ライフサイエンスコーパス: tri-

1 Bis-[tri-(3,5-di-tert-butyl)phenylmethyl]-peroxide 2 was test

2 detail: the highly effective inhibitor 1,3,5-tri-[5-(1-quinolinum)-pent-1-yn-1-yl]-benzene tribromide

3 tPyQB) and the less potent antagonist 1,3,5,-tri-{5-[1-(2-picolinium)]-pent-1-yn-1-yl}benzene tribrom

4 at the designed alpha-helical peptide family TRI [(Ac-G(LKALEEK)4G-CONH2)], containing single site su

5 Frequency of di-(AG/CT), tri-(AGG/CTT), tetra-(AAAT), penta-(AGAGG), and hexa-(AG

6 Most Phase 3 tri- als have adopted virologically confirmed symptomati

7 ed for the regioselective synthesis of 1,3,5-tri- and 1,3,4,5-tetrasubstituted pyrazoles by the react

8 3 patients (40%) at 3 to 4 months, including tri- and bilineage responses.

9 Tri- and di(pentafluorocyclopropyl) derivatives 2 also u

10 successive action of exo-peptidases, mainly, tri- and di-peptidylpeptidases, aminopeptidases and carb

11 successive action of exo-peptidases (mainly, tri- and di-peptidylpeptidases, aminopeptidases and carb

12 Lumenal ecto-nucleoside tri- and di-phosphohydrolases (ENTPDases) of the secreto

13 A series of tri- and dibrominations were accomplished for a range of

14 Recently, tri- and difluoromethyl ethers have received increasing

15 ght photoredox catalysis in the synthesis of tri- and difluoromethyl ethers.

16 thylation of chlorosilanes is reported using tri- and difluoromethyl sulfides, sulfoxides, and sulfon

17 nes using magnesium metal-mediated reductive tri- and difluoromethylation of chlorosilanes is reporte

18 and efficient method for the preparation of tri- and difluoromethylsilanes using magnesium metal-med

19 detected in both the presence and absence of tri- and dihydroxy bile salts in rats, WT mice, and CELK

20 h1, which can specifically demethylate H3K36 tri- and dimethyl modification states.

21 both parental alleles had similar levels of tri- and dimethylated H3K4 within the Gsalpha first exon

22 n containing 2A), which is selective towards tri- and dimethylated histone H3 lysyl residues 9 and 36

23 lso called JARID1A or KDM5A) can demethylate tri- and dimethylated lysine 4 in histone H3, which are

24 ndent demethylases remove methyl groups from tri- and dimethylated lysine 4 of histone H3.

25 g oxygenase JMJD2A specifically demethylates tri- and dimethylated lysine-9 and lysine-36 of histone

26 KDM4 subfamily of demethylases removes H3K9 tri- and dimethylation and contributes to the regulation

27 KDM4A is a histone demethylase that targets tri- and dimethylation marks on histone H3 lysines 9 and

28 For example, tri- and diorganophosphates (e.g., adenosine triphosphat

29 Orf153 (ymfB) is a nonspecific nucleoside tri- and diphosphatase and atypically releases inorganic

30 ng 2'-(3')-O-(2,4,6-trinitrophenyl)adenosine tri- and diphosphate.

31 ng stimulates self-association of NrdR, with tri- and diphosphates stimulating oligomerization more e

32 lyzes the phosphodiester bonds of nucleoside tri- and diphosphates, but not monophosphates, thus disp

33 pyrase, an enzyme that hydrolyzes nucleoside tri- and diphosphates, each normalized ischemic leukoseq

34 ase that hydrolyzes extracellular nucleoside tri- and diphosphates, has seven potential N-glycosylati

35 This enzyme hydrolyzed all tri- and diphosphonucleosides but not AMP or diadenosine

36 Furthermore, the excesses of tri- and hexanucleotide coding repeats appear to be cont

37 Tri- and hexanucleotide repeats are found in consistent

38 n the same way, suggesting binding modes for tri- and hexanucleotide-repeat RNAs in two neurodegenera

39 ese had unique sequences due to variation in tri- and hexapeptide repetitive motifs.

40 shed and are illustrated by the formation of tri- and pentablock and scarf architectures with cylinde

41 Galactosylated tri- and pentamannosides, representing the structure of

42 Methods have been developed to synthesize tri- and pentapeptide thioesters containing one or more

43 r carry out the total syntheses of heparosan tri- and pentasaccharides and heparin di-, tetra-, hexa-

44 have previously investigated the binding of tri- and pentasaccharides of N-glycan with a GlcNAc at t

45 ain glycopeptides carrying two N-linked core tri- and pentasaccharides was achieved.

46 optimized in order to generate arsanes from tri- and pentavalent inorganic arsenic species (iAs(III)

47 on of plasmids with loxP sites: a model with tri- and possibly multimeric co-integrates comprising th

48 a higher percentage in DBA/2 mice, and more tri- and quad-nucleated cells were in C57BL/6 mice.

49 Both tri- and tetra(ethylene glycol) linked bis-chromium carb

50 4,4'-)-dicarbomethoxydibenzo-27-crown-9 with tri- and tetra-(ethyleneoxy) linkages transposed were sy

51 compared with our previously reported cyclic tri- and tetra-amine disulfides.

52 hown to be correlated with the expression of tri- and tetra-antennary beta1,6-N-acetylglucosamine (be

53 he high-pI fractions, nor were predominantly tri- and tetra-antennary glycans associated with low-pI

54 MALDI-MS data revealed several fucosylated tri- and tetra-antennary glycans which were significantl

55 reduced content and structural diversity of tri- and tetra-antennary N-glycans and of O-glycans, 2)

56 pecificity and activity of human FUT8 toward tri- and tetra-antennary N-glycans in the forms of glyco

57 ed glycoproteins, such as ASOR, that contain tri- and tetra-antennary N-linked oligosaccharides.

58 lycans as PrP(C), but a higher proportion of tri- and tetra-antennary sugars.

59 ized acyl chains, phosphatidic acids (PAs)), tri- and tetra-galactosyldiacylglycerols (TrGDGs and TeG

60 s efficient preparation of hindered biaryls (tri- and tetra-ortho-substituted), functions effectively

61 played high activity in the hydrogenation of tri- and tetra-substituted alkenes with TON > 8000 for t

62 tituted isocyanides incorporating contiguous tri- and tetra-substituted centers.

63 relative amount of biantennary glycan versus tri- and tetraantennary glycans was different at separat

64 In addition, significantly higher amounts of tri- and tetraantennary glycans were observed.

65 iantennary glycans, N83 containing primarily tri- and tetraantennary glycans, and N247 containing exc

66 entified carry more biantennary glycans than tri- and tetraantennary glycans, and the relative amount

67 a decrease in the amount of highly branched tri- and tetraantennary N-glycans, whereas monoantennary

68 Fractionation of complex tri- and tetraantennary N-linked glycoforms from bianten

69 rtho PCBs [OR = 4.55 (95% CI: 1.48, 13.95)], tri- and tetrachloro PCBs [OR = 3.66 (95% CI: 1.37, -9.7

70 A computational analysis of the reaction of tri- and tetracoordinate boron azides R2BN3 (R = H, Me,

71 A four-step synthesis of tri- and tetracyclic 1,2-dihydroquinolin-2(1H)-ones via

72 synthesis of complex, functional group-rich tri- and tetracyclic lactams.

73 Tri- and tetrafunctional DNA adducts of 5 were detected.

74 ased hepatic BA hydrophilicity by increasing tri- and tetrahydroxylated and decreasing the dihydroxyl

75 ed the ability of these proteins to generate tri- and tetraketide lactone products using N-acetylcyst

76 e potent inhibitors, monosulfated benzofuran tri- and tetrameric homologues of the parent designed di

77 Herein, we report that the thermal tri- and tetramerizations of pyridoannulated silylene 1

78 to Plasmodium chitinases: the enzymes cleave tri- and tetramers of GlcNAc from penta- and hexameric o

79 Tri- and tetramethyl-substituted acridones had the highe

80 oading for such reactive olefins as styrene, tri- and tetramethylethylene.

81 Between three and six tri- and tetranucleotide repeat microsatellite loci were

82 t base-stacking interactions; analyses of 62 tri- and tetranucleotide repeat-containing genes associa

83 tial for extension of the dinucleotide AC to tri- and tetranucleotides.

84 ta-glucan from oat and wheat brans mainly to tri- and tetraoligosaccharides.

85 as specificity for muropeptides that possess tri- and tetrapeptide stems on muramyl residues.

86 wall but not the wall of S. aureus contained tri- and tetrapeptide units, suggesting the presence of

87 but novel penta- and hexapeptides as well as tri- and tetrapeptides are released.

88 coid, peptidoglycan dipeptides increased and tri- and tetrapeptides decreased.

89 recovered support was utilized to synthesize tri- and tetrapeptides that contain amino acids other th

90 ctures of the complexes formed with selected tri- and tetrapeptides.

91 he oxygen- and novel carbon-linked adenosine tri- and tetraphosphate analogues are stable from pH 3 t

92 The method uses nucleoside tri- and tetraphosphate derivatives carrying 4-methylumb

93 With the first two approaches, no tri- and tetraphosphopeptides were identified in either

94 re mono-, 20% di-, and approximately 1% were tri- and tetraphosphopeptides, and 78 novel phosphorylat

95 conciled this issue using a panel of minimal tri- and tetrasaccharide sequences of variable but well

96 text] Syntheses of fluorinated mucin core 2 tri- and tetrasaccharides modified at the C-3 or C-4 pos

97 urves were generated for a series of related tri- and tetrasaccharides to evaluate their relative eff

98 ol carbamates and Grignard reagents to yield tri- and tetrasubstituted acrylates is reported.

99 ral amino acids and geometrically controlled tri- and tetrasubstituted acrylic acids.

100 urally complex and synthetically challenging tri- and tetrasubstituted alkene building blocks.

101 electrophiles, a broad range of mono-, di-, tri- and tetrasubstituted alkenes are compatible in thes

102 f terminal, geminal, disubstituted internal, tri- and tetrasubstituted alkenes using pinacolborane (H

103 Tri- and tetrasubstituted alkenes, including the challen

104 efficient intramolecular cyclopropanation of tri- and tetrasubstituted alkenes.

105 efficient regio- and stereospecific route to tri- and tetrasubstituted alkenes.

106 ocess is the ability to directly couple di-, tri- and tetrasubstituted alkenyl cyanohydrin pronucleop

107 In tri- and tetrasubstituted allenes, steric issues concern

108 odology for the stereoselective synthesis of tri- and tetrasubstituted allylic amines based on Pd-cat

109 A selective and convenient synthesis of tri- and tetrasubstituted alpha,beta-unsaturated ketones

110 ntioselective syntheses of challenging alpha-tri- and tetrasubstituted alpha-amino acids including an

111 Tri- and tetrasubstituted anilines are formed in good to

112 chemo- and stereoselective access to various tri- and tetrasubstituted conjugated alkenones and alken

113 vertheless, a diverse range of unsymmetrical tri- and tetrasubstituted cyclobutane structures can be

114 of these reactions which form unsymmetrical tri- and tetrasubstituted cyclobutanes through a heterod

115 roalkenes, giving access to the synthesis of tri- and tetrasubstituted double bonds in Rauhut-Currier

116 yl amides to form nonpropenyl disubstituted, tri- and tetrasubstituted enamides with excellent geomet

117 A Bronsted acid-catalyzed method to prepare tri- and tetrasubstituted furans efficiently from cycloi

118 n ring closure sequence for the formation of tri- and tetrasubstituted furans is presented.

119 Tri- and tetrasubstituted hydrazines could be formed by

120 lysis and proceeds using sterically hindered tri- and tetrasubstituted olefins to give products conta

121 ds on palladium, can direct the arylation of tri- and tetrasubstituted olefins.

122 , thus bestowing a powerful avenue to access tri- and tetrasubstituted pyridines including carbo- and

123 uide, analogues were synthesized in both the tri- and tetrasubstituted pyrrolidine series by means of

124 A series of tri- and tetrasubstituted spiro-oxaphosphetanes stabiliz

125 the cascade reactions of naturally occurring tri- and tetrasubstituted tetraenes (in agreement with c

126 component synthesis of highly functionalized tri- and tetrasubstituted thiophenes has been reported i

127 electivity and syn-stereoselectivity to form tri- and tetrasubstituted vinylboronic esters from comme

128 0' interprotomer cross-links, including di-, tri- and tetrasulfide bonds, which allosterically inhibi

129 to ETP, damping the spontaneous formation of tri- and tetrasulfides.

130 ses that convert these diphosphates into the tri- and tetraterpene precursors of sterols, hopanoids,

131 deltaD values of specific di-, tri- and tetraunsaturated C37 alkenones produced by an E

132 ding, the binding of a series of mono-, bi-, tri- and tetravalent carboxylate ligands to Ca(II) was e

133 The presence of both tri- and tetravalent Ce, contrary to formulation, was co

134 (4)L(6) through self-assembly reactions with tri- and tetravalent metal ions such as Ga(III), Fe(III)

135 rentiate HPAEC peak fractions containing the tri- and tri'-antennary branching isomers and two tetraa

136 e salts (TAA), benzylamines (mono-, di-, and tri-), and illicit drugs (MA, MDEA, and haloperidol).

137 he addition of dialkylzincs and (E)-di-, (E)-tri-, and (Z)-disubstituted vinylzinc reagents to alpha-

138 lpha-casein sample, while 19 mono-, 8 di-, 4 tri-, and 3 tetraphosphopeptides were identified in the

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

140 R screening of a comprehensive panel of di-, tri-, and high-mannose oligosaccharides establish that h

141 In contrast, di-, tri-, and longer unpaired ribonucleotide stretches, as w

142 nt and selective (>or=98%) syntheses of di-, tri-, and oligoenes containing regio- and stereodefined

143 train synthesizing cross-bridges with mono-, tri-, and pentaglycyl as well as tetraglycyl-monoseryl,

144 We also detected di-, tri-, and pentasaccharides with one sulfate group.

145 allows for synthesizing both mono- and di-, tri-, and poly( p-carboxyphenyl)siloxanes with p-carboxy

146 everal unique LOS glycoforms containing di-, tri-, and poly-N-acetyllactosamine repeats added to the

147 We expect that the bi-, tri-, and quad-cistronic vectors constructed here and ou

148 e, and outer arm), and galactosylation (di-, tri-, and tetra-) between striatum and SN N-glycans with

149 ional ensembles of unacetylated, mono-, di-, tri-, and tetra-acetylated H4 histone tails using Replic

150 can reach a tetra-anionic state, mono-, di-, tri-, and tetra-anionic complexes likely dominate as the

151 ble, for the first time, to prepare any bi-, tri-, and tetra-antennary asymmetric N-glycan from a sin

152 nt strategy for the rapid production of bi-, tri-, and tetra-antennary complex type N-glycans with an

153 t of fully galactosylated or sialylated bi-, tri-, and tetra-antennary N-glycans was largely equivale

154 saccharide compositions with sialylated bi-, tri-, and tetra-antennary structures.

155 are common building blocks, a family of di-, tri-, and tetra-histidine-catecholic adducts, that were

156 he Sir proteins to reconstituted mono-, di-, tri-, and tetra-nucleosomal chromatin templates and show

157 nthesis of sterically hindered biaryls (di-, tri-, and tetra-ortho substituted).

158 Di-, tri-, and tetra-substituted acrylic acid derivatives wit

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

160 Di-, tri-, and tetra-substituted bromoallenes were prepared t

161 Et2N:BH3 (10) and representative mono-, di-, tri-, and tetra-substituted olefins were carried out at

162 The synthesis of a series of di-, tri-, and tetraalkyl beta-thiolactones and beta-lactones

163 ul chemoselectivity in the synthesis of di-, tri-, and tetraamines (62 examples) by use of Buchwald-H

164 toward the chemoselective synthesis of di-, tri-, and tetraamines was achieved.

165 lycosylation sites, each varying in its bi-, tri-, and tetraantennary glycan content.

166 iency, affecting neutral and sialylated bi-, tri-, and tetraantennary N-glycans.

167 wenty-amino acid PSA fragments carrying di-, tri-, and tetrabranched complex-type glycans were prepar

168 Bi-, tri-, and tetracyclic isoquinoline salts were readily sy

169 ation intermediates and accumulation of bi-, tri-, and tetracyclic sesterterpenes, revealing the cycl

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

171 l alpha-D-mannopyranoside residues, and di-, tri-, and tetrameric analogs possessing terminal 3, 6-di

172 -(1->3)-glucan mimetics and synthesized di-, tri-, and tetramers in an enantiomerically pure form by

173 A series of three short oligomers (di-, tri-, and tetramers) of cis-2-(aminomethyl)cyclobutane c

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

175 Applications to four different sets of di-, tri-, and tetranucleotide loci from a number of human po

176 the repeat structure including abundant di-, tri-, and tetranucleotide microsatellite loci yielded ac

177 is model and use it to fit DNA data for di-, tri-, and tetranucleotide repeats in humans, mice, fruit

178 ons in 10 microsatellite loci including di-, tri-, and tetranucleotide repeats were evaluated.

179 howed that the mutation rate differs in di-, tri-, and tetranucleotide repeats, how mutation rate dis

180 g SSRs composed of iterations of mono-, di-, tri-, and tetranucleotides are mostly restricted to host

181 imple sequences consisting of repeating di-, tri-, and tetranucleotides, which allow the maximum reso

182 atalyzes template-directed synthesis of di-, tri-, and tetranucleotides.

183 ))-H bonds of N-terminal amino acids in di-, tri-, and tetrapeptides without installing a directing g

184 had a narrow substrate specificity with di-, tri-, and tetrapeptides, and it hydrolyzed only basic N-

185 e having a decreased ability to utilize di-, tri-, and tetrapeptides.

186 chsticks" self-assemble into multipods (bi-, tri-, and tetrapods) of varying coordination number and

187 nditions, regioselective methylation of di-, tri-, and tetrasaccharide substrates proceeded in isolat

188 vels of elongation of fucose-O-Thr61 to di-, tri-, and tetrasaccharides, not previously observed in r

189 Di-, tri-, and tetrasubstituted allenes were synthesized in m

190 Di-, tri-, and tetrasubstituted carbon-carbon double bonds re

191 broad range of N-allyl amides to form Z-di-, tri-, and tetrasubstituted enamides with exceptional geo

192 Di-, tri-, and tetrasubstituted enones are amenable to annula

193 ocess shows functional group tolerance; di-, tri-, and tetrasubstituted N-vinylazoles were obtained i

194 regioselective incorporation of mono-, di-, tri-, and tetrasubstituted olefins at the alpha-carbon o

195 nversion of structurally diverse mono-, di-, tri-, and tetrasubstituted olefins to N-H aziridines usi

196 method providing a concise synthesis of di-, tri-, and tetrasubstituted pyrroles is described.

197 the desired product, including isomeric di-, tri-, and tetrasubstituted species previously believed t

198 sts for the asymmetric hydrogenation of di-, tri-, and tetrasubstituted unfunctionalized alkenes.

199 quent MS(2) and MS(3) spectra of mono-, di-, tri-, and tetrasulfated KS oligosaccharides and sialylat

200 lorimetry (ITC) data for the binding of di-, tri-, and tetravalent carbohydrate analogues possessing

201 from our previous report for binding of di-, tri-, and tetravalent carbohydrate analogues possessing

202 ever, Hill plots for the binding of the di-, tri-, and tetravalent trimannoside analogues to both lec

203 nism, the estimates are highest in di-, then tri-, and then tetranucleotide repeats.

204 8 for monomethylated lysine, and 84 for di-, tri-, and unmethylated lysine) have been effectively use

205 In addition, bis-, tri-, and up to octaadducts of Sc3N@C80 were detected by

206 079) in the risk of PCSM in men treated with tri- as compared with bimodality therapy.

207 reveal a "trans-tail" regulation of H3-Lys-4 tri- but not dimethylation by H2B-Lys-123 ubiquitination

208 tion (mono-, di-, and tetra-), fucosylation (tri-, core, and outer arm), and galactosylation (di-, tr

209 A-Ni(II)-Zn(II) inhibitor complexes bound to tri-, di- and monomethyl forms of H3K9 and the trimethyl

210 osine-based nucleotides, including adenosine tri-, di-, and mono-phosphate, are controlled through th

211 colipase, human PLRP2 hydrolyzed long-chain tri-, di-, and monoglycerides.

212 in fatty acid uptake, lipid droplet size, or tri-, di-, or monoacylglycerol levels when compared with

213 ignalling, including the histone H3 lysine 9 tri-/di-methyl HDM enzyme KDM4B.

214 our peptide nomenclature, the prefixes di-, tri-, etc. refer to the number of amino acid residues in

215 Six loci (one tri-, four tetra- and one pentanucleotide) were assemble

216 und throughout the genome, di- (H3K4me2) and tri- (H3K4me3) methylated H3K4 are enriched at specific

217 alency of H3K79 methylation (mono-, di-, and tri-) is determined by nucleosome turnover rates.

218 tial histone H3 methylation (mono-, di-, and tri-) is still not understood, and the involvement of do

219 ed unique mono- (K16Ac), di- (K12Ac, K16Ac), tri- (K8Ac, K12Ac, K16Ac), and tetra-acetylated (K5Ac, K

220 Tri- l-menthyl pyromellitate (27b) was obtained by catal

221 Sialylated bi-, tri- [mainly the (2,4)-branched isomer], tetraantennary

222 isplays rate accelerations of up to 3900 for tri- n-propyl orthoformate.

223 being a pyranopyran nitrile synthesized from tri- O-acetyl-d-galactal by Ferrier cyanoglycosidation,

224 rmed in eight individuals with CAS affecting tri- or bileaflet aortic valves revealed considerable ol

225 ted prior to making a decision on the use of tri- or di-enzyme treatment.

226 a its chromodomain, binds histone H3 peptide tri- or di-methylated at lysine 9 (H3K9me3/H3K9me2) in s

227 innate immune sensor RIG-I distinguishes 5' tri- or diphosphate containing viral double-stranded (ds

228 d primers produced products with 5'-terminal tri- or diphosphate groups, indicating that genuine unpr

229 pin ribozyme appears to take up at least one tri- or divalent cation or two monovalent cations upon l

230 idges such as truncations of pentaglycine to tri- or monoglycine.

231 utinin is a homotrimeric receptor, and thus, tri- or oligovalent ligands should have a high binding a

232 ritical in the oxidative process involving a tri- or tetra-coordinate gold(I) with the oxidizing reag

233 t the accessibility of the gold(I) center to tri- or tetra-coordination is critical in the oxidative

234 ed on 3,5-dihydroxybenzyl alcohol containing tri- or tetrafunctional chiral central cores and allyl e

235 H(4) in the presence of catalytic amounts of tri- or tetraglyme were developed.

236 We reconstitute cohesin as tri- or tetrameric assemblies and use those as physiolog

237 their ability to promote selective ethylene tri- or tetramerization in combination with chromium.

238 Since it works with di-, tri- or tetranucleotide models supplied as external file

239 l levels, using 14 new markers consisting of tri- or tetranucleotide repeats.

240 ts do not contain any particular unique di-, tri- or tetranucleotide sequences, but are frequently co

241 tion mutations lacking either the C-terminal tri- or tetrapeptide exhibit apparent size increases of

242 ons and have been identified as dinucleoside tri- or tetraphosphates.

243 glycoside (mono- or disaccharide) to form a tri- or tetrasaccharide in high overall yield.

244 process gave access to highly functionalized tri- or tetrasubstituted dihydropyranones featuring an u

245 The sterically encumbered tri- or tetrasubstituted olefins yielded 1,2- or 1,4-dih

246 itopic 2-pyridinyl aromatic carboxylates and tri- or tetratopic phenols gave the corresponding ester-

247 Di-, tri-, or even tetrasubstituted allenes together with lac

248 ng different glycine branch lengths (penta-, tri-, or monoglycine), while PBP2a can only cross-link p

249 n the expression of proteins encoded in bi-, tri-, or quad-cistronic constructs.

250 no-dicarboxylic acids containing either di-, tri-, or tetramethylene spacers.

251 0, ApoB), and 27 microsatellite loci of di-, tri-, or tetranucleotide repeats.

252 cally hindered substrates which gave di- and tri -ortho-substituted biaryls in up to 92% yield.

253 d at hospitals with moderate and high use of TRI (P=0.01).

254 Factors potentially limiting use of TRI (renal failure, shock, cardiac arrest, and mechanica

255 letions (genetic instabilities) of repeating tri-, tetra- and pentanucleotide repeating sequences ass

256 Macrocyclization of suitably functionalized tri-, tetra- and pentapeptides via Suzuki-Miyaura cross-

257 that the major N-glycans were monosialylated tri-, tetra-, and penta-antennary oligosaccharides conta

258 classical methods, giving a wide variety of tri-, tetra-, and penta-substituted pyridines in high, o

259 Thus, a series of tri-, tetra-, and pentacarbonyl synthons was successfull

260 In this way, selectively substituted di-, tri-, tetra-, and pentachloro-BODIPYs 2-5 were prepared.

261 surface sites by evidencing the presence of tri-, tetra-, and pentacoordinated Y-surface sites.

262 iana yielded fungal-type sesterterpenes with tri-, tetra-, and pentacyclic scaffolds, and notably (-)

263 Here we present a series of tri-, tetra-, and pentadentate rotaxane-based ligands an

264 is enzymatic synthesis yielded predominantly tri-, tetra-, and pentaglutamyl species for the [(3)H]fo

265 f short chain condensed polyphosphates: di-, tri-, tetra-, and pentapolyphosphate.

266 the early PGC-LC elution of smaller glycans (tri-, tetra-, and pentasaccharides) at low organic solve

267 elevant noncovalent interactions stabilizing tri-, tetra-, hexa-, and octameric cyclic peptoids (as f

268 sulfane ring structure predominates, and the tri-, tetra-, hexa-, hepta-, and nonasulfanes were prese

269 that differ in the length of their peptides (tri-, tetra-, or pentapeptides with or without mono- or

270 nthesized having hydrophilic spacers of di-, tri-, tetra-, penta(ethylene glycol) and tri(propylene g

271 ns, all types of microsatellite (mono-, di-, tri-, tetra-, penta-, and hexanucleotide repeats) are fo

272 tellite mutations involving the expansion of tri-, tetra-, penta-, or hexanucleotide repeats cause mo

273 The separation of myo-inositol mono-, di-, tri-, tetra-, pentakis-, and hexakisphosphate (InsP1, In

274 the native epitope becomes larger across the tri-, tetra-, pentasaccharide series, entropy contributi

275 inhibition of PPE can be effected by simple tri-, tetra-and pentapeptides terminating in a carboxyli

276 ) into mono- (MAs(III)), di- (DMAs(III)) and tri- (TMAs(III)) methylarsenicals.

277 Eleven polybrominated diphenyl ether (tri- to deca-BDE) congeners and 2,2',4,4',5,5'-hexabromo

278 Tri- to decabrominated diphenyl ethers (tri-decaBDEs), i

279 and analyzed using GC-negative ion MS for 26 tri- to decabromodiphenyl ethers (BDEs), as well as othe

280 A variety of tri- to decabromodiphenyl ethers, phosphorus flame retar

281 he 5' end of transcribed genes in a 5'-to-3' tri- to di- to monomethyl gradient and promotes associat

282 roximal tubules there was a greater ratio of tri- to dimethylated H3K4 of Gsalpha exon 1 in the more

283 es reversibly transfer phosphate groups from tri- to diphosphate nucleosides.

284 abetic db/m mice) and increased the ratio of tri- to disulfated disaccharides in hepatic HSPGs (P < 0

285 We analyzed 10 tri- to hepta-BDE congener levels in blood collected fro

286 h-resolution mass spectrometry to measure 10 tri- to heptabrominated diphenyl eithers in serum sample

287 the arithmetic mean serum concentrations of tri- to hexaBDEs were lower in NHANES 2007/08 than in 20

288 ion contributed to the body burden of mostly tri- to hexachlorobiphenyls and produced a distinct prof

289 nriched vapor, body tissues mainly contained tri- to hexachlorobiphenyls.

290 from the human Y chromosome was searched for tri- to hexanucleotide microsatellites.

291 ified highly polymorphic BES-SSRs containing tri- to hexanucleotides motifs and bringing together rel

292 cases significantly correlated (P < 0.05) to tri- to nona-BDE homologues, and the strength of the cor

293 up to 52% and the aqueous concentrations of tri- to nonachlorobiphenyl PCB congeners by as much as 9

294 leven standard oligosaccharides ranging from tri- to nonasaccharide (3'-sialyllactose, 6'-sialyllacto

295 ngeners of 2,3,7- and 2,3,7,8-Br-substituted tri- to octabromodibenzo-p-dioxins and -furans, and all

296 attached support has been used to synthesize tri- to octapeptides in 28 to 97% yields using only 1.2

297 ibrary of 31 free HMOs, ranging in size from tri- to octasaccharide, was screened against three human

298 entic oligosaccharide standards ranging from tri- to octasaccharides, and their identities were confi

299 ermodynamic data demonstrate that the native tri- to pentasaccharides have free energies of binding i

300 The tri- versus diphosphate specificity of the two receptors