ライフサイエンスコーパス: decreased expression

1 pid metabolic genes, with most genes showing decreased expression.

2 reas transforming growth factor-beta1 caused decreased expression.

3 oters of stem cell genes, resulting in their decreased expression.

4 ctivation of resting T cells resulted in its decreased expression.

5 nover were overrepresented in the genes with decreased expression.

6 g genes showing, respectively, increased and decreased expression.

7 sed vitamin B-12 in liver and cord blood and decreased expression and activity of MS in liver point o

8 Either intravenous or gastric loading led to decreased expression and activity of renal Pi transporte

9 Immunohistochemistry highlighted decreased expression and changes in KCC2 subcellular loc

10 ure neutrophils with functional deficits and decreased expression and storage of S100A12.

11 DICER1 gene alterations and decreased expression are associated with developmental d

12 educed H3K36me3 enrichment, concomitant with decreased expression at shared genes which function to m

13 creating gene lists with variably increased/decreased expression compared with steady state/baseline

14 pression is abnormal in psoriatic skin, with decreased expression correlating with recruitment of T-c

15 We also found evidence for decreased expression divergence of the homoeologous gene

16 these clusters included genes with initially decreased expression followed by increased expression at

17 suppressor in the normal mammary gland with decreased expression in breast cancer.

18 We discovered that FTO has decreased expression in failing mammalian hearts and hyp

19 to ischemia and DIO3, MT1G and CMA1 showed a decreased expression in females compared to males due to

20 veral SMALL AUXIN UP RNA (SAUR) genes showed decreased expression in mutant plants defective in these

21 3 snoRNA was one of a number of snoRNAs with decreased expression in osteoarthritic cartilage and ost

22 2 disease risk variants were associated with decreased expression in peripheral and mucosal tissues a

23 For NURR1 such decreased expression is associated with treatment with a

24 to the syncytiotrophoblast layer, and showed decreased expression later in gestation.

25 cer suggested a tumor-suppressive role where decreased expression led to increased metastasis.

26 apoptosis (IAPs) family member, exhibited a decreased expression level after DHM treatment, which ma

27 We also observed, from a separate study, a decreased expression level of DNA mismatch repair genes

28 Decreased expression level of phosphorylated AKT suggest

29 ermore, association between inflammation and decreased expression levels of MAGI3, PTEN, and TJP1 in

30 mortem DLPFC expression data analysis showed decreased expression levels of NURR1 and ERR1 in patient

31 classic M1 proinflammatory macrophages) and decreased expression levels of proinflammatory and profi

32 Immunochemical analysis revealed decreased expression levels of the NMDA receptor subunit

33 ervations, soluble extracts of PRF membranes decreased expression levels of the osteoclast marker gen

34 ng phenotype of Trem2 R47H knock-in mice was decreased expression levels of Trem2 in microglia, which

35 s associated with reduced cell viability and decreased expression levels of vimentin.

36 e ER genome wide-binding pattern, leading to decreased expression of 'classical' oestrogen-regulated

37 ted genes, and we confirm experimentally the decreased expression of 19 microRNAs with 11 correspondi

38 We identified decreased expression of 37/67 kDa laminin receptor (LAMR

39 l limitation to relaxin-based IPF therapy is decreased expression of a relaxin receptor, relaxin/insu

40 s a critical imbalance in RAS represented by decreased expression of ACE in combination with increase

41 The effects of increased or decreased expression of ACYL-COENZYME A:DIACYLGLYCEROL A

42 derailment at this early age is suggested by decreased expression of adiponectin, the fat mass and ob

43 wth on formate increased fhl1 expression but decreased expression of all other hydrogenases.

44 sing antifibrotic effect as indicated by the decreased expression of alpha smooth muscle actin, when

45 ic N-methyl-D-aspartate (NMDA) receptors and decreased expression of alpha-amino-3-hydroxy-5-methylis

46 ophosphamide was sufficient to normalize the decreased expression of alpha-smooth muscle actin in der

47 aginal cell DNA which may be associated with decreased expression of an estrogen-responsive gene.

48 d with OA derived extracellular vesicles had decreased expression of anabolic genes and elevated expr

49 lpha-Klotho in association with enhanced BP, decreased expression of angiotensin converting enzyme 2,

50 Extracts decreased expression of anti-apoptotic proteins (survivi

51 sufficient for infection in cell lines with decreased expression of antiviral IFN genes at baseline.

52 osmolality in mice that was associated with decreased expression of aquaporin (AQP)-2 in the renal i

53 A2, overexpression of ZmHSBP2 in Arabidopsis decreased expression of AtGOLS1, AtGOLS2 and AtRS5, decr

54 in Brown Norway rats showed a trend towards decreased expression of ATP5H.

55 Additionally, loss of Id2 resulted in decreased expression of aTreg-associated markers, includ

56 Epas1 deficiency led to the decreased expression of atypical mitochondrial subunits

57 This was associated with decreased expression of Bcl-xL and increased acetylated

58 ra-tumoral expression of the p16 and p53 but decreased expression of Bcl-xL and SMAD4.

59 that the relA knockout strains demonstrated decreased expression of beta-hemolysin/cytolysin, an imp

60 s, androgen deprivation in the medium led to decreased expression of both androgen receptor and its t

61 glycosylation end product (RAGE), exhibited decreased expression of both HMGB1 and MX1 after UVB exp

62 ading glioblastoma 2 (GLI2), followed by the decreased expression of both smoothened and GLI2.

63 These effects were paralleled by decreased expression of c-Myc and stemness-related genes

64 dingly, immunohistochemistry staining showed decreased expression of CARD14 in patients' skin, as wel

65 the other hand, CTK-1 overexpression led to decreased expression of CAT-3.

66 mbers of intra-tumoral activated T cells and decreased expression of Ccl17, Ccl22, and Foxp3.

67 bits TAM tumor infiltration, consistent with decreased expression of CCL2.

68 ts with high sST2, flow cytometry identified decreased expression of CD14 (4.27 x 10(5) +/- 2,950 arb

69 ations have immature CD56(dim) NK cells with decreased expression of CD16, perforin, CD57, and impair

70 tometry to characterize AMs, a significantly decreased expression of CD163, an M2 marker, was seen in

71 Cl-OCH3 also decreased expression of CD3(+)/CD4(+)/CD25(+)/FoxP3(+) r

72 ls, T cell subsets from methadone users show decreased expression of CD69 and CD25 in response to TCR

73 The strains exhibit decreased expression of CDKN2A (both p16(INK4a) and p19(

74 (2+) overload, mitochondrial depolarization, decreased expression of cell-cycle genes and reduced tum

75 IgG or phosphate-buffered saline (PBS), had decreased expression of chitin synthetase, CHS1, CHS2, a

76 Plants with decreased expression of class-I TCPs and plants that exp

77 This was associated with significantly decreased expression of claudin-5 in the vasculature of

78 This protection was associated with decreased expression of cleaved (activated) caspases 9 a

79 the phosphorylation of ERK, together with a decreased expression of cleaved caspase-3 in mice treate

80 creased ribosomal content was accompanied by decreased expression of cMYC, a positive regulator of ri

81 of A(2B) adenosine receptors correlated with decreased expression of Col1 and was associated with poo

82 depleted cardiomyocyte secretome resulted in decreased expression of collagen I and III in fibroblast

83 In vitro cultures of synthetic VSMCs showed decreased expression of contractile markers CNN-1 (calpo

84 This was accompanied by decreased expression of costimulatory and activating rec

85 itory factors CTLA-4, PD-1, and Blimp-1, and decreased expression of costimulatory molecules CD40L, C

86 isplayed enhanced expression of IL-1beta and decreased expression of counter-regulatory IL-1RA.

87 The results identify that in old males decreased expression of CRABP2 leads to cell proliferati

88 These differences were due to significantly decreased expression of crtOPQMN and aur Previous studie

89 BXD2-p19(-/-) GC B cells was associated with decreased expression of CSR-related novel base excision

90 (Tcm), evidence of Type I polarization, and decreased expression of CTLA-4 and PD-1 in BAL Tregs, su

91 Furthermore, we identified decreased expression of CXCR3 in nonresponding mice and

92 of cyclin-dependent kinase inhibitor p21 and decreased expression of cyclin B1.

93 This was likely due to decreased expression of cytokine and chemokine genes in

94 l cell-specific NRP1 knockout mice exhibited decreased expression of DDAH1 and slightly increased exp

95 Decreased expression of DGAT1 led to an increased percen

96 Infection with NiggV but not NiggA led to decreased expression of Dicer and Ago 2, suggesting that

97 In the TCGA CRC cohort, decreased expression of DNA repair genes associated with

98 Decreased expression of EGFR and RELA was validated by b

99 Accordingly, decreased expression of eIF5a elicited by Klf5 down-regu

100 We also showed a decreased expression of ELOVL5 in patients' blood at 40

101 defective LTbetaR signaling correlated with decreased expression of endothelial and angiogenic marke

102 nd differentiation pathways, suggesting that decreased expression of EPB41L4A is a mechanism in the p

103 EAC cells incubated with trastuzumab decreased expression of epithelial markers (CD24, CD29,

104 xifen as a result of increased autophagy and decreased expression of estrogen receptor-alpha.

105 ting enhanced cytolytic activity, as well as decreased expression of exhaustion markers in CD4(+) and

106 on of proteolysis in endothelial cells, with decreased expression of extracellular matrix remodeling-

107 id not affect lifespan, and was coupled with decreased expression of extracellular signal-regulated k

108 s downregulated in HCC patient specimens and decreased expression of FBP1 associated with poor progno

109 monstrated by reduced collagen abundance and decreased expression of fibronectin-1, collagen I, alpha

110 chors mGluR5 to the cell surface, as well as decreased expression of FKBP5, implicating aberrant gluc

111 educing sensory glutamate release results in decreased expression of GABA-synthesizing enzymes GAD65

112 ort-term or long-term cocaine administration decreased expression of Gas5 in NAc.

113 At 3 days post-injury (dpi), decreased expression of genes associated with cell proli

114 T(reg) cells deficient in complex III showed decreased expression of genes associated with T(reg) fun

115 a transcriptomic signature characterized by decreased expression of genes critical for mitochondrial

116 Impaired differentiation was associated with decreased expression of genes encoding critical hematopo

117 Decreased expression of genes encoding putative cell wal

118 nscriptional regulators TCF4 and NEUROD6 and decreased expression of genes involved in long-term pote

119 This deficit can be explained by decreased expression of genes involved in mature neuron

120 AHL4-OE seedlings displayed decreased expression of genes involved in TAG hydrolysis

121 essing CD38 and ICOS and was associated with decreased expression of genes that regulate cell-cycle a

122 eta, ERK 1/2, NF-kappaBp65, and NF-kappaBp50 decreased expression of GLUT4 mRNA were observed in the

123 ation of IKKbeta/NF-kappaB, resulting in the decreased expression of GLUT4.

124 ference silencing of GmMYB29A2 increased and decreased expression of GmNAC42-1, GmMYB29A1, and glyceo

125 MENT-BINDING2A mutant (zmdreb2a) lines, with decreased expression of GRETCHEN HAGEN3.2 (ZmGH3.2, enco

126 higher fasting insulinemia, concomitant with decreased expression of hepatic gluconeogenic genes.

127 osis, and the antiangiogenic factor GAX, and decreased expression of HIF-1alpha and proangiogenic fac

128 Emphysematous lungs exhibit decreased expression of HIF-2alpha (hypoxia-inducible fa

129 eased protein expression of MUC16, SIRPA and decreased expression of HLA-DRB1 was further demonstrate

130 s, reduced colony-forming activity in vitro, decreased expression of Hox genes in the hematopoietic s

131 TDF also increased expression of GFAP and decreased expression of IBA1 in the wt and gp120-tg mice

132 on, as TICAM2 deficient neutrophils have the decreased expression of ICAM1, CD11b, PD-L1, and the red

133 After ATI, decreased expression of IFN genes in pDCs inversely corr

134 BIIB059 administration in patients with SLE decreased expression of IFN response genes in blood, nor

135 R274W mice was associated with paradoxically decreased expression of IFN-stimulated genes (ISGs) and

136 are uniformly anti-inflammatory despite the decreased expression of IL-10.

137 ence of nuclear translocation of RelA with a decreased expression of IL-6, IL-12p40, and IL-17A.

138 ortant for iNKT17 differentiation, including decreased expression of IL-7Ralpha, BATF and c-Maf and i

139 EET decreased expression of IL6 (P < 0.05), C/EBPbeta (P < 0

140 Here we report that CTA was associated with decreased expression of immediate early genes in rat GC

141 sed expression of myelin-related genes and a decreased expression of immediate early genes.

142 We consistently observed decreased expression of inflammation-related genes NLRP3

143 monstrated improved urine output (P = .009), decreased expression of injury biomarker NGAL (P = .012)

144 levant neuropeptides in the hypothalamus and decreased expression of insulin receptor signaling genes

145 ormality; however, VHR-knockout cells showed decreased expression of integrins and FAK but stronger F

146 of programmed death-ligand 1 and IL-10, and decreased expression of interferon-gamma.

147 ssive antibiotic therapy was associated with decreased expression of interleukin-2 high-affinity rece

148 mic inflammation, nutrient malabsorption and decreased expression of intestinal and pancreatic genes

149 r effects through inhibition of lipogenesis; decreased expression of invasion associated proteins thr

150 RNAs encoding isoform 1 of RNF128 (Iso1) and decreased expression of Iso2 of RNF128.

151 in Fx-/- mice fed standard chow, leading to decreased expression of its target Hes1.

152 d a profound loss of tissue differentiation, decreased expression of keratin 4 (KRT4) and cornulin (C

153 Furthermore, residual Rora(sg/sg) ILC3s have decreased expression of key signature genes, including R

154 levels of ERK, RSK, ELK1 and DR5 along with decreased expression of Ki67.

155 of the proliferation marker Ki-67 as well as decreased expression of leptin-regulated genes.

156 o and JEG3 cells under hypoxia significantly decreased expression of LIN28B and LIN28A, SYN-1, and EL

157 ctivation and increased granulocytes; and 4) decreased expression of lymphocyte related genes and lym

158 blood samples, while nasal samples also had decreased expression of many genes associated with cilia

159 creased with advancing age concurrently with decreased expression of MEIS1.

160 umors, activation of RhoA is correlated with decreased expression of melanocyte lineage genes.

161 ltage-gated potassium channel gene Kcna1 and decreased expression of metabotropic glutamate receptor

162 h may be post-transcriptionally modulated by decreased expression of microRNA-155 in Treg-DC.

163 Decreased expression of miR-92 in CSCs led to higher exp

164 We noted that APN(-/-) mice showed decreased expression of mitochondrial biogenesis regulat

165 humans carrying the ADAMTS9 risk allele have decreased expression of mitochondrial markers.

166 In the brains of wt and gp120-tg mice, TDF decreased expression of mitochondrial transcription fact

167 elates with impaired DNA mismatch repair and decreased expression of Mlh1 and Msh2 genes, defects fre

168 Furthermore, PIM inhibition decreased expression of molecules engaged in shaping the

169 sd10 and Acaa2, and blunted VLDL export with decreased expression of Mttp and its product microsomal

170 ere also associated with either increased or decreased expression of multiple additional classes of t

171 unding the cuticle of the abdomen results in decreased expression of multiple HSR genes in proximal a

172 Consistently, we found that decreased expression of mutant p53 by FDXR deficiency in

173 ockdown resulted in increased E-cadherin and decreased expression of N-cadherin and snail transcripti

174 netic variants in NBEAL1 are associated with decreased expression of NBEAL1 in arteries and increased

175 iology associated with neuroinflammation and decreased expression of neuronal activity marker, which

176 ear factor-kappaB (NF-kappaB) activation and decreased expression of NF-kappaB target genes matrix me

177 genetic inhibition of sestrin 2 resulted in decreased expression of NKG2D and DAP12 and restored TCR

178 ardiomyocyte-related genes, and simultaneous decreased expression of nodal cardiomyocyte-related gene

179 ultiple sclerosis that were characterized by decreased expression of NRF2 and increased expression of

180 We found that constitutive NIK expression decreased expression of numerous Treg signature genes an

181 Furthermore, Cav3.2 inhibition decreased expression of oncogenes (PDGFA, PDGFB, and TGF

182 ed optic nerve pathological states, we found decreased expression of one major metalloproteinase prot

183 Immunofluorescence staining showed decreased expression of PADI3 in biopsy samples of scalp

184 ELENA1 knockdown plants show decreased expression of PATHOGENESIS-RELATED GENE1 (PR1)

185 ns This increase in survival correlated with decreased expression of pattern recognition receptors on

186 RNAi-mediated silencing of NR4A1 decreased expression of PAX3-FOXO1A and its downstream e

187 Likewise, decreased expression of PCDHA7 in the brain is linked to

188 against melanoma in a syngeneic model, with decreased expression of PD-L1 and of matrix metallo-prot

189 -4-hydroxy-5-methoxyphenyl)methane (Cl-OCH3) decreased expression of PD-L1 mRNA, promoter-dependent l

190 esenchymal stem/stromal cells, likely due to decreased expression of PDGF-AA and BMP2.

191 mural cells, an effect that associated with decreased expression of PDGFRbeta and p57kip2, a cyclin-

192 The CD56(dim) NK cell subset had decreased expression of perforin and CD16 and a greater

193 etastases exhibited cisplatin resistance and decreased expression of phosphorylated CREB1.

194 In DR, we found decreased expression of PKM2 and Pde6beta expression, bu

195 dominal aortic aneurysms and correlated with decreased expression of predicted miR-181b targets, tiss

196 t under glucose deprivation (GD) conditions, decreased expression of presenilin 1 (PS1) results in de

197 en of the striatum of xCT(-/-) mice revealed decreased expression of presynaptic proteins and abnorma

198 ith elevated expression of osteogenic genes, decreased expression of pro-inflammatory cytokine genes,

199 induces NEFM, RET, and VACHT and results in decreased expression of proapototic (BMF, BIM), adrenerg

200 3) A tendency for decreased expression of progesterone receptor co-activat

201 D8(+) T cells with an effector phenotype and decreased expression of programmed death receptor-1 (PD-

202 APAP-treated mice, with necrotic hepatocytes decreased expression of proinflammatory cytokines.

203 This enhanced adhesion was associated with decreased expression of protein kinase A regulatory subu

204 thione (GSH) was upregulated in chRCC due to decreased expression of proteins involved in GSH degrada

205 and DNA replication and damage repair, and a decreased expression of proteins responsible for core ex

206 ture silencing of Ptch1 These cells also had decreased expression of Pten, which encodes a negative r

207 blocks primitive hematopoiesis, as shown by decreased expression of pu.1, mpo, and l-plastin; and di

208 However, the zmdreb2a seeds, with decreased expression of RAFFINOSE SYNTHASE (ZmRAFS) and

209 ssues of HFD-fed UtxAKO female mice revealed decreased expression of rate-limiting enzymes of triacyl

210 nslates into reduced histone lactylation and decreased expression of reparative macrophage genes.

211 ocalization and decrease in visual pigments, decreased expression of retinoic acid-responsive genes a

212 Functional follow-up implied that decreased expression of REV3L may lower the probability

213 IgM also decreased expression of RIM101 and HOG1, genes encoding

214 We identified decreased expression of RNASET2 as a component of TL1A-m

215 rc, coding for stereocilin, and dramatically decreased expression of Rps4l, coding for a ribosome sub

216 ngevity pathways exhibit small nucleoli, and decreased expression of rRNA, ribosomal proteins, and th

217 ells (definitive hematopoiesis), as shown by decreased expression of runx1 and c-myb However, adtrp1

218 ld-type at 29 degrees C, suggesting that the decreased expression of SAUR genes is partly responsible

219 in differentiating neural cells we observed decreased expression of schizophrenia-associated gene Fe

220 Decreased expression of SDH-A and COX-I demonstrated tha

221 ts with OA undergoing total knee replacement decreased expression of senescent and inflammatory marke

222 portant stimuli for TNFalpha expression, and decreased expression of several M2 markers, including in

223 Decreased expression of SLC25A46 results in increased st

224 sed expression of VLDLR, as well as 1.5-fold decreased expression of SMARCA2, located 388 kb away.

225 blocked the activation of primary HSCs, with decreased expression of smoothened, GLI2 and ILK compare

226 ted substantial activation of p53 and STAT3, decreased expression of SOCS7, and increase in profibrot

227 , increased expression of WNT4 and FOXL2 and decreased expression of SRY and SOX9.

228 Uterine tumor epithelium was associated with decreased expression of steroid biosynthesis genes, incr

229 luteinizing hormone/testosterone ratio, and decreased expression of steroidogenic mRNAs, appropriate

230 K9.361 injection also decreased expression of stimulatory Fcgamma receptors, e

231 BRB decreased expression of survival/proliferation-associate

232 and Bifidobacterium-colonized mice exhibited decreased expression of synapse-promoting genes and incr

233 terferon-gamma, and fractalkine as well as a decreased expression of synaptophysin, a neuronal activi

234 rence affected viral splicing and, like 1C8, decreased expression of Tat, Gag and Env.

235 of eIF4E-binding protein (4EBP1) resulted in decreased expression of TCF7L2.

236 Decreased expression of TGFB pathway signaling ligands w

237 sed the immunosuppressive nature of MDSC and decreased expression of TGFbeta1 and arginase 1.

238 sverse aortic constriction, corresponding to decreased expression of the angiogenic factor VEGF.

239 ed inflammation under high-SS conditions and decreased expression of the antiinflammatory factor KLF-

240 l BA, colonocytes from WD-fed mice exhibited decreased expression of the BA transporters FABP6, OSTbe

241 A2AAR-KO mice had decreased expression of the beta-cell-specific markers p

242 rliest signaling alterations in CRC, and the decreased expression of the bile acid apical transporter

243 mponent protein expression, they demonstrate decreased expression of the calcium-dependent protein ki

244 d spread of bacteria in infected leaves, and decreased expression of the central defense gene TaNPR1

245 tumors have elevated T cell infiltrates and decreased expression of the CLEC2D receptor, which may p

246 ity associated with infection sites, and had decreased expression of the early auxin responsive gene

247 pressive Tregs in the injured myocardium and decreased expression of the gene encoding IFN-gamma, a k

248 Disc1-KD in astrocytes also led to decreased expression of the glutamatergic and increased

249 specification of hemangioblasts, as shown by decreased expression of the hemangioblast markers, etsrp

250 n mice is cell intrinsic and associated with decreased expression of the high affinity IL-2 receptor

251 of the IL23 subunits IL23p19 and IL12p40 but decreased expression of the IL12 subunit IL12p35 in cerv

252 ed expression of proinflammatory factors and decreased expression of the immunosuppressive cytokine I

253 nic hepatitis C virus (HCV) infection causes decreased expression of the iron hormone hepcidin, which

254 ression of the iron exporter ferroportin and decreased expression of the iron importer transferrin re

255 These amiCOX19 plants, however, showed decreased expression of the low-copper responsive miRNA

256 s and microglial accumulation accompanied by decreased expression of the LPC receptor G2A, whereas MS

257 aternal PolyI:C exposure was associated with decreased expression of the maternally imprinted genes M

258 The increase in PP2A activity is caused by decreased expression of the MID1 ubiquitin ligase that m

259 Here, we demonstrate decreased expression of the mitochondrial Na(+)/Ca(2+)/L

260 morphine tolerant mice, contributing to the decreased expression of the mouse and human MOR-1B3 and

261 Furthermore, we found decreased expression of the MR and downstream molecules

262 normal human diploid fibroblasts results in decreased expression of the mTOR inhibitor DDIT4 (REDD1)

263 city to use glycolysis, a function linked to decreased expression of the NAD(+)-dependent protein dea

264 xpression of the anti-oxidant marker CAT and decreased expression of the pro-oxidant marker NOX-4.

265 more complete inhibition of p-S6, leading to decreased expression of the pro-survival protein MCL-1,

266 This resistance correlated with decreased expression of the senescence regulator, DNMT1,

267 Furthermore, DOCA treatment led to decreased expression of the slit diaphragm-associated pr

268 ng in cystinosis was found to associate with decreased expression of the small GTPase Rab11 and the R

269 pecific proteins, rhodopsin and cone opsins, decreased expression of the specific inflammatory marker

270 miscarriage is associated with significantly decreased expression of the T-cell co-receptor CD8 and t

271 terations in this group are likely driven by decreased expression of the transcription factor FOXM1 a

272 Previous studies have reported decreased expression of the transcription factor SOX9 (s

273 ds to rapid cell de-differentiation, without decreased expression of the transcription factors NKX2-1

274 Mutant kidneys also had decreased expression of the UT-A urea transporter and co

275 Overexpression of CD44-ICD also resulted in decreased expression of these chondrocyte genes.

276 ersely, overexpression of HDAC11 resulted in decreased expression of these genes.

277 ne (CHS), whereas the mybs2 mutant exhibited decreased expression of these genes.

278 for pulmonary endothelial HIF-2alpha and how decreased expression of this endogenous factor causes em

279 regulation of GLI transcription factors also decreased expression of TIC marker CD24.

280 echanisms play a role in drug resistance via decreased expression of TOP2alpha/170.

281 Decreased expression of TRANK1 perturbed expression of m

282 how that Treg cells in food allergy (FA) had decreased expression of transforming growth factor beta

283 d with promoter hypermethylation, leading to decreased expression of tumor suppressor genes, as well

284 giogenic factor thrombospondin 1 (Tsp-1) and decreased expression of two critical pro-angiogenic fact

285 d activation of microglia and astrocytes and decreased expression of tyrosine hydroxylase in periglom

286 lotting analyses showed that MEOX1 knockdown decreased expression of tyrosine kinase 2 (TYK2), signal

287 zed by decreased energy expenditure (EE) and decreased expression of uncoupling protein 1 (UCP1) in b

288 S promoters, enhanced ICAM-1 expression, and decreased expression of upstream regulators of KLF2 (ERK

289 Clinically, decreased expression of USP49 in patients with pancreati

290 revealed a decreased copy number of UT2 and decreased expression of UT2 in genomic and transcriptomi

291 idenced by a reduced clinical disease score, decreased expression of various inflammatory cytokines,

292 Under the same condition, the decreased expression of vascular endothelial cadherin, p

293 pression of E-cadherin and beta-catenin, and decreased expression of vimentin and snail, which is par

294 ction, GYY4137 treatment was associated with decreased expression of viral proteins and mRNA, suggest

295 nes showed 1.2-fold significantly (P < 0.04) decreased expression of VLDLR, as well as 1.5-fold decre

296 We show that decreased expression of VPS29 in the brain may increase

297 expression of the AtlA murein hydrolase and decreased expression of wall-teichoic acids.

298 r collagen deposition and myofibroblasts and decreased expressions of MMP-1.

299 ite branches and total neurite length, and a decreased expression on RhoA and neurodegenerative prote

300 rugs, metabolites, or toxins and reverse the decreased expression under disease conditions.