i

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

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

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

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

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

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

97 study via the Langendorff preparation under basal conditions and during IR.

98 e voltage-gated calcium channel Cav2.3 under basal conditions and following activity.

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

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

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

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

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

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

105 ational regulator of Cav2.3 expression under basal conditions and in response to GpI mGluR stimulatio

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

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

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

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

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

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

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

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

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

117 EK293 cells, calmodulin bound to NCKX4 under basal conditions and induced a ~2.5-fold increase in NCK

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

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

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

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

122 ng over to restrict insulin oversecretion in basal conditions and preserve the insulin pool that can

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

124 f synaptic vesicle pools is maintained under basal conditions and regulated by neural activity.

125 ions empower HSF1 to both repress AMPK under basal conditions and restrain its activation by diverse

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 nd mitochondrial Parkin protein levels under basal conditions and upon exposure to mitochondrial toxi

129 to higher cytosolic Parkin protein levels at basal conditions and upon exposure to mitochondrial toxi

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

131 e genes in primary mouse cortical neurons in basal conditions and upon overexpression and knockdown o

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

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

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

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

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

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

138 e, associated with increased adiposity under basal conditions, and glucose intolerance and insulin re

139 Remarkably, under basal conditions, and having accounted for false site lo

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

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

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

143 creted abundant inflammatory cytokines under basal conditions, and this was also greatly reduced by B

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

145 Under basal conditions ANKRD9 is largely segregated from the c

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

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

148 terfered with nociceptive input to RVM under basal conditions, as well as in acute inflammation.

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

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

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

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

153 Under basal conditions at pH ~6.6, calculated paracellular HCO

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

155 Under basal conditions, autophagosomes are continuously genera

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

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

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

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

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

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

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

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

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

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

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

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

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

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

170 3 alleles appear phenotypically normal under basal conditions, but show marked hyperacetylation of se

171 Data from mouse model show that in basal condition, butyrate up-regulated the expression of

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

173 Under basal conditions, calculated paracellular HCO(3) (-) flu

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

175 (R)-channels are constitutively active under basal conditions carrying tonic inward current and synap

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

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

178 Under basal conditions, CK1delta OE mice exhibited horizontal

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

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

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

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

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

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

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

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

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

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

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

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

191 nnel activity is dynamically modulated under basal conditions, during beta-adrenergic stimulation, an

192 interact to regulate channel activity under basal conditions, during beta-adrenergic stimulation, an

193 activity of cardiac Ca(V)1.2 channels under basal conditions, during sympathetic activation, and in

194 Under basal conditions, DYRK1A is a negative regulator of Wnt/

195 Under basal conditions, endocytosed AMPA receptors are rapidly

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

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

198 s of human intestinal epithelial cells under basal conditions, exposure to cytokines TNFalpha, IFNgam

199 Patch clamped VMs under basal conditions from TABs but not Shams exhibited outwa

200 Under basal conditions, hemodynamic parameters, cardiac anatom

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

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

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

204 Under basal conditions, immunofluorescence assays showed signi

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

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

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

208 DA) -DeltaCa(2+) response was observed under basal conditions in HF compared to sham rats.

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

210 receptor tyrosine kinase endocytosis, under basal conditions in monolayer keratinocyte cultures.

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

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

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

214 -cellular gene expression pattern of TSPO at basal conditions in the adult mouse hippocampus.

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

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

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

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

219 We also found that apical hTf uptake under basal conditions is receptor-associated protein (RAP)-se

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

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

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

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

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

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

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

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

228 In basal conditions, MSNs are more excitable in parkinsonia

229 Under basal conditions, myeloid-specific KLF2 knockout mice (K

230 Under basal conditions, neuronal expression of HRI is barely d

231 Under the basal condition, NFATc1 is phosphorylated.

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

233 Under basal conditions, NHERF2 and NHE3 exhibited robust FRET

234 In basal conditions, no overt dystonic movements or posture

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

236 Under basal conditions, NRF2 is continuously ubiquitylated by

237 Under basal conditions, Nrf2 is polyubiquitinated by the Keap1

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

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

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

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

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

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

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

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

246 ssentially undetectable in these cells under basal conditions or following TSH-stimulation.

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

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

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

250 pheral blood mononuclear cells (PBMCs) under basal conditions or in situations that promote oxidative

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

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

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

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

255 Under basal conditions, plasma and urine osmolalities and urin

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

257 Under basal conditions, pNEC cultures from patients with CRSwN

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

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

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

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

262 Under basal conditions, receptors and G proteins form activity

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

264 Under basal conditions, selective inhibition of alpha3 using a

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

266 Under basal conditions, Slitrk5 interacts primarily with a tra

267 -155, which is the most abundant miRNA under basal conditions, specifically required CD154 for furthe

268 Under basal conditions, such overexpression of iNOS causes mar

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

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

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

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

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

274 In basal conditions, the majority of the mutations confer P

275 Under basal conditions, the mitochondrial structure of WT and

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

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

278 nic effects evoked by a low level of Nrf2 at basal condition; the other is responsible for the induci

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

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

281 Under basal conditions, this phosphorylation is maintained at

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

283 Intriguingly, under basal conditions TMX2 occurs in both reduced and oxidize

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

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

286 Under basal conditions, TRAF6 is methylated by the methyltrans

287 ltered zinc transport or proliferation under basal conditions, under activation, these KO cells showe

288 Under basal conditions very few platelets bound to the endothe

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

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

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

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

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

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

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

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

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

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