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1       In NK cells, CD16a stimulation induced increased expression of 276 transcripts (FC > 2x, false
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
6                        The loss of macroH2A1 increased expression of a panel of stemness-associated g
7                        KDM5i treatment alone increased expression of a small number of genes, whereas
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
10              Transcriptomics analyses showed increased expression of A20 (tumor necrosis factor alpha
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
16            FAK activation is associated with increased expression of alpha-smooth muscle actin (alpha
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
22              HNF-1beta mutant kidneys showed increased expression of aquaporin-2 mRNA but mislocalize
23 iosynthetic pathways is partially due to the increased expression of AR splice variants.
24                                Intriguingly, increased expression of Arf in tumor stromal cells, as i
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,
28                               Meanwhile, the increased expression of ATF4 and HO-1 mRNAs were observe
29 sion of HuR, Bcl2, cyclin E, and Bcl-XL with increased expression of Bax and p27 in CMLD-2-treated NS
30                                We found that increased expression of Bcl-6 in CD4(+) Th cell populati
31 expression of IL-7Ralpha, BATF and c-Maf and increased expression of Bcl11b and Lef1.
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
35 , Wnt3a and NP12 stabilized beta-catenin and increased expression of both Nanog and VEGFR2.
36 activation of Elk-1 transcription factor and increased expression of c-Fos gene.
37                                 MUC1 induces increased expression of c-myc in EVs that induces prolif
38 e damage during ischemia was associated with increased expression of C3/C3 fragments primarily in the
39                            In particular, an increased expression of Cad-11 can be detected on the pl
40            The mpk3 and mpk6 mutants display increased expression of CBF genes and enhanced freezing
41       Constitutive activation of RhoA led to increased expression of CCL2, IL6, TNF-alpha, and CXCL10
42 an essential autophagy gene, FIP200, in NSCs increased expression of Ccl5 and Cxcl10 in a p53-indepen
43               Also, patients' DCs present an increased expression of CD62L and a tendency to overexpr
44 immune cells, especially CD8(+) T cells, and increased expression of cell proliferation markers.
45  reduced expression of pluripotency factors, increased expression of cell-lineage-affiliated developm
46                    Using this model, we show increased expression of cellular prion protein (PrP(C))
47 racterized by infiltration with neutrophils, increased expression of chemokine (C-X-C motif) ligand (
48              For duplications, we found that increased expression of CHRNA7 mRNA is associated with h
49  adaptation by S. aureus to obesity/T2D with increased expression of clfA that is associated with the
50         We found that low SES was related to increased expression of conserved transcriptional respon
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
54         We could demonstrate mechanistically increased expression of Cxcl10 by hepatocytes, and conse
55 t the loss of Twist1 in IPF lung fibroblasts increased expression of CXCL12 downstream of increased e
56 ced pulmonary fibrosis, which is mediated by increased expression of CXCL12.
57 and induced cell cycle arrest accompanied by increased expression of cyclin-dependent kinase inhibito
58                                          The increased expression of cyp1a (2.49 +/- 0.28-fold), udpg
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 (
67            Both CSE and CS treatment induced increased expression of Duox-1, and silencing of Doux-1
68 phenotypic inversion of EMT, correlated with increased expression of E-cadherin and beta-catenin, and
69            Loss of atypical E2Fs resulted in increased expression of E2F target genes, including E2f1
70              We therefore speculated whether increased expression of EBI2 would lead to an expanded B
71                                              Increased expression of EGFR in myeloid cells from the c
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
75            In addition, HDAC11KO T cells had increased expression of Eomesodermin (Eomes) and TBX21 (
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
78                            In Hjv(-/-) mice, increased expression of exogenous MT2 in the liver signi
79       Aortic tissue from Micu2(-/-) mice had increased expression of extracellular matrix remodeling
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
82 therapeutic agent for HCC cases that exhibit increased expression of FGF19.
83                      DEX-Ac treatment led to increased expression of fibronectin, collagen I, and alp
84  of TSP1 activation of TGFbeta, reversed the increased expression of fibrotic molecules.
85 and monocytes/macrophages in capillaries and increased expression of five biologically relevant genes
86 1 showed increased suppressive function, and increased expression of Foxp3 and TGF-beta.
87           In the setting of viral hepatitis, increased expression of Gal-9 drives the expansion of re
88 ponse, but PD-L1-expressing ILC2s stimulated increased expression of GATA3 and production of IL-13 by
89                                  We observed increased expression of GATA3 by lamina propria T cells
90 conate levels in loz1Delta cells result from increased expression of gcd1 By analyzing the activity o
91                                  We observed increased expression of genes associated with inflammato
92 volved in mature neuron function, along with increased expression of genes atypical of the olfactory
93                In contrast, obeticholic acid increased expression of genes encoding enzymes involved
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
99                                          MCH increased expression of genes regulating hypoxia signall
100                                          MCH increased expression of genes regulating sodium (SCNN1-B
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
103                  CP was characterized by the increased expression of genes related to responses to ex
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
107                  To determine the effects of increased expression of human aldosterone synthase (hAS)
108 ing metagenomic sequencing related SAMHD1 to increased expression of human endogenous retrovirus K (H
109                                  We observed increased expression of IFN-beta, IFN-lambda1/IL-29, OAS
110                 RNASET2 knockdown in T cells increased expression of IFNG and intercellular adhesion
111        De novo DSA ABMR was characterized by increased expression of IFNgamma-inducible, natural kill
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
114                             We confirmed the increased expression of IL-36alpha in the renal tubular
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
120                       In a regression model, increased expression of IL5 and IL17A mRNAs distinguishe
121            These changes were accompanied by increased expression of immune genes in adipose tissue a
122            In vivo, mAAQ was associated with increased expression of immune modulators PD-L1 (program
123 ol feeding decreased miR181b-3p in liver and increased expression of importin alpha5 in nonparenchyma
124            Treatment of BMDCs with oxLDL ICs increased expression of inflammasome-related genes Il1a,
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
131                     ConA-treated HSCs showed increased expression of interferon-beta, tumor necrosis
132                                              Increased expression of Interleukin (IL)-33 has been det
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
137                       We further demonstrate increased expression of KATII and KMO, but not IDO, in v
138                                     We found increased expression of KIBRA and phosphorylated YAP pro
139            This current is likely due to the increased expression of Kir2.1 channels.
140  In UN-KC-6141 cells, PI3K and MEK signaling increased expression of KLF5; a high level of KLF5 incre
141 of keratin 4 (KRT4) and cornulin (CRNN), and increased expression of KRT5 and KRT14.
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
146                   The chemical exposure also increased expression of major inflammatory cytokines, in
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
153                                              Increased expression of MCM8 in prostate cancer is assoc
154                                              Increased expression of mcr-1 results in decreased growt
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
158                                          The increased expression of miR-323-3p and noncoding RNA nc8
159                                           An increased expression of miR-323-3p in PBMCs from patient
160  lacking A2AR develop an 'OA phenotype' with increased expression of Mmp13 and Col10a1.
161                  The OX lines also displayed increased expression of Mn transporters and were more se
162 s increased protease activity coincided with increased expression of mRNA for kallikreins (KLKs), wit
163                                 We validated increased expression of multiple miRNAs, including miR12
164            RNA-sequencing analysis showed an increased expression of MYBL1 in tumor cells with OGT kn
165 up of double-expressor lymphomas, which have increased expression of MYC and BCL-2 and/or BCL-6 by im
166 n, enhanced its transcriptional activity and increased expression of MYC-regulated genes.
167 aH222P/H222P mice, which was associated with increased expression of myocardial connexin 43.
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
170        We demonstrate that ES contributes to increased expression of neural differentiation biomarker
171 lly examined CM gene expression and observed increased expression of neuronal markers Dcx, Map2, and
172                                              Increased expression of neurotensin receptor 1 (NTR1) ha
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
175                           We now report that increased expression of NKG2D ligands after virus infect
176                  We observed a significantly increased expression of NKG2D ligands on cells infected
177                        These data suggest an increased expression of NLRP12 in association with prost
178         Our results demonstrate distinctive, increased expression of NLRP3, caspase-1, and IL-1beta i
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
181                            We found that LPS increased expression of Nox4, TNF-alpha, and proliferati
182  clinically relevant doses of FTY720 to mice increased expression of NPC1 and -2 in brain and liver a
183                               FTY720 greatly increased expression of NPC1 and -2 in human NPC1 mutant
184    Real-time RT-PCR also showed dramatically increased expression of osteogenesis marker genes only i
185                               Interestingly, increased expression of osteogenic differentiation-relat
186  combination treatment remarkably (P < 0.05) increased expression of p-Akt and anti-apoptotic protein
187 ited AKT phosphorylation, activated PTEN and increased expression of p-eIF2a.
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.
192                         Single ATP injection increased expression of phospho-STAT3 and GAP43, two mar
193                      JUNV infection leads to increased expression of PKR as well as its redistributio
194 ased phosphorylation of STAT3 on Ser727, and increased expression of PML, a STAT3 transcriptional tar
195 aloside IV treatment, as demonstrated by the increased expression of PPARalpha and SERCA2a.
196                                              Increased expression of PPP1R11 in p53-deficient CRC cel
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
199                  This was associated with an increased expression of profibrotic genes and transformi
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
203          Hippo-deficient cardiomyocytes have increased expression of proliferative genes and stress r
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
207          Immunohistochemical staining showed increased expression of pSMAD158 and VEGF in the MCC and
208 l as UC mucosa, and between inflammation and increased expression of PTPN22 in colonic IBD mucosa, wa
209         We found that lal(-/-) ECs displayed increased expression of Rab7, a late endosome/lysosome-a
210         Smurf2-deficient osteoblasts display increased expression of RANKL, the central osteoclastoge
211                                     We found increased expression of RTN1A and ER stress markers in t
212  and is also bound by RBM3, which drives the increased expression of RTN3.
213 l analysis, we found that IPF MPCs displayed increased expression of S100 calcium-binding A4 (S100A4)
214                                     We found increased expression of S100A12 in the epidermis of huma
215 on in the Wnt pathway, and qPCR confirmed an increased expression of secreted frizzled-related protei
216                                        Thus, increased expression of sEH is a key determinant in the
217           The antennae of R. prolixus showed increased expression of several chemosensory-related gen
218                                ATP injection increased expression of several markers for regenerative
219 id content were enhanced in roots along with increased expression of several nitrate assimilatory gen
220         MEAN suppressed C-MYC expression and increased expression of several tumor suppressor genes,
221 ation of nuclear factor-kappaB, resulting in increased expression of SMAD6 and SMAD7.
222                     This was correlated with increased expression of soluble Frizzled-related protein
223        We found that Msx gene overexpression increased expression of specific blastemal markers and e
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
228              After radiation, the CD8(+) DCs increased expression of surface molecules required for N
229 ion reduced levels of phosphorylated tau and increased expression of synaptophysin.
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
236                  In MG63 osteoblastic cells, increased expression of the 1,25(OH)2D target gene CYP24
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
239         VIVIT treatment in 5xFAD mice led to increased expression of the astrocytic glutamate transpo
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.
247                       Previously we observed increased expression of the critically important beta-ce
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
252                                              Increased expression of the EGR1-regulated cardioprotect
253 ot account for all the actions observed with increased expression of the enzyme.
254 F-alpha- and TRAIL-mediated apoptosis due to increased expression of the ER stress mediator tribbles-
255 sitivity to Wnt stimulation, associated with increased expression of the FZD4 receptor.
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
260        The Igf1r-deficient mice exhibited an increased expression of the IGF system and surfactant ge
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
265                      Consistently, SCH772984 increased expression of the mitochondrial transcriptiona
266 m airway hyperresponsiveness, due in part to increased expression of the murine ortholog of human chy
267                                              Increased expression of the mutant GlyR alpha1(Q177K) su
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
270                 Additionally, we observed an increased expression of the NLRP3 gene in macrophages an
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
274                                              Increased expression of the pluripotency gene Klf4 in th
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
284                                Moreover, the increased expression of the transcription factors GLI1/G
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
288 nd PDCD1LG2/PD-L2, and copy number-dependent increased expression of these ligands.
289                                              Increased expression of TLR4 and myeloid differentiation
290 n of oncogenes (PDGFA, PDGFB, and TGFB1) and increased expression of tumor suppressor genes (TNFRSF14
291                                  We observed increased expression of type 1 IFN-stimulated genes (ISG
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-
294 ion, formation of a continuous EC layer, and increased expression of VE-cadherin.
295 ice, a model of post-traumatic OA in humans, increased expression of VEGF is associated with cataboli
296 ement and activity, ultimately leading to an increased expression of virulence.
297 n in murine and human macrophages results in increased expression of with-no-lysine kinase 1 (WNK1),
298                             Furthermore, the increased expression of Wnt4 elevated the phosphorylatio
299 NFkappaBIZ, in the Treg-DC, together with an increased expression of Wnt5a, a negative regulator of D
300                      Here we determined that increased expression of XRN2 induced EMT and promoted me

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