ライフサイエンスコーパス: stimulate

1 onstimulated, obese nonstimulated, and obese stimulated).

2 nates they can be protective when adequately stimulated.

3 rication of these cascaded logic circuits to stimulate a transformative generation of energy-efficien

4 ry cyclic nucleotide-gated (CNG) channel and stimulates a depolarizing chloride current by opening th

5 ement in the TST in stress-naive mice, while stimulating above the carrier frequency of this circuit

6 e isoform 8 (ACA8) and that this interaction stimulates ACA8 activity.

7 especially the auxiliary factor(s) that can stimulate accurate and timely repair, have remained elus

8 r near the ubiquinone binding site of SDH to stimulate activity and contributes to plant stress signa

9 f the angiotensin II receptor type 1 (AT1R), stimulates acute catecholamine secretion through couplin

10 , consistent with reports that CO2 directly stimulates adenylyl cyclase.

11 orticoid receptor (GR), is routinely used to stimulate adipogenesis in culture.

12 se that LKB1 acts as a safeguard against HPV-stimulated aerobic glycolysis and tumor progression.

13 In contrast, loss of CTRP6 enhanced insulin-stimulated Akt activation in adipose tissue.

14 In this novel cascade, RIT1 stimulates Akt-dependent phosphorylation of Sox2 at T118

15 nique motility organelles of spirochetes, in stimulating an innate immune response.

16 hagosomes and identified an interferon-gamma-stimulated and Rab20-dependent membrane trafficking path

17 human cancer cells that IMP2 overexpression stimulates and IMP2 elimination diminishes proliferation

18 e PF-deficient mutants lacked the ability to stimulate, and the complemented PF-positive T. denticola

19 MbR assembly is ligand-stimulated, and we show that only 6-carbon molecules wit

20 d, both hypertrophic and hypoxic signals can stimulate angiogenesis, both of which stimulated SRC-2 e

21 ower socioeconomic status relative to others stimulates appetite and food intake.

22 When stimulating at 2 mA, cortical electric fields reach 0.8

23 EV biology and methodology with the goal of stimulating authors, reviewers, editors and funders to p

24 he impairment in autophagic flux and further stimulated autophagy.

25 ATG4B stimulates autophagy by promoting autophagosome formatio

26 hyla, we found that potent Nod-like receptor-stimulating bacteria in the upper airway (Staphylococcus

27 lity and increased TJP expression in the Mtb-stimulated BBB co-cultures.

28 onsistently enhanced the ability of HMGA1 to stimulate beta-catenin-dependent transcription, suggesti

29 versely, Wnt1 overexpression from osteocytes stimulated bone formation by increasing osteoblast numbe

30 We stimulated both eyes simultaneously with large sinusoida

31 tment of IL-1beta-producing monocytes, which stimulated brain endothelial IL-1R1.

32 Both nitrogen sources stimulated bulk phytoplankton, bacterial and DOM product

33 sults show that ZntB mediates Zn(2+) uptake, stimulated by a pH gradient across the membrane, using a

34 tional differentiation compared with T cells stimulated by a vaccine.

35 6K), downstream kinases whose activities are stimulated by AKT, or by mutating a residue in MRE11 tha

36 eins and malondialdehyde (MDA) contents were stimulated by all tested irradiation doses.

37 be noticeably more effective when cells were stimulated by collagen without the non-helical telopepti

38 Ascorbate degradation was stimulated by darkness, and the degradation rate was eva

39 litates ATR activation and HR, but how it is stimulated by DNA damage is still unclear.

40 INPP4A activity is stimulated by high membrane curvature and synergizes wit

41 accompanying loss of fluid, is not normally stimulated by intestinal distension as the meal passes t

42 N2O production with both production pathways stimulated by low O2, independent of NO2(-) concentratio

43 ciency ameliorates the inflammatory response stimulated by LPS and attenuates the inflammatory impact

44 ed that JCV DNA replication in G144 cells is stimulated by myristoylated (i.e., constitutively active

45 ction by hydroxylamine oxidation was further stimulated by NH4(+), whereas nitrifier denitrification

46 trifier denitrification at low O2 levels was stimulated by NO2(-) at levels as low as 0.2 mM.

47 Stimulated by our 2015 Current Biology paper [1], Zambon

48 scale structures with CM2, whose assembly is stimulated by Plk1 phosphorylation in vitro.

49 Angiotensin II also reduced vasoconstriction stimulated by Psora-4 or 4-aminopyridine, another KV cha

50 erphotoreceptor retinoid-binding protein and stimulated by retinoic acid 6 protein showed significant

51 Production of secreted proteases is stimulated by secreted signals that convey information a

52 fficking block in anergic B cells repeatedly stimulated by self-antigen.

53 esults were seen when lytic reactivation was stimulated by the KSHV protein replication and transcrip

54 In contrast, IL-1beta release stimulated by the TLR4 agonist LPS is independent of bot

55 In vitro, AGR2 expression was stimulated by tunicamycin-induced endoplasmic reticulum

56 sence of noncognate Gq protein enhances cAMP stimulated by two Gs-coupled receptors, beta2-adrenergic

57 n of StarD10 in mice led to impaired glucose-stimulated Ca(2+) dynamics and insulin secretion and rec

58 These compounds stimulate cAMP levels and raise mature let-7 levels to s

59 preferentially expressing D1 receptors that stimulate cAMP/cGMP synthesis.

60 diates hormone and neurotransmitter receptor-stimulated cAMP generation.

61 We found that 2-PAA stimulated cAMP synthesis and enhanced gap junction coup

62 ad to increased intensity and duration of D1-stimulated cAMP/cGMP signaling; conversely, the increase

63 Epidermal growth factor (EGF) was found to stimulate CAR homodimerization, thus constraining CAR in

64 (NuRD) complex, which associate with ZNF281, stimulates cardiac gene expression.

65 Here, we show that palmitate-stimulated CD11b(+)F4/80(low) hepatic infiltrating macro

66 y, the uptake of exosomes, derived from IL-2 stimulated CD4+ T cells, effectively promoted reactivati

67 inks the myofibroblast phenotype to TGFbeta1-stimulated CD44V6/ERK/EGR1 signaling.

68 er: while TOR-dependent energy signals alone stimulate cell proliferation, the development of a norma

69 Whereas activation of ERalpha stimulates cell proliferation and cell survival, ERbeta

70 Interestingly, while CpG-stimulated cells activated the mTOR pathway via TLR9 rec

71 to show that exosomes derived from poly(I:C) stimulated cells induce in vivo macrophage M1-like polar

72 tion, yet how EGF is stored or released from stimulated cells is undefined.

73 TLR9 receptor to induced MMP-7, beta-glucan-stimulated cells were mTOR-independent and used Dectin-1

74 HDM stimulated cellular reactive oxygen species production,

75 esters, which is required for its ability to stimulate CerS activity.

76 d during reactivation from latency, and they stimulate certain viral promoters and productive infecti

77 3 expression and activity is critical for NO-stimulated cGMP production and vasodilation.

78 as interactions between pH, SOM, and drought stimulate chemodenitrification.

79 reased IFN-beta, IFN-lambda1, and interferon-stimulated chemokine gene expression.

80 Calcitonin gene-related peptide (CGRP) stimulated CLR endocytosis and activated protein kinase

81 e seafloor accompanies methane emissions and stimulates CO2 consumption by photosynthesizing phytopla

82 ion of asymmetrically projecting neurons was stimulated collectively, only downward eye rotations wer

83 INT-777 also stimulated colonic HbetaD1 and HbetaD2 release from wild

84 yses of DF-1 and CEFs, under both normal and stimulated conditions using chicken interferon-alpha (ch

85 either 55 unstimulated and muramyl dipeptide-stimulated conditions.

86 plying that iRhom2 is a primary regulator of stimulated cytokine and growth factor signalling.

87 d that the Mcm10-4A mutant was defective for stimulating DDK phosphorylation of Mcm2, binding to eigh

88 etion, increases serum glucose levels, which stimulates de novo lipogenesis (DNL) in the liver.

89 the gamma134.5 protein, a virulence factor, stimulates dendritic cell (DC) maturation which is depen

90 plant safeners, which are nontoxic chemicals stimulating detoxification pathways in plants.

91 plasma membrane and clemastine fumarate can stimulate differentiation of oligodendrocyte precursor c

92 keeps their cycles out of phase in order to stimulate directional motility.

93 resolve the telomeric replication stress by stimulating DNA end resection and homologous recombinati

94 stemic AMPH administration reduced both AMPH-stimulated dopamine overflow and AMPH-induced locomotor

95 f all recorded hydraulically fractured wells stimulated during 2014 exist within 2 km of at least one

96 Electrically stimulating early visual cortex results in a visual perc

97 Chromatin per se can stimulate efficient enhancer-promoter communication (EPC

98 F-actin demonstrate low toxicity and enable stimulated emission depletion (STED) nanoscopy in neuron

99 By transforming stimulated emission depletion microscopy into a time-res

100 le tumor antigens in a fashion that potently stimulates endogenous immune responses against those ant

101 Ectopic p53 stimulates endogenous LMP1 expression.

102 tly influences the skin barrier integrity by stimulating endogenous proteolytic activity and defines

103 We found that platelets stimulated EOMA proliferation but did not mitigate apopt

104 omonas gingivalis lipopolysaccharide (PgLPS)-stimulated epithelial supernatant was investigated in HM

105 Of note, topical mevastatin stimulated epithelialization and angiogenesis in vivo Me

106 en metabolite profile (2-OH:16alpha-OH), and stimulated equol production in postmenopausal women with

107 analyzed HK biosynthesis in human leukocytes stimulated ex vivo and defined the biosynthetic roles of

108 ine apparently has no effect on electrically stimulated excitatory inputs.

109 visiae proteins, we show that Rrp47 and Mpp6 stimulate exosome-mediated RNA decay, albeit with unique

110 upplementation of culture medium with Neu5Ac stimulated expression of IL-6 and IL-8 and rescued the t

111 DNA repair in melanocytes exposed to UVB and stimulated expression of p53 phosphorylated at Ser-15.

112 miR-337-3p stimulates expression of cholangiocyte genes and repress

113 of certain objects that did not activate the stimulated face patch at all.

114 ve protein 1 (MCP-1), and granulocyte colony-stimulating factor (G-CSF) levels in the amniotic fluid

115 rculation by the cytokine granulocyte colony-stimulating factor (G-CSF) through complex mechanisms.

116 y factors including IL-8, granulocyte-colony stimulating factor (G-CSF), IL-33, IL-11, IL-1alpha, and

117 e to the up-regulation of granulocyte-colony stimulating factor (G-CSF); these effects are reversed f

118 Granulocyte-macrophage colony-stimulating factor (GM-CSF), mainly produced by MDSCs, w

119 hage glucose metabolism by macrophage colony-stimulating factor (M-CSF; inflammation resolving) and g

120 h gamma interferon (IFN-gamma) DNA or colony-stimulating factor 1 (CSF-1) DNA prior to ocular infecti

121 -to-tumour heterogeneity, response to colony-stimulating factor 1 receptor (CSF-1R) blockade and nano

122 and CD1a with granulocyte-macrophage colony-stimulating factor and transforming growth factor beta a

123 depletion and granulocyte-macrophage colony-stimulating factor blockade.

124 ons in CSF3R encoding the granulocyte colony-stimulating factor receptor (G-CSFR) in approximately 80

125 id IL-1alpha, IL-6, IL-8, granulocyte colony-stimulating factor, and GM-CSF levels.

126 cell adhesion molecule-1, granulocyte colony-stimulating factor, and soluble Fas.

127 bine plus cytarabine plus granulocyte colony-stimulating factor, mitoxantrone plus cytarabine, or hig

128 ismatched, unrelated, and granulocyte colony-stimulating factor-mobilized peripheral blood stem cell

129 of hypothalamic responses involving appetite-stimulating fasting-responsive hypothalamic neurons expr

130 Fpk1 phosphorylates and stimulates flippases that translocate aminoglycerophosph

131 outi-related peptide (AgRP) neurons potently stimulate food intake, whereas proopiomelanocortin (POMC

132 t this conceptual mechanistic framework will stimulate fruitful research that aims at unraveling the

133 These breakthroughs have stimulated further design and stabilization of Env trime

134 Munc13-4 promoted the Ca(2+)-stimulated fusion of VAMP8-containing liposomes with lip

135 tocatalysis are abridged to reinvigorate and stimulate future investigations.

136 eration was evident, while decreased mitogen-stimulated gamma interferon (IFN-gamma) production sugge

137 ssing cell lines did not activate interferon-stimulated gene (ISG) transcription following treatment

138 ds to persistently high levels of type I IFN-stimulated gene expression and to increased resistance t

139 riptional activator that, in prostate cells, stimulates gene expression required for various cellular

140 Pol II recruitment to the IRF3-dependent IFN-stimulated genes (ISGs).

141 ll line THP-1 results in an induction of IFN-stimulated genes in these cells.

142 IFN-stimulated genes were hypo-expressed in the liver of pat

143 keletal muscle is the major site for insulin-stimulated glucose disposal, and muscle insulin resistan

144 Thus, insulin secreted into the circulation stimulated glucose uptake by the liver spheroids, while

145 insulin-responsive compartment, and insulin-stimulated glucose uptake in adipocytes is suppressed.

146 Loss of Rab20 impairs insulin-stimulated glucose uptake in human and mouse skeletal mu

147 These results expand the model of insulin-stimulated glucose uptake in skeletal muscle cells by im

148 alance between insulin secretion and insulin-stimulated glucose utilization in the neonate which prob

149 n (EGP) are markedly more sensitive than for stimulating glucose disposal (Rd).

150 f nicotinamide phosphoribosyltransferase and stimulates glycolysis in cardiomyocytes.

151 eraction between the Gi1 protein and the non-stimulated GPCRs.

152 Strikingly, hH3R365 was completely unable to stimulate GSK3beta phosphorylation, an endpoint robustly

153 The ability of FSL-1 to stimulate hematopoiesis is critical, as hematopoietic dy

154 ng glucose effectiveness to suppress EGP and stimulate hepatic glucose uptake; activation of glucokin

155 with human brittle bone disease and thyroid stimulating hormone receptor hyperactivity.

156 n hormones (luteinizing hormone and follicle-stimulating hormone) from the pituitary.

157 hance the levels of SEC-P-TEFb also potently stimulated HSV reactivation from latency both in a senso

158 e methods preserved the ability of yolkin to stimulate human whole blood cells to release anti-inflam

159 In thrombin-stimulated HUVECs, Kindlin-2 and cortical actin dissocia

160 When the stimulated ictal onset area was hyperperfused, 82% of st

161 levels of IL-18 and are unable to optimally stimulate IFN-gamma production by NK cells.

162 d pannexin-1 and P2X7 receptor activation to stimulate IL-1beta release.

163 ether exposure to a previous pandemic strain stimulates immunity to a pandemic strain identified deca

164 acetylates Nav1.5 at lysine 1479 (K1479) and stimulates INa via lysine-deacetylation-mediated traffic

165 ated with differences in their ability to re-stimulate influenza-specific CD4 T cells ex vivo.

166 ated at the transition zone (TZ) in Hedgehog-stimulated Inpp5e(-/-) cells, which was associated with

167 Although glucose is known to stimulate insulin secretion by beta cells, whether it di

168 Antagonist 5d not only blocked exendin-4-stimulated insulin release in islets but also lowered in

169 le it is known that ghrelin inhibits glucose-stimulated insulin secretion (GSIS), the effect of obest

170 ose homeostasis, partly by enhancing glucose-stimulated insulin secretion (GSIS).

171 MIN6 beta-cells increases basal and glucose-stimulated insulin secretion and Ca(2+) uptake in the pr

172 naling in adult islets, since Ex-4 treatment stimulated insulin secretion by both juvenile and adult

173 re reduced by approximately 60%, and glucose-stimulated insulin secretion was eliminated.

174 crucial activator of muscarinic M3 receptor-stimulated insulin secretion.

175 mitochondrial bioenergetics control glucose-stimulated insulin secretion.

176 induced receptor internalization, and ligand-stimulated intracellular cAMP accumulation.

177 the formation of cellular protrusions and to stimulate invasive migration.

178 A2 degradation, whereas over-expressed Plk1 stimulates it, support our conclusion that the delay in

179 m multiple outcrops and that their optically stimulated luminescence (OSL) age of about 20,000 years

180 The optically stimulated luminescence ages suggest that Neandertals re

181 We conclude that ESAT-6 stimulates macrophage IL-6 production through STAT3 acti

182 hanism for IL-10-mediated suppression in LPS-stimulated macrophages and that inhibited genes can be d

183 Furthermore, IL-4-stimulated macrophages from female mice exhibited more t

184 ncreases nitric oxide (NO) production, which stimulates matrix metalloprotease-2 (MMP-2) and MMP-9 ac

185 Ectopic delivery of miR-194 stimulated migration, invasion, and epithelial-mesenchym

186 imary corneal epithelial cells, 24,25(OH)2D3 stimulated migration.

187 , insulin decreases dynein binding to APC to stimulate minus end-directed transport, which could modu

188 n the MBH hypersecrete TNFalpha that in turn stimulate mitochondrial ATP production in POMC neurons,

189 ng to impaired insulin signaling and insulin-stimulated mitochondrial respiration and glycolysis.

190 The observation that DMF stimulates mitochondrial biogenesis, gene expression and

191 Thus LPS stimulated monocytes are partially permissive lytic gene

192 dephosphorylates MYPT1(pThr696) and thereby stimulates MP activity inducing dephosphorylation of eNO

193 Stimulating mPFC D2R+ neurons disrupts normal social int

194 The molecular mechanism of how TPX2 stimulates MT assembly remains unknown because structura

195 framework for ecophysiological understanding stimulated much research into plant physiological traits

196 as restored and insulin action was improved, stimulating muscle glucose uptake in association with de

197 y, plasma cell differentiation of sorted LPS-stimulated MZ B cells was impaired, and aged bumble mice

198 e supernatant sialidase activity, largely by stimulating nanI transcription.

199 ved exosomes in recovering cardiac function, stimulating neovascularization, and promoting myocardial

200 Here an immunomodulatory approach to stimulating nerve repair in a nerve-guidance scaffold wa

201 Immune cell activation stimulates neuronal circuits that regulate innate and ad

202 well as between resting and physiologically stimulated neurons.

203 asize the importance of APP in AD and should stimulate new studies to elucidate APP-related targets s

204 The discovery of alpha-Gal stimulated new discussions and investigations regarding

205 NKG2D-ligand interaction between cytokine-stimulated NK cells increases the activity of the metall

206 of embryonic kidney rudiments, retinoic acid stimulated Nrip1 expression, whereas a pan-RAR antagonis

207 In vivo, the DDC-stimulated number of cytokeratin-19-positive cells in th

208 gonin mimicked the effects of F4 in IL-1beta-stimulated OA chondrocytes.

209 The enhanced myelination capacity of the SMF stimulated oligodendrocytes was validated in a dorsal ro

210 c receptor on osteoclastic lineage cells and stimulates osteoclastogenesis in vitro and in vivo.

211 unlike its mouse orthologue (mG9a) potently stimulated p53 transcriptional activity.

212 eta in biopsy samples and Leishmania antigen-stimulated peripheral blood mononuclear cells from patie

213 Both exercise and nitrate stimulated PGC1alpha-mediated gamma-aminobutyric acid (G

214 acting as a nucleotide exchange factor, can stimulate phosphorylation of KaiC, and how the different

215 Ablation of Gnb5 impaired M3R-stimulated phosphorylation of ERK1/2.

216 timulation of tracheal smooth muscle tissues stimulates phosphorylation of the NM myosin heavy chain

217 CaM binds to and stimulates PI3Kalpha/Akt signaling, promoting cell growt

218 ulates PRKCB promoter function in CLL cells, stimulating PKCbeta gene transcription via increased ass

219 did not normalize the differences in hormone-stimulated PLC activity, indicating calcium-dependent PL

220 We found stimulated polymerization of F-actin is not required for

221 nce of PPi, suggests that nucleotide binding stimulates PPi dissociation and occurs before polymerase

222 In addition, IL-7-stimulated pro-B cell cultures revealed a reduced differ

223 eIF4E stimulates production of enzymes that synthesize the bui

224 This in turn stimulates production of type III interferons and hence

225 These were successful in stimulating production of virus-targeted antibodies that

226 Cancer cells exploit Spy1 to stimulate proliferation through inappropriate activation

227 platelet-derived growth factor-BB (PDGF-BB)-stimulated proliferation of human venous smooth muscle c

228 VEGF-A stimulated proliferation of MM cells in monolayer and in

229 oncentrations, and that initiation with them stimulates promoter escape.

230 sociated with sensitization to food fails to stimulate protective tolerogenic pathways, leading to th

231 the nature of the mutation, CBZ application stimulated proteolysis of misfolded collagen X by either

232 Femtosecond stimulated Raman spectroscopy (FSRS) is a vibrational sp

233 Histamine, IL-17, and IL-22 stimulated RANKL expression in RA monocytes and JNJ77771

234 miR-193b also stimulated reactive oxygen species signaling by targetin

235 ac disease underwent oral wheat challenge to stimulate recirculation of gluten-specific T cells.

236 ic mediators and pharmacologic agonists that stimulate resolution of inflammation and infection.

237 at vaccination with the VC2-EHV-1-gD vaccine stimulated robust IgG1 and IgG2a antibodies after three

238 To stimulate, Sec17 needs its central residues which bind t

239 topology necessary for transcription process stimulates secondary structure-formation thereby amplify

240 New compounds that stimulate sGC show clinical promise, but where these sti

241 In vitro, hnRNP F overexpression stimulated Sirtuin-1 and Foxo3alpha with downregulation

242 s through enhancement of ERK activity, which stimulates SMAD3 expression and nuclear translocation.

243 ls can stimulate angiogenesis, both of which stimulated SRC-2 expression in vitro Furthermore, SRC-2

244 ype I EBV infection, particularly type I BL, stimulates strong responses of innate immune cells.

245 lycemia and insulinemia by enhancing insulin-stimulated suppression of endogenous glucose production.

246 Chronically stimulated surfaces of the body, in particular the gut m

247 paired NMDAR-dependent insertion of GluA1 at stimulated synapses.

248 nates DC metabolism and function to limit DC-stimulated T-cell responses.

249 r-induced sensitization of TRPA1 nociceptors stimulates targeted modification of the receptor.

250 We confirmed that the TL stimulates termination rate, but found that stabilizing

251 trointestinal motility, and metabolites that stimulate the "gut-brain axis" to alter neural circuits,

252 ption factor that can inhibit the growth, or stimulate the death, of developing cancer cells.

253 ding allergens and endotoxin, in urban homes stimulate the development of cytokine responses in early

254 UL8 has been reported to stimulate the helicase and primase activities of the com

255 1-palmitoyl-2-oleoyl diacylglycerol (PODAG) stimulate the IMD pathway of ticks.

256 chemical analysis reveals that RPA serves to stimulate the primase activity of PrimPol.

257 uction of innate inflammatory mediators that stimulate the production of matrix metalloprotease, infl

258 aberrant hormone-evoked Ca(2+) increases may stimulate the production of mitochondrial reactive oxyge

259 ghly inflammatory state that enables them to stimulate the recruitment of monocytes.

260 "alpha-(1,3)-Glucan-educated" DCs stimulated the activation of naive T cells and polarized

261 e production of anti-inflammatory IL-10, and stimulated the secretion of IL-6.

262 ociation of RNaseH1 with RNA:DNA hybrids and stimulates the activity of RNaseH1 on R loops.

263 ATR stimulates the BRCA1-PALB2 interaction after DNA damage

264 , first-in-class, agonist CD27 antibody that stimulates the CD27 pathway, which results in T-cell act

265 degradation affect a signaling pathway that stimulates the development of the digestive tract.

266 s of growth over time demonstrates that PLA1 stimulates the duration of leaf elongation by maintainin

267 l of hepcidin due to inflammatory conditions stimulates the ferroportin (FPN) transporter internaliza

268 hypothalamus, the fat-derived hormone leptin stimulates the growth of axons from the arcuate nucleus

269 Here, we report that MYC stimulates the transcription of DANCR, a long noncoding

270 omote assembly of branched actin networks by stimulating the filament-nucleating activity of the Arp2

271 itochondrial fission via GPR91, consequently stimulating the hMSC migration through mtROS-induced F-a

272 Where slippage is stimulated, the resulting products have one or more addi

273 with metalloprotease-containing exosomes and stimulates their secretion.

274 Stimulating these glutamate receptors increases nitric o

275 ating waves of gamma oscillations in the non-stimulated tissue.

276 Implantation of tension-stimulated tissues results in neotissues that are morpho

277 33 (1-100 ng/mL) in combination also greatly stimulate TNF secretion (by 4,500-fold).

278 activity than WT 26S, and this activity was stimulated to a greater extent by adenosine 5'-O-(thiotr

279 ersensitive patients, but not controls, were stimulated to secrete IgG and increase CD27 expression w

280 In contrast, stimulating Toll-like receptor signaling in medaka enhan

281 ion elongation factor that both inhibits and stimulates transcription elongation in metazoans.

282 esents the first documented protein known to stimulate transforming growth factor (TGF)-beta1 to -bet

283 habilitation can be increased by 'plasticity-stimulating' treatments that enhance experience-dependen

284 DK) binding-defective mutants are capable of stimulating treslin phosphorylation.

285 ctor (AMF) is a tumor-secreted cytokine that stimulates tumor cell motility in vitro and metastasis i

286 We find that Sir2/4 stimulates Ubp10 DUB activity on nucleosomes, likely thr

287 (PGC)-1alpha as well as attenuated forskolin-stimulated uncoupled respiration.

288 s from healthy controls and viremic KTR were stimulated using BK virus peptide libraries loaded or no

289 required in cases where rapamycin is used to stimulate vaccine-induced immunity.

290 id not affect WT cell proliferation, but did stimulate VDR KO cell proliferation.

291 In stimulated versus unstimulated organoid cultures, elevat

292 the breeding season (BS), angiogenic VEGF-A stimulates vessel growth in the infundibulum, aiding vas

293 HIV-1 establishes chronic infection and stimulates vigorous immune responses in the human host;

294 as ruxolitinib and JAK inhibitor I) strongly stimulate VSV replication and oncolysis in all resistant

295 PBMCs from MS patients stimulated with a TLR-9 agonist showed reduced expressio

296 However, it did not do so when ILC2s were stimulated with IL-7 and thymic stromal lymphopoietin (T

297 P2X7-deficient macrophages were isolated and stimulated with lipopolysaccharide, ATP, or both.

298 Aortic EC were stimulated with low-dose TNFalpha (0.3 ng/ml) in a micro

299 ranscriptome data from human blood monocytes stimulated with various immune stimuli and provide a tim

300 Ligase-dead UBE3A did not stimulate Wnt pathway activation.