ライフサイエンスコーパス: aerobic

1 which becomes zero when metabolism is fully aerobic (100% aerobiosis).

2 oup of organisms considered to belong to the aerobic actinomycetes.

3 g the minimum amount of moderate to vigorous aerobic activity per week.

4 species are proposed as key intermediates in aerobic alcohol oxidation.

5 s undertaken in community facilities (30 min aerobic and 30 min resistance) and handwriting at home,

6 operties of conventional culture techniques (aerobic and anaerobic agars and thioglycolate broth) com

7 e hydrogen isotope fractionation during both aerobic and anaerobic biodegradation of 1,2-dichloroetha

8 al isotope analysis to differentiate between aerobic and anaerobic biodegradation pathways of 1,2-DCA

9 Modeled heat sources include energy from aerobic and anaerobic biodegradation, anaerobic metal co

10 line's PA fraction included taxa known to be aerobic and anaerobic chemoorganotrophs.

11 all intestine causes a systemic dysbiosis of aerobic and anaerobic commensal bacteria.

12 Hg bioreporter capable of functioning under aerobic and anaerobic conditions and exhibiting no physi

13 me from germination to young seedlings under aerobic and anaerobic conditions revealed 82% similarity

14 ysteine in diverse species of bacteria under aerobic and anaerobic conditions.

15 ratory-scale biofilm reactors operated under aerobic and anaerobic conditions.

16 ymidine were treated with trimethoprim under aerobic and anaerobic conditions.

17 reases resistance to trimethoprim under both aerobic and anaerobic conditions.

18 embrane space that seems to function in both aerobic and anaerobic conditions.

19 ompared metagenomic sequencing with standard aerobic and anaerobic culture in 97 sonication fluid sam

20 Prokaryotes have aerobic and anaerobic electron acceptors for oxidative f

21 These metabolic alterations increase both aerobic and anaerobic energy expenditure.

22 tor of lipid homeostasis that regulates both aerobic and anaerobic energy metabolism.

23 he effects of gender and prior experience on aerobic and anaerobic energy systems contributions, and

24 Comparison between aerobic and anaerobic results showed that ferrihydrite p

25 The relationship between telomere length and aerobic and muscular fitness is not well characterized.

26 he methods tested, weight loss plus combined aerobic and resistance exercise was the most effective i

27 ed more in the combination group than in the aerobic and resistance groups (27.9 to 33.4 points [21%

28 The WL + E group incorporated aerobic and resistance muscle training, whereas the WL +

29 c training, resistance training, or combined aerobic and resistance training - or to a control group

30 however, the waters around Sapelo Island are aerobic and well-mixed.

31 ngemia in four bottle types, SA and FA Plus (aerobic) and SN and FN Plus (anaerobic), was performed i

32 ns (anaerobic, aerobic, sequential anaerobic-aerobic), and the extracellular oxidoreductase enzyme ho

33 cally important gram-negative, gram-positive aerobic, and facultative bacteria including most of thos

34 xidative, thermal, photochemical, catalytic, aerobic, and the less common ones) in the light of effic

35 Coupled aerobic-anoxic nitrous decomposition operation (CANDO) i

36 molecular oxygen is released, maintaining an aerobic atmosphere and creating the ozone layer.

37 h an acridinium photoredox catalyst under an aerobic atmosphere.

38 catalyst and trimethylsilyl cyanide under an aerobic atmosphere.

39 olatile fatty acids, ideal substrate to feed aerobic bacteria and produce more PHA.

40 with malonate as the sole carbon source.Some aerobic bacteria contain a biotin-independent malonate d

41 dimethyl disulfide was related to the total aerobic bacteria count.

42 Pseudomonas species and other aerobic bacteria have a biotin-independent malonate deca

43 hane production in the MPPC, the presence of aerobic bacteria suggests that H2O2 diffusion to the ano

44 d anode biofilm for the two operating modes, aerobic bacteria were significant only on the side of th

45 and 10 or more colony-forming units (CFU) of aerobic bacterial growth on either sampling location.

46 e that combining electrolytic treatment with aerobic biodegradation may be a promising synergistic ap

47 hat combining electrochemical oxidation with aerobic biodegradation produces an overadditive treatmen

48 mpounds that are relatively more amenable to aerobic biodegradation.

49 re and after treatment in a laboratory-scale aerobic bioreactor.

50 do not satisfy their metabolic demands using aerobic biosynthesis from glucose.

51 hos capacity that is insufficient to support aerobic biosynthesis from glucose.

52 - 4 per thousand and -38 +/- 4 per thousand (aerobic C-Cl bond cleavage via hydrolytic dehalogenation

53 silonbulk(H)) were -115 +/- 18 per thousand (aerobic C-H bond oxidation), -34 +/- 4 per thousand and

54 e results explain the unique features of the aerobic C-H imidoylation of N-methoxybenzamides and have

55 mportant implications for other Pd-catalyzed aerobic C-H oxidation reactions.

56 O) and respiratory capacity compared to high aerobic capacity (high capacity runner; HCR) rats.

57 We recently reported that rats bred for low aerobic capacity (low capacity runner; LCR) displayed su

58 epatic steatosis; however, rats bred for low aerobic capacity developed greater hepatic inflammation,

59 Intrinsic aerobic capacity had no impact on WD-induced hepatic ste

60 results confirm epidemiological reports that aerobic capacity impacts progression of liver disease an

61 Myricetin significantly potentiated aerobic capacity in mice, as evidenced by their increase

62 reversing cardiac remodeling and increasing aerobic capacity in patients with heart failure with red

63 Low intrinsic aerobic capacity in the low capacity runner (LCR) rat in

64 ABSTRACT: Low aerobic capacity increases risk for non-alcoholic fatty

65 deficit in elite race walkers increases peak aerobic capacity independent of dietary support.

66 KEY POINTS: Low intrinsic aerobic capacity is associated with increased all-cause

67 Here we tested the impact of aerobic capacity on susceptibility for progressive liver

68 Higher aerobic capacity was associated with better performance

69 T in changing left ventricular remodeling or aerobic capacity, and its feasibility remains unresolved

70 ty of life, lung function, body composition, aerobic capacity, muscle strength, and inflammatory/anti

71 Genes for aerobic carbon monoxide (CO) oxidation, polysulfide meta

72 These aerobic catalytic systems comprise an inexpensive Cu(II)

73 e-resolved metagenomics demonstrated that an aerobic cellulolytic consortium cultivated from compost

74 re-oxygenation did not reflect those seen in aerobic coleoptiles, but instead, reverted to a pattern

75 ted, contrasting with a reduced abundance of aerobic commensals.

76 ef was 5-6days for AP samples packaged under aerobic conditions and 14-15days for AP samples in high-

77 explain the excess lactate generation under aerobic conditions characteristic of the Warburg effect.

78 nd NNO(H2) in the presence of base and under aerobic conditions generates FeCl2(NNO(ISQ)) (1), featur

79 Iron that precipitates under aerobic conditions in natural aquatic systems scavenges

80 o the benzoisothiazolones under Cu-catalyzed aerobic conditions to complete the catalytic cycle.

81 se-free oxidative isocyanide insertion under aerobic conditions with intramolecular bis-amine nucleop

82 (anaerobic conditions) versus cell division (aerobic conditions) in the coleoptiles.

83 Under aerobic conditions, 4-MCHM isomers degraded to nondetect

84 Under aerobic conditions, glucose is generally assumed to be b

85 , we demonstrate that ArcA overexpression in aerobic conditions, results in downregulation of respira

86 her under anaerobic conditions compared with aerobic conditions, suggesting that higher Fe(2+) availa

87 Under aerobic conditions, the budding yeast Saccharomyces cere

88 sulting from the oxidation of NO by O2 under aerobic conditions.

89 dentification after culture in anaerobic and aerobic conditions.

90 ree electrons to NO under both anaerobic and aerobic conditions.

91 itoNEET [2Fe-2S] clusters under anaerobic or aerobic conditions.

92 t MRSA and menaquinone utilizing bacteria in aerobic conditions.

93 This transformation occurs via aerobic copper-catalyzed alkene aminooxygenation where m

94 ction compared to the wild-type strain under aerobic culturing conditions.

95 both anaerobic reductive dechlorination and aerobic degradation occurred concurrently.

96 In this study, aerobic degradation of BPA, BPAF, and BPS at 100 mug/kg

97 Furthermore, we could measure the aerobic degradation of dissolved organic carbon (DOC) ad

98 ) and very different from those reported for aerobic degradation pathways in a previous laboratory st

99 robenzodioxolone core by palladium-catalyzed aerobic dehydrogenation.

100 fied a bacterial gene (arsI) responsible for aerobic demethylation of methylarsenite (MAs(III)).

101 ve DeltaP increased the risk of O2 entry and aerobic deterioration during feed-out phase.

102 a critical global feedstock, but is prone to aerobic deterioration.

103 The obligate aerobic diazotroph, Azotobacter vinelandii, employs a mu

104 numerous treatment technologies (air drying, aerobic digestion, mesophilic anaerobic digestion, therm

105 However, the universal MSP is inherently aerobic due to a requirement of molecular oxygen for one

106 NOB were continually washed out using aerobic duration control strategy (ADCS).

107 aken into consideration along with its known aerobic effects in the skeletal muscle.

108 The aerobic electron acceptors include oxygen and cytochrome

109 alysis revealed that among components of the aerobic electron transport chain (ETC), only genes invol

110 As a result of the adaptation of life to an aerobic environment, nature has evolved a panoply of met

111 ficile is strictly anaerobic, it survives in aerobic environments and transmits between hosts via spo

112 oscillations, VC is degraded via coexisting aerobic ethenotrophic and anaerobic reductive dechlorina

113 Aerobic exercise (AE) and non-aerobic neuromuscular elec

114 The study aimed to assess whether aerobic exercise (AEx) training and a fibre-enriched die

115 significant decreases in these measures, but aerobic exercise alone did not.

116 aerobic exercise, caloric restriction alone, aerobic exercise alone, or usual care.

117 t the inflammatory response and improve peak aerobic exercise capacity in patients with recently deco

118 econdary outcomes: left ventricular EF, peak aerobic exercise capacity, and N-terminal pro-brain natr

119 ion, 4-month dietary calorie restriction and aerobic exercise had significant, albeit clinically mode

120 Aerobic exercise improved various neurophysiological dys

121 s have traditionally been observed following aerobic exercise interventions; that is, sustained sessi

122 at implementation of caloric restriction and aerobic exercise is feasible and can improve the proinfl

123 to hot environments, and studies evaluating aerobic exercise performance in such environments across

124 Aerobic exercise training combined with fibre-enriched d

125 Aerobic exercise was performed in 99% of attended sessio

126 andomized to receive caloric restriction and aerobic exercise, caloric restriction alone, aerobic exe

127 nt in peak rate of oxygen consumption during aerobic exercise, respectively.

128 Bactec Plus Aerobic/F and BacT/Alert FA Plus BC bottles were inocula

129 stage than in initial aerobic phase or later aerobic feed-out phase.

130 Longer LTL was associated with higher aerobic fitness and better trunk muscle endurance in mod

131 We examined the association between aerobic fitness and neurocognitive outcomes at young adu

132 crease neural stem cell populations, whereas aerobic fitness has beneficial effects on the adult brai

133 This evidence suggests that aerobic fitness levels are associated with hippocampal D

134 Moreover, aerobic fitness levels were positively associated with d

135 rained participants had significantly higher aerobic fitness measures than untrained participants.

136 86-1987, underwent a graded exercise test of aerobic fitness to measure maximal oxygen uptake (VO2Max

137 dults, we tested the working hypothesis that aerobic fitness, as a physiological indicator of enduran

138 mere length (LTL) with objective measures of aerobic fitness, muscle strength, and muscle endurance,

139 e sample (n = 75) based on a median split of aerobic fitness, the higher fitness group had better dis

140 Mammalian embryos transiently exhibit aerobic glycolysis (Warburg effect), a metabolic adaptat

141 ols help to dissect the relationship between aerobic glycolysis and anabolic metabolism in the retina

142 Aerobic glycolysis and enhanced reliance on glutamine ut

143 Here, we report that aerobic glycolysis and glutaminolysis co-operatively red

144 Thus, a primary function of aerobic glycolysis and glutaminolysis is to co-operative

145 L-2 restores Myc expression in RTEs, driving aerobic glycolysis and IFN-gamma production to the level

146 Whereas IPF fibroblasts are enriched for aerobic glycolysis and innate immune receptor activation

147 1 acts as a safeguard against HPV-stimulated aerobic glycolysis and tumor progression.

148 rate of biosynthesis implies a selection for aerobic glycolysis and uncoupling biosynthesis from NADH

149 helial to mesenchymal transition, increasing aerobic glycolysis by upregulating the glycolytic enzyme

150 TEs are impaired in their ability to perform aerobic glycolysis following activation.

151 nd presumably all astrocytes, can survive by aerobic glycolysis for an extended period of time in the

152 Endothelial cells typically rely on aerobic glycolysis for angiogenesis.

153 To grow faster cancer cells must activate aerobic glycolysis for energy generation and uncouple NA

154 Tumor cells preferentially adopt aerobic glycolysis for their energy supply, a phenomenon

155 Although Otto Warburg first described aerobic glycolysis in cancer cells >90 years ago, the pr

156 ariant M1 isoform is considered critical for aerobic glycolysis in cancer cells.

157 drial Calcium Uptake 1 (MICU1/CBARA1) drives aerobic glycolysis in ovarian cancer.

158 egment maintenance and provide evidence that aerobic glycolysis is part of a metabolic program that s

159 We have previously shown that aerobic glycolysis is required for the regulated prolife

160 hat efforts to block the oncogenic effect of aerobic glycolysis must target reactions upstream of PKM

161 lls switch from oxidative phosphorylation to aerobic glycolysis plus glutaminolysis, markedly increas

162 and mainly derive their cellular energy from aerobic glycolysis rather than oxidative phosphorylation

163 Aerobic glycolysis supports proliferation through unreso

164 use the metabolic conditions established by aerobic glycolysis to both synthesize and accumulate hig

165 Cancer cells actively promote aerobic glycolysis to sustain their metabolic requiremen

166 Metabolic reprogramming toward aerobic glycolysis unavoidably favours methylglyoxal (MG

167 tes metabolic adaptations of lipogenesis and aerobic glycolysis under the control of Akt2 activity, b

168 due to inefficient energy production (i.e., aerobic glycolysis) and depletion of resources for adapt

169 tic deficiency, mammalian cells up-regulated aerobic glycolysis, a process mediated by AMP-activated

170 bolism from oxidative phosphorylation toward aerobic glycolysis, also known as the Warburg effect.

171 increased cytosolic calcium ([Ca(2+)]cyto), aerobic glycolysis, and mitochondrial fission.

172 ation increases PFKP expression and promotes aerobic glycolysis, cell proliferation, and brain tumor

173 remodeling from oxidative phosphorylation to aerobic glycolysis, during which glucose is converted in

174 zyme associated with tumour cell reliance on aerobic glycolysis, in promoting tumour cell exosome rel

175 metabolism characterized by a preference for aerobic glycolysis.

176 g a switch from oxidative phosphorylation to aerobic glycolysis.

177 vent cell migration, which relies instead on aerobic glycolysis.

178 oreceptors maintain their ability to perform aerobic glycolysis.

179 uscle isozyme 2 (PKM2) is a key regulator of aerobic glycolysis.

180 roduce an acidic environment via upregulated aerobic glycolysis; and (ii) noninvasive cells that were

181 The aerobic glycolytic phenotype of hepatocellular carcinoma

182 The aerobic glycolytic preference in NLRX1(-/-) effector T c

183 kg [19% increase], respectively) than in the aerobic group (265 to 270 kg [4% increase]) (P<0.001 for

184 ombination and resistance groups than in the aerobic group (56.5 to 54.8 kg [3% decrease] and 58.1 to

185 inute) increased more in the combination and aerobic groups (17.2 to 20.3 [17% increase] and 17.6 to

186 n investigation of a shift from anaerobic to aerobic growth for the bacterium Escherichia coli.

187 Our calculation demonstrates that aerobic growth from glucose is feasible up to a minimum

188 Remarkably, spxA1 was essential for aerobic growth, demonstrating that L. monocytogenes SpxA

189 hereas the Tenacibaculum-like as free-living aerobic heterotroph, densely colonizing the mesogleal ax

190 Metabolic modelling predicted an aerobic heterotrophic lifestyle for the chlamydia, which

191 osphere and thus its availability to support aerobic life.

192 , eudoraenol and adriaticol, produced by the aerobic marine heterotrophic bacterium Eudoraea adriatic

193 de evidence for the emergence of a pervasive aerobic marine nitrogen cycle.

194 ted anaerobic plates to primary quadrants of aerobic media during specimen planting yielded a colonia

195 ial stability of the patties, delaying total aerobic mesophilic, and lactic acid bacteria growth, esp

196 signals the presence of eukaryotes, but also aerobic metabolic processes.

197 also the temperature providing the greatest aerobic metabolic scope and body condition across all tr

198 to changes in upper critical thermal limits, aerobic metabolic scope and thermal preference.

199 ed the upper critical thermal limit, neither aerobic metabolic scope nor thermal preference exhibited

200 rination potential suppresses development of aerobic metabolic VC oxidation potential.

201 Under oxic atmosphere, aerobic metabolic VC oxidation was absent in sediments w

202 Aerobic metabolism also generates superoxide (O2()) and

203 ctive oxygen species (ROS) are byproducts of aerobic metabolism and contribute to both physiological

204 g is essential for bacterial survival during aerobic metabolism and host infection.

205 ults indicated the exogenous GAs lowered the aerobic metabolism including the oil metabolisms during

206 the high energy requirements and reliance on aerobic metabolism render it particularly susceptible to

207 duction by spheroids upon suppression of the aerobic metabolism was observed.

208 pecies (ROS) are toxic by-products of normal aerobic metabolism.

209 Here, the response of the deep-sea aerobic methanotroph Methyloprofundus sedimenti to metha

210 mulation of significant amount of PHA inside aerobic microbial cells occurs when a surplus of an easi

211 ts indicated that CAPB markedly improved the aerobic microorganism activities.

212 These organic halides can be degraded by aerobic microorganisms, where the initial steps of vario

213 conditions on separate days: after a 60-min aerobic moderate-intensity exercise session, after a hig

214 To our knowledge, while aerobic 'moss banks' have often been examined, waterlogg

215 Aerobic exercise (AE) and non-aerobic neuromuscular electric stimulation (NMES) are co

216 Our present study implies that aerobic NH3 oxidation by AOB occurs via two obligate int

217 phonate is a source of methane in the upper, aerobic ocean, where phosphorus-starved microbes catabol

218 Blood was added to paired aerobic or anaerobic bottles, with the volume in each bo

219 hibitory influence on the endogenous rate of aerobic or anaerobic microbial respiratory activity.

220 avin-dependent monooxygenase, HadA, from the aerobic organism Ralstonia pickettii DTP0602, identifyin

221 ous polyketides are known to be derived from aerobic organisms, only a single family of polyketides h

222 toxic trace element that is required by all aerobic organisms.

223 tion and biosynthetic precursor synthesis in aerobic organisms.

224 Highly aerobic organs like the kidney are innately susceptible

225 have important implications for Pd-catalyzed aerobic oxidation catalysis: (1) The reaction tolerates

226 ent iodine reagents will expand the scope of aerobic oxidation chemistry in chemical synthesis.

227 -H bonds para to the CH2N(CH3)2 group in the aerobic oxidation of 4-alkyl-N,N-dimethylbenzylamines ca

228 cts of the N-heterocyclic carbenes catalyzed aerobic oxidation of aldehydes shares important similari

229 ion strategy highlighted by a Cu(I) mediated aerobic oxidation of betulin, a highly selective PIFA me

230 Ubiquitous tyrosinase catalyses the aerobic oxidation of phenols to catechols through the bi

231 ol revealed the formation of aldehyde during aerobic oxidation of the arylmethanes.

232 ave been used to support palladium-catalyzed aerobic oxidation reactions and, where possible, describ

233 The former catalyst was used in batch aerobic oxidation reactions with different primary alcoh

234 ificant expansion of the scope of accessible aerobic oxidation reactions.

235 The use of aryl iodides as mediators of aerobic oxidation underpins an oxidase catalysis platfor

236 te for N-hydroxyphthalimide in the catalytic aerobic oxidations of aliphatic hydrocarbons characteriz

237 l oxide catalysts are widely studied for the aerobic oxidations of C1-C4 alkanes to form olefins and

238 The aerobic oxidative cleavage of 1,2-diols using a heteroge

239 A photocatalytic method for the aerobic oxidative cleavage of C=C bonds has been develop

240 celeration effect of Cu(OTf)2 in the C-H/C-H aerobic oxidative coupling of o-xylene.

241 t compositions that are highly effective for aerobic oxidative methyl esterification of primary alcoh

242 Of 5,709 bottle sets (52.5% aerobic pairs and 47.5% anaerobic pairs), 430 (7.5%) wer

243 and ion regulation, respiratory function and aerobic performance in aquatic animals.

244 High aerobic performance is linked to oxidative damage in mus

245 anaerobic fermentation stage than in initial aerobic phase or later aerobic feed-out phase.

246 ously undescribed role of saNOS in S. aureus aerobic physiology was reported.

247 g step and rinsates were applied to estimate aerobic plate count (APC) and Campylobacter as well as S

248 The treated juice exceeded total aerobic plate count of 2 log10 (cfu/ml) on 15th day of s

249 leading to only intermittent observation of aerobic plate positivity), and laboratory factors (novel

250 t a work rate estimated to require 110% peak aerobic power reduced VO2, muscle phosphocreatine breakd

251 sor exercise (estimated to require 110% peak aerobic power) continuously and with three different int

252 ing between O2 production and consumption by aerobic processes under apparent anoxic conditions.

253 evealed the enhanced expression of genes for aerobic processes, such as nitrite oxidation.

254 ls share several metabolic traits, including aerobic production of lactate from glucose (Warburg effe

255 lonization is typified by both expansions in aerobic Proteobacteria and decreases in anaerobic Firmic

256 evolution by facilitating the development of aerobic respiration and complex multicellular life.

257 , the CydAB bd-type oxidase is essential for aerobic respiration and intracellular replication, and c

258 uvate metabolism, resulting in a decrease in aerobic respiration at the location of injury following

259 Altogether, our results identify aerobic respiration by bacteria as a previously unknown

260 Therefore, we reasoned that inhibiting aerobic respiration by inducing systemic hypoxaemia woul

261 ry complexes, supporting the hypothesis that aerobic respiration evolved after oxygenic photosynthesi

262 In this system, aerobic respiration generally maintains anoxic groundwat

263 AB aa 3-type oxidase is required neither for aerobic respiration in air nor for intracellular growth.

264 gulator for the switch between anaerobic and aerobic respiration in Escherichia coli and many other b

265 ted mandelalides are effective inhibitors of aerobic respiration in living cells.

266 ing revealed bacterial formate oxidation and aerobic respiration to be overrepresented metabolic path

267 hypoxia, leads to reduced ATP production by aerobic respiration, driving cells to rely more on fatty

268 tochondrial homeostasis, including decreased aerobic respiration, increased oxidant stress, and mitoc

269 h, saNOS also plays a modulatory role during aerobic respiration.

270 cal gas normally produced in the body during aerobic respiration.

271 ycling in upland soils is entirely driven by aerobic respiration; the impact of anaerobic microsites

272 existing cardiomyocytes, and is regulated by aerobic-respiration-mediated oxidative DNA damage.

273 unctions as the initial electron acceptor in aerobic respiratory chains of most organisms.

274 hat all three classes independently acquired aerobic respiratory complexes, supporting the hypothesis

275 ate a key contribution of saNOS to S. aureus aerobic respiratory metabolism.

276 Specifically, aerobic S. aureus nos mutant cultures presented with ele

277 ogical traits (such as extracellular pCO2 or aerobic scope) cannot be distinguished.

278 ents, different redox conditions (anaerobic, aerobic, sequential anaerobic-aerobic), and the extracel

279 key constituent of excess sludge produced by Aerobic Sewage Sludge Treatment plants.

280 ns act as participating ligands at Pd(II) in aerobic sp(3)-C-H bond acetoxylation processes and are i

281 suppressed microbial activity and supported aerobic stability, the negative DeltaP increased the ris

282 ion BNR, LMW-DON is released during the post-aerobic step following the preanoxic step, which does no

283 to measure multiple realms of function (eg, aerobic, strength, balance, and even cognition) that are

284 ut added moderate physical activity (PA; 80% aerobic; supervised/free gym membership).

285 rsity and biogeochemical cycling between the aerobic surface layer and the anaerobic core in nitrite-

286 s for cj1377c in formate metabolism, nuoK in aerobic survival and oxidative respiration, and cj1368-7

287 To further reduce costs, an aerobic thermal sorbent regeneration step was also exami

288 Given that the myocardium is an obligate aerobic tissue and consumes large amounts of O2, the dat

289 cultures to demonstrate that the switch from aerobic to anaerobic metabolism is brought about by chan

290 nges from membrane-associated patterns under aerobic to diffuse patterns under anaerobic conditions.

291 e also demonstrated that fasting and chronic aerobic training negatively modulated the ACSL6 mRNA and

292 - 7.0 mug/L, respectively; P = 1.00).Regular aerobic training reduces the apparent effectiveness of i

293 ifestyle intervention included 5 to 6 weekly aerobic training sessions (duration 30-60 minutes), of w

294 rogram plus one of three exercise programs - aerobic training, resistance training, or combined aerob

295 draw conclusions about the effectiveness of aerobic training, resistance training, or tai chi for im

296 ansfer and electron transfer-oxygen transfer aerobic transformations, there a few examples of apparen

297 anced performance of the STAD system for WAS aerobic treatment.

298 ere packaging conditions (MAP), in our case, aerobic, vacuum or high O2, to extend the shelf life of

299 However, the identity of aerobic VC degradation pathways (cometabolic vs metaboli

300 Free-draining biofilters remained aerobic with negligible greenhouse gas production during