ライフサイエンスコーパス: N2

1 N2 -fixing N. azollae, we conclude, dominated the microb

2 N2 O was not detectably released from surface-sterilized

3 N2-fixing symbionts progressively outcompete isogenic no

4 The square pyramidal Fe(0)(N2)(P4N2) complex catalyzes the conversion of N2 to N(Si

5 ge, {K(crypt)}2{[(R2N)3Sc]2[mu-eta(1):eta(1)-N2]} (crypt = 2.2.2-cryptand, R = SiMe3), has been isola

6 med {K(crown)}2{[(R2N)3Sc]2[mu-eta(1):eta(1)-N2]}.

7 nitrogen fertilizer concentrations (N1:100, N2:200 and N3:300 kg ha(-1)N) on starch properties (tota

8 (15) N2 incorporation was active in ferns with N. azollae but

9 The application of this strategy to a (15) N2 -diazirine-containing choline derivative demonstrates

10 erivative demonstrates the potential of (15) N2 -diazirines as molecular imaging tags for biomedical

11 As recently reported, (15) N2 -diazirine can be hyperpolarized by the SABRE-SHEATH

12 af tissue under simulated sunlight, and [(15)N2]DNAN yielded (15)NO2(-) in leaves.

13 metastases were present in 68% (44% N1, 24% N2).

14 Horizon oil spill using a combination of (29)N2 and (30)N2 production (isotope pairing), denitrificat

15 spill using a combination of (29)N2 and (30)N2 production (isotope pairing), denitrification potenti

16 hat the presence of a single 5'p-rN1-(2'-5')-N2 unit in the antisense strand does not alter the 'clov

17 scores in two independent datasets (N1 = 97, N2 = 176).

18 sun illumination, at 60 degrees C, and in a N2 atmosphere.

19 rain constellation of G1-P[8]-I2-R2-C2-M2-A3-N2-T6-E2-H3, with most of the gene segments having a clo

20 N-back task accuracy (N2 and N3) improved after real-rTMS (and not after sham-

21 ing a small molecule, N1-(3-acetamidophenyl)-N2-(2-(4-methyl-2-(p-tolyl)thiazol-5-yl)ethyl)oxalamide.

22 lites: 6-hydroxymelatonin (6-OHM), N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK), N-acetylserotonin

23 increased denitrification potential affected N2 O fluxes under WTL conditions.

24 They are responsible for up to 50% of all N2 released from marine ecosystems into the atmosphere a

25 n, where at least four PLN are needed for an N2 diagnosis, this threshold may be inadequate for accur

26 The iron complex is in equilibrium with an N2-free species.

27 (HR: 0.68, CI95%: 0.62-0.76, P = 0.007) and N2 (HR: 0.59, CI95%: 0.54-0.64, P = 0.04).

28 colonization, root phosphatase activity and N2 fixation increased in the N2 fixers, allowing them to

29 cifically inhibited AOB growth, activity and N2 O production.

30 rom silicon kerf in two atmospheres: air and N2, under a regime of no-diffusion-limitation.

31 was minor for CO2 emissions, whereas CH4 and N2 O fluxes displayed strong and asynchronous seasonal d

32 ion and ebullition fluxes of CO2 , CH4 , and N2 O from a restored emergent marsh ecosystem.

33 rconversions of H(+)/H2, O2/H2O, CO2/CO, and N2/NH3, is an ongoing challenge.

34 ient cycling, including pathways for CO2 and N2 fixation, anaerobic respiration, sulfur oxidation, fe

35 HG transport, accounting for >99% of CO2 and N2 O emissions, and 71% of CH4 emissions.

36 N0) disease and N2|3 (vs.

37 EFC) that is able to produce NH3 from H2 and N2 while simultaneously producing an electrical current.

38 stic features of multivalency between H3 and N2 with SA receptors and show that the stability of the

39 gh dry weather decreased NO3(-) leaching and N2 O emissions in isolation, 2-year cumulative N losses

40 SARS-CoV-2 RNA targets N1 and N2 concentrations correlated positively and significantl

41 Analysis of IAVs carrying N1 and N2 mutants demonstrated that the N-linked glycosylation

42 s developed for the more nucleophilic N1 and N2 positions.

43 mprising basic residues from both the N1 and N2 subdomains, that directly contributes to 30S-binding

44 (NSCLC), distinguishing between N0, N1, and N2 or N3 (N2|3) disease is important.Objectives: To deve

45 can estimate the probability of N0, N1, and N2|3 disease in patients with NSCLC.

46 or estimating the probability of N0, N1, and N2|3 disease.Methods: Consecutive patients with clinical

47 sequences in the SH3 domain to yield N1- and N2-Src.

48 Adding N2O and N2 effluxes to catchment nitrogen output not only reduce

49 aggregated N loss (sum of NO3(-) , NH3 , and N2 O, totaling 84 kg N/ha); (ii) UI in rice-paddy system

50 The remaining six accumulated NO and N2 O to varying degrees and genome sequencing of four in

51 growth and turnover of nitric oxide (NO) and N2 O at low cell densities of Nitrosomonas europaea (AOB

52 esis that AOB dominate ammonia oxidation and N2 O production under conditions of high inorganic ammon

53 In unamended soils, ammonia oxidation and N2 O production were lower and resulted mainly from ammo

54 understanding of soil N cycling pathways and N2 O production.

55 nsembles to predict jointly productivity and N2 O emissions at field scale is discussed.

56 erest in water splitting, CO2 reduction, and N2 fixation.

57 ains, cell-specific rates of NO turnover and N2 O production reached maxima near O2 half-saturation c

58 ction model errors predicted both yields and N2 O emissions within experimental uncertainties for 44%

59 imental uncertainties of observed yields and N2 O emissions.

60 Hbl features two inner protons bound at N2 and N4 of the corrin ligand, as discovered in Hby.

61 ional analysis show that 2'-O methylation at N2, another abundant mRNA modification, is also detrimen

62 the highest turnover number of any Fe-based N2 silylation catalyst to date (up to 65 equiv N(SiMe3)3

63 For 116 structural discrepancies between N2 and VC2010, 97 structures matching VC2010 (84%) were

64 le analytical approach to measure biological N2 fixation rates directly without a proxy or isotopic l

65 mino acids did not significantly affect bulk N2 fixation rates, N2 fixation was enhanced by amino aci

66 D s of accessible pores estimated by N2 desorption is greater than that for N2 adsorption for

67 )(H)x systems that are active for catalytic N2 -to-NH3 conversion.

68 hey have not been shown to mediate catalytic N2-to-NH3 conversion (N2RR), nor have M-NxHy complexes b

69 Features detected within the (DT)CCS(N2) and m/ z ranges of the analyzed standards are flagge

70 on-cross-section values in nitrogen ((DT)CCS(N2)), and retention times of the species found are compa

71 es are seen in CCMM membranes for CO2 /CH4 , N2 /CH4 , He/CH4 , and H2 /CH4 separations.

72 lfur clusters in complex I, [4Fe-4S] cluster N2.

73 lidene (BAC) to provide PhB((i)Pr2Im)3Fe(CN)(N2)(BAC).

74 degrees C and 0.15 bar), extraordinary CO2 /N2 selectivities (98-205 at 25 degrees C), and excellent

75 ions with CO2 permeance of 1,020 GPU and CO2/N2 selectivity as high as 680, demonstrating its potenti

76 ile coating process for highly efficient CO2/N2 separation under wet conditions.

77 8 Robeson upper bounds for O2/N2, H2/N2, CO2/N2, H2/CH4 and CO2/CH4, with the potential for biogas pu

78 At 0.15 bar CO2 partial pressure, the CO2/N2 selectivity was 49 (corresponding to 91% purity of th

79 n the ecophysiology and SNF rate of a common N2 -fixing tree in eastern US forests.

80 nusual Fe-Ct(N2)-Fe angle of 150 degrees (Ct(N2) = centroid of N(2)), a geometry that approximates th

81 a bridging N(2) ligand with an unusual Fe-Ct(N2)-Fe angle of 150 degrees (Ct(N2) = centroid of N(2)),

82 dry-wet sequence decreased 2-year cumulative N2 O emissions while the wet-dry sequence increased 2-ye

83 wet-dry sequence increased 2-year cumulative N2 O emissions.

84 omic differences concentrated in CDR3's N1-D-N2 region, which allowed the prediction of public and pr

85 ERPs revealed decreased N2 amplitudes reflecting poorer response selection for b

86 The 2'-deoxyguanosin-N2-yl radical (dG(N2-H)(.) ) formed was proposed to rapi

87 ethods can presumably also be used to detect N2 fluxes by denitrification from ecosystems to the atmo

88 dG(N2-H)(.) is directly observed upon nanosecond laser flas

89 eport the first independent generation of dG(N2-H)(.) in high yield via photolysis of 1.

90 The absorption spectrum of dG(N2-H)(.) is corroborated by DFT studies, and anti- and s

91 showed no evidence for tautomerization of dG(N2-H)(.) to dG(N1-H)(.) within hundreds of microseconds.

92 The 2'-deoxyguanosin-N2-yl radical (dG(N2-H)(.) ) formed was proposed to rapidly tautomerize to

93 borated by DFT studies, and anti- and syn-dG(N2-H)(.) are resolved for the first time.

94 ts that the generation of dG(N1-H)(.) via dG(N2-H)(.) following hydrogen atom abstraction from dG is

95 enase catalyzes the reduction of dinitrogen (N2) to two ammonia (NH3) at its active site FeMo-cofacto

96 pated to influence the growth of dinitrogen (N2)-fixing phytoplankton, which contribute a large fract

97 We hypothesized that dinitrogen (N2 )- and non-N2 -fixing tropical trees would have disti

98 ed inhibitor of AOB, was used to distinguish N2 O production resulting from archaeal and bacterial am

99 , or PCL5 survey) in the awake state, during N2 sleep, and in a hybrid BCM incorporating both awake a

100 Yield-scaled N2 O emissions (N2 O emissions divided by crop yields) were ranked accur

101 N-depleted surface waters, which encourages N2 fixation, the dominant N input to the ocean.

102 dissociation activation energy to be 4.74 eV/N2, with Fe as the active site on the surface.

103 esis and characterization of new P2(P'Ph) Fe(N2 )(H)x systems that are active for catalytic N2 -to-NH

104 Here we show that a nitrogen-fixing Fe-N2 catalyst can be protonated to form a neutral Fe(NNH2)

105 es derived from the direct protonation of Fe-N2 and Fe-CN species at the terminal N atom (e.g., Fe ho

106 tivity profiles of early stage protonated Fe-N2 and Fe-CN species.

107 These same Fe-N2 and Fe-CN systems are functionally active for N2-to-N

108 ONALE: Estimating the probability of finding N2 or N3 (prN2/3) malignant nodal disease on endobronchi

109 row aerobically and diazotrophically (fixing N2 to grow) while containing functional nitrogenase.

110 ed gases with a precision better than 1% for N2, O2, CO2, He, Ar, 2% for Kr, 8% for Xe, and 3% for CH

111 nd Fe-CN systems are functionally active for N2-to-NH3 and CN-to-CH4/NH3 conversion, respectively, wh

112 and to a lesser and more variable extent for N2 O emissions.

113 ifics and whether the intimate mechanism for N2-to-NH3 conversion involves a distal pathway, an alter

114 rval above this minimum CO2 mixing ratio for N2 fixation rate calculations.

115 phic denitrification was the main source for N2 O production, and was not impacted by the application

116 suggest potential mitigation strategies for N2 O emissions from fertilised agricultural soils.

117 ed by N2 desorption is greater than that for N2 adsorption for each linear section of each tested sam

118 Data from N2 -physisorption and rotation electron diffraction prov

119 mbly of VC2010, a modern strain derived from N2.

120 entical withN species have been derived from N2.

121 We demonstrate the synthesis of NH3 from N2 and H2O at ambient conditions in a single reactor by

122 The Haber-Bosch method of NH3 synthesis from N2 and H2 is notoriously energy intensive.

123 ectable amounts of the strong greenhouse gas N2 O.

124 es the desired sulfonyl amidines, generating N2 and CO2 as the only reaction byproducts.

125 Small molecules such as H2, N2, CO, NH3, O2 are ubiquitous stable species and their

126 model was validated experimentally with H2, N2, Ar and CH4 on three classes of microporous materials

127 the 2008 Robeson upper bounds for O2/N2, H2/N2, CO2/N2, H2/CH4 and CO2/CH4, with the potential for b

128 te collision cross sections (Omega) with He, N2, Ar, CO2, and N2O were measured for the 20 common ami

129 seedling experiment: the N2 fixer with high N2 fixation and root phosphatase activity grew best on o

130 oxidising archaea (AOA), due to their higher N2 O yield under oxic conditions and denitrification in

131 st levels were recorded for I100-N1 and I100-N2 treatments.

132 In N2 patients, this threshold was not associated with surv

133 % of CO2 in N2 when using an ionic liquid having a preorganized anio

134 o outgroup strains, implying deficiencies in N2.

135 probability of identifying at least 4 PLN in N2 patients.

136 extensive study of siderophore production in N2 -fixing A. vinelandii under a variety of trace metal

137 r upstates than theta bursts or spindles, in N2 than N3, in posterior than anterior HC, in frontal th

138 lated with wetland sediment and suspended in N2-purged artificial groundwater.

139 ccurred frequently with posterior HC-SWRs in N2).

140 ated whether eszopiclone could both increase N2 spindle density and improve memory.

141 nbenzodiazepine sedative hypnotic, increased N2 spindle density (number/minute) but did not significa

142 Different luminance-polarities increased N2 amplitude only, suggesting that shape but not numeros

143 cascade reaction features an intramolecular N2-arylation of pyrazoles with allenes at the C-beta pos

144 in surface V2O5 compared to exposure to just N2).

145 ordinated in situ metabolism of the keystone N2-fixing cyanobacterium Crocosphaera, as well as the br

146 dentified genes, namely PKN2 (protein kinase N2), PTK2 (protein tyrosine kinase 2), and ALPP (alkalin

147 and random configurations and found a larger N2 component for shape over lateral-occipital electrodes

148 haustible or easy-to-generate chemicals like N2, O2, CO2, CO, H2, or methane gas to value-added produ

149 With azine-linked N2-COF photosensitizer, chloro(pyridine)cobaloxime co-ca

150 mpound 2 is only stable at cryogenic (liquid N2) temperatures, and frozen solutions as well as solid

151 essing (freezing at -196 degrees C in liquid N2, FN sample; freeze-drying at -50 degrees C and 30Pa,

152 xes been derived from protonation of their M-N2 precursors.

153 r wheat and 129 kg ha(-1) for summer maize), N2 (240 kg ha(-1) for winter wheat and 185 kg ha(-1) for

154 (n = 633) had a 25% prevalence of malignant N2 or N3 disease.

155 chemical implications in an important marine N2 -fixer, as well as advancing evolutionary theory exam

156 etween nifH transcript abundance and maximal N2 fixation, as well as sepF transcript abundance and ce

157 haracterized derivative, [Fe(III)S2(Me2)N(Me)N2(amide)(Pr,Pr)](-) (8), shows that oxo atom donor reac

158 stics of a robust network with a microdomain N2-adsorption profile.

159 anipulate the dryland microbiome to mitigate N2 O emissions in situ using emerging technologies with

160 0-T3, N0-N2c, M0 (AJCC 8th edition T0-T3, N0-N2, M0), (2) being p16 positive, and (3) reporting minim

161 In total, 344 patients with T1-T4, N0-N2 breast cancer (352 lesions) were included.

162 We used existing N1, N2, and RP primer and probe sets by the Centers for Dise

163 including an N-back task (3 task loads: N1, N2, N3; control condition: N0) inside the MR scanner.

164 nserved potential N-glycosylation sites (N1, N2 and N3).

165 qPCR (Pearson coefficients > 0.7 for the N1, N2 and RPP30 genes).

166 cceptors (R,R)M and (S,S)M [where M = (N1,N1,N2,N2-tetramethylcyclohexane-1,2-diamine)Pd(NO(3))(2)] h

167 assified using different terms, including N1/N2 neutrophils, tumor-associated neutrophils, and polymo

168 distinguishing between N0, N1, and N2 or N3 (N2|3) disease is important.Objectives: To develop a pred

169 CO2 mixing ratio might be needed for natural N2 fixation and only used the time interval above this m

170 sorption of several small gases (H2, D2, Ne, N2, CO, CH4, C2H6, Ar, Kr, and Xe) on the metal-organic

171 two weakly coupled exchangeable protons near N2.

172 By contrast, negligible N2 O was produced following nitrate application to eithe

173 H3N2): hemagglutinin (H3) and neuraminidase (N2).

174 carbon source in an argon (Ar) and nitrogen (N2) atmosphere.

175 enzymes known to reduce molecular nitrogen (N2 ) to ammonia (NH3 ).

176 leguminosae family and hundreds of nitrogen (N2)-fixing bacterial species.

177 xhibited higher reduction of NO to nitrogen (N2) comparing to the predictions by the kinetic simulati

178 dinium) to shuttle electrons to nitrogenase, N2 reduction to NH3 can be mediated at an electrode surf

179 addition with reaction only across C4/N1 (no N2/N5 cycloaddition observed), proceed with a predictabl

180 izing effects (e.g., exposure to 250 ppmv NO/N2 resulted in an 2.4 times increase in surface V2O5 com

181 hypothesized that dinitrogen (N2 )- and non-N2 -fixing tropical trees would have distinct phosphorus

182 fixers, allowing them to outcompete the non-N2 fixers regardless of P source.

183 etitive ability of N2 fixers relative to non-N2 fixers.

184 (AM) colonization among two N2 - and two non-N2 -fixing seedlings, and grew them alone and in competi

185 P, whereas the poor N2 fixer and the two non-N2 fixers with high AM colonization grew best on inorgan

186 evels of tRNA-specific modified nucleosides (N2,N2-dimethylguanosine, N1-methylinosine), tricarboxyli

187 surpass the 2008 Robeson upper bounds for O2/N2, H2/N2, CO2/N2, H2/CH4 and CO2/CH4, with the potentia

188 Over 98% of N2 genes encoded unchanged products in VC2010; moreover,

189 gies may increase the competitive ability of N2 fixers relative to non-N2 fixers.

190 ratio, 3.38; 95% CI, 1.30-9.09), absence of N2 sleep transients (3.69; 1.69-8.20), predominant delta

191 ly implies that the metal-free activation of N2 with frustrated Lewis pairs may be achievable in the

192 unities on the production and consumption of N2 O, we have limited knowledge of the biological pathwa

193 2)(P4N2) complex catalyzes the conversion of N2 to N(SiR3)3 (R = Me, Et) at room temperature, represe

194 roach was taken complemented by detection of N2 O released and nitrogen isotope determinations of fer

195 This cut-point enabled improved detection of N2 patients and stage III disease (58% versus 37%, p = 0

196 ptimal staging through improved detection of N2/stage III disease.

197 otential energy surfaces for dissociation of N2 on an Fe-doped Au(111) surface.

198 I) complexes reveals that the free energy of N2 binding across three oxidation states spans more than

199 used to obtain thermodynamic measurements of N2 binding.

200 enitrification were the dominant pathways of N2 O production, and application of the nitrification in

201 catalytic activity for the photoreduction of N2 to NH3 in water at 25 degrees C under visible-light i

202 The dependent variable was the presence of N2 or N3 disease (vs. N0 or N1) as assessed by EBUS-TBNA

203 ification, a potential significant source of N2 O production in agricultural soils.

204 We determined the X-ray crystal structure of N2, combined with monitoring secretion efficiency in cel

205 n NO3(-) leaching but had a lesser effect on N2 O emissions.

206 nts with resectable high-risk T3, T4, and/or N2 CC on baseline computed tomography (CT) scan.

207 hrough water splitting, CO2 reduction and/or N2 fixation using photo- and photo(electro)catalytic pro

208 ents at a high risk of recurrence (T4 and/or N2), adjuvant chemotherapy should be offered for a durat

209 s used to predict the presence of N0, N1, or N2|3 disease.

210 Protonation of Os-N2(-) affords a structurally characterized Os=NNH2(+) hy

211 Nitrous oxide (N2 O) is a potent, globally important, greenhouse gas, p

212 Nitrous oxide (N2 O) is a powerful greenhouse gas with ozone depletion

213 AOB) are thought to emit more nitrous oxide (N2 O) than ammonia oxidising archaea (AOA), due to their

214 of the potent greenhouse gas nitrous oxide (N2 O), which is generated during denitrification and, in

215 e (CO2 ), methane (CH4 ), and nitrous oxide (N2 O).

216 Compartment and patch N2 O production was measured both before and after addit

217 had pathologic N1, 122 (78%) had pathologic N2 (pN2), and 4 (3%) had pathologic N3 (pN3) disease.

218 In node-positive patients, N2-class, but not LNR, was a significant predictor of su

219 m Xanthobacter autotrophicus, which performs N2 and CO2 reduction to solid biomass.

220 ity grew best on organic P, whereas the poor N2 fixer and the two non-N2 fixers with high AM coloniza

221 sition and pH-dependent reduction potential, N2 has long been considered a candidate for the elusive

222 ing bacteria (AOB) and archaea (AOA) produce N2 O, their relative activities in soil are unknown.

223 ticide and phosphor bronze, and the produced N2 might be collected and used as a protective gas or be

224 es decompose rapidly upon warming, producing N2.

225 ddition, two substitutions, H274Y and R292K (N2 numbering), were introduced into each NA gene for com

226 significantly affect bulk N2 fixation rates, N2 fixation was enhanced by amino acids in individual co

227 was hypothesized that AMF hyphae may reduce N2 O production.

228 ron-rich nitrogenases, with which it reduces N2 .

229 Ab to the Notch2-negative regulatory region (N2-NRR Ab).

230 lines widely used by C. elegans researchers (N2 hermaphrodite and male stocks).

231 e oxygen uptake, related Ni(mu-E(PhX))(mu-S'(N2))Fe (E = S or Se, Fe = (eta(5)-C(5)H(5))Fe(II)(CO)) c

232 four-membered ring core, Ni(mu-E(PhX))(mu-S'(N2))Fe, to a five-membered ring Ni-O-E-Fe-S', where an O

233 a 17-fold higher binding affinity for the SA-N2 bond with respect to that of SA-H3.

234 e in D3 symmetry involving two degenerate Sc-N2-Sc bonding orbitals.

235 Yield-scaled N2 O emissions (N2 O emissions divided by crop yields) w

236 ved tridomain unit that contains its second (N2) and third (N3) NEAT domains joined by a helical link

237 eria is an important contributor to sediment N2 production.

238 etion efficiency in cell culture of selected N2 single-domain mutants, finding that mutations located

239 ons of stage 2 non-rapid eye movement sleep (N2), mediate memory consolidation.

240 Soil N2 O and CH4 fluxes were measured for five crop-years (2

241 Both area- and yield-scaled soil N2 O emissions were greater with stover retention compar

242 guished from SARS-CoV-2 (SARS-CoV-2-specific N2 target).

243 , during non-rapid eye movement (NREM) stage N2 sleep, and in a hybrid BCM incorporating both awake a

244 terns was then reapplied during sleep stages N2 and SWS coupled to slow oscillations in a closed-loop

245 during non-rapid eye movement sleep (stages N2 and N3) and rapid eye movement sleep (stage R) were s

246 turnover required to reach 2.5% of starting N2 concentration (-0.88; 95% CI, -1.40 to -0.37; P = 0.0

247 embly employed a standard C. elegans strain (N2), it used sequence data from several laboratories, wi

248 from a cross between the laboratory strain (N2) and a wild strain (CB4856).

249 d so far in the laboratory reference strain (N2), grown at 20 degrees temperature.

250 ected by the head domain glycans, suggesting N2 is more amenable to glycan additions.

251 affect N1 stability more than N2, suggesting N2 is more accommodating to glycan additions.

252 rought frequency, which may affect symbiotic N2 fixation (SNF), a process that facilitates ecosystem

253 to the rational design of improved synthetic N2 fixation catalysts.

254 se (NA)-like protein (NA-F144C and NA-T342A, N2 numbering) that increased the virus titers in three m

255 domain glycans affect N1 stability more than N2, suggesting N2 is more accommodating to glycan additi

256 We found that N2-NRR Ab reduced TNF-induced osteoclastogenesis in PAR1

257 opes from the South China Sea indicates that N2 fixation covaried with sea level.

258 The N2 reduction reaction proceeds at a low driving force wi

259 tress-response function of scb-1 between the N2 and CB4856 strains, thereby leading to differences in

260 e second VWA domain of the alpha3 chain, the N2 domain, harbors several such mutations.

261 ed P sources in the seedling experiment: the N2 fixer with high N2 fixation and root phosphatase acti

262 o involve hydrogen atom abstraction from the N2-amine.

263 se activity and N2 fixation increased in the N2 fixers, allowing them to outcompete the non-N2 fixers

264 -configuration was evidenced earlier, in the N2 time-window.

265 nitrification inhibitor DMPP can inhibit the N2 O production from nitrifier-induced denitrification,

266 .012) and shorter latency (p = .029) of the N2 component of event-related brain potential, for 60 mi

267 gate structure-function relationships of the N2 mutations to shed light on their possible myopathy me

268 ctors that may have driven the spread of the N2-fixation mutualistic trait.

269 ycosylated on N1 and N3 sites but not on the N2 site.

270 e phosphate (DMPP) significantly reduced the N2 O production from these pathways; this is probably du

271 Thus, the N2 assembly has many differences from any C. elegans ava

272 enetically divergent strains compared to the N2 reference strain.

273 A mechanistic understanding of these N2 O production biological pathways in complex soil envi

274 Pharmacologic inhibition of IP6K by TNP [N2-(m-Trifluorobenzyl), N6-(p-nitrobenzyl)purine] recapi

275 Relative contributions of AOA and AOB to N2 O production, therefore, reflect their respective con

276 found that a monovalent SA receptor binds to N2 with a significantly higher bond lifetime (270 ms) co

277 ude that the histidine is hydrogen-bonded to N2, tuning its reduction potential.

278 trous oxide (N2O); and (3) N2O conversion to N2 with energy generation.

279 ate flux, suggesting that denitrification to N2 and not facultative nitrate reduction by Geobacter sp

280 Our VC2010 assembly has 99.98% identity to N2 but with an additional 1.8 Mb including tandem repeat

281 eutrons to probe pore spaces inaccessible to N2 and mercury.

282 s they have the ability to oxidize NH4(+) to N2 under anoxic conditions using NO2(-).

283 Conversion of nitrate to N2 by denitrification in sediments accounts for half or

284 Model denitrifiers convert NO3- to N2 , but it appears that a significant fraction of natur

285 s were available to completely reduce NOx to N2, resulting in increased N2O accumulation.

286 diameter intervals) inaccessible porosity to N2 was determined using SANS and LPNP data.

287 ular mycorrhizal (AM) colonization among two N2 - and two non-N2 -fixing seedlings, and grew them alo

288 l betalains on the lifespan of the wild-type N2 strain was carefully studied using the automatic plat

289 tment with 2.5 uM dietary flavonoid or 10 uM N2-(m-trifluorobenzyl), N6-(p-nitrobenzyl) purine], to i

290 In the absence of CO (under N2 atmosphere), the reaction did not proceed, and only s

291 logical pathways and mechanisms underpinning N2 O emissions from drylands, which are estimated to acc

292 Unlike N2 (another group 2NA), H274Y conferred highly reduced i

293 quantified the loss of bioluminescence using N2 reference worms and eat-2 mutants, and found a nearly

294 Similarly, in vitro N2-NRR Ab reduced RANKL-induced osteoclastogenesis in PA

295 ogenic non-fixers within root nodules, where N2-fixation occurs, even when they share the same nodule

296 at germ extract translation systems, whereas N2-methylguanosine (m2G) moderately impeded translation.

297 terocyclic carbene=C[((i) Pr)NC(Me)]2 ) with N2 O furnishes the first Si-metalated iminosilane, [Dipp

298 ELN was independently associated with N2-status (OR 1.27, p < 0.001).

299 vant radiation therapy for each patient with N2 disease.

300 patients with N1 stage, eight patients with N2 stage, and two patients with N3 stage.

301 ctrophilic borylene such as 1 can react with N2 reversibly and with CO irreversibly under photochemic