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

6 3 patients (40%) at 3 to 4 months, including tri- and bilineage responses.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Tri- and hexanucleotide repeats are found in consistent

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

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

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

36 Galactosylated tri- and pentamannosides, representing the structure of

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

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

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

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

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

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

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

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

45 4,4'-)-dicarbomethoxydibenzo-27-crown-9 with tri- and tetra-(ethyleneoxy) linkages transposed were sy

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 In vitro antimalarial screening of both tri- and tetracyclic analogs was conducted using the W-2

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

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

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

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

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

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

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

75 Tri- and tetramethyl-substituted acridones had the highe

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

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

78 Di-, tri- and tetranucleotide repeat microsatellite markers l

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

80 Two thousand nine hundred and thirty-one tri- and tetranucleotide short tandem repeat polymorphis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 Tri- and tetrasubstituted alkenes, including the challen

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

100 efficient intramolecular cyclopropanation of tri- and tetrasubstituted alkenes.

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

102 In tri- and tetrasubstituted allenes, steric issues concern

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

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

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

106 Tri- and tetrasubstituted anilines are formed in good to

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

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

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

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

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

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

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

114 Tri- and tetrasubstituted hydrazines could be formed by

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

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

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

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

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

120 0' interprotomer cross-links, including di-, tri- and tetrasulfide bonds, which allosterically inhibi

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

122 s are green and blue-green in color, contain tri- and tetrasulfonated moieties, compared to the disul

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 alysis revealed 24 lactosamine species (bi-, tri-, and tetraantennary structures), with all branches

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

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

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

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

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

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

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

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

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

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

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

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

169 with no increase in stutter artifact on di-, tri-, and tetranucleotide repeats.

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

171 Comparisons use relative abundances of di-, tri-, and tetranucleotides from entire genomes.

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

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

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

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

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

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

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

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

180 and molecular weight of asialo-, mono-, di-, tri-, and tetrasialotransferrin variants was obtained fr

181 The focused protein zones of di-, tri-, and tetrasialotransferrins are eluted by combining

182 ferences in isoelectric point (pI), the di-, tri-, and tetrasialotransferrins are separated and resol

183 nal transferrin variants within each of di-, tri-, and tetrasialotransferrins, differing in their mol

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 8 for monomethylated lysine, and 84 for di-, tri-, and unmethylated lysine) have been effectively use

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

238 0, ApoB), and 27 microsatellite loci of di-, tri-, or tetranucleotide repeats.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

279 The tri- versus diphosphate specificity of the two receptors