ライフサイエンスコーパス: ethylene

1 ing coordination-insertion polymerization of ethylene.

2 ioxo catalyst to terephthalic acid (PTA) and ethylene.

3 s a molecule that is able to reversibly bind ethylene.

4 ave been particularly notable when targeting ethylene.

5 ays, particularly between those of auxin and ethylene.

6 ia transcriptional repression in response to ethylene.

7 of the main product propylene and by-product ethylene.

8 alkyl ethylene intermediates is catalyzed by ethylene.

9 intermediates for more selective CO(2)RR to ethylene.

10 reased fruit firmness and increased internal ethylene.

11 luorinated MOFs for capturing acetylene from ethylene.

12 assayed by the reduction of acetylene gas to ethylene.

13 an inhibition of shoot growth in response to ethylene.

14 ared to the reaction of maleic anhydride and ethylene.

15 tom), thereby favouring further reduction to ethylene.

16 icroelectrodes were inkjet-printed onto poly(ethylene 2,6-naphthalate) substrates, with dimensions of

17 ly explains the long-standing observation of ethylene accumulation in oxygen-depleted soils.

18 Ethylene acts as an inverse agonist by inhibiting its re

19 (286.1-474.4) for separating acetylene from ethylene along with high thermal and water stability, co

20 ntheses have been demonstrated with olefins (ethylene and 1-hexene) which produce amorphous or crysta

21 concentration of 16.7% in output gas (12.1% ethylene and 4.6% ethane) is achieved while the methane

22 Ethylene and a derived methylidene complex can also adva

23 enetic and pharmacological interference with ethylene and auxin pathways outlines the hierarchy of re

24 ted gravity flame reactor (IGFR) operated on ethylene and ethane.

25 odel for ripening regulation, which requires ethylene and master TFs including NAC-NOR and the MADS-b

26 l production of gaseous hydrocarbons such as ethylene and methane affects soil environments and atmos

27 tle or no product formation, it is best that ethylene and methylidene complex formation is avoided al

28 shows significantly enhanced selectivity to ethylene and suppressed coke formation.

29 involved in sensing the balance of auxin and ethylene and that affect pectin degradation during absci

30 nalyze the different scenarios through which ethylene and the involvement of methylidene complexes ca

31 cited changes in levels of jasmonic acid and ethylene and the magnitude of induced defense responses,

32 smax1 mutants release increased amounts of ethylene and their root phenotype is rescued by treatmen

33 and the plant immune system; how plants use ethylene and ubiquitin systems to control growth and dev

34 hat are similarly affected by treatment with ethylene and with various dormancy release stimuli.

35 Ethylene- and cytokinin-insensitive mutants were partly

36 significant interaction was recorded between ethylene antagonists and ozone application in cold stora

37 results suggest that BC and NC are potential ethylene antagonists in Cripps Pink and Granny Smith app

38 The effects of two new ethylene antagonists namely 1H-cyclopropabenzene (BC) an

39 ates (Coa) (i.e., a tertiary complex of poly(ethylene argininylaspartate diglyceride) (PEAD) polycati

40 ith 100% conversion and 85.1% selectivity to ethylene at 80 degrees C.

41 ll fall below the values required to produce ethylene at cost-competitive prices.

42 root phenotype is rescued by treatment with ethylene biosynthesis and signaling inhibitors.

43 re exposure to induce autocatalytic system 2 ethylene biosynthesis and subsequent fruit ripening.

44 NTHASE7, an ACC synthase homolog involved in ethylene biosynthesis, and ELONGATED HYPOCOTYL5 (HY5), a

45 rocesses, such as basal metabolic processes, ethylene biosynthesis, and the activation of polysacchar

46 hanol application after CA storage decreased ethylene biosynthesis, respiration rate and membrane per

47 , NO production apparently regulates hypoxic ethylene biosynthesis.

48 of ERF3, which is involved in regulation of ethylene biosynthesis.

49 S7), which encodes a rate-limiting enzyme in ethylene biosynthesis.

50 developed for enrichment of maneb (manganese ethylene-bisdithiocarbamate) with a supramolecular solve

51 % for aqueous solutions of 1,2-bis(4-pyridyl)ethylene (BPE), the lowest reported to date.

52 yields a similar bimetallic product with an ethylene bridge.

53 A dimeric ethylene-bridged PH/BH system reduced carbon monoxide to

54 he weak exciton delocalization while the cis-ethylene-bridged picenophane exhibits dual emission rend

55 cohol)), and a processable rubber (a styrene-ethylene-butylene-styrene derivative) to demonstrate wid

56 amework NTU-65, the gate-opening pressure of ethylene (C(2) H(4) ), acetylene (C(2) H(2) ), and carbo

57 Purification of ethylene (C(2)H(4)), the largest-volume product of the c

58 However, because ethylene can be converted to a methylidene complex, whic

59 In some cases, introducing excess ethylene can increase reaction rate owing to faster cata

60 Application of exogenous ethylene, carbon dioxide and treatment to high temperatu

61 ress this issue, we propose the additions of ethylene carbonate (EC) to the imaging buffer, sequence

62 ic efficiencies and cycle lives of LMBs with ethylene carbonate (EC), dimethyl carbonate, ethylene su

63 Applied to dimethoxyethane (DME) and ethylene carbonate (EC), the present methodology shows t

64 iFePO(4)/Li cell using a 1 M LiAsF(6) in 1:1 ethylene carbonate/dimethyl carbonate (EC/DMC) electroly

65 ogenation and reforming of ethane to produce ethylene, CO, and H(2), and a RhCo(x)/MCM-41 catalyst (s

66 ex blends of low molar mass polyethylene and ethylene-co-1-octene copolymers were separated with high

67 To achieve this, a telechelic poly(ethylene-co-butylene) was end-functionalized with diphen

68 As demonstrated for poly(ethylene-co-cyclohexane-1,4-dimethanol terephthalate) (P

69 mer demonstration, a commodity polymer, poly(ethylene-co-vinyl alcohol) (PEOH), was silylated with tr

70 Both isomers of the methyl ethylene complex can be generated and observed at low te

71 howed the isomerization rate is dependent on ethylene concentration.

72 Although ethylene controls hyponasty and aerenchyma formation, NO

73 room-temperature activities per Rh atom for ethylene conversion in the presence of H(2), but the SAP

74 duction and that the selectivity of CO(2)-to-ethylene conversion is further enhanced in the CV-treate

75 acetylene pai-adsorption, but also enhanced ethylene desorption.

76 Herein, we report the anionic surfactant, ethylene diamine tetraacetic acid (EDTA), mediated synth

77 ed species, comprise the soot observed in an ethylene diffusion flame.

78 the zeolite-supported catalyst selective for ethylene dimerization; correspondingly, the catalyst on

79 68%), norbornene (DPF.norbornene, 73%), and ethylene (DPF.C(2)H(4), 80%) under ambient conditions.

80 We report stable ethylene electrosynthesis for 190 hours in a system base

81 outlines the hierarchy of responses, placing ethylene epistatic to the auxin signaling pathway.

82 salicylic acid (SA), jasmonic acid (JA) and ethylene (ET) pathways.

83 n salicylic acid (SA) and jasmonic acid (JA)/ethylene (ET) signalling resulting in trade-offs between

84 nly 10% WT concentrations of carotenoids and ethylene (ET) were synthesized.

85 etween the plant hormones jasmonate (JA) and ethylene (ET).

86 We demonstrate that biogenic methane and ethylene from terrestrial and freshwater bacteria are di

87 n of economically desirable products such as ethylene from the carbon dioxide reduction reaction (CO(

88 lowed by autocatalytic reduction of Ag(+) by ethylene glycol (and not solvent oxidation products) to

89 g and graphite composite target submerged in ethylene glycol (EG) to form AgNPs decorated 2-D GNs-EG

90 re conducted with the cryoprotectants (CPAs) ethylene glycol (EG), propylene glycol (PG), dimethyl su

91 le, iodine yields the bis-bisulfate ester of ethylene glycol (HO(3)SO-CH(2)-CH(2)-OSO(3)H, EBS), wher

92 sent method was applied for determination of ethylene glycol and diethylene glycol in 701 beer sample

93 method for the simultaneous determination of ethylene glycol and diethylene glycol in beer was develo

94 ively) and quantification (15.0 mg.L(-1) for ethylene glycol and diethylene glycol) obtained were app

95 mits of detection (10.0 and 5.0 mg.L(-1) for ethylene glycol and diethylene glycol, respectively) and

96 e Ag-decorated 2-D graphene nanocomposite in ethylene glycol based nanofluid by laser liquid solid in

97 erization approach with BTA-Glc, BTA-Man, or ethylene glycol BTA (BTA-OEG(4)) to give 1D fibers with

98 ), which is cleaved to terephthalic acid and ethylene glycol by MHETase.

99 ized, differing in the distribution of their ethylene glycol chains that are tethered to the conjugat

100 In a typical example, the diol ethylene glycol decreased the overall system modulus.

101 h each step of the Schiff-base process: poly(Ethylene glycol Dimethacrylate-co-Glycidyl methacrylate)

102 al therapy against genetic hyperoxaluria and ethylene glycol poisoning.

103 system, CO(2) was efficiently captured by an ethylene glycol solution of the base and subsequently hy

104 acid, TAT, via noncleavable bonding to poly(ethylene glycol) (PEG(400)) (P) might allow for effectiv

105 self-assembly of diblock copolymers of poly (ethylene glycol) (PEG) and poly (propylene sulfide) (PPS

106 Two hydrophilic polymers, poly(ethylene glycol) (PEG) and poly(vinyl alcohol) (PVA), ar

107 and A-B-A nanowires with a solvophilic poly(ethylene glycol) (PEG) corona, an inner crystalline core

108 naling moiety linked with a hydrophilic poly(ethylene glycol) (PEG) passivation chain, the reporters

109 ) (PLGA) or poly(lactide-coglycolide)-b-poly(ethylene glycol) (PLGA-PEG) for gene delivery by a robus

110 lymer, poly(triol dicarboxylic acid)-co-poly(ethylene glycol) (TDP), is achieved by hydrolysis of est

111 egates coated with poly(L-lysine)-block-poly(ethylene glycol) block copolymer (s-MNPs).

112 In particular, we report the use of poly(ethylene glycol) diacrylate (PEGDA) aqueous droplets for

113 -1), in thiolated gelatin (gelatin-SH)/ poly(ethylene glycol) diacrylate (PEGDA) interpenetrating net

114 Finally, we use poly(ethylene glycol) diacrylate microgels, excellent reactan

115 (mIPNs) comprised of Collagen I, HA and poly(ethylene glycol) diacrylate.

116 lling the pores of a PTFE matrix with a poly(ethylene glycol) dimethacrylate (PEGDMA) hydrogel; this

117 electrode through its modification with poly(ethylene glycol) for determination of tannic acid in bee

118 zed by the polyol method, where the solvent (ethylene glycol) is considered the reducing agent and po

119 icate grid poly (epsilon-caprolactone)-poly (ethylene glycol) microfibrous scaffold and infuse the sc

120 a graphitic carbon shell decorated with poly(ethylene glycol) provide an MPI signal intensity that is

121 ing sites for glyphosate-functionalized poly(ethylene glycol) SCPs.

122 graft polymer chains controllably from poly(ethylene glycol) showcasing the potential application of

123 By tethering this photoswitch to a poly(ethylene glycol) star polymer, we can tune the stiffness

124 ein, we report a polymer gel comprising poly(ethylene glycol) star polymers linked by Cu(24) L(24) me

125 he carbon paste electrode improved with poly(ethylene glycol) was effectively implemented in the quan

126 Utilizing biodegradable poly(ethylene glycol)-b-poly(d,l-lactide) (PEG-PDLLA) block c

127 (PEO) fibers that incorporated methoxy poly(ethylene glycol)-b-poly(lactide-co-glycolide) (mPEG-PLGA

128 -3-8 lipid conjugate (LDC) into methoxy poly(ethylene glycol)-block-poly(2-methyl-2-carboxyl-propylen

129 Poly(ethylene glycol)-block-poly(D,L-lactic acid) (PEG-b-PLA)

130 k-poly(D,L-lactic acid) (PEG-b-PLA) and poly(ethylene glycol)-block-poly(epsilon-caprolactone) (PEG-b

131 previously reported the synthesis of a poly(ethylene glycol)-haloperidol (PEG-haloperidol) conjugate

132 composite consisting of up to 0.20 wt% poly(ethylene glycol)-modified gold nanorods (AuNRs) without

133 )-poly(propylene sulfide) (PEG-PPS) and poly(ethylene glycol)-oligo(ethylene sulfide) (PEG-OES) that

134 ed amphiphilic block copolymers made of poly(ethylene glycol)-poly(propylene sulfide) (PEG-PPS) and p

135 isting commercial markets including polyols (ethylene glycol, 1,2-propanediol, 1,3-propanediol, glyce

136 dition of the water-miscible organic reagent ethylene glycol, which radically alters the properties o

137 ls, (b) two different permeability enhancers ethylene glycol-bis(2-aminoethylether)-N,N,N',N'-tetraac

138 Polymeric micelles composed of poly(ethylene glycol-block-caprolactone) (mPEG-CL) and poly(e

139 lycol-block-caprolactone) (mPEG-CL) and poly(ethylene glycol-block-lactide) (mPEG-LA) were unstable i

140 Ethylene glycol-derived, oligomeric ethers were found to

141 o methanol with high yields in a solution of ethylene glycol.

142 e for the direct conversion of ethane toward ethylene glycol.

143 impinged on a 450 nm sheet of flowing liquid ethylene glycol.

144 se were entrapped in a photopolymerized poly(ethylene) glycol diacrylate (PEG-DA) hydrogel that was c

145 catalysts in Li-O(2) batteries with a tetra(ethylene)glycol dimethyl ether electrolyte.

146 (BCat = catecholatoboryl), and -[Beg] (Beg = ethylene glycolatoboryl) promote the hydrogenation of tr

147 ion transforms into rotation of the terminal ethylene groups in the photoproduct 1,3,5-hexatriene on

148 High-grade propylene and ethylene (>99.999%) can be generated using temperature-c

149 The phytohormone ethylene has numerous effects on plant growth and develo

150 addition reactions of trans-1,2-di(2-pyridyl)ethylene have been studied.

151 ed additional ERFs that respond similarly to ethylene, HC, azide and hypoxia.

152 cation) for the methyl signal from SCB in an ethylene-hexene copolymer (EH, 3.6 mol % H) in 3.5 min w

153 he SAPO-supported catalyst was selective for ethylene hydrogenation and the zeolite-supported catalys

154 for the selective conversion of acetylene to ethylene, i.e., with high conversion (95%), high selecti

155 study, using a porous and cross-linked poly(ethylene imine) structure under marine and fouling envir

156 situ electrochemical oxidation of methane to ethylene in a solid oxide electrolyzer under ambient pre

157 core set of 255 genes uniquely regulated by ethylene in R. bourboniana AZ.

158 that most of the genes are down-regulated by ethylene in shoots, and a DNA binding motif was identifi

159 Here, we demonstrate that ACC exhibits ethylene-independent signaling in Arabidopsis thaliana r

160 We revealed that both cytokinin and ethylene induce the MSP in similar and distinct cell typ

161 Necrosis- and ethylene-inducing peptide 1 (Nep1)-like proteins (NLP) h

162 lymerase subunit II (RPB2), and necrosis and ethylene-inducing proteins 1 and 2 (NEP1 and NEP2) genes

163 Ethylene initiates ripening of mature green fruit, upreg

164 hich the master transcriptionactivator EIN3 (Ethylene Insensitive 3)-mediated transcriptional activat

165 tein of unknown biochemical activity, called ethylene-insensitive 2 (EIN2); and transcription factors

166 SULFUR LIMITATION1 (SLIM1), a member of the ETHYLENE-INSENSITIVE3-LIKE (EIL) transcription factor fa

167 atory mechanism at EIN2 requiring two genes: ETHYLENE-INSENSITIVE6 (EIN6), which is a H3K27me3 demeth

168 ct the balance of hormonal signaling through ethylene interaction with SA and cytokinin networks.

169 rect proof that isomerization in these alkyl ethylene intermediates is catalyzed by ethylene.

170 calculated SF rate is very large but the two ethylenes interpenetrate.

171 Ethylene is a gas and a plant hormone with wide ranging

172 Ethylene is a gaseous phytohormone and the first of this

173 Ethylene is an important plant hormone that regulates pl

174 y 1-indanones are commercially available and ethylene is inexpensive, this strategy simplifies synthe

175 and thus highly controlled polymerization of ethylene is observed, leading to lightly branched ultra-

176 netic selectivity, making it preferable that ethylene is removed while being generated.

177 Unfortunately, the Faradaic efficiency for ethylene is still low in neutral media (60 per cent at a

178 Ethylene is the byproduct of olefin metathesis reactions

179 One of the earliest reported responses to ethylene is the triple response.

180 The phytohormone ethylene is widely involved in many developmental proces

181 stigation of the equilibration of the methyl ethylene isomers in the presence of excess ethylene show

182 model, according to which in the absence of ethylene, its cognate receptors signal to CTR1, which in

183 rabidopsis accession Col-0 and ein2/jar1, an ethylene/jasmonic acid-signaling deficient mutant that e

184 The ethylene ligands were readily replaced with CO, giving s

185 ed [2,2](5,8)picenophanediene 8 with two cis-ethylene linkers was explored using X-ray crystallograph

186 mple of analyzing saturated chain ends in an ethylene-octene copolymer sample with a hard 180 degrees

187 lm and a maleic anhydride (MAH) grafted poly(ethylene-octene) (MAHgEO) sample, was directly analyzed

188 y examined the effects of elevated auxin and ethylene on the metabolome of Arabidopsis roots using a

189 scription factors and key enzymes related to ethylene or carotenoid pathways potentially targeted by

190 the immediate precursor to methionine, while ethylene or methane is released into the environment.

191 assembly of polydimethylsiloxane-block-poly(ethylene oxide) (PDMS-b-PEO) BBCPs with phenol-formaldeh

192 nanoscopy studies of few-nanometer-thin poly(ethylene oxide) (PEO) films which reveal marked spectral

193 hanism is reproduced here by an aqueous poly(ethylene oxide) (PEO) solution, which solidifies at ambi

194 ygen vacancies to demonstrate two oxide/poly(ethylene oxide) (PEO)-based polymer composite electrolyt

195 e and thermosensitive hydrogel based on poly(ethylene oxide) (PEO)-poly(propylene oxide) (PPO)-PEO po

196 ic, disordered, water-soluble polymers: poly(ethylene oxide) (PEO).

197 boxyanhydrides (NCAs) using alpha-amino-poly(ethylene oxide) as a macroinitiator to protect the NCA m

198 of PS-block-poly(2-vinylpyridine)-block-poly(ethylene oxide) were used to interact with H(4) TPPS(2-)

199 of vesicles through incorporation of a poly(ethylene oxide)-b-poly(butadiene) diblock copolymer, we

200 sium hydroxide electrolyte (pH ~ 15) with an ethylene partial current density of 1.3 amperes per squa

201 anges in gene methylation were linked to the ethylene pathway and ripening processes.

202 ciated with large scale up-regulation of the ethylene pathway but prominent suppression of the JA, au

203 an ethylene receptor antagonist that blocks ethylene perception and downstream ripening responses in

204 involvement of various components regulating ethylene perception and signaling in establishing Arabid

205 h which cyst nematodes exploit components of ethylene perception and signaling to affect the balance

206 New neutral nickel and palladium ethylene polymerization catalysts have been prepared tha

207 minium, cobalt-alloys, stainless steel, poly-ethylene, polyurethanes, polyglycolide and polylactides)

208 n electrode) and a cathodic-side (half-cell) ethylene power conversion efficiency of 55 +/- 2 per cen

209 between pre- and post-veraison with a clear ethylene precursor (aminocyclopropane-1-carboxylic acid,

210 , as well as 1-methylcyclopropene (1-MCP) on ethylene production and fruit quality of Cripps Pink and

211 n of ERF3 expression, which is turn promotes ethylene production and loss of fruit firmness.

212 ith BC and NC exhibited significantly lowest ethylene production and respiration, whilst the Granny S

213 (ACO4), which may in part explain increased ethylene production and signaling in RPW8.1-expressing p

214 Anaerobic ethylene production by this pathway apparently explains

215 th fruit treated with 1-MCP exhibited lowest ethylene production followed by NC and BC treatments.

216 ntained higher levels of sugars but elevated ethylene production in both the apple cultivars.

217 irreversibly obstructs the onset of system 2 ethylene production resulting in perpetually unripe frui

218 ontaining 1% OA showed significantly reduced ethylene production than that coated with 2% and 3% OA a

219 eater anaerobic metabolism resulted in lower ethylene production, ACC oxidase activity, membrane perm

220 1b advanced ripening initiation, climacteric ethylene production, and fruit softening, whereas SlLHP1

221 and ozone application in cold storage on the ethylene production, respiration and other fruit quality

222 d antioxidant activity, and a lower level of ethylene production, respiration, weight loss, phenylala

223 of ERF4 or TPL4 promoted fruit ripening and ethylene production.

224 y breakthrough experiments, giving excellent ethylene productivities (121 mmol/g from 1/99 mixture, 9

225 ity of nickel enables the oligomerization of ethylene, propylene, and butenes into a wide range of ol

226 version reaction also produces light olefins ethylene, propylene, and butenes, totalling a yield of 8

227 ata analysis showed that polyamide (39%) and ethylene-propylene-diene rubber (23%) were the most abun

228 kynes and efficient separations of acetylene/ethylene, propyne/propylene, and butyne/1,3-butadiene mi

229 rom multiscale porous polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS) supporti

230 1-methylcyclopropene (1-MCP) in an ethylene receptor antagonist that blocks ethylene percep

231 These components include a family of ethylene receptors in the membrane of the endoplasmic re

232 Although it is largely accepted that ethylene regulates plant responses to nematode infection

233 Because ethylene responding factors (ERF) are natural candidates

234 om the flowering induction pathway, APETALA2/ETHYLENE RESPONSE FACTOR (AP2/ERF) family genes, and jas

235 nt binding protein, a member of the APETALA2/ethylene response factor (AP2/ERF) superfamily, is a tra

236 The ETHYLENE RESPONSE FACTOR (ERF) genes of Arabidopsis thal

237 xture, we identified a mutation (C-G) in the ethylene response factor-associated amphiphilic repressi

238 We have identified ETHYLENE RESPONSE FACTOR12 (ERF12) as the Arabidopsis or

239 Arabidopsis ETHYLENE RESPONSE FACTOR12 (ERF12), the rice MULTIFLORET

240 EAR) motif in the coding region of the apple ETHYLENE RESPONSE FACTOR4 (ERF4) gene.

241 to exogenous hypoxia are driven by group VII ethylene response factors (ERF-VIIs).

242 n factors such as EIN3, EIN3-like (EIL), and ethylene response factors (ERFs).

243 EIN3-mediated transcriptional repression in ethylene response is unknown.

244 Transcriptional Repressor of EIN3-dependent Ethylene-response 1 (TREE1) interacts with EIN3 to regul

245 Their root transcriptome reveals elevated ethylene responses and expression of ACC Synthase 7 (ACS

246 ng cascade, alternative pathways also affect ethylene responses.

247 anscription and translation, leading to most ethylene responses.

248 ACC is often used to induce ethylene responses.

249 ated genes were enriched for cis-elements of ethylene-responsive and heat shock factor transcription

250 B1 is a C2H2 zinc finger encoding gene with ethylene-responsive element binding factor-associated am

251 3 localized to the nucleus and functioned as ethylene-responsive element binding factor-associated am

252 Ethylene-responsive element binding protein, a member of

253 cid metabolism, organic acid metabolism, and ethylene-responsive pathways.

254 fragrant roses such as Rosa bourboniana are ethylene-sensitive and undergo rapid petal abscission wh

255 l abscission while hybrid roses show reduced ethylene sensitivity and delayed abscission.

256 Their efficiency in acetylene/ethylene separation is confirmed by breakthrough experim

257 nfection, a mechanistic understanding of how ethylene shapes plant-nematode interactions remains larg

258 l ethylene isomers in the presence of excess ethylene showed the isomerization rate is dependent on e

259 s a link between PAP/SAL retrograde pathway, ethylene signaling and Fe metabolism in Arabidopsis.

260 hat there is a link between PAP/SAL pathway, ethylene signaling and Fe metabolism.

261 Ethylene signaling appears critical for grape bud dorman

262 r and distinct cell types with ETR1-mediated ethylene signaling controlling MSP output specifically i

263 hese alternative pathways, and discusses how ethylene signaling has been manipulated for agricultural

264 s, we reveal a connection between KAR/KL and ethylene signaling in which the KAR/KL signaling module

265 In return, ACO4 and other key components of ethylene signaling negatively regulate RPW8.1-mediated c

266 coordination of phytochrome B with auxin and ethylene signaling pathways and uncover differential hyp

267 he pathogen suggests that salicylic acid and ethylene signaling pathways mediate resistance.

268 Ethylene signaling regulates the relative abundance of t

269 Here, we show that RPW8.1 activates ethylene signaling that, in turn, negatively regulates R

270 -signaling pathway, in which RPW8.1 enhances ethylene signaling, and the latter, in return, negativel

271 view summarizes our current understanding of ethylene signaling, including these alternative pathways

272 (ERF) are natural candidates for targets of ethylene signaling, we initially characterized the behav

273 pmental responses to KAR treatment depend on ethylene signaling.

274 regulatory circuit connecting RPW8.1 and the ethylene-signaling pathway, in which RPW8.1 enhances eth

275 the identification of many components of the ethylene-signaling pathway.

276 e) (PEG-PPS) and poly(ethylene glycol)-oligo(ethylene sulfide) (PEG-OES) that can self-assemble into

277 ethylene carbonate (EC), dimethyl carbonate, ethylene sulfite (ES), and their combinations as electro

278 and post-transcriptional levels that lead to ethylene synthesis and downstream ripening events determ

279 Ethylene synthesis inhibition revert the constitutive Fe

280 trodes were fabricated on the bio-based poly(ethylene terephthalate) (Bio-PET) substrates for the dev

281 revealed consistent polyethylene (PE), poly(ethylene terephthalate) (PET), and polypropylene (PP) co

282 polymers in Lake Michigan samples were poly(ethylene terephthalate) (PET), high-density polyethylene

283 emically functionalized conical shaped poly-(ethylene terephthalate) nanopore (PET nanopore) as a sto

284 we designed a sensing platform based on poly(ethylene terephthalate) substrates to which polyacrylate

285 polymerized onto surface-functionalized poly(ethylene terephthalate), resulting in the formation of c

286 s losses, respiration rate and production of ethylene than controls.

287 y (ELISA) was developed for the detection of ethylene thiourea (ETU); a metabolite of ethylenebisdith

288 I2-MAX2-SMAX1) regulates the biosynthesis of ethylene to fine-tune root and root hair development, wh

289 ene-treated petals of R. bourboniana and 8 h ethylene-treated AZ (R. hybrida) identified a core set o

290 f petal abscission zones (AZ) of 0 h and 8 h ethylene-treated flowers from R. bourboniana was perform

291 Further comparisons with ethylene-treated petals of R. bourboniana and 8 h ethyle

292 transcriptome was observed between 0 and 8 h ethylene-treated R. bourboniana petal AZ.

293 drogen transfer to produce the main product (ethylene) via a key -CH-CH(2) intermediate.

294 Teflon filters to polyethylene terephthalate-ethylene vinyl acetate (PET-EVA) substrates by a tempera

295 re packed in multilayer metalized (MET), and ethylene vinyl alcohol (EVOH) based pouches and stored a

296 D printed mimics that performed similarly to ethylene-vinyl acetate shoe materials in quasi-static lo

297 ic efficiency as high as 57.7 and 52.0 % for ethylene when the CuNWs are oxidized by the O(2) from ai

298 t of this strategy, we report the CO(2)RR to ethylene with a Faradaic efficiency of 72 per cent at a

299 e learning, that efficiently reduce CO(2) to ethylene with the highest Faradaic efficiency reported s

300 of CO; reaction of the silylene complex with ethylene yields a similar bimetallic product with an eth