ライフサイエンスコーパス: be upregulated during

1 that Il25 and its receptor subunit, Il17rb, were upregulated during a primary infection and a second

2 ophages, T cells, and cells expressing CCR2, is upregulated during acute and chronic inflammation.

3 The inflammatory microRNA-155 is upregulated during acute myocarditis, contributes to

4 Surprisingly, although IFN-beta is upregulated during acute SIV infection, we found that

5 r program consisting of more than 1000 genes was upregulated during acute exacerbations in comparison

6 Transcription of the S. scabies HBGC was upregulated during aerial growth, which suggests a l

7 ikely to be involved in anaerobic metabolism were upregulated during aerobic growth, and the mutant e

8 132 cluster (Mirc19) is enriched in HSCs and is upregulated during aging.

9 served that production of IL-6 and IFN-gamma was upregulated during allograft rejection in untreated

10 AAT/enhancer-binding protein-alpha and -beta were upregulated during anagen, then downregulated in ca

11 er targeting alpha(v)beta(3) integrin, which is upregulated during angiogenesis soon after acute myoc

12 nd that cyclin-dependent kinase-5 expression is upregulated during apoptosis induced by bacterial inf

13 The Kip/Cip CKIs, p27(Kip1) and p21(Cip1), are upregulated during arterial repair and negatively re

14 ce marker of ASCs, CD138 (syndecan-1), which is upregulated during ASC maturation, is required in a c

15 The glutamate transporter 1 (GLT1) is upregulated during astrocyte development and maturati

16 mics show that the unfolded protein response is upregulated during Aze treatment implicating that Aze

17 Mlp-9 or Mlp-10, all three of the mlp genes were upregulated during B. burgdorferi replication at 37

18 m the human pathogen Neisseria meningitidis, is upregulated during bacterial-host cell contact.

19 in 1) is a nuclear receptor coregulator that is upregulated during breast cancer progression to metas

20 identified a set of BAT-specific miRNAs that are upregulated during brown adipocyte differentiation a

21 re we show that spleen tyrosine kinase (SYK) is upregulated during brown adipocyte differentiation an

22 nd that the expression of the ZBED6 and IGF2 were upregulated during C2C12 differentiation.

23 Expression of these AR circRNAs was upregulated during castration-resistant progression

24 The expression of both receptors is upregulated during cell growth; however, Y2 appears t

25 m and activates the expression of genes that are upregulated during chlamydosporulation, an asexual p

26 Herein we report that ADAMTS-7 is upregulated during chondrocyte differentiation and de

27 Although Minpp1 expression is upregulated during chondrocyte hypertrophy, normal ch

28 Two of these lncRNAs are upregulated during chondrogenic differentiation of m

29 of magnocellular oxytocin neurone activation are upregulated during chronic morphine treatment, and t

30 Specific immunoglobulin E (IgE) responses are upregulated during chronic schistosome infection and

31 and protein expression, indicating that Fyn is upregulated during chronic inflammatory conditions.

32 We have previously shown that her9 is upregulated during chronic rod photoreceptor degenera

33 uman disease states, Mdm1, Mlf1, and Dyx1c1, are upregulated during ciliogenesis and localize to cent

34 ocalizes to the basal body of the cilium and is upregulated during ciliogenesis.

35 inal dendritic cells in the steady state and is upregulated during colitis in mouse models and inflam

36 Expression of the PGE(2) receptor EP4 is upregulated during colorectal carcinogenesis.

37 Importantly, we observed that TAK1 is upregulated during compensatory hypertrophy but downr

38 Expression of late chlamydial genes is upregulated during conversion from the replicating to

39 retina, but the expression did not appear to be upregulated during corneal infection.

40 In myeloid cells, p15(INK4b) mRNA is upregulated during cytokine-induced differentiation a

41 ke 1 (FSTL1) is a matricellular protein that is upregulated during development and disease, including

42 Bin2 is upregulated during differentiation of granulocytes, s

43 ZC3H4 is upregulated during differentiation, and its knockdown

44 Fbxo40 is muscle specific in expression and is upregulated during differentiation.

45 expressed in proliferating C2C12 cells that is upregulated during differentiation.

46 t RhoA was downregulated, and Cdc42 and Rac1 were upregulated during differentiation of primary oligo

47 erosclerosis, we found that CXCL5 expression was upregulated during disease progression, both locally

48 thymidine-kinase 1 enzyme expression, which is upregulated during DNA synthesis.

49 the function of autophagy and how autophagy is upregulated during drought stress.

50 on, we identified transcription factors that were upregulated during drought conditions and that may

51 However, RGS14 protein and mRNA are upregulated during early postnatal development, with

52 osition to obesity through the FTO locus and is upregulated during early adipogenesis in risk-allele

53 Expression from the trapped allele is upregulated during early myoblast fusion and downregu

54 Approximately 900 genes were upregulated during early infection in vivo, includi

55 as to investigate whether PLCgamma1 activity is upregulated during EGF-induced proliferation of RCECs

56 Several Kv genes are upregulated during embryogenesis in parallel with in

57 In humans, telomerase is upregulated during embryogenesis and in cancers, and

58 lved in extracellular matrix remodeling that are upregulated during EMT and are highly expressed in p

59 In this article, we show that miR-223 is upregulated during eosinophil differentiation in an e

60 CASZ1 expression is upregulated during epidermal terminal differentiation

61 iptional regulator LIM-only protein 4 (LMO4) is upregulated during ErbB2-induced mouse mammary gland

62 t in erythroid cells and that its expression is upregulated during erythroid differentiation.

63 sed as a housekeeping gene in all cells, but is upregulated during erythropoiesis.

64 We show that GLI1 is upregulated during esophageal carcinogenesis, and GLI

65 -inducible factors (HIF1alpha and HIF2alpha) was upregulated during EVT differentiation mediated by l

66 thway that maintains cellular homeostasis(2)-is upregulated during exercise, and a core autophagy pro

67 IRF4 expression, however, is upregulated during exit from the GC reaction and has

68 gest that leptin receptor binding in the ARC is upregulated during fasting and that fasting changes t

69 Here we report that SIRT3 expression is upregulated during fasting in liver and brown adipose

70 umerous novel genes and candidate biomarkers were upregulated during fibrosis, specifically in myofib

71 in filamentous growth, and their expression is upregulated during filamentation in an Ecm22/Upc2-dep

72 tified a cDNA, gsp1, whose transcript levels are upregulated during flagellar adhesion.

73 e ligands for CCR2 (MCP-1, MCP-3, and MCP-5) were upregulated during Fr98 infection of the brain.

74 d that the p57(Kip2) cyclin kinase inhibitor is upregulated during G(1)/G(0) in a subset of retinal p

75 oglycan, is a component of the brain ECM and is upregulated during glial cell motility.

76 er of aggressive and metastatic disease, and is upregulated during glioblastoma progression.

77 tional studies showed that the ilvE promoter is upregulated during growth at low pH.

78 d characterization of a serine protease that is upregulated during growth of the adrenal cortex.

79 The ccf genes of B. fragilis are upregulated during gut colonization, preferentially

80 at is highly specific for activated T cells, is upregulated during GvHD, and mediates disease pathoge

81 ether, our results demonstrated that miR-373 is upregulated during HCV infection and negatively regul

82 In addition, alpha9 integrin was upregulated during healing, and changes were observe

83 These data show that BST-2 is upregulated during HIV infection, consistent with its

84 pk16 are cotranscribed as a single mRNA that is upregulated during homeostatic plasticity.

85 rotein inhibitor of activated STAT 4 (PIAS4) is upregulated during HSV-1 infection and localizes to n

86 adult human neurons and astrocytes, and they are upregulated during human stem cell differentiation t

87 Our data demonstrates cGAS to be upregulated during human and murine colitis.

88 expression and plasma membrane localization are upregulated during hypertension induced by angiotens

89 or IIB (TFIIB) and cyclin-dependent kinase 9 are upregulated during hypertrophy, both targeted by mic

90 In this study, we show that JMY is upregulated during hypoxia in a HIF-1alpha-dependent

91 c-Myc expression is upregulated during ILC2 activation.

92 This recombination event is upregulated during immune responses by a regulatory r

93 expressed in mature human NK cells (mNK) and was upregulated during in vitro differentiation of NK ce

94 Lymphangiogenesis is upregulated during incidents of trauma, thereby coinc

95 ytokinin-responsive response regulator genes were upregulated during incubation on cytokinin-rich SIM

96 ing cytokinin-independent shoot development, were upregulated during incubation on SIM.

97 ion of the polyamine spermine to spermidine, is upregulated during infection and is associated with i

98 erone and posttranscriptional regulator Hfq, is upregulated during infection of porcine lungs.

99 ritic episodes suggests that OspA expression is upregulated during infection with B. burgdorferi.

100 Unlike in mouse macrophages, in which CRAMP is upregulated during infection, camp gene expression wa

101 ere mostly downregulated, except H2AX, which was upregulated during infection.

102 C oxidase during Inflammation" (MOCCI) that is upregulated during inflammation and infection to prom

103 Fat10 is upregulated during inflammation, and its substrates u

104 ich is expressed by diverse immune cells and is upregulated during inflammation-including during toxi

105 By contrast, TRPV1 appears to be upregulated during inflammatory conditions.

106 xpressed at a low level in healthy brain and is upregulated during inflammatory processes that may oc

107 The cytokine TNF-alpha is upregulated during inflammatory reactions associated

108 We conclude that TRPM7 is upregulated during inflammatory renal damage and prop

109 Finally, we show that FRC VEGF expression is upregulated during initiation and that dendritic cell

110 s is genotype-dependent and that these genes are upregulated during intestinal inflammation in IBD.

111 . phagocytophilum-infected ticks on mice and is upregulated during invasion of HL-60 cells.

112 dentified several new JAK1 target genes that are upregulated during involution.

113 Interestingly, a cleaved form of TWEAK is upregulated during involution.

114 III secretion system genes was also found to be upregulated during iron starvation in both B. pertuss

115 of microRNAs (miRNAs); for example, miR-214 is upregulated during ischemic injury and heart failure,

116 Expression of PBP by E. chaffeensis was upregulated during its intracellular life cycle.

117 is highly expressed in KS spindle cells and is upregulated during KSHV infection of endothelial cell

118 giogenic repressive lncRNA, LINC00313, which is upregulated during KSHV reactivation, interacts with

119 is not expressed in virgin mammary gland but is upregulated during lactation and is expressed in mous

120 data demonstrate that S1943 phosphorylation is upregulated during lamellar protrusion, and that CK-I

121 SpNot is upregulated during larval development, in the invagin

122 Expression of the B-Myb transcription factor is upregulated during late G1 phase of the cell cycle by

123 iated genes (DMGs), such as NAC016 and SEN1, are upregulated during leaf senescence, and found an inv

124 Expression of nor was upregulated during low-oxygen growth and dependent o

125 IRF-4 expression is upregulated during lymphocyte activation and IRF-4-de

126 We report that cell surface IL-15 expression is upregulated during lymphopenia induced by total body

127 Identification of genes that are upregulated during mammary epithelial cell morphogen

128 The histone chaperone FACT is upregulated during mammary tumorigenesis and necessar

129 ated by Notch1 in T cells and show that they are upregulated during maturation into both single posit

130 vealed two major pools of polyribosomes that were upregulated during memory formation: one pool in de

131 lysis, we first showed that PRMT1 expression was upregulated during metamorphosis when both TR and T3

132 expressed in all mouse tissues examined and is upregulated during mid-G(1) in serum-stimulated fibro

133 ied a novel histone deacetylase complex that is upregulated during mitosis and is associated with cyc

134 f GluA1 subunits of glutamate AMPA receptors were upregulated during morphine withdrawal, and viral k

135 GRASLND, a primate-specific lncRNA, is upregulated during MSC chondrogenesis and appears to

136 Skeletal alpha-actin), and two KLF3 isoforms are upregulated during muscle differentiation.

137 mitochondria-associated apoptotic signalling is upregulated during muscle denervation.

138 Mfn2 expression is upregulated during myoblast differentiation in vitro

139 CHC22 protein is upregulated during myoblast differentiation into myot

140 e oxidized low-density lipoprotein receptors are upregulated during myocardial ischemia-reperfusion,

141 - and skeletal muscle-enriched microRNA that is upregulated during myocyte differentiation and cardio

142 region of myogenic cells and its expression is upregulated during myogenesis.

143 Furthermore, CERS1 is upregulated during myogenic differentiation.

144 ctin family of proteins, galectin-9 (Gal-9), is upregulated during natural HCMV-reactivated infection

145 CMTR1 was found to be upregulated during neural differentiation and there w

146 Although Bcl11b expression is upregulated during NK maturation from CD56(bright) to

147 ine whether several important growth factors were upregulated during OB in the mouse heterotopic trac

148 prisingly, most microtubule-binding proteins are upregulated during only one process, suggesting that

149 cell-related markers have been described to be upregulated during operational tolerance in kidney al

150 kidneys of young animals in which Ang-2 had been upregulated during organogenesis, increased apoptos

151 The Myb gene is upregulated during oxidative stress and development,

152 including an E. histolytica Myb gene, which is upregulated during oxidative stress response.

153 Taken together, our findings show that RET is upregulated during pancreas tumorigenesis and its act

154 ive inflammation and T cell differentiation, was upregulated during pancreatic cancer progression, an

155 hat hematopoietic progenitor kinase 1 (HPK1) was upregulated during pancreatic injury and ADM.

156 Further, Ron protein expression was upregulated during papilloma formation.

157 ancer specimens revealed that RET expression is upregulated during PDAC tumorigenesis.

158 as low in B220(-) bone marrow precursors and was upregulated during pDC differentiation, concomitant

159 of levansucrase and amylovoran biosynthesis, were upregulated during pear tissue infection.

160 for recycling intracellular components that is upregulated during periods of cell stress.

161 The ess genes are upregulated during persistent infection, and the sec

162 also identified 4 bioactive metabolites that were upregulated during PF (spermidine, 1-methylnicotina

163 the host, suggesting that virulence factors are upregulated during phase transition.

164 ical activities of GH131 enzymes whose genes were upregulated during plant-tissue colonization in a s

165 d in situ hybridization which PNN components are upregulated during PNN formation in rat cerebellar p

166 GnRH excitability is upregulated during positive feedback, perhaps driving

167 europrotective chemokine, fractalkine, which is upregulated during postnatal development.

168 We found that all three family members were upregulated during postnatal development coinciding

169 Macula densa NOS1B was upregulated during pregnancy, resulting in blunted T

170 rmone response genes, such as Aux/IAA genes, were upregulated during preincubation on auxin-rich CIM,

171 bserved that numerous hormone response genes were upregulated during preincubation on CIM.

172 BCAT1 is upregulated during progression of CML and promotes BC

173 crometastases, and stress response signaling was upregulated during progression.

174 SOCS7 is upregulated during projection neuron migration, and u

175 alpha7-nAChR was upregulated during proliferation, by hypoxia in vitr

176 atency, whereas K9/vIRF1 and K10/vIRF4 mRNAs are upregulated during reactivation.

177 d in normal kidneys and that this expression is upregulated during renal disease, in a TGF-beta-depen

178 The Notch pathway is upregulated during retinal regeneration in both fish

179 pt abundance of the glycolysis pathway genes was upregulated during ripening.

180 , we identify B. thetaiotaomicron genes that were upregulated during Salmonella-induced gut inflammat

181 Numerous vasoactive cytokines are upregulated during sepsis, including angiopoietin 2

182 CD39 expression is upregulated during sepsis in mice, as well as in both

183 whereas the energy-dependent zinc importers are upregulated during severe zinc deficiency.

184 Eight genes that are upregulated during sexual development in the heterot

185 of the MEF2 family of transcription factors are upregulated during skeletal muscle differentiation a

186 on, MAZ transcripts and DNA-binding activity are upregulated during skeletal myocyte differentiation.

187 e, FOXG_18438 (abbreviated as Fo18438), that is upregulated during soybean infection in the presence

188 Several cytokines relevant to healing were upregulated during storage.

189 Several family members are upregulated during stress, and some are strongly cyt

190 homeostasis and is a survival mechanism that is upregulated during stress or starvation.

191 Neuronal expression of both transporters is upregulated during synapse development, and ABTS-1 ex

192 3 is a death domain-containing receptor that is upregulated during T cell activation and whose overex

193 P9 mRNA encoding the MARylating PARP9 enzyme was upregulated during TB in humans and mice and provide

194 and a coreceptor for certain growth factors, is upregulated during TGF-beta1-driven EMT in lung cance

195 Furthermore, Itk is upregulated during Th2 differentiation, while Rlk, a

196 focused on the analysis of 2 proteins, which are upregulated during the alternative activation and ar

197 tosis and differentiation to determine which are upregulated during the assembly of each network.

198 eover, it remains unclear how levels of p202 are upregulated during the cell growth arrest.

199 lacking cyanobacteriochrome sensory domains, are upregulated during the differentiation of hormogonia

200 four repressors of cytokinin signaling that are upregulated during the floral transition in ful1 ful

201 sed in all tissues, while almost all SlPP2Cs are upregulated during the flowering stage.

202 found in oligodendrocytes where transcripts are upregulated during the maturation of these cells.

203 acrophages to apolipoprotein A-1 and HDL and are upregulated during the phagocytosis of apoptotic cel

204 ator of cellular stresses, was also shown to be upregulated during the early period of infection.

205 CM ligand fibronectin (FN) are both known to be upregulated during the formation of neo-vasculature.

206 tivity is downregulated in somatic cells but is upregulated during the activation of cells of the imm

207 We found that N(6)-mA is upregulated during the development of mouse trophobla

208 is, the expression of several of these genes is upregulated during the early stages of infection-rela

209 1) is an intracellular adaptor molecule that is upregulated during the induced granulocytic different

210 MiR21 functionally targets CCL20 and is upregulated during the infection, thus contributing t

211 The chr.8q24.3 amplicon-resident gene TONSL is upregulated during the initial steps of tumorigenesis

212 apl-1 expression is upregulated during the last larval stage in hypoderma

213 p27(Kip1) is upregulated during the late G(2)/early G(1) phase of

214 t direct evidence that cardiac iNOS activity is upregulated during the late phase of ischemic PC in r

215 mbrane receptor for parasite attachment that is upregulated during the mid-S phase of the host cell c

216 In the developing retina, TK+ receptor mRNA is upregulated during the period of retinal ganglion cel

217 Cortactin, but not its related protein HS1, is upregulated during the phorbol 12-myristate 13-acetat

218 dicated that a specific retinue of molecules is upregulated during the rejection response, and they s

219 NCAM is upregulated during the remodeling period of hypertrop

220 additional chromosomal type 2 TA system that is upregulated during the SOS DNA damage response.

221 t of (p)ppGpp, and that expression of xdhABC is upregulated during the stringent response to promote

222 Expression of the protein is upregulated during the terminal differentiation of ep

223 e enzyme in PA and that cfas gene expression is upregulated during the transition to stationary phase

224 oredoxin reductase, and cellular thioredoxin was upregulated during the decarbonylation phase.

225 the zinc finger transcription factor cKrox, was upregulated during the differentiation of CD4(+) but

226 NRP/B expression was upregulated during the differentiation of murine Neu

227 entified a cationic peroxidase, VviCP1, that was upregulated during the priming and postpathogen chal

228 on, at both the mRNA and the protein levels, was upregulated during the repair phase (2-3 days postin

229 ate filament protein nestin whose expression was upregulated during the repair phase.

230 ion machinery, including ribosomal proteins, was upregulated during the T cell clonal-expansion phase

231 study, we show by promoter fusions that iraD was upregulated during the transition from exponential g

232 five of 97 differentially expressed proteins were upregulated during the 96-h time course and most of

233 contrast, 5.7% (4,028) of the T. ni unigenes were upregulated during the early period (0 to 6 h p.i.)

234 We identified specific pathway members that were upregulated during the early phase of the infection

235 NFalpha, IFNgamma, and IL-4 mRNA and protein were upregulated during the evolution of ARN in HSV-1-in

236 These proteins were upregulated during the period of DPCP monotherapy,

237 In particular, cadherin-11 is upregulated during tumour and inflammatory cell invas

238 These receptors are upregulated during vascular injury.

239 everal distal sodium reabsorptive mechanisms are upregulated during vasopressin escape; this may help

240 IL-15 is upregulated during viral infections and drives the ex

241 e regulators of NF-kappaB, IkappaBa and A20, were upregulated during viral infection.

242 rated view of the inflammatory networks that are upregulated during virus-induced asthma exacerbation

243 In rodents, mammary lymphangiogenesis was upregulated during weaning-induced mammary gland inv

244 GPD1L was found to be upregulated during weight loss and weight maintenance

245 dition, although both TbetaR-I and TbetaR-II are upregulated during wound repair, they appear to be d

246 , which all belong to the miR-17~92 cluster, are upregulated during wound repair.

247 Additionally, several host ncRNAs are upregulated during yHV infection and play integral r

248 While ATF3 is known to be upregulated during ZIKV infection, the mode by which