ライフサイエンスコーパス: normoxic

1 ISL1) in the secondary heart field (SHF) are normoxic.

2 al hemorrhage (49%) of whom 1,084 (38%) were normoxic, 1,316 (46%) were hypoxic, and 450 (16%) were h

3 or antagonist, while awake hamsters breathed normoxic (21% O(2) in N(2)), hypoxic (10% O(2)in N(2)) a

4 +/-SD) years old were randomly assigned to a normoxic (21% O2) and hypoxic (10% O2) trial with measur

5 tilated TBI patients, of whom 403 (33%) were normoxic, 553 (46%) were hypoxic and 256 (21%) were hype

6 Normoxic 7 degrees C goldfish (ILCM present) possessed s

7 f oxygen supplementation was equivalent to a normoxic 94% or higher target for infants admitted to ho

8 line rats are hyperproliferative and display normoxic activation of hypoxia-inducible factor-1alpha (

9 Mitochondrial fragmentation and normoxic activation of hypoxia-inducible factor-1alpha (

10 ps (n = 11/group), including air (controls), normoxic air with 5% CO2 (therapeutic hypercapnia), air

11 e volunteers were exposed to 10 min bouts of normoxic and hypoxic (FIO2 0.12) rest and exercise (100

12 cells and mediate the communication between normoxic and hypoxic areas of tumors to facilitate cance

13 ivity was induced by serum depletion both in normoxic and hypoxic cells and that activation of SREBP

14 ns, but also has HIF-independent activity in normoxic and hypoxic cells.

15 hibited this hypertrophy response under both normoxic and hypoxic conditions (26% lower than control

16 sion of fur protected Salmonella grown under normoxic and hypoxic conditions against the bacteriostat

17 s, and stabilized HIF-1alpha protein in both normoxic and hypoxic conditions by blocking its proteaso

18 d delivery strategy was evaluated under both normoxic and hypoxic conditions in normal tissues as wel

19 ral metabolic rate of oxygen (CMRO(2)) under normoxic and hypoxic conditions in rats.

20 min addition to these MCT-disrupted cells in normoxic and hypoxic conditions induced a rapid drop in

21 In addition, cell lines cultured under normoxic and hypoxic conditions were used.

22 cine receptors in rat cortical neurons under normoxic and hypoxic conditions with major differences b

23 sformed human mammary epithelial cells under normoxic and hypoxic conditions, and applying in silico

24 formability, increasing sRBC occlusion under normoxic and hypoxic conditions, and increasing sRBC adh

25 ng, lowers HIF-1alpha protein levels in both normoxic and hypoxic conditions, consistent with a role

26 However, both under normoxic and hypoxic conditions, glucose was critical fo

27 xic effects after 72 h of incubation in both normoxic and hypoxic conditions, unlike sulfonamide CA i

28 verexpressing CA IX and XII was tested under normoxic and hypoxic conditions, using 2D and 3D in vitr

29 eloma cell-specific signaling pathways under normoxic and hypoxic conditions.

30 radation, thereby stabilizing HIF under both normoxic and hypoxic conditions.

31 of maintaining high levels of ROS under both normoxic and hypoxic conditions.

32 glucose uptake, CBF, and CMRO(2) under both normoxic and hypoxic conditions.

33 l melanocytes to melanoma cell lines in both normoxic and hypoxic conditions.

34 portantly, this regulation occurs under both normoxic and hypoxic conditions.

35 ss is known about pVHL regulation under both normoxic and hypoxic conditions.

36 d biologically active Epo protein under both normoxic and hypoxic conditions.

37 dent proliferation of tumor cells under both normoxic and hypoxic conditions.

38 unoprecipitation, and colocalization in both normoxic and hypoxic conditions.

39 with important cellular functions under both normoxic and hypoxic conditions.

40 etaining the molecule's cytotoxicity in both normoxic and hypoxic conditions.

41 ce, plant growth, and development under both normoxic and hypoxic conditions.

42 ration, and function of EM CD4(+) T cells in normoxic and hypoxic conditions.

43 pups using whole-body plethysmography under normoxic and hypoxic conditions.

44 by fetal and newborn rat preparations under normoxic and hypoxic conditions.

45 ons achievable by dietary intervention under normoxic and hypoxic conditions; a moderate dose of nitr

46 aptation to hypoxia, we performed RNA-Seq of normoxic and hypoxic head and neck cancer cells.

47 lastoma), we quantified miR-124 abundance in normoxic and hypoxic regions in glioblastoma patient tis

48 ibrary from 4(th) instar larvae subjected to normoxic and hypoxic treatments (respectively), and perf

49 ion (NG-monomethyl-L-arginine; L-NMMA) under normoxic and normocapnic hypoxic (80% arterial O2 satura

50 to the cytotoxic effects of this agent under normoxic and oxygen deficient conditions.

51 Adult guinea pigs were divided into control (normoxic) and hypoxic groups; a separate group of hypoxi

52 Here, we investigated decorin during normoxic angiogenic signaling.

53 ed ventilatory responses to acute hypoxia in normoxic animals without altering the output of the CB (

54 The expression pattern corresponded to the normoxic animals, as far as verifiable due to the existi

55 In the group of control (normoxic) animals, apoptotic neurons were not observed i

56 he animals were mechanically ventilated with normoxic artificial air with or without 2.5% methane.

57 tly increased fetal plasma SOD activity from normoxic baseline (-8.9 +/- 6.5 vs. 15.0 +/- 6.6% inhibi

58 concentration ratio of nitrate:nitrite from normoxic baseline (DeltaNO3(-):NO2(-); 0.15 +/- 0.30 vs.

59 he 3rd week of hypoxia regressed back toward normoxic baseline as the duration of re-oxygenation cont

60 mory (EM) CD4(+) T cells recirculate between normoxic blood and hypoxic tissues to screen for cognate

61 rat hearts (n = 5/group) were perfused with normoxic buffer for 30 min and then hypoxic buffer for 4

62 d acclimatization using four groups of rats: normoxic, caffeine-treated normoxic, chronically hypoxic

63 thetic pathway activation, favor hypoxic and normoxic cancer cell survival and correlate with pancrea

64 alpha accumulation induced by doxorubicin in normoxic cancer cells.

65 om hypoxic cancer cells favors the growth of normoxic cancer cells.

66 ing data on the effects of oxygen therapy in normoxic cardiac patients.

67 In vivo, normoxic cardiac retention of (64)Cu-CTS was significant

68 in hypoxic cells, whereas STAT3 knockdown in normoxic cells also reduces cell proliferation, motility

69 alised to distinct cytoplasmic aggregates in normoxic cells and underwent redistribution to the leadi

70 of de novo lipogenesis can be reproduced in normoxic cells by Ras activation.

71 ible to NK cell-mediated lysis compared with normoxic cells expressing a moderate level of Cx43.

72 Normoxic cells remotely regulate the acid-base balance o

73 cells, and we propose that, via this route, normoxic cells supply hypoxic neighbors with acid-neutra

74 ubicin-induced accumulation of HIF-1alpha in normoxic cells was caused by increased expression and ac

75 generate both DNA breaks and cross-links in normoxic cells, a low oxygen environment represses the f

76 c drug can induce HIF-1alpha accumulation in normoxic cells, an efficacy-limiting activity.

77 f fluorescent CA IX signal in hypoxic versus normoxic cells, which could be blocked by 60%-70% with u

78 rly 3-fold more cytotoxic to hypoxic than to normoxic cells.

79 and killed the hypoxic cells, but spared the normoxic cells.

80 Compared with a normoxic, chow-fed control mouse heart, hypoxia decrease

81 r groups of rats: normoxic, caffeine-treated normoxic, chronically hypoxic (12% O(2), 15 days), and c

82 omplex under hypoxic condition but not under normoxic condition.

83 proteins, BAX and BIM, down-regulated under normoxic condition; (2) beta1 Integrin/FAK signaling pat

84 ion of NF-kappaB, S6, c-Myc, and c-Jun under normoxic condition; (2) blocked myeloma cell migration a

85 ent XCI, we derived six new hESC lines under normoxic conditions (UCLA1-UCLA6).

86 is up-regulation of HIF-1 alpha occurs under normoxic conditions and could be inhibited with wortmann

87 egradation, stabilized HIF-1 activity during normoxic conditions and elevated miR-429 levels, demonst

88 the alpha subunit of HIF1 (HIF1alpha) under normoxic conditions and enhances HIF1alpha accumulation

89 n results in myocardial ischemia under basal normoxic conditions and in acute cardiac decompensation

90 ominant HIF-hydroxylase in neutrophils under normoxic conditions and link intrinsic regulation of gly

91 rexpressing cancer cells stabilize HIF under normoxic conditions and require HIF-1 for ERBB2-mediated

92 ive oxygen species-mediated phototoxicity in normoxic conditions and small molecule uncaging in hypox

93 ence and respond to CD44-ICD induction under normoxic conditions and therefore independent of Hif1alp

94 rom GBM cells grown at hypoxic compared with normoxic conditions are potent inducers of angiogenesis

95 erfused with 26 mm [1,6-(13)C2]glucose under normoxic conditions at 37 degrees C and monitored by (13

96 HIF-1 activity is usually suppressed under normoxic conditions because of rapid oxygen-dependent de

97 r a restricted time interval after return to normoxic conditions blocked the progression of OIR.

98 1 promoter silencing persisted in subsequent normoxic conditions but could be reversed by treatment w

99 axis that is dispensable for survival under normoxic conditions but is critical for non-replicating

100 HIF-1alpha is rapidly degraded under normoxic conditions by ubiquitin-mediated proteasome pat

101 RNA and protein, the reversal of which under normoxic conditions decreased T-cell-suppressive effects

102 ntra-arterially with 3.4 mug.g(-1) FLX under normoxic conditions displayed a transient tachycardia an

103 e slowed in metastatic melanomas, even under normoxic conditions due to the persistence of a high nuc

104 itrogen in the presence of acetate and under normoxic conditions is accompanied by a marked increase

105 ic inhibition of complex II by atpenin A5 in normoxic conditions mimics hypoxia and induces hypoxic t

106 tag), we found that exposure to NO2(-) under normoxic conditions or exposure to ischemia alone result

107 How Toxoplasma activates HIF-1 under normoxic conditions remains unknown.

108 eriods of hypoxia and recover development if normoxic conditions resume, an ability rarely found in m

109 exosomes derived from hypoxic compared with normoxic conditions showed increased autocrine, promigra

110 tion of HIF1A transcriptional activity under normoxic conditions through regulation of succinate dehy

111 f HIF-1alpha using Ad-VP16- HIF-1alpha under normoxic conditions up-regulated miR-210 expression, dow

112 , human RBCs constitutively produce NO under normoxic conditions via an active eNOS isoform, the acti

113 mber of ribosomes per transcript relative to normoxic conditions was not enhanced.

114 d factor 1alpha (HIF1alpha) mRNA, even under normoxic conditions, and markedly upregulate HIF1alpha p

115 le, even under deviations from physiological normoxic conditions, and show minimal interference from

116 ncreased HIF-2alpha protein expression under normoxic conditions, and up-regulated HIF-dependent gene

117 In normoxic conditions, BACH2 was able to modulate HIF-1alp

118 e indistinguishable from control cells under normoxic conditions, but are unable to survive and proli

119 ly more able to exploit food resources under normoxic conditions, but at the cost of being more sensi

120 marginally important to generate LG3 during normoxic conditions, cathepsin B activity was found to b

121 yl-hydroxylated by EglN family members under normoxic conditions, causing its rapid degradation.

122 end to utilize aerobic glycolysis even under normoxic conditions, commonly called the "Warburg effect

123 eactive oxygen species in these cells and in normoxic conditions, decreased the mitochondrial oxygen

124 In normoxic conditions, Gd@C82(OH)22 mediates these effects

125 When cells proliferate under normoxic conditions, glucose provides the acetyl-CoA tha

126 Under normoxic conditions, HdHIF-1alpha and HdHIF-1beta mRNAs

127 Here, we show that, under normoxic conditions, HIF-1alpha is upregulated in tumor

128 Under normoxic conditions, hypoxia-inducible factor (HIF)-1alp

129 Under normoxic conditions, it undergoes oxygen-dependent degra

130 In roots of plants grown under normoxic conditions, loss of function of GOX3 induces me

131 Under normoxic conditions, PGC-1alpha also strongly induces mi

132 Under normoxic conditions, proline hydroxylation of HIF-1alpha

133 It also plays a crucial role under normoxic conditions, such as in inflammation, where its

134 ctivity and trigger a hypoxic response under normoxic conditions, such as iron chelators and inhibito

135 or of this process, but its activation under normoxic conditions, termed pseudohypoxia, is not well d

136 ogenesis of renal cell carcinoma (RCC) under normoxic conditions, through the loss of the Von Hippel-

137 rogenase lead to the inactivation PHDs under normoxic conditions, which can be overcome by treatment

138 hance MDSC-mediated T-cell suppression under normoxic conditions, while targeting hypoxia-induced miR

139 (+) and the accumulation of HIF-1alpha under normoxic conditions, with parallels to Warburg reprogram

140 pression induced CD24 mRNA and protein under normoxic conditions, with this effect traced to a recrui

141 ation rate in osteosarcoma cells grown under normoxic conditions.

142 s hypoxia marker genes under both anoxic and normoxic conditions.

143 by uracil-rich 3'-untranslated regions under normoxic conditions.

144 2%, and 29.7% retention, respectively, under normoxic conditions.

145 omyocyte apoptosis under hypoxic compared to normoxic conditions.

146 ventilator-induced ALI in vivo occurs under normoxic conditions.

147 r from ER to mitochondria through IP3R under normoxic conditions.

148 transcription and protein levels even under normoxic conditions.

149 re efficiently under hypoxic conditions than normoxic conditions.

150 relative to the same level of exercise under normoxic conditions.

151 ble of inducing target gene expression under normoxic conditions.

152 levels under hypoxic conditions compared to normoxic conditions.

153 and SIRT3-dependent stabilization of HIF1 in normoxic conditions.

154 production and erythropoiesis in vivo under normoxic conditions.

155 lutamine-derived alpha-ketoglutarate even in normoxic conditions.

156 specially as it switches between hypoxic and normoxic conditions.

157 rowth resumes when seedlings are returned to normoxic conditions.

158 is not required for sensory processing under normoxic conditions.

159 ochondrial-specific lipids, cardiolipins, in normoxic conditions.

160 tained in low oxygen (hypoxic) compared with normoxic conditions.

161 reduces TNFR2 but not TNFR1 expression under normoxic conditions.

162 3a is present in the nucleus of HDMECs under normoxic conditions.

163 an in mice treated with cells cultured under normoxic conditions.

164 ere more remarkable in hypoxic compared with normoxic conditions.

165 to hypoxic conditions followed by return to normoxic conditions.

166 TX-loaded MSNR was observed when compared to normoxic conditions.

167 K stimulated CSC development under softer or normoxic conditions.

168 were isolated and cultured under hypoxic or normoxic conditions.

169 on of the cellular hypoxic response, despite normoxic conditions.

170 e induction of HIF1alpha in such cells under normoxic conditions.

171 iently generating reactive oxygen species in normoxic conditions.

172 IF) signaling, leading to HIF degradation in normoxic conditions.

173 d with exosomes secreted by CPCs grown under normoxic conditions.

174 were isolated and cultured under hypoxic or normoxic conditions.

175 metabolism were compared under hyperglycemic normoxic conditions; 51% of the energy came from oxidati

176 TSM provided significant gains in hypoxic-to-normoxic contrast (14:1 for (64)Cu-2,3-butanedione bis(t

177 hold, only (64)Cu-CTS delivered a hypoxic-to-normoxic contrast of 3:1, and it therefore warrants in v

178 o be significantly lower in OIR mice than in normoxic control mice (P = 0.0048).

179 m hyperoxic retinas compared with those from normoxic control mice.

180 stress (4-hydroxynonenal, 141.1 +/- 17.6% of normoxic control), reduced superoxide dismutase (60.7 +/

181 immunohistochemistry in four groups of ewes: normoxic control, normoxia + ketamine, hypoxic control a

182 er and lesser, respectively, relative to the normoxic control, thus leading to an increased T/E2 rati

183 ndothelial dysfunction (70.9 +/- 5.6% AUC of normoxic control; all P < 0.05).

184 Whereas normoxic controls showed normal magnetic resonance imagi

185 %, 32%, and 38%, respectively, compared with normoxic controls.

186 ung and right ventricle tissue compared with normoxic controls.

187 d in adult hypoxic-reared mice compared with normoxic controls.

188 dent insulin secretion comparable to that in normoxic controls.

189 icantly altered in OIR retinas compared with normoxic controls.

190 lation whenever it was increased relative to normoxic controls; i.e. acute hypoxia in CON and CSH, an

191 apy resistance, in hypoxic cells compared to normoxic counterparts.

192 We show that in Saccharomyces cerevisiae, normoxic COX activity measured in the presence of ATP is

193 evolution, a CO2-sAC-cAMP-PKA axis regulates normoxic COX activity.

194 A balance between hypoxic and normoxic CSCs may be present in the young heart, althoug

195 emonstrate mesenchymal cell morphology under normoxic culture conditions (21% O(2)).

196 te ischemic exposure was reduced compared to normoxic culture conditions (P < 0.01).

197 damage and apoptosis under both hypoxic and normoxic culture conditions.

198 MICOS subunit Mic19) in contrast to its even normoxic distribution.

199 sites was enhanced approximately 20-fold at normoxic DNAse1 hypersensitivity sites (irrespective of

200 element (HRE)-driven luciferase activity in normoxic ECs.

201 gnaling was recapitulated in hypoxic but not normoxic endothelial cells, and was associated with decr

202 prostate cancer cell line under hypoxic and normoxic environments.

203 y increased value in comparison to that from normoxic ERYs of 0.60 +/- 0.04 microM (p < 0.001, n = 4

204 ons employed, NO and PGs have little role in normoxic exercise hyperaemia whereas combined NO-PG inhi

205 in DeltaFVC (% change compared to respective normoxic exercise trial) between the older subjects (pre

206 idual dilator responses to hypoxia alone and normoxic exercise.

207 enhanced induction by hypoxic compared with normoxic exosomes of tumor vascularization, pericyte ves

208 red in 6% O(2) showed 31% less PR death than normoxic explants.

209 For the normoxic fetus, CBF was closely related to ECoG state, b

210 In the normoxic fetus, LD-CBF and CMRO(2) correlated highly wit

211 delivery remained unchanged from baseline in normoxic fetuses.

212 as wash-in MR imaging during inhalation of a normoxic fluorinated gas mixture (perfluoropropane) and

213 o a threshold panic challenge (ie, 20% CO(2)/normoxic gas).

214 (+)/CD11c(+)) are significantly increased in normoxic Gata6-KO mice.

215 when oxygen-stable HIF1alpha is expressed in normoxic glioma cells CD133 is induced.

216 ronment, we incorporated the interactions of normoxic glioma cells, hypoxic glioma cells, vascular en

217 cantly reduced in both hyperoxic compared to normoxic groups (P<0.05).

218 ed function in neonatal hypoxic and neonatal normoxic groups compared with saline-treated controls.

219 rvival of class I nuclei are compatible with normoxic hESC derivation, and that chemical supplementat

220 r HIF1A in lung protection during ALI, where normoxic HIF1A stabilization and HIF-dependent control o

221 f succinate dehydrogenase (SDH) in mediating normoxic HIF1A stabilization, concomitant increases in g

222 Normoxic HIF1alpha protein expression was also dependent

223 ly, C2 and B4 mAbs bound to hypoxic, but not normoxic, human endothelial cells in vitro.

224 In wakefulness, the ventilatory response to normoxic hypercapnia is higher in young SHRs (mean +/- S

225 e authors administered a series of identical normoxic hyperpolarized gas breaths to the subject; afte

226 The effect of CB normoxic hypocapnia, normocapnia and hypercapnia (caroti

227 mitochondria in vitro and in vivo, promoting normoxic hypoxia inducible factor-1alpha activation and

228 Measurements were made in normoxic, hypoxic, and hypercapnic conditions.

229 by retinal pigmented epithelial cells under normoxic, hypoxic, and lutein-pretreated conditions in a

230 Normoxic inducers of HIF (CoCl(2), desferrioxamine, and

231 ypoxia (three, 5 min hypoxic episodes, 5 min normoxic intervals) induced phrenic long-term facilitati

232 oxide donor reduced HIF-1alpha expression in normoxic IPAH-ECs.

233 of dual-specificity phosphatase 16 increased normoxic levels of IL-6 and IL-1beta and reduced the hyp

234 pression until the miR-429 levels drop below normoxic levels.

235 Normoxic littermates were kept in the same room outside

236 d higher amounts of mature IL-1beta than did normoxic macrophages after treatment with crystalline ch

237 6 inhibits VEGF IRES-mediated translation in normoxic MCF-7 extract.

238 that the NK cell immune synapse formed with normoxic melanoma cells is more stable and contains a hi

239 metabolism following hypoxia due to abnormal normoxic metabolism, which was associated with a functio

240 D19 (term approximately D20.5), relative to normoxic mice in 21% O2.

241 he olfactory bulb (OB) at P48, compared with normoxic mice.

242 cells derived ex vivo from hypoxic, but not normoxic, mice were able to form pluripotent, long-term

243 omplex III inhibitor, has similar effects in normoxic monocytes.

244 We found that miR-210 was induced in normoxic myoblasts upon myogenic differentiation both in

245 In conclusion, miR-210 is induced in normoxic myofibers, playing a cytoprotective role.

246 33% lower in hypoxic/NaCl rats compared with normoxic/NaCl controls.

247 hypoxic cells onto metabolically altruistic normoxic neighbors.

248 ed cardiac function; however, mechanisms for normoxic neonatal CPC exosomes improved function indepen

249 Constitutive normoxic NO formation was abolished by NOS inhibition an

250 aining CB to maintain normal CB blood gases (normoxic, normocapnic perfusate), to inhibit (hyperoxic,

251 Relative to CB control conditions (normoxic, normocapnic perfusion), we found that CB chemo

252 No changes in the retina were found in normoxic Ntn-4(-/-) mice.

253 ts were divided into 3 groups (n = 5/group): normoxic (Nx), HI and HI pre-treated with Src kinase inh

254 erved in hypoxic eosinophils compared to the normoxic ones.

255 Under normoxic or hypoxic conditions, SAD inhibited cell survi

256 ical venous endothelial cells cultured under normoxic or hypoxic conditions.

257 isolated islets and adenomas cultured under normoxic or hypoxic conditions.

258 ampal development and synaptic function in a normoxic or hypoxic environment, possibly by modifying c

259 xation to acetylcholine in aged offspring of normoxic or hypoxic pregnancy but not in young offspring

260 g (4 mo) and aged (15 mo) adult offspring of normoxic or hypoxic pregnancy with or without maternal a

261 aused phenylephrine pre-constricted UtA from normoxic or hypoxic pregnant mice to dilate and this dil

262 f monocytes, but this was independent of the normoxic or hypoxic state.

263 del simulating high-density encapsulation to normoxic or ischemic culture for 12 hours, after which v

264 ment (Rank) in SCD mice compared with either normoxic or single-H/R-episode SCD mice.

265 pring of hypoxic, relative to offspring from normoxic or undernourished, pregnancies.

266 dies suggest that iron chelators can prevent normoxic oxidative neuronal death through selective inhi

267 not HIF-1alpha, regulates susceptibility to normoxic oxidative neuronal death.

268 Direct normoxic PARP1 activation by a DNA alkylating agent enha

269 mining the effects of supplemental oxygen in normoxic patients with acute presentations of coronary a

270 osphatidylglycerol species were increased in normoxic pellets, whereas phosphatidylinositol species w

271 C increased birth weight in both hypoxic and normoxic pregnancies.

272 5.1 +/- 3.8%) in aged vs. young offspring of normoxic pregnancy (P < 0.05).

273 Pregnant rats were subjected to normoxic pregnancy or 13% O2 chronic hypoxia for most of

274 lphide-synthesis blockers on HPV and also on normoxic pulmonary vasoconstriction (NPV) stimulated by

275 Multivariate regression of hypoxic/normoxic ratios of electrophysiological parameters and c

276 yruvate treatment reduced infarct volumes in normoxic rats but not in IH-exposed rats.

277 pared with those in ATII cells isolated from normoxic rats.

278 (at approximately 30%) after 1 or 2 weeks of normoxic recovery.

279 nervation steadily decreased over 2 weeks of normoxic recovery.

280 ction to isolate RNA from viable hypoxic and normoxic regions of 9L experimental gliomas.

281 nstituted for 2 hours followed by 4 hours of normoxic reoxygenation.

282 n independently of polycythemia and enhanced normoxic respiration similar to Chuvash patients, furthe

283 ies in transformed cell lines suggested that normoxic stabilization of HIF-1alpha explains the persis

284 ns in von Hippel-Lindau (VHL) and subsequent normoxic stabilization of hypoxia-inducible factor (HIF)

285 n of VHL ubiquitin ligase is associated with normoxic stabilization of hypoxia-inducible factor-1alph

286 nt metabolic alterations are associated with normoxic stabilization of hypoxia-inducible factors (HIF

287 l (CSC) function is regulated by the hypoxic/normoxic state of the cell is currently unknown.

288 e ATP-mediated regulation of COX through the normoxic subunit Cox5a, homologue of human COX4i1, in a

289 (18)F-FMISO equilibrates in normoxic tissues but is retained under hypoxic condition

290 al volume density (Mito(VD)) over equivalent normoxic training.

291 n hypoxia (Delta18%) was greater than in the normoxic trials (Delta5-9%)(P <0.05).

292 tion, doxorubicin enhanced VEGF secretion by normoxic tumor cells and stimulated tumor angiogenesis.

293 Conversely, when overexpressed in normoxic tumor cells, Cx43 improves their susceptibility

294 eased RAD51 protein levels in hypoxic versus normoxic tumor regions.

295 Normoxic Ucp2KO-PASMCs had mitochondrial hyperpolarizati

296 tocellular carcinoma cells recapitulated the normoxic up-regulation of HIF-1 alpha observed in HEK ce

297 e in an Illumina HumanWG-6 v3.0 48k array of normoxic vs. hypoxic osteoclasts differentiated from hum

298 that in systems with MeHg production in the normoxic water column eutrophication can increase phytop

299 tic Sea MeHgT budget, we inferred an average normoxic water column Hg(II) methylation rate constant o

300 hypoxia was not significantly different from normoxic WT mice and much lower than the RVSP values see