ライフサイエンスコーパス: conditioned medium

1 ppression of Ly6C(high) cells induced by GEM-conditioned medium.

2 butors to fibroblast migration caused by HRV-conditioned medium.

3 or stimulated with amoeba-derived cell-free conditioned medium.

4 ium with Wnt5a activity, and FrzB containing conditioned medium.

5 ve bone into DBM affects the activity of the conditioned medium.

6 00- to 1000-nm diameter) or vesicle-depleted conditioned medium.

7 pon trophic factors present in Lymnaea brain-conditioned medium.

8 N)-beta neutralizing antibody to MLO-Y4 cell conditioned medium.

9 lturing with U937 cells and exposure to U937-conditioned medium.

10 tect natural, cell-derived AbetaO present in conditioned medium.

11 blocked by depleting CXCL1 and IL-8 from the conditioned medium.

12 6 conditioned medium and lower in the APP-KO conditioned medium.

13 (iii) It decreased the amount of HA in the conditioned medium.

14 the cardioprotective effects of shPHD2-ADSC-conditioned medium.

15 TF reduced the astrogenic effects of YAP 5SA-conditioned medium.

16 s, or by culturing LNCaP cells in adipocytes-conditioned medium.

17 r the secretome of PRF membranes, termed PRF conditioned medium.

18 tokines in the presence of S. aureus biofilm-conditioned medium.

19 n response to LLC or C26 adenocarcinoma cell conditioned medium.

20 s and cultured with DMEM or endothelial cell-conditioned medium.

21 when presented to Torso-expressing cells in conditioned medium.

22 ding a TGFbeta1-neutralizing antibody in the conditioned-medium.

23 lactic acid, since pH neutralization of the conditioned medium aborted the antibacterial effect.

24 We found that astrocyte conditioned medium (ACM) applied directly to tumor cells

25 days in the absence or presence of astrocyte-conditioned medium (ACM).

26 otective signal present in retinal astrocyte conditioned medium (ACM).

27 cient to activate the inflammasome, as wound-conditioned medium activates caspase-1 and induces relea

28 Here we show that p40-conditioned medium activates EGFR in young adult mouse c

29 In vitro studies revealed that AEC-conditioned medium (AEC-CM) enhanced AM SOCS3 secretion

30 Myocilin-containing conditioned medium also increased proliferation of unmod

31 Notably, activated-microglia-conditioned medium altered metabolism in cINs and iPSCs

32 ne the isoelectric point of Wnt3A protein in conditioned medium and after purification and applied th

33 This protocol describes how to prepare conditioned medium and how to culture stem cell-enriched

34 ion in axonal growth when incubated in HUVEC-conditioned medium and in direct co-culture with HUVECs.

35 CD55 expression in HCV-infected cell culture-conditioned medium and inhibits C3 convertase activity.

36 vels of cystatin C were higher in the Tg2576 conditioned medium and lower in the APP-KO conditioned m

37 K increased collagen degradation in pericyte-conditioned medium and purified type IV collagen.

38 thy articular chondrocytes release ACVs into conditioned medium and show significant levels of ongoin

39 ation was potently induced by PDGF-D and CCA conditioned medium and was significantly inhibited by PD

40 tuberculosis-infected macrophages using Wnt6 conditioned medium and Wnt6-deficient macrophages uncove

41 re supernatants of live schistosome egg (egg-conditioned medium), and in particular by IPSE/alpha-1,

42 MSC cultures was less angiogenic than PA MSC conditioned medium, and had little effect on endothelial

43 MDSCs could be enhanced by exposure to tumor-conditioned medium, and IL1beta was identified as one of

44 for gametocyte production by the addition of conditioned medium, and they are then exposed to the tre

45 data revealed that bacterial-fungal derived conditioned medium (BF-CM) significantly increased the g

46 Co-cultured BMFs or BMF-conditioned medium (BMF-CM) induced the formation of sph

47 ion from the cell-associated matrix into the conditioned medium, but primarily by inducing HA synthes

48 MSC migration was stimulated by epithelial-conditioned medium, but was significantly inhibited by e

49 e of cell culture and ENP isolation from the conditioned medium by ultracentrifugation (UC) can take

50 STAT5A-induced PRL in the conditioned medium can activate STAT5, STAT1, and to a l

51 to release MCP-1, MIP1alpha, and RANTES into conditioned medium causing HSC chemotaxis, which was inh

52 igodendrocyte lines induced MN death through conditioned medium (CM) and in coculture.

53 ion of human satellite cells (HMuSC) using a conditioned medium (CM) cell culture model.

54 We have found that conditioned medium (CM) collected from painful SWN tumor

55 Here, we have shown that conditioned medium (CM) containing gelsolin fragments or

56 The activities of suPAR were replicated by conditioned medium (CM) from EGFRvIII-positive GBM cells

57 Furthermore, conditioned medium (CM) from embryonic endothelial proge

58 ytes (BMMs) and OBs after treatment with the conditioned medium (CM) from lamin A/C-deficient muscle

59 nd that CD169 labels M1 macrophages and that conditioned medium (CM) from M1 macrophages, but not fro

60 Conditioned medium (CM) from Ocy454 (both Gsalpha(cont)

61 Conditioned medium (CM) from PA-treated PRHs was applied

62 Conditioned medium (CM) from RANKL-treated WT, but not K

63 When hepatocytes were pretreated with conditioned medium (CM) from RAW 264.7 or Kupffer cells

64 Conditioned medium (CM) from senescent human preadipocyt

65 Conditioned medium (CM) from stationary-phase cultures o

66 TNF-alpha-activated EC-conditioned medium (CM) increased transmigration across

67 cells express all 19 Wnts and CD8(+) T cell-conditioned medium (CM) induced canonical Wnt signaling

68 (miPSCs) for four weeks in the presence of a conditioned medium (CM) of cancer cell lines, which func

69 aluated the effects of O. formigenes culture conditioned medium (CM) on apical (14)C-oxalate uptake b

70 n vitro with a papillary TC or ATC cell line conditioned medium (CM) or with a normal thyroid CM as c

71 We show that injection of HLSCs and of HLSC-conditioned medium (CM) significantly attenuates mouse m

72 The U937 Mvarphi-conditioned medium (CM) significantly decreased the tran

73 igated the trophic potential of DPSC-derived conditioned medium (CM) to protect and regenerate isolat

74 After 3 to 14 d, conditioned medium (CM) was collected.

75 LIF was elevated in C26 conditioned medium (CM), but IL-6, OSM, TNFalpha, and my

76 d inhibited adipocyte UCP1 mRNA induction by conditioned medium (CM).

77 on, THP-1 macrophages were treated with HMEC-conditioned medium (CM).

78 WT but not Porcn-null bone marrow macrophage-conditioned medium (CM).

79 rafenib in the presence of Ln-332 and of HSC conditioned medium (CM).

80 erapeutic potential of mesenchymal stem cell-conditioned medium (CM-MSC) as an alternative to cell th

81 Astrocyte-conditioned medium collected from DS astroglia causes to

82 Direct treatment of fibroblasts with conditioned medium collected from stratified keratinocyt

83 a constitutively active YAP mutant, and the conditioned medium collected from these cells activated

84 ells failed to form tubes in the presence of conditioned medium collected from TNF-alpha-stimulated P

85 more, immunodepletion of cystatin C from the conditioned medium completely removed the ability of the

86 Exosomes isolated from neuron-conditioned medium contain abundant microRNAs and small

87 Further, we used conditioned medium containing eGFP-Wnt-3a to visualize i

88 Breast cancer-derived conditioned medium containing elevated concentrations of

89 Interestingly, we found that pituitary-conditioned medium contains a factor that inhibits actio

90 We verified that neurofibroma SC conditioned medium contains macrophage chemo-attractants

91 T cells, TCR-stimulated under a tolerogenic conditioned medium, could be ex vivo reprogrammed to FOX

92 Double conditioned medium (DCM) from the activated THP-1 cells

93 phatase to cell cultures or stationary phase conditioned medium decreases polyphosphate levels and ab

94 small interfering RNA suppresses MKalpha3(+) conditioned medium-dependent induction of Cox-2 expressi

95 talized HSCs (LX2 cells) were incubated with conditioned medium derived from HCV-exposed human macrop

96 Conditioned medium derived from macrophages increased th

97 Additionally, treatment either with conditioned medium derived from myofibroblasts or with h

98 Further, conditioned medium derived from NF-kappaB activated LNCa

99 Mass spectrometry analysis of conditioned medium derived from PIFA-stimulated splenic

100 Conditioned medium derived from RLIP76-depleted tumor ce

101 +) cells cultured in HNSCC cell line-derived conditioned medium differentiated into myeloid derived s

102 The activity of conditioned medium directly correlated with radiation-in

103 Tumor-conditioned medium down-regulated C/EBPalpha expression,

104 However, the hHF-MSC conditioned medium enhanced cell organization and multil

105 port of M2 polarization, PRF lysates and PRF conditioned medium enhanced the expression of arginase-1

106 Transwell and conditioned-medium experiments showed that MDSCs inhibit

107 On starvation, the cells secrete conditioned medium factors that initiate cAMP signal tra

108 dance was selectively elevated in the active conditioned medium fraction.

109 stinal stem cells can be propagated by using conditioned medium from a supportive cell line (L-WRN).

110 Cellular PIgR expression was induced by conditioned medium from activated human leukocytes, as w

111 increased in cardiac fibroblasts exposed to conditioned medium from aldosterone-treated cardiomyocyt

112 We also found that conditioned medium from alpha3-expressing mouse keratino

113 Conditioned medium from amebic parasites contained parti

114 Conditioned medium from antigen-stimulated bone marrow-d

115 Finally, conditioned medium from astrocytes in which HuR or TDP-4

116 The conditioned medium from B16F10 cultures induced the acti

117 Conditioned medium from both conditions were tested as c

118 ng mouse induced pluripotent stem cells with conditioned medium from breast cancer cell lines.

119 growth or differentiation in the presence of conditioned medium from breast cancer cells, but under t

120 Finally, conditioned medium from C1P-stimulated keratinocytes sho

121 C2C12 myotubes treated with conditioned medium from C26 cancer cells induced atrophy

122 -supported angiogenesis, we also showed that conditioned medium from CAF treated with E2 and G-1 prom

123 Conditioned medium from CD271+ MSC cultures was less ang

124 Conditioned medium from cells exposed to 17-HDHA inhibit

125 Conditioned medium from cells expressing NT-PGC-1alpha r

126 enic differentiation of precursor cells than conditioned medium from chondrocytes treated with IL-1be

127 This phenotype is rescued by conditioned medium from control muscle cells and by reco

128 EA.hy926 cells treated with conditioned medium from Corin-deficient HK-2 cells had i

129 nthase (eNOS) in EA.hy926 cells treated with conditioned medium from Corin-siRNA- or ANP-siRNA-transf

130 Moreover, conditioned medium from CR-treated cells transmits the l

131 We then assessed MSC migration induced by conditioned medium from CRE-challenged human epithelium

132 Similarly, conditioned medium from CSCs cultured from the cardiac b

133 Conditioned medium from CSCs of patients with diabetes m

134 Conditioned medium from cytokine-treated smooth muscle c

135 is model, resuspension of wild-type cells in conditioned medium from DeltabsrA cultures also resulted

136 Conditioned medium from ERalpha-null adipocytes and medi

137 Conditioned medium from F. nucleatum-infected HCT116 cel

138 Conditioned medium from fibroblasts and CAFs enhanced Er

139 inib provided by these growth factors and by conditioned medium from fibroblasts that produce NRG1 an

140 The conditioned medium from fibrocyte-like cells (FcCM) has

141 e number of IL-10(+) CD4(+) T cells, and the conditioned medium from FSD-C10-treated microglia promot

142 We also show that astrogliosis-conditioned medium from GAP43 knock-down astrocytes inhi

143 from monocytes/microglial cells treated with conditioned medium from glioma cells.

144 In contrast, conditioned medium from GM-CSF-treated murine macrophage

145 Here we show that conditioned medium from HCC cell lines, Hep3B and HepG2,

146 a neutralizing antibody, when incubated with conditioned medium from HCV-infected hepatocytes, inhibi

147 Conditioned medium from HCV-infected hepatoma cells (Huh

148 Next, we demonstrated that conditioned medium from HCV-infected human hepatocytes a

149 f WT bone marrow stromal cells cultured with conditioned medium from Hdac3-deficient osteoclasts was

150 Conditioned medium from HPMCs cultured with IL-6 and sIL

151 We sought to investigate whether conditioned medium from HRV-infected epithelial cells ca

152 Most importantly, we show that conditioned medium from human reactive A1-like astrocyte

153 Finally, conditioned medium from IL-1beta and P15-1-treated human

154 Mass spectrometric analysis of conditioned medium from immortalized keratinocytes showe

155 Conditioned medium from injured, 1,25-VitD3-treated arte

156 tuberculosis-infected macrophages exposed to conditioned medium from KGF-treated alveolar type II cel

157 addition, an anti-inflammatory effect of the conditioned medium from Lactobacillus rhamnosus L34 was

158 isassemble late in their life cycle and that conditioned medium from late-stage biofilms inhibits bio

159 tal cancer cells or systemic delivery of the conditioned medium from LOX-overexpressing colorectal ca

160 that M1 macrophage apoptosis was promoted by conditioned medium from macrophages polarized into an M2

161 Conditioned medium from mesenchymal stem cells (MSC-CM)

162 The in vivo Matrigel plug assay showed that conditioned medium from miR-184-expressing HLEKs elicite

163 Human dermal microvascular cells exposed to conditioned medium from miR-184-overexpressing HLEKs wer

164 In the bone marrow cell culture, the conditioned medium from MLO-Y4 cells decreased the capab

165 n bronchial epithelials were stimulated with conditioned medium from monocytes infected with virulent

166 l cells that were unstimulated or exposed to conditioned medium from monocytes not exposed to TB.

167 Mouse serum rich in irisin and the conditioned medium from myotubes exposed to palmitate fo

168 Conditioned medium from native bone chips can activate t

169 Conditioned medium from NICD3-expressing cells enhanced

170 We also found that conditioned medium from nociceptors treated with the wel

171 hagy modulators on ACV number and content in conditioned medium from normal adult porcine and human o

172 Recombinant Nuc and conditioned medium from Nuc-containing N. gonorrhoeae de

173 Conditioned medium from optogenetically stimulated corti

174 Conditioned medium from organoids induced neutrophil mig

175 docosahexaenoic acid) were increased in the conditioned medium from peroxisome-induced macrophages,

176 Conditioned medium from PS1 null neuronal cultures at 8

177 Conditioned medium from rat brain slice cultures with ne

178 Recombinant VEGF added to conditioned medium from RLIP76-knockdown tumor cells res

179 Conditioned medium from senescent cells treated with ant

180 Conditioned medium from shPHD2-ADSCs decreased cardiomyo

181 Conversely, conditioned medium from Spg-miR145-transfected non-TICs/

182 ion in unpolarized monocytes stimulated with conditioned medium from spinal-injured tissue explants.

183 Conditioned medium from stretched AVICs was sufficient t

184 Conditioned medium from TECs exposed to the virulent Rlo

185 Conditioned medium from the intact smooth muscle of the

186 Conditioned medium from these cells failed to support CT

187 cells showed increased secretion of bFGF and conditioned medium from these cells induced increased an

188 Conditioned medium from these macrophages was antichlamy

189 Conditioned medium from TKO microglia cultures inhibits

190 itogenic T-cell clone (LCN-8), we found that conditioned medium from TNF-stimulated Gal-9(+/+) but no

191 response, but an increase in Vegfa+Ang2- or conditioned medium from tumor cell-stimulated cellular/a

192 We performed secretome analysis of the conditioned medium from tumor-induced bone to identify p

193 effect of peripheral blood mononuclear cell conditioned medium from vaccinated cattle upon apical-ba

194 Conditioned medium from W(sh)/W(sh) osteoclasts had elev

195 ld be restored following incubation with Tat-conditioned medium from wild-type DCs, (vi) impaired the

196 Conditioned-medium from NF2-null ACs or exogenous NRG1 s

197 SC-derived smooth muscle-like cells or their conditioned medium further increased the induction of VC

198 R-29 conditioned medium, whereas pre-miR-30c conditioned medium had a prohypertrophic effect.

199 Conditioned medium harvested from IL1R2-overexpressing C

200 tro studies demonstrated that senescent-cell conditioned medium impaired osteoblast mineralization an

201 uction of myeloid cells induced by adipocyte-conditioned medium in vitro.

202 hymal stromal cells or with their secretome (conditioned medium) in a transwell system.

203 PMF-conditioned medium increased the migration and tubulogen

204 ulturing primary mouse cardiomyocytes in LEC-conditioned medium increases cardiomyocyte proliferation

205 Endothelial cell-conditioned medium induced downregulation of miR-145 in

206 migration of fibroblasts, but only adipocyte conditioned medium induced fibroblast differentiation in

207 found that both adipocyte and pre-adipocyte conditioned medium induced the migration of fibroblasts,

208 Furthermore, a testis-conditioned medium induced the migration of REH and NALM

209 Adipocyte-conditioned medium-induced CD11b(+)Gr1(+) cells express

210 F-differentiated macrophages and in melanoma-conditioned medium-induced macrophages (MCMI/Mphi) in co

211 from IL-1 receptor knockout mice blocked the conditioned medium-induced upregulation of proinflammato

212 h OP9 stromal cells, we found that adipocyte-conditioned medium induces the generation of CD11b(+)Gr1

213 Here, we demonstrate that neuron-conditioned medium induces the transcriptionally mediate

214 ng specific siRNAs we observed that LLC cell-conditioned medium (LCM)-treated C2C12 myotubes underwen

215 eated THP-1 macrophages to IGFBP-3-deficient conditioned medium led to a 20-fold increase in palmitat

216 Within epithelial cell-conditioned medium, low amounts of glucocorticoids were

217 ced, 5823 +/- 2192 MMP14-positive MVs/muL of conditioned medium; means +/- SEM; n = 6; P < 0.01).

218 etion of lcn2 by immunoprecipitation reduced conditioned medium-mediated neurotoxicity.

219 -167 cell lines) were stimulated by IL-6, MF-conditioned medium (MF-CM) or MFs, with or without TGF-b

220 ocytes activated with MDP in the presence of conditioned medium obtained from CD3 bead-isolated T cel

221 Moreover, conditioned medium obtained from commercial human DBM mo

222 l fibroblasts were exposed to the respective conditioned medium obtained from DBM (DBCM).

223 Strikingly, conditioned medium obtained from developing oligodendroc

224 opic Indian clade C HIV-1 (93IN101) from the conditioned medium of 293 cells.

225 Soluble c-Met was studied in the conditioned medium of 9 uveal melanoma cell lines and in

226 e of ribosomes and full-length tRNAs in cell-conditioned medium of a variety of mammalian cell lines.

227 a because in vitro studies demonstrated that conditioned medium of both mouse and human wounds upregu

228 his fragmentation event is released into the conditioned medium of cells expressing recombinant NOTCH

229 Reporters secreted into the conditioned medium of cells in culture or into blood in

230 ost abundant labeled protein detected in the conditioned medium of choroid or sclera had an apparent

231 5A-dependent proangiogenic activity from the conditioned medium of EC.

232 ncreased in endothelial cells exposed to the conditioned medium of FHL2(-/-) versus wild-type (WT) EO

233 The conditioned medium of GEM-treated tumor cells enhances d

234 tly, CD33(+) myeloid and T cells cultured in conditioned medium of HNSCC cells in which Sema4D was kn

235 Conditioned medium of IL-12-incubated cells proved to co

236 Conditioned medium of inflammasome-activated RPE cells p

237 Accordingly, conditioned medium of isolated acinar cells from old WT

238 Co-precipitation of serglycin from conditioned medium of MM cells using a CD44-Fc chimera s

239 We searched for tau in the conditioned medium of N2a cells, induced pluripotent ste

240 4 in the lungs of OxPAPC-treated mice and in conditioned medium of OxPAPC-exposed pulmonary endotheli

241 llular domain (sVLDLR-N) was detected in the conditioned medium of retinal pigment epithelial cells,

242 F-1) levels were significantly higher in the conditioned medium of shPHD2-ADSCs versus ADSCs, and dep

243 t, Endoplasmic Reticulum/Golgi apparatus and conditioned medium of T24 vs. its metastatic subclone T2

244 We also set up cocultures between a conditioned medium of treated keratinocytes and naive T

245 in the serum samples from pregnant women or conditioned medium of trophoblast cells promoted endomet

246 The conditioned medium of uveal melanoma cell lines and the

247 atory effects of ERalpha-deficient adipocyte-conditioned medium on BrCA cells was reversed by Lcn2 de

248 This effect was inhibited by incubation with conditioned medium or exosomes (40- to 100-nm diameter)

249 Exosomes purified from either conditioned medium or human plasma could partially rescu

250 in ultracentrifugation supernatants of cell-conditioned medium or mammalian blood serum.

251 In contrast, cFb-conditioned medium or transwell coculture did not signif

252 s alone or in the presence of autologous PMN-conditioned medium (PCM) on poly(ethylene glycol) hydrog

253 he angiogenic properties of endothelial cell-conditioned medium-preconditioned ASCs; whereas, overexp

254 eted MMP9 under pathological conditions, and conditioned medium prepared from the stressed OPCs weake

255 Conditioned medium prepared from YAP 5SA-expressing cell

256 carried out by simple fine filtering of cell-conditioned medium prior to a non-NTA-determined (i.e.,

257 BMP4, identified in PDX-conditioned medium, promoted EC-to-OSB conversion of 2H1

258 Furthermore, mature adipocyte conditioned medium promotes MM growth, whereas co-cultur

259 ally, adding ANP to the Corin-deficient HK-2 conditioned medium rescued the above defects, indicating

260 by AKR1B10-overexpressing keratinocytes into conditioned medium resulted in up-regulation of transfor

261 After removal of activated-microglia-conditioned medium, SCZ cINs but not HC cINs showed prol

262 human amniotic mesenchymal stromal cells or conditioned medium showed comparable protective effects

263 cells, we demonstrate that S. aureus biofilm-conditioned medium significantly attenuated the capacity

264 that treatment of endothelial cells with EVT conditioned medium significantly increased production of

265 ophages co-cultured with cancer cells or TAM-conditioned medium significantly reduced apoptosis and a

266 The addition of anti-Sema4D Ab to HNSCC conditioned medium significantly reduced the expansion o

267 nocytes, or addition of IL-10-containing M14-conditioned medium, significantly enhanced their express

268 Trunk and Torso-like were also taken up from conditioned medium specifically by cells expressing Tors

269 s showed that second-trimester human decidua conditioned medium stimulated transendothelial PMN invas

270 In co-culture and conditioned medium studies, cMSCs markedly inhibited hum

271 l-filtration chromatography, we identified a conditioned medium subfraction, which specifically displ

272 5-blocking Ab inhibited erythrocyte lysis by conditioned medium, suggesting that CD55/sCD55 impairs c

273 PMSC-conditioned medium suppressed caspase activity in apopto

274 Recombinant TGF-beta1 or tumour cell conditioned medium (TCM) elevated alpha-SMA, calponin 1

275 urther, aerobactin was the primary factor in conditioned medium that enhanced the growth/survival of

276 ese cultures in the fully defined serum-free conditioned medium that is required to sustain organoid

277 g gamma rays, and is the major factor in the conditioned medium that leads to the inhibition of cell

278 We report here that PRF lysates and PRF conditioned medium, the latter containing the secretome,

279 f prechordal mesoderm microcultures to Nodal-conditioned medium, the Nodal inhibitor CerS, or to an A

280 Addition of conditioned medium to fresh and low cell density culture

281 medium completely removed the ability of the conditioned medium to increase NSPC proliferation.

282 om microglial cells treated with glioma cell-conditioned medium to induce angiogenesis.

283 in PAECs and inhibited the capacity of PAEC-conditioned medium to induce the proliferation of pulmon

284 direct coculture and direct addition of PMSC-conditioned medium to the staurosporine-induced apoptoti

285 wn, but we demonstrate that endothelial cell conditioned medium upregulates these genes in ex vivo fr

286 -/anti-miR of miR-29b and miR-30c, and their conditioned medium was analyzed by mass spectrometry.

287 HRV-conditioned medium was chemotactic for fibroblasts.

288 The pericyte-conditioned medium was collected and the collagen proteo

289 and (3) the proneurogenic effect of TgCRND8-conditioned medium was counteracted by blockade of the r

290 Keratinocyte-conditioned medium was insufficient to induce this pheno

291 Consistent with these experiments, conditioned medium was shown to induce and maintain cond

292 HUVEC-conditioned medium was sufficient to enhance axonal grow

293 Experiments in which conditioned medium was swapped between cultures showed t

294 Using nonpropagating viruses or conditioned medium, we demonstrate a paracrine effector

295 ryonic stem cells atrophied under pre-miR-29 conditioned medium, whereas pre-miR-30c conditioned medi

296 e detected WT MESD in cell lysate but not in conditioned medium, whereas the converse was true for mu

297 heparin or heparan sulfate, pretreatment of conditioned medium with heparinase III, or growth of cel

298 tein induction were analzyed after butryate, conditioned medium with Wnt5a activity, and FrzB contain

299 tion were unaffected by the presence of PBMC conditioned medium, with no observable differences betwe

300 ar cells (PBMCs) pretreated with Whole Smoke-Conditioned Medium (WS-CM) or Smokeless Tobacco Extracts