ライフサイエンスコーパス: mono-

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

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

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

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

5 the PFA(Bi) group (18/18 PFA(Bi), 10/18 PFA(Mono), 3/6 radiofrequency, P=0.002).

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

7 s post-processed using kurtosis (ADC(k), K), mono- (ADC(m)), and biexponential functions (f, D(p), D(

8 polar PFA was performed with monophasic (PFA(Mono)) and biphasic (PFA(Bi)) waveforms in 7 and 7 swine

9 rategy is a highly efficient regiospecific 7-mono- and 7,12-di-phenoxy bay substitution at the "imide

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

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

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

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

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

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

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

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

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

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

20 ppressive role of TP53, patients harbor both mono- and biallelic mutations(10).

21 mutations increased RHV replication of both mono- and bicistronic constructs, and CpG/UpA-dinucleoti

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

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

24 Vi monomer both de-O- and de-N-acetylated by mono- and bidimensional Nuclear Magnetic Resonance spect

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

26 py, propagating surface phonon polaritons in mono- and bilayer hBN microcrystals are imaged.

27 as with small mode volumes coupled to atomic mono- and bilayers of WSe[Formula: see text].

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

29 ing experiments through detection of protein mono- and bilayers, where the geometrical parameters fav

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

31 The mono- and biradicals produce abundant thiomethyl abstrac

32 nitoring proton transfer from the protonated mono- and biradicals to reference bases with known proto

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

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

35 Dissociated bipyridyl ligand is oxidized to mono- and bis- N-oxide species under the reaction condit

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

37 s why the Ge atom can form the corresponding mono- and bis-AlBr(3) Ge -> Al Lewis adducts [Si(II)(Xan

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

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

40 hat tetradentate Fe(III) complexes formed by mono- and bis-catechol species are important Fe sources

41 moieties, providing access to 6 selectively mono- and bis-fucosylated oligosaccharides.

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

43 ed by oriented photografting of a variety of mono- and bis-imidazolium host monomers at subzero tempe

44 A simple method for the direct mono- and bis-organylselenylation of N-substituted pyrro

45 l energy surface, which allows separation of mono- and bis-peroxide tricyclic products, also explains

46 d crystal structures of 14-3-3sigma bound to mono- and bis-phosphorylated APN-derived peptides, which

47 tripodal molecule that acts as receptor for mono- and bis-phosphorylated PIPs in a cell free environ

48 nd stabilizing distinct plant phenol-derived mono- and bis-quinone methide intermediates during diffe

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

50 Two regioisomeric pairs of heptahelical mono- and biscoumarins that are differentiated by "inwar

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

52 vealed atomic details of the binding mode of mono- and bivalent 14-3-3 interactions.

53 computational results indicate that both the mono- and co-catalytic processes proceed via stepwise [4

54 Most mono- and co-culture bioprocess applications rely on lar

55 try, we characterized the growth patterns of mono- and co-cultures using a mathematical model of intr

56 le CD163 and neopterin were decreased in HCV mono- and coinfected persons.

57 y used OCA and ELA to compare the effects of mono- and combination therapies on metabolic and histolo

58 ight loss over time when compared to chronic mono- and combined-treated groups, without affecting GLP

59 is general and allows for synthesizing both mono- and di-, tri-, and poly( p-carboxyphenyl)siloxanes

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

61 Synthesis of mono- and di-heteroarylation of quinoxaline was performe

62 Mild mono- and di-hydrodehalogenative reductions of gem-dibro

63 talyze N-demethylation of N-methylated (both mono- and di-methylated) arginine residues of histones a

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

65 terminate developmental plasticity, through mono- and di-methylation of H3K9 (me1/me2), and promotes

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

67 findings were also applied in unprecedented mono- and di-N-arylation of amino acid derivatives (lysi

68 Mono- and di-nucleotide repeats motifs were found in a h

69 enotypes on lactose, but also on a number of mono- and di-saccharides that involve the glucose-PTS or

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

71 me regulates brassinosteroid homeostasis via mono- and diacetylation of castasterone

72 show that the ATAD2B bromodomain recognizes mono- and diacetyllysine modifications on histones H4 an

73 e concentration, and reaction temperature on mono- and diacylglycerol production and I(t) are all ass

74 olyricinoleate (PGPR), citric acid esters of mono- and diacylglycerols (CITREM) and ammonium phosphat

75 The production of mono- and diacylglycerols rich in polyunsaturated fatty

76 C, producing a content of 24.8% and 51.9% of mono- and diacylglycerols, respectively, over an I(t) of

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

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

79 systems shows a time-dependent formation of mono- and dianionic species, and the latter was isolated

80 Mono- and dianions of 2-tert-butyl-3a(2) -azapentabenzo[

81 ew routes toward selective synthesis of both mono- and diaryl maleimides have been innovated.

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

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

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

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

86 Mono- and dichlorinated PCBs were released from the colo

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

88 ion years ago during the early divergence of mono- and dicotyledonous clades.

89 DAC*), along with carbazolyl (Cz) as well as mono- and dicyano-substituted Cz derivatives.

90 This protocol is compatible with both mono- and dienes and exhibits a good functional group to

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

92 were significantly higher than those of the mono- and diesters.

93 The mono- and diformylated azaBODIPYs were treated with pyrr

94 eported, allowing access to a broad range of mono- and difunctionalized products.

95 eup, which is dominated by the galactolipids mono- and digalactosyldiacylglycerol (MGDG and DGDG).

96 caseinate, diacetyl tartaric acid esters of mono- and diglycerides (DATEM), and/or modified DATEMs w

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

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

99 ared di-m-benzipentapyrrane with appropriate mono- and diheterocyclic dialcohols selectively produced

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

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

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

103 The diffusion constants of both mono- and diinterstitials are measured and found to be s

104 The higher abundance of mono- and dimeric sites for the Mo system, their ease of

105 iques to dissect the biosynthetic pathway of mono- and dimethyl FuFAs and their intermediates in two

106 esidues, 12,13-difluorocyclopropyl moieties, mono- and dimethylated macrolactones, and 1-keto macrocy

107 Maximum thiolation of mono- and dimethylated oxyarsenates was about 70% and 10

108 e position of a single methyl group for both mono- and dimethylated variants.

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

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

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

112 his catalytic reaction involves both nonheme mono- and dinitrosyl diiron(II) species as the key inter

113 We present a set of 13 new stable mono- and dinitroxide PAs for MAS DNP NMR where this pri

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

115 e chemistry afford various CF(3)-substituted mono- and dinucleoside oligophosphates in good yields.

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

117 Finally, we identify a cluster of mono- and dioxygenase fourth-level enzyme classes that m

118 simultaneous quantification of thiamine, its mono- and diphosphate derivatives and its precursors 4-m

119 resence of phosphate-containing minerals, 5'-mono- and diphosphates also form selectively in one-pot

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

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

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

123 We report persistent chiral organic mono- and diradical cations based on bicarbazole molecul

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

125 tal sugars (i.e., total grams of all dietary mono- and disaccharides per day) and sweets (i.e., handf

126 utes by which G. stearothermophilus utilizes mono- and disaccharides such as galactose, cellobiose, l

127 ilic Janus glycodendrimers containing simple mono- and disaccharides that mimic glycolipids are known

128 lations, we determined the effect of sugars (mono- and disaccharides) on caffeine self-association an

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

130 -di-tert-butyl-9,9-dimethylxanthene) towards mono- and disubstituted arenes is reported.

131 he parent 2-aminobenzimidazole (ABZ, 1), the mono- and disubstituted derivatives (2, 3), 2-aminonapht

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

133 bstituted amines couple with a wide range of mono- and disubstituted enynes in a nonenantioselective

134 ed benzimidazoles were prepared from various mono- and disubstituted ortho-phenylenediamines (OPD) by

135 A series of mono- and disubstituted thiophenes can be difunctionaliz

136 e, two standard compounds, representative of mono- and disulfated peptides, were used to compare the

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

138 Increased mono- and divalent salt concentrations counteracted this

139 this context, we also studied the effects of mono- and divalent salts on the flipping dynamics.

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

141 Mono- and doubly reduced forms of [3]TrTol were isolated

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

143 al platform for the HER, rather than that of mono- and few-layer graphene.

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

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

146 ylic substrates, providing high yield of the mono- and geminal bis-borylation products.

147 s determine the operation of slip systems in mono- and high-entropy carbides at room temperature.

148 1)(,)(2) and embody two main configurations: mono- and holocentromeres, referring, respectively, to l

149 Mono- and multi-functionalised gamma-butyrolactones were

150 These results present a mono- and multi-inhibitor management strategy effective

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

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

153 tery, acidic and bitter than those made from mono- and multi-varietal juices.

154 single nucleus sequencing, we revealed both mono- and multiclonal origins in the separate type cHCC-

155 e same Svalbard population were incubated as mono- and multistrain cultures.

156 the formation of 2',3'-cyclic phosphate RNA mono- and oligonucleotides from monophosphorylated precu

157 range of conditions and capable of retaining mono- and oligonucleotides.

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 and other substrates through the addition of mono- and poly(ADP-ribose) (PAR)(1-5).

162 use NAD(+) to modify numerous proteins with mono- and poly(ADP-ribose) signals that are important fo

163 cities, interpolating, for instance, between mono- and poly-centric organization.

164 nt synergy mechanism of gamma-terpinene with mono- and poly-phenolic antioxidants is discussed and it

165 ter (CAPE), used as models, respectively, of mono- and poly-phenols were demonstrated by differential

166 apped, water-soluble, fluorescent cage binds mono- and poly-phosphoric esters, including nucleotides.

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

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

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

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

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

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

173 These mono- and polysynaptic circuits may underlie polarized m

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

175 lationships between EES inputs that modulate mono- and polysynaptic outputs from spinal circuitry whi

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

177 as the delivery and destruction of both the mono- and polyubiquitinated forms of the G protein.

178 ts 4 lysine residues on Zta, leading to both mono- and polyubiquitination of Zta.

179 Galpha undergoes both mono- and polyubiquitination, and these modifications ha

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

181 and Brazil nut oils presented high levels of mono- and polyunsaturated fatty acids, displaying low at

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

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

184 For this, we quantified leaf mono- and sesquiterpene amount, richness, and diversity

185 Differences among the mono- and sesquiterpenoids, appear to be related to eith

186 in-mediated mitophagy predominantly exploits mono- and short-chain polyubiquitin, in which phosphoryl

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

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

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

190 Mono- and triethylene glycol aminooxy derivatives were r

191 T2C mutations correlated with a loss of H3K4 mono- and trimethylation by immunohistochemistry.

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

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

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

195 ands (HX = NH(2)Alk) form selectively either mono- (ArNHAlk) or diarylated (Ar(2)NAlk) products in th

196 a class of networks that are "structurally (mono) attractive" meaning that they are incapable of exh

197 mechanistic details behind the synthesis of mono-, bi-, and multimetallic nanoframes, as well as het

198 y retrieving the parameters used to generate mono-, bi-, and tri-exponential TRFAs from the global an

199 hesion energies were compared with those for mono-, bi-, and tri-layer graphene, as well as SiO(2) su

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

201 quinoline-based sigma-type (carbon-centered) mono-, bi-, and triradicals toward dimethyl disulfide (D

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

203 ar monomers is designed and synthesized with mono- (BTA-beta-d-glucose; BTA-Glc and BTA-alpha-d-manno

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

205 heckpoint blockade therapies administered as mono-, combo- and sequential therapies, to show how diff

206 the vaginal metabolome in the context of CT mono (CT+) and CT/MG co-infection (CT+/MG+) may identify

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

208 plantarum AVEF17, leading to high levels of mono, di-, and tri-hydroxy-octadecenoic acids.

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

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

211 h-yielding, catalytic transformations of the mono-, di-, and oligosaccharides.

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

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

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

215 nd oligomannose type N-glycans, sialylation (mono-, di-, and tetra-), fucosylation (tri-, core, and o

216 find that the valency of H3K79 methylation (mono-, di-, and tri-) is determined by nucleosome turnov

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

218 Here, we synthesized a panel of mono-, di-, and tri-meric fatty acid-conjugated siRNAs t

219 -23, 20-49 and 64-124ngmL(-1) for nucleotide mono-, di-, and tri-phosphates, respectively, were found

220 ram preparation of side-chain functionalized mono-, di-, and trifluoromethylisoxazoles, for example,

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

222 lycomb Repressive Complex 2 (PRC2) catalyzes mono-, di-, and trimethylation of lysine 27 on histone H

223 atin-associated methyltransferase catalyzing mono-, di-, and trimethylation of lysine 27 on histone H

224 mopeptides with 1-100 residues and adenosine mono-, di-, and triphosphate nucleotides are used as mod

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

226 This protocol comprises mono-, di-, and trisubstituted aliphatic, alpha-amino, a

227 ough Suzuki cross-coupling reactions to give mono-, di-, and trisubstituted bullvalenes.

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

229 iciency and broad substrate scope, including mono-, di-, and trisubstituted tertiary, secondary, and

230 (VI)(mu-O(Ar))(2)M(n+) cores with a range of mono-, di-, and trivalent Lewis acids (M(n+)).

231 ous identification and quantification of all mono-, di-, oligosaccharides and cyclitols observed in g

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

233 triflates as electrophiles, a broad range of mono-, di-, tri- and tetrasubstituted alkenes are compat

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

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

236 ild models for predicting methylation types (mono-, di-, tri-methylation).

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

238 re enzymes that deposit histone H3 Lys4 (K4) mono-/di-/tri-methylation and regulate gene expression i

239 onoid compounds, such as flavanols, flavonol mono-/di-glycosides, proanthocyanidin dimers, and phenol

240 rous organosilica nanoparticles (HMONs) with mono, double, triple, and even quadruple framework hybri

241 6(-) monocytes, TSLPR(+) monocytes (TSLPR(+) mono), expresses TSLPR complex upon LPS stimulation in a

242 Mono-, few-, and multilayer graphene is explored towards

243 e recombinant cyclophilin 1 monomer (rTvCyP1 mono) from the human pathogen Trichomonas vaginalis.

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

245 Rituximab monotherapy (R-Mono) in unselected patients has shown a lack of durable

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

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

248 Here, by forming a mono-/multi-layer nano-bridge multi-heterojunction struc

249 On-demand formation of mono-/multiple epoxides is achieved at different voltage

250 nge of aryl and alkyl sulfonamides undergoes mono- N-alkylation in excellent isolated yields (32 exam

251 rved with an interquartile range increase in mono- n-butyl phthalate.

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

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

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

255 Mono- or biexponential functions were fitted to measured

256 and/or P1-benzene ring with fluorine scan of mono- or bis-fluorine atoms around DRV's scaffold.

257 e (TAML(red) or TAML(sq)) determines whether mono- or bis-nitrene radical complexes are formed.

258 diorganyl diselenide used in the reactions, mono- or bis-organylselenylation products were efficient

259 the stereo- and regioselective formation of mono- or bis-silylated adducts from commercially availab

260 y liver fibrosis compared to two-dimensional mono- or co-cultures.

261 ession analyses to determine whether HIV/HCV mono- or co-infection were associated with PASP and PH c

262 al development have shown promise, either as mono- or combination therapy, in refractory and difficul

263 that drives resistance to ERK inhibitors in mono- or combined regimens, suggesting that resistance w

264 locks for further use in synthesis, but also mono- or di-deuterated analogues.

265 reverse transcription model shows that both mono- or di-methylated cytosine bases could specify the

266 SHL2 position when ISW1a is bound to either mono- or di-nucleosomes, there are major differences in

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

268 NMR studies clarified the mechanism, with a mono- or dianionic key intermediate, depending on the am

269 by hydrogen bond-mediated imprinting of the mono- or dianions of phenyl phosphonic acid (PPA), pheny

270 e readily transformed into the corresponding mono- or difluoromethylated compounds through proto- or

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

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

273 An analogous mechanism of O(2) activation at mono- or dinuclear iron centers is rare in the synthetic

274 enzymes with the ability to perform precise mono- or dioxygenation reactions on a variety of substra

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

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

277 D8 T cell intracellular signaling network by mono- or dual-costimulation.

278 multispecies biofilm communities rather than mono- or dual-species biofilms.

279 First, we looked for strong, potentially mono- or oligogenic variants for ischemic stroke, and se

280 ution and its lower expression levels and is mono- or oligomorphic unlike the highly polymorphic UAA

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

282 acid residues of target proteins, leading to mono- or poly-ADP-ribosylation (MARylation or PARylation

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

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

285 ization level, 22 patients were allocated in Mono- or Poly-sensitized groups, excluding patients alle

286 ence of the patient sensitization phenotype (Mono- or Poly-sensitized).

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

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

289 ect cross-chiral polymerases that use either mono- or trinucleotide substrates that are activated as

290 atty acyl-CoA biosynthesis and elongation of mono-, poly-unsaturated and saturated fatty acids and en

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

292 this gap, we site-specifically radiolabeled mono- (scFv) and bivalent (mAb) affinity ligands specifi

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

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

295 Specifically, diversifying plant litter from mono- to mixed-species increases decomposition rate by 3

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

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

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

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

300 sic quaternary two-state allosteric model of Monod, Wyman, and Changeux to include tertiary conformat