ライフサイエンスコーパス: ethylene

1 y active catalysts for the polymerization of ethylene.

2 ts in BIG or ARF1 result in insensitivity to ethylene.

3 (111) catalyst recombines to yield ethane or ethylene.

4 d, uncatalyzed reactivity toward H2, CO, and ethylene.

5 aintenance phase downstream of plant hormone ethylene.

6 ear to influence nodulation independently of ethylene action, as SL-deficient and ethylene-insensitiv

7 ciated with regulation of soluble sugars and ethylene activities were also increased during para- to

8 ts show fast kinetics, with more than 90% of ethylene adsorption occurring within 30 s after dosing.

9 exes with a borate cocatalyst are active for ethylene + amino olefin [AO; H2 C=CH(CH2 )n NR2 ] copoly

10 The plant hormones ethylene and auxin play key roles during apical hook dev

11 lutarate-derived intermediate occurs to give ethylene and carbon dioxide.

12 he ethylene biosynthesis pathway and reduced ethylene and CO2 production, thus delaying fruit ripenin

13 Analogous eta(2)-ethylene and eta(2)-cyclohexene complexes were also synt

14 za-derivatives in Diels-Alder reactions with ethylene and fumaronitrile were investigated with densit

15 he kinetics and pathways for major products (ethylene and methane) and minor products (ethanol, glyox

16 Homolog F, signaling components involved in ethylene and other hormone-mediated pathways, photosynth

17 d(10) metals, such as Cu(I) and Ni(0), with ethylene and other olefins, complexation of d(10) Zn(II)

18 This new species reacts with ethylene and phenyl acetylene to give the [2+2] cycloadd

19 nding enthalpies, below 55 and 70 kJ/mol for ethylene and propylene, respectively, indicate that thes

20 hytoalexins, and the stress-related hormones ethylene and salicylic acid (SA).

21 egulating H3K14Ac and H3K23Ac in response to ethylene and uncover a unique mechanism by which ENAP1 i

22 nd PsACO (encode enzymes that convert ACC to ethylene), and ethylene evolution were developmentally,

23 irect and single-step conversion of benzene, ethylene, and a Cu(II) oxidant to styrene using the Rh(I

24 with saturation at higher concentrations of ethylene, and a zero-order dependence on the concentrati

25 nt routes to the major products, methane and ethylene, and identify the key intermediates where branc

26 r gaseous compounds, oxygen, carbon dioxide, ethylene, and nitric oxide, change during the submergenc

27 din A-inhibited GEF (BIG) family and GNOM in ethylene- and auxin-mediated control of hook development

28 that jasmonates acting synergistically with ethylene are the key molecular triggers of tyloses.

29 Auxin, cytokinin, and ethylene are three important hormones that regulate many

30 ms the C-H silylation product C6F5SiMe3 with ethylene as a byproduct ([(i)Pr2Im] = 1,3-di(isopropyl)i

31 ase the selectivity of all electrodes toward ethylene at E > -0.45 V vs RHE, but methane is favored a

32 ibed here suggests that conversion of 2OG to ethylene, atypical among Fe(II)/2OG oxygenases, is facil

33 junction with structural characterization of ethylene binding in Co2(m-dobdc) and Co2(p-dobdc) via in

34 of the EPiR response reveals a modulation in ethylene biosynthesis and signaling, metal ions deficien

35 d synthase gene, the first committed step in ethylene biosynthesis compared with wild type.

36 ed to treat tuberculosis, as an inhibitor of ethylene biosynthesis in Arabidopsis thaliana, using a c

37 Specific ethylene biosynthesis inhibitors would help to decrease

38 These data support the hypothesis that ethylene biosynthesis is regulated in reproductive tissu

39 KEY MESSAGE: Ethylene biosynthesis is regulated in reproductive tissu

40 CNFC coating delayed the ethylene biosynthesis pathway and reduced ethylene and C

41 t PC suppressed CI symptoms and induced more ethylene biosynthesis than the other treatments.

42 The genes involved in ethylene biosynthesis were differentially regulated by L

43 ver, genes related to auxin, gibberellin and ethylene biosynthesis were significantly up-regulated.

44 s (ACS), generally the rate-limiting step in ethylene biosynthesis, which is regulated both transcrip

45 egulators of plant metabolism, in particular ethylene biosynthesis.

46 of relevant genes of the phenylpropanoid and ethylene biosynthetic pathways during elicitation of res

47 and rapid access to various chain lengths of ethylene-bridged BODIPY motifs was discovered.

48 liquid chromatography, whereby the selected ethylene-bridged hybrid phenyl ultra-high-performance li

49 The normal ethylene burst in the stigma/style and petals following

50 in legumes is regulated by the plant hormone ethylene, but it has remained unclear whether and how it

51 ng of pore size (3.4 A) to effectively block ethylene (C2 H4 ) molecules but to take up a record-high

52 iv) toluenediisocyanate (TDI), and (v) oligo(ethylene) ([C2H4O]n) as well as p-toluenesulfonic acid.

53 Use of ethylene can also cause adventitious olefin isomerizatio

54 ve potential (+2.0 V) to these PCPs promotes ethylene capture, and subsequent dose of negative potent

55 ore how an electrolyte additive (fluorinated ethylene carbonate - FEC) mediates the thickness and com

56 , which is a copolymer of ethylene oxide and ethylene carbonate, was synthesized by ring-opening poly

57 t are observed after cycling in the standard ethylene carbonate-based electrolyte are suppressed in t

58 ynthesized by ring-opening polymerization of ethylene carbonate.

59 e concentration, a first-order dependence on ethylene concentration with saturation at higher concent

60 -order that varies with both temperature and ethylene concentration, a first-order dependence on ethy

61 ting the complexity in auxin, cytokinin, and ethylene crosstalk requires a combined experimental and

62 ayers of complexity in auxin, cytokinin, and ethylene crosstalk.

63 Thus, ETR1 and ETR2 have both ethylene-dependent and -independent roles in plant cells

64 nal regulator of these chaperone genes in an ethylene-dependent manner, and that MADS-RIN protein-reg

65 We established a sensitive ethylene detection system for Lotus japonicus and found

66 ce obtained by electrochemical patterning of ethylene diamine and terminal amine polyethylene glycol

67 ethylene diamine tetraacetic acid and serum dilution imp

68 dilution to detect high-level IgG, and after ethylene diamine tetraacetic acid treatment to obviate c

69 omparison with perovskites grown on poly(3,4-ethylene dioxy thiophene) polystyrene sulfonate.

70 Electrodeposition of poly(3,4-ethylene dioxythiophene) (PEDOT)/graphene oxide (GO) ont

71 gomer formation during the polymerization of ethylene due to the presence of a N-donor ligand.

72 strated to be transcriptionally regulated by ethylene during mature green (MG) fruit transition into

73 )PdCH2 CHF2 (lutidine) and inserts multiple ethylene (E) units to generate polyethylene that contain

74 ry and breeding wheat cultivars with reduced ethylene effects on yield under heat stress.

75 the absence of ethylene; in the presence of ethylene, EIN2 interacts with ENAP1, elevating the level

76 Diels-Alder cycloaddition of butadiene with ethylene, electrocyclic ring-opening of cyclobutene, ele

77 at perception of Nod factor was required for ethylene emission, while downstream transcription factor

78 Specifically, in the presence of ethylene, ENAP1-binding regions are more accessible upon

79 activity for a kinetically driven reaction, ethylene epoxidation, giving rise to a 20-fold selectivi

80 (CH2CH3)(CHCH2)Ar((i)Pr4) (4) featuring five ethylene equivalents, one of which is dehydrogenated to

81 salicylic acid (SA), jasmonic acid (JA), and ethylene (ET) pathways suggest the involvement of a comp

82 anscripts involved in jasmonic acid (JA) and ethylene (ET) signaling pathways were also accumulated a

83 formation when combined with JA depended on ethylene (ET) signaling, as shown by a decrease in the r

84 an and non-host Arabidopsis treated with the ethylene (ET)-synthesis inhibitor aminoethoxyvinylglycin

85 rameworks, Fe2(m-dobdc) displays the highest ethylene/ethane (>25) and propylene/propane (>55) select

86 Ethylene, ethanol, and n-propanol are the major C2-C3 pr

87 Amorphous poly(ethylene ether carbonate) (PEEC), which is a copolymer o

88 O in the pedicels was correlated with higher ethylene evolution and ovary senescence and pedicel absc

89 e enzymes that convert ACC to ethylene), and ethylene evolution were developmentally, environmentally

90 t profiles in a manner that suppressed ovary ethylene evolution.

91 tential less than -0.60 V (RHE), the rate of ethylene formation decreases, mainly due to the loss of

92 anaerobic MSP that couples MTA metabolism to ethylene formation in the phototrophic bacteria Rhodospi

93 The rate-determining step to methane and ethylene formation is CO hydrogenation, which is conside

94 CO), the enzyme catalysing the final step of ethylene formation.

95 al may hinder such a ferryl flip and promote ethylene formation.

96 The ethylene-forming enzyme (EFE) from Pseudomonas syringae

97 formance for the physisorptive separation of ethylene from ethane and propylene from propane relative

98 he discovery of new materials for separating ethylene from ethane by adsorption, instead of using cry

99 This material can kinetically separate ethylene from ethane with an unprecedented selectivity o

100 on of the chromates reduction carried out by ethylene from the subsequent polymerization.

101 Ethylene gas is essential for developmental processes an

102 straight access to indoles from anilines and ethylene glycol by heterogeneous catalysis, based on an

103 VPP; a resin of N-vinyl-2-pyrrolidinone with ethylene glycol dimethacrylate and triallyl isocyanurate

104 c acid or methyl methacrylate as monomer and ethylene glycol dimethacrylate as cross-linker at differ

105 ve molecularly imprinted poly[acrylamide-co-(ethylene glycol dimethacrylate)] polymer particles (MIPs

106 ZnO have been found to slowly dehydrogenate ethylene glycol generating, after condensation with the

107 Acylation with PEG containing five ethylene glycol units led to the largest gain in ESI res

108 Ms) of thiol-terminated derivatives of oligo(ethylene glycol) (HS(CH2CH2O)nCH3; HS(EG)nCH3); these SA

109 n, the N-terminal leptin conjugate with poly(ethylene glycol) (LepNPEG5K), and two conjugates of lept

110 odification is the attachment of methoxypoly(ethylene glycol) (mPEG), termed PEGylation, which has le

111 ymer poly(amidoamine)-polyvalerolactone-poly(ethylene glycol) (PAMAM-PVL-PEG).

112 Pre-existing and induced anti-poly(ethylene glycol) (PEG) antibodies (abs) have been shown

113 e synthesis of 12 variations of the PLA-poly(ethylene glycol) (PEG) based precision-polyester (P2s) p

114 The influence of the poly(ethylene glycol) (PEG) chain length on the performance o

115 polyion complex of SOD1 with polycation poly(ethylene glycol) (PEG)-polylysine (single-coat (SC) nano

116 on of natural clay mineral particles in poly(ethylene glycol) (PEG)/dextran (Dx) aqueous two-phase sy

117 ly, poly(p-phenylene) beta-cyclodextrin poly(ethylene glycol) (PPP-CD-g-PEG) combined with gold nanop

118 hydrogel by combining dopamine-modified poly(ethylene glycol) and the nanosilicate Laponite, without

119 particle surface functionalization with poly(ethylene glycol) and/or immunological modulators, preven

120 ve a critical value of approximately 20 poly(ethylene glycol) chains (MW 5 kDa) per 100 nm(2) prolong

121 In nanoparticles with low poly(ethylene glycol) coverage, adsorption of apolipoproteins

122 rance of nanoparticles, irrespective of poly(ethylene glycol) density.

123 novel effects of the amyloid-binding tetra (ethylene glycol) derivative of benzothiazole aniline, BT

124 intramolecular anhydride formation of oligo(ethylene glycol) diacids gives macrocycles analogous to

125 el fibers consist of poly(acrylamide-co-poly(ethylene glycol) diacrylate) cores functionalized with p

126 (HS(CH2)nH) demonstrates that SAMs of oligo(ethylene glycol) have values of beta (beta(EG)n = 0.29 +

127 Herein, the polymer conformation of poly(ethylene glycol) is detailed and compared with those of

128 ox-insensitive), which consist of poly(oligo(ethylene glycol) methacrylate) (POEG) hydrophilic blocks

129 introducing an acetic acid terminated poly (ethylene glycol) methyl ether (aaPEG) onto the Thr resid

130 es (SPE) through a blend formation with poly(ethylene glycol) methyl ether (mPEG) to prevent its leac

131 es by functionalizing the nanorods with poly(ethylene glycol) methyl ether thiol (PEG-thiol) prior to

132 The versatile new poly(oligo(ethylene glycol) vinyl acetate)s are presented with exce

133 lactose, glucose, carboxybetaine, and oligo(ethylene glycol) were installed via postpolymerization t

134 hexahistidine tagged OPH (His6-OPH) and poly(ethylene glycol)-b-poly(l-glutamic acid) diblock copolym

135 rogels (poly(lactic-co-glycolic acid)-b-poly(ethylene glycol)-b-poly(lactic-co-glycolic acid); PLGA-P

136 ell as conventional carboxy-terminated oligo(ethylene glycol)-based alkanethiolate self-assembled mon

137 ilamellar and tubular polymersomes from poly(ethylene glycol)-bl-poly(propylene sulfide) block copoly

138 nd its polymer-drug conjugate, methoxy-poly (ethylene glycol)-block-poly (2-methyl-2-carboxyl-propyle

139 poly(d,l-lactic-co-glycolic acid)-block-poly(ethylene glycol)-block-poly(d,l-lactic-co-glycolic acid)

140 While poly(ethylene glycol)-block-poly(lactic-co-glycolic acid) (PE

141 and doxorubicin (Dox) co-loaded Methoxy poly(ethylene glycol)-poly(epsilon-caprolactone) (MPEG-PCL) n

142 ; the resulting DA-TAT is conjugated to poly(ethylene glycol)-poly(epsilon-caprolactone) (PEG-PCL, PE

143 Specifically, biodegradable poly(ethylene glycol)-poly(lactic-co-glycolic acid) (PEG-PLGA

144 iol-activated terminal such as four-arm poly(ethylene glycol)-thiol (PEG-SH) via chemisorption.

145 een alpha-truxillic acid and diols including ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pe

146 products (ethanol, glyoxal, glycolaldehyde, ethylene glycol, acetaldehyde, ethane, and methanol).

147 rements carried out on methanol isotopomers, ethylene glycol, and acetone.

148 hydraulic fracturing compounds (2-propanol, ethylene glycol, propargyl alcohol, 2-butoxyethanol, and

149 Four compounds (2-propanol, ethylene glycol, propargyl alcohol, and 2-butoxyethanol)

150 rate, PVP-DEGMA-TAIC; and poly(acrylamide-co-ethylene glycol-dimethacrylate), PA-EGDMA) to remove fum

151 emerged, where replacing Bpin with Beg (eg = ethylene glycolate) was predicted to significantly impro

152 dying in-house prepared, low dispersity poly(ethylene glycols)s (PEGs), also known as poly(ethylene o

153 of the reactions of monoacceptor-substituted ethylenes (H2C horizontal lineCH-Acc, 1) and styrenes (P

154 ework (MOF) catalyst for the dimerization of ethylene has a combination of selectivity and activity t

155 evelopmental responses of plants mediated by ethylene has been demonstrated.

156 ses the turnover frequency (TOF) relative to ethylene homopolymerization, but still remarkably high T

157 electron oxidation of 2-oxoglutarate to give ethylene in an arginine-dependent reaction.

158 1 single and double mutants still respond to ethylene in light-grown seedlings.

159 anscriptional and developmental responses to ethylene in light-grown seedlings.

160 lexity in crosstalk of auxin, cytokinin, and ethylene in root development.

161 onse to elevated levels of the plant hormone ethylene in roots from light-grown Arabidopsis (Arabidop

162 n metathesis of methyl acrylate, styrene, or ethylene in the presence of either DBU, or enolates form

163 source, generating stoichiometric amounts of ethylene in the process.

164 t program, and reinforced the role played by ethylene in the ripening receptacle.

165 chemically controlled capture and release of ethylene in the solid state.

166 tion allows for the direct polymerization of ethylene in water to nanocrystal dispersions of disentan

167 the open chromatin regions in the absence of ethylene; in the presence of ethylene, EIN2 interacts wi

168 Necrosis and ethylene-inducing peptide 1-like (NLP) proteins constitu

169 Ethylene induction experiments using 2-(methylthio)ethan

170 These data suggest a NO-ethylene influenced regulatory node in polyamine biosynt

171 Ethylene influences many aspects of plant growth and dev

172 or example, PHYTOALEXIN DEFFICIENT 4 (PAD4), ETHYLENE-INSENSITIVE 3-LIKE 1 (EIL3), and ETHYLENE RESPO

173 ntly of ethylene action, as SL-deficient and ethylene-insensitive double mutant plants display essent

174 We used ethylene-insensitive or sensitive mutants to provide mor

175 Ljein2b double mutant that exhibits complete ethylene insensitivity and confirms that these two genes

176 Ethylene is a gaseous plant hormone perceived by a famil

177 Ethylene is a major plant hormone mediating developmenta

178 We show here that ethylene is also produced during systemic inflammation i

179 Ethylene is an important phytohormone that promotes the

180 The biosynthesis of ethylene is highly regulated by a variety of internal an

181 Ethylene is important in industry and biological signali

182 they also suggest a possible route by which ethylene is produced by microbes in anoxic environments.

183 In plants, ethylene is produced by oxidation of 1-aminocyclopropane

184 al studies reveal that fragmentation to give ethylene is promoted by binding of l-arginine in a nonox

185 Of these gases, ethylene is seen as the most consistent, pervasive, and

186 and separation of olefin/paraffin, acetylene/ethylene, linear/branched alkanes, xenon/krypton, etc.

187 ctivation nor beta-Si elimination but either ethylene loss or reductive elimination of cis-disposed a

188 Reversible ethylene loss was not observed with 1b, which suggests t

189 In vivo ethylene measurement showed that UHb plants significantl

190 se transcription factor, EIN3, is central to ethylene-mediated development, the roots of ein3 and eil

191 nsitive mutants to provide more evidence for ethylene-mediated signaling.

192 prompted a reinvestigation of the effects of ethylene on the circadian oscillator.

193 illator proteins and can mask the effects of ethylene on the circadian system, identifying novel mole

194 ing states but are in rapid equilibrium with ethylene-opened chelates, (alpha-diimine)Ni(R)(C2H4)(+)

195 -2,4,6-(i)Pr3)2) (1a) reacts with 2 equiv of ethylene or t-butylethylene at ca. 25 degrees C to yield

196 e can be generated at 60 degrees C, 600 psig ethylene over 4 h with a productivity of 560 kg copolyme

197 theory help to understand how cations favor ethylene over methane at low overpotentials on Cu(100).

198 nd an isoprenyl ether type PCE (PCEI-P) with ethylene oxide (EO) unit numbers (P) of 25, 34 and 25, r

199 r carbonate) (PEEC), which is a copolymer of ethylene oxide and ethylene carbonate, was synthesized b

200 standard high-level disinfection followed by ethylene oxide gas sterilization (HLD/ETO).

201 , including organic solvents, proteases, and ethylene oxide gas sterilization.

202 osed of a dendron with two monodisperse poly(ethylene oxide) (PEO) branches terminated by a hydroxyap

203 Preformed poly(ethylene oxide) (PEO) single crystals were used as the t

204 y(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) triblock copolymers, and t

205 riblock copolymers containing a central poly(ethylene oxide) block and terminal polycarbonate blocks

206 riblock copolymers containing a central poly(ethylene oxide) block and terminal trimethylene carbonat

207 using singly charged sodium adducts of poly(ethylene oxide) monomethyl ether (CH3O-PEO-H) for positi

208 crylamide; acrylonitrile; 1,3-butadiene; and ethylene oxide) than combustible cigarette-only, dual co

209 the common issue of low conductivity of poly(ethylene oxide)(PEO)-based solid polymer electrolytes at

210 rystallization of block copolymer (BCP) poly(ethylene oxide)-b-poly(4-vinylpyridine) (PEO-b-P4VP), wh

211 w%) of two amphiphilic thermoresponsive poly(ethylene oxide)-b-poly(N,N-diethylacrylamide)-b-poly(N,N

212 We find that the soluble poly(ethylene oxide)-like linear oligomeric electrolyte break

213 The stretchable LEDs consist of poly(ethylene oxide)-modified poly(3,4-ethylenedioxythiophene

214 are composed of alpha-cyclodextrins and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxid

215 thylene glycols)s (PEGs), also known as poly(ethylene oxide)s (PEOs) depending on the classification

216 to form both soluble and insoluble branched ethylene-oxide-based polymers.

217 sectors of the signaling network, jasmonate, ethylene, PAD4, and salicylate, are disabled, the hypers

218 characterized by a lack of induction of the ethylene pathway.

219 The gaseous phytohormone ethylene plays an important role in spike development in

220 Ethylene plays vital roles in plant development and abio

221 We found that the sites involved in ethylene polymerization are mainly divalent Cr ions in a

222 duced Cr(VI) species are also present during ethylene polymerization as well as reduced Cr species (e

223 in the Cr(VI)/SiO2 Phillips catalyst during ethylene polymerization.

224 eral plant hormones especially auxin and the ethylene precursor aminocyclopropane-carboxylic acid.

225 Polymerizations are first-order in ethylene pressure and inverse-order in silane concentrat

226 roups whose ratios depend on temperature and ethylene pressure.

227 ntly used cryogenic distillation process for ethylene produced through steam cracking.

228 l symptoms related to chilling injury, while ethylene production and ammonium content resulted associ

229 howed that UHb plants significantly decrease ethylene production and expression of aminocyclopropane-

230 Coated plums showed a delay in ethylene production and respiration rate at 20 degrees C

231 yclopropane-1-carboxylate) oxidase activity, ethylene production and respiration rate of apples store

232 ntative products were induced, which reduced ethylene production and respiration rate; however, it di

233 as sulfur sources further indicate anaerobic ethylene production from 2-(methylthio)ethanol requires

234 on system for Lotus japonicus and found that ethylene production increased as early as 6 hours after

235 These results demonstrate that ethylene production is an early and sustained nodulation

236 Light (LBL) induces changes in phenolics and ethylene production of sweet oranges, and whether they p

237 al quality, physiological (respiration rate, ethylene production, ammonium content) and chemical (ant

238 Bacteria catalyze ethylene production, but via the four-electron oxidation

239 atory quotient 1.3 (DCA-RQ 1.3) showed lower ethylene production, respiration rate, mealiness and hig

240 n combination with rosehip oil (RO) at 2% on ethylene production, respiration rate, quality parameter

241 ating mutants was also sufficient to elevate ethylene production.

242 balbicans increased the ACCO mRNA levels and ethylene production.

243 While ethylene promotes the emergence and growth of ARs, gravi

244 Transcript abundance profiles of ethylene receptor and signaling-related genes acted as q

245 ncreases were observed in Neverripe (Nr), an ethylene receptor mutant.

246 e development marker genes GLABRA2 (GL2) and Ethylene Receptor2 (ETR2) is not affected in the glh1 mu

247 developmental marker genes GLABRA2 (GL2) and Ethylene Receptor2 (ETR2) were not affected in the glh1

248 receptor mutants revealed that, of the five ethylene receptors, ETR1 controls lateral root and root

249 how crosstalk between auxin, cytokinin, and ethylene regulates patterning in root development.

250 edented high-energy conformation that favors ethylene, relative to succinate formation.

251 Our results highlight that ethylene release is an early and integral component of i

252 c root bending is inhibited by the group VII ethylene response factor (ERFVII) RAP2.12, as rap2.12-1

253 proteins, which were regulated by Group VII Ethylene Response Factor (ERFVII) transcription factors,

254 ), ETHYLENE-INSENSITIVE 3-LIKE 1 (EIL3), and ETHYLENE RESPONSE FACTOR 1 (ERF1)] clustered into salicy

255 -regulated Nodulation Signaling Pathway2 and Ethylene Response Factor Required for Nodulation1 early

256 gh oxygen-dependent degradation of group VII Ethylene Response Factor transcription factors (ERFVIIs)

257 Recent studies indicate that the ETHYLENE RESPONSE FACTOR VII (ERF-VII) transcription fac

258 transcription factors belonging to group VII ethylene response factors (ERF-VII) that, together with

259 ranscription factors, encoding predominantly ethylene response factors, active during early MTI, and

260 th dark-grown seedlings, where the canonical ethylene response transcription factor, EIN3, is central

261 ter inoculation with Mesorhizobium loti This ethylene response was dependent on Nod factor production

262 Arabidopsis (Arabidopsis thaliana) including ETHYLENE RESPONSE1 (ETR1) and ETR2.

263 l closure in the wild type, but not Nr, with ethylene responses attenuated in the are mutant.

264 Transcripts of representative ethylene-responsive and ripening-modulated genes confirm

265 Additionally, a subset of these clusters of ethylene-responsive transcripts were enriched in targets

266 ss responses; however, little is known about ethylene's role in reproductive tissues during developme

267 -Alder cycloaddition of cyclopentadiene with ethylene serves, in pedagogical detail, to describe the

268 tion and the genomic regions governing spike ethylene (SET) production in wheat under long-term heat

269 We demonstrate that ethylene shortens the circadian period, conditional on t

270 hylene signaling, the mechanism by which the ethylene signal is transduced remains largely unknown.

271 genes acted as qualitative markers of tissue ethylene signaling events.

272 Ethylene signaling is controlled by EIN2, which is dupli

273 f ETR1 and ETR2 do not require the canonical ethylene signaling pathway.

274 stitutive activity of MPK3 can bypass SA and ethylene signaling to activate defense responses.

275 ines, which are impaired in SA synthesis and ethylene signaling, respectively, retain most of the CA-

276 membrane-bound protein EIN2 is critical for ethylene signaling, the mechanism by which the ethylene

277 n is strictly regulated by jasmonic acid and ethylene signaling, while only AtPMEI11 expression is co

278 ripening-related regulators and elements of ethylene signaling.

279 LE RESPONSE1 (CTR1), a negative regulator of ethylene signaling.

280 irms that these two genes act redundantly in ethylene signaling.

281 wild type and ACS2-antisense fruit with the ethylene-signaling inhibitor, 1-methylcyclopropane (1-MC

282 and we found no evidence that SLs influence ethylene synthesis or vice versa.

283 ell devices made on an indium tin oxide/poly(ethylene terephthalate) substrate via a low temperature

284 lied potential (U) greater than -0.6 V (RHE) ethylene, the major product, is produced via the Eley-Ri

285 certed pathways for [2 + 2] cycloaddition of ethylene to all 10 of the cumulenes with the formula X h

286 ons of oxidative gold catalysis, exposure of ethylene to aryl silanes and alcohols generates products

287 As simple model reactions, cycloaddition of ethylene to formaldehyde, thioformaldehyde, and formaldi

288 6(C6H3-2,6-(i)Pr2)2) (1b) reacts with excess ethylene to give Ar((i)Pr4)(CH2CH3)2Sn(CH2CH2)Sn(CH2CH3)

289 ing substituents allow for polymerization of ethylene to higher molecular weights with reduced branch

290 Inability of ethylene to suppress sHSP genes in rin/rin mutant, which

291 Notably, ethylene treatment of the MG fruit led to significant sH

292 Ethylene treatment of wild-type tomato plants increased

293 wer levels of ROS due to elevated flavonols, ethylene treatments decreased ABA-induced stomatal closu

294 tively expressed genes both with and without ethylene treatments.

295 mild potentials and reacts with O2, CO2, and ethylene via formal [4+2] cycloaddition to the central d

296 The significance and features of ethylene-vinyl acetate (EVA) copolymers in initial resea

297 In humans, ethylene was detected prior to the increase of blood lev

298 Traces of ethylene were detected by laser spectroscopy both in vit

299 Direct coordinative copolymerization of ethylene with functionalized co-monomers is a long-sough

300 Copolymerizations of ethylene with vinyltrialkoxysilanes using cationic (alph