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8 oplasmic tRNAs tK(UUU), tQ(UUG) and tE(UUC), is down-regulated in a proteasomal dependent fashion.
9 xpression of glutathione peroxidase 3 (GPx3) is down-regulated in a variety of human malignancies.
11 at of miR-661 and its activator, c/EBPalpha, were down-regulated in a breast cancer progression model
13 ed that many genes of flavonoid biosynthesis were down-regulated in a tissue-specific manner in M. tr
15 ression status, and the majority of the rest were down-regulated in abiotic stresses and up-regulated
16 proximately miR-27a approximately miR-24-2), was down-regulated in acute leukemia cell lines and prim
17 mma (PPAR-gamma) and downstream target genes were down-regulated in adipose tissue from participants
19 PKD family of signal transduction proteins, is down-regulated in advanced prostate cancer and intera
21 iogenesis, including c-MYC, c-MYB, and VEGF, were down-regulated in association with a decline in hyp
25 and qPCR indicated that the expression of FT is down-regulated in both OsbHLH068-overexpressing Arabi
26 e 3 (Sec14l3) - a putative target of Creb1 - was down-regulated in both asthma models and in NHBE cel
27 hese targets, such as Axin2, Fgf8 and Wnt3a, is down regulated in Brachyury mutant embryos and we dem
28 dings demonstrate that mGlu2 mRNA expression is down-regulated in brain cortical regions of 5-HT2A kn
30 trates that SOX7 mRNA and protein expression are down-regulated in breast cancer tissues and cell lin
35 a possible tumor suppressor microRNA (miR), is down-regulated in breast tumors compared with normal
38 one in cancer; these tended to be genes that are down-regulated in cancer and that function in develo
44 ed with cancer cell invasion and metastasis, were down-regulated in cell homogenates following cystat
45 mediated by the DNA methylase, DNMT3A, which is down-regulated in cells lacking p38alpha, but once re
47 hatidylinositol 3-kinase/Akt activation that was down-regulated in cells that lack annexin-A6, one of
49 ich miR-494, one of the miR species found to be down-regulated in cholangiocarcinoma (CCA), participa
50 c cells, is a candidate tumor suppressor and is down-regulated in chronic lymphocytic leukemia (CLL).
51 ral drug metabolism and BA transporter genes were down-regulated in Cic-L(-/-) liver, and that BA was
53 teractions and NK cell-mediated cytotoxicity were down-regulated in cKO decidua compared with control
54 c stress responses, as kaempferol glycosides were down-regulated in cml42, and impaired in ultraviole
57 Interestingly, the proapoptotic protein p73 is down-regulated in colon cancer cells expressing p53.
60 ferator-activated receptor-gamma (PPARgamma) was down-regulated in control animals after AMI and up-r
66 g ducts of mice and rats, and its expression is down-regulated in Dahl salt-sensitive rats fed a high
72 Analysis revealed that this target gene set is down-regulated in DS-AMKL patients highly expressing
73 regulated, whereas tissue inhibitors of MMPs are down-regulated, in dystrophic muscle of mdx mice.
74 rized, the mechanism by which Rag expression is down-regulated in early B cell development has not be
76 3GalT4 gene, responsible for Gg4 expression, is down-regulated in EMT; and Gg4 has a regulatory funct
78 miR-214, and LHX6 expression was detected to be down-regulated in erlotinib-resistant HCC827 cells.
79 canonical Wnt/beta-catenin signaling pathway was down-regulated in ERMS cells compared with normal my
80 induced MMP-9 and MMP-13 promoter activities were down-regulated in ETS-1 siRNA-transfected cells.
82 we show that major antioxidant defense genes are down-regulated in FA patients, and that gene down-re
83 anscript; miR-198 expression in healthy skin is down-regulated in favor of FSTL1 upon wounding, which
89 important role in tumor cell proliferation, were down-regulated in Foxm1-deficient PCa tumors in viv
94 man specimens showed that miR-34a expression is down-regulated in glioblastoma tissues as compared wi
95 in neural development and has been shown to be down-regulated in glioma and medulloblastoma, suggest
98 contrast to other cancers, PICK1 expression is down-regulated in grade IV astrocytic tumor cell line
101 analyzed miR-133b expression and found it to be down-regulated in HCC patient samples and induced in
110 mMRP-5 (all orthologs of HRGs in C. elegans) are down-regulated in heme-treated B. malayi, as compare
114 rce this result, we also show that Tif1gamma is down-regulated in HSCs during aging in 20-mo-old wild
116 sis, and expression of IKKalpha was found to be down-regulated in human and murine skin squamous cell
119 We also found that expression of miRNA-200b is down-regulated in human breast cancer during lymph no
120 we showed that caveolin-1 (Cav-1) expression is down-regulated in human breast cancer-associated fibr
126 array expression studies, we found that Per1 is down-regulated in human prostate cancer samples compa
127 glandin E2 (PGE2), through its receptor EP4, is down-regulated in human systemic inflammatory disease
131 results, both RAD52 and RAD23B were found to be down-regulated in hypoxia, but in both cases, the hyp
132 Muscular secreted frizzled-related protein 2 is down-regulated in ICU-acquired weakness patients and
133 ne expression data sets indicates that DOT1L is down-regulated in idiopathic DCM patient samples comp
135 2',5'-oligoadenylate synthetase (2',5'-OAS) were down-regulated in IFN-alpha-treated HEV-A549 cells.
140 , (ii) murine TETs, especially TET2 and TDG, are down-regulated in islets during postnatal differenti
141 cates that basic processes of DNA metabolism are down-regulated in its absence, and the blocked T-cel
142 e level of RNA expression of these TCP genes is down-regulated in jaw-D and elevated in miR319a(129).
145 defense priming in systemic plant immunity, was down-regulated in leaves by joint stress and conferr
146 ogy practice; and CPS1 expression appears to be down-regulated in liver cancer tissue and cell lines.
148 IRF5 in HCV-induced HCC, as IRF5 expression was down-regulated in livers from HCV-positive versus HC
151 RNA processing and the endoplasmic reticulum were down-regulated in LRRK2 G2019S mice compared with K
152 TGFbeta pathway, including pSMAD2 and pERK, were down-regulated in LTBP4 mutant human dermal fibrobl
159 of a number of known ERalpha-regulated genes was down-regulated in MED1-mutant mammary epithelial cel
160 xpressed endogenous chemoattractant protein, is down-regulated in melanoma as well as other human tum
163 xpressed in many cancers, including RCC, and is down-regulated in metastatic versus primary ccRCC.
166 :0)-ceramide was gradually reduced and CerS6 was down-regulated in mitochondria, thereby implicating
167 owed that expression of miR-128b and miR-221 is down-regulated in MLL-rearranged ALL relative to othe
168 Additionally, miR-126, miR-145, and miR-335 were down-regulated in monolayers of tissue-cultured cho
169 t in short-term hematopoietic stem cells and is down-regulated in more differentiated hematopoietic c
170 nuclear factor 4A-driven gene network, which was down-regulated in mouse hepatocyte nuclear factor 4A
171 The expression of the fbpB gene is found to be down-regulated in Mtb cells upon infection when these
172 in A, and Growth factor-independent 1 (Gfi1) were down-regulated in Mtgr1(-/-) whole intestines and M
174 nits and membrane translocation of p47(phox) are down-regulated in murine and human G6PC3-deficient n
175 he activity of the insulin signaling pathway was down-regulated in myocytes isolated from the femoral
176 e we report that the activity of Rho GTPases is down-regulated in non-malignant MECs in three-dimensi
177 tein claudin 1 (Cldn-1) has been reported to be down-regulated in nonlesional skin of atopic dermatit
179 e 2 of the gibberellin biosynthesis pathway, is down-regulated in OsbZIP48(OE) and up-regulated in Os
182 RT-PCR results revealed that VEGF expression was down-regulated in Osx-null calvarial cells and that
185 The functionally essential sGC beta1-subunit was down-regulated in patients with COPD and in CS-expos
190 ies in PGK mutants showed that PGK1 and PGK3 were down-regulated in pgk3.2 and pgk1.1, respectively.
193 vels in the pre-TCR signaled thymocytes, and is down-regulated in post-beta-selection thymocytes.
194 olved in gametogenesis in Chlamydomonas pCRY is down-regulated in pregametes and gametes, and in the
201 181a, miR-199a-5p) predicted to target GRP78 are down-regulated in prostate, colon and bladder tumors
202 eration, whereas the beta(1C) variant, which is down-regulated in prostate cancer, inhibits tumor gro
204 lly, we demonstrated that phosphorylated Akt is down-regulated in Raji cells transduced with EPHB4.
206 cial role in muscle growth and regeneration, was down-regulated in regenerating Trpc1(-/-) muscles.
207 ression, but the extent to which TMPRSS2:ERG is down-regulated in response to androgen deprivation th
209 deacetylase and activator of fat oxidation, is down-regulated in response to high fat feeding, the r
210 hich surface expression of the Vbeta5(+) TCR is down-regulated in response to Mtv-8 and recombination
211 primary methyltransferase acting on H3K9me2, was down-regulated in response to (*)NO, and changes in
213 owed high levels of LRRc17 expression, which was down-regulated in response to the pro-osteoclastogen
215 ntified a serine protein kinase, SRPK3, that was down-regulated in RMS cells and found that expressio
216 In prior work, we identified 48 genes that were down-regulated in SCCs compared with high-grade squ
217 Importantly, we show that iso3, known to be down-regulated in several cancers, competes with RBBP
219 BPdelta, and in contrast to cyclin D1, Cdc27 was down-regulated in several breast cancer cell lines,
220 tate histidine exonuclease whose transcripts are down-regulated in sexual ovules entering meiosis whi
222 ibitor, secreted frizzled-related protein 2, was down-regulated in skeletal muscle of ICU-acquired we
223 show that the p53-induced genes DDB2 and p21 are down-regulated in skin cancer, and in the mouse mode
224 vity of ATR, which regulates the cell cycle, was down-regulated in SLE patients compared with control
230 many glycosylation sites on surface proteins were down-regulated in statin-treated cells compared to
231 on cross section serving PSII photochemistry was down-regulated in T. pseudonana through induction of
232 Th2) and T regulatory (Treg) differentiation were down-regulated in T cells stimulated in the presenc
234 samples revealed that microRNA-101 (miR-101) is down-regulated in TCC, and we showed that miR-101 inh
236 f Runx2 and Osterix as well as Dlx5 and Msx2 were down-regulated in Tgfbr2-deleted cultures compared
237 Finally, we demonstrate that Rheb levels are down-regulated in the AD brain, which is consistent
238 are up-regulated and downstream SRF targets are down-regulated in the hearts of MCKCUG-BP1 mice, whi
239 IA, are transcriptionally induced by BRs and are down-regulated in the loss-of-function BR mutant bri
241 tiple DNA repair pathways have been shown to be down-regulated in the tumor microenvironment, whereas
243 yoD, a master regulator of myogenesis, which is down-regulated in the absence of MASTR and MRTF-A.
246 ecifically, basal transcription factor Taf4b is down-regulated in the CNCC-derived intramembranous bo
248 the most widely characterized family member, is down-regulated in the depressed brain and plays a pro
249 in 3 (Ucn3), a marker for mature beta cells, is down-regulated in the early stages of T2D in mice and
250 we report that miR-24 (miRNA-24) expression is down-regulated in the ischemic border zone of the mur
251 transforming growth factor-beta1 expression is down-regulated in the Lamc3(-/-) retina, and SMAD sig
252 es with a QTL for rice blast resistance, and is down-regulated in the ospal4 mutant line; this may ex
253 an endothelial-specific, proangiogenic miR, is down-regulated in the peripheral muscles of patients
254 rticoid regulated kinase 1 (SGK1) expression is down-regulated in the postmortem PFC of PTSD subjects
255 angiogenic protein, thrombospondin-1 (TSP-1) is down-regulated in the prostate and liver of U19/EAF2
261 ation found that BMP/Smad4 signaling pathway was down-regulated in the K14-cre;Bmp2(f/f);Bmp4(f/f)ame
266 xpression of multiple enamel matrix proteins was down-regulated in the mutant ameloblasts, the cleava
267 ately 2 Mb mapping interval whose expression was down-regulated in the mutant pool was subsequently d
268 rs (VCDs) and thickened choroids, while BMP2 was down-regulated in the RPE from eyes wearing -10 D le
269 s were up-regulated whereas 36% of LPE genes were down-regulated in the absence of this receptor.
271 Interestingly, these mitochondrial proteins were down-regulated in the CTX model thereby linking oxi
272 paraoxonase 2 and glutathione peroxidase 3, were down-regulated in the eye angle tissue of 18-month-
273 ins were differentially up-regulated and 400 were down-regulated in the fast muscle compared with slo
274 0.75, respectively; P < 0.05); both pathways were down-regulated in the greatest-ADG compared with le
275 script as well as protein levels, while they were down-regulated in the GSH-depleted phytoalexin defi
276 Specifically, let-7d, miR-210, and -221 were down-regulated in the in situ and up-regulated in t
277 etylase sirtuin 1, a ChREBP-negative target, were down-regulated in the liver of alcohol-fed mice, th
278 f the beta cell transcriptional network that were down-regulated in the Nkx2.2(KO) mice, were maintai
279 three of these genes, Zic1, Hnf1b and Foxd3, were down-regulated in the posterior hindbrain, where ca
281 le control and 9 genes involved in apoptosis were down-regulated in the treatment tumor tissues versu
287 Among those, miR-24, miR-145, and miR-210 were down-regulated in Tregs compared with controls and
289 ntitative RT-PCR: 14 were up-regulated and 4 were down-regulated in tumors with a higher Gleason scor
292 ors to activate the expression of mRNAs that are down-regulated in various neurological and psychiatr
293 ult to reconcile observations that profilin1 is down-regulated in various invasive adenocarcinomas an
295 e expression of synapsin genes SYN1 and SYN2 was down-regulated in vivo and in vitro by alphaSyn olig
296 rate xenografts in which EGFRvIII expression was down-regulated in vivo, uPAR assumed a major role in
297 sis and fatty acid biosynthesis; these genes were down-regulated in wild-type or WRI1-overexpressing
299 zymes in EAE spinal cords showed that PARP-1 was down-regulated in WT mice and that PARP-3 but not PA
300 %) of S-palmitoylation sites on 254 proteins were down-regulated in Zdhhc13-deficient mice, represent
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