ライフサイエンスコーパス: formaldehyde

1 olymers is the reduction of the carcinogenic formaldehyde.

2 N-methyl group, resulting in the release of formaldehyde.

3 has evolved systems to perceive and detoxify formaldehyde.

4 hemicals, such as chemotherapeutic drugs and formaldehyde.

5 tochemical ozone creation potential, such as formaldehyde.

6 n the Prato reaction with N-ethylglycine and formaldehyde.

7 radical scavenger and measuring its product, formaldehyde.

8 methoxybenzene, 1,3,5-trimethoxybenzene, and formaldehyde.

9 ase, catalysing the oxidation of methanol to formaldehyde.

10 fectively killed through exposure to heat or formaldehyde.

11 oduced by treating live poliovirus (PV) with formaldehyde.

12 CO2 can be used as a C1 feedstock to produce formaldehyde.

13 thanol and its subsequent dehydrogenation to formaldehyde.

14 ton transfer steps to reduce formic acid and formaldehyde.

15 ing the cage vertices with carbonyls such as formaldehyde.

16 H, significantly underestimate the levels of formaldehyde.

17 espond to Zn(II), RcnR to cobalt and FrmR to formaldehyde.

18 tu iodination-based oxidative elimination of formaldehyde.

19 nsient exposure to natural concentrations of formaldehyde.

20 NO3)3 and La2O3 were found to be superior to formaldehyde.

21 cation via reductive amination with isotopic formaldehydes.

22 low target levels of adulterations including formaldehyde (0.074g.L(-1)), hydrogen peroxide (21.0g.L(

23 a coli can convert TMAO to dimethylamine and formaldehyde (1 TMAO --> 1 dimethylamine + 1 formaldehyd

24 perimental animals to stable isotope-labeled formaldehyde ([(13)CD2]-formaldehyde) by inhalation and

25 -column addition of isopropanol solutions of formaldehyde, 2,2-dimethylpropanal, ethyl methanoate, an

26 r with the common terpene oxidation products formaldehyde, 4-acetyl-1-methylcyclohexene (4-AMCH), 3-i

27 Maximum 2 h averaged concentrations of formaldehyde, 4-AMCH, 6-MHO, and IPOH would not give ris

28 This cycle might also release formaldehyde, a potent protein and DNA crosslinking agen

29 re known to produce toxic byproducts such as formaldehyde, acetaldehyde and acrolein.

30 in the presence of buffer and air to produce formaldehyde, acetaldehyde, and the aldehydes correspond

31 tative determination of six toxic compounds (formaldehyde, acetaldehyde, ethyl carbamate, furan, furf

32 1 compounds, including nicotine, nicotyrine, formaldehyde, acetaldehyde, glycidol, acrolein, acetol,

33 ditionally, we present genetic evidence that formaldehyde-activating enzyme (FAE) homologs might be i

34 es show promise for general use in reversing formaldehyde adducts in clinical specimens.

35 OR), and Adh5(-/-) mice therefore accumulate formaldehyde adducts in DNA.

36 es and phosphanilates) speed the reversal of formaldehyde adducts of mononucleotides over standard bu

37 es are cross-linked by short treatments with formaldehyde after reaching binding equilibrium.

38 The illegal addition of formalin (37% formaldehyde and 14% methanol) to foods to extend their

39 m vaping amounted to as much as 12 mug m(-3) formaldehyde and 2.6 mug m(-3) acrolein.

40 Formaldehyde and acetaldehyde are the dominant HAP conce

41 Carbonyls such as formaldehyde and acetaldehyde dominated VOC emissions, m

42 Formaldehyde and acetaldehyde were the most abundant car

43 However, formaldehyde and acetaldehyde, which are formed in the a

44 e intermediates as well as different oximes (formaldehyde and acetone oxime) were considered.

45 When formaldehyde and ammonia were simultaneously present, Ph

46 for the efficient PEC methanol oxidation to formaldehyde and concomitant hydrogen evolution.

47 The fixation was carried out with formaldehyde and does not damage lipid membranes.

48 at this benefit is absent in combinations of formaldehyde and epirubicin, which cannot form stable ox

49 und to be active for CO2 and CO reduction to formaldehyde and even methane.

50 milarly, the oxidation of methanol generates formaldehyde and formic acid which then condense with me

51 into bromonitromethane, bromochloromethane, formaldehyde and formic acid.

52 Further, we use a tandem reversible formaldehyde and irreversible covalent chemical capture

53 is lesions are likely produced by endogenous formaldehyde and malondialdehyde with lysine.

54 tential health risks inflicted by endogenous formaldehyde and may inform improved disease prevention

55 ent with trends in satellite observations of formaldehyde and NO2, but much slower than the explosive

56 that oxidizes the pyocyanin methyl group to formaldehyde and reduces the pyrazine ring via an unusua

57 The peptides are reacted with formaldehyde and sodium cyanoborohydride to dimethylate

58 By (13)C, D2-formaldehyde and sodium cyanoborohydride, the reductive

59 e adulterants water, starch, sodium citrate, formaldehyde and sucrose in milk samples containing from

60 se findings identify an unexpected source of formaldehyde and, more generally, indicate that the deto

61 sotopic reagents ((18)O water and deuterated formaldehyde) and requires no postlabeling cleanup or is

62 ium salt of alpha,alpha'-o-xylene dibromide, formaldehyde, and 5-tolyl-, 4-phenyl-5-methyl-, and 4,5-

63 g aromatics, terpenes, chlorinated solvents, formaldehyde, and acrolein.

64 terfacial tension of reacting methylglyoxal, formaldehyde, and ammonium sulfate aqueous mixtures with

65 me trend of increased ethanol, acetaldehyde, formaldehyde, and CH4 emissions and decreased NMHC and b

66 (OSCs) by reductive amination with (13)C, D2-formaldehyde, and developed an isotope dilution analysis

67 acteria, that converts methanethiol to H2O2, formaldehyde, and H2S, an activity not previously known

68 ulk electrolysis, including formate, aqueous formaldehyde, and methanol.

69 Three paths were considered, and the O3, formaldehyde, and NO2 anthropogenic increments were appo

70 ethyl)-9H-pyrido[3,4-b]indole-3-carboxylate, formaldehyde, and primary amines.

71 r lipoic acid), a melatonin-like isocyanide, formaldehyde, and tacrine derivatives, according to the

72 In this work, the apparent HLCs for formaldehyde aqueous solutions were determined in the co

73 Two relevant pathways for desorption of formaldehyde are found with intrinsic barriers for the r

74 Results for formaldehyde are more complex.

75 Advantages of formaldehyde as a cross-linking reagent include cell per

76 Using formaldehyde as a model analyte, air-liquid interface cu

77 rch on Cancer controversially has classified formaldehyde as causing nasopharyngeal carcinoma and mye

78 ylation yielding N-methyl-4-cyanoaniline and formaldehyde as primary products.

79 on has a broad substrate scope, encompassing formaldehyde as well as aryl and alkyl aldehydes.

80 its Ras-transformed derivative (EpRas) using formaldehyde-assisted isolation of regulatory element (F

81 orm for small molecule screening, we adapted formaldehyde-assisted isolation of regulatory elements (

82 Formaldehyde-assisted isolation of regulatory elements (

83 maldehyde cross-link reversal based upon the Formaldehyde-Assisted Isolation of Regulatory Elements (

84 To address this limitation, we have applied formaldehyde-assisted isolation of regulatory elements (

85 Here we used formaldehyde-assisted isolation of regulatory elements t

86 breakdown of N,N-dimethylformamide (DMF) to formaldehyde at high temperature under mildly acid condi

87 Most anatomy departments use a traditional formaldehyde-based embalming method, but formalin embalm

88 Moreover, we describe a modification of formaldehyde-based fixatives that prevents bead formatio

89 Many aspects of formaldehyde behavior in cells are unknown or undocument

90 biochemical literature, important aspects of formaldehyde behavior in cells have not been well descri

91 double resonance spectroscopy establish that formaldehyde binds close to the active site.

92 or-promoter, and repression is alleviated by formaldehyde but not manganese, iron, cobalt, nickel, co

93 nd buffer capacity and not limited to BDD or formaldehyde, but can be generalized to different electr

94 pling with the irreversible sequestration of formaldehyde by 3-hexulose-6-phosphate synthase (Hps) an

95 udies, we disclose the selective trapping of formaldehyde by in situ condensation with a primary amin

96 ted result to the demonstrated production of formaldehyde by sarcosine dehydrogenase and dimethylglyc

97 able isotope-labeled formaldehyde ([(13)CD2]-formaldehyde) by inhalation and performed ultrasensitive

98 esent the first examples of enantioselective formaldehyde C-C coupling beyond aldol addition.

99 roxidation, it is unclear whether endogenous formaldehyde can initiate and/or promote diseases in hum

100 nsation of two different alkoxybenzenes with formaldehyde catalyzed by a Bronsted acid (trifluoroacet

101 Formaldehyde caused a dose-dependent inhibition of amilo

102 ses to beta-/delta-staphylobilin isomers and formaldehyde (CH2O).

103 d to be important for its response against a formaldehyde challenge.

104 Here, we highlight features of formaldehyde chemistry relevant to its use in analyses o

105 Optimum conditions included an increased formaldehyde concentration and more robust glycine-quenc

106 The influences of the formaldehyde concentration, temperature, agitation rate,

107 Median formaldehyde concentrations of 626 mug/m(3) in e-cigaret

108 nking by performing experiments with varying formaldehyde concentrations.

109 formaldehyde (1 TMAO --> 1 dimethylamine + 1 formaldehyde), confirming that it encodes a bona fide TM

110 h the anthracycline's ability to form cyclic formaldehyde conjugates as oxazolidine moieties and that

111 These data suggest that formaldehyde contributes to edematous acute lung injury

112 nking and potent synergy in combination with formaldehyde correlate with the anthracycline's ability

113 While the kinetics of formaldehyde cross-link formation have been well-establi

114 here a method for measurement of the rate of formaldehyde cross-link reversal based upon the Formalde

115 TF profiling is commonly carried out by formaldehyde cross-linking and sonication followed by ch

116 developing a biochemical protocol involving formaldehyde cross-linking.

117 In addition, formaldehyde cross-links are reversible, which has the a

118 Fresh cells, formaldehyde-cross-linked cells or cells recovered from

119 etics (CLK) assay, which uses time-dependent formaldehyde-cross-linking data to extract kinetic param

120 results that better define the properties of formaldehyde-cross-linking in budding yeast cells.

121 Notably, we observed that formaldehyde-cross-linking rates can vary dramatically f

122 Analysis of global formaldehyde-cross-linking studies indicated that the Ig

123 Formaldehyde-cross-linking underpins many of the most co

124 Formaldehyde crosslinking is routinely employed for dete

125 V RNA-protein complexes preserved in vivo by formaldehyde crosslinking, and coupled with mass spectro

126 However, formaldehyde dehydrogenase (FDH) catalyzed reduction of

127 olate and subsequent formation of formate by formaldehyde dehydrogenase.

128 ction of formaldehyde using NAD(+) dependent formaldehyde dehydrogenase.

129 ii) transient expression of frmRAB, encoding formaldehyde dehydrogenase; and (iii) downregulation of

130 formaldehyde modification as a function of [formaldehyde] demonstrates that FrmR reactivity is optim

131 methyl)glutathione, yet glutathione inhibits formaldehyde detection by FrmR in vivo and in vitro Quan

132 erivatization of samples is not required for formaldehyde detection.

133 and enhance formaldehyde reactivity in vitro Formaldehyde detoxification by FrmA requires S-(hydroxym

134 Furthermore, we find that formaldehyde detoxification in human cells generates for

135 f formaldehyde, permitting expression of the formaldehyde detoxification machinery (FrmA and FrmB, wh

136 Formaldehyde, diluted in either phosphate-buffered salin

137 logation of pyridine-4-carboxaldehydes using formaldehyde dimethyl thioacetal monoxide (FAMSO), and a

138 useful chemicals including syngas, methanol, formaldehyde, dimethyl ether, heavier hydrocarbons, arom

139 We report that adding formaldehyde during biomass pretreatment produces a solu

140 anisms are exposed to the genotoxic chemical formaldehyde, either from endogenous or environmental so

141 t are both important parameters for modeling formaldehyde emissions from aqueous solutions.

142 example, E85 resulted in high acetaldehyde, formaldehyde, ethanol, ethene, and acetylene emissions w

143 pression patterns emerge for 0.1 and 0.5 ppm formaldehyde exposure, which is reflected in significant

144 barriers for the cycloaddition as well as a formaldehyde expulsion steps were computed, and a multis

145 Endogenous and exogenous formaldehyde (FA) has been linked to cancer, neurotoxici

146 Formaldehyde (FA) is a reactive carbonyl species (RCS) p

147 Formaldehyde (FA) is a reactive signaling molecule that

148 Formaldehyde (FA) is an environmental and occupational c

149 the endogenous and environmental carcinogen formaldehyde (FA) that binds to cytosolic and nuclear pr

150 rmation of DNA double-strand breaks (DSB) by formaldehyde (FA) that forms histone adducts and replica

151 Formaldehyde (FA), in the 0.2-0.4 mM range, is produced

152 phone was developed to quantitatively detect formaldehyde (FA).

153 The method uses formaldehyde fixation to stabilize protein complexes.

154 NTHi on lectin-derivatized chips followed by formaldehyde fixation, rendering the bacteria an integra

155 open chromatin profiling on both native and formaldehyde-fixed cells.

156 en retrieval agents improve the detection of formaldehyde-fixed proteins, but how they work is not we

157 on chromatography, in the presence of CO2 or formaldehyde form mutual, methylene-bridged cross-links

158 We report here that these formaldehyde formulations can induce bead formation in t

159 posed nano-sniffer could successfully detect formaldehyde from 0.001 to 100000ng/mL (R(2) = 0.9339) b

160 he first time the production of methanol and formaldehyde from CO hydrogenation on Ni(110) and confir

161 ein we report the direct observation of free formaldehyde from the borane reduction of CO2 catalyzed

162 example is the unimolecular dissociation of formaldehyde (H2CO), in which the "normal" reaction proc

163 We show that inactivation with formaldehyde has an effect on early steps of viral repli

164 yzes the primary oxidation of methylamine to formaldehyde has been examined in great detail.

165 Formaldehyde has been used for decades to probe macromol

166 Formaldehyde (HCHO) is the most important carcinogen in

167 Formaldehyde (HCHO), a strong electrophile and a rapid a

168 HONO), hydrogen peroxide (H2O2), ozone (O3), formaldehyde (HCHO), and acetaldehyde (CH3CHO).

169 We found that formaldehyde hemiacetals are a considerable fraction of

170 The formaldehyde hemiacetals derived from these solvents wer

171 The reason for this is that formaldehyde hemiacetals follow other reaction pathways,

172 In the study described herein, the formaldehyde hemiacetals were found at higher levels tha

173 Among the seventeen systems tested, Mn(IV)-formaldehyde-hexametaphosphate was considered to be the

174 ydrogenase (Mdh), which converts methanol to formaldehyde, highly favors the reverse reaction.

175 cludes addition of toxic substances, such as formaldehyde, hydrogen peroxide, hypochlorite, dichromat

176 ss model, which considered unadulterated and formaldehyde-, hydrogen peroxide-, citrate-, hydroxide-

177 species (ROS) was elevated significantly by formaldehyde in addition to markedly augmented membrane

178 ethylglyoxal relative to carbon monoxide and formaldehyde in agricultural biomass burning plumes inte

179 ternary solutions of both methylglyoxal and formaldehyde in aqueous ammonium sulfate, indicating a m

180 Levels of formaldehyde in food samples were compared with publishe

181 urate methods and the ubiquitous presence of formaldehyde in foods make the detection of illegally ad

182 It could also detect formaldehyde in fruit juice and wine samples indicating

183 idated for the quantitative determination of formaldehyde in mango, fish and milk.

184 c mechanism of FrmR is triggered directly by formaldehyde in vitro Sensitivity to formaldehyde requir

185 Relative to FrmR, RcnR is less responsive to formaldehyde in vitro, and RcnR does not sense formaldeh

186 rmaldehyde in vitro, and RcnR does not sense formaldehyde in vivo, but reciprocal mutations FrmR(P2S)

187 derivatives by condensation of indoles with formaldehyde in water under microwave irradiation.

188 The aqueous solutions tested included formaldehyde in water, formaldehyde-water with nonionic

189 a shock sensor for bioactive compounds (e.g. formaldehyde) in water.

190 tible cotton rat challenge model compared to formaldehyde inactivated RSV (FI-RSV) and live RSV exper

191 accine to a whole-inactivated-virus vaccine (formaldehyde-inactivated HSV-2 [FI-HSV-2]).

192 , carbon dioxide promoted migration and only formaldehyde increased slightly due to sunlight.

193 More widespread formaldehyde-induced DNA damage also causes karyomegaly

194 e stability, but previous methods to measure formaldehyde-induced DPCs were incapable of discriminati

195 n, together with the finding that endogenous formaldehyde-induced DPCs were present in all tissues ex

196 Filtering and formaldehyde inhibition confirmed the biological nature

197 Formaldehyde intake from 100 daily puffs was higher than

198 Formaldehyde interacts with anthracyclines to enhance an

199 Instead, Fe-bound formaldehyde is a metal-hydrido mimic, a locked, inhibit

200 Unsaturated oxidative formaldehyde is a noxious aldehyde in cigarette smoke th

201 Endogenous formaldehyde is abundantly present in our bodies, at aro

202 istic features in formose chemistry by which formaldehyde is converted to higher sugars under credibl

203 Notably, formaldehyde is generated from oxidative decomposition o

204 situ, since cotreatment with doxorubicin and formaldehyde is highly cytotoxic to dox-resistant tumor

205 Formaldehyde is one such compound that can irreversibly

206 Endogenous formaldehyde is produced by numerous biochemical pathway

207 Here we show that endogenous formaldehyde is removed by the enzyme alcohol dehydrogen

208 Formaldehyde is therefore an important source of endogen

209 Formaldehyde is universally used to fix tissue specimens

210 actions with acidic permanganate enhanced by formaldehyde (KMnO4-COH), acidic cerium (IV) and rhodami

211 roteins following in vivo cross-linking with formaldehyde (known as ChIP-seq) has been used extensive

212 ion with ion mobility spectrometry (IMS) and formaldehyde labeling, this novel strategy enables quali

213 from the ortho isomer underwent an exclusive formaldehyde loss.

214 re, we show that fluorescent malondialdehyde-formaldehyde (M2FA)-lysine adducts are immunogenic witho

215 While such high steady state levels of formaldehyde may be derived by enzymatic reactions inclu

216 tailpipe emissions of ethanol, acetaldehyde, formaldehyde, methane, and ammonia increased; NOx and NM

217 Thirty-five melamine-formaldehyde (MF) monolithic materials with bimodal pore

218 mber of FrmR molecules per cell and modeling formaldehyde modification as a function of [formaldehyde

219 pectra showing different ratios of (13)C, D2-formaldehyde-modified and H2-formaldehyde-modified compo

220 os of (13)C, D2-formaldehyde-modified and H2-formaldehyde-modified compounds.

221 eaction monitoring (MRM) to detect (13)C, D2-formaldehyde-modified OSCs by ultrahigh-performance liqu

222 alyzes the carboligation of three one-carbon formaldehyde molecules into one three-carbon dihydroxyac

223 generated from the disproportionation of two formaldehyde molecules).

224 The use of formaldehyde N,N-dialkylhydrazones as neutral C1-nucleop

225 s than 2.5 mum aerodynamic diameter (PM2.5), formaldehyde, nitrogen dioxide (NO2), nicotine, carbon d

226 s such as nitrite, 4-nitro-2,4-diazabutanal, formaldehyde, nitrous oxide, formate, and ammonia corres

227 However, the mechanistic effects of formaldehyde on lung fluid transport are still poorly un

228 Formaldehyde (on average 135 mug m(-3)) and acrolein (28

229 served for glycolaldehyde, acetaldehyde, and formaldehyde only at elevated temperatures in thermograv

230 mouse and chicken cells that cannot detoxify formaldehyde or that lack DNA crosslink repair.

231 t on the emissions of nitrogen oxides (NOx), formaldehyde, or acetaldehyde.

232 face layers), soluble metabolites (methanol, formaldehyde, organic acids, and ectoine), lipids (biodi

233 mostly from PG, while other compounds (e.g., formaldehyde) originated from both.

234 l data to support source modeling for indoor formaldehyde originating from the use of household produ

235 By applying the measured HLCs, the formaldehyde overall liquid-phase mass transfer coeffici

236 ofuran analog was proposed to be involved in formaldehyde oxidation in Alphaproteobacteria.

237 he tetrahydromethanopterin (H4MPT)-dependent formaldehyde oxidation pathway but not a complete tetrah

238 xF), the tetrahydromethanopterin pathway for formaldehyde oxidation, the serine cycle and the ethylma

239 c acid (TFA) with two Criegee intermediates, formaldehyde oxide and acetone oxide, decrease with incr

240 ation en route to regioisomeric allyliridium-formaldehyde pairs, yet single constitutional isomers ar

241 specifically inactivated in the presence of formaldehyde, permitting expression of the formaldehyde

242 m, we established FDF-PAGE (fully-denaturing formaldehyde polyacrylamide gel electrophoresis) to prev

243 till limited to the wet processing of phenol-formaldehyde polycondensation, which involves soluble to

244 ic acid coordination polymer or a resorcinol-formaldehyde polymer.

245 ign, synthesis, and biological evaluation of Formaldehyde Probe 1 (FP1), a new fluorescent indicator

246 In particular, Formaldehyde Probe 573 (FAP573), based on a resorufin sc

247 Formaldehyde probe-1 (FAP-1) is capable of detecting phy

248 als are a considerable fraction of the total formaldehyde produced in electronic cigarette that canno

249 ction of dimethylamine in culture medium and formaldehyde production when cell-free extracts were inc

250 ntigen retrieval process through reversal of formaldehyde-protein adduct formation.

251 RcnR(S2P), respectively, impair and enhance formaldehyde reactivity in vitro Formaldehyde detoxifica

252 Our results showed that formaldehyde reduced mouse transalveolar fluid clearance

253 ADH scavenger, thereby preventing reversible formaldehyde reduction.

254 We examined how formaldehyde regulates human epithelial sodium channels

255 tone and non-histone fragments, resulting in formaldehyde release.

256 m the use of household products that contain formaldehyde-releasing biocides.

257 ctly by formaldehyde in vitro Sensitivity to formaldehyde requires a cysteine (Cys(35) in FrmR) conse

258 ompounds for manufacturing modified melamine formaldehyde resins and other polymer building blocks.

259 plus CstR, which responds to persulfide, and formaldehyde-responsive FrmR.

260 a sphere attached to a mesoporous resorcinol-formaldehyde (RF) sphere.

261 Here, we perform formaldehyde RNA immunoprecipitation (fRIP-Seq) to surve

262 We demonstrate that formaldehyde scavenging represents a key characteristic

263 Formaldehyde selectively depletes BRCA2 via proteasomal

264 ysical data suggests a mechanistic model for formaldehyde-sensing and derepression of frmRA(B) expres

265 A crystal structure of metal- and formaldehyde-sensing FrmR(E64H) reveals that an FrmR-spe

266 Cys(35), and these residues form the deduced formaldehyde-sensing site.

267 La cells before and after fixation by either formaldehyde solution or by chilled ethanol.

268 teen small-chamber tests were conducted with formaldehyde solutions in small pools.

269 tabolite and ubiquitous environmental toxin, formaldehyde, stalls and destabilizes DNA replication fo

270 inescence of manganese(IV)-hexametaphosphate-formaldehyde system was greatly enhanced by plant polyph

271 modified and frmRA is derepressed at lower [formaldehyde] than required to generate S-(hydroxymethyl

272 Protonation of 3(-) liberates H2 gas and formaldehyde, the latter of which is rapidly consumed by

273 odel reactions, cycloaddition of ethylene to formaldehyde, thioformaldehyde, and formaldimine is also

274 gins with the dehydrogenation of methanol to formaldehyde through a new ligand-ligand bifunctional me

275 ling of branched allylic acetates 1a-1o with formaldehyde to form primary homoallylic alcohols 2a-2o

276 indole ester beta-lactone intermediate with formaldehyde to introduce the requisite C16 hydroxymethy

277 mary amine groups were reacted with isotopic formaldehydes to synthesize ISs and standards.

278 eding intermediates, namely, formic acid and formaldehyde, to ultimately form CH3OH.

279 The X-ray structure of the formaldehyde-treated Escherichia coli FrmR (EcFrmR) prot

280 Studies with formaldehyde-treated RNA oligonucleotides show that the

281 , and Cu(I), and moreover metals, as well as formaldehyde, trigger an allosteric response that weaken

282 3.8 to 4.8 V, users were predicted to inhale formaldehyde (up to 49 mg day(-1)), acrolein (up to 10 m

283 was applied for the successful detection of formaldehyde using NAD(+) dependent formaldehyde dehydro

284 ydomonas reinhardtii [FeFe]-hydrogenase with formaldehyde using pulsed-EPR techniques including elect

285 h between RDX and TNT as well as acidity and formaldehyde vapors.

286 re found at higher levels than those of free formaldehyde via an orthogonal sample collection protoco

287 When formaldehyde was added to a mixture of phenylacetaldehyd

288 on where the free and total concentration of formaldehyde was determined in car exhaust using a porta

289 Formaldehyde was produced by thermal degradation of phen

290 with nonionic surfactant Tergitol NP-9, and formaldehyde-water with anionic surfactant sodium dodecy

291 tions tested included formaldehyde in water, formaldehyde-water with nonionic surfactant Tergitol NP-

292 Glyoxal enhancements relative to formaldehyde were 30 times lower than previously reporte

293 ratios of other species such as methane and formaldehyde were consistent with previous measurements,

294 resence of propionaldehyde, acetaldehyde and formaldehyde were correlated, corroborating previous wor

295 ntially lower concentrations of limonene and formaldehyde were observed.

296 s (e.g., acetic acid, methanol, ethanol, and formaldehyde) were synthesized in a one-step process fro

297 three to seven times those obtained without formaldehyde, which prevented lignin condensation by for

298 which is consumed by alcohol oxidase to form formaldehyde while simultaneously reducing oxygen to hyd

299 Methanol is oxidized on alpha-Fe2O3 to formaldehyde with near unity Faradaic efficiency.

300 tor that modulates H. influenzae response to formaldehyde, with two cysteine residues (Cys54 and Cys7