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

4 All experiments were performed under normoxic (21%) and hyperoxic (>95%) conditions.

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 AH (P(50) = 16 +/- 1 mmHg), had them perform normoxic and acute hypoxic (15% inspired oxygen) maximal

10 lmonary and renal mitochondria isolated from normoxic and chronically hypoxic rats were infused into

11 OE MRI used two sequential 3.5-minute normoxic and hyperoxic steady-state free-breathing UTE a

12 vascular density of the labrynthine zone in normoxic and hypoxic (Hx) conditions, and mean vascular

13 The same measurements were repeated under normoxic and hypoxic (normobaric (NH) and hypobaric (HH)

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

15 quinoline), which is phototoxic towards both normoxic and hypoxic cancer cells.

16 remarkable destructive effects against both normoxic and hypoxic cancers.

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

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

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

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

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

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

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

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

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

26 umor cells with low light fluence under both normoxic and hypoxic conditions, after activation by int

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

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

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

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

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

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

33 monoxide (CO) in live mammalian cells under normoxic and hypoxic conditions.

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

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

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

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

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

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

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

41 pHi, metabolic flux, and cytotoxicity under normoxic and hypoxic conditions.

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

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

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

45 ystem is validated by testing the effects of normoxic and hypoxic culture conditions on healthy and t

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 ow- and high-affinity HBOCs would perform in normoxic and hypoxic tumors.

50 Here, we investigated decorin during normoxic angiogenic signaling.

51 There were 4 groups: CON-normoxic animals with placebo (n=18); PH-Su/Hx rats+plac

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

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

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

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

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

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

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

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

60 alpha accumulation induced by doxorubicin in normoxic cancer cells.

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

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

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

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

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

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

67 Normoxic cells remotely regulate the acid-base balance o

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

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

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

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

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

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

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

75 ncreased endothelial tube length compared to normoxic CM.

76 resence of functional VHL-wt protein under a normoxic condition, which might then result in increasin

77 omplex under hypoxic condition but not under normoxic condition.

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

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

80 cipients of T(C)2 cells differentiated under normoxic conditioning.

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

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

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

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

85 ly within cardiac myocyte mitochondria under normoxic conditions and is consistently associated with

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

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

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

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

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

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

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

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

94 n factor HIF-1alpha, which is degraded under normoxic conditions by HIF-prolyl hydroxylase (HIF-PHD).

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

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

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

98 lly, all female offspring were maintained in normoxic conditions into early adulthood.

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

100 egradation by prolyl hydroxylase (PHD) under normoxic conditions is emerging as a promising option in

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

102 and extracellular Ca(2+) to mPTP opening in normoxic conditions or after anoxia-reoxygenation.

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

104 Restoring animals to normoxic conditions results in cytosolic dispersion of P

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

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

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

108 vate anaerobic genes but are destabilized in normoxic conditions through the action of oxygen-sensing

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

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

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

112 on hydrogen cyanamide (HC) application under normoxic conditions, and their levels peak at deepest do

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

114 We have previously shown that in normoxic conditions, ASS1 downregulation facilitates can

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

116 Under normoxic conditions, both healthy female and male diaphr

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

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

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

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

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

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

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

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

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

126 In CGNPs cultured under normoxic conditions, HIF1alpha is posttranslationally st

127 Under normoxic conditions, it undergoes oxygen-dependent degra

128 essed under hypoxia, is down-regulated under normoxic conditions, leading to an increase in dephospho

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

130 not cause unfolded protein response and, in normoxic conditions, only marginally affects proinflamma

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

132 ibitor PLX5622, while having no effect under normoxic conditions, profoundly increased vascular leak

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

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

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

140 Restoration of normoxic conditions-either ex vivo during NMP or in vivo

141 sR- strain fitness even in biofilms grown in normoxic conditions.

142 rowth resumes when seedlings are returned to normoxic conditions.

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

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

145 K stimulated CSC development under softer or normoxic conditions.

146 were isolated and cultured under hypoxic or normoxic conditions.

147 nificant changes in (64)Cu-ATSM signal under normoxic conditions.

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

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

150 iently generating reactive oxygen species in normoxic conditions.

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

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

153 res of the BPD phenotype in PCLS cultured in normoxic conditions.

154 ation rate in osteosarcoma cells grown under normoxic conditions.

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

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

157 2%, and 29.7% retention, respectively, under normoxic conditions.

158 controls, but this effect disappeared under normoxic conditions.

159 omyocyte apoptosis under hypoxic compared to normoxic conditions.

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

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

162 transcription and protein levels even under normoxic conditions.

163 re efficiently under hypoxic conditions than normoxic conditions.

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

165 ble of inducing target gene expression under normoxic conditions.

166 levels under hypoxic conditions compared to normoxic conditions.

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

168 ompared responses for each hypoxia regime to normoxic conditions.

169 eq data on cultured HUVECs under hypoxic and normoxic conditions.

170 on, and spheroid formation under hypoxic and normoxic conditions.

171 ethylated lysine (K) 224 of PGC-1alpha under normoxic conditions.

172 ls and a metabolic shift to glycolysis under normoxic conditions.

173 were isolated and cultured under hypoxic or normoxic conditions.

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

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

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

177 e pre-BotC of CIH rats, when compared to the normoxic control and hypoxic group with daily acute inte

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

179 In normoxic control mice, HIF-1alpha deletion in the CNS or

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

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

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

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

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

185 tational hypoxia-exposed animals compared to normoxic controls (P < 0.01).

186 Whereas normoxic controls showed normal magnetic resonance imagi

187 icantly altered in OIR retinas compared with normoxic controls.

188 %, 32%, and 38%, respectively, compared with normoxic controls.

189 ung and right ventricle tissue compared with normoxic controls.

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

191 dent insulin secretion comparable to that in normoxic controls.

192 posed to 48 hours of hyperoxia together with normoxic controls.

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

194 inct functional areas (the rim, hypoxic, and normoxic cores) were clearly discernible based on spatia

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

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

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

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

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

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

201 ble albumin secretion for up to 6 days under normoxic culture conditions.

202 -1-induced contraction of UtA in hypoxic and normoxic dams equivalently.

203 tal labyrinthine zone in hypoxic compared to normoxic dams.

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

205 prostate cancer cell line under hypoxic and normoxic environments.

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 delivery remained unchanged from baseline in normoxic fetuses.

209 uring hypoxic flights was not higher than in normoxic flights.

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

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

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

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

214 Recent studies have revealed, in normoxic growth conditions, an interface made exclusivel

215 /tissue treated with Ndufs2 siRNA) decreased normoxic H(2)O(2), prevented hypoxic increases in [Ca(2+

216 In this study, we show that normoxic HC increases viral replication, lung injury, an

217 lind randomized manner, while breathing: (i) normoxic helium-oxygen (HEL) to reduce the work of breat

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

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

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

221 Normoxic HIF1alpha protein expression was also dependent

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

223 ~43 mmHg, P(a) CO(2) ~33 mmHg, pH ~7.39), or normoxic hypercapnia (S(a) O(2) ~98%, P(a) O(2) ~105 mmH

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 aque axoplasmic sentinels are arranged along normoxic/hypoxic interfaces in OHM2.

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

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

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

234 Normoxic littermates were kept in the same room outside

235 modulates O(2) delivery to hypoxic (FME) and normoxic (LOX) human melanoma xenografts in a murine win

236 Mitochondria-conditioned media from normoxic lungs contained more H(2)O(2) than mitochondria

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

238 6 inhibits VEGF IRES-mediated translation in normoxic MCF-7 extract.

239 alpha, which was pathologically activated in normoxic MCT-RVfib.

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

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

242 In normoxic mice and oligodendrocytes, exposure to a mitoch

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

244 nd increased uterine artery contractility in normoxic mice, providing evidence that physiological lev

245 2) , and there were no changes in the HVR in normoxic mice.

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

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

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

249 ) medium (+/- fetal bovine serum, FBS) under normoxic (N, p(O(2)) = 20%) or hypoxic (H, p(O(2)) < 2%)

250 33% lower in hypoxic/NaCl rats compared with normoxic/NaCl controls.

251 hypoxic cells onto metabolically altruistic normoxic neighbors.

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

253 Constitutive normoxic NO formation was abolished by NOS inhibition an

254 capable of increasing circulating Epo under normoxic, nonanemic conditions in a previously unrecogni

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

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

257 he superficial inner retina, whether this is normoxic (OHM1), hypoxic (OHM2), or anoxic (OHM3).

258 erved in hypoxic eosinophils compared to the normoxic ones.

259 Under normoxic or hypoxic conditions, SAD inhibited cell survi

260 sies and on A549 LUAD cell lines cultured in normoxic or hypoxic conditions, we identified a subset o

261 or associated transcriptional activity under normoxic or hypoxic conditions.

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

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

264 (64)Cu][Cu(ATSM)] pharmacokinetics in either normoxic or hypoxic hearts, beyond decreasing cardiac ox

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

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

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

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

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

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

271 Direct normoxic PARP1 activation by a DNA alkylating agent enha

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

273 5.1 +/- 3.8%) in aged vs. young offspring of normoxic pregnancy (P < 0.05).

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

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

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

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

278 nervation steadily decreased over 2 weeks of normoxic recovery.

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

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

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

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

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

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

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

286 forest fish to four DO levels, ranging from normoxic to hypoxic (8.7, 6.0, 4.1, and 2.2 mg O(2) /L).

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

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

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

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

291 nosis association was particularly strong in normoxic tumor samples and was linked to an increased ri

292 nd R-state PolyhHbs led to worse outcomes in normoxic tumors.

293 umors and significantly worsened outcomes in normoxic tumors.

294 oxia and compared the results with those for normoxic turtles (25 degrees C) and mouse hearts exposed

295 Normoxic Ucp2KO-PASMCs had mitochondrial hyperpolarizati

296 ropriate to maintain CDO(2) at normothermic, normoxic values.

297 ha deletion had no effect on the increase in normoxic ventilation with acclimatization to CH, indicat

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