ライフサイエンスコーパス: mono-

1 Consistent with theoretical predictions, the mono-(13)C ((13)C identical with(12)C) and bis-(13)C ((1

2 nd 225 depicted hypermethylation, whereas in Monos, 155 hypomethylated loci and 247 hypermethylated l

3 o (2-ethyl-5-oxohexyl) phthalate (MEOHP) and mono (2-ethyl-5-hydroxyhexyl) phthalate (MEHHP).

4 MBzP), mono (2-ethylhexyl) phthalate (MEHP), mono (2-ethyl-5-oxohexyl) phthalate (MEOHP) and mono (2-

5 hthalate (MBP), monobenzyl phthalate (MBzP), mono (2-ethylhexyl) phthalate (MEHP), mono (2-ethyl-5-ox

6 Mono-(2,3-manno-epoxide) alpha-, beta-, and gamma-CDs we

7 di-2-ethylhexyl phthalate (DEHP) metabolites mono-(2-ethyl)-hexyl phthalate (MEHP) and mono-(2-ethyl-

8 es mono-(2-ethyl)-hexyl phthalate (MEHP) and mono-(2-ethyl-5-carboxypentyl) phthalate (MECPP), as wel

9 us preterm births were examined alone, MEHP, mono-(2-ethyl-5-oxohexyl) phthalate, MECPP, Sigma DEHP,

10 allocated 587 participants to OT (291) or PI-mono (296).

11 exyl) phthalate, MECPP, Sigma DEHP, MBP, and mono-(3-carboxypropyl) phthalate metabolite levels were

12 nthetic approaches for the preparation of 5'-mono-, 5'-di-, and 5'-triphosphorylated nucleosides, als

13 The particles, consisting of the mixtures of mono- (acetic, propanoic, p-toluic, and cis-pinonic acid

14 In order to visualise both Poly-, and Mono-, ADP-ribosylation in vivo, we engineered specific

15 The increasing complexity of both mono, and particularly combination therapies presents a

16 activity on ribo- and deoxyribonucleoside 5'-mono- and 5'-diphosphates with a substrate specificity d

17 X-ray characterization of a mono- and a disubstituted derivative as a racemic mixtur

18 ovides access to the minimalist core of beta-mono- and beta,beta'-disubstituted porphyrins from readi

19 e we used the CRISPR/Cas9 system to generate mono- and bi-allelic null mutations in the Tyr locus by

20 mework that allows selective introduction of mono- and bi-allelic sequence changes with high efficien

21 Similarly, the mono- and bi-exponential short and long T2 relaxation ti

22 y-controllable devices realized with undoped mono- and bi-layer 2D materials.

23 In addition, using a trilayer graphene, mono- and bi-layer graphene could be successfully fabric

24 ar precursors in the controlled synthesis of mono- and bi-layer WS2 leads to superior material qualit

25 We create point-like strain perturbations in mono- and bi-layer WSe2 which locally modify the band-ga

26 ms of this structural transformation in both mono- and bi-layered MoS2 using density functional theor

27 nitride and transition metal dichalcogenide mono- and bi-layers.

28 significant amount of Bid in the cytosol is mono- and bi-ubiquitinated.

29 were able to achieve the highest Th wt % in mono- and biactinide frameworks with minimal structural

30 We then compare mono- and biallelic genes at three distinct scales.

31 ture chemically diverse structures, spanning mono- and bicyclic compounds, that either inhibited or a

32 A number of mono- and bidentate ligands have also proven to be effec

33 imultaneous quantification of bitter-tasting mono- and bidesmosidic saponins in fresh and processed a

34 The mono- and biexponential models were fitted pixel-wise to

35 by introducing various phase-separated lipid mono- and bilayers to the MACs.

36 Shown herein is that mono- and binuclear organoscandium complexes with a bora

37 rk, N-nitro- and N-nitroamino-functionalized mono- and bis(1,2,4-triazoles) were synthesized and char

38 Mono- and bis(imidazolidinium ethynyl) cations have also

39 However, in recent years, a few mono- and bis(Lewis base)-stabilized borylenes have been

40 ucts of C70, which are the precursors of the mono- and bis-adduct final products.

41 ime of catalysis, the in situ formed neutral mono- and bis-alkynylated iron(II)-SciOPP complexes are

42 A time dependent selective mono- and bis-aroylation can be achieved.

43 Syntheses and optical properties of mono- and bis-chromene-annulated bacteriochlorins are de

44 bacteriochlorin-type optical spectra of the mono- and bis-chromene-annulated bacteriochlorins are mo

45 aminal derivatives in various ratios to form mono- and bis-functionalized quaternary ammonium salts.

46 ed that enable access to a variety of unique mono- and bis-heterocyclic scaffolds.

47 Both mono- and bis-ligation modes were studied (n = 1 and 2).

48 pectively, but XANES data revealed that both mono- and bis-nitrene species are six-coordinate O(h) sp

49 The mono- and bis-nitrene species were initially expected to

50 Importantly, mono- and bis-phenylated iron(II)-SciOPP species that fo

51 Regiospecific C-N photocyclization of mono- and bis-styryl-substituted N-heterocycles was inve

52 Mono- and bis-terphenyl complexes of molybdenum and tung

53 erocyclic compounds was accomplished through mono- and bis[3 + 2]-cycloaddition reactions of (2E,4E)-

54 A series of Hoechst 33258 based mono- and bisbenzimidazoles have been synthesized and th

55 lorins to morpholine moieties yields ruffled mono- and bismorpholinobacteriochlorins with broadened a

56 trically driven critical bifurcation between mono- and bistability.

57 s, we were able to differentiate between the mono- and bivalent binding modes during individual antib

58 o non-MC-producing Microcystis strains under mono- and co-culture conditions.

59 Mono- and cross-reactive CD8 T cells use distinct TCRB C

60 Mono- and di-(18)F-labeled derivatives of phenolsulfonph

61 encoded in the pyoluteorin gene cluster into mono- and di-chlorinated phloroglucinols.

62 ind that KDM3A, a histone H3 lysine 9 (H3K9) mono- and di-demethylase, plays a pivotal role in anoiki

63 tructural and functional characterization of mono- and di-domain ARO/CYCs in bacterial type II polyke

64 ed the best in oil enrichments compared with mono- and di-glycerides.

65 rms several monounsaturated fatty acids into mono- and di-hydroxylated derivatives.

66 We have identified the histone H3 lysine 9 mono- and di-methyl demethylase enzyme KDM3A as a positi

67 Enhancers are marked by histone H3K4 mono- and di-methylation (H3K4me1/2).

68 ible for the majority of histone H3 lysine 9 mono- and di-methylation (H3K9me1/me2).

69 ) CICs, by directly regulating the levels of mono- and di-methylation of histone H3 lysine-4 at the p

70 ressor MLL4 (KMT2D) is a major enhancer H3K4 mono- and di-methyltransferase with a partial functional

71 able precursors for selective preparation of mono- and di-N-protected C-functionalized cyclams and C-

72 g., aromatic substituents, halides, isolated mono- and di-substituted double bonds, esters, silyl eth

73 the presence of Agave fructans that had been mono- and diacylated with lauric acid.

74 Unlike diacetyl tartaric esters of mono- and diacylglycerols (DATEM, used as control), lipa

75 in the presence of potassium carbonate gave mono- and dialkylation products, and treatment of the fo

76 Various mono- and diamines are oxidized into corresponding monon

77 e highest-occupied molecular orbitals of the mono- and dianionic clusters consist of a combined pi*-f

78 ube which is capable of binding a variety of mono- and dianionic guests within an enclosed cavity gre

79 c)2 as the catalyst and AgO as the promoter, mono- and diarylation of anilides were realized in up to

80 Both mono- and diarylations were performed under ambient oxyg

81 We synthesized a series of mono- and dibenzoates and identified three dibenzoates [

82 ving formation and isomerization of the acyl mono- and dicarbonyl intermediates and their hydrogenoly

83 hy-mass spectroscopy technique to measure 11 mono- and dicarboxylic acids from plain and KOH impregna

84 tic character, but upon protonation aromatic mono- and dicationic species were generated.

85 The reaction was utilized for the late-stage mono- and dichlorination of a range of target compounds

86 approximately 10(11)-fold for both phosphate mono- and diester hydrolysis by each enzyme indicated th

87 troscopy, 11 Po species were detected in the mono- and diester region.

88 tope effects (KIEs) for a range of phosphate mono- and diester substrates.

89 of a series of cyclitol derivatives, namely mono- and diesters of 1,2:5,6-di-O-isopropylidene-myo-in

90 phthyrid in-6-one (5), and related cis-diols mono- and diesters were designed and synthesized.

91 The mono- and diformylated azaBODIPYs were treated with pyrr

92 built up sequentially using a combination of mono- and difunctionalized clusters, giving an unprecede

93 ersion that is selective for mixtures of the mono- and difunctionalized TFA esters.

94 Through molecular docking studies mono- and dihaloacetates are identified as potent PDK2 b

95 The halopyrrole moieties of mono- and dihalopyrrole-containing compounds arise from

96 lable in the literature allow one to prepare mono- and diheteroporphyrins and their functionalized de

97 The gold-catalyzed mono- and dihydrofluorination of alkynes using the DMPU/

98 Additionally, mono- and dihydroxy-GDGT analogs (including novel specie

99 Mono- and dihydroxy-metabolites, together with glucuroni

100 These include mono- and dihydroxylated TBECH and mono- and dihydroxyla

101 e include mono- and dihydroxylated TBECH and mono- and dihydroxylated TriBECH as well as an alpha-oxi

102 and suggesting discrete biological roles for mono- and dimethylarginine-modified proteins.

103 e show here that the PikR1 and PikR2 enzymes mono- and dimethylate, respectively, the N6 amino group

104 -2 binding highly correlates with histone H3 mono- and dimethylated at lysine 9 (H3K9me1 and H3K9me2)

105 ethylase 1, also known as KDM1) demethylates mono- and dimethylated H3K4 in peptide substrates, but r

106 idylethanolamine (PE) or chemically by using mono- and dimethylated PE.

107 to activation of poised (histone H3 lysine 4 mono- and dimethylated) enhancers, as evidenced by the a

108 ming the MLL1 core complex required for H3K4 mono- and dimethylation and transcriptional activation.

109 que pathway of PRMT5-MEP50 catalyzed histone mono- and dimethylation of chromatin at key metastasis s

110 (MLL1) core complex predominantly catalyzes mono- and dimethylation of histone H3 at lysine 4 (H3K4)

111 G9a form a heterodimer complex and catalyze mono- and dimethylation of histone H3 lysine 9 and nonhi

112 The G9a/GLP complex mediates mono- and dimethylation of Lys9 of histone H3 at specifi

113 EHMT1/2 catalyze mono- and dimethylation of lysine 9 on histone 3 (H3K9),

114 While DFT studies of mono- and dinuclear copper dinitrogen complexes suggest

115 We compared a number of different mono- and dinuclear geometries, in some cases enhanced w

116 We report the synthesis of novel mono- and dinucleotide cap analogues containing dihaloge

117 espondingly phenocopied by overexpression of mono- and diphosphomimetic RLC mutants.

118 des are innocuous to all the cell lines, the mono- and diphosphorylated D-tetrapeptides selectively i

119 d central SF viscoelastic properties through mono- and diphosphorylation of RLC, offering new quantit

120 n't Hoff analysis of the equilibrium between mono- and dipyridine adducts (extrapolated Keq,0 approxi

121 n A consists of a 20-membered macrolide with mono- and disaccharide moieties.

122 SWEETs carry mono- and disaccharides across vacuolar or plasma membra

123 le constituents and increased the release of mono- and disaccharides by up to 94%.

124 uorescence microscopy to study the effect of mono- and disaccharides on membranes that phase separate

125 method works well with both sugars (such as mono- and disaccharides) and nonsugars (such as inositol

126 ed fatty acids, polyunsaturated fatty acids, mono- and disaccharides, protein, cholesterol, dietary f

127 lent cross-links were glycosylated with both mono- and disaccharides, whereas the mature, trivalent c

128 have prepared a range of highly enantiopure mono- and disubstituted alpha-sulfinyl benzoates, some b

129 lyzed cross-coupling reactions provides both mono- and disubstituted derivatives, the latter obtained

130 The stability of mono- and disubstituted disulfides was determined to be

131 The ability of CD-MOF to separate various mono- and disubstituted haloaromatic compounds appears t

132 rly distinguishing between the reactivity of mono- and disulfide-derived (vicinal or neighbors-throug

133 ng of diazonium salts or by self assembly of mono- and dithiolated hydrazide linkers, resulting in fi

134 quantification of thiol pKa values for both mono- and dithiols in water.

135 the mouth, dietary fat constituents such as mono- and diunsaturated fatty acids give rise to taste s

136 topology, can be induced by the addition of mono- and divalent cations to aqueous U60 solutions.

137 dylethanolamine (DOPE), with the addition of mono- and divalent salts.

138 30 mo of postnatal life from eight pairs of mono- and dizygotic Malawian twins concordant for health

139 ibutions of site-specific phosphorylation of mono- and doubly phosphorylated forms on MEK1 activity.

140 With FITC as the reference signal, the mono- and dual-color emission allow efficient in situ di

141 followed by electrophilic quench affords exo-mono- and exo,exo-bis-substituted derivatives of Troger'

142 report that high-quality single-crystalline mono- and few-layer BN nanosheets are one of the stronge

143 thermore, it was possible to prove that both mono- and few-layer hydrogenated/deuterated graphene can

144 Atomic force microscopy reveals mono- and few-layer island growth, while conducting atom

145 However, the electron mobility of mono- and few-layer MoS2 has so far been substantially b

146 elease of indole is essential for priming of mono- and homoterpenes in systemic leaves of attacked pl

147 ntial and toxic element concentrations in 34 mono- and multi-floral honey samples from four geographi

148 re defined to check the authenticity of both mono- and multi-floral honey.

149 e parameters for bulk 2H-MX2 (our work) with mono- and multi-layer MX2 (published), we found that sta

150 Mono- and multi-layered molybdenum disulfide (MoS2) is c

151 Upon visible-light irradiation, typical mono- and multi-substituted aromatic olefins could be co

152 Rotaxane mono- and multilayers are shown to reversibly switch in

153 strates the successful deposition of ordered mono- and multilayers of chemically switchable rotaxanes

154 have calculated the electronic structures of mono- and multiple layers (bulk) of CuSbS2 using the hyb

155 reduction in the steady-state levels of the mono- and nonglycosylated forms of PrP in the brain.

156 stributive mode is employed by TUT7 for both mono- and oligo-uridylation in the absence of Lin28.

157 ing a large number of carbohydrates, several mono- and oligosaccharides could be identified as substr

158 composition of the POS mixtures in terms of mono- and oligosaccharides was assessed at the molecular

159 anomeric selectivities for both anomers with mono- and oligosaccharides, deoxysugars, saccharides wit

160 nanoparticle receptors for a wide variety of mono- and oligosaccharides.

161 lation and de-PARylation, respectively) from mono- and poly(ADP)-ribosylated proteins, respectively.

162 to match the total normalized impacts of the mono- and poly-Si, CIGS, CdTe, and a-Si devices, the SWC

163 Mono- and poly-SUMOylations of target proteins provide d

164 Applying our method to the detection of mono- and poly-Ub molecules, we show that we can analyze

165 responding HAs in a larger contribution from mono- and polyaromatic hydrocarbons and heterocyclic hyd

166 e results agreed within error for saturates, mono- and polyaromatics.

167 ant to influenza A virus infections, to both mono- and polybasic subtypes.

168 dependent transcription terminators for both mono- and polycistronic transcripts.

169 nzene as a suitable reference, the AIs of 30 mono- and polycyclic conjugated hydrocarbons are calcula

170 MTHFD2L uses the mono- and polyglutamylated forms of CH2-THF with similar

171 ay results in the instantaneous formation of mono- and polyhydroxylated aromatic rings (PHA) and chro

172 ylated aromatic rings (PHA) and chromophoric mono- and polyhydroxylated quinones (PHQ), a different c

173 ligands available, the applications of their mono- and polynuclear metal complexes are very diverse a

174 adienyl and M=Ir or Rh) with pillar[5]arene, mono- and polynuclear pillar[5]arenes, a new class of me

175 and immunological differences exist between mono- and polysensitized subjects.

176 e termination sites are consistent with both mono- and polysynaptic connections between these afferen

177 and leads to increased spasms and excessive mono- and polysynaptic low threshold spinal reflexes in

178 Unexpectedly, all mono- and polysynaptic ST afferent pathways to NTS-CeA n

179 ary gustatory cortex (GC) is connected (both mono- and polysynaptically) to primary olfactory (pirifo

180 By mono- and polyubiquitinating target proteins, parkin reg

181 ts, and PCNA phosphorylation was followed by mono- and polyubiquitination.

182 vels of malic and fumaric acids, sucrose and mono- and polyunsaturated fatty acids (MUFA and PUFA).

183 ds (FFA) and the concentration of saturated, mono- and polyunsaturated fatty acids.

184 sed plasma concentrations of LPCs containing mono- and polyunsaturated fatty acyl chains, indicative

185 ng the specificity of MFSD2A for LPCs having mono- and polyunsaturated fatty acyl chains.

186 and (13)C NMR spectra of mixtures of racemic mono- and prochiral bis-deuterated glycine-2-(13)C were

187 ny places the enzyme with two-domain TPSs of mono- and sesqui-terpene biosynthesis.

188 By contrast, the mono- and sesquiterpene synthases represent a distinct c

189 Here, 2D culture and 3D mono- and stromal co-culture models of increasing comple

190 numerous residues are critical for both the mono- and the poly-ADP-ribosylhydrolase activity of ARH3

191 crystallization in the presence of sorbitan mono- and triesters or canola oil was investigated.

192 d mono- to hexafluoroalkyl carboxylic acids, mono- and trifluoroalkyl carboxylic acid ethers, and nov

193 les detection of histone modifications (H3K4 mono- and trimethylation) and two yeast histone demethyl

194 lustered particles (Dh,DLS = 195 nm) and the mono- and trinuclear Cu sites of bilirubin oxidases.

195 cil and cytosine 2'-deoxyribonucleosides and mono- and triphosphates were synthesized through aqueous

196 nstrate their therapeutic potential in vivo, mono- and trivalent Abeta-specific DARPins (D23 and 3xD2

197 dec exhibited reversible interaction between mono- and-di-hexamer forms.

198 hat are available in ultrathin forms such as mono-, bi- and multilayers, which are commonly known as

199 onstrated by the controlled production of 22 mono-, bi- and trilayer graphene stacks encapsulated in

200 leading to the formation of enantioenriched mono-, bi-, and tricyclic products.

201 de (TIPS-CC-MgBr) leads to a distribution of mono-, bis-, and tris-alkynylated iron(II)-SciOPP specie

202 man astrocytes, and human brain pericytes in mono-, co-, and tricultures.

203 The nucleosides were converted to 5'-O-mono-(dA(SR)MP) or triphosphates (dA(SR)TP) by phosphory

204 ermine the relationship between methylation (mono, di, and tri) of this residue and nucleosome turnov

205 ion of unmodified nucleosides and nucleotide mono-, di- and tri-phosphates by capillary electrophores

206 in acetonitrile was also performed yielding mono-, di- and tri-stearic ester derivatives.

207 e)2Cu complex the reaction mixture generated mono-, di- and tri-substituted sugar complexes and their

208 The ion signal intensities of mono-, di-, and oligohexosylceramides were enhanced by u

209 igurational assignment of substances bearing mono-, di-, and perfluoroalkyl rather than trifluorometh

210 n to separate diesel samples into saturates, mono-, di-, and polyaromatics by gas chromatography, wit

211 ach to the construction of highly oxygenated mono-, di-, and polycyclic carbocycles from the reaction

212 fully applied to a variety of alpha- or beta-mono-, di-, and polythiosugar derivatives to synthesize

213 The successive oxyfunctionalization to mono-, di-, and tetraepoxy derivatives is accomplished u

214 The final mono-, di-, and tetravalent ligands were resistant to en

215 lammonium bromide salts (TAA), benzylamines (mono-, di-, and tri-), and illicit drugs (MA, MDEA, and

216 -23, 20-49 and 64-124ngmL(-1) for nucleotide mono-, di-, and tri-phosphates, respectively, were found

217 ysis of the photolysis of this and six other mono-, di-, and triazastilbenes in solid and solution st

218 pellers, fluidic and multicompartments) with mono-, di-, and tricomponents configurations were achiev

219 The synthesis of mono-, di-, and trifluoromethyl aryl ethers by fluorodec

220 A wide range of readily available mono-, di-, and trifluoromethyl heteroaryl sulfones can

221 ange process was used to prepare a series of mono-, di-, and trifunctionalized mesoporous metal-organ

222 ometric analysis to differentiate a panel of mono-, di-, and triglycerides.

223 The stability of seven mono-, di-, and trihaloacetonitriles was examined under

224 e-triphosphinate) and NODAGA, we synthesized mono-, di-, and trimeric conjugates of the alphavbeta6 i

225 e-triphosphinate) and NODAGA, we synthesized mono-, di-, and trimeric conjugates of the alphavbeta6 i

226 pic, and azelaic acid) acid with alkylamine (mono-, di-, and trimethylamines), represent those common

227 active histone methyltransferase catalyzing mono-, di-, and trimethylation of the H3K4 mark.

228 e sole lysine methyltransferase required for mono-, di-, and trimethylation of this site.

229 Mono-, di-, and triPAPs, including several diPAP homolog

230 In this study, mono-, di-, and triPAPs, perfluorinated alkyl acids (PFA

231 C25A36 cytosine and uracil (deoxy)nucleoside mono-, di-, and triphosphates by uniport and antiport.

232 Three different phosphoinositide phosphates (mono-, di-, and triphosphorylated inositides), a phospha

233 dentified binding to the oligosaccharides of mono-, di-, and trisialylated gangliosides.

234 s in the surfactant, including PEO(n)-glucam mono-, di-, and tristearates as well as free and esterif

235 A range of mono-, di-, and trisubstituted olefins as well as alkyl-

236 An array of olefins, including mono-, di-, and trisubstituted olefins, are all smoothly

237 The present method allows the synthesis of mono-, di-, and trisubstituted pyrroles with appropriate

238 nworm (Manduca sexta), which uses a blend of mono-, di-, and uncommon triunsaturated fatty acid (3UFA

239 , with suggestions of a dinuclear Fe site or mono-, di-, or trinuclear Cu sites.

240 y, a library of 20 CBMs was synthesized with mono-, di-, or trisaccharides at each site for compariso

241 he conformational ensembles of unacetylated, mono-, di-, tri-, and tetra-acetylated H4 histone tails

242 binding of the Sir proteins to reconstituted mono-, di-, tri-, and tetra-nucleosomal chromatin templa

243 s the direct regioselective incorporation of mono-, di-, tri-, and tetrasubstituted olefins at the al

244 ospecific conversion of structurally diverse mono-, di-, tri-, and tetrasubstituted olefins to N-H az

245 The separation of myo-inositol mono-, di-, tri-, tetra-, pentakis-, and hexakisphosphat

246 SAv constructs having controlled valencies (mono-, di-, trivalent in terms of biotin-binding sites)

247 nctional diversity at the ring and featuring mono, double, or spiro substitution at the sp(3) positio

248 6(-) monocytes, TSLPR(+) monocytes (TSLPR(+) mono), expresses TSLPR complex upon LPS stimulation in a

249 lution-based approaches for the synthesis of mono-, few-, and multiple layers of CuSbS2.

250 m autochthonous and nonautochthonous grapes, mono- from the plurivarietals, and identifying, in part,

251 146 participants (75 PI-mono) had neurocognitive testing (median time after rand

252 ous 3D models including adherent/suspension, mono-/heterocellular cultures and several disease types.

253 lysis revealed specific features of TSLPR(+) mono, including higher CCL17 and IL-10 production and in

254 y methylated loci were common in both WB and Monos, including thioredoxin-interacting protein (TXNIP)

255 rases that methylates inorganic As(III) into mono- (MAs(III)), di- (DMAs(III)) and tri- (TMAs(III)) m

256 systematically studied under a wide range of mono- (NaCl) and divalent (CaCl2) electrolytes and using

257 DNA-me was also profiled in blood monocytes (Monos) of the same patients obtained during EDIC Study y

258 on converting NAE 12:0-glucoside to NAE 12:0-mono- or -dimalonylglucosides providing direct evidence

259 d pinacol ester, additions to ketones with a mono- or a difluoromethyl group were highly enantioselec

260 es or other members of the HR pathway and if mono- or bi-allelic alterations of HR-related genes have

261 tential of these materials and the growth of mono- or bi-layers with high crystal quality is yet to s

262 re obtained from 11 patients carrying either mono- or biallelic variants, including 1 case harboring

263 Mono- or biexponential functions were fitted to measured

264 ity may reveal novel strategies suitable for mono- or combinatorial cancer therapies.

265 hether the former group of CCOs functions as mono- or di-oxygenases.

266 e selectively ortho-alkylated to give either mono- or dialkylated products by simply adjusting the am

267 he allylating agent used, selectively either mono- or diallylated products were readily synthesized.

268 hromatic color discrimination opposed to the mono- or dichromacy found in other lampreys.

269 Selective mono- or difluorination of oxalyl amide-protected benzyl

270 by N-tert-butyl amides, is achieved to avail mono- or dihydroarylated amide products selectively in a

271 itriles selectively provide stable NHC-boryl mono- or dinitriles, depending on the nitrile source.

272 Crystal structures have shown a mono- or dinuclear Cu site, but the resolution was low a

273 xy acids with C8 to C10 carbon backbones and mono- or diperoxy acid functionality.

274 CD) fragmentation of glycopeptides generates mono- or disaccharide ions called oxonium ions that carr

275 uinone (BQ) can be controlled to give either mono- or disubstituted BQ, including the installation of

276 the RNA conformation as a function of either mono- or divalent ion concentration.

277 Herein, we investigated the effect of mono- or divalent small-molecule albumin binders for hal

278 After treatment with ceftriaxone mono- or dual therapy (with azithromycin or doxycycline)

279 a carbohydrate-destroying chemical (NaIO4), mono- or oligosaccharides (N-acetylneuraminic acid, gala

280 the different domains that interpret either mono- or poly-ADP-ribosylation and the implications for

281 This modification can occur as mono- or poly-ADP-ribosylation.

282 ools to dissect pathways depending on either mono- or poly-SUMOylation are largely missing.

283 e ion serves as a core upon which up to nine mono- or polycyclic aromatic hydrocarbon ligands are exo

284 immunostained with antibodies to histone H3 mono- or tri-methylated at lysine 4 (H3K4me1, H3K4me3).

285 trast to its hypoxia-regulated activity, VHL mono-, rather than poly-ubiquitinates AURKA, in a PHD-in

286 th herbs and pepper include large amounts of mono-, sesqui- and diterpenes as well as various terpeno

287 nfalpha alleles, which was necessary for the mono- to biallelic switch in gene expression.

288 ectionality of electron transfer, i.e., from mono- to bidirectional, between the redox-active metal c

289 Human dermal absorption of eight mono- to deca-brominated diphenyl ethers (PBDEs) was inv

290 non-acylated anthocyanins was increased from mono- to di- to triglycosyl moieties, possibly due to st

291 The identified candidates included mono- to hexafluoroalkyl carboxylic acids, mono- and tri

292 tennary, core and terminal fucosylation, and mono- to trisialylation.

293 have previously reported increased monocyte (Mono) trafficking into the retinas of diabetic animals.

294 sing IMS MS, the entire series starting from mono- up to octasialylated GGs was detected in FL37.

295 Formation of mono- versus diborylated methane is tunable as a functio

296 id oxygenase, a site predicted to govern the mono- versus dioxygenase tendency of CCOs, greatly reduc

297 ential features of the E2 that differentiate mono- versus polyubiquitinating E2 enzymes remain unclea

298 integer (non-Kramers) spin states and (iii) mono- vs. multi-frequency EPR spectra.

299 r-boosted protease inhibitor monotherapy (PI-mono); we recommended ritonavir (100 mg)-boosted darunav

300 emoglobin: the quaternary two-state model of Monod, Wyman, and Changeux; the tertiary two-state model