ライフサイエンスコーパス: increased expression

1 the YY1 and GABPA transcription factors and increased expression.

2 ins such as BMP2, COL1a1 and OCN, all showed increased expression.

3 ong these, BHLHE40, MIR210HG, and HILPDA had increased expression among winter births (Bonferroni P <

4 In this study, we observed increased expression and activation of YAP (yes-associat

5 In particular, MDR is characterized by increased expression and activity of ATP-binding cassett

6 lation in macrophages was associated with an increased expression and activity of glutamine fructose

7 e of neurodevelopmental TF binding sites and increased expression and binding capacity of activity-re

8 This effect depends on increased expression and chromatin loading of PRIMPOL an

9 Increased expression and nuclear localization of LEF1 ar

10 in of function due either to mutations or to increased expression can disrupt critical cellular proce

11 Moreover, its increased expression correlates with poor prognosis in A

12 with several nonhistone substrates and their increased expression has been highlighted in specific di

13 ) release channel in cholangiocytes, and its increased expression has been related to the pathogenesi

14 Overall, our results show that increased expression heterogeneity is a characteristic o

15 IV(6)Neu5Ac-nLc(4)Cer had increased expression in both CSCs and non-CSCs of both c

16 e we show that NOTCH1 gene amplification and increased expression in CAFs are an attractive target fo

17 differentiated intestinal Caco-2 cells, but increased expression in hepatic Huh7 cells.

18 We demonstrate that 15-PGDH shows areas of increased expression in patients with IPF.

19 The genes with most markedly increased expression included members of the erythrocyte

20 11H cells showed lower apoptosis rates at an increased expression level of MT2A after cisplatin treat

21 a challenge with LPS treatment significantly increased expression levels of alpha7nAChR in monocytes,

22 Furthermore, depletion of DYRK1A increased expression levels of cyclin L2.

23 and human primary cells led to dramatically increased expression levels of HS3ST1, a key enzyme invo

24 dicating that tissue remodelling rather than increased expression might contribute to their presence

25 LDH) and was oxidative in nature as shown by increased expression of 8-hydroxydeoxyguanosine (8-OHdg,

26 onsistent with this explanation, we observed increased expression of a GABA transporter, GABA transpo

27 in refractive index in the lens nucleus and increased expression of a particular crystallin protein

28 In addition, increased expression of a serine protease inhibitor, the

29 MLL1) gene rearrangement is characterized by increased expression of a set of homeodomain transcripti

30 risk for schizophrenia and bipolar disorder, increased expression of a ST3GAL3 transcript with risk f

31 VEP is sensitive to changes mediated by the increased expression of alpha-synuclein and especially w

32 compared to naive MDSC control, evMDSC have increased expression of an anti-angiogenic factor thromb

33 pt with risk for schizophrenia and ADHD, and increased expression of an XPNPEP3 transcript with risk

34 iated reduction in drug sensitivity involves increased expression of antiapoptotic proteins and susta

35 ic survivors, nonsurvivors had significantly increased expression of any checkpoint molecule on any c

36 ney HEK293 cells and examined the effects of increased expression of APOL1 (G0, G1, G2, G0G0, G0G1, o

37 arrest, reduced proliferation, migration and increased expression of apoptotic markers.

38 Increased expression of Atg5, Atg16, Irgm1, Tlr4, and Ly

39 The increased expression of Atoh1 mRNA after LKB1 loss from

40 anced Zip14-dependent zinc uptake by muscle, increased expression of Atrogin1 and MuRF1 and markedly

41 of Ras, inhibition of Akt/mTOR pathways, and increased expression of autophagy markers, leading to an

42 d cell growth and induced apoptosis and also increased expression of Bax as well as cleaved caspase-3

43 increased brain capillary pericyte density, increased expression of BBB tight junction proteins, red

44 In addition, we find increased expression of beta-site cleaving enzyme (BACE1

45 ersus tumor-infiltrating monocytes and found increased expression of both pro- and anti-inflammatory

46 eads that could not pass the plasma membrane increased expression of both TCSn::GFP and Cytokinin Res

47 We detected increased expression of both tumor-associated truncated

48 SIK1) stabilized the deacetylase, leading to increased expression of c-Myc, which in turn stimulated

49 ediated synaptic engulfment is enhanced with increased expression of C4.

50 These changes are preceded by increased expression of calcium/calmodulin kinase IV (CA

51 d with amplification of Myc target genes and increased expression of canonical Wnt signaling in treat

52 This coincided with increased expression of caspase-8-associated protein 2,

53 Next, we show a significantly increased expression of caspase-mediated apoptosis by si

54 n AAA tissues obtained from surgery revealed increased expression of CCR2 that was co-localized with

55 g repertoires as a result of infection, with increased expression of CD103 in colon NK cells and curt

56 cells (Tregs), in contrast, demonstrated an increased expression of CD28 with aging and CTLA4-Ig tre

57 reater competitive advantage as evidenced by increased expression of CD5 and IL-7Ralpha.

58 BCG infection increased expression of CD54, MHC Class I and II molecul

59 , CRP level was 12.5mg/dl and the remarkably increased expression of CD64 on neutrophils was found.

60 Larger and more irregular tumors showed increased expression of cell cycle and DNA damage checkp

61 Diseased endothelium had increased expression of chemokine and alarmin genes incl

62 ylation, aberrant metabolic profiles, and an increased expression of chemokines, indicative of a pers

63 NA-sequencing of DAC-treated tumors revealed increased expression of Chi3l3 (Ym1), reflecting an incr

64 DXR induced increased expression of Cldn2 and Cldn4 in murine small

65 hosphorylation state, as demonstrated by the increased expression of Collagen-I by HSCs incubated wit

66 d that during desiccation, all three species increased expression of common protective genes.

67 CD11c(+) cells from Sema3E KO mice displayed increased expression of costimulatory molecules and IL-1

68 ation of mouse, human, and porcine APC, with increased expression of costimulatory molecules and secr

69 the brain may increase risk to SCZ only and increased expression of CSE1L is associated with SCZ and

70 criptomic analysis linked elevated injury to increased expression of Cybb, the gene encoding the cata

71 ployed a model of murine BSM tissue in which increased expression of desmin or vimentin was induced b

72 Increased expression of diffuse mHtt sequesters the CREB

73 TBI increased expression of DNA sensors cyclic GMP-AMP synth

74 reatment of MDSC-like cells activated STAT3, increased expression of DNMT1 and DNMT3b, and enhanced s

75 migraine trigger, nitroglycerin, we observed increased expression of DOR in cortex, hippocampus, and

76 F-beta3, phospho-AKT and phospho-PRAS40, but increased expression of E-cadherin.

77 a result of tumour cell re-wiring leading to increased expression of EGFR, MAPK, CDK4, CDK2, CDK7, CC

78 in reduced muscle expression of miR-379 and increased expression of EIF4G2 and DAPIT.

79 Ilea of mutant mice displayed increased expression of enterocyte markers, but reduced

80 We identified increased expression of envelope (Env) trimers at the ce

81 Importantly, increased expression of epithelial-derived GSDMD is obse

82 staining of joints from the HFD group showed increased expression of ER stress and apoptotic markers

83 The increased expression of ER stress-associated proteins in

84 Breast cancer progression is accompanied by increased expression of extracellular and cell-surface p

85 esistance but increased cell migration, with increased expression of extracellular matrix-related gen

86 and the transcriptomic level, indicated that increased expression of factors such as interferon-gamma

87 Increased expression of FcgammaRIIB correlated with free

88 from smokers and subjects with COPD display increased expression of ferroportin as well as hepcidin.

89 for acquired resistance to EGFR TKIs through increased expression of FGFR1.

90 ed skeletal muscles, which were confirmed by increased expression of fibroblast growth factor-inducib

91 Increased expression of Filamin-B in podocytes in biopsy

92 Our findings indicate that increased expression of FMR1 mRNA isoforms, including Is

93 ion of primate-conserved LINE-1s, as well as increased expression of full-length hominid-specific LIN

94 nerating crypts from patient biopsies showed increased expression of Gal-9, indicating these processe

95 otrophic factor (GDNF) in injured muscle and increased expression of GDNF family receptor alpha1 (GFR

96 qPCR confirmed increased expression of GDPD1 and increased expression o

97 e WT EBV- versus Delta3A-infected tumors and increased expression of genes associated with T cells, s

98 eq and quantitative RT-PCR analyses revealed increased expression of genes associated with tumor cell

99 Livers of Nod2(-/-) tumorigenic mice had increased expression of genes involved in cell prolifera

100 ssion revealed that downregulation of Rab27a increased expression of genes involved in epithelial-to-

101 ng the pancreas of humans with T1D exhibited increased expression of genes located on misfolded loci

102 ced B cell IgA production in vitro, with the increased expression of genes related with class-switchi

103 r overnight fasting, BAT lacking ALK7 showed increased expression of genes responsive to nutrient str

104 educed EZH2 mRNA and protein levels but also increased expression of genes silenced by EZH2, such as

105 tissues from patients with liver disease had increased expression of genes that define PMC identity c

106 Expansion of tuft cells was associated with increased expression of genes that regulate the tricarbo

107 th primary muscle afferent sensitization and increased expression of glial cell line-derived neurotro

108 enitor cells promotes cell proliferation and increased expression of glial markers and glia-enriched

109 ation of mutant TLR4 marrow cells results in increased expression of gluconeogenic genes and impaired

110 ncreased levels of glycolytic intermediates, increased expression of glycolysis genes, and increased

111 In patients with lung cancer, increased expression of HACE1 correlated with reduced le

112 blood glucose levels that is associated with increased expression of hepatic gluconeogenic enzymes in

113 /-) mutant zebrafish exhibited significantly increased expression of hepatocyte markers with no impac

114 Vs of the HERV-K and -H families, as well as increased expression of HERV-K envelope protein.

115 Stimulation of fibroblasts with TGFbeta1 increased expression of HVEM; subsequent stimulation wit

116 -gamma production in mesenteric lymph nodes, increased expression of Ido1 in the cecum, and a complet

117 nflammatory response that is associated with increased expression of IFN-beta and other IFN-related g

118 NOX2 deficiency results in increased expression of IFN-stimulated genes in response

119 er of bronchoalveolar lavage eosinophils and increased expression of IL-13 mRNA but not expression of

120 ay 6 before RV-A2 infection on day 13 showed increased expression of IL-13, IL-5, Gob5, Muc5b, and Mu

121 We found increased expression of IL15RA and IL21 in duodenal tiss

122 Increased expression of IL17A and associated cytokines w

123 We observed increased expression of IL22 and the IL22 receptor (IL22

124 Increased expression of IL22 by PDACs is associated with

125 g shotgun metagenome sequencing and observed increased expression of immune-modulating microbiota, su

126 86 with a serine (VbrK C86S mutant) leads to increased expression of inflammatory cytokines in infect

127 sive tissue infiltration by immune cells and increased expression of inflammatory cytokines.

128 NMT3A mutations demonstrated a significantly increased expression of inflammatory genes compared with

129 st commonly found mutations in CHIP, lead to increased expression of inflammatory genes in innate imm

130 transfected to overexpress LPCAT2 exhibited increased expression of inflammatory genes in response t

131 tory receptor Ly49D on educated NK cells and increased expression of inhibitory receptor NKG2A/CD94 o

132 share a common core phenotype including the increased expression of inhibitory receptors, associated

133 uppressed by the tumor microenvironment, and increased expression of inhibitory receptors, including

134 firmed decreased ERBB3/ERBB4 while revealing increased expression of insulin-like growth factor recep

135 [LLV]) or point mutations in Lpro result in increased expression of interferon (IFN) and IFN-stimula

136 g, we reveal rapid viral replication and the increased expression of interferon-associated genes and

137 Increased expression of interferon-stimulated genes (ISG

138 Removal of SLP increased expression of K1, K10 and K2 in 2D and 3D cult

139 nontarget microRNA control ZIKV demonstrated increased expression of key cytokines and chemokines cri

140 levated extracellular acidification rate and increased expression of key glycolytic genes (GLUT1, HK2

141 inct in young and older adults; for example, increased expression of killer cell lectin-like receptor

142 bility of release associated with an overall increased expression of L-type voltage-gated Ca(2+) chan

143 human ortholog of MaTAR25, and importantly, increased expression of LINC01271 is associated with poo

144 n revealed that rs2242367 is associated with increased expression of LRRK2 and two long intergenic no

145 Here we demonstrate increased expression of LTbetaR ligands in adaptive and

146 ls results in activation of beta-catenin and increased expression of lymphoid enhancer-binding factor

147 s and Sjogren's syndrome patients identified increased expression of lysosome-associated membrane pro

148 cterized by decreased expression of NRF2 and increased expression of MAFG, which cooperates with MAT2

149 onse to cornea debridement wounding, we find increased expression of MAGP1 throughout the central cor

150 nd that NPCs cultured in BrainPhys displayed increased expression of markers for cortical deep-layer

151 nts during HSC activation and accompanied by increased expression of markers of fibrogenesis; incubat

152 o ductal metaplasia, stem cell features, and increased expression of markers of the epithelial-mesenc

153 llagen due to impaired TGFbeta signaling and increased expression of matrix metalloproteinases drivin

154 quencing of engrafted hESC-CMs confirmed the increased expression of matured ventricular cardiomyocyt

155 Indeed, SHIP1 activation mediated the increased expression of Mcl-1 and HSP27, two Akt-depende

156 Mutant-clone HSPCs have increased expression of megakaryocyte-associated genes c

157 hagocytic states, such as IL-6 and IL-4, and increased expression of microglial chemokines, such as m

158 on the promoter region of miR-1185-1, which increased expression of miR-1185-1 and further repressed

159 Furthermore, increased expression of miR-9-3p and miR-9-5p in chemore

160 nterocytes isolated from mice given IL1B had increased expression of MIR200C-3p and decreased levels

161 PGE(2) increased expression of miR675-5p by activating expressi

162 nt accumulation of pyruvate, corroborated by increased expression of mitochondrial enzymes and transp

163 tomas with MYCN amplification, 17q gain, and increased expression of mitochondrial ribosome and elect

164 Based on the increased expression of MLO in mycorrhizal roots and its

165 Increased expression of MMPs have been described in trau

166 ssues progressed from BE to HGD to EAC, they increased expression of mRNAs encoding isoform 1 of RNF1

167 ogressive fibrosis and bronchiolization with increased expression of Muc5b in peripheral airways, hon

168 tory response in the lungs, characterized by increased expression of multiple inflammatory markers an

169 igodendrocyte precursor cells (OPCs) rapidly increased expression of myelin genes and myelin proteins

170 maternally separated (MS) pups identified an increased expression of myelin-related genes and a decre

171 rived from JAK2V617F erythrocytes identified increased expression of myeloperoxidase as the likely me

172 reatment increased I(Na) in association with increased expression of Na(V)1.5.

173 heightened transcription factor binding, and increased expression of neighboring genes.

174 This includes increased expression of neuronal-associated transcriptio

175 Here, we observed increased expression of NPY5 receptor (Y5R) in HCC, whic

176 with decreased GULP1 expression, we observed increased expression of NRF2, HMOX1, and other candidate

177 ssion of ER stress and apoptotic markers and increased expression of nuclear protein 1 and tribbles r

178 Muscles of mice with CKD have increased expression of nucleolar protein 66 (NO66), as

179 rrupt protein-coding genes, resulting in the increased expression of one gene and modest truncation i

180 tance to pathogen infection accompanied with increased expression of one-third of the 207 NLR genes i

181 f cytosolic p16(INK4A) and HMGB1, as well as increased expression of p16Ink4a, p21, and MMP-9.

182 R3(injury) displayed increased expression of parenchymal injury transcripts (

183 The data show increased expression of particular invasion-related gene

184 splayed excess mitochondrial fission and had increased expression of PDK isoforms 1 and 3 that persis

185 Increased expression of perilipin (PLIN) proteins and co

186 Increased expression of PFKFB3 is mediated by binding of

187 addition, Hipk2 (-/-) neurons and MEFs show increased expression of PGC-1alpha (peroxisome prolifera

188 ns and mouse embryonic fibroblasts also show increased expression of PGC-1alpha (peroxisome prolifera

189 We detected increased expression of phosphorylated eIF4E, eIF4G, and

190 Our results demonstrated an increased expression of pik3ca, pik3cb, pik3r5 and pik3r

191 motherapy induces BCSC specification through increased expression of pluripotency factors, but how th

192 However, we found that the increased expression of Polkappa was not excessively mut

193 e membrane depolarization and calcium influx increased expression of primiR-199a2 but not of primiR-1

194 violet light exposure and is associated with increased expression of pro-cancer genes and reduced exp

195 There was increased expression of pro-inflammatory markers in cort

196 Chronic tendinopathy was associated with increased expression of pro-inflammatory markers PTX3, C

197 DHA-deficient mice were characterized by an increased expression of pro-inflammatory molecules, name

198 19 and B cell-activating factor receptor and increased expression of proapoptotic BIM.

199 This is due to a microbiota-dependent increased expression of proinflammatory factors and decr

200 TBI increased expression of proinflammatory mediators in the

201 on and proliferation of human aortic SMC and increased expression of proinflammatory molecules and ac

202 Increased expression of protein kinase ULK1 was reported

203 HIF1A-knockout pancreatic cancer cells had increased expression of protein phosphatase 1 regulatory

204 yses revealed that genetic silencing of TBK1 increased expression of proteins and genes essential for

205 Increased expression of proximal AP genes was associated

206 These effects were associated with increased expression of purported BMAL1-target genes med

207 s (including those involved with pectin) and increased expression of putative cellulose synthases ind

208 igh-fat diet-fed ApoE(-/-) mice displayed an increased expression of Rap1 both in aortas and circulat

209 These findings are further substantiated by increased expression of S100A8 and S100A9 mRNA in whole

210 ical symptoms relative to wild-type mice and increased expression of S100A9 and S100A8 proteins in ke

211 Increased expression of SARS-CoV-2 receptors was blocked

212 Torin1 significantly increased expression of selected sarcomere proteins (inc

213 hese results, transcriptome profiling showed increased expression of several direct p53 targets, redu

214 Here, we report increased expression of several ligands in NF2-null huma

215 her investment into reproduction (including, increased expression of sexually dimorphic traits in mal

216 echanistically, loss of mTORC2 results in an increased expression of signature genes representing imm

217 betaR1, Col1alpha1, and cMyb expression, and increased expression of SMAD7, C/EBPalpha, and C/EBPdelt

218 CO2 activity was significantly elevated, and increased expression of SRC-2 with concomitant reduction

219 cholesterol movement to the ER, evidenced by increased expression of SREBP2-regulated genes.

220 ormation and invasive activity, resulting in increased expression of stem-associated transcription fa

221 We confirmed the increased expression of survivin in CD20(+) lymphocytes

222 te subset of DNMT3A mutation carriers showed increased expression of T-cell stimulating immunoglobuli

223 on 1 upregulation, which subsequently causes increased expression of T-cell-attracting chemokines suc

224 l signature between health and disease, with increased expression of Th17-associated factors in perio

225 Increased expression of the 3.1 isoform of the KCNH2 pot

226 hoice-induced abstinence was associated with increased expression of the activity marker Fos in the O

227 -signaling mode (adipocytes and muscle) with increased expression of the ADAM10/17 metalloprotease th

228 ocrine signaling in adipocytes that promotes increased expression of the adipokine adiponectin and su

229 proliferation, which could be maintained by increased expression of the alternative amino acid trans

230 inflammatory cytokines IL10 and IL12P40, and increased expression of the angiogenic and neurotrophic

231 ion of channel transcripts revealed modestly increased expression of the ATXN1 co-repressor Capicua (

232 ation, was misregulated in male kidneys with increased expression of the canonical Wnt target lymphoi

233 ental infection by P. vranovensis results in increased expression of the cysteine synthases cysl-1 an

234 We found that increased expression of the Drosophila PICALM orthologue

235 ay elevated aminoglycoside resistance due to increased expression of the efflux pump, MexXY.

236 e endothelial activation molecule VCAM-1 but increased expression of the endothelial tight junction p

237 1/Kir5.1 and Nedd4-2 in the kidney exhibited increased expression of the epithelial sodium channel al

238 ecreased expression of the glutamatergic and increased expression of the GABA-ergic synaptic markers,

239 , it declines during ageing concomitant with increased expression of the gap junction protein Gja1.

240 HsmR senses vertebrate heme, leading to increased expression of the hsmRA operon and subsequent

241 rough a positive feed-forward loop involving increased expression of the IL-2 receptor alpha-subunit

242 Increased expression of the immune gene C4 has been link

243 micronuclei formation, reduced Lamin B1, and increased expression of the immune regulators IL6 and IL

244 We also found that Stat3 inactivation led to increased expression of the inflammatory chemokines CCL5

245 ased growth of xenograft tumors in mice, and increased expression of the integrin subunits ITGA3 and

246 TAZ-KO cells exhibited increased expression of the iron exporter ferroportin an

247 as risk variants in STX6 are associated with increased expression of the major transcripts in disease

248 ited the loss of mitochondrial integrity and increased expression of the microtubule-associated prote

249 d fission, decreased membrane potential, and increased expression of the mitochondria-specific protei

250 creases in MDSC accumulation correlated with increased expression of the myeloid cell lineage-specifi

251 hetic neurons: microbiota depletion leads to increased expression of the neuronal transcription facto

252 This however occurs despite increased expression of the nuclear-encoded transcriptio

253 virus infection of the mosquito led to an in increased expression of the odorant binding protein 22 (

254 ibited interleukin 10 (IL-10) expression and increased expression of the p40 subunit shared by IL-12

255 g alveolar bone is resorbed when there is an increased expression of the pro-osteolytic factor termed

256 creased alpha-hemolysin (Hla) production but increased expression of the proteases SspAB and aureolys

257 confirmed increased expression of GDPD1 and increased expression of the retinal enhancer that enters

258 sing age as well as non-cell-autonomously by increased expression of the retinoic acid-degrading enzy

259 These results demonstrate that increased expression of the schizophrenia-associated gen

260 peripheral blood eosinophils accompanied by increased expression of the severe acute respiratory syn

261 We recently demonstrated that increased expression of the stress response protein regu

262 ation carriers were further characterized by increased expression of the T-cell alpha receptor consta

263 Using an RNA-seq approach, we identified the increased expression of the tetraspanin family member, C

264 re, we show that pre-TCR signalling leads to increased expression of the transcriptional repressor Bc

265 by immunohistochemical validation identified increased expression of the TTSP family member, TMPRSS13

266 However, IEC organoids have increased expression of the type I IFN receptor relative

267 notably, the fusA1 mutant displayed greatly increased expression of the Type III secretion system (T

268 otic resistance against tetracycline through increased expression of the xenobiotic transporters mexE

269 While increased expression of these cellular genes defines a p

270 Increased expression of these genes after 3 months' endo

271 at alpha-Syn pathology is reduced due to the increased expression of this protein.

272 tactin, a nonhistone substrate of HDAC8, and increased expression of three fibrotic markers: alpha-sm

273 esult in increased serine degradation and in increased expression of threonine biosynthetic enzymes s

274 On the basis of increased expression of thymidylate synthase (TYMS), thy

275 cell invasion, clinical studies demonstrated increased expression of TIMP-1 and its association with

276 NF-kappaB c-Rel and TonEBP essential for the increased expression of TonEBP-dependent osmoprotective

277 e to oxidative stress, which correlated with increased expression of tpx, a gene essential for defens

278 Treatment of hEECs with bovine CAPG increased expression of transcripts previously known to

279 Functional microbiome analysis revealed increased expression of Treg-cell-inducing genes in the

280 AAI is associated with increased expression of TrkA by eosinophils; however, th

281 LPS further increased expression of TSPO and IL-6 in SNCA mice.

282 eptors (PRs) of diseased individuals display increased expression of two key glycolytic genes, sugges

283 Moreover, Th2 cells in presence of IL-3 show increased expression of type 2 effector cytokines, such

284 a transcriptional signature characterized by increased expression of type I and type II IFN-stimulate

285 combinant HMPVs and virion RNAs that induced increased expression of type I interferon, which was dep

286 t dermal endothelial cells in rosacea had an increased expression of VCAM1 and hypothesized that LL-3

287 fected astrocytes were inducible, leading to increased expression of viral proteins upon reactivation

288 amatergic receptor activity, consistent with increased expression of voltage-gated potassium channel

289 We found that increased expression of WDR-48, but not WDR-20, promotes

290 ly, Tbx3 (+/-) atrioventricular nodes showed increased expression of working myocardial gene programs

291 -mesenchymal transition (EMT) coordinated by increased expression of ZEB-1, an EMT activator.

292 t with 1, while GM3 (II(3)Neu5Ac-LacCer) had increased expression only on both cell subpopulations in

293 -coupled receptor kinase 4 (GRK4), caused by increased expression or genetic variants (eg, GRKgamma14

294 SHA [95%], DICER [17%], TARBP2 [38%]) showed increased expression patterns in MDD subjects.

295 as hypocalcemia-associated missense variants increased expression, plasma membrane targeting, and/or

296 ified a number of oncogenic factors, with an increased expression upon radiation exposure, including

297 tion, Mx proteins are known to show markedly increased expression via an interferon-responsive promot

298 in the SGs of 54% of pSS patients, and this increased expression was correlated with low unstimulate

299 This increased expression was due at least in part to reduced

300 Of note, most of the genes with increased expression were known to be regulated by perox