ライフサイエンスコーパス: aerobic

1 ed from human subjects before and after step aerobics.

2 individuals before and after 30-minute step aerobics.

3 mestic wastewater were operated under stable aerobic (+195 +/- 25 mV), anoxic (-15 +/- 50 mV), and an

4 nfection caused by gram-positive filamentous aerobic actinobacterium Tropheryma whipplei occurs class

5 However, higher aerobic activity and genetic drift impose strong mutatio

6 , with impacts on the resulting capacity for aerobic activity.

7 copper(I/II) shuttle, as exemplified with an aerobic alcohol oxidation.

8 Here, we report a mechanistic study of aerobic allylic acetoxylation of allylbenzene with a cat

9 stimulations, such as knee loading and step aerobics, altered urinary metabolism and downregulated W

10 lso play a crucial role in the metabolism of aerobic and anaerobic ammonia oxidizers by converting hy

11 Germination under aerobic and anaerobic conditions showed very low correla

12 nisms in regulating isotopic compositions in aerobic and anaerobic conditions, respectively.

13 Similar findings were obtained from both aerobic and anaerobic cultivations.

14 s are metabolized with equal affinity during aerobic and anaerobic growth conditions, suggesting that

15 de or (2-methylthio)acetaldehyde during both aerobic and anaerobic growth.

16 stinal epithelium with stable communities of aerobic and anaerobic human gut microbiota, using a micr

17 different growth conditions, including both aerobic and anaerobic metabolisms.

18 ses with a relatively constant ratio between aerobic and anaerobic oil decomposition rates even after

19 idases are transmembrane enzymes involved in aerobic and anaerobic respiration.

20 ized by a subset of prokaryotes via distinct aerobic and anaerobic routes.

21 ed the proposed concepts of control over the aerobic and anoxic phases collectively.

22 often requires high chemical stability under aerobic and aqueous conditions for practical application

23 robe B. fragilis have diverged from those of aerobic and facultative anaerobic pathogenic bacteria.

24 Aerobic and nitrite-dependent methanotrophs make a livin

25 We aimed to determine if a program of aerobic and resistance exercise could safely achieve bod

26 Women were randomized to either a combined aerobic and resistance exercise training program followi

27 cle lipids are impacted by acute and chronic aerobic and resistance exercise training.

28 Exercise group completed 12-weeks of aerobic and resistance training (n = 20), while the cont

29 Moderate-intensity combined aerobic and resistance training is safe in physically un

30 tested the role of FDX5 in both the initial aerobic and subsequent anaerobic phases of S-deprivation

31 p. WSUCF1 is a Gram-positive, spore-forming, aerobic and thermophilic bacterium, isolated from a soil

32 a more ancient lineage of DMSORs compared to aerobic arsenite oxidase catalytic subunits, which evolv

33 Aerobic ATP synthesis unavoidably produces reactive oxyg

34 n in the GB samples of 1st, and 9th-week old aerobic biofilms.

35 New aerobic bioreactor designs are needed, ideally employing

36 n to dioxane, unraveling its pivotal role in aerobic biostimulation that utilizes propane, isobutane,

37 significant pathogens that were negative in aerobic blood cultures and supports the routine collecti

38 automatic anaerobic blood culture alongside aerobic blood cultures in a pediatric emergency departme

39 ve cultures in the postimplementation phase, aerobic blood cultures recovered 7.6% (349/4,615), where

40 716 blood samples, was negative in all 1,312 aerobic bottles and 810 bacterial culture-negative anaer

41 d left ventricular function at rest, maximal aerobic capacity ( V O(2) max) and submaximal exercise t

42 c output at rest (echocardiography), maximal aerobic capacity ( V O(2) max) and the speed-duration re

43 Aerobic capacity (VO(2)max) is a critical performance tr

44 e that HAH attenuates the decline in maximal aerobic capacity and preserves pulmonary gas exchange du

45 e impact of physical activity, exercise, and aerobic capacity compared with caloric restriction on re

46 shows that physical activity, exercise, and aerobic capacity have profound effects on regulating int

47 emonstrated an attenuated decline in maximal aerobic capacity in acute hypoxia.

48 k could be used as a reference for assessing aerobic capacity in studies on exercise intervention wit

49 determinant of the age-dependent decline in aerobic capacity that ultimately limits functional indep

50 riteria fatigue, reduced resistance, reduced aerobic capacity, and weight loss.

51 FRAIL scale: fatigue, poor strength, reduced aerobic capacity, having >=5 chronic illnesses, and weig

52 the FRAIL scale: fatigue, poor strength, low aerobic capacity, having >=5 illnesses, and >=5% weight

53 scale: fatigue, reduced resistance, reduced aerobic capacity, having >=5 illnesses, and weight loss

54 n fraction (HFpEF) and is linked to impaired aerobic capacity.

55 tion (HFpEF) and is associated with impaired aerobic capacity.

56 synthetic models of the Mo/Cu active site of aerobic carbon monoxide dehydrogenase (CODH) has been a

57 aining F. nucleatum viability under standard aerobic cell culture conditions.

58 omic instability and phenotypic evolution in aerobic cells.

59 me, and thus has lost the ability to perform aerobic cellular respiration.

60 While receiving little attention so far, aerobic chemolithoautotrophic bacteria that operate the

61 high-efficiency preparative method based on aerobic Co-/ N-hydroxysuccinimide (NHSI) catalyzed oxida

62 The reaction proceeds under aerobic condition at room temperature.

63 The reaction proceeds in aerobic conditions and does not require any sacrificial

64 iving radical polymerizations under apparent aerobic conditions by first consuming dissolved oxygen v

65 and guidance on how to measure and maintain aerobic conditions during the test.

66 f bacterial growth under hypoxia compared to aerobic conditions in the presence of these inhibitors.

67 Moreover, under aerobic conditions in which the Fe(III) oxidation state

68 biochemical analyses of CopG purified under aerobic conditions indicate that it is a green copper-bi

69 Incubation of this strain under aerobic conditions resulted in the emergence of a novel

70 il in which the maintaining and measuring of aerobic conditions was possible without the loss of vola

71 ly, although they still failed to grow under aerobic conditions without mevalonate.

72 X, is required for CO ligand synthesis under aerobic conditions, and preliminary in vivo data indicat

73 Under thermal and aerobic conditions, the consecutive and pH-dependent tra

74 Under aerobic conditions, they participate in the citric acid

75 of stem-cell activity in plants grown under aerobic conditions, which suggests that the spatially di

76 racterized by enhanced glycolysis even under aerobic conditions.

77 e citrate under anaerobic conditions but not aerobic conditions.

78 ds photobiological hydrogen production under aerobic conditions.

79 n is rapidly scavenged or precipitated under aerobic conditions.

80 No QTL effects were observed under aerobic conditions.

81 g sifnificant fermentation rates even during aerobic conditions.

82 nd easily available starting materials under aerobic conditions.

83 tion and nitrosative stress resistance under aerobic conditions.

84 aterials, and performing the reactions under aerobic conditions.

85 ylene blue (MB) wastewater for 9 weeks under aerobic conditions. The COD of MB wastewater showed a re

86 land Mollisol-with added litter under either aerobic (control) or anaerobic conditions for 1 year.

87 datively trimerize phenols using a catalytic aerobic copper system is described.

88 luenga-Valdes cross-coupling, followed by an aerobic, copper-catalyzed, radical cyclization to form C

89 C accumulation in peatlands due to enhanced aerobic decay in the acrotelm, which would lead to a slo

90 is reported based on a rhodium(II)-catalyzed aerobic decomposition process.

91 m), it is difficult to project how much more aerobic decomposition will take place before the younger

92 Herein, we report the first complete aerobic dehydrogenation pathway to large-scale productio

93 physiological fitness through metabolic and aerobic depression and changes to anti-predator behavior

94 central carbon and nitrogen metabolism in an aerobic diazotroph for the first time.

95 RP4-gfp-bearing cells disappeared rapidly in aerobic ecosystems (~2.0 log reduction after 72 h), espe

96 Most of it is recycled within aerobic ecosystems, but some is lost to the system and i

97 adaptation required to support the NQ-driven aerobic electron transport chain.

98 oupling extracellular manganese oxidation to aerobic energy conservation and autotrophic CO(2) fixati

99 fness does not appear to alter the volume of aerobic energy consuming muscle in the soleus, or any ot

100 For each condition, we quantified athlete aerobic energy expenditure and performed biomechanical a

101 fiber plates to shoes soles reduces athlete aerobic energy expenditure during running (improves runn

102 th ecophysiological limits to acquisition of aerobic energy(4) for a global cross-section of the biod

103 exercise intervention that was comprised of aerobic exercise (AE) or a combination of aerobic exerci

104 ined the effects of acute moderate-intensity aerobic exercise (MAE) on inhibitory control and resting

105 of aerobic exercise (AE) or a combination of aerobic exercise and resistance training (CE).

106 ISS-like CM exercise (modelled as 2 x 30-min aerobic exercise at 75% VO(2max), 6-d/week).

107 Aerobic exercise elicits increases in cerebral blood flo

108 verall, we highlight the importance of acute aerobic exercise for children with ADHD as a potential m

109 Aerobic exercise further resulted in more effective conf

110 mice They also show that lifelong voluntary aerobic exercise has remarkable protective effects on va

111 mic and cardiorespiratory recovery following aerobic exercise in normotensive individuals with differ

112 ts engaged in aerobic exercise training, and aerobic exercise interventions improve arterial stiffnes

113 of this cardiovascular-protective effect of aerobic exercise is likely due to its vascular health-en

114 However, acute aerobic exercise may not modulate sympathovagal balance

115 tes seated at rest, followed by a submaximal aerobic exercise on a treadmill and then remaining seate

116 suggest that the beneficial effects of acute aerobic exercise on inhibitory control are sustained for

117 Lifelong aerobic exercise prevented age- and WD-related vascular

118 engage patients awaiting LT in an intensive aerobic exercise program with a signal of improvement in

119 ted from 48 college-aged participants during aerobic exercise sessions along with mental distress and

120 Aerobic exercise training (AT) improves endothelial func

121 Here we show that aerobic exercise training up-regulates DICER in adipose

122 e is attenuated in healthy adults engaged in aerobic exercise training, and aerobic exercise interven

123 ired for whole-body metabolic adaptations to aerobic exercise training, in part, by allowing controll

124 e remarkable protective effects of voluntary aerobic exercise, and the underlying mechanisms.

125 are key mechanisms underlying the voluntary aerobic exercise-associated preservation of vascular fun

126 r presence (voluntary wheel running, VWR) of aerobic exercise.

127 sity and some anthropometric elements during aerobic exercise.

128 sin-containing BacT/Alert FA Plus and Bactec Aerobic/F blood culture bottles.

129 te uptake rates accompanied by a switch from aerobic fermentation to respiration, with glycerol and a

130 vention comprised of high-intensity interval aerobic fitness and strength training paired with a nove

131 2 and folic acid] to high-intensity interval aerobic fitness and strength training paired with a stan

132 a multimodal intervention that incorporates aerobic fitness and strength training with a novel nutri

133 n between total leukocyte count and not only aerobic fitness but also parts of anaerobic fitness in y

134 Aerobic fitness was assessed by the time for a 3-kilomet

135 Aerobic fitness was evaluated by 3000-meter run test, an

136 (CSA), muscle density, balance, flexibility, aerobic fitness, inflammation, oxidative stress, bone an

137 plementation improves vascular and therefore aerobic function in health and disease is presented.

138 in situ cellulolytic enzyme production by an aerobic fungus next to facultative anaerobic lactic acid

139 d significantly colocated with prior maps of aerobic glycolysis (AG), AG-related gene expression, pos

140 bolism in vertebrate retinas is dominated by aerobic glycolysis (the "Warburg Effect"), which allows

141 Most tumor cells use aerobic glycolysis (the Warburg effect) to support anabo

142 s including dysregulated androgen signaling, aerobic glycolysis (Warburg effect), and aberrant activa

143 g-resistant CSC- and EMT-like phenotype with aerobic glycolysis and fatty acid beta-oxidation-mediate

144 Aerobic glycolysis and glutaminolysis are two of the mos

145 ated osteoclasts heavily relies on increased aerobic glycolysis and glycolysis-derived lactate produc

146 nstrates a reciprocal stimulation of Myc and aerobic glycolysis and identifies the Pfk2-Pfk governed

147 pa B-dependent metabolic pathway, leading to aerobic glycolysis and polarization of macrophages.

148 BCAP deficiency also results in defective aerobic glycolysis and reduced lactate production.

149 in a wide range of human cancers and drives aerobic glycolysis and tumor growth by inhibiting pyruva

150 PKM2 catalytic activity and thereby promotes aerobic glycolysis and tumor growth.

151 Increased glucose uptake and aerobic glycolysis are striking features of many cancers

152 Finally, skewing T cell metabolism toward aerobic glycolysis by deleting mitochondrial pyruvate ca

153 cells exhibiting the Warburg effect rely on aerobic glycolysis for ATP production and have a notable

154 he neural retina metabolizes glucose through aerobic glycolysis generating large amounts of lactate.

155 Mechanistically, aerobic glycolysis genes are elevated in T cells during

156 nine N-methyltransferase 6 (PRMT6) regulates aerobic glycolysis in human hepatocellular carcinoma (HC

157 Cancer cells are known to adopt aerobic glycolysis in order to fuel tumor growth, but th

158 phorylation in mitochondria, complemented by aerobic glycolysis in the cytoplasm.

159 nate metabolic changes have been compared to aerobic glycolysis in tumour cells.

160 These findings reveal that aerobic glycolysis is a process functionally distinct fr

161 , targeting glucose transporters to regulate aerobic glycolysis is an attractive approach to identify

162 Aerobic glycolysis or the Warburg effect (WE) is charact

163 This metabolic reprogramming, known as aerobic glycolysis or the Warburg effect, allows tumor c

164 Dividing lymphocytes typically rely on aerobic glycolysis over oxidative phosphorylation for en

165 glucose and metabolically reprogram to favor aerobic glycolysis over oxidative phosphorylation.

166 extensive metabolic remodeling to engage in aerobic glycolysis prior to delamination.

167 Warburg effect or aerobic glycolysis provides selective growth advantage t

168 erior elongation(1), exhibit a high level of aerobic glycolysis that is reminiscent of the metabolic

169 ed lactate production from glucose, known as aerobic glycolysis when oxygen is abundant, is also crit

170 This argues that cells engage in aerobic glycolysis when the demand for NAD(+) is in exce

171 n of Glut1 in osteoclast progenitors reduces aerobic glycolysis without compromising OXPHOS, but none

172 ) accounts for the fermentative component of aerobic glycolysis, a near ubiquitous metabolic alterati

173 ed macrophages undergo a metabolic switch to aerobic glycolysis, accumulating Krebs' cycle intermedia

174 t of rapamycin (AKT-mTOR) pathway, increased aerobic glycolysis, favored Th17 cell differentiation ov

175 Aerobic glycolysis, or preferential fermentation of gluc

176 Aerobic glycolysis, originally identified by Warburg as

177 IL-2 promoted effector-like metabolism and aerobic glycolysis, robustly inducing lactate dehydrogen

178 In response, hMDMs shift their metabolism to aerobic glycolysis, which directly triggers an M1-like p

179 is shifted from oxidative phosphorylation to aerobic glycolysis, which is considered important for pr

180 nd Tumor cells frequently show high rates of aerobic glycolysis, which provides the glycolytic interm

181 expression, which is a critical regulator in aerobic glycolysis.

182 volving the enhancement of key indicators of aerobic glycolysis.

183 rheostat that mediates exquisite control of aerobic glycolysis.

184 appear to uncouple rapid proliferation from aerobic glycolysis.

185 ex remodeling of cellular metabolism towards aerobic glycolysis.

186 erate ATP, while bloodstream cells switch to aerobic glycolysis.

187 poxia, and a metabolic profile skewed toward aerobic glycolysis.

188 a broad array of multidrug-resistant (MDR), aerobic Gram-negative bacilli.

189 Listeria monocytogenes that is essential for aerobic growth and pathogenesis.

190 lacking the two dehydrogenases essential for aerobic growth exhibited a severe growth defect with an

191 ase (kat) were required for L. monocytogenes aerobic growth in rich medium.

192 We previously reported that aerobic growth on citrate (Cit(+)) evolved in an Escheri

193 oteome allocation, during both anaerobic and aerobic growth on glucose.

194 xygen-related fitness benefits: it increases aerobic growth yield by increasing oxygen diffusion, and

195 During aerobic growth, the Gram-positive facultative anaerobe a

196 er NarK whose gene is silent during standard aerobic growth.

197 (henceforth: Haloarchaea) are predominantly aerobic halophiles that are thought to have evolved from

198 nary proteins, knee loading in mice and step aerobics in humans markedly reduced WNT1-inducible signa

199 cium homeostasis in the presence of complete aerobic inhibition.

200 roxide (H(2)O(2)) as a normal constituent of aerobic life in eukaryotic cells.

201 Aerobic life is possible because the molecular structure

202 animals invaded when conditions permitted an aerobic life style at the seafloor.

203 r oxygen that occur as a normal attribute of aerobic life.

204 as a key driver of the evolution of O(2) and aerobic life.

205 Aerobic lifeforms, including humans, thrive because of a

206 ate metabolic profile analysis suggests that aerobic mechanism is better supported under high perfusa

207 Here we show that diverse aerobic members of communities in SPG sediments (4.3-101

208 oxygen species (ROS) produced during normal aerobic metabolism and by the innate immune systems.

209 gical constraints on oxygen supply affecting aerobic metabolism of aquatic ectotherms, ecological the

210 oli, which conferred resistance by using its aerobic metabolism to compete with Salmonella for resour

211 As oxygen is central to all aerobic metabolism, hypoxia is now recognized to contrib

212 effective preservation strategy to maintain aerobic metabolism, protect mitochondria, and achieve an

213 All MV420 sites showed the presence of aerobic methane oxidation (MOx)- and anaerobic methane o

214 Aerobic methane oxidation is catalyzed by particulate me

215 ters distant) communities with gene-inferred aerobic, microaerophilic, and anaerobic metabolisms are

216 In aerobic natural surface water, a silver ion (Ag(+)) exis

217 rbon, nitrogen, and sulfur assimilation, and aerobic nitrogen cycling.

218 ex regulates HIF-1alpha protein levels under aerobic (normoxia) or anaerobic (hypoxia) conditions.

219 n of the oxidized form of the catalyst under aerobic/O(2) oxidation makes this protocol eco-friendly

220 where organisms were only recovered from an aerobic or an anaerobic bottle in the paired cultures we

221 h occurs in coal and oil, can be degraded by aerobic or anaerobic microorganisms.

222 idative stress is a ubiquitous threat to all aerobic organisms and has been implicated in numerous pa

223 Aerobic organisms evolved conserved mechanisms controlli

224 Aerobic organisms have successfully found solutions to t

225 Most aerobic organisms, including nearly all eukaryotes, have

226 al cofactor for many biological processes in aerobic organisms, which can synthesize it de novo throu

227 Instead, they suggest a predominantly aerobic organoheterotrophic lifestyle, perhaps based on

228 y converted into crotonic acid via catalytic aerobic oxidation (62 % yield).

229 dative carbocyclization of dienallenes under aerobic oxidation conditions has been developed to affor

230 Aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,

231 shows exceptional catalytic activity for the aerobic oxidation of alcohols to produce aldehydes in ne

232 n visible light photoredox catalysis for the aerobic oxidation of arylboronic acids to phenols under

233 high catalytic activity for the solvent-free aerobic oxidation of benzyl alcohol.

234 drogel layers resulting in the GOx catalyzed aerobic oxidation of glucose to gluconic acid.

235 he reactions discussed include CO oxidation, aerobic oxidation of monohydric and polyhydric alcohols,

236 vent for a nitric acid and FeCl(3)-catalyzed aerobic oxidation of secondary alcohols to ketones.

237 on, the main underlying factor hindering the aerobic oxidation of tetrahydroisoquinolines, is relieve

238 lopment and a key step in the development of aerobic oxidation reactions.

239 Co(salophen)-HQ] as hybrid ETM gave a faster aerobic oxidation than the use of separated ETMs, indica

240 in-fused pentacycles B were found to undergo aerobic oxidation to give the corresponding hydroxypyrro

241 pplication of a ring-closing copper(I)/TEMPO aerobic oxidation to the pyrrolobenzodiazepine ring syst

242 the first use of phd to support Pd-catalyzed aerobic oxidation.

243 While aerobic oxidations with Fe and Cu are well precedented,

244 onal study of N-hydroxyphthalimide-catalyzed aerobic oxidative cleavage of alkenes is carried out emp

245 zed for developing a Co(II)[salen]-catalyzed aerobic oxidative cross-coupling of phenols in a recycla

246 (phd) as the ancillary ligand, that enables aerobic oxidative homocoupling of 2-bromothiophenes and

247 successful applications in red-light-induced aerobic oxidative hydroxylation of arylboronic acids and

248 rete multicellular spheroids capable of both aerobic (oxygen producing) and hypoxic (hydrogen produci

249 Three sentinel parameters of aerobic performance are the maximal oxygen uptake ( VO2m

250 Aerobic phase contributed to N(2)O production/emission p

251 t, electron spin-resonance spectroscopy, and aerobic photo-oxidation of benzylamine.

252 Regular aerobic physical exercise of moderate intensity is unden

253 localized anoxic microsites in the otherwise aerobic porous bulk soil causing reduction of ferrihydri

254 ive muscle volume (p = 0.538; d = 0.241), or aerobic power (p = 0.458; d = 0.04) during running.

255 ion of the alk-1-enyl ether bond involves an aerobic process in animal cells and thus is fundamentall

256 mmonia oxidation in a wastewater reactor and aerobic pyrite oxidation in acid mine drainage.

257 zoan abundances were over 20 times higher in aerobic reactors relative to anaerobic reactors, and pro

258 of an anaerobic blood culture alongside the aerobic remains controversial.

259 type 1 and type 2 pathways, alleviating the aerobic requirement for PDT.

260 All DOM sources significantly enhanced aerobic respiration and denitrification of the biofilm w

261 disorganized mitochondrial networks, reduced aerobic respiration and increased reactive oxygen specie

262 transformed eukaryotic life, from providing aerobic respiration and photosynthesis to enabling colon

263 ned a large number of genes and expanded its aerobic respiration and salt/UV resistance gene repertoi

264 ated intimate attachment is not required for aerobic respiration but for hydrogen peroxide (H(2)O(2))

265 pathways, already present in bacteria before aerobic respiration evolved, offer a solution to the str

266 s more efficient than O(2) metabolism during aerobic respiration in foraminifera from the Peruvian OM

267 Modern day aerobic respiration in mitochondria involving complex I

268 Although aerobic respiration is a hallmark of eukaryotes, a few u

269 Aerobic respiration is essential to almost all eukaryote

270 s rise to molecular oxygen that supports the aerobic respiration of E. coli.

271 olisms at specific environmental conditions: aerobic respiration of glucose in freshwater, anaerobic

272 thways and determined that genes involved in aerobic respiration or mitochondrial DNA replication wer

273 hydroperoxyl (superoxide) as a byproduct of aerobic respiration, and the demonstrated cytoprotective

274 ions by first consuming dissolved oxygen via aerobic respiration, and then directing extracellular el

275 icantly enhanced, including sugar transport, aerobic respiration, pyruvate breakdown, and the glyoxyl

276 chment provides C. rodentium with oxygen for aerobic respiration.

277 ore carbon when oxygen becomes available for aerobic respiration.

278 within a shell of bacterial cells undergoing aerobic respiration.

279 or Q8) mediates electron transfer within the aerobic respiratory chain, mitigates oxidative stress, a

280 functions as an initial electron acceptor in aerobic respiratory chains that reduces quinone and pump

281 y into an electrochemical proton gradient in aerobic respiratory chains, powering energy-requiring pr

282 Both species exhibited decreases in aerobic scope (as a function of reduced maximum metaboli

283 e predict that global warming will limit the aerobic scope of aquatic ectotherms and may place a grea

284 resting and active metabolic rate and hence aerobic scope of aquatic ectotherms.

285 duced critical swimming speeds (U(crit)) and aerobic scopes (reductions of ~40 and 61%, respectively)

286 (anaerobic screenhouse, anaerobic tray, and aerobic screenhouse) to establish the relationship among

287 losum and Stagonospora sp., we observed that aerobic Se(IV and VI) bioreduction to Se(0) and Se(-II)

288 Aerobic sludge digestion of waste activated sludge (WAS)

289 alues of delta(13) C increased with depth in aerobic soil layers (0-40 cm) but slightly decreased in

290 jor stressor that generally subverts life of aerobic species and is a prominent feature of pathologic

291 Amongst those, only the aerobic species were efficient methylators.

292 ention (active treatment) (n = 105) included aerobic, strength, balance, and functional training.

293 Evidence that facultatively aerobic SUP05 are more active and respire nitrate when o

294 d inexpensive source for catalytic NO(2) for aerobic TEMPO oxidations of alcohols, diols, and ethers.

295 mice, which have evolved a high capacity for aerobic thermogenesis, to determine the mechanisms of mi

296 standing the evolutionary transition from an aerobic to an exclusive anaerobic metabolism.

297 substrate complexation, charge transfer, and aerobic turnover, involving high-valent Fe(IV) intermedi

298 tive PCR (qPCR) assay, including testing for aerobic vaginitis (AV), Candida, sexually transmitted in

299 ing antibiotic treatment or in patients with aerobic vaginitis.

300 for rapid and simple quantification of total aerobic viable counts of bacteria (TVC) in food and envi