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2 xplained by immunohistochemical data showing increased expression of 5-HT2CR in non-GABAergic BLA cel
3 ne expression, as the mybs1 mutant displayed increased expression of a hexokinase gene (HXK1), chloro
4 Cells expressing the iTango system exhibit increased expression of a marker gene in the presence of
5 omyocytes from Gas2l3-deficient mice exhibit increased expression of a p53-transcriptional program in
8 e expression profiling analysis demonstrates increased expression of a specific set of transcription
9 ration of epithelial KIT(+) progenitors, and increased expression of a target gene, Disco-interacting
11 deaminases gene cluster APOBEC3 resulting in increased expression of A3A, which is shown to be of cli
12 resistin, fed-state and fasting insulin and increased expression of adipogenic transcription factors
13 emonstrated that this compound significantly increased expression of Ah-responsive genes such as Cyp1
14 sceptibility to IPF was also associated with increased expression of AKAP13 mRNA in lung tissue from
15 nd adipose tissue, which was associated with increased expression of aldehyde dehydrogenase family 1
17 ire a profibrotic phenotype characterized by increased expression of alpha-smooth muscle actin and co
18 g hepatotropic viral infection and displayed increased expression of alternative Mvarphi activation m
19 2 suppressed expression of CYP24A1, but also increased expression of an exon 10-skipped CYP24A1 splic
20 steroids improved sarcolemmal repair through increased expression of annexins A1 and A6, which mediat
21 ismatch repair subtypes were associated with increased expression of antitumor immunity, including ac
25 nses in liver and spleen, as associated with increased expression of arginase I and the cytokines IL1
26 increased immunosuppression as evidenced by increased expression of arginase-1 in CD11b(+)Gr1(+) cel
27 ng apoE inducible mouse models, we show that increased expression of astrocytic apoE4, but not apoE3,
29 sion of HuR, Bcl2, cyclin E, and Bcl-XL with increased expression of Bax and p27 in CMLD-2-treated NS
32 t 8 weeks, we observed two distinct waves of increased expression of beta cell functional and prodiff
33 inactive Cas9 (dCas9) in MVM-infected cells increased expression of both cyclin B1 protein and RNA,
34 fter repeated cocaine exposure, resulting in increased expression of both genes in D2-type medium spi
38 e damage during ischemia was associated with increased expression of C3/C3 fragments primarily in the
42 an essential autophagy gene, FIP200, in NSCs increased expression of Ccl5 and Cxcl10 in a p53-indepen
45 reduced expression of pluripotency factors, increased expression of cell-lineage-affiliated developm
47 racterized by infiltration with neutrophils, increased expression of chemokine (C-X-C motif) ligand (
49 adaptation by S. aureus to obesity/T2D with increased expression of clfA that is associated with the
51 This resulted in sustained, several-fold increased expression of CRRY in the RPE, which significa
52 l CD4(+) T cells from patients with ALF have increased expression of CTLA4 compared to individuals wi
53 palmar epidermis demonstrated significantly increased expression of CTSB, as well as stronger staini
55 t the loss of Twist1 in IPF lung fibroblasts increased expression of CXCL12 downstream of increased e
57 and induced cell cycle arrest accompanied by increased expression of cyclin-dependent kinase inhibito
59 riments of immunohistochemistry (IHC) showed increased expression of cytoplasmic HMGB1 in dengue-extr
60 ed ADSC differentiation, characterized by an increased expression of cytoplasmic lipids and perilipin
61 This respiratory burst was associated with increased expression of cytosolic components of the NADP
62 essing plants after elf18 treatment confirms increased expression of defense-related genes compared w
63 evious findings in schizophrenia to identify increased expression of developmentally and genetically
64 mesenchymal to epithelial transition (MET), increased expression of differentiation markers and pres
65 last resulted in decreased proliferation and increased expression of differentiation markers, includi
66 4166 induced phosphorylation of NFkappaB and increased expression of dual specificity phosphatase 6 (
68 phenotypic inversion of EMT, correlated with increased expression of E-cadherin and beta-catenin, and
72 nal reprogramming is shown to be mediated by increased expression of eIF4E and its increased availabi
73 ology, including mitochondrial architecture, increased expression of electron transport chain protein
74 OTCH1 signalling in tumour xenografts led to increased expression of endothelial FABP4 that decreased
76 ariants; both mouse and human tumors exhibit increased expression of epigenetic reprogramming factors
77 signal regulated kinase proteins and with an increased expression of epithelial-to-mesenchymal transi
80 3H in tumorigenesis have been interested and increased expression of FAM83H and MYC in hepatocellular
81 f mice with the ADRB3 agonist CL316,243 (CL) increased expression of fatty acid synthase (FASN) and m
85 and monocytes/macrophages in capillaries and increased expression of five biologically relevant genes
88 ponse, but PD-L1-expressing ILC2s stimulated increased expression of GATA3 and production of IL-13 by
90 conate levels in loz1Delta cells result from increased expression of gcd1 By analyzing the activity o
92 volved in mature neuron function, along with increased expression of genes atypical of the olfactory
94 uscle mass in PINTA745-MCAO mice involved an increased expression of genes encoding myofibrillar prot
95 upregulated in the outer retina and there is increased expression of genes involved in glucose metabo
96 Initial responses to P limitation showed increased expression of genes involved in P uptake and a
97 the inoculum suspension concomitant with an increased expression of genes involved in stress respons
98 r osteogenic differentiation, perhaps due to increased expression of genes involved in the control of
101 iptomes from orange morphs had significantly increased expression of genes related to immune response
102 s, while single-cell RNA-seq analyses showed increased expression of genes related to reactive oxygen
104 ses indicated that IPF lung fibroblasts have increased expression of genes that are targets of mEV-en
105 luding higher CCL17 and IL-10 production and increased expression of genes with important immune func
106 rcinoma (PDAC) and generally correlates with increased expression of HER2, the underlying mechanism r
108 ing metagenomic sequencing related SAMHD1 to increased expression of human endogenous retrovirus K (H
112 erbated pathology of skin inflammation, with increased expression of IL-17-induced keratinocyte-deriv
113 that STAT1-deficient mice had significantly increased expression of IL-33 and IL-23, cytokines that
115 posure of HTEpC cells to both CSE and IL-17A increased expression of IL-6 and IL-8 in a concentration
116 adhesion, and transendothelial migration via increased expression of IL-6 and monocyte chemoattractan
117 odel (mEER) caused systemic inflammation and increased expression of Il1b in the brain while inducing
118 rast, CD4 T cells of nonresponders exhibited increased expression of IL2 and STAT5 genes, which are k
119 atients with IBD, and mice with colitis, had increased expression of IL28 compared with controls; lev
123 ol feeding decreased miR181b-3p in liver and increased expression of importin alpha5 in nonparenchyma
125 ated genes in these cells was examined, with increased expression of inflammatory (NLR family pyrin d
126 atment of control HEEs with arachidonic acid increased expression of inflammatory cytokines, 12-hydro
127 al pneumonia, Miwi2-deficient mice exhibited increased expression of inflammatory mediators and incre
128 trate an exhausted phenotype associated with increased expression of inhibitory receptors, decreased
129 smoke accelerated development of colitis and increased expression of interferon gamma in the small in
130 te smoke developed ileitis, characterized by increased expression of interferon gamma, compared to wi
133 Downregulated miRNAs were associated with increased expression of interleukin 8 (IL-8), CXCL2, IL-
134 stretch to RAW 264.7 macrophages resulted in increased expression of interleukin receptor 1 messenger
135 nsion of Th17-type CD4 T cells was seen with increased expression of interleukin-17 and interleukin-2
136 pr of liver X receptor-alpha (LXRalpha) with increased expression of its lipogenic targets Srebp1c, C
140 In UN-KC-6141 cells, PI3K and MEK signaling increased expression of KLF5; a high level of KLF5 incre
142 t brains following neonatal infection showed increased expression of kynurenine amino transferase II
143 t LCE3B/C-del was associated with a markedly increased expression of LCE3A, a gene directly adjacent
144 ANX - A1 (-/-) mice exhibited significantly increased expression of LV pro-inflammatory and pro-fibr
145 reases in tumor-infiltrating lymphocytes and increased expression of lymphocyte-homing signals in the
147 l nonrepressed 2 serine/threonine kinase and increased expression of mammalian target of rapamycin, s
148 adherence compared to the wild type, due to increased expression of mannose-sensitive type 1 pili.
149 ndent deposition of hyaluronic acid (HA) and increased expression of markers for alternative activati
150 cells in skin and digit joints as well as by increased expression of matrix metalloproteases and bone
151 : enhanced invasion and migration, including increased expression of matrix metalloproteinases and ac
152 ng cells obtained after H1152 treatment show increased expression of mature beta cell markers and imp
155 at have lost epithelial characteristics with increased expression of mesenchymal genes, have decrease
156 occurring in PLNs of T1D patients, involving increased expression of miR-125a-5p on Treg cells which
157 mia-reperfusion injury (IRI) associated with increased expression of miR-146a in both allografts and
162 s increased protease activity coincided with increased expression of mRNA for kallikreins (KLKs), wit
165 up of double-expressor lymphomas, which have increased expression of MYC and BCL-2 and/or BCL-6 by im
168 and immunofluorescence results indicating an increased expression of Nav1.7 associated with spontaneo
169 ilitated by tumour-associated macrophages or increased expression of negative regulators of cytotoxic
171 lly examined CM gene expression and observed increased expression of neuronal markers Dcx, Map2, and
173 , with FOXJ2 phosphorylation associated with increased expression of newly identified NEK6 transcript
174 ed with control (P <0.001) and significantly increased expression of NF-kappaB mRNA in neutrophils (P
179 d that cutaneous leishmaniasis patients have increased expression of NLRP3, leading to high levels of
180 odocytes in vitro with TGF-beta1 resulted in increased expression of Notch-1, ErbB4, pErbB4, and pEGF
182 clinically relevant doses of FTY720 to mice increased expression of NPC1 and -2 in brain and liver a
184 Real-time RT-PCR also showed dramatically increased expression of osteogenesis marker genes only i
186 combination treatment remarkably (P < 0.05) increased expression of p-Akt and anti-apoptotic protein
188 te-derived DCs (MDDCs) is associated with an increased expression of p21cip1/waf, a cell cycle regula
189 reatment marrow samples revealed a trend for increased expression of PD-L1 in responding patients and
190 cluster and miR-125a-5p are downregulated by increased expression of PDGFR-alpha or PDGFR-beta in NSC
191 ne causes FOXO1 localization in the nucleus, increased expression of pERK1/2, and drug resistance.
194 ased phosphorylation of STAT3 on Ser727, and increased expression of PML, a STAT3 transcriptional tar
197 istent with in vitro findings, significantly increased expression of proapoptotic and proinflammatory
198 d TGF-beta1-induced enhanced ROS production, increased expression of profibrotic and proinflammatory
200 e-treated SPL-overexpressing cells exhibited increased expression of prohibitin 2 (Phb2), involved in
201 tes incubated with L. infantum significantly increased expression of proinflammatory genes for IL-6,
202 nd IL-17C+KO primary keratinocytes confirmed increased expression of proinflammatory molecules, sugge
204 he lung myeloid compartment characterized by increased expression of prometastatic genes, including i
205 ith differences in structural remodeling and increased expression of proteins involved in cardiac fun
206 tes, activation of FXR with obeticholic acid increased expression of proteins that regulate amino aci
208 l as UC mucosa, and between inflammation and increased expression of PTPN22 in colonic IBD mucosa, wa
213 l analysis, we found that IPF MPCs displayed increased expression of S100 calcium-binding A4 (S100A4)
215 on in the Wnt pathway, and qPCR confirmed an increased expression of secreted frizzled-related protei
219 id content were enhanced in roots along with increased expression of several nitrate assimilatory gen
224 ivities results in robust HSR induction with increased expression of specific heat shock proteins tha
225 differentially hydroxymethylated regions and increased expression of specific potassium channels in t
226 d colon tissues from Mefv-/-, which also had increased expression of stem cell markers (OLFM4, BMI1,
227 ytes transiently exposed to the SASP exhibit increased expression of stem cell markers and regenerati
230 M. tuberculosis-infected IL-21R KO mice had increased expression of T cell inhibitory receptors, red
231 th the lowest mortality was characterized by increased expression of T-cell immunoglobulin and mucin
232 gn3 stability and DNA binding, promoting the increased expression of target genes that drive differen
233 st, the RIP1-deficient cells were defined by increased expression of tartrate-sensitive prostatic aci
234 ould promote acute skin wound healing though increased expression of TGF beta leading to enhanced for
235 ge >2 and false discovery rate < 0.05), with increased expression of Th2, Th9, Th17/Th22 polar cytoki
237 associated with disease risk correlate with increased expression of the 7p21 gene TMEM106B and no ot
238 mportant, these changes were associated with increased expression of the antifibrotic protein Smad7 a
240 aberrant cortical positioning of neurons and increased expression of the astrocytic marker GFAP in th
241 s via divergent regulation of two processes: increased expression of the AtlA murein hydrolase and de
242 strated hypomethylation of MPO and PRTN3 and increased expression of the autoantigens; in remission,
243 -iPSC-CMs under catecholamine-induced stress increased expression of the cardiac stress marker NR4A1;
244 n led to enhanced G2/M cell-cycle arrest and increased expression of the CDK inhibitor 1B (p27Kip1) a
245 increased levels of Il1b, we did measure an increased expression of the chemokine-encoding gene Ccl2
246 in the lung-draining lymph node, as well as increased expression of the costimulatory molecule CD86.
248 ed beta-galactosidase (SA-betagal) activity, increased expression of the cyclin-dependent kinase (CDK
249 ptor co-agonist d-serine were accompanied by increased expression of the d-serine degrading enzyme d-
250 ic markers pdx1, glut2, mafA, and nkx6.1 and increased expression of the dedifferentiation markers so
251 methylation, resulting at least in part from increased expression of the DNA methyltransferase DNMT1
254 F-alpha- and TRAIL-mediated apoptosis due to increased expression of the ER stress mediator tribbles-
256 wn-regulation of diabetes-related genes, and increased expression of the genes encoding the myokines
257 Apc-mutant adenomas were characterized by increased expression of the glial nexin Serpine2, the hu
258 ification of the MYC gene is correlated with increased expression of the homologous DNA recombination
259 transcription 1 in the liver and spleen and increased expression of the IFN-gamma-inducible chemokin
261 ted with brain insulin resistance and showed increased expression of the key downstream messenger ins
262 ced efferocytosis, which was associated with increased expression of the macrophage efferocytosis rec
263 ilial PD patient fibroblasts, accompanied by increased expression of the mitochondrial calcium transp
264 vated mitochondrial-to-nuclear DNA ratio and increased expression of the mitochondrial markers transc
266 m airway hyperresponsiveness, due in part to increased expression of the murine ortholog of human chy
268 sion of angiotensin converting enzyme 2, and increased expression of the Na(+)-K(+)-2Cl(-) cotranspor
269 rimary cortical neurons in culture, ketamine increased expression of the neural plasticity-related pr
271 increased expression of CXCL12 downstream of increased expression of the noncanonical NF-kappaB trans
272 calization of the NRF2 transcription factor, increased expression of the NRF2-related antioxidant res
273 post-synaptic SMB motor neuron partners via increased expression of the odr-2 glycosylated phosphati
275 ecause both C57BL/6J and Pde11a KO mice show increased expression of the pro-inflammatory cytokine in
276 n premature depletion of the progenitors and increased expression of the proapoptotic protein Bim (al
277 uent translocations of 9p24.1 and associated increased expression of the programmed cell death protei
278 o kidneys with IRI, which was accompanied by increased expression of the proinflammatory molecules.
279 systems biology approach, is responsible for increased expression of the splicing factor PTBP1 (polyp
280 M-specific TH17 cell differentiation through increased expression of the TH17-instructing cytokines I
281 titis-like phenotype that is triggered by an increased expression of the thymic stromal lymphopoietin
282 otic lesions lacking myeloid CaMKIIgamma had increased expression of the transcription factor ATF6.
283 Analysis of transcriptomes indicated that increased expression of the transcription factor PHYTOCH
285 The hearts of FGFR1(DT-cKO) mice showed increased expression of the transient receptor potential
286 re(ERTM);LSL-Kras(G12D);Klf5(fl/fl) mice had increased expression of the tumor suppressor NDRG2 and r
287 e expression, whereas either no change or an increased expression of these genes was observed in mice
290 n of oncogenes (PDGFA, PDGFB, and TGFB1) and increased expression of tumor suppressor genes (TNFRSF14
292 A recent study from our group showed an increased expression of uncoupling protein-2 (UCP2) in p
293 trols, no change in tumour angiogenesis, but increased expression of vascular cell adhesion molecule-
295 ice, a model of post-traumatic OA in humans, increased expression of VEGF is associated with cataboli
297 n in murine and human macrophages results in increased expression of with-no-lysine kinase 1 (WNK1),
299 NFkappaBIZ, in the Treg-DC, together with an increased expression of Wnt5a, a negative regulator of D
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