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1 ve bone into DBM affects the activity of the conditioned medium.
2 00- to 1000-nm diameter) or vesicle-depleted conditioned medium.
3 pon trophic factors present in Lymnaea brain-conditioned medium.
4 N)-beta neutralizing antibody to MLO-Y4 cell conditioned medium.
5 tect natural, cell-derived AbetaO present in conditioned medium.
6 6 conditioned medium and lower in the APP-KO conditioned medium.
7   (iii) It decreased the amount of HA in the conditioned medium.
8  the cardioprotective effects of shPHD2-ADSC-conditioned medium.
9 ns and secreted nerve growth factor (NGF) in conditioned medium.
10  when presented to Torso-expressing cells in conditioned medium.
11 ggered by oligomer-enriched APP(LDN)-derived conditioned medium.
12 ing their bone marrow cells in IL-3-enriched conditioned medium.
13 mal cell line End2 by co-aggregation or End2-conditioned medium.
14  also occurred to a lesser extent with glial conditioned medium.
15 REF feeder layers could be replaced with REF conditioned medium.
16 butors to fibroblast migration caused by HRV-conditioned medium.
17  or stimulated with amoeba-derived cell-free conditioned medium.
18 ium with Wnt5a activity, and FrzB containing conditioned medium.
19 ding a TGFbeta1-neutralizing antibody in the conditioned-medium.
20                      We found that astrocyte conditioned medium (ACM) applied directly to tumor cells
21 E13 brainstem slices together with astrocyte-conditioned medium (ACM) obtained from E16 brainstems an
22 otective signal present in retinal astrocyte conditioned medium (ACM).
23 days in the absence or presence of astrocyte-conditioned medium (ACM).
24 cient to activate the inflammasome, as wound-conditioned medium activates caspase-1 and induces relea
25                        Here we show that p40-conditioned medium activates EGFR in young adult mouse c
26           In vitro studies revealed that AEC-conditioned medium (AEC-CM) enhanced AM SOCS3 secretion
27                                     Cells or conditioned medium after light exposure induced apoptosi
28                          Myocilin-containing conditioned medium also increased proliferation of unmod
29 ne the isoelectric point of Wnt3A protein in conditioned medium and after purification and applied th
30       This protocol describes how to prepare conditioned medium and how to culture stem cell-enriched
31 ion in axonal growth when incubated in HUVEC-conditioned medium and in direct co-culture with HUVECs.
32 CD55 expression in HCV-infected cell culture-conditioned medium and inhibits C3 convertase activity.
33 vels of cystatin C were higher in the Tg2576 conditioned medium and lower in the APP-KO conditioned m
34 n-1, present in large amounts in lung cancer conditioned medium and lung cancer patient sera, mimicke
35 ely abrogated the inductive effects of tumor-conditioned medium and PGE2 on p19 transcription, wherea
36 K increased collagen degradation in pericyte-conditioned medium and purified type IV collagen.
37 AGE), inhibited responses to cell debris and conditioned medium and reduced the numbers of migrating
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 ponsible because TSP1 mimicked the effect of conditioned medium, and gabapentin, a high-affinity anta
42 otaxis assays and responded to cell lysates, conditioned medium, and HMGB-1.
43 for gametocyte production by the addition of conditioned medium, and they are then exposed to the tre
44  data revealed that bacterial-fungal derived conditioned medium (BF-CM) significantly increased the g
45                      Co-cultured BMFs or BMF-conditioned medium (BMF-CM) induced the formation of sph
46 ion from the cell-associated matrix into the conditioned medium, but primarily by inducing HA synthes
47   MSC migration was stimulated by epithelial-conditioned medium, but was significantly inhibited by e
48                    STAT5A-induced PRL in the conditioned medium can activate STAT5, STAT1, and to a l
49 to release MCP-1, MIP1alpha, and RANTES into conditioned medium causing HSC chemotaxis, which was inh
50 igodendrocyte lines induced MN death through conditioned medium (CM) and in coculture.
51                                              Conditioned medium (CM) collected from immortalized huma
52 e results obtained from cultivating ECs with conditioned medium (CM) collected from macrophages sugge
53                     Here, we have shown that conditioned medium (CM) containing gelsolin fragments or
54   The activities of suPAR were replicated by conditioned medium (CM) from EGFRvIII-positive GBM cells
55                                 Furthermore, conditioned medium (CM) from embryonic endothelial proge
56 nd that CD169 labels M1 macrophages and that conditioned medium (CM) from M1 macrophages, but not fro
57                                              Conditioned medium (CM) from PA-treated PRHs was applied
58                                              Conditioned medium (CM) from RANKL-treated WT, but not K
59        When hepatocytes were pretreated with conditioned medium (CM) from RAW 264.7 or Kupffer cells
60                                              Conditioned medium (CM) from senescent human preadipocyt
61                                              Conditioned medium (CM) from stationary-phase cultures o
62 e cultured with angiogenic growth factors or conditioned medium (CM) from uNK cells or EVT or uNK cel
63                       TNF-alpha-activated EC-conditioned medium (CM) increased transmigration across
64                                              Conditioned medium (CM) of tumor-activated EMPhis (tEMPh
65 aluated the effects of O. formigenes culture conditioned medium (CM) on apical (14)C-oxalate uptake b
66  We show that injection of HLSCs and of HLSC-conditioned medium (CM) significantly attenuates mouse m
67                             The U937 Mvarphi-conditioned medium (CM) significantly decreased the tran
68                                              Conditioned medium (CM) was collected from adult and fet
69                             After 3 to 14 d, conditioned medium (CM) was collected.
70                      LIF was elevated in C26 conditioned medium (CM), but IL-6, OSM, TNFalpha, and my
71 d inhibited adipocyte UCP1 mRNA induction by conditioned medium (CM).
72 on, THP-1 macrophages were treated with HMEC-conditioned medium (CM).
73 WT but not Porcn-null bone marrow macrophage-conditioned medium (CM).
74 rafenib in the presence of Ln-332 and of HSC conditioned medium (CM).
75 erapeutic potential of mesenchymal stem cell-conditioned medium (CM-MSC) as an alternative to cell th
76                                    Astrocyte-conditioned medium collected from DS astroglia causes to
77         Direct treatment of fibroblasts with conditioned medium collected from stratified keratinocyt
78 ells failed to form tubes in the presence of conditioned medium collected from TNF-alpha-stimulated P
79  delayed time points (6 h and 24 h), whereas conditioned medium collected from TNF-alpha-treated NPCs
80 more, immunodepletion of cystatin C from the conditioned medium completely removed the ability of the
81                Exosomes isolated from neuron-conditioned medium contain abundant microRNAs and small
82 d fragments of 25, 21, 18, and 13 kDa, while conditioned medium contained full length 38- and a 21-kD
83                        Breast cancer-derived conditioned medium containing elevated concentrations of
84       Interestingly, we found that pituitary-conditioned medium contains a factor that inhibits actio
85             We verified that neurofibroma SC conditioned medium contains macrophage chemo-attractants
86                                       Double conditioned medium (DCM) from the activated THP-1 cells
87  measure the responses to chemokines, injury-conditioned medium, dead cell debris, and high mobility
88 phatase to cell cultures or stationary phase conditioned medium decreases polyphosphate levels and ab
89                                 Furthermore, conditioned medium derived from eNOS(-/-) glomerular end
90 talized HSCs (LX2 cells) were incubated with conditioned medium derived from HCV-exposed human macrop
91             Injection of mice with cell-free conditioned medium derived from hypoxic mammary tumor ce
92                                              Conditioned medium derived from macrophages increased th
93                                              Conditioned medium derived from mPGES-1-deficient macrop
94          Additionally, treatment either with conditioned medium derived from myofibroblasts or with h
95                                     Further, conditioned medium derived from NF-kappaB activated LNCa
96                Mass spectrometry analysis of conditioned medium derived from PIFA-stimulated splenic
97                                              Conditioned medium derived from RLIP76-depleted tumor ce
98 (+) CPCs in a dose-dependent manner, but the conditioned medium did not, indicating that direct conta
99 +) cells cultured in HNSCC cell line-derived conditioned medium differentiated into myeloid derived s
100 hen cultured in the presence of fetal kidney conditioned medium, differentiated along mesenchymal lin
101                              The activity of conditioned medium directly correlated with radiation-in
102                                        Tumor-conditioned medium down-regulated C/EBPalpha expression,
103 tment of BM mononuclear cells with adipocyte conditioned medium dramatically inhibited their differen
104                         However, the hHF-MSC conditioned medium enhanced cell organization and multil
105                                Transwell and conditioned-medium experiments showed that MDSCs inhibit
106             On starvation, the cells secrete conditioned medium factors that initiate cAMP signal tra
107 MM cells grown in the presence of UB-derived conditioned medium failed to undergo differentiation.
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 actor (BDNF) released nitric oxide (NO), and conditioned medium from activated astrocytes had detrime
111  increased in cardiac fibroblasts exposed to conditioned medium from aldosterone-treated cardiomyocyt
112                                              Conditioned medium from antigen-stimulated bone marrow-d
113                                     Finally, conditioned medium from astrocytes in which HuR or TDP-4
114                                          The conditioned medium from B16F10 cultures induced the acti
115                                              Conditioned medium from both conditions were tested as c
116 ng mouse induced pluripotent stem cells with conditioned medium from breast cancer cell lines.
117        To model breast cancer TAMs in vitro, conditioned medium from breast cancer cells was used to
118 growth or differentiation in the presence of conditioned medium from breast cancer cells, but under t
119                                     Finally, conditioned medium from C1P-stimulated keratinocytes sho
120                  C2C12 myotubes treated with conditioned medium from C26 cancer cells induced atrophy
121                            We found that the conditioned medium from CA-STAT5A but not from dominant-
122       Similarly, the ability of concentrated conditioned medium from CA-STAT5A transfected EC to indu
123                                We found that conditioned medium from CA-STAT5A- but not from DN-STAT5
124 -supported angiogenesis, we also showed that conditioned medium from CAF treated with E2 and G-1 prom
125                                              Conditioned medium from cells exposed to 17-HDHA inhibit
126                                              Conditioned medium from cells expressing NT-PGC-1alpha r
127                                              Conditioned medium from cells pretreated with CoPP confe
128                 This phenotype is rescued by conditioned medium from control muscle cells and by reco
129                                    Moreover, conditioned medium from CR-treated cells transmits the l
130    We then assessed MSC migration induced by conditioned medium from CRE-challenged human epithelium
131                                   Similarly, conditioned medium from CSCs cultured from the cardiac b
132                                              Conditioned medium from CSCs of patients with diabetes m
133                                              Conditioned medium from cytokine-treated smooth muscle c
134 is model, resuspension of wild-type cells in conditioned medium from DeltabsrA cultures also resulted
135 rowth factor-binding proteins (IGFBP) in the conditioned medium from endoglin-deficient PrSCs and tha
136    Here we show that macrophages cultured in conditioned medium from ER-stressed tumor cells become a
137                                              Conditioned medium from ERalpha-null adipocytes and medi
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                            Here we show that conditioned medium from HCC cell lines, Hep3B and HepG2,
145 a neutralizing antibody, when incubated with conditioned medium from HCV-infected hepatocytes, inhibi
146                                              Conditioned medium from HCV-infected hepatoma cells (Huh
147                   Next, we demonstrated that conditioned medium from HCV-infected human hepatocytes a
148                                              Conditioned medium from Hep3B-SND1 cells stably overexpr
149                                              Conditioned medium from HPMCs cultured with IL-6 and sIL
150             We sought to investigate whether conditioned medium from HRV-infected epithelial cells ca
151                     Here we demonstrate that conditioned medium from human MSCs (MSC-CM) reduces func
152                                              Conditioned medium from hypoxia-reoxygenation explants a
153                                              Conditioned medium from injured, 1,25-VitD3-treated arte
154                          Upon treatment with conditioned medium from iPFK2-overexpressing adipocytes,
155 d NRVMs, as well as in NRVMs stimulated with conditioned medium from isoproterenol-stimulated cardiac
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 ession in C2C12 myotubes was up-regulated by conditioned medium from Lewis lung carcinoma cells or C2
160 tal cancer cells or systemic delivery of the conditioned medium from LOX-overexpressing colorectal ca
161 that M1 macrophage apoptosis was promoted by conditioned medium from macrophages polarized into an M2
162              Furthermore, cells treated with conditioned medium from mammary glands in which Akt had
163                                              Conditioned medium from mesenchymal stem cells (MSC-CM)
164  The in vivo Matrigel plug assay showed that conditioned medium from miR-184-expressing HLEKs elicite
165  Human dermal microvascular cells exposed to conditioned medium from miR-184-overexpressing HLEKs wer
166         In the bone marrow cell culture, the conditioned medium from MLO-Y4 cells decreased the capab
167 n bronchial epithelials were stimulated with conditioned medium from monocytes infected with virulent
168 l cells that were unstimulated or exposed to conditioned medium from monocytes not exposed to TB.
169           Mouse serum rich in irisin and the conditioned medium from myotubes exposed to palmitate fo
170                                              Conditioned medium from native bone chips can activate t
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  docosahexaenoic acid) were increased in the conditioned medium from peroxisome-induced macrophages,
175                                              Conditioned medium from PS1 null neuronal cultures at 8
176                                              Conditioned medium from rat brain slice cultures with ne
177                                      Choroid conditioned medium from recovering choroids inhibited pr
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                                              Conditioned medium from these macrophages was antichlamy
188                                              Conditioned medium from TKO microglia cultures inhibits
189 itogenic T-cell clone (LCN-8), we found that conditioned medium from TNF-stimulated Gal-9(+/+) but no
190       We performed secretome analysis of the conditioned medium from tumor-induced bone to identify p
191                                              Conditioned medium from W(sh)/W(sh) osteoclasts had elev
192 ld be restored following incubation with Tat-conditioned medium from wild-type DCs, (vi) impaired the
193 augmented in the presence of MM cell-derived conditioned medium, glial-derived neurotrophic factor (G
194 R-29 conditioned medium, whereas pre-miR-30c conditioned medium had a prohypertrophic effect.
195 reatment of OP9 stromal cells with adipocyte conditioned medium had no effect on B lymphopoiesis.
196                Conversely, CA-STAT5A-induced conditioned medium had no effect on EC proliferation.
197                                       Adding conditioned medium harvested from cultures of wild-type
198                                              Conditioned medium harvested from IL1R2-overexpressing C
199                                  Analysis of conditioned medium identified that keratinocyte growth f
200  introducing them into the irradiated embryo conditioned medium (IECM) alone, i.e., without partnerin
201 tro studies demonstrated that senescent-cell conditioned medium impaired osteoblast mineralization an
202 -Synuclein secreted from neuronal cells into conditioned medium in the form of exosomes can be transm
203 uction of myeloid cells induced by adipocyte-conditioned medium in vitro.
204 hymal stromal cells or with their secretome (conditioned medium) in a transwell system.
205                                          PMF-conditioned medium increased the migration and tubulogen
206 nic, but not acute, treatment with astrocyte-conditioned medium, indicating that a soluble factor is
207                     However, UB cell-derived conditioned medium induced MM cell migration.
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              C2C12 myotubes treated with LLC-conditioned medium (LCM) rapidly activates p38 MAPK and
215 ng specific siRNAs we observed that LLC cell-conditioned medium (LCM)-treated C2C12 myotubes underwen
216 eated THP-1 macrophages to IGFBP-3-deficient conditioned medium led to a 20-fold increase in palmitat
217                       Within epithelial cell-conditioned medium, low amounts of glucocorticoids were
218 ced, 5823 +/- 2192 MMP14-positive MVs/muL of conditioned medium; means +/- SEM; n = 6; P < 0.01).
219 etion of lcn2 by immunoprecipitation reduced conditioned medium-mediated neurotoxicity.
220 -167 cell lines) were stimulated by IL-6, MF-conditioned medium (MF-CM) or MFs, with or without TGF-b
221  in LAC cells cocultured with MSCs or in MSC-conditioned medium (MSC-CM).
222                                    Moreover, conditioned medium obtained from commercial human DBM mo
223 l fibroblasts were exposed to the respective conditioned medium obtained from DBM (DBCM).
224                                  Strikingly, conditioned medium obtained from developing oligodendroc
225 opic Indian clade C HIV-1 (93IN101) from the conditioned medium of 293 cells.
226             Soluble c-Met was studied in the conditioned medium of 9 uveal melanoma cell lines and in
227 a because in vitro studies demonstrated that conditioned medium of both mouse and human wounds upregu
228                                          The conditioned medium of BV2 cells exposed to OGD contained
229        On transfection with pre-miR-29b, the conditioned medium of cardiac fibroblasts lost its abili
230                  Reporters secreted into the conditioned medium of cells in culture or into blood in
231 on of the Gaussia luciferase reporter in the conditioned medium of cells.
232 ost abundant labeled protein detected in the conditioned medium of choroid or sclera had an apparent
233 5A-dependent proangiogenic activity from the conditioned medium of EC.
234 5A-dependent proangiogenic activity from the conditioned medium of EC.
235 ncreased in endothelial cells exposed to the conditioned medium of FHL2(-/-) versus wild-type (WT) EO
236 tly, CD33(+) myeloid and T cells cultured in conditioned medium of HNSCC cells in which Sema4D was kn
237                                              Conditioned medium of IL-12-incubated cells proved to co
238                                              Conditioned medium of inflammasome-activated RPE cells p
239                                 Accordingly, conditioned medium of isolated acinar cells from old WT
240           Co-precipitation of serglycin from conditioned medium of MM cells using a CD44-Fc chimera s
241                   We searched for tau in the conditioned medium of N2a cells, induced pluripotent ste
242   Importantly, treatment of macrophages with conditioned medium of NP cells treated with TNFalpha or
243 4 in the lungs of OxPAPC-treated mice and in conditioned medium of OxPAPC-exposed pulmonary endotheli
244 llular domain (sVLDLR-N) was detected in the conditioned medium of retinal pigment epithelial cells,
245 F-1) levels were significantly higher in the conditioned medium of shPHD2-ADSCs versus ADSCs, and dep
246 t, Endoplasmic Reticulum/Golgi apparatus and conditioned medium of T24 vs. its metastatic subclone T2
247          We also set up cocultures between a conditioned medium of treated keratinocytes and naive T
248  in the serum samples from pregnant women or conditioned medium of trophoblast cells promoted endomet
249                                          The conditioned medium of uveal melanoma cell lines and the
250 atory effects of ERalpha-deficient adipocyte-conditioned medium on BrCA cells was reversed by Lcn2 de
251                             The effect of NP-conditioned medium on macrophage migration was measured
252 mimicked the inductive effect of lung cancer conditioned medium on the expression and ectodomain shed
253 blocked by immunodepletion of Jagged-1 in EC-conditioned medium or blockade of ADAM17 activity.
254 This effect was inhibited by incubation with conditioned medium or exosomes (40- to 100-nm diameter)
255                Exosomes purified from either conditioned medium or human plasma could partially rescu
256 s alone or in the presence of autologous PMN-conditioned medium (PCM) on poly(ethylene glycol) hydrog
257 eted MMP9 under pathological conditions, and conditioned medium prepared from the stressed OPCs weake
258 carried out by simple fine filtering of cell-conditioned medium prior to a non-NTA-determined (i.e.,
259                      BMP4, identified in PDX-conditioned medium, promoted EC-to-OSB conversion of 2H1
260                Furthermore, mature adipocyte conditioned medium promotes MM growth, whereas co-cultur
261                           Interestingly, 4T1-conditioned medium reduced myeloid cell NGP expression b
262 by AKR1B10-overexpressing keratinocytes into conditioned medium resulted in up-regulation of transfor
263  human amniotic mesenchymal stromal cells or conditioned medium showed comparable protective effects
264 irmed by the analysis of lipid vesicles from conditioned medium showing that amyloid peptide induced
265 that treatment of endothelial cells with EVT conditioned medium significantly increased production of
266 ophages co-cultured with cancer cells or TAM-conditioned medium significantly reduced apoptosis and a
267      The addition of anti-Sema4D Ab to HNSCC conditioned medium significantly reduced the expansion o
268  depletion of these molecules from astrocyte-conditioned medium significantly reduces its ability to
269 nocytes, or addition of IL-10-containing M14-conditioned medium, significantly enhanced their express
270 Trunk and Torso-like were also taken up from conditioned medium specifically by cells expressing Tors
271 s showed that second-trimester human decidua conditioned medium stimulated transendothelial PMN invas
272 l-filtration chromatography, we identified a conditioned medium subfraction, which specifically displ
273 5-blocking Ab inhibited erythrocyte lysis by conditioned medium, suggesting that CD55/sCD55 impairs c
274  endothelial cells promoted by mammary gland conditioned medium, suggesting that lymphangiogenesis in
275 helial cell migration activated by flagellin-conditioned medium, suggesting that TLR-5 ligation can m
276 the addition of transmigrated neutrophils or conditioned medium, taken from transmigrated neutrophils
277 urther, aerobactin was the primary factor in conditioned medium that enhanced the growth/survival of
278 ese cultures in the fully defined serum-free conditioned medium that is required to sustain organoid
279 g gamma rays, and is the major factor in the conditioned medium that leads to the inhibition of cell
280 ocd-/- hearts were cultured ex vivo in BMP10-conditioned medium, the defects in cardiomyocyte prolife
281 f prechordal mesoderm microcultures to Nodal-conditioned medium, the Nodal inhibitor CerS, or to an A
282                                  Addition of conditioned medium to fresh and low cell density culture
283 e use biochemical fractionation of astrocyte-conditioned medium to identify glypican 4 (Gpc4) and gly
284 medium completely removed the ability of the conditioned medium to increase NSPC proliferation.
285 om microglial cells treated with glioma cell-conditioned medium to induce angiogenesis.
286  in PAECs and inhibited the capacity of PAEC-conditioned medium to induce the proliferation of pulmon
287 ve form of beta-catenin or by LiCl or Wnt-3a conditioned medium treatment induced hTERT mRNA expressi
288 wn, but we demonstrate that endothelial cell conditioned medium upregulates these genes in ex vivo fr
289 -/anti-miR of miR-29b and miR-30c, and their conditioned medium was analyzed by mass spectrometry.
290                                          HRV-conditioned medium was chemotactic for fibroblasts.
291                                 The pericyte-conditioned medium was collected and the collagen proteo
292  and (3) the proneurogenic effect of TgCRND8-conditioned medium was counteracted by blockade of the r
293           Consistent with these experiments, conditioned medium was shown to induce and maintain cond
294                                        HUVEC-conditioned medium was sufficient to enhance axonal grow
295              Using nonpropagating viruses or conditioned medium, we demonstrate a paracrine effector
296                                  Using Wnt3a-conditioned medium, we demonstrated that ZMIZ2 can enhan
297 d differentiated when FGF4, heparin, and REF conditioned medium were removed.
298 ryonic stem cells atrophied under pre-miR-29 conditioned medium, whereas pre-miR-30c conditioned medi
299  heparin or heparan sulfate, pretreatment of conditioned medium with heparinase III, or growth of cel
300 tein induction were analzyed after butryate, conditioned medium with Wnt5a activity, and FrzB contain

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