戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 tase, which appeared to be essential for the proliferative effect.
2  polyphosphate levels and abrogates the anti-proliferative effect.
3 hibits MMP activity, has no significant anti-proliferative effect.
4 ro IGF-I induced both an antiapoptotic and a proliferative effect.
5 in they undergo apoptosis, counteracting the proliferative effect.
6 t-dependent, manifesting both inhibitory and proliferative effects.
7 nt but does not significantly alter the anti-proliferative effects.
8 reonine kinase which has anti-viral and anti-proliferative effects.
9 rr virus (EBV) oncogenes exert potent B cell proliferative effects.
10 ects of insulin, whereas IR-A rather signals proliferative effects.
11 eta-cells versus possible adverse pancreatic proliferative effects.
12  that this property is essential to its anti-proliferative effects.
13 ogenous PR abrogated progestin-mediated anti-proliferative effects.
14 atherosclerotic, anti-inflammatory, and anti-proliferative effects.
15 ptide mimetic that exhibits significant anti-proliferative effects against erbB-2-dependent breast ca
16 ts and vegetables, has shown remarkable anti-proliferative effects against various malignant cell lin
17                   This protein also exhibits proliferative effects, although little is known about th
18 in either order resulted in synergistic anti-proliferative effects, although the mechanism of synergy
19 e E (GE) was found to exhibit excellent anti-proliferative effects among the tested xanthones.
20 r transcription factor, which possesses anti-proliferative effects and is frequently silenced in ovar
21 cytes is a pathway by which Shh produces its proliferative effects and offers a potential therapeutic
22                                     The anti-proliferative effects and related changes in cell cycle
23                                     The anti-proliferative effects and the selective killing of HSCs,
24 s, such as rheumatoid arthritis, without the proliferative effect associated with traditional estroge
25 f rheumatoid arthritis without the classical proliferative effects associated with estrogens.
26 ression of MAST1 or MAST2 gene fusions has a proliferative effect both in vitro and in vivo.
27 ective inhibitor of CARM1 that exhibits anti-proliferative effects both in vitro and in vivo and, to
28  the permissive temperature does not exert a proliferative effect but causes p53-mediated apoptosis,
29 in the liver can have both antiapoptotic and proliferative effects, but it is unclear which liver cel
30              Progesterone did not alter E2's proliferative effects, but testosterone reduced E2-induc
31 ve glucose homeostasis, TZDs also exert anti-proliferative effects by a mechanism that is unclear.
32 e results suggest that adiponectin can exert proliferative effects by activating Ras signaling pathwa
33 at quinoxaline antibiotics could exert anti- proliferative effects by inhibition of chromosomal DNA r
34 t anti-inflammatory, anti-apoptotic and anti-proliferative effects by modulating intracellular signal
35                            These genetic and proliferative effects can be induced by activation of re
36 y and G(2)-M phase to contribute to its anti-proliferative effect, degradation of activated Akt and B
37 uses p53-mediated apoptosis, i.e., the tal-1 proliferative effect depends on the integrity of the cel
38                                              Proliferative effects due to overexpression of processed
39  pathways correlates with a significant anti-proliferative effect, due to cell-cycle regulation leadi
40        However, the casual link between cell proliferative effects during liver regeneration and meta
41 s mediate prominent differentiative and weak proliferative effects; (iii) the antiproliferative and a
42 IGF-I receptor alone but had an even greater proliferative effect in cells overexpressing both the IG
43                        CDO had a potent anti-proliferative effect in colorectal cell lines, yet, a si
44 that TM is not cytotoxic, but exerts an anti-proliferative effect in ECC-1 cells.
45 these in males commensurate with a decreased proliferative effect in male hPASMCs.
46        Ectopic expression of BLM causes anti-proliferative effect in p53 wild type, but not in p53-de
47                        PPARgamma has an anti-proliferative effect in pre-adipocytes and mammary epith
48  have been associated primarily with an anti-proliferative effect in vitro and in vivo.
49                               KLF5 has a pro-proliferative effect in vitro and is induced by mitogeni
50 lism or activity level and exhibited an anti-proliferative effect in vitro.
51 ins of BRD4, have been shown to exhibit anti-proliferative effects in a range of malignancies.
52 d PL and TRAIL demonstrated significant anti-proliferative effects in a triple-negative breast cancer
53                              Acid exerts pro-proliferative effects in Barrett's-associated esophageal
54 fore and during the treatment suggested that proliferative effects in BM may have preceded effects on
55 ve metabolite of vitamin D(3), mediates anti-proliferative effects in cells by regulating the express
56 synthetic processing intermediates also have proliferative effects in colonic mucosa and in some oeso
57 l program causes potent, NOTCH-specific anti-proliferative effects in cultured cells and in a mouse m
58   This is associated with anti-apoptotic and proliferative effects in epithelial progenitors, whereas
59 hese data indicate that Nef induces multiple proliferative effects in podocytes in culture and that n
60 ate that a key event in the artemisinin anti-proliferative effects in prostate cancer cells is the tr
61 nstrated previously to have significant anti-proliferative effects in several leukemia models.
62 ing human amphiregulin was examined for anti-proliferative effects in the human skin-severe combined
63  receptor (ER)-beta is thought to exert anti-proliferative effects in the normal prostate but support
64 verexpression of the H30N enzyme causes anti-proliferative effects in vitro and anti-tumor effects in
65 ignaling pathways mediating CAMKII-dependent proliferative effects in vivo are poorly understood.
66 These early-age neurotrophic and neurogenic (proliferative) effects in the Arg-61 mouse may be an ina
67                             In addition, the proliferative effects induced by E2 and G-1 in these cel
68 ZD4547 (1-5 microM) demonstrated potent anti-proliferative effects, inhibition of stemness, and suppr
69 ement of neuronal nitric-oxide synthase, the proliferative effect is mediated via an NO/cyclic guanos
70                   Dexamethasone-induced anti-proliferative effects may confer protection from radioth
71 y through which estrogen, independent of its proliferative effect, may induce heparanase overexpressi
72 rapamycin pathway and/or by facilitating the proliferative effect mediated by growth factors such as
73 Ras (N17) failed to significantly reduce the proliferative effect mediated by the sst(4) receptor but
74  PI3K effectors, it is able to reproduce the proliferative effect of activated Ras.
75                                         Anti-proliferative effect of AICAR is mediated through activa
76        The objective was to compare the anti-proliferative effect of anthocyanin-rich plant extracts
77                                     The anti-proliferative effect of asTORi in vitro and in vivo is t
78 vestigated whether TGFbeta mediates the anti-proliferative effect of atRA and BMS453 in normal breast
79                                      The pro-proliferative effect of BDNF was attenuated by TrkB kina
80                                 However, the proliferative effect of Bmp signaling appears to be inde
81 teins (cdk6R31C) was found to inactivate the proliferative effect of cdk6 and increase cytoplasmic lo
82                                     The anti-proliferative effect of CO in vitro requires the activat
83 gainst IGF-II to cell cultures inhibited the proliferative effect of CRD-BP knockdown, suggesting tha
84  rather than c-myc mRNA levels, mediates the proliferative effect of CRD-BP knockdown.
85                                          The proliferative effect of elevated [Ca2+]o was associated
86                                          The proliferative effect of estradiol requires the availabil
87 id (EPA, C20:5) shifted the pro-survival and proliferative effect of estrogen to a pro-apoptotic effe
88                          To further test the proliferative effect of FGF-4 in cardiac cushion expansi
89                                    Thus, the proliferative effect of fibronectin in combination with
90             FK506 competitively reversed the proliferative effect of FK1012 but had no influence on t
91 tes is unclear, we hypothesize that the anti-proliferative effect of FOXO3 was dependent on lowering
92                                          The proliferative effect of glial growth factor (GGF) does n
93                             In addition, the proliferative effect of GRP on neuroblastoma cells (SK-N
94 /Akt pathway, at least in part, mediates the proliferative effect of HIMF.
95 are interchangeable for IRS to transduce the proliferative effect of IL-4.
96 ed the antiapoptotic effect of IGF-I and the proliferative effect of IL-6 in the myeloma cell lines.
97                        Here we show that the proliferative effect of IL-7 is more pronounced on CD4(+
98 ing the renewal of T cells by inhibiting the proliferative effect of IL-7.
99 tivity is necessary for the IRS-1/2-mediated proliferative effect of IL-9 and IL-4, Akt activation is
100 effect of FK1012 but had no influence on the proliferative effect of interleukin 3.
101         These results demonstrate the marked proliferative effect of intravenously infused EGF in the
102   Bilateral nephrectomy did not diminish the proliferative effect of KGF on urothelium, suggesting th
103  R2 receptor-blocking antibody prevented the proliferative effect of low-dose TNF-alpha.
104 H]thymidine incorporation, thus ruling out a proliferative effect of malignant cells on the surroundi
105  not dorsal growth, and that it mediates the proliferative effect of midline N signaling in a ventral
106 anslation in polysomes, and reduces the anti-proliferative effect of mTOR kinase inhibitors.
107                                         This proliferative effect of NECA was inhibited by the additi
108 ts is one possible mechanism to modulate the proliferative effect of Notch in the committed osteoblas
109 l rat hippocampal cultures, we show that the proliferative effect of NPY on nestin(+) precursor cells
110 significantly suppressed, confirming an anti-proliferative effect of PAI-2.
111 flammatory cytokines in vivo can inhibit the proliferative effect of PDGF on human RPE and, at the sa
112  Formation of heterodimers enhances the anti-proliferative effect of PF4 on endothelial cells in cult
113                      Here we report a direct proliferative effect of platelets on cancer cells both i
114                                          The proliferative effect of platelets was not dependent on d
115                                          The proliferative effect of platelets was reduced by fixing
116 small molecule inhibitor, augmented the anti-proliferative effect of RAPA on EBV+ B cell lymphomas.
117                Knockdown of c-myc blocks the proliferative effect of RNA interference with parafibrom
118  the SCF-treated tissue, suggesting a direct proliferative effect of SCF; conversely, treatment with
119 monstrate that cyclin A1 is required for the proliferative effect of Six1.
120 lized p27-null cells to demonstrate that the proliferative effect of Spy1 depends on the presence of
121    Furthermore, forskolin abolished the anti-proliferative effect of tannic acid on cholangiocyte pro
122                                     The anti-proliferative effect of tannic acid was associated with
123            Finally we demonstrate a distinct proliferative effect of TFF2 protein on an AGS gastric c
124 strin decreased during hypergastrinemia, the proliferative effect of TGF-alpha on ECL cells was speci
125                 We now demonstrate that this proliferative effect of TGF-beta is mediated through the
126 , Sulf1 siRNA transfection enhanced the anti-proliferative effect of TGF-beta1.
127     We find that the combination of the anti-proliferative effect of the cytokine TGF- beta and the i
128 1-C, a matrix assembly domain, increased the proliferative effect of these Fn-fs.
129                                     The anti-proliferative effect of TM-FKHRL1 was partially reversed
130 of alpha2beta1 integrin or JAG1, reduced the proliferative effect of TNC on BTIC.
131              Hence, it is suggested that the proliferative effect of TPO is more related to activatio
132  (HER2) to determine if it modifies the anti-proliferative effect of transforming growth factor (TGF)
133 o-L-arginine methyl ester prevented both the proliferative effect of VEGF and Raf-1 activation by VEG
134                                          The proliferative effect of VEGF was inhibited by the extrac
135 orporation were reduced, suggesting that the proliferative effect of VEGF was restricted developmenta
136 anti-AR small interfering RNA, inhibited the proliferative effect of VIP.
137                                  To test the proliferative effect of Wnt-3a in vivo, we ectopically e
138                                      The pro-proliferative effects of 11beta-HSD2 were abrogated by 1
139  lines revealed that sensitivity to the anti-proliferative effects of 1alpha, 25(OH)2D3 was strongly
140 r, our data support a model whereby the anti-proliferative effects of 1alpha,25(OH)2D3 are mediated,
141  the use of uridine, which reverses the anti-proliferative effects of A77 1726 caused by inhibition o
142      In this study, we investigated the anti-proliferative effects of adaphostin in the human prostat
143                                      The pro-proliferative effects of Agr2 may explain its actions in
144  783, and leucine 784) largely abolished the proliferative effects of alphavbeta6, but none of the mu
145 ot significantly elevated, suggesting direct proliferative effects of Ang II.
146 nsplant atherosclerosis is the result of the proliferative effects of anti-HLA Abs.
147 SCRT-I), as an important determinant of anti-proliferative effects of anti-miR-21.
148 Abl-deficient mice are hyporesponsive to the proliferative effects of B cell Ag receptor (BCR) stimul
149                                          The proliferative effects of bFGF and OSM may be via their r
150                                     The anti-proliferative effects of BMP4 occur more rapidly than th
151        Thus, in osteoblastic cells the acute proliferative effects of both estradiol and strain are E
152                     Interestingly, while the proliferative effects of both FK1012 and AP1510 were rev
153                                     The anti-proliferative effects of BTK inhibition in human AML are
154 posure, are reassuring and contrast with the proliferative effects of conventional combined hormone t
155                                     The anti-proliferative effects of COX inhibition are rescued spec
156                       Additionally, the anti-proliferative effects of deoxyanthocyanidins, have been
157 D cells and reduced their sensitivity to the proliferative effects of E2, while having no effect on t
158                     TGFbeta can override the proliferative effects of EGF and other Ras-activating mi
159 ctivated protein kinases as mediators of the proliferative effects of EGF is well established.
160 mor cells may provide resistance to the anti-proliferative effects of EGR-1.
161 and investigated their role in mediating the proliferative effects of endothelin-1 (ET-1) on distal h
162 se abrogated the increased lipid content and proliferative effects of ephrin-A1 knockdown.
163 wth suppression in MCF-7 cells, but the anti-proliferative effects of ERbeta1 could be overridden by
164 tionally hyperactive AR, suggesting that the proliferative effects of ERG and PRMT5 are mediated thro
165                                       Direct proliferative effects of estrogen (E(2)) on estrogen rec
166 r prevention and treatment by inhibiting the proliferative effects of estrogen that are mediated thro
167 tulated role of ERbeta as a modulator of the proliferative effects of estrogen.
168 rapeutic target because ERalpha mediates the proliferative effects of estrogens on the mammary gland
169 in vitro, and that BRCA1 is required for the proliferative effects of EZH2.
170 pression of AhR expression reversed the anti-proliferative effects of flutamide.
171 se results demonstrate that rac mediates the proliferative effects of G-protein coupled receptors thr
172                     Ras proteins mediate the proliferative effects of G-protein-coupled receptors (GP
173                                          The proliferative effects of galanin were via activation of
174 g protein DNA-binding activity prevented the proliferative effects of galanin.
175  a potential candidate to counterbalance the proliferative effects of gastrin.
176 olorectal cancers, its role in mediating the proliferative effects of gastrin1-17 (G-17) on these can
177  as a primer to sensitize hepatocytes to the proliferative effects of growth factors and offers a mec
178 tomas are known to produce GRP; however, the proliferative effects of GRP on neuroblastomas have not
179 naling pathway, we hypothesize that the cell proliferative effects of hamartin and tuberin are partly
180         Despite a clear understanding of the proliferative effects of HBx on cell cycle, a mechanisti
181  biologically active, and it neutralized the proliferative effects of human CSF-1 in a dose-dependent
182 l line as a relevant model to study the anti-proliferative effects of ICI182,780 and identified the n
183  ng/mL; furthermore, huIL-4 counteracted the proliferative effects of IL-7.
184                                         Anti-proliferative effects of immunotherapy produce prolongat
185 is a key mediator of the anti-viral and anti-proliferative effects of interferon.
186 of events that functionally connect the anti-proliferative effects of interferons with the IRF1-depen
187 apamycin and deferoxamine, mimicked the anti-proliferative effects of K+ channel blockers.
188                   Because of the potent anti-proliferative effects of KRAS(G12D) in granulosa cells,
189                          We also demonstrate proliferative effects of leptin alone and in combination
190                                          The proliferative effects of leptin seem to be at the level
191                                          The proliferative effects of MIF may involve CD74 together w
192 -gamma-positive spots on ELISPOT, and 7) the proliferative effects of MIG/CXCL9 were mediated via an
193 ICD in the c57MG cell line recapitulated the proliferative effects of MMP7 in vitro and in vivo.
194                The anti-tumorigenic and anti-proliferative effects of N-alpha-tosyl-l-phenylalanyl ch
195 ings that RU-486 could partially prevent the proliferative effects of N-CAM, inhibition of MAP kinase
196                     One approach to blocking proliferative effects of nicotine and ACh on growth of l
197 knockdown diminished the transcriptional and proliferative effects of NUP98-HOXA9.
198       Recent studies have suggested that the proliferative effects of p21(ras) may depend on signalin
199                                          The proliferative effects of P2RX7 blockade were associated
200                In unstressed cells, the anti-proliferative effects of p53 are restrained by mouse dou
201 tors RIIA and RIIB are required for the full proliferative effects of Pdx-1 in rat islets.
202              In addition, the protective and proliferative effects of plasminogen activator inhibitor
203 ating that both factors are required for the proliferative effects of progastrin.
204  by TRAF6-binding peptide abrogated the anti-proliferative effects of RANKL, suggesting the critical
205  Our results indicate that the pro- and anti-proliferative effects of ROS can be independently modula
206  antagonism in vitro significantly decreases proliferative effects of Shh in cultured CGNPs.
207 ors, but how cells become insensitive to the proliferative effects of Shh is not well understood.
208         In contrast, shYY2 reversed the anti-proliferative effects of shYY1, and shYY2 particularly a
209 yeloid cell lines respond to the synergistic proliferative effects of SLF plus other cytokines in a m
210                                          The proliferative effects of sodium ascorbate on the male ra
211 eptor was first suggested by the strong anti-proliferative effects of soluble heparin-like molecules
212 ether with classic ER signaling, mediate the proliferative effects of synthetic estrogens such as tam
213                      In conclusion, the anti-proliferative effects of tannic acid in cholangiocytes i
214 ferate slowly and are refractory to the anti-proliferative effects of TGF beta1.
215 ted against IL-1alpha could abate the growth proliferative effects of TGF-beta without compromising i
216 odies against IL-1alpha prevented the growth proliferative effects of TGF-beta.
217 t1-expressing neural crest and that the anti-proliferative effects of Tgfbeta depend on Arf in vivo.
218 ours were particularly sensitive to the anti-proliferative effects of the agent.
219  the role of this receptor in the peroxisome proliferative effects of the endogenous steroid dehydroe
220 nsgenic mice were also hypersensitive to the proliferative effects of the skin tumor promoter, 12-0-t
221 increase in active TGFbeta mediates the anti-proliferative effects of these retinoids, a TGFbeta-bloc
222 uggests an additional mechanism for the anti-proliferative effects of this drug.
223  human and murine cells, suggestive that the proliferative effects of TNF-alpha may be limited to ery
224 ingle TP53 target gene required for the anti-proliferative effects of TP53 during pharmacological act
225 sensitizes prostate cancer cells to the anti-proliferative effects of vitamin E and that this activit
226 nd forced expression of MBP-1 exerts an anti-proliferative effect on a number of human cancer cells.
227 is factor (TNF) ligand superfamily and has a proliferative effect on both normal and tumor cells.
228 kt phosphorylation and showed a greater anti-proliferative effect on EBV+ B lymphoma lines compared t
229 ietin-1 as well as angiopoietin-2 exhibit no proliferative effect on endothelial cells.
230 tion of this pathway abrogates adiponectin's proliferative effect on HSCs.
231 confirmed initially that EVO exerted an anti-proliferative effect on human epithelial ovarian cancer
232 pression of p202 was associated with an anti-proliferative effect on human prostate cancer cells.
233 ogen activator inhibitor (PAI)-2 has an anti-proliferative effect on keratinocytes.
234                     IL-7 has a predominantly proliferative effect on mature CD4(+)CD3(+)CD8(-) and CD
235                           In contrast to its proliferative effect on primary B cells, SGN-14 inhibite
236               CNTF does not, however, have a proliferative effect on responsive cells, but rather enh
237                        EMD had a significant proliferative effect on SVF cells, when compared with 2%
238 ctor (KGF or FGF7) has a differentiative and proliferative effect on the epithelium of the developing
239 lls and downstream signaling, as well as its proliferative effect on the MK lineage.
240 nd that has recently been shown to have anti-proliferative effects on a number of human cancer cell t
241 b (SCH727965, MK-7965), exhibits potent anti-proliferative effects on a panel of NB cell lines by blo
242 oliferative effects on Namalwa cells and pro-proliferative effects on CD34+ cells, whereas p21WAF-1 e
243 m cell factor (SCF) is a molecule with known proliferative effects on hematopoietic cells.
244 n gene, R-spondin1, with potent and specific proliferative effects on intestinal crypt cells.
245 rowth factor I (IGF-I) are distinct from its proliferative effects on myoblasts.
246 e indicates that extracellular factors exert proliferative effects on neurogenetic precursors in vivo
247 let-derived growth factor were found to have proliferative effects on Schwann cells, but they had no
248 st cell-derived bFGF might exert fibrogenic, proliferative effects on smooth muscle cell/myofibroblas
249 eviously shown that RSpo proteins can induce proliferative effects on the gastrointestinal epithelium
250 ional inflammatory zone but also more global proliferative effects on the liver.
251 2 and E2F3 mutant backgrounds alleviated Myc proliferative effects on the pregnant mammary gland, red
252 ve hematopoietic cells and its ligand exerts proliferative effects on these cells in vitro in synergy
253  mAbs C225 and 4D5 resulted in additive anti-proliferative effects on these cells, which was accompan
254 it is noteworthy that it had no demonstrable proliferative effects on these cells.
255                 Other family members have no proliferative effects on these cells.
256 active form of vitamin D, has selective anti-proliferative effects on tumor-derived endothelial cells
257 ependent protein kinase II inhibitors showed proliferative effects only on cardiomyocytes in early de
258                     Individual stimuli cause proliferative effects (PHH3(+) mitotic cells, YAP transl
259 ese data indicate that the ouabain-activated proliferative effect previously observed in canine VSMCs
260 bservations indicate that progastrin induces proliferative effects, primarily in colonic progenitor c
261 nism(s) by which adaphostin elicits its anti-proliferative effect(s).
262 nM, with a concentration of 100 nM achieving proliferative effects similar to those of 1 nM estradiol
263  of exogenous interleukin (IL)-2 also had no proliferative effect, suggesting that the mPEG-modified
264 to PL with hPL did not have significant anti-proliferative effects, suggesting that hPL is not membra
265 BRAF and MEK inhibition may reduce cutaneous proliferative effects that arise on BRAF inhibitor monot
266 constriction but also exerts profibrotic and proliferative effects that change vessel architecture, w
267                            To exert its anti-proliferative effects, this factor must ultimately contr
268 stem/progenitor cells TKIs exert potent anti-proliferative effects through a poorly understood mechan
269 mediates its potent anti-thrombotic and anti-proliferative effects through its G protein-coupled rece
270 line) ectopic tal-1 expression induces (i) a proliferative effect under suboptimal culture conditions
271                                         This proliferative effect was blocked by an ER antagonist, in
272                                          The proliferative effect was confirmed by a tetrazolium dye-
273                                         This proliferative effect was down-regulated by the arginase
274 SN5 knockdown signature showed that the anti-proliferative effect was driven by a common subset of mo
275                                         This proliferative effect was suppressed by dimethylsphingosi
276                                     FK1012's proliferative effect was sustained and reversible.
277                         Notwithstanding this proliferative effect, we have shown that a novel isoform
278      The principal mechanisms for their anti-proliferative effects were also described.
279                                              Proliferative effects were determined by cell count, tox
280                                        These proliferative effects were modulated by a phosphoinositi
281                                         Anti-proliferative effects were observed in all cell lines at
282 east tumour explants, and had increased anti-proliferative effects when coupled with an ERalpha antag
283  human cancers and pro-apoptotic and/or anti-proliferative effects when re-expressed in tumor cell li
284 ression of securin resulted in a significant proliferative effect, whereas high levels of securin exp
285 tant being that FGF19 has both metabolic and proliferative effects, whereas FGF21 has only metabolic
286 ctivation was found to be essential for this proliferative effect, which was further confirmed by in
287 lar activation of p-ERK, p-AKT, and cellular proliferative effects, which were abrogated following Kl

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top