ライフサイエンスコーパス: unstimulated

1 ere compared to a control coculture that was unstimulated.

2 This fragment causes GLUT4 translocation in unstimulated 3T3-L1 adipocytes.

3 CD95 expression on unstimulated A-T lymphocytes was high, and the apoptotic

4 ular compartments of both GIP-stimulated and unstimulated adipocytes.

5 ccumulate adjacent to the plasma membrane of unstimulated adipocytes.

6 ese/type 2 diabetic mice, whereas the basal (unstimulated) adiponectin release level was elevated two

7 Simultaneously, unstimulated airway mucosal lining fluid was obtained an

8 A predictive model analysis using unstimulated analytes discriminated best between the con

9 tion correlate with RPE apoptosis induced by unstimulated and activated mononuclear phagocytes.

10 lize the spatial organization of granules in unstimulated and activated platelets.

11 s glycolysis and oxidative respiration, both unstimulated and after inflammatory conditions.

12 network analyses were applied utilizing the unstimulated and background-corrected plasma analyte con

13 ondly, this effect is greater when cells are unstimulated and finally, resting and stimulated samples

14 arly placed FPR2 peptides were identified in unstimulated and fMLF + cytochalasin B-stimulated sample

15 notype-specific expression of 17q21 genes in unstimulated and HRV-stimulated peripheral-blood mononuc

16 edia were sampled and RNA was extracted from unstimulated and IL-4/IL-13-stimulated cultures.

17 In vitro cytokine production by both unstimulated and lipopolysaccharide-stimulated PBMCs fro

18 In vitro, both unstimulated and LPS-stimulated HSCs upregulated Fas (CD

19 here it interacts with ZNRF4 under either 55 unstimulated and muramyl dipeptide-stimulated conditions

20 FPR1 (NFPRb) in dodecylmaltoside extracts of unstimulated and N-formyl-Met-Leu-Phe (fMLF) + cytochala

21 and their immune responses were assessed in unstimulated and stimulated blood specimens, using flow

22 The pileup of polymerases was similar in unstimulated and stimulated cells from Ung(-/-) and Aid(

23 Calcineurin binds to B-Raf in both unstimulated and stimulated cells.

24 teogenesis were present in the cocultures in unstimulated and stimulated conditions.

25 dynamics using single-cell RNA sequencing of unstimulated and stimulated naive and effector memory CD

26 Interaction between oral bacteria and both unstimulated and stimulated saliva was examined in vitro

27 hibited expression of GATA3 messenger RNA by unstimulated and stimulated T cells, and distributed thr

28 on an interrogation of the transcriptomes of unstimulated and TNF-alpha- and IFN-gamma-stimulated pri

29 responsible for neutrophil crawling in both unstimulated and TNF-alpha-activated venules.

30 for 48 h (anti-CD3/anti-CD28 stimulation or unstimulated), and IL-37 concentrations in supernatants

31 contains approximately 90% of the PerC MO in unstimulated animals but disappears rapidly from PerC fo

32 orrelated with basal NF-kappaB activation in unstimulated B cells and monocytes and regulated the sen

33 l-intrinsic inflammation upregulated in aged unstimulated B cells and negatively associated with AID

34 n existed in a preformed complex with Syk in unstimulated B cells and underwent Syk-dependent phospho

35 Our results showed that unstimulated B cells from old BALB/c mice make significa

36 recombination, miR-155 and miR-16, in human unstimulated B cells from young and elderly individuals

37 diet, ex vivo IgM and IgG were elevated with unstimulated B cells.

38 noninvasive imaging agent to directly detect unstimulated BAT and quantify the core mechanism of mito

39 vantage of (18)F-FBnTP not only in detecting unstimulated BAT at high contrast but also in quantifyin

40 -alpha genes are constitutively expressed in unstimulated bat tissues and cells and their expression

41 Unstimulated beta(1)- and beta(2)AR were highly confined

42 No paradigm induced LLSR changes in the unstimulated brachioradialis muscle.

43 3, we performed extensive ChIP-sequencing in unstimulated breast cancer cells and following estrogen

44 e coactivated both in stimulated rats and in unstimulated but injured rats.

45 neuron, while an antagonist muscle fiber is unstimulated by a pause and step from the antagonist neu

46 Unstimulated c-Abl knockout MEFs are less responsive to

47 points of NF-kappaB regulation revealed that unstimulated c-Abl knockout MEFs do not exhibit an incre

48 roposed crucial role of PKA in modulation of unstimulated Ca(2)(+) current in the absence of beta-adr

49 g a significant increase in the frequency of unstimulated Ca(2+(i)) events and the development of alt

50 Unstimulated Ca(2+) influx was greater in E than CA.

51 Unstimulated CD4(+) CBMCs that lack CCR5/CD45RO showed r

52 data derived from either whole blood (WB) or unstimulated CD4(+) T lymphocytes (CD4), and a self-repo

53 we analyzed clock gene expression by qPCR in unstimulated CD4+ T cells and immune responses of PMA/io

54 Primary, unstimulated CD8(+) T cells insignificantly suppress vir

55 ted neuron; it could also be produced in the unstimulated cell.

56 man umbilical vein endothelial cells than to unstimulated cells and 14x more than nontargeted microbu

57 eta, which maintains Stat1 protein levels in unstimulated cells and acts in an autocrine/paracrine ma

58 orylation, serving both to inhibit PDE4D3 in unstimulated cells and also to mediate a cAMP-induced po

59 evel of Ser15 phosphorylation occurs in both unstimulated cells and cells stimulated pharmacologicall

60 UG enhances its function to trap GSVs within unstimulated cells and enhances insulin-stimulated gluco

61 nucleosomes in stimulated cells compared to unstimulated cells and identified 24 318 loci.

62 vesicles and tethers them intracellularly in unstimulated cells and in which insulin mobilizes this p

63 ed the homodimeric fraction of ErbB3 even in unstimulated cells and induced a ~2-fold reduction in th

64 7 on the IRAK-M promoter is trimethylated in unstimulated cells and that this silencing epigenetic ma

65 that VSV-G-pseudotyped virus cannot fuse to unstimulated cells because the viral particles cannot be

66 YOD1 associates with TRAF6 in unstimulated cells but is released upon IL-1beta stimula

67 ternative NF-kappaB pathway is restricted in unstimulated cells by a cIAP1/2:TRAF2:TRAF3:NIK complex.

68 dation of NIK limits NF-kappaB activation in unstimulated cells by the ubiquitin:NIK E3 ligase compri

69 levels and mRNA expression were measured in unstimulated cells by using flow cytometry and qRT-PCR,

70 Although unstimulated cells experienced apoptosis following anti-

71 We found that in unstimulated cells GIV does not co-fractionate with its

72 ntrast, steady-state endocytosis of Kv1.2 in unstimulated cells is cholesterol dependent.

73 The results of our study showed that unstimulated cells of UC patients had a decreased viabil

74 lular localization in ligand-stimulated and -unstimulated cells overexpressing the seven transmembran

75 Translational silencing of MCPIP1 mRNA in unstimulated cells resulted from the combined suppressiv

76 able network through the cytoskeleton allows unstimulated cells to move persistently and, for cells i

77 ulated RhoGEFs are found in the cytoplasm of unstimulated cells, and PM recruitment is a critical asp

78 In unstimulated cells, association of TPL-2 with NF-kappaB1

79 Notably, in unstimulated cells, bat ISGs were expressed more highly

80 A, and UNC5B were expressed at low levels in unstimulated cells, but they increased following mitogen

81 In unstimulated cells, each BDNF 5'- and 3'UTR determined a

82 In unstimulated cells, ERK-mediated negative feedback reduc

83 lated linearly with G-actin concentration in unstimulated cells, even at concentrations much higher t

84 In unstimulated cells, FKBP51 forms endogenous complexes wi

85 In unstimulated cells, GLUT4 is incorporated into specializ

86 0 protein interactions in IFN-stimulated and unstimulated cells, many of which involve proteins assoc

87 of 21 +/- 3 um/day compared to the rate for unstimulated cells, of 5 +/- 4 um/day.

88 nd p63RhoGEF(619) is strikingly different in unstimulated cells, p63RhoGEF(580) is located at the pla

89 In unstimulated cells, pathway activity is inhibited by the

90 Thus, in unstimulated cells, the increased phosphorylation and ac

91 SF2 (ASF) bound chemokine mRNA in unstimulated cells, whereas the SF2 (ASF)-mRNA interacti

92 r intracellular retention of these cargos in unstimulated cells.

93 e to C5a induced the cleavage of the C5aR on unstimulated cells.

94 nsiderable cell-to-cell variability, even in unstimulated cells.

95 ry (i.e., past social status), especially in unstimulated cells.

96 with proinflammatory mediators compared with unstimulated cells.

97 hagocytosed significantly more bacteria than unstimulated cells.

98 ted as CD4(+)CD25(high)CD127(low) cells from unstimulated cells.

99 calized predominantly at lateral clusters in unstimulated cells.

100 of HIV-1 is found within the cell nucleus in unstimulated cells.

101 t, contributed to increased cell survival in unstimulated cells.

102 eases significantly in comparison to that of unstimulated cells.

103 g allows for constitutive IL-2 expression in unstimulated cells.

104 all desensitization with respect to those of unstimulated cells.SIGNIFICANCE STATEMENT The efferent s

105 oncanonical nuclear factor kappaB pathway in unstimulated cells; (ii) RIP1 polyubiquitination is not

106 and -9 are basally persulfidated in resting (unstimulated) cells and become depersulfidated during th

107 Compared to normal, unstimulated CF cells or normal cells treated with CFTR

108 omal plasma membrane-enriched fractions from unstimulated CHT(+/-) animals matched those observed in

109 mice and wild-type littermates revealed that unstimulated Cl(-) secretion reflected approximately 50%

110 A, however, appeared to contribute little to unstimulated Cl(-) secretion, whereas studies with cysti

111 ulatory activity and simultaneously inhibits unstimulated cleavage, we now provide evidence that esca

112 induced apoptosis of IgM-stimulated but not unstimulated CLL cells in a dose- and time-dependent man

113 d pSTAT3 and pJAK2 in IgM-stimulated but not unstimulated CLL cells, suggesting that activation of th

114 ntal cell miRNA content and control EVs from unstimulated CLL cells.

115 Regarding functionality, under unstimulated conditions HIV-infected patients showed a h

116 ded by the ubiquitin proteasome under normal unstimulated conditions, but its degradation is accelera

117 Under unstimulated conditions, endogenous TAK1 is stably assoc

118 In unstimulated conditions, larvae spend most of their time

119 3beta destruction complex (DC), which, under unstimulated conditions, targets cytoplasmic beta-cateni

120 However, under unstimulated conditions, the Pro32Pro33 mutation led to

121 cretion of cyclic GMP (cGMP) under baseline, unstimulated conditions.

122 y in non-raft membrane fractions under basal/unstimulated conditions.

123 bicarbonate, revealing a role of KSper under unstimulated conditions.

124 d expression of NF-kappaB-dependent genes in unstimulated conditions.

125 n in the expression of dsRNA receptors under unstimulated conditions.

126 ilar actin stress fiber staining patterns in unstimulated conditions.

127 increase in immobile integrins compared with unstimulated conditions.

128 ressed, this methylation exists under basal (unstimulated) conditions and is further augmented upon i

129 smic reticulum Ca(2+) load and by increasing unstimulated contractions and Ca(2+) waves.

130 pronounced in TLR4-stimulated cells than in unstimulated control cells.

131 At week 3, the unstimulated control cocultures developed the expression

132 estored M-responses at earlier times than in unstimulated controls in both TA and Sol muscles.

133 fold improvements in tensile properties over unstimulated controls, may allow the engineering of mech

134 as markedly lower than in M2 macrophages and unstimulated controls.

135 hils exposed to poly(A:U), relative to their unstimulated counterpart.

136 HLDB1 displayed a cytoplasmic disposition in unstimulated cultured adipocytes but translocated to the

137 Although these unstimulated DCs induced T cell function in vivo, there

138 Unstimulated DeltaF508CFTR channels or those inhibited b

139 lation by first decreasing the size of their unstimulated dendrites and then increasing the size of t

140 s (either dorsal or ventral) resulted in the unstimulated dendrites losing total dendritic branch len

141 evealed by electron microscope tomography in unstimulated, dissociated rat hippocampal neurons.

142 s induced cytoplasmic localization of YAP in unstimulated ECs and, strikingly, blocked the nuclear im

143 In unstimulated ECs, YAP localized mainly in the cytoplasm.

144 ovel, EHD1- and RUSC2-dependent transport of unstimulated EGFR from the Golgi compartment to the cell

145 cellular mRNA export that is not met by the unstimulated enzyme, suggesting a possible mechanism by

146 ase in intragranule pH, underwent detectable unstimulated exocytosis, and was very poorly responsive

147 oup (P < 0.05) but no significant changes in unstimulated expression.

148 specific; it is predominantly cytoplasmic in unstimulated fibroblasts and some muscle cell types and

149 ls but increased TIMP-1 levels compared with unstimulated fibroblasts.

150 in which participants estimate the number of unstimulated fingers between two touched fingers or a lo

151 ion of CRY1; phyB Pr interacts only with the unstimulated form of CRY1 but not with the photostimulat

152 pported CD4(+) T-cell proliferation, whereas unstimulated FRC did not.

153 tion functions as initiator and amplifier of unstimulated HCMV MIE gene expression and cooperatively

154 ubiquitin chains when it is bound to Axin in unstimulated HEK293 cells.

155 AR1-PAR4 heterodimers were not detected when unstimulated; however, when the cells were stimulated wi

156 In unstimulated human as well as mouse lung ECs, ROCK2 acti

157 dosomes and the trans-Golgi network (TGN) in unstimulated human colonic epithelial cells.

158 d for the global phosphoproteome analysis of unstimulated human Jurkat leukemia T cells (E6.1).

159 C3 and C5b-9 deposits than control serum on unstimulated human microvascular endothelial cells (HMEC

160 We did not observe human CD83 on unstimulated human natural regulatory T cells (Treg), in

161 When tested in whole human blood and unstimulated human saliva maximum power densities of 73

162 (H3K27ac), a marker of active enhancers, in unstimulated HUVECs and HUVECs stimulated with VEGFA for

163 eta-arrestin1 by promoting degradation of an unstimulated IGF-1R, but protecting the receptor against

164 Unstimulated IL-2 and IFN-gamma were ranked at or near t

165 In contrast, unstimulated IL1B displayed very low levels of both TBP

166 dopsis (Arabidopsis thaliana) remain largely unstimulated in nrt2 mutants.

167 le to isolate highly purified populations of unstimulated in vivo latent cells.

168 ve stress and CVB3 copy number compared with unstimulated infected cells.

169 e cases triggers barrage firing in a nearby, unstimulated interneuron.

170 networks that resisted fibrinolysis, whereas unstimulated intravascular (endothelial) cells produced

171 In unstimulated IRAP knockdown adipocytes, plasma membrane

172 Here we demonstrate that in unstimulated J774A.1 macrophages, caspase-1 and Nalp1b a

173 We show that modulation of UBASH3A levels in unstimulated Jurkat cells leads to altered amounts of to

174 The ability to isolate unstimulated latent cells from infected individuals enab

175 emonstrated that CK11 is not chemotactic for unstimulated leukocyte populations from central immune o

176 terized by shorter telomeres with high TA in unstimulated leukocytes would show signs of high allosta

177 NS produced linear increases in V(I)max from unstimulated levels at flow capture to peak flow thresho

178 h-throughput protein analysis, we found that unstimulated licensed NK cells have increased expression

179 enomic footprinting of the PRDM1 promoter in unstimulated lymphoma and myeloma cells reveals multiple

180 e range of 10 and 100 pmol per mg protein in unstimulated macrophage-like RAW 264.7 cells.

181 ar corepressor NCoR is bound to HIV-1 LTR in unstimulated macrophages and is released from the LTR af

182 are encoded on the Z chromosome of chickens, unstimulated macrophages from the female birds expressed

183 , nitric oxide (NO) and PGE(2) production in unstimulated macrophages, RAW264.7 cells.

184 Although unstimulated MC constitutively released CD9(+) EV, degra

185 ed tetramers via its transmembrane domain in unstimulated membranes and octamers in membranes stimula

186 Despite this, 50% fewer leukocytes rolled on unstimulated mesenteric venous endothelium of Tph1(-/-)

187 -HT2AR and downstream signaling molecules in unstimulated MIA prefrontal cortex (PFC).

188 ted clear changes in polarization markers in unstimulated monocytes from patients with SJIA and MAS,

189 opy, we show that baseline TLR expression in unstimulated monocytes is greater for TLR2 than for TLR8

190 ated with IFNalpha Exos or Exos derived from unstimulated monocytes.

191 and apoptotic changes in RPE cells than did unstimulated mononuclear phagocytes.

192 e fatty-acyl species of PtdIns(3,4,5)P(3) in unstimulated mouse and human cells (>/=10(5)) or tissues

193 d that some TCR microclusters are present in unstimulated murine T cells, indicating that the mechani

194 that catalytically active Lck was present in unstimulated naive T cells and thymocytes and was readil

195 We show that previously unstimulated (naive) Id-specific B and T cells collabora

196 res exhibit a random spatial distribution in unstimulated neuroendocrine PC12 cells.

197 ed ROS generation and DNA externalisation by unstimulated neutrophils.

198 sequestered in intracellular compartments in unstimulated NK cells, translocates to the cell surface

199 mide did not trigger IFN-gamma production in unstimulated NK cells.

200 endocervix and ectocervix revealed that (i) unstimulated/not activated immune cells gene sets positi

201 Cord blood mononuclear cells were cultured unstimulated or after stimulation with lipid A, peptidog

202 In this study, using unstimulated or cytokine-activated EC, we observed signi

203 ng a substrate-free NanoCulture system under unstimulated or drug pressure conditions.

204 Controls were epithelial cells that were unstimulated or exposed to conditioned medium from monoc

205 profiles of the expanded NK cells and their unstimulated or IL-2-stimulated counterparts showed mark

206 NK cells were significantly more potent than unstimulated or IL-2-stimulated NK cells against acute m

207 activated RAW264.7 cells versus the Golgi in unstimulated or ISP1-inhibited cells.

208 IL-24, canine mda-7 mRNA is not expressed in unstimulated or lipopolysaccharide (LPS), concanavalin A

209 icant increase in IL-10 levels compared with unstimulated or live P. gingivalis-stimulated cells from

210 Live imaging revealed unstimulated or purine-induced microglial motilities, in

211 monocytes and neutrophils in blood-perfused unstimulated or TNF-alpha-activated venules.

212 urite outgrowth by three-fold as compared to unstimulated or wild-type (WT) controls.

213 In stimulated versus unstimulated organoid cultures, elevated IFN-gamma reduc

214 fission yeast Schizosaccharomyces pombe than unstimulated OSPW.

215 alcium signal intensity in stimulated versus unstimulated parts.

216 ced IFN signature exhibited by the patients' unstimulated PBMCs parallels the hyperinflammatory state

217 nes and chemokines and increased survival of unstimulated PBMCs.

218 ed in HRV-stimulated PBMCs, as compared with unstimulated PBMCs.

219 significantly elevated relative to those in unstimulated PBMCs.

220 However, as compared with unstimulated pDCs, Dll4(high) i-DCs expressed higher lev

221 ABT-199 is strongly cytotoxic against unstimulated peripheral blood CLL cells in vitro but is

222 ucleotide exchange factors Tiam1 and Vav1 in unstimulated peripheral blood CLL cells with almost comp

223 In unstimulated peripheral monocytes, IFN-induced gene expr

224 for measurable voltage-gated H(+) current in unstimulated phagocytes.

225 ssessed: ADP-stimulated platelet P-selectin, unstimulated platelet fibrinogen binding, and light tran

226 PF), TRAP-stimulated platelet surface CD42b, unstimulated platelet surface P-selectin, and platelet f

227 with the cytoplasm and membrane fraction of unstimulated platelets, and these fractions were functio

228 In unstimulated platelets, we detected little to no interac

229 ge size of EVs compared to those produced by unstimulated platelets.

230 nd PP1c co-immunoprecipitated with Gbeta1 in unstimulated platelets.

231 Unstimulated PMNs express minimal quantities of surface

232 Here, we compared the ability of unstimulated primary CD4+ and CD8+ effector T cells to s

233 half-life, whereas overexpression of HuR in unstimulated primary mouse astrocytes doubles the half-l

234 7 tumor cell lines as well as stimulated and unstimulated primary murine macrophages.

235 O-357 cells, which tended to normalize to an unstimulated profile.

236 strongly inverse correlated with IFN-gamma (unstimulated, r = -0.7, P = 0.111; LpA stimulation, r =

237 n E2 increased mucin release to ~400% of the unstimulated rate.

238 one stimulated mucin release to ~300% of the unstimulated rate.

239 n nucleus accumbens (NAc) dopamine levels in unstimulated rats.

240 0 min of the equilibration period to measure unstimulated release rate.

241 und both HA and HC-HA/PTX3 were not toxic to unstimulated RPE cells.

242 (NGS) technology for profiling miRNAs in two unstimulated saliva samples collected by passive drool m

243 yme-linked immunosorbent assay (ELISA) using unstimulated saliva samples obtained from patients with

244 Clinical periodontal parameters and unstimulated saliva were collected at screening, baselin

245 saliva was lower than that to proteins from unstimulated saliva.

246 gene fold change (FC) for stimulated versus unstimulated samples or the interaction between outcome

247 Unstimulated samples showed higher analyte concentration

248 92 and 11.42 +/- 2.66 for the stimulated and unstimulated samples, respectively (p < 0.05).

249 single compartment primarily responsible for unstimulated secretion of tPA or, in cells exposed to in

250 l sensory pathway carrying excitation to the unstimulated side and record from its neurons.

251 s lesioned, swimming starts later and on the unstimulated side.

252 or is lesioned, swimming starts later on the unstimulated side.

253 nses and augmented host defense at adjacent, unstimulated skin through a nerve reflex arc.

254 WP2-FL leading to increased activity against unstimulated Smad2 and Smad3, and that Smad7 is a prefer

255 uitin ligase activity causing degradation of unstimulated Smad2 and Smad3.

256 igoadenylate synthetase (OAS) and viperin in unstimulated sputum cells in 57 asthmatics (including 16

257 calize to plasma membrane lipid rafts in the unstimulated state and that IL-1beta signals caveolin-1-

258 mean beta activity amplitude compared to the unstimulated state, this was achieved by a selective eff

259 uired for comparable effects relative to the unstimulated state.

260 the prevention of Bcl10 binding in the basal unstimulated state.

261 differences in HD monocytes in their basal, unstimulated state.

262 ing on whether their ON (stimulated) or OFF (unstimulated) steady states exhibit noise.

263 aged (21-28 months) mice, LTP was relayed to unstimulated synapses, blemishing its synapse specificit

264 nally, we harness the impedance signature of unstimulated T cells to set a boundary separating activa

265 Notably, also unstimulated T cells were stably genetically modified.

266 l as immune function was further analyzed in unstimulated T cells which were cultured in serum-free m

267 Five experimental groups were prepared: unstimulated T cells, stimulated T cells, CA46 cells, an

268 on while elevating baseline proliferation in unstimulated T cells.

269 pathways including GATA-3, MAL and FcER1 in unstimulated T-cells.

270 with an MMP-9 activity assay in 1 microL of unstimulated tear fluid.

271 y strong degranulation after an encounter of unstimulated TECs, represented by a high cell surface ex

272 appropriate targets to a greater extent than unstimulated Tib axons.

273 DeltaF508) were measured under 5 conditions: unstimulated (to determine basal secretion), stimulated

274 Unstimulated trained macrophages displayed evidence of m

275 A cleavage, but instead efficiently inhibits unstimulated transcript cleavage by RNAPII.

276 Remarkably, in unstimulated TUG-depleted cells, the exocytic rate is si

277 pheral blood mononuclear cells were cultured unstimulated (U), with phorbol 12-myristate 13-acetate/i

278 240 bpm, 0.8 V, 0.05-ms pulses) or were left unstimulated (UNSTIM; n=10).

279 ng; however, the LFA-1-dependent crawling in unstimulated venules becomes Mac-1 dependent upon inflam

280 in microvessels are neutrophils; however, in unstimulated venules, a greater percentage of the total

281 Comparing unstimulated versus TLR4-stimulated monocytes reveals 1,

282 a killing assays with thrombin-stimulated or unstimulated washed platelets and saw a similar decrease

283 Unstimulated WBCCs served as negative controls.

284 Secondary aims were to study unstimulated whole and stimulated glandular (i.e., parot

285 ients with dry mouth (DMPs) consistently had unstimulated whole mouth saliva (UWMS) spinnbarkeit belo

286 Unstimulated whole saliva (5 ml) was collected every 2 t

287 Serum and unstimulated whole saliva (UWS) collected from 92 AMI pa

288 The cytokine profile in unstimulated whole saliva (UWS) of patients with prediab

289 increased expression was correlated with low unstimulated whole saliva flow rate.

290 on were done on harvested bone particles and unstimulated whole saliva in a group of 30 patients unde

291 nterviews, anthropomorphic measurements, and unstimulated whole saliva sample collection.

292 In addition, unstimulated whole saliva samples might reflect a synerg

293 Unstimulated whole saliva samples were collected, and un

294 Unstimulated whole saliva samples were collected, unstim

295 ted whole saliva samples were collected, and unstimulated whole salivary flow rate (UWSFR) was determ

296 mulated whole saliva samples were collected, unstimulated whole salivary flow rate (UWSFR) was determ

297 hose without anti-SSA/SSB, and those with an unstimulated whole salivary flow rate of <0.1 ml/minute

298 e, 0.58-1.18] mL/min, P = 0.003), as well as unstimulated whole- and stimulated glandular flow rates

299 linical parameters (plaque/gingival indices, unstimulated whole-mouth salivary flow rate, gingival cr

300 ling by TNF-deficient macrophages to that of unstimulated wild-type macrophages.