ライフサイエンスコーパス: unstimulated

1 ere compared to a control coculture that was unstimulated.

2 translocation and enhances glucose uptake in unstimulated 3T3-L1 adipocytes, similar to insulin.

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

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

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

6 ccumulate adjacent to the plasma membrane of unstimulated adipocytes.

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

8 Simultaneously, unstimulated airway mucosal lining fluid was obtained an

9 healthy individuals have low frequencies of unstimulated alpha3(IV)NC1-reactive T cells with similar

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

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

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

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

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

15 in this study, the localization of HCF-1 in unstimulated and induced latently infected sensory neuro

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

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

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

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

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

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

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

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

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

25 n compared with the +2018TT genotype in both unstimulated and stimulated PBMCs (P=0.01 by analysis of

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

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

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

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

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

31 Mutation of lysine 3016 does not affect unstimulated ATM kinase activity but does abolish upregu

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 essed on both cytolytic lymphocytes and some unstimulated CD4+ T cells.

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

56 Although undetectable on unstimulated CD8(+) T cells, it is uniformly up-regulate

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

58 However, in every (unstimulated) cell studied to date, endogenous proton ch

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

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

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

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

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

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

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

66 7 on the IRAK-M promoter is trimethylated in unstimulated cells and that this silencing epigenetic ma

67 ls was slower than that of GFP-Stat3alpha in unstimulated cells and was slowed further following cyto

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

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

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

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

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

73 n of the NADPH oxidase or ClC-3 in otherwise unstimulated cells elicited a phenotype similar to that

74 Although unstimulated cells experienced apoptosis following anti-

75 OS-mediated priming, but basal oxidants kept unstimulated cells from becoming primed.

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

77 le in controlling centrosome organization in unstimulated cells in addition to its known function as

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

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

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

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

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

83 he intranuclear mobility of GFP-Stat3beta in unstimulated cells was slower than that of GFP-Stat3alph

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

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

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

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

88 calized and constitutively activates SOCE in unstimulated cells, displayed a relatively higher partit

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

90 In unstimulated cells, ERK-mediated negative feedback reduc

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

92 In unstimulated cells, FKBP51 forms endogenous complexes wi

93 In unstimulated cells, GLUT4 is incorporated into specializ

94 R did not differ between TLR9-stimulated and unstimulated cells, inhibition of ATM/ATR and Chk1/Chk2

95 In unstimulated cells, NF-kappaB proteins are sequestered i

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

97 In unstimulated cells, pathway activity is inhibited by the

98 of colocalization of FPR with FcepsilonRI in unstimulated cells, shown by computer simulation to be a

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

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

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

102 with proinflammatory mediators compared with unstimulated cells.

103 hagocytosed significantly more bacteria than unstimulated cells.

104 calized predominantly at lateral clusters in unstimulated cells.

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

106 well as enhanced low-level Ca2+signaling in unstimulated cells.

107 ly shuttles between cytoplasm and nucleus in unstimulated cells.

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

109 r intracellular retention of these cargos in unstimulated cells.

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

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

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

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

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

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

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

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

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

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

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

121 ed RTKs, is associated with Ret under basal, unstimulated conditions in neurons.

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

123 Under unstimulated conditions, endogenous TAK1 is stably assoc

124 In unstimulated conditions, larvae spend most of their time

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

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

127 ilar actin stress fiber staining patterns in unstimulated conditions.

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

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

130 increase in immobile integrins compared with unstimulated conditions.

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

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

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

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

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

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

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

138 degranulate and express IFN-gamma in ex vivo unstimulated culture.

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

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

141 Unstimulated DeltaF508CFTR channels or those inhibited b

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

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

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

145 burgdorferi and IFN-gamma, as compared with unstimulated endothelial monolayers.

146 ty pattern to more closely resemble control, unstimulated endothelium.

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

148 vation leads to increased phosphorylation of unstimulated EphB2, which we show is caused by down-regu

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

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

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

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

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

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

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

156 e is limb-specific: it does not occur in the unstimulated hand, nor in the ipsilateral foot.

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

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

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

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

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

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

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

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

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

166 The resultant bscAb redirected unstimulated human T cells to lyse EphA2-expressing tumo

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

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

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

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

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

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

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

174 In unstimulated IRAP knockdown adipocytes, plasma membrane

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

176 ow report a new adhesion pathway that allows unstimulated leukocytes to adhere to and migrate through

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

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

179 Conclusion: Unstimulated liver pDCs exist in a latent state with the

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

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

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

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

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

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

186 Increased PTEN expression in unstimulated MCF-7 breast cancer cells results in a 51%

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

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

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

190 milliliter concentrations in the serum from unstimulated mice, but differences in affinity and half-

191 Unstimulated microglial cells, subcultured from an astro

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

193 These enzymes are cytoplasmic in unstimulated monocytes.

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

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

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

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

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

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

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

201 CF-1 was localized to the Golgi apparatus in unstimulated neurons, a unique location for a transcript

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

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

204 Unstimulated NKCC1 was expressed on basolateral membrane

205 g siRNA-mediated knockdown of either gene in unstimulated OA cartilage.

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

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

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

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

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

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

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

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

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

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

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

217 fission yeast Schizosaccharomyces pombe than unstimulated OSPW.

218 tatin reduced (i) the human PBMC response to unstimulated (P<0.05) and (ii) the human and baboon PBMC

219 alcium signal intensity in stimulated versus unstimulated parts.

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

221 significantly elevated relative to those in unstimulated PBMCs.

222 nes and chemokines and increased survival of unstimulated PBMCs.

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

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

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

226 In unstimulated peripheral monocytes, IFN-induced gene expr

227 evels of proinflammatory gene transcripts in unstimulated peripheral-blood neutrophils and mononuclea

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

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

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

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

232 In unstimulated platelets, we detected little to no interac

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

234 Unstimulated PMNs express minimal quantities of surface

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

236 t in vivo on the CSF-1R proximal promoter in unstimulated primary macrophages.

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

238 7 tumor cell lines as well as stimulated and unstimulated primary murine macrophages.

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

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

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

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

243 0 min of the equilibration period to measure unstimulated release rate.

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

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

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

247 92 and 11.42 +/- 2.66 for the stimulated and unstimulated samples, respectively (p < 0.05).

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

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

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

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

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

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

254 olated from wild-type mice, as compared with unstimulated SMCs.

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

256 ma) and CD107a expression by NK cells in the unstimulated state and after stimulation by the major hi

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

258 igher IFN-gamma and CD107a expression in the unstimulated state compared to those who do not possess

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

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 pproximately 40% of the total ADF/cofilin in unstimulated tissues is phosphorylated.

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

275 Unstimulated total ROS levels did not differ between pat

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 cy results in increased leukocyte rolling on unstimulated veins and increased leukocyte adhesion in i

280 e number of leukocytes rolling per minute in unstimulated veins was increased by 2.5-fold in Prdx1(-/

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

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

283 Comparing unstimulated versus TLR4-stimulated monocytes reveals 1,

284 Unstimulated WBCCs served as negative controls.

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

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

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

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

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

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.