ライフサイエンスコーパス: dose-dependently

1 by the addition of natural mosquito extract dose dependently.

2 n anesthetized rats reduced renal blood flow dose dependently.

3 r, reducing cell size induces premature ZGA, dose dependently.

4 , flow rate and urinary pH were not affected dose dependently.

5 isoforms equally regulate macrophage numbers dose-dependently.

6 .5-5 mg/kg) suppressed tumor growth of NSCLC dose-dependently.

7 the humoral immune reaction after OVA recall dose-dependently.

8 donor, xanthine (X) + xanthine oxidase (XO), dose-dependently.

9 duced osteoclast formation and TRAP activity dose-dependently.

10 unctions thought to be controlled by the PFC dose-dependently.

11 65, p-MEK and p-IkappaB-alpha were inhibited dose-dependently.

12 lammatory activity of the whole hydrolysates dose-dependently.

13 -80 to 0mV) in naive DRG neurons was reduced dose dependently (0.002-200microM) by icilin (18-80%).

14 ach protectin and resolvin sulfido-conjugate dose dependently (0.1-10 nM) stimulated human macrophage

15 WIN55,212-2, dose-dependently (0.5-2 mg/kg, i.p.) impaired short-term

16 Shikonin dose-dependently (0.5-50 mg/kg, per os) prevented DM/hyp

17 TP-10 administration dose-dependently (0.562, 1.0 mg/kg; subcutaneously) redu

18 In cellular assays, SAR-20347 dose dependently (1 nM-10 muM) inhibited JAK1- and/or TY

19 minal epoxides 17,18-EEQ-EA and 19,20-EDP-EA dose-dependently abated proinflammatory IL-6 cytokines w

20 All proteasome inhibitors dose-dependently abrogated IgM and IgG production by act

21 pplication of parthenolide in wild-type mice dose-dependently acceleratedin vivoaxon regeneration and

22 n transmission at spinal C-fiber synapses by dose dependently acting on distinct mu-opioid receptor s

23 RPamide neuropeptides dose-dependently activate the GnRH/AKH-like receptors GN

24 ZINC40099027 (10-1000 nM) dose-dependently activated FAK phosphorylation, without

25 The xanthine derivative rapidly and dose-dependently activates Kir6.2/SUR1 with a half-effec

26 All four proteins specifically and dose dependently adhered to bovine fibrinogen.

27 s follows: absolute tolerance was selective, dose dependently affecting a small group of powerful eff

28 ral dorsal premotor cortex further increased dose-dependently after 1800 pulses of iTBS over M1.

29 Whole-body net protein balance increased dose-dependently after ingestion of 0, 15, 30, or 45 g p

30 into de novo mitochondrial protein increased dose-dependently after ingestion of 15, 30, and 45 g pro

31 Consequently, anti-AREG antibody treatment dose-dependently ameliorated GN.

32 furthermore, finasteride (10-100 mg/kg, IP) dose-dependently ameliorated PPI deficits, hyperactivity

33 he adult beta-cell reduces glucose tolerance dose dependently and impairs glucose-stimulated insulin

34 whereas TAC inhibited this T-cell population dose dependently and significantly.

35 Recombinant IsdB bound Vn dose dependently and specifically.

36 posi's sarcoma-associated herpesvirus (KSHV) dose dependently and synergistically.

37 a nonspecific adenosine receptor antagonist, dose-dependently and at high doses completely blocked et

38 -CSF reduces hippocampal neuronal cell death dose-dependently and attenuates sensorimotor deficits af

39 Consumption of 100, 300 and 1000 mg NR dose-dependently and significantly increased whole blood

40 CRP and SAP dose-dependently and substoichiometrically inhibited bot

41 ts loss-of-function nature, the A allele was dose dependently associated with elevated basal AEA leve

42 Statin users, except lovastatin users, are dose-dependently associated with a decreased incidence o

43 Life-threatening disease was dose-dependently associated with carbohydrate ingestion

44 activity, longer sedentary bout duration was dose-dependently associated with increased homeostatic m

45 Cotinine-based measurements were dose-dependently associated with mortality and graft fai

46 ve as an alternative to self-report and were dose-dependently associated with poor late outcomes in R

47 The SST agonist OCT dose dependently attenuated the METH-induced accumulatio

48 phalin in dorsal horn homogenates, which was dose-dependently attenuated by selective D1LR antagonist

49 tered intraperitoneally or intragastrically, dose-dependently attenuated cocaine self-administration,

50 amine D1-like receptor antagonist, SCH23390, dose-dependently attenuated cocaine-seeking behavior in

51 athecal ondansetron administration after TBI dose-dependently attenuated nociceptive sensitization.

52 etaII, PKCdelta, and PKC given intrathecally dose-dependently attenuated paclitaxel-induced mechanica

53 Clozapine dose-dependently attenuated the absolute S-(+)-ketamine

54 nociceptive behaviors, while ROS scavengers dose-dependently attenuated the secondary response.

55 ntriguingly, dynorphin A(1-17) (10-100 nmol) dose-dependently attenuates both beta-endorphin- and GRP

56 The uptake of (18)F-UCB-H was dose dependently blocked by pretreatment with LEV (0.1-1

57 self-stimulation (ICSS) behavior, which was dose-dependently blocked by DA receptor antagonists, but

58 )H-Lu AE92686 to striatum was completely and dose-dependently blocked by the structurally different P

59 Topical administration of SRPK inhibitors dose-dependently blocked CNV with an EC50 of 9 muM.

60 rst, that the full TAAR1 agonist, RO5256390, dose-dependently blocked cocaine-induced inhibition of D

61 e PAC1R antagonist PACAP(6-38) into the BNST dose-dependently blocked excessive alcohol intake in eth

62 Pretreatment with R-MOD dose-dependently blocked nicotine-induced dopamine (DA)

63 ncentration of 5.89 nM (SD: +/- 1.80 nM) and dose-dependently blocked oocyst development in the mosqu

64 ell-derived factor-1alpha-mediated migration dose-dependently but minimally affected cell viability.

65 se (5% and 20% w/v) stimulated the secretion dose dependently, but vascular glucose was without signi

66 neration of hippocampal neurons is prevented dose-dependently by intracerebral injection of NAD(+).

67 Injections of the TRPA1 agonist dose-dependently caused pain with a half-maximal effecti

68 either Tnfaip3(CD11c) or Tnfaip3(LysM) mice dose-dependently controlled development of TH17-mediated

69 tro ADME and pharmacokinetics properties and dose-dependently counteracted acute lung eosinophilia in

70 creased alpha2,6-linked CD31 sialylation and dose-dependently counteracted NEU1-mediated inhibition o

71 A-988315 dose-dependently dampened stress-induced increases in co

72 cted for behavioral studies and was shown to dose-dependently decrease cocaine self-administration in

73 c-Jun dose dependently decreased activity of the human ITPR2 p

74 stration of SB-334867 (0, 7.5, 15, 30 mg/kg) dose dependently decreased cocaine intake specifically i

75 Yohimbine dose-dependently decreased advantageous responding in fe

76 ADX71441 dose-dependently decreased alcohol self-administration o

77 Memantine dose-dependently decreased binge-like eating and fully b

78 BNST PACAP38 dose-dependently decreased body weight, as well as food

79 Hunger and prospective consumption dose-dependently decreased by 15% and 13% for MHP and by

80 These were dose-dependently decreased by feeding D-PDMP.

81 d cell stiffness, while EP2 and EP4 agonists dose-dependently decreased cell stiffness 47% and 23% wi

82 M-5MPEP, Br-5MPEPy, and MTEP dose-dependently decreased cocaine self-administration a

83 Both drugs dose-dependently decreased food-maintained responding.

84 ate that systemically administered NBI-80713 dose-dependently decreased heroin self-administration in

85 esponded, with their frequencies rapidly and dose-dependently decreased in the blood, then returning

86 EDP-305 dose-dependently decreased macrophage infiltration as me

87 IN insulin dose-dependently decreased plasma glucose concentrations

88 FE 204038 dose-dependently decreased PP, did not modify mean arter

89 ed by immunoprecipitation, and purified Mfn2 dose-dependently decreased Ras activity in a cell-free a

90 In Exp. 1, we show that SalB dose-dependently decreased spontaneous and cocaine-induc

91 nhibited HIV-1 syncytia-inducing ability and dose-dependently decreased supernatant p24 antigen level

92 s and found that bath application of ethanol dose-dependently decreased the firing rate of low-freque

93 Both agonists dose-dependently decreased the impedance as a result of

94 , and 3 mg/kg, bid) given orally for 14 days dose-dependently decreased voluntary alcohol intake in M

95 injection of the Cdk5 inhibitor roscovitine, dose-dependently decreased wheel running.

96 ncident rate ratio compared with placebo was dose-dependently decreased with amiselimod (0.1 mg 0.53

97 pallidal Gs signaling and in this regard CNO dose-dependently decreases spontaneous locomotor activit

98 Weight loss dose-dependently decreases visceral adipose tissue and l

99 Both propofol and isoflurane dose dependently depressed force from low doses (propofo

100 In vitro binding showed that PIP2 dose-dependently disrupted Syn-1A.SUR1 complexes, corrob

101 cellular access without membrane disruption, dose-dependently dissociates both p53/HDM2 and p53/HDMX

102 ration of ADAMTS13 5 minutes after occlusion dose-dependently dissolved these t-PA-resistant thrombi

103 ate sodium salt (8-Br-cGMP), or pioglitazone dose-dependently downregulated podocyte injury-induced T

104 -endorphin (10-100 nmol) and GRP (1-10 nmol) dose-dependently elicit the same degree of robust itch s

105 tin setting, whereas overexpression of Olfm2 dose dependently enhanced SRF binding.

106 ults of the present study showed that CXCL12 dose-dependently enhanced angiogenesis in chorioallantoi

107 Erythrocyte membranes dose-dependently enhanced calcification in murine aortic

108 In addition, VK4-116 pretreatment dose-dependently enhanced the antinociceptive effects of

109 stration of a GABA(B)R antagonist, CGP55845, dose-dependently enhanced working memory in aged rats.

110 In contrast, diabetic cardiac damage was dose-dependently exacerbated by beclin 1 overexpression.

111 ever, only allopregnanolone (5-15 mg/kg, IP) dose-dependently exacerbated TS-like manifestations in D

112 ve mu opioid receptor (MOR) agonist fentanyl dose-dependently facilitates gregarious song and reduces

113 Protein increased dose-dependently glucagon-like peptide-1 (GLP-1), peptid

114 opsis (Arabidopsis thaliana), HD-ZIP III TFs dose-dependently govern the patterning of the xylem axis

115 In the present study, H2O2 dose-dependently impaired the adenosine triphosphate (AT

116 or, immediately after the extinction session dose-dependently impaired the consolidation of fear exti

117 us encoding for catalytically active WT NEU1 dose-dependently impaired tube formation, whereas overex

118 CRF dose-dependently impaired working memory performance whe

119 Oily fish dose-dependently improved cognitive function, especially

120 the nonselective CRF antagonist, D-Phe-CRF, dose-dependently improved working memory performance.

121 We found that DNCB activates human TRPA1 dose dependently in FLIPR experiments with an EC50 of 16

122 Diastolic blood pressure increased dose dependently in males, but not in females.

123 Saa3 appeared dose dependently in plasma after LPS injection.

124 ine increased FXN transcript and FXN protein dose-dependently in FA cells and brains of animal models

125 The tracer accumulates dose-dependently in GLP-1R-positive tumors.

126 ncreas and spleen and could be competed away dose-dependently in nondiabetic pigs and nonhuman primat

127 , the reduction of LPS-induced NO production dose-dependently in RAW 264.7 cell indicates the extract

128 ic acid metabolites significantly increased, dose-dependently, in serum and 24-h urine (P < 0.01 and

129 We found that CA1 pyramidal neurons could be dose-dependently inactivated by clozapine-n-oxide (CNO).

130 Particulate matter was found to dose-dependently increase cellular viability, activate t

131 lly, we show that anti-psychotic medications dose-dependently increase claudin-5 expression in vitro

132 ally microinjected into the NAc and found to dose-dependently increase drinking in nondependent (CTL)

133 ADM dose dependently increased ex vivo lipolysis.

134 C6' generated NO, increased cGMP, and dose dependently increased NO metabolites.

135 Specific serum IgG and IgG4 levels were dose dependently increased.

136 nction integrity or barrier function, but it dose-dependently increased acetaldehyde-mediated tight j

137 High glucose dose-dependently increased ADAM17 promoter activity, tra

138 Both methylone and MDPV dose-dependently increased brain temperature, but even a

139 Satiety and fullness dose-dependently increased by 7% and 6% for MHP and 16%

140 cted by bafilomycin A1 treatment, but it was dose-dependently increased by UPS inhibitors bortezomib

141 A selective FFA2 agonist dose-dependently increased DBS, unaffected by DPPIV inhi

142 ured endothelial cells, globular adiponectin dose-dependently increased endothelial nitric oxide synt

143 ADP dose-dependently increased force production in the absen

144 As expected, MDMA dose-dependently increased heart rate and blood pressure

145 Dose-response studies revealed that PEGPH20 dose-dependently increased insulin sensitivity in DIO mi

146 -7 -carboxamide), that activated the ISR and dose-dependently increased levels of ATF4 in transformed

147 Nitrite dose-dependently increased local cGMP production at the

148 nistration of R-MOD alone (10-30 mg/kg i.p.) dose-dependently increased locomotor activity and electr

149 Ethanol dose-dependently increased NREM sleep, which was consist

150 Luteolin, dose-dependently increased osteoblast cell counts.

151 PDE9-I dose-dependently increased plasma cyclic guanosine monop

152 sion of lipid emulsion in the isolated heart dose-dependently increased rate pressure product, dP/dt,

153 In vitro, cisplatin dose-dependently increased ROS generation in LLC-PK1 cel

154 Protein dose-dependently increased satiety and GLP-1, PYY 3-36,

155 Glucose dose-dependently increased the dihydroxyacetone phosphat

156 ces from kisspeptin-GFP mice showed that AVP dose-dependently increased the firing rate of most kissp

157 U-50488 dose-dependently increased the frequency of stimulation

158 Use of strong ACs dose-dependently increased the risk of AD in terms of in

159 Doxorubicin selectively and dose-dependently increased this value in the standard-do

160 ulture-based angiogenesis assays, IL-32gamma dose-dependently increased tube formation up to 3-fold;

161 PDE9-I dose-dependently increased urinary cGMP in both states (

162 In Wistar Kyoto, C-21 dose-dependently increased urine Na(+) excretion from 0.

163 ain tissue insulin and insulin signaling was dose-dependently increased, but ISF Abeta was unchanged

164 thionine, betaine, and homocysteic acid were dose-dependently increased, while S-adenosylmethionine,

165 CRs calculated for 130 children dose-dependently increased.

166 We further demonstrate that WIN 55,212-2 dose-dependently increases dopamine release and accelera

167 blockade of LDTg GLP-1Rs with exendin-(9-39) dose-dependently increases food intake and attenuates th

168 Doxorubicin dose-dependently increases LV MRGlu, particularly in the

169 parations, we found that CX1739 (10-100 muM) dose-dependently increases the frequency of respiratory

170 rate, using myography, that ADP and ADPbetaS dose-dependently induce mouse BSM contraction, and ADP-i

171 More importantly, bile acids dose-dependently induce PTB with minimal hepatotoxicity.

172 A (but not intra-basolateral amygdala) PACAP dose-dependently induced anorexia and body weight loss w

173 necrotic tumor material, S100A4 and UA both dose-dependently induced chemotaxis of MSCs with synergi

174 ivity testing data, cebranopadol itself also dose-dependently induced hyperactivity in rats at doses

175 l in dog, both piperidine 3 and azetidine 13 dose-dependently induced increases in blood flow and inh

176 We show here that dimethyl fumarate (DMF) dose-dependently induces mitochondrial biogenesis and fu

177 chanistic analyses reveal that the compounds dose dependently inhibit the formation of pregenomic RNA

178 and simian Vero E6), we found that both IFNs dose-dependently inhibit SARS-CoV-2.

179 n of bupropion or hydroxybupropion with 5-HT dose dependently inhibited 5-HT-induced currents in hete

180 tor 17-N-allylamino-17-demethoxygeldanamycin dose dependently inhibited A3G and A3B mutational activi

181 dhesion and chemotaxis of MCL cell lines and dose-dependently inhibited BCR, stromal cell, and CXCL12

182 In comparison with medium controls, BEL dose-dependently inhibited both lymphoproliferation and

183 nwhile, the resurgent hERG tail currents are dose-dependently inhibited by AMD without altering the k

184 required vitamin K supplementation, and was dose-dependently inhibited by racemic warfarin at a phys

185 res IFN-beta induction by viral dsRNA and is dose-dependently inhibited by VP35 expression.

186 SNF472 dose-dependently inhibited calcium phosphate crystalliza

187 xA4 in human embryonic kidney (HEK)293 cells dose-dependently inhibited cAMP levels after direct stim

188 identified five diverse small molecules that dose-dependently inhibited CGG RAN translation, while re

189 Strikingly, pretreatment with JJC8-016 dose-dependently inhibited cocaine-enhanced locomotion,

190 Similar to 2, these diarylureas dose-dependently inhibited CP55,940-induced intracellula

191 Riluzole dose-dependently inhibited cue- and cocaine-primed reins

192 cted DLK localization in our primary screen, dose-dependently inhibited DLK palmitoylation in follow-

193 Moreover, slow-releasing ATRA potently and dose-dependently inhibited HCC growth in mice.

194 iD) analogs, lenalidomide, and pomalidomide, dose-dependently inhibited hiPSC mesendoderm differentia

195 ly selective CB2R agonist, significantly and dose-dependently inhibited intravenous cocaine self-admi

196 Importantly, annexin A5 dose-dependently inhibited lipopolysaccharide binding to

197 imilar effects were observed with SIV, which dose-dependently inhibited neutrophil elastase and short

198 Thymol dose-dependently inhibited PCA when administered topical

199 Intrathecal administration of IL4-10 dose-dependently inhibited persistent inflammatory pain

200 elial dedifferentiation, exogenous TGF-beta1 dose-dependently inhibited pIgR production, whereas pIgR

201 Only HC-HA/PTX3 dose-dependently inhibited proliferation and EMT of stim

202 y-selective RORgammat inverse agonist, which dose-dependently inhibited RORgammat-driven transcriptio

203 Pretreatment with VK4-116 (5-25 mg/kg, i.p.) dose-dependently inhibited the acquisition and maintenan

204 In addition, pretreatment with 19 also dose-dependently inhibited the acquisition of oxycodone-

205 ome c When tested in cellular assays, ADDA 5 dose-dependently inhibited the proliferation of chemosen

206 peptide corresponding to this decorin region dose-dependently inhibited the response to myostatin in

207 Finally, TM2 dose-dependently inhibited thrombin-induced impairment o

208 HA dose-dependently inhibited TLR2-induced TNF-alpha produc

209 nstrated that the novel compound EOAI3402143 dose-dependently inhibited Usp9x and Usp24 activity, inc

210 ed as a potent 5-HT1A receptor antagonist by dose-dependently inhibiting 8-OH-DPAT-stimulated (35)S-G

211 alidations indicate that they are capable of dose-dependently inhibiting GEF catalytic activity, bind

212 model receptor system, we found that ethanol dose-dependently inhibits 5-HT1AR internalization and th

213 Phospholipid-conjugated A10Cp dose-dependently inhibits formation of A10TmCp homodimer

214 vandetanib, a multitarget kinase inhibitor, dose-dependently inhibits invasion.

215 Both CRY proteins dose-dependently lengthen the intrinsic, high-frequency

216 igen, we confirmed that 8a significantly and dose-dependently lengthens G(2) phase.

217 produced analgesic and anti-scratch effects dose-dependently, like the prototypic KOR agonist U50,48

218 ewer's and Baker's yeast products and Epicor dose-dependently lowered IFN-gamma, demonstrating that E

219 inhibitors of phosphatidylinositol 3-kinase dose dependently modulate platelet thrombus dynamics.

220 Dose-dependently, MYC increased output at minimal promot

221 indicate that Civacir potently, broadly, and dose-dependently neutralizes all tested patient variants

222 Both isoforms are dose-dependently nitrated and inactivated by peroxynitri

223 iabetic subjects, where it increased the UPR dose dependently over the entire physiologic insulin ran

224 an airway smooth muscle (ASM) cells, Sul-121 dose-dependently prevented cigarette smoke extract-induc

225 lia, we demonstrated that Sul-121 inhalation dose-dependently prevented LPS-induced airway neutrophil

226 Dabigatran etexilate (DE) dose-dependently prolonged diluted thrombin time and tai

227 We observed that GUWE dose-dependently promoted DC maturation and cytokine sec

228 NaCl dose-dependently promoted lipid oxidation as measured by

229 Importantly, DC-EV significantly and dose-dependently promoted MSC recruitment across a trans

230 ous (obesity) or exogenous (infusion) leptin dose-dependently raised CYP11B2 expression and aldostero

231 mice with Ang II and the NPR-C agonist cANF dose dependently reduced AF inducibility by preventing s

232 NE antagonism of either region dose dependently reduced approach-avoidance conflict beh

233 In addition, muscimol dose dependently reduced open-field locomotor activity,

234 and in cells that endogenously express LRH-1 dose dependently reduced the expression of cyclin-D1 and

235 1 agonists (e.g., 87), which efficiently and dose dependently reduced the number of circulating lymph

236 ancy, whereas LY2456302 (0.05 and 0.3 mg/kg) dose-dependently reduced (11)C-EKAP-specific binding, th

237 ntration of 0.31 mum Coinjection of A-967079 dose-dependently reduced and at a high concentration abo

238 ion of mGluR1, mGluR5 and PLC inhibitors all dose-dependently reduced binge intake, without influenci

239 Naltrexone and GSK1521498 dose-dependently reduced both cue-controlled alcohol see

240 rats, systemic administration of PF-04859989 dose-dependently reduced brain KYNA to as little as 28%

241 In conscious rats, renal cortical PO2 was dose-dependently reduced by intravenous AngII.

242 thermal pain behavior were observed and were dose-dependently reduced by meloxicam.

243 her, specific binding of (11)C-LY2459989 was dose-dependently reduced by the selective KOR antagonist

244 Intravenous injection of tat-cyclotraxin-B dose-dependently reduced cocaine intake, motivation for

245 ave anti-fibrotic activity; indeed, apigenin dose-dependently reduced collagen I in the human HSC lin

246 Further, capsaicin markedly and dose-dependently reduced coronary flow.

247 Acute treatment with A-705253 dose-dependently reduced cue-induced reinstatement of al

248 MDPV dose-dependently reduced functional connectivity.

249 Unexpectedly, CXL146 treatment rapidly and dose-dependently reduced GRP78 protein in MDR cancer cel

250 EDP-305 also dose-dependently reduced interstitial fibrosis as assess

251 ment with a pharmacological inhibitor of FAK dose-dependently reduced invasion, indicating a crucial

252 CNQX dose-dependently reduced motivation for cocaine in the e

253 Varenicline dose-dependently reduced responding maintained by nicoti

254 Importantly, 4 and two analogs dose-dependently reduced the Emax of the agonist curve i

255 In SSc fibroblasts, DZNep dose-dependently reduced the expression of profibrotic g

256 Lesogaberan also dose-dependently reduced the mean number of acid reflux

257 POM dose-dependently reduced the number of spontaneously act

258 (10 to 200 mug/ml) showed significantly and dose-dependently reduced TNF-alpha secretion induced by

259 Additionally, BI 749327 dose dependently reduces renal fibrosis and associated g

260 n receptors by the agonist salmon calcitonin dose-dependently reduces body weight, food intake, and m

261 In cynomolgus monkeys, ARGX-117 dose-dependently reduces free C2 levels and classical pa

262 potecan, a topoisomerase 1 (TOP1) inhibitor, dose-dependently reduces the expression of extremely lon

263 le anti-fibrotic agents that were capable of dose-dependently reducing connective tissue growth facto

264 Here, we demonstrate that SIRT1 dose-dependently regulates cellular glutamine metabolism

265 m cells, we show that CTCF is absolutely and dose-dependently required for looping between CTCF targe

266 Amylin dose-dependently reversed DAMGO-induced hyperphagia; 3 n

267 following administration of edoxaban (60 mg) dose-dependently reversed edoxaban's effects on bleeding

268 The 4F-PCC dose-dependently reversed the effects of edoxaban (60 mg

269 r-Antidote dose-dependently reversed the inhibition of fXa by direc

270 We now report that VU0152100 dose-dependently reverses amphetamine-induced hyperlocom

271 In addition, highly purified PF were able to dose dependently stimulate cytokine TNF-alpha, IL-1beta,

272 Norepinephrine also dose dependently stimulated isoketal formation in cultur

273 Uric acid dose-dependently stimulated aldose reductase expression

274 mary fat pad, and we observed that TNF-alpha dose-dependently stimulated Py230 cell growth in vitro.

275 Cch and CCK-8 both dose-dependently stimulated secretory responses from hum

276 ial lipopolysaccharide (LPS) can rapidly and dose-dependently suppress interleukin-2 (IL-2) productio

277 SH-11037 dose-dependently suppressed angiogenesis in the choroida

278 llagen-induced arthritis model, JNJ-54271074 dose-dependently suppressed joint inflammation.

279 entricular nucleus of the hypothalamus (PVN) dose-dependently suppressed lumbar SNA (LSNA) and its ba

280 TRAM-34 dose-dependently suppressed proliferation of wild-type C

281 ysaccharide-activated peritoneal macrophages dose-dependently suppressed the expression and release o

282 Noradrenaline and adrenaline dose-dependently suppressed the release of IL-27p28 in L

283 7,8-hexahydro-quinoline -3-carboxamide; MQC) dose-dependently suppressed the response to CCh but not

284 n of flagellin and QX-314 (flagellin/QX-314) dose-dependently suppresses mechanical allodynia after c

285 cal application of TNF to the cortex reduced dose-dependently the amplitude of CSD.

286 bioactive compounds significantly inhibited, dose-dependently, the expression of iNOS mRNA and protei

287 The model responded dose-dependently to androgens, with highest sensitivity

288 FH and FH19-20 bound dose-dependently to mGEnCs and TNF-alpha treatment incre

289 we found that properdin in human serum bound dose-dependently to solid-phase myeloperoxidase.

290 tudy, we apply the effects of dopamine (DA), dose-dependently, to both models on the basis of an exha

291 In cultured macrophages, recombinant CTRP6 dose-dependently up-regulated the expression and product

292 Short-term incubation with IL-3 dose-dependently upregulated MRGPRX2 expression in both,

293 Moreover, we found that 5-HT dose dependently upregulates the expression of AhR targe

294 rcumin improved disease activity index (DAI) dose-dependently, while the anti-inflammatory efficacy o

295 Risk magnified dose dependently with exposure to multiple fevers after

296 Delay frequency increased dose dependently with shorter recommended interval: 11 (

297 Lp(a) molar concentration was associated dose-dependently with CAD risk, peripheral artery diseas

298 ygen species generation was mildly elevated, dose dependently, with SiNPs, but no significant decreas

299 alogue Taltirelin (TAL) stimulated breathing dose-dependently, with greater effects in BN versus cont

300 Additionally, the cross-linking reagent dose-dependently yielded a band corresponding to the tet