ライフサイエンスコーパス: di-

1 he reactions are compatible with various 1,1-di- and 1,1,3-trisubstituted allenes and N-hydroxyanilin

2 ether+10% tris-(2-ethylhexyl) phosphate+10% di-(2-ethylhexyl) phosphate; pH of the sample solution,

3 NMR experiments showed them to be N(1),N(10)-di-(E)-caffeoyl-N(5)-p-(E)-coumaroyl spermidine, N(1)-(E

4 ne dibromide ([(VIM)(2)C(8)] 2[Br]) and 1,12-di (3-vinylimidazolium) dodecane dibromide ([(VIM)(2)C(1

5 the hydrophilicity and peptide length of 153 di- to tetrapeptides.

6 (1,2-di-(tert-butyl)-dpp-BIAN)(2)] (7), (1,2-di-(tert-butyl)-dpp-BIAN) (8), and (1-(tert-butyl)-2-OH-

7 theses and characterizations of [Li(4)][(1,2-di-(tert-butyl)-dpp-BIAN)(2)] (7), (1,2-di-(tert-butyl)-

8 nd injection of 8-OH-DPAT [(+/-)-8-hydroxy-2-di-(n-propylamino) tetralin hydrobromide; 5-HT(1A) agoni

9 Of these sites 79% were mono-, 20% di-, and approximately 1% were tri- and tetraphosphopept

10 lished impact on global histone H3 lysine 27 di- and trimethylation (H3K27me2/3), the relevance of th

11 )(3)N)U(IV)}(2)(mu-eta(2)(C4):eta(1)(C1)-1,3-di-(p-(t)Bu-phenyl)butadi ene))] (5), are formed.

12 rase SDG8, implicated in histone 3 lysine 36 di- and trimethylation (H3K36me2 and me3), is involved i

13 MT2B mediates hippocampal histone 3 lysine 4 di- and trimethylation and is a critical player for memo

14 wed a specific deficit in histone 3 lysine 4 di- and trimethylation, while histone 3 lysine 4 monomet

15 lites of high-molecular-weight phthalates, 4 di-(2-ethylhexyl) phthalate (DEHP) metabolites (Sigma4DE

16 jugates, including the glucuronides of 3',4'-di- and 3',4',5'-trihydroxyphenyl-gamma-valerolactone, t

17 Rod-like 4,4'-di-(1,4-buta-1,3-diynyl)-benzoic acid (BDBA) and iron at

18 proaches for the preparation of 5'-mono-, 5'-di-, and 5'-triphosphorylated nucleosides, also known as

19 Cy3G) was more instable than delphinidin 3,5-di (Dp3,5dG) and cyaniding 3,5-diglucosides (Cy3,5dG).

20 and improve the electrical conductivity, 2,5-di-(2-thienyl)-1-pyrrole-1-(p-benzoic acid) and chloroau

21 With the EDTA-2D-RP/RP approach, 13 mono-, 6 di-, and 3 triphosphopeptides were identified in the alp

22 (2+) (Ru = Ru complex with one 4-t-butyl-2,6-di-(1',8'-naphthyrid-2'-yl)-pyridine ligand and two 4-pi

23 r the double-asymmetric hydrogenation of 2,6-di-(1-phenylethenyl)-4-methylaniline to produce the C2-s

24 of the 4-(nitrophenyl)phenoxyl radical, 2,6-di-(t)butyl-4-(4'-nitrophenyl) phenoxyl radical ((t)Bu2N

25 n the alpha-casein sample, while 19 mono-, 8 di-, 4 tri-, and 3 tetraphosphopeptides were identified

26 onic liquid-based cross-linkers, namely, 1,8-di (3-vinylimidazolium) octane dibromide ([(VIM)(2)C(8)]

27 Three xanthones, 1,3,7-trihydroxy-2,8-di-(3-methylbut-2-enyl)xanthone, 1,3,7-trihydroxy-4,8-di

28 hylbut-2-enyl)xanthone, 1,3,7-trihydroxy-4,8-di-(3-methylbut-2-enyl)xanthone a previously undescribed

29 often associates with the neighboring Lys-9 di- or tri-methylations, they are not required for the a

30 nascent RNAs to initiate histone H3 lysine 9 di- and trimethylation (H3K9me2 and H3K9me3, respectivel

31 Four series of 7,9-di- and 2,7,9-trialkyl guanine derivatives were synthesi

32 aluminum foil (VACNT-Al foil) with poly (9,9-di-(2-ethylhexyl)-fluorenyl-2,7-diyl)-end capped with 2,

33 as alkyl-substituted electrophiles bearing a di- or trisubstituted alkene may be employed.

34 pecificity from a monomethyltransferase to a di- and a trimethyltransferase, respectively.

35 E,Z-configured conjugated diene linked to a di- or triyne chain.

36 We report an efficient means to access di- and trisubstituted pyridines in an efficient and hig

37 ere observed of which 4-sinapoylquinic acid, di- and tri-methoxycinnamoylquinic acids, two isomers of

38 th weakly activating groups reveal analogous di- and trisolvated monomer-based metalations.

39 rystal phases are observed for the analogous di- and tetracationic compounds without an ion shelterin

40 her, tris-(2-ethylhexyl) phosphate (10%) and di-(2-ethylhexyl)phosphate (10%) as the extraction solve

41 r analysis of di-n-butyl phthalate (DBP) and di-(2-ethylhexyl) phthalate (DEHP) in soft drinks.

42 is also potentially diastereoselective, and di- and trisubstituted tetraenes often undergo cascade r

43 he likely in vivo substrates are NAD(P)H and di-, poly-, and persulfide derivatives of coenzyme A, al

44 H3 tails mono- and dimethylated on H3K4 and di- and trimethylated on H3K36, an H3 methylation patter

45 Both mono- and di- hydroxyl metabolites were identified for parent HBCD

46 Mono- and di-(18)F-labeled derivatives of phenolsulfonphthalein (p

47 so quantified along with different mono- and di-(Z)-isomers of lycopene which were tentatively assign

48 or TGs having a combination of saturated and di- or triunsaturated fatty acyls in sn-1 and sn-3 posit

49 ASP-1 associated with UHRF1, G9a, Snail1 and di- and tri-methylated histoneH3 in a CXCL12-dependent m

50 ed with sequences with identical coding and (di-)nucleotide composition but disrupted RNA secondary s

51 ation and quantification of antihypertensive di- and tri-peptides in fermented milk products was esta

52 NMDARs are di- or tri-heteromeric complexes of NR1 and NR2 subunits

53 ed with activation of transcription, such as di- or trimethylation of histone 3 on lysine 4 (H3K4me2/

54 s, hopanoids, and carotenoids; the betagamma di- and triterpene synthases; the zeta head-to-tail cis-

55 f total anthocyanins and high ratios between di- and tri-substituted forms.

56 lexibility is involved in the switch between di- and pentapeptide hydrolysis.

57 etylase complex have both been shown to bind di- and trimethylated histone H3 Lys-36 stimulated by Ea

58 aches to show that the Set3 PHD finger binds di- and trimethylated states of H3K4 with comparable aff

59 This antibody optimally binds di- and trisaccharide epitopes, whereas larger oligomers

60 mono- and dimethylated lysines, SFMBT1 binds di- and trimethyl H3K4, both of which are enriched at ac

61 Moreover, several potentially bioactive di- and tripeptides were identified in oryzacystatin pep

62 D,D-carboxypeptidase, which hydrolyzes both di- and pentapeptide.

63 substituted (chlorinated BPA; mono- [BPAMC], di-[BPADC], and trichloride [BPATrC]) forms of BPA were

64 llular exposure of the TLR2 PAMPs carried by di- and triacylated SVLP cores, which indicates subset-d

65 Only SVLPs carrying di- and triacylated lipopeptide cores induced DC activat

66 Syntheses of certain di- and mono-oxygenated derivatives (e.g., 2 and 3, resp

67 n the mechanism of inhibition of hRNR by ClF di- and triphosphates (ClFDP and ClFTP) are presented.

68 regioselective monoepoxidation of conjugated di- and trienes using 30% H2O2 at or below room temperat

69 also methylated other l-histidine-containing di- and tripeptides.

70 en beta-CN derived C-terminal Pro-containing di-, tri, and tetrapeptides which were predicted in sili

71 In contrast, di- and trimethylation of lysine 9 of histone 3 (H3K9) a

72 In contrast, di-, tri-, and longer unpaired ribonucleotide stretches,

73 ightly less effective than the corresponding di- and triguanidinocalix[4]arene derivatives, most like

74 ng partners giving rise to the corresponding di- or trisubstituted alkenes, typically in high yield a

75 is process is the ability to directly couple di-, tri- and tetrasubstituted alkenyl cyanohydrin pronu

76 molecular mechanism underlying Na(+)-coupled di- and tricarboxylate transport by this family is under

77 Cyclic di- and linear oligo-nucleotide signals activate defense

78 Cyclic di-(3':5')-guanosine monophosphate (c-di-GMP) is a major

79 uitous bacterial secondary messenger, cyclic di-(3',5')-guanosine monophosphate (c-di-GMP), represent

80 Moreover, c-di-GMP, but not cyclic di-(3':5')-adenosine monophosphate, induced stalk gene e

81 ses (DGCs) that catalyze formation of cyclic di-(3',5')-guanosine monophosphate (c-di-GMP) from GTP.

82 to hydrophobic phthiocerol dimycocerosates, di- and pentaacyl trehaloses and sulfoglycolipids.

83 ssociated alpha-glucosidase that breaks down di- and oligosaccharides to absorbable monosaccharides.

84 hod for the addition of dialkylzincs and (E)-di-, (E)-tri-, and (Z)-disubstituted vinylzinc reagents

85 Ps can encompass multiple orientations; each di- and triphosphorylated species binds with comparable

86 ubiquitin chain cleavage was comparable for di- and tri-ubiquitin, the Km value was lower for tri-ub

87 orded from m/z 167 and 168 ions obtained for di- and tri-deuterio isotopologues showed peak pairs at

88 yl-(oim)2][1,5-NDS] displays selectivity for di- over monocarboxylate anions.

89 ort chain monoglycerides was larger than for di- and triglycerides when Tween 80 was used as surfacta

90 Whereas many GPCRs have been shown to form di-/oligomers, the size and stability of such complexes

91 The method forms di-, tri-, and even tetrasubstituted acetones with high

92 ndividual bases, but also contributions from di- and trinucleotides at various positions within or ne

93 set of covalently linked homo-oligomers from di- to tetramers serve as proof-of-principle test cases.

94 evalent folding of small oligopeptides (from di- to tetramers) composed of 2-aminocyclobutane-1-carbo

95 panes and oxepane-containing polyethers from di- and trisubstituted epoxides.

96 med over the (1-->5)-beta-d-galactofuranosyl di- and trisaccharide derivatives 12 and 13.

97 I)-mediated isomerization process that gives di- or trisubstituted allylic boronic esters with high E

98 ophila E(z) homolog, were deficient in H3K27 di- and trimethylation, with no detectable replication s

99 Here we show that the levels of H3K27 di- and trimethylation (H3K27me2 and H3K27me3) are reduc

100 nes with altered expression as well as H3K36 di- and trimethylation in H3.3K36M cells are enriched in

101 lation (H3K27me3) rarely coexists with H3K36 di- or tri-methylation (H3K36me2/3) on the same histone

102 the major monoubiquitination-dependent H3K4 di- and trimethylase in Drosophila.

103 ithout obvious changes in the levels of H3K4 di- and trimethylation.

104 egions, coupled to a modest decrease in H3K9 di- and trimethylation at the rDNA promoter.

105 rchitecture, with significantly reduced H3K9 di- and tri-methylation at specific chromatin sites.

106 to the DSB, where local levels of histone H4 di- and tri-methylation at lysine 20 (H4K20me2, 3) and H

107 arosan tri- and pentasaccharides and heparin di-, tetra-, hexa-, and octasaccharide analogues.

108 Here, di- and monozinc catalysts, coordinated by bis(imino)dip

109 Homogenous di- and tetravalent dendrimers incorporating the alpha7-

110 ta-fructofuranosidase capable of hydrolyzing di- and trisaccharides containing a terminal, non-reduci

111 ding large hydrophobic peptides, hydrophilic di-/tripeptides and glycopeptides.

112 CZE-MS for the analysis of small hydrophilic di-/tripeptides, large hydrophobic peptides, glycopeptid

113 tes inorganic As(III) into mono- (MAs(III)), di- (DMAs(III)) and tri- (TMAs(III)) methylarsenicals.

114 (sp(3))-H bonds of N-terminal amino acids in di-, tri-, and tetrapeptides without installing a direct

115 Decreases were observed in di- and triacylglycerides, sphingomyelins (SMs), lysopho

116 -Cys60' interprotomer cross-links, including di-, tri- and tetrasulfide bonds, which allosterically i

117 ger-associated molecular patterns, including di- and triacylated lipopeptides.

118 acyl chains across lipid species, including di- and triacylglycerols, phospholipids, cholesteryl est

119 en the accessions were related to metal ion (di-, trivalent inorganic cation) transmembrane transport

120 The (1-->2)-beta-linked di-, tri-, and tetramannosides bind in helical conformat

121 or site-specific incorporation of K48-linked di- or tetra-Ub chains onto the side chain of Lys12 of a

122 sine 27 trimethylation and histone H3 lysine di- and trimethylation.

123 The main di- and tribromophenols detected were 2,4-diBP > 2,5-diB

124 n to Ag (111) facets can be expanded to many di- and tricarboxylate compounds whose two nearest carbo

125 ate into large clusters in water, but merely di- or trimerize in chloroform.

126 dified individual amino acids, Fmoc-modified di- and tripeptides, and Fmoc-modified tetra- and pentap

127 5-Bromouracil ((Br)U) modified di- and hexanucleotides having (Br)U flanked on the 5' o

128 Mono-, di- and trisubstituted lanthanide amidinate and guanidin

129 Mono-, di-, and trinucleoside conjugates of glutamate or peptid

130 Mono-, di-, and triPAPs, including several diPAP homologues, we

131 Mono-, di-, and triphosphorylated phosphatidylinositol phosphat

132 Mono-, di-, and trisubstituted arenes lacking a directing group

133 manent increase of histone 3 lysine 4 mono-, di-, and trimethylation and decrease of H3K9 trimethylat

134 tive form of the drug (Gemcitabine 5'-mono-, di- and triphosphates) by specific enzymatic activities,

135 d azelaic acid) acid with alkylamine (mono-, di-, and trimethylamines), represent those commonly foun

136 Engineering HMS2 reveals alternative mono-, di- or tri-cistronic and antisense transcription units (

137 minate between lysine acetylation and mono-, di-, or trimethylation in a site-specific and quantitati

138 A wide range of readily available mono-, di-, and trifluoromethyl heteroaryl sulfones can thus be

139 Histone H3 lysine 4 (H3K4) can be mono-, di-, and trimethylated by members of the COMPASS (comple

140 nd histone residue that could also be mono-, di-, and trimethylated by PRDM9 as efficiently as H3K4.

141 onal assignment of substances bearing mono-, di-, and perfluoroalkyl rather than trifluoromethyl grou

142 um bromide salts (TAA), benzylamines (mono-, di-, and tri-), and illicit drugs (MA, MDEA, and haloper

143 pplied to a variety of alpha- or beta-mono-, di-, and polythiosugar derivatives to synthesize efficie

144 analysis showed that rRP789 catalyzed mono-, di-, and trimethylation of lysine, while rRP027-028 cata

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

146 d to the production of singly charged mono-, di-, and trisaccharide fragments.

147 gene expression through demethylating mono-, di-, or trimethylated lysines.

148 ic conversion of structurally diverse mono-, di-, tri-, and tetrasubstituted olefins to N-H aziridine

149 r simultaneous quantitation of eleven mono-, di-, and triphosphates of thioguanosine, methylthioinosi

150 The final mono-, di-, and tetravalent ligands were resistant to enzymatic

151 lysine methyltransferase required for mono-, di-, and trimethylation of this site.

152 omplex the reaction mixture generated mono-, di- and tri-substituted sugar complexes and their hydrol

153 e surfactant, including PEO(n)-glucam mono-, di-, and tristearates as well as free and esterified PEO

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

155 The separation of myo-inositol mono-, di-, tri-, tetra-, pentakis-, and hexakisphosphate (InsP

156 and the exposed alpha-amino group is mono-, di-, or trimethylated by NRMT, a recently identified N-t

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

158 unmodified nucleosides and nucleotide mono-, di- and tri-phosphates by capillary electrophoresis coup

159 -49 and 64-124ngmL(-1) for nucleotide mono-, di-, and tri-phosphates, respectively, were found.

160 ves access to the naturally occurring mono-, di-, and trisaccharide substructures.

161 The ion signal intensities of mono-, di-, and oligohexosylceramides were enhanced by up to 10

162 ch allowed us to produce a variety of mono-, di-, and triarylimidazoles using diverse bromo- and chlo

163 The synthesis of mono-, di-, and trifluoromethyl aryl ethers by fluorodecarboxyl

164 ocess was used to prepare a series of mono-, di-, and trifunctionalized mesoporous metal-organic fram

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

166 for the stereoselective synthesis of mono-, di-, and trihydroxylated indolizidines is presented in f

167 ed binding to the oligosaccharides of mono-, di-, and trisialylated gangliosides.

168 oxyamination reaction of a variety of mono-, di-, and trisubstituted alkenes.

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

170 resent method allows the synthesis of mono-, di-, and trisubstituted pyrroles with appropriate substi

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

172 ffinities and signaling capacities of mono-, di-, or triglycosylated NKp30, suggesting that the degre

173 All members of this library of mono-, di-, tri-, and tetramethyl-substituted derivatives were

174 irect regioselective incorporation of mono-, di-, tri-, and tetrasubstituted olefins at the alpha-car

175 ukaryotic proteins, lysines are often mono-, di-, or trimethylated, which may signal different biolog

176 Various olefins, mono-, di-, and trisubstituted, are epoxidized chemoselectively

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

178 the photolysis of this and six other mono-, di-, and triazastilbenes in solid and solution states.

179 the construction of highly oxygenated mono-, di-, and polycyclic carbocycles from the reaction of dis

180 ifferent phosphoinositide phosphates (mono-, di-, and triphosphorylated inositides), a phosphatidic a

181 iciresinol monoglycoside, pinoresinol mono-, di- and triglycoside, sesaminol, sesaminol triglycoside,

182 ne H3, but not by histones previously mono-, di-, or trimethylated at H3K4.

183 of the Sir proteins to reconstituted mono-, di-, tri-, and tetra-nucleosomal chromatin templates and

184 parate diesel samples into saturates, mono-, di-, and polyaromatics by gas chromatography, with selec

185 The stability of seven mono-, di-, and trihaloacetonitriles was examined under a varie

186 ites can reach a tetra-anionic state, mono-, di-, tri-, and tetra-anionic complexes likely dominate a

187 In this study, mono-, di-, and triPAPs, perfluorinated alkyl acids (PFAAs), sa

188 osphinate) and NODAGA, we synthesized mono-, di-, and trimeric conjugates of the alphavbeta6 integrin

189 osphinate) and NODAGA, we synthesized mono-, di-, and trimeric conjugates of the alphavbeta6 integrin

190 ases comprises 27 members that target mono-, di-, and trimethylated lysine residues of histone (or no

191 sing numbers of the PEG groups in the mono-, di-, and tri-PEG chlorin conjugates increased the water

192 Finally, the mono-, di-, and triglycosylceramides were characterized as gala

193 he successive oxyfunctionalization to mono-, di-, and tetraepoxy derivatives is accomplished using hy

194 ons as part of the COMPASS complex to mono-, di-, and tri-methylate H3K4.

195 ormational ensembles of unacetylated, mono-, di-, tri-, and tetra-acetylated H4 histone tails using R

196 e the discrimination of unmethylated, mono-, di-, and trimethylated lysines on a single histone tail

197 lex with peptides bearing unmodified, mono-, di-, and trimethylated lysines illustrate the roles of a

198 trates, respectively, to form unusual mono-, di-, and tetranuclear titanium(III) complexes.

199 RFCRYS utilizes mono-, di-, and tri-peptides amino acid compositions, frequenci

200 nstructs having controlled valencies (mono-, di-, trivalent in terms of biotin-binding sites) are stu

201 tetrasubstituted calix[4]arene, whose mono-, di-, and triprotonated forms are slightly less effective

202 , fluidic and multicompartments) with mono-, di-, and tricomponents configurations were achieved, and

203 brary of 20 CBMs was synthesized with mono-, di-, or trisaccharides at each site for comparison of bi

204 tonitrile was also performed yielding mono-, di- and tri-stearic ester derivatives.

205 In contrast, most di- and tri-methylation PTMs are enriched on old histone

206 ich are presumed to be PG fragments (muramyl di- and tripeptides).

207 trometry, confirming the presence of muramyl di- and tripeptides in Chlamydia-infected cell lysate fr

208 lows for the synthesis of unsymmetrical N,N'-di- and N,N,N'-trisubstituted ureas in one pot and is to

209 Cp*(Cl)Ti(N,N-di-(t)Bu-eta(1),eta(2)-diimine) (2), in the presence of

210 ioanisole, diphenyl ether, phenol, naphthol, di- and trimethoxy benzenes, xylene, mesitylene, N,N-dim

211 cil, thymine, and cytosine (deoxy)nucleoside di- and triphosphates by an antiport mechanism and SLC25

212 s that catalyze the hydrolysis of nucleotide di- and triphosphates, thereby modulating extracellular

213 MS fragmentation, clustered in flavonol-3-O-di-/tri-glycosides-7-O-rhamnosides and other flavonol-gl

214 e body by mediating intestinal absorption of di- and tripeptides.

215 ioselective redox-relay Heck alkynylation of di- and trisubstituted alkenols to construct propargylic

216 were identified as having reduced amounts of di- and trimethylated myricetins and increased monomethy

217 ess is useful for the convergent assembly of di- through penta-substituted pyridines with complete re

218 e O antigen would be capped by attachment of di- or tri-O-methylated fucose as catalyzed by glycosylt

219 (intra ligand-ligand), (ii) the building of di- or oligonuclear complexes (inter ligand-ligand), (ii

220 presence/absence of specific combinations of di- and trinucleotides, (iii) nucleotide interactions by

221 hocyanin profiles differently constituted of di- and tri-substituted forms.

222 These GPCRs showed very different degrees of di-/oligomerization, lowest for beta(1)ARs (monomers/dim

223 elective synthesis of either diastereomer of di- and trisubstituted cyclopropanes.

224 d, we compare here the removal efficiency of di-(2-ethylhexyl)phthalate (DEHP) on hands by handwashin

225 Emissions of di-(2-ethylhexyl) phthalate (DEHP) from one type of poly

226 atalysts for the asymmetric hydrogenation of di-, tri-, and tetrasubstituted unfunctionalized alkenes

227 onstrated high microsatellite instability of di- and tetranucleotides (EMAST), and immunohistochemica

228 ead, one-electron reduction and isolation of di- and trinuclear [UO(2)(BIPMH)(mu-Cl)UO(mu-O){BIPMH}]

229 benzyl phthalate (MBzP), four metabolites of di-(2-ethylhexyl) phthalate (DEHP), and BPA.

230 on conditions, regioselective methylation of di-, tri-, and tetrasaccharide substrates proceeded in i

231 We prepared a number of di- and trifunctionalized quinolines by selective metala

232 The synthesis of a series of di-, tri-, and tetraalkyl beta-thiolactones and beta-lac

233 Stability of di- and tri-saccharide conjugates of anthocyanidins slig

234 This procedure can be used for synthesis of di-, tri-, and tetra-substituted allenes.

235 useful chemoselectivity in the synthesis of di-, tri-, and tetraamines (62 examples) by use of Buchw

236 2)/L1 toward the chemoselective synthesis of di-, tri-, and tetraamines was achieved.

237 for chloroacetamide but higher than those of di- and trichloroacetamide.

238 orters (POTs) couple the inward transport of di- or tripeptides with an inwardly directed transport o

239 he large PTR family facilitate the uptake of di- and tripeptides to provide cells with amino acids fo

240 ily, functioning in proton-coupled uptake of di- and tripeptides.

241 nation of T3 and rT3 to produce a variety of di- and monoiodo derivatives.

242 guided pathway to develop a large variety of di- and trinuclear 1,2,4-triazolate-based clusters for u

243 avoid gluten, or reduce fermentable oligo-, di-, and mono-saccharides and polyols.

244 ate diet and diet low in fermentable oligo-, di-, and monosaccharides and polyols.

245 tain fructans, a type of fermentable oligo-, di-, monosaccharides and polyols.

246 ort-chain carbohydrates (fermentable oligo-, di-, monosaccharides, and polyols [FODMAPs]) has been re

247 rt-chain carbohydrates (fermentable, oligo-, di-, monosaccharides, and polyols [FODMAPs]) in subjects

248 A series of three short oligomers (di-, tri-, and tetramers) of cis-2-(aminomethyl)cyclobut

249 Furthermore, the presence of one di- and two monohydroxylated octachlorinated biphenyls (

250 Summed metabolites of butyl phthalates or di-(2-ethylhexyl) phthalates were significantly associat

251 bryos accumulate large numbers of single (or di-) ribonucleotides embedded in their genomic DNA (>1,0

252 ort of the formation of opioid receptor (OR) di-/oligomers suggests previously unknown mechanisms use

253 e mainly zerovalent, such as thiols, organic di- and polysulfides, or heterocycles.

254 The distinction of oxidized di- and triterpenes, for example, is hindered by the sup

255 2B lysine 123 by Bre1, which in turn permits di- and trimethylation of histone H3 lysine 79 by Dot1.

256 This analogue was used to make potent di- and trivalent binders of ASGPR.

257 Modeling color vision of potential di- and trichromatic fish predators of cuttlefish corrob

258 ic ester, a variety of selectively protected di- and trisaccharide derivatives can be accessed in an

259 iazo compounds and terminal alkynes provides di- and trisubstituted allenes.

260 In the presence of slow reacting di- and tricarboxylic acids (oxalic, malonic, succinic,

261 Agonist stimulation did not alter receptor di-/oligomerization, but increased the mobility of GABA(

262 SHL and EBS recognize di- and trimethylated histone H3 at lysine 4 and bind re

263 Initially, the enzyme removes di- or trinucleotides from viral DNA ends to expose 3'-h

264 distinct mechanisms, including the reported (di-)polar, axial, and a previously undescribed mechanism

265 o, taxanes, epothilones, statins, retinoids, di-/triterpenes, noviose deoxysugar, and antibiotics der

266 vosyldiacylglycerols (SQDGs), sphingolipids, di- and tri-acylglycerols (DAGs and TAGs), and sterol de

267 In this way, selectively substituted di-, tri-, tetra-, and pentachloro-BODIPYs 2-5 were prep

268 nd the stereoselectivity with which terminal di- and trisubstituted tetraenes are known to react bios

269 The method is compatible with terminal, di-, and trisubstituted alkenes.

270 showed a higher resistance against heat than di- and non-acylated.

271 Computations indicate that di- and trisubstituted tetraenes undergo facile but less

272 The di- and trivalent p21-based antagonists bind to PCNA wit

273 otosensitized mechanism is suggested for the di- and tri-PEG chlorin conjugates; however, a more comp

274 em products 12 and 14 were isolated from the di- and trimethylated substrates 1k and 1l, respectively

275 prepared in six steps and 29% yield from the di-(tert-butoxycarbonyl) precursor of 11.

276 tions in kis cause a global reduction in the di- and tri-methylation of histone H3 on lysine 36 (H3K3

277 current effect, which is also present in the di- and trisulfide species.

278 Antibody recognition of the di- and trisaccharide is primarily dependent on the mann

279 We found that the di- and trimethylated states both contribute to activati

280 nt activation, and further indicate that the di- and trimethylation states play distinct roles in the

281 ce inhibitors structurally dissimilar to the di- and tripeptide-based HCV protease inhibitors in adva

282 (8), and bionectin A (9)--starting with the di-(tert-butoxycarbonyl) derivative 17 of the trioxopipe

283 yltransferase activity but differed in their di- and trimethylation activities.

284 3-carboxypropyl) phthalate (MCPP), and three di-(2-ethylhexyl) phthalate metabolites (SigmaDEHP) had

285 00 ppm) of LiCl diverts the reaction through di- and trisolvated monomer-based pathways for metalatio

286 fragment and has been designed to access to di- and multivalent sugar-oligoamides.

287 /5/7 specifically stimulates NuA4 binding to di- and trimethylated histone H3 Lys-36 and that this bi

288 d Dx; and glutamatergic output from DC/Dx to di-, mes-, and rhombencephalic nuclei.

289 ted anthocyanins was increased from mono- to di- to triglycosyl moieties, possibly due to steric inte

290 is process shows functional group tolerance; di-, tri-, and tetrasubstituted N-vinylazoles were obtai

291 silver-catalyzed aminations which transform di- and trisubstituted homoallylic carbamates into [4.1.

292 ase, human PLRP2 hydrolyzed long-chain tri-, di-, and monoglycerides.

293 LLE using di-(2-ethylhexyl)phosphoric acid (D2EHPA) extracted 97%

294 llows: organic solvent: 1-octanol+2.5% (V/V) di-(2-ethylhexyl) phosphate, applied voltage: 70V, extra

295 od yields and selectivities, especially with di- and trisubstituted arenes.

296 is indeed a result of complex formation with di- and polyols, specific binding.

297 t the strongest interactions took place with di- and tetra-acetylated peptides derived from the histo

298 VLPs) carrying hydrophobic TLR2 PAMPs within di- and triacylated lipopeptide cores (P2Cys-SVLPs and P

299 ked to the N atom of proline residues within di- and tripeptides.

300 of a broad range of N-allyl amides to form Z-di-, tri-, and tetrasubstituted enamides with exceptiona