ライフサイエンスコーパス: elevated level of

1 They then show that elevated levels of 2-HG are correlated with mutations in

2 Elevated levels of 5'-methylthioadenosine (MTA), which p

3 approximately 21,000 loci with consistently elevated levels of 5-hydroxymethycytosine.

4 e fed a high fat/sucrose diet also exhibited elevated levels of activated JNK as well as enhanced p70

5 weight loss after 9 weeks, whereas mice with elevated levels of activin A lost 11% of their body weig

6 to increased stability of miRNPs along with elevated levels of Ago2-bound cytokine mRNA in Ld-infect

7 in memory, DN, and naive B cells in SLE show elevated levels of Aiolos, whereas Ikaros levels are unc

8 pared with the wild-type mice accompanied by elevated levels of alanine aminotransferase, a marker of

9 Elevated levels of alpha-synuclein (alpha-Syn) appear to

10 essed in PD brains within neurons containing elevated levels of alpha-synuclein or Lewy bodies.

11 the patients with parkinsonism demonstrated elevated levels of alpha-synuclein.

12 ered in ovariectomized recipients, including elevated levels of AMH and estradiol.

13 Elevated levels of Ang II may confer protection against

14 arine inhabitants of the area are exposed to elevated levels of anthropogenic underwater sound, parti

15 thway, regulated miR-125B1 and miR-29B1, and elevated levels of antioxidants glutathione S-transferas

16 and alveolar macrophage transcriptomes, and elevated levels of apoptotic endothelial cell microparti

17 We observed that beta-adrenergic activation elevated levels of approximately fifty lipid species, in

18 Moreover, ALDH(high) tumor cells expressing elevated levels of aromatase stimulated tumor/host estro

19 Recently, elevated levels of aromatase, the rate-limiting enzyme f

20 mosaicism in disease pathogenesis; although elevated levels of ASC, IL-6, and IL-18 in patients' ser

21 At optimal thresholds, elevated levels of at least one of these two peptides wa

22 These data indicate that elevated levels of autotaxin and soluble markers of immu

23 ma1-induced IL-10-producing Bregs, expressed elevated levels of B and T lymphocyte attenuator (BTLA)

24 on in CD4(+) and CD8(+) T cells dominated by elevated levels of B cell-supporting cytokines.

25 We have reported that NP contain elevated levels of B cells and antibodies, making NP an

26 It is therefore possible that the elevated levels of background radiation in Chernobyl aff

27 have utility in the treatment of SLE, where elevated levels of BAFF and Aiolos may prime CD27(+) mem

28 osis tissue from patients with NF1 and found elevated levels of beta-catenin compared to unaffected b

29 sucrose consumption might be associated with elevated levels of beta-glucuronidase, an enzyme previou

30 Elevated levels of bioactive TGF-beta1 are associated wi

31 the impacts of artificial topography contain elevated levels of biogenic elements and heavy metals, i

32 These mice exhibit elevated levels of blood- and brain-resident Foxp3(+) T-

33 tasis but that sustained inflammation due to elevated levels of both HDPs and MRGPRX2-expressing mast

34 including ceh1, a mutant with constitutively elevated levels of both the stress-specific plastidial r

35 Wastewaters in coastal regions may contain elevated levels of bromide (Br(-)) and iodide (I(-)) fro

36 Here, we show that elevated levels of c-di-AMP, a ubiquitous second messeng

37 Elevated levels of C-reactive protein (CRP), a sensitive

38 ted metabolite measurements, we found highly elevated levels of CAM-cycle enzyme transcripts and thei

39 rdingly, in the myocardium of Des(-/-) mice, elevated levels of cardiac actin correlated with alterat

40 Elevated levels of cardiac troponin, and especially thei

41 tients with acute ischemic stroke (AIS) have elevated levels of cardiac troponins (cTn).

42 Elevated levels of cardiac troponins are associated with

43 ZDF islets contain elevated levels of CB1R, interleukin-1beta, tumor necros

44 ompanied by reduced levels of p27 as well as elevated levels of CCAAT/enhancer-binding protein beta (

45 inical specimens of glioblastoma multiforme, elevated levels of CCL2 expression correlated with reduc

46 Elevated levels of CCN1 mRNA were confirmed in lung tiss

47 Distinct isotope fingerprints, combined with elevated levels of CCR tracers, provide strong evidence

48 other hand, Tollip deficient neutrophils had elevated levels of CCR5, responsible for their homing to

49 reduced class-switched memory B cells and an elevated level of CD21(lo) B cells (Freiburg 1a), and ma

50 Instead, they expressed elevated levels of CD80, indicating that B cells may con

51 Elevated levels of cell death (necrosis) and occurrence

52 and CRAF is substantially increased under an elevated level of cellular Hsp90 and in the presence of

53 Elevated levels of cholesteryl ester (CE)-enriched apoB

54 The elevated level of chymases and other serine proteases is

55 We subsequently demonstrated that elevated levels of CIB1 resulted in full neoplastic tran

56 Accordingly, we observed elevated levels of CIDEC and its acetylated form in HDAC

57 Elevated levels of Cif in bronchoalveolar lavage fluid w

58 th an inflammatory response characterized by elevated levels of circulating CD14(+), CD16(+), CD4(+),

59 hat both wild-type and Per3(-/-) mice showed elevated levels of circulating corticosterone and increa

60 Osteoblast ablation was associated with elevated levels of circulating inflammatory cytokines, i

61 like behavior, reduction of body weight, and elevated levels of circulating interleukin 6.

62 ted monocytes with an IFNalpha phenotype and elevated levels of circulating LPS.

63 tosis, an antiangiogenic plasma profile, and elevated levels of circulating monocytes and T, but not

64 less atherosclerosis, despite having highly elevated levels of circulating proinflammatory cytokines

65 s associated with low-grade inflammation and elevated levels of circulating saturated fatty acids, wh

66 revealed that SLE patients had significantly elevated levels of circulating U1 and/or Y1 RNA compared

67 ion data revealed a high correlation between elevated levels of CNTD2 and decreased overall survival

68 Enterocytes sense highly elevated levels of (conjugated) bile acids in the system

69 of psychedelic phenomenology constitutes an elevated level of consciousness - as measured by neural

70 North Dakota is remarkably persistent, with elevated levels of contaminants observed in spills sites

71 lar counterparts of the viral oncogene v-Crk Elevated levels of Crk and CrkL have been observed in ma

72 Elevated levels of CRP are common and relevant in CSU pa

73 ing questions: (i) What is the prevalence of elevated levels of CRP in CSU?

74 One-third of CSU patients had elevated levels of CRP.

75 (ii) Why do CSU patients show elevated levels of CRP?

76 Elevated levels of CXCL1 did not influence the generatio

77 increased oxidative stress (as reflected in elevated levels of CYP2E1 and protein carbonyls).

78 sfunction, increased neurological score, and elevated levels of cytokines.

79 n the general population and, in the case of elevated levels of depressive symptoms, persist into you

80 caused by an impaired glyoxalase system and elevated levels of dicarbonyl species, such as MG.

81 Elevated levels of dieldrin, chlordane- and DDT-related

82 nts with anxiety disorders, individuals with elevated levels of dispositional anxiety are prone to in

83 ring extraskeletal tumors show significantly elevated levels of Dkk1 in bone microenvironment relativ

84 Elevated levels of DNA ligase IIIalpha (LigIIIalpha) hav

85 We report elevated levels of DNA-RNA hybrids (R-loops) and double

86 synthesis in rad53-1 cells is suppressed by elevated levels of dNTPs in vivo, and the activity of Po

87 3 is overexpressed in breast cancer and that elevated levels of DPP3 mRNA correlate with increased NR

88 the insulin signaling (IS) pathway revealed elevated levels of Drosophila insulin-like peptide 2 (Di

89 anscription factor E2F3, we demonstrate that elevated levels of E2F3 drive ectopic proliferation in m

90 Elevated levels of each biomarker were associated signif

91 All had elevated levels of EBV in the blood; 2 of 3 patients tes

92 and other epithelial tumors associated with elevated levels of EGFR and especially those demonstrati

93 Old fibroblasts also demonstrated elevated levels of endogenous DNA damage that were incre

94 PM2.5 exposure was associated with the elevated levels of endothelial microparticles (annexin V

95 However, females had elevated levels of Env-specific IgG1, IgG2, and IgG3 Abs

96 e in M-ILK-deficient mice is correlated with elevated levels of epithelial Stat3 activation and proli

97 Consistently, significantly elevated levels of ErbB2 were confirmed in the hippocamp

98 Consistent with elevated levels of Erdr1, germfree mice have increased s

99 xenografts and DEN-induced-HCC tumors showed elevated levels of ERK, RSK, ELK1 and DR5 along with dec

100 location-specific information that revealed elevated levels of essential lipids to be related to inf

101 differential cholesterol profile, including elevated levels of esterified cholesterol, that is consi

102 On the other hand, aberrant, elevated levels of FA are implicated in disease states r

103 oliferation-infected primary B cells express elevated levels of factors associated with plasma cell (

104 Lupus neutrophils produce elevated levels of factors known to fuel autoantibody pr

105 onfirmed undiagnosed diabetes was defined as elevated levels of fasting glucose (>/=7.0 mmol/L [>/=12

106 secretion of glucagon and insulin positions elevated levels of fatty acids as potential triggering f

107 Patients with elevated levels of fetal hemoglobin (HbF, alpha2gamma2)

108 Fenretinide normalised elevated levels of FGF21 in both high-fat diet-induced o

109 The blood of cKO mice had an elevated level of fibroblast growth factor 23 and reduce

110 Elevated levels of fine particulate matter <2.5 microm i

111 esult in the exposure of the cancer cells to elevated levels of flow-based shear stress.

112 Recent work suggests that elevated levels of free cell hemoglobin in blood plasma

113 es is often accompanied by dyslipidemia with elevated levels of free fatty acids (FFAs).

114 tinct metabolic reaction profiles but shared elevated levels of free fatty acids.

115 Abnormally elevated levels of gamma-aminobutyric acid (GABA) in the

116 aT- and Th17-cells; yet in the CNV eye, only elevated levels of gammadeltaT-cells were observed.

117 p with early replicating fragile sites, show elevated levels of gammaH2AX, and suffer frequent mutati

118 Elevated levels of geogenic and anthropogenic arsenic ar

119 Elevated levels of glucose, free fatty acids, and inflam

120 nal activity by whole-cell patch-clamp shows elevated levels of glutamatergic transmission and change

121 in the chorioamnion was also associated with elevated levels of granulocyte colony-stimulating factor

122 in increased spontaneous DNA damage foci and elevated levels of H2AK15ub and impairs DNA damage respo

123 These findings indicate that elevated levels of helicase perturb replication initiati

124 taining, and HGF ELISA assays confirmed that elevated levels of HGF protein were present only in U87M

125 Elevated level of homocysteine (Hcy) is considered a ris

126 We demonstrate elevated levels of homocysteine and concomitantly reduce

127 eiofaunal species have been reported to have elevated levels of horizontal gene transfer (HGT) events

128 l proliferation and carcinogenesis resulting elevated levels of host antibodies (e.g., anti-HPV16 E7

129 ound that HP1gamma is upregulated in PCa and elevated levels of HP1gamma in PCa predict poor outcome.

130 ae as a model eukaryote, we demonstrate that elevated levels of Hsp90 attenuate efficient DNA damage

131 Finally, we detected elevated levels of HSPCs in the circulation of newly dia

132 essing hTDP1 and rhabdomyosarcoma cells with elevated levels of hTdp1 were more sensitive to histone

133 potential therapeutic agents for tumors with elevated levels of hTdp1.

134 is dramatically enhanced in the presence of elevated levels of human alpha-syn.

135 Elevated levels of human lipoprotein-associated phosphol

136 hat decreased Herpud1 protein levels lead to elevated levels of hypertrophic markers in cultured rat

137 in which ADAM10 is deleted only on B cells, elevated levels of ICOSL were seen.

138 hypersensitivity skin of Sash mice exhibited elevated levels of IFN-gamma, IL-17alpha, and IL-23, as

139 implanted with MPM cells expressing EPCR had elevated levels of IFNgamma and TNFalpha compared to mic

140 There is a strong link between CSU and elevated levels of IgG antithyroid autoantibodies (AAbs)

141 number of these B cell subsets, we detected elevated levels of IgG3 natural Abs and a striking incre

142 ternatively-activated macrophages, displayed elevated levels of IL-13, and extensive fibrosis, wherea

143 nes, activated inflammatory macrophages, and elevated levels of IL-17 and TNF.

144 d disease severity, which is associated with elevated levels of IL-1beta and checkpoint kinase 1 phos

145 ated with the activation of inflammasome and elevated levels of IL-1beta at primary and metastatic si

146 combined deletions of YopJ and YopM induces elevated levels of IL-1beta/IL-18 in vitro and in vivo a

147 Mice with elevated levels of IL6 exhibited 8.1% weight loss after

148 HCV-viremic PWID have elevated levels of immune activation when compared to he

149 who previously were PWID continue to harbor elevated levels of immune activation, as defined by incr

150 of refractory/relapsed AML patients contains elevated levels of immunosuppressive exosomes which inte

151 Unhelped CD8(+) T cells expressed elevated levels of inhibitory receptors and exhibited tr

152 germination of seeds from plants exposed to elevated levels of ionizing radiation.

153 of the cytosolic protein damage sensor HSF1, elevated levels of K48-polyubiquitinated cytoplasmic pro

154 , leukopenia in 59%; lymphopenia in 45%; and elevated levels of lactate dehydrogenase in 82%, asparta

155 Although single HSP90 mutants showed subtly elevated levels of lesions, double mutant analysis disag

156 expression significantly correlated with the elevated levels of Lin28B expression and subsequently in

157 onset retinal degeneration, associated with elevated levels of lipofuscin and its bis-retinoid compo

158 Microbial translocation, characterized by elevated levels of lipopolysaccharide (LPS) and related

159 tered microbiota metagenome characterized by elevated levels of lipopolysaccharide and flagellin.

160 -mediated KDM1A eviction was associated with elevated levels of local histone H3 lysine 4 dimethylati

161 etic disorder, is characterized by extremely elevated levels of low-density lipoprotein cholesterol (

162 ra from symptomatic pregnant patients showed elevated levels of M2-skewed immunosuppressive cytokines

163 g and production of shorter transcripts with elevated levels of m6A that are rapidly degraded.

164 n NF2-mutant cells renders them sensitive to elevated levels of malonyl-CoA, as occurs following bloc

165 Placentas from preterm Nrf2(-/-) mice showed elevated levels of markers of inflammation, oxidative st

166 at bexarotene treatment reduced neuron loss, elevated levels of markers of synaptic integrity that wa

167 llergy was associated with increased odds of elevated levels of maternal-reported symptoms of depress

168 In this study, we identified elevated levels of matrix metalloproteinase (MMP)-12 in

169 We also show elevated levels of MCJ in the liver of patients with ace

170 COPD AMs had elevated levels of Mcl-1, an antiapoptotic B-cell lympho

171 is a functional polymorphism that results in elevated levels of MDM2 (due to enhanced SP1 binding to

172 gle serving-sizes or when substrate contains elevated levels of metal(loid)s.

173 g treatment of S. stercoralis infection, the elevated levels of microbial translocation markers, acut

174 Previously, it was suggested that elevated levels of miR-27 in T cells isolated from patie

175 ing mneP are Mn(II) sensitive and accumulate elevated levels of Mn(II), and these effects are exacerb

176 The ECL1i signal was associated with an elevated level of mouse lung monocytes.

177 et-like cells were depleted of mucus and had elevated levels of MUC2 mRNA expression after G. duodena

178 Exhausted CD4 population expressed elevated levels of multiple inhibitory receptors concomi

179 e transcriptional profiles and significantly elevated levels of multiple pro-inflammatory molecules.

180 the hot-spot p53R172H mutation described an elevated level of mutant p53 in non-cancerous mouse tiss

181 ugh mitochondrial genomes (mtDNA) accumulate elevated levels of mutations in cancer cells, the origin

182 xpression led to high expansion activity and elevated levels of MutSbeta complex, indicating that Mut

183 em from other breast cancer cells, including elevated levels of N-acetylaspartate, a metabolite prima

184 ults in increased transcription of c-Myb and elevated levels of neutrophil infiltration, thereby alle

185 elated kinase A (TrkA) is linked to pain and elevated levels of NGF (the ligand for TrkA) are associa

186 n contrast, immune-intact 5xfAD mice exhibit elevated levels of nonamyloid reactive IgGs in associati

187 Elevated levels of NT-proBNP, high-sensitive troponin-T,

188 nces, high and-or regular precipitation, and elevated levels of organic matter.

189 Elevated levels of oxidative phosphorylation were requir

190 ions found in SPG5 patients, indicating that elevated levels of oxysterols might be key pathogenic fa

191 Exposure to elevated levels of ozone leads to yield reduction in agr

192 with pancreatic or brain cancer suggest that elevated levels of PAI-1 may contribute to VTE.

193 Preventing ATX-2 function leads to elevated levels of PAR-5, enhanced chromatin and centros

194 n, people with prediabetes had significantly elevated levels of PDFF and total and visceral fat.

195 Psen1-/- cells, and this was associated with elevated levels of phospho-p38 consistent with decreased

196 th activating mutations of EGFR, we observed elevated levels of phospho-Y153 IKBKE.

197 essive MS patients exhibited a significantly elevated level of phosphorylated NF-kappaB (p-P65) follo

198 In human gastric tissues, elevated levels of phosphorylated EGFR were observed thr

199 tivity, a marker of cellular senescence; and elevated levels of phosphorylated H2AX (gamma-H2A.X), a

200 mutations in the kinase domain that lead to elevated levels of PI(3,5)P2 and impair the interaction

201 ify mutations in the CCR domain that lead to elevated levels of PI(3,5)P2 Together these findings rev

202 ng from alterations in clot architecture and elevated levels of plasma FXIII and PAI-1.

203 ived cultures contain approximately 1.5-fold elevated levels of PMP22 mRNA, exhibit reduced mitotic p

204 We show that elevated levels of PPARG strongly correlate with elevati

205 Consistent with this, we observe elevated levels of PRC2-mediated histone H3K27 methylati

206 Elevated levels of PRL associate with metastasis and poo

207 of macrophages with damaged RPE also elicits elevated levels of pro-angiogenic proteins that promote

208 exhibit high proportions of immune cells and elevated levels of pro-inflammatory cytokines predict po

209 Cerebral spinal fluid analysis revealed elevated levels of proinflammatory cytokines before trea

210 onists and (10)Panx1 and are associated with elevated levels of proinflammatory cytokines in cord sli

211 ns causes immune activation characterized by elevated levels of proinflammatory cytokines, including

212 in the developing brain have indicated that elevated levels of proinflammatory mediators leading to

213 lated, as in lactating mice with chronically elevated levels of prolactin, the rate of (125)I-prolact

214 rates of single-strand break repair but also elevated levels of protein ADP-ribosylation.

215 ation, reduced markers of T-cell exhaustion, elevated levels of proteins associated with antigen pres

216 This, together with elevated levels of proteins associated with electron tra

217 revealed that val1 mutant seeds accumulated elevated levels of proteins compared with the wild type,

218 Concussed athletes had significantly elevated levels of quinolinic acid (QUIN) and significan

219 Yet recent studies report elevated levels of reactive oxygen species and abnormal

220 athione depletion and associated with highly elevated levels of reactive oxygen species and induction

221 sed requirement of ubiquinone is to mitigate elevated levels of reactive oxygen species generated by

222 opmental and neurological abnormalities, and elevated levels of reactive oxygen species have been fou

223 a have abnormal membrane potentials, produce elevated levels of reactive oxygen species, are fragment

224 GNPTAB(-/-) cells exhibited elevated levels of reactive oxygen species, known to ina

225 ve stress and PRP-overexpressing plants have elevated levels of reactive oxygen species, PRP may conn

226 riched breast carcinomas display evidence of elevated levels of replication stress-associated DNA dam

227 ced levels of gangliosides and significantly elevated levels of rhEPO sialylation.

228 We previously reported elevated levels of sAPPalpha in ASD and FXS vs. CONTROLS

229 h ASD and typically developing controls, and elevated levels of sAPPalpha in ASD and FXS vs. CONTROLS

230 Moreover, elevated levels of secreted MDA-modified vimentin were d

231 that are at least partially attributable to elevated levels of Ser57 phosphorylated ubiquitin.

232 The elevated level of serum creatinine in CNI groups was abo

233 in an asymptomatic individual who exhibited elevated levels of serum autoantibodies and defective pe

234 ne responses that result in autoimmunity and elevated levels of serum IgE.

235 s and plasmablasts in the spleen, and led to elevated levels of serum IgM and enhanced renal glomerul

236 expression of vanin-1 in skin and blood and elevated levels of serum pantothenic acid that correlate

237 Elevated levels of sFlt-1 are associated with adverse ou

238 Elevated levels of single-stranded DNA were necessary bu

239 In addition, elevated levels of SIRT2 sensitized breast cancer cells

240 Elevated levels of SIRT2 sensitized breast cancer cells

241 ch MLL2 gene deletion can be induced display elevated levels of sister chromatid exchange, gross chro

242 affinity maturation occurred as evidenced by elevated levels of somatic hypermutation (SHM) in Ab seq

243 Elevated levels of SOX5/6/21 promoted SVZ cells to exit

244 ing a delay in epiboly, depleted S1P levels, elevated levels of sphingosine, and resistance to sphing

245 t mice with reduced levels of MDC1 showed an elevated level of spontaneous tumors in aged animals.

246 esis, ribosomal protein gene expression, and elevated levels of stress response genes such as the act

247 how a highly reduced quinone pool caused by elevated levels of succinate is likely responsible for t

248 MRL/lpr and NZM2410 mice accumulate markedly elevated levels of surface-bound nuclear self-antigens.

249 In dengue-infected patients, elevated levels of syndecan-1 and chondroitin sulfate ar

250 strongly associated with plasma leakage, and elevated levels of syndecan-1 and claudin-5 are strongly

251 In this study, we identified elevated levels of T cell Ig and mucin-domain containing

252 At elevated levels of TAF treatment to match TFV intracellu

253 Low hippocampal volumes or elevated levels of tau or ptau in isolation may not accu

254 cerbated in cells also engineered to express elevated levels of TbNTR or TbCPR.

255 sciatic nerve lesion in adult mice leads to elevated levels of Tet3 and 5-hydroxylmethylcytosine in

256 Although elevated levels of TF(+) MVs have been observed in patie

257 -NICC xenografts from treated mice expressed elevated levels of TGF-beta, IL-10 and IFN-gamma.

258 cytes are hyperactivated in vivo and secrete elevated levels of Th1 and Th2 cytokines after TCR ligat

259 icient mdx muscle, which correlates with the elevated levels of the alpha7beta1 integrin observed in

260 is well documented that aging patients with elevated levels of the amino acid metabolite homocystein

261 ice retain the remaining p73 allele, exhibit elevated levels of the antiapoptotic protein Bcl2 and th

262 actor also contained cells with low MITF and elevated levels of the AXL kinase.

263 Elevated levels of the beta-amyloid peptide (Abeta) are

264 own syndrome (DS) and AD, which is caused by elevated levels of the beta-cleaved carboxy-terminal fra

265 hormones and contribute to the substantially elevated levels of the catabolic hormone cortisol.

266 ed transgenic CGRP-sensitized mice that have elevated levels of the CGRP receptor hRAMP1 subunit in n

267 t MI-induced titin stiffening is mediated by elevated levels of the cytokine interleukine-6.

268 When P2-HNF4alpha-only mice (which have elevated levels of the cytokine resistin-like beta, RELM

269 revealed an association of LOXL2 action with elevated levels of the EMT regulatory transcription fact

270 clinical study of nasal secretions in which elevated levels of the human forms of these antimicrobia

271 on of the complement cascade as reflected by elevated levels of the key regulator C3a.

272 n clinical specimens of human breast cancer, elevated levels of the mammalian paralogs MMP2, MMP9, an

273 Further investigation revealed elevated levels of the metabolite urea in the OVT73 stri

274 transcript abundance changes in response to elevated levels of the plant hormone ethylene in roots f

275 Elevated levels of the proinflammatory cytokine IL6 are

276 overexpressed in pancreatic cancer producing elevated levels of the RON tyrosine kinase receptor prot

277 ncreased nuclear localization of YAP/TAZ and elevated levels of the target genes in the endothelium i

278 the presence of glucose that correlates with elevated levels of the toxic catabolite methylglyoxal.

279 rom human volunteers exposed to O3 contained elevated levels of these oxysterol species.

280 The elevated levels of this proinflammatory cytokine may exp

281 hionine tRNA and cancer progression, whereby elevated levels of this tRNA specifically drive synthesi

282 neuroprotection via increased BBB integrity (elevated levels of tight-junction protein, Claudin 5, an

283 r-276a-binding site in the tim 3' UTR causes elevated levels of TIM and approximately 50% arrhythmici

284 Elevated levels of TIMP3 and vitronectin, acting downstr

285 risk of autoimmune disorders, accompanied by elevated levels of tissue necrosis factor (TNF) alpha.

286 erresponsiveness and displayed significantly elevated levels of TNF-alpha in lung tissue.

287 An elevated level of topoisomerase I is found in many carci

288 iles in strains lacking Spt4 reveal globally elevated levels of transcribing RNA Polymerase II (Pol I

289 ome loss impacts core metabolism, leading to elevated levels of tricarboxylic acid cycle intermediate

290 levels, increased caspase-3 activation, and elevated levels of tubulin cleavage.

291 , a class of inflammatory diseases marked by elevated levels of tumor necrosis factor (TNF)-alpha and

292 thermore, we found that ant ail6 plants have elevated levels of two defense hormones: salicylic acid

293 DBDC patients had an elevated level of type 17 immune responses and the frequ

294 that produce defective CD11b associate with elevated levels of type I interferon (IFN-I) in lupus, s

295 We hypothesize that elevated levels of vascular markers, placental-like grow

296 We also found elevated levels of VEGF receptor 3 together with reduced

297 We found elevated levels of viral lytic gene expression when Kapo

298 d viral polymerase activity that resulted in elevated levels of viral transcription and virus output.

299 However, a key difference is the elevated levels of vitamin C in SunGold (161mg/100g edib

300 rminal fibroblast growth factor 23 (cFGF23), elevated levels of which are also prospectively associat