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1 nd 12 metabolites (methylated, glucuronided, sulfated).
2 S was significantly increased and abnormally sulfated.
3  primary CD4(+) T cells is inherently highly sulfated.
4 nd this glycosaminoglycan was 2,6-O- and 3-O-sulfated.
5 e remaining 23, 21 were tested, and all were sulfated.
6                                   The highly sulfated (1-->3)-alpha-l-fucan from S. cichorioides was
7                                              Sulfated 2-acrylamido-2-methyl-1-propanesulfonic acid (A
8                                     A highly sulfated 3-linked beta-arabinan (Ab1) with arabinose in
9  in the fibromodulin N-terminal domain are O-sulfated, a posttranslational modification often involve
10 f trisulfated glucosamine [N-, 3-O-, and 6-O-sulfated] (A*) is bifurcated, owing to the presence of A
11 rbed on Bronsted acidic sulfated ZrO2 (ZrS), sulfated Al2O3 (AlS), and ZrO2-WO3 (ZrW).
12                        To discover promising sulfated allosteric modulators (SAMs) of glycosaminoglyc
13                             Carrageenans are sulfated alpha-1,3-beta-1,4-galactans found in the cell
14 r(CH(3))(3) adsorbed on Bronsted superacidic sulfated alumina (AlS).
15 CR5 mutants severely damaged in the tyrosine-sulfated amino terminus or extracellular loop 2.
16 ] with aqueous sulfuric acid to generate its sulfated analogue, MOF-808-2.5SO4 [Zr6O5(OH)3(BTC)2(SO4)
17           To limit intestinal absorption, C7-sulfated analogues designed to avoid active and passive
18                               We discover 20 sulfated and 4 acetylated N-glycans on IgGs.
19                      This library covers 4-O-sulfated and 6-O-sulfated oligosaccharides ranging from
20 lso identified an HPLC peak corresponding to sulfated and glucuronidated estradiol in serum from wild
21  both sources, including structures carrying sulfated and methylated variants of the histo-blood grou
22 n TPST and peptides around tyrosines of both sulfated and non-sulfated proteins to differentiate them
23 the heparan sulfate chains of GPC3, both the sulfated and nonsulfated portions.
24   Based on the controlled production of both sulfated and nonsulfated variants in plants, we could un
25 ular assemblies containing various original, sulfated, and carboxylated polysaccharides.
26 ormones and processes it to a unique, triple-sulfated, and N-terminally truncated product distinct fr
27 These results show that this novel pyranosic sulfated arabinan Ab1 exerts its anticoagulant activity
28                                         Less sulfated arabinans obtained from the same seaweed have l
29  up to dodecasaccharide, as well as a highly sulfated Arixtra-like heptamer.
30 ed library led to the identification of 6, a sulfated aromatic mimetic of heparin.
31 one composed of 3-alpha-Glc1 units partially sulfated at 2- and 4-positions and branches of Pyr(4,6)a
32  of which two are sulfated at C-3 and one is sulfated at C-2.
33 dihydroxypent-4-enoic acid, of which two are sulfated at C-3 and one is sulfated at C-2.
34 of repetitive disaccharide units that can be sulfated at specific positions by heparan sulfate O-sulf
35                        Our work presents the sulfated benzofuran scaffold as a promising framework to
36 gnition between the two structurally related sulfated benzofurans.
37 because of the unique positioning of the 3-O-sulfated beta-galactose headgroup.
38  method is illustrated by the synthesis of a sulfated beta-mannuronic acid disaccharide.
39       Loading also increased with content of sulfated BP in microspheres.
40                                              Sulfated BP-PLGA microspheres were capable of loading LY
41                  The peak at m/z 433 is also sulfated, but it contains an additional oxygen, as confi
42 eas the major bile salts in adult liver were sulfated C27 bile alcohols.
43 ited, leading to accumulation of more highly sulfated C4S, which binds less galectin-3, a beta-galact
44  of Siglec-8 toward different sialylated and sulfated carbohydrate ligands and determined the structu
45 structures, langerin has the ability to bind sulfated carbohydrate ligands as 6-sulfated galactosides
46 HIV-1 entry by adding or removing a tyrosine-sulfated CCR5 peptide from the culture medium.
47 fluenza virus particles using novel magnetic sulfated cellulose particles is presented and compared t
48 rifugation method, use of the novel magnetic sulfated cellulose particles reduced the influenza A vir
49 ) B cells release ACh after stimulation with sulfated cholecystokinin but not norepinephrine.
50 ions and increased concentrations of the non-sulfated chondroitin disaccharide D0a0 and the disacchar
51  This nematode produces large amounts of non-sulfated chondroitin in addition to low-sulfated chondro
52 method to modify cell surfaces with specific sulfated chondroitin sulfate (CS) glycosaminoglycans usi
53  non-sulfated chondroitin in addition to low-sulfated chondroitin sulfate chains.
54  for these complexes; indeed, for the highly sulfated chondroitin sulfate motifs, CS-E and CS-D, ther
55 parated mixtures, with a particular focus on sulfated compounds.
56 were identified in biological fluids, mainly sulfated conjugates of caffeic and ferulic/isoferulic ac
57     We have examined the effect of increased sulfated content of galactosylceramides (sulfatides) on
58 2 as the site of binding for the most potent sulfated coumarin.
59                                     Overall, sulfated coumarins represent first-in-class, sub-maximal
60 thrombin was impaired in the presence of the sulfated coumarins suggesting that allosteric partial in
61  We synthesized a focused library of some 36 sulfated coumarins to discover two agents that display s
62 eport demonstrates the use of differentially sulfated CS chains for neuronal navigation.
63  M NaCl) were found to predominantly contain sulfated CS disaccharides, including disulfated disaccha
64  (0.1-0.5 M NaCl) contained unsulfated and 4-sulfated CS disaccharides.
65 M NaCl and found to contain unsulfated and 4-sulfated CS disaccharides.
66                       We could indeed detect sulfated CS in both wild type and mutant nematodes.
67 ere analyzed for their reactivity with the 4-sulfated CS linkage region antibody (2B6).
68 also describe the synthesis of unnatural 6-O-sulfated CS pentasaccharides containing either a 6-O-sul
69                        Here, we identified a sulfated derivative of the Escherichia coli polysacchari
70  polysaccharide revealed that the highly N,O-sulfated derivative prevents the binding of p17 to both
71 iched in galactosylceramide (GalCer) and its sulfated derivative sulfatide.
72  group of LC-PCBs and their hydroxylated and sulfated derivatives by selective displacement of the fl
73 rmore, analysis of a minilibrary of variably sulfated derivatives of Escherichia coli K5 polysacchari
74 ccharide to be converted into 12 differently sulfated derivatives.
75 -sulfotransferases-1 (3-OST1) to provide 3-O-sulfated derivatives.
76 companied by a decrease in iduronic acid 2-O-sulfated disaccharide structures.
77 ts displayed a relative increase in mono-6-O-sulfated disaccharides accompanied by a decrease in idur
78  parallel increase in iduronic acid mono-2-O-sulfated disaccharides.
79                                 The tyrosine-sulfated domain and the leucine-rich repeat domain both
80 gth fibromodulin and its N-terminal tyrosine-sulfated domain purified from tissue, as well as recombi
81  pro-pathogenic activity is dependent on 2-O-sulfated domains in HS, indicating that the effects of s
82           These results demonstrate that 2-O-sulfated domains in syndecan-1 HS halt disease progressi
83  VEGFA and proteoglycan co-receptors require sulfated domains in the HS chains.
84 d length are used as chemical analogs of the sulfated domains of heparan sulfate and examined for the
85                        Altering specific 3-O-sulfated epitopes provides a mechanism to rapidly respon
86  effects of different PGs and their assorted sulfated epitopes.
87 s for urinary estrus signals, as well as for sulfated estrogen (SE) compounds.
88        Thus we have shown that excess overly sulfated extracellular HS binds, and sequesters CXCL12,
89 posed mechanisms of sulfatase catalysis is a sulfated FGly intermediate.
90                               Interestingly, sulfated fibulin 2 significantly reduced the rate of cel
91  gene, dehydroepiandrosterone (DHEA) and its sulfated form (DHEA-S), and characteristics of attention
92 CFH binds more strongly to heparin (a highly sulfated form of HS) than CCP19-20, and that their sulfa
93 portantly, the peptide is only active in the sulfated form, further confirming the importance of the
94 aran sulfate occurring in N-acetylated and N-sulfated forms, and as the unmodified amine.
95 te OH stretches, as a means to differentiate sulfated from phosphorylated peptides within the framewo
96 es, including the characterization of labile sulfated functional groups.
97                           Surprisingly, even sulfated fungal Myc-LCOs and Sinorhizobium meliloti Nod-
98 y controlling Wnt3a availability through its sulfated GAG chains.
99 emely mild matrix for the analysis of highly sulfated GAG disaccharides by infrared matrix-assisted l
100 several micrograms), particularly for highly sulfated GAG ions.
101                                          The sulfated GAG oligosaccharides derived from cartilage pos
102       This research establishes that chicken sulfated GAG polysaccharides can enhance iron uptake by
103                  Both the cartilage and skin sulfated GAG polysaccharides showed greater ferritin for
104                     Heparin, the most highly sulfated GAG, binds sCT in the pH interval 3-7.
105 nt positive charge, and its interaction with sulfated GAG-polymers were quantitatively investigated u
106                       Enzymatic digestion of sulfated GAGs canceled their effects on trigeminal neuro
107                                     While no sulfated GAGs have been found in marine sponges, chondro
108 ate highly informative EDD spectra of highly sulfated GAGs on the liquid chromatography (LC) timescal
109                         HSV-1 recognized all sulfated GAGs, but not the nonsulfated hyaluronan, indic
110 several classes of GAGs; however, the highly sulfated GAGs, such as heparins, have remained a relativ
111 n inexpensive, colorimetric urinary assay of sulfated GAGs.
112 ghput, de novo structural analyses of highly sulfated GAGs.
113 tain polyanionic, low-methylated pectins and sulfated galactans, a feature shared with the cell walls
114 alactosamine dominated, we also detected 6-O-sulfated galactosamine residues.
115 rmed by unique loop regions, recognizing 6-O-sulfated galactose dictates tight specificity distinct f
116  group antigens, and glycans with terminal 6-sulfated galactose.
117 y to bind sulfated carbohydrate ligands as 6-sulfated galactosides in the Ca(2+)-dependent binding si
118                                              Sulfated galactosylceramides (sulfatides) are glycosphin
119 o receive the N-acetyl and sulfate groups of sulfated GalNAc residues of glycosaminoglycans such as c
120 tion and possible developmental roles of 2-O-sulfated GlcA (GlcA2S).
121 epolymerized for compositional analysis, 3-O-sulfated glucosamine at the reducing ends appears to be
122 hat specifically degrades HS chains with 3-O-sulfated glucosamine at the reducing-end.
123 critically depend on the distribution of 6-O-sulfated glucosamine residues, which is generated by glu
124 in the peptide backbone and acid sensitive O-sulfated glycan chains.
125 ycopeptide containing aspartic acid and an O-sulfated glycan was synthesized.
126 ed Bacteroides species, to metabolize highly sulfated glycans (i.e. mucins and glycosaminoglycans (GA
127       Human naive and memory B-cells express sulfated glycans as high affinity CD22 ligands, which ar
128  similar applications based on permethylated sulfated glycans have not been fully investigated.
129               Siglec-F recognizes sialylated sulfated glycans in glycan-binding assays, but the ident
130 based nanoLC-MS/MS analysis of permethylated sulfated glycans in negative ion mode and demonstrate th
131 ) are a class of heterogeneous, often highly sulfated glycans that form linear chains consisting of u
132                                              Sulfated glycans were selectively recovered from the aqu
133 ed mucin preparations carried sialylated and sulfated glycans, bound to eosinophils and induced their
134 an easy way to separate and hence enrich the sulfated glycans.
135 exchange cartridges facilitated detection of sulfated glycans.
136  pathways and action mechanisms via distinct sulfated glycoconjugate-mediated processes.
137 ted to suggest that the shifting between the sulfated glycoconjugates as distinct targets of CTX A2,
138 ins as well as enhanced expression of MECA79 sulfated glycoepitope at the luminal aspect of HEVs, thu
139 ugh interactions with adhesion receptors and sulfated glycolipids (Figure 1, bottom).
140             We report here on supramolecular sulfated glycopeptide nanostructures, which display a tr
141 ursor to produce a variety of differentially sulfated glycopolymers.
142 oprotective factor prosaposin (also known as sulfated glycoprotein-1), we purified full-length prosap
143                                   Food grade sulfated glycosaminoglycan (GAG) polysaccharides were su
144 osition of AF-specific extracellular matrix (sulfated glycosaminoglycan and collagen type I), indicat
145 result from differences in intracellular HA, sulfated glycosaminoglycan concentration, apoptosis, or
146 ed by 36 and 30%, respectively, and SDC4 and sulfated glycosaminoglycan in the culture medium were in
147                          Heparin is a highly sulfated glycosaminoglycan that shares a common biosynth
148 K is promoted by chondroitin sulfate (CS), a sulfated glycosaminoglycan.
149 that specifically degrade heparan sulfate, a sulfated glycosaminoglycan.
150 riments (BIAcore) determined that DMAV binds sulfated glycosaminoglycans (e.g. heparin, KD ~100 nmol/
151                        Degraded fragments of sulfated glycosaminoglycans (GAGs) are key reporters for
152        Structural characterization of highly sulfated glycosaminoglycans (GAGs) by collisionally acti
153 y langerin was demonstrated to interact with sulfated glycosaminoglycans (GAGs), in a Ca(2+)-independ
154 importance of tissue-specifically expressed, sulfated glycosaminoglycans (GAGs), like HS, in determin
155 ients that are achieved by interactions with sulfated glycosaminoglycans (GAGs).
156        Proteoglycans are proteins that carry sulfated glycosaminoglycans (GAGs).
157 ned by our demonstrated N6L interaction with sulfated glycosaminoglycans and consequently the control
158 IMP-3 K26A/K45A retained higher affinity for sulfated glycosaminoglycans than K42A/K110A and exhibite
159                                       Highly sulfated glycosaminoglycans within the cartilage matrix
160 g of CpClec-Fc was specifically inhibited by sulfated glycosaminoglycans, particularly heparin and he
161 osomal sulfatases involved in degradation of sulfated glycosaminoglycans.
162 e and sialyl-globotetraosylceramide, and the sulfated glycosphingolipids sulfatide, sulf-lactosylcera
163 ochemistry, and electron microscopy, whereas sulfated glycosphingolipids were only found in intracell
164 fication of various fucosylated, sialylated, sulfated glycotopes and definitive determination of the
165 ct patients revealed that circulating highly sulfated heparan fragments persisted for greater than 3
166  lines of evidence suggested the role of 3-O-sulfated heparan sulfate (3-OS HS) during HCMV-mediated
167 lope glycoprotein D (gD) to the receptor 3-O-sulfated heparan sulfate (3-OS HS) mediates viral entry.
168 of cells in sodium chlorate, indicating that sulfated heparan sulfate chains are required for nuclear
169  both NDST1 and NDST2, expressing a very low sulfated heparan sulfate, can take the initial step towa
170  decreased glomerular expression of a highly sulfated HS domain, and albuminuria.
171 ografts we found increased expression of 6-O-sulfated HS domains in tubular epithelial cells during c
172 e cleaves at the non-reducing side of highly sulfated HS domains, exposing cryptic growth factor bind
173                   To examine the role of 6-O-sulfated HS in the development of fibrosis, we generated
174  GAGs from Idua(-/-) BM and specifically 2-O-sulfated HS, elevated in Idua(-/-) BM, both inhibited CX
175 thelial cells and that these effects require sulfated HS.
176    Enzymes generating a specific type of 3-O-sulfated-HS (3-O-HS) are enriched, and fibroblast growth
177 ed binding region to chondroitin sulfate and sulfated hyaluronan but not to the non-sulfated hyaluron
178 e and sulfated hyaluronan but not to the non-sulfated hyaluronan, confirming binding specificity.
179 fate) and compared our results to chemically sulfated hyaluronan.
180 ot require compounds such as hydrocarbons or sulfated hydrocarbons, however, it cannot be explained o
181  Four new metabolites of PCMC (hydroxylated, sulfated/hydroxylated, sulfated PCMC, and glucuronidated
182 rides, suggesting that the disaccharide; 2-O-sulfated iduronic acid linked to 6-O-sulfated N-glucosam
183             Both antibodies were efficiently sulfated in planta on coexpression of an engineered huma
184 ally modified by tyrosine sulfation, and the sulfated isoform is present outside the cell, whereas th
185  the HS structure revealed that the highly O-sulfated K5 polysaccharides inhibited HMPV infection, id
186                           Heparan sulfate, a sulfated linear polysaccharide modified in a complex var
187 s to HA, suggesting that the CS containing 4-sulfated linkage region structures and disulfated disacc
188 face via interactions with surface-localized sulfated lipid and protein receptors.
189             Thus, other, as-yet unidentified sulfated macromolecules must contribute to infection.
190 e mass measurement confirmed m/z 417 to be a sulfated metabolite of glyceollins.
191                        Interactions of these sulfated metabolites of LC-PCBs with HSA, however, have
192     Several acetylated, hydroxylated, and/or sulfated metabolites were identified, some of which were
193 etabolites, together with glucuronidated and sulfated metabolites, were detected.
194            Here, we report superacidity in a sulfated metal-organic framework (MOF) obtained by treat
195 ed by tremendous structural heterogeneity of sulfated modifications.
196        We conclude that interaction with the sulfated N terminus of CCR2 destabilizes the dimerizatio
197 de; 2-O-sulfated iduronic acid linked to 6-O-sulfated N-glucosamine, which contains a free amine at p
198 sferase-1 (GlcNAc6ST-1) failed to synthesize sulfated N-glycans and exhibited abnormal myelination an
199                         Here, we report that sulfated N-glycans are involved in peripheral nervous sy
200                                        Major sulfated N-glycans were identified in both porcine and m
201 ie-Tooth neuropathy, has abundant GlcNAc-6-O-sulfated N-glycans.
202 myelin glycoproteins contain highly abundant sulfated N-glycans.
203 to be responsible for the degradation of 3-O-sulfated N-sulfoglucosamine residues of heparan sulfate
204 se residues as well as from an authentic 3-O-sulfated N-sulfoglucosamine standard.
205 ping using the MCP-1 mutants showed that the sulfated N-terminal region of CCR2 binds to the same reg
206 of human-, swine-, and avian-origin viruses; sulfated Neu5Acalpha2-3 substructures were associated wi
207                                      Because sulfated neurosteroids also modulate NMDARs, here we exa
208 ilar to cationic channel blockers but unlike sulfated neurosteroids, DPA antagonism was voltage depen
209 n-6) polyunsaturated fatty acids (PUFAs), 2) sulfated neurosteroids, which play a role in brain devel
210 re essential for growth and development; low sulfated neurosteroids, which play a role in brain devel
211 y a mechanism indistinguishable from that of sulfated neurosteroids.
212 d both undersulfated (NA) domains and highly sulfated (NS) domains as well as very well defined non-r
213                     Also, nearly 100% of the sulfated O-linked glycans were recovered in the aqueous
214 ed to carry high densities of sialylated and sulfated O-linked glycans.
215 try (MALDI MS), for quantitative analysis of sulfated oligosaccharides in biological samples.
216                                        Three sulfated oligosaccharides of natural origin were chosen
217     This library covers 4-O-sulfated and 6-O-sulfated oligosaccharides ranging from trisaccharides to
218                                       First, sulfated oligosaccharides such as chondroitin-4-sulfate
219 tures of oligo-porphyrans, a class of highly sulfated oligosaccharides.
220 method for detection and characterization of sulfated oligosaccharides.
221          It comprised major amounts of units sulfated on C-2 and C-4 and constitutes the first polysa
222  receptors are commonly post-translationally sulfated on tyrosine residues in their N-terminal region
223 s expand the "cationic" metal center-anionic sulfated oxide surface distances, and this separation/we
224 f PCMC (hydroxylated, sulfated/hydroxylated, sulfated PCMC, and glucuronidated PCMC) were identified
225                     But only one metabolite, sulfated PCMC, was confirmed in wastewater and in urine.
226                       We recently introduced sulfated pentagalloylglucopyranoside (SPGG) as an allost
227                  We present the discovery of sulfated pentagalloylglucoside (6) as a highly selective
228 e-sulfated region) when the soluble tyrosine-sulfated peptide is present, we show that HIV-1JRCSF wit
229 nthomonas oryzae pv. oryzae (Xoo) produces a sulfated peptide named RaxX, which shares similarity to
230          In two-dimensional NMR experiments, sulfated peptides derived from the N-terminal region of
231 at variations in sequences and structures of sulfated peptides.
232  measurements of self-binding forces of this sulfated polysaccharide and their chemically desulfated
233                  Heparin is a linear, highly sulfated polysaccharide consisting of alternating glucos
234  and of purified calcium spirulan (Ca-SP), a sulfated polysaccharide contained therein.
235                                  Fucoidan, a sulfated polysaccharide from Fucus vesiculosus, decrease
236 rotein 2 significantly more than the natural sulfated polysaccharide heparin, and promoted regenerati
237                    Heparan sulfate (HS) is a sulfated polysaccharide that decorates cell surface and
238             Heparan sulfate (HS) is a linear sulfated polysaccharide that is a component of the cell
239                Chondroitin sulfate (CS) is a sulfated polysaccharide that plays essential physiologic
240                                          Its sulfated polysaccharide units, which were characterized
241 ferent from those found previously for other sulfated polysaccharides and glycosaminoglycans.
242  with binding domains for the highly diverse sulfated polysaccharides are important growth factors in
243 m-dependent multivalent self-interactions of sulfated polysaccharides components of extracellular mem
244                                          The sulfated polysaccharides from brown algae - the fucoidan
245                                   The highly sulfated polysaccharides heparin and heparan sulfate (HS
246             Heparan sulfates (HS) are linear sulfated polysaccharides that modulate a wide range of p
247 glycosaminoglycans (GAGs), a class of linear sulfated polysaccharides which are present on most anima
248 in infection in relevant models, we utilized sulfated polysaccharides, heparan sulfate mimetics, and
249 ysaccharides alginates and fucose-containing sulfated polysaccharides.
250 n between ICP-associated levels of the 3beta-sulfated progesterone metabolite epiallopregnanolone sul
251                Here we report that the 3beta-sulfated progesterone metabolite epiallopregnanolone sul
252                           Our discovery that sulfated progesterone metabolites are a prognostic indic
253 t cause cholestasis are not known but 3alpha-sulfated progesterone metabolites have been shown to be
254 ed in ICP, leading us to study the impact of sulfated progesterone metabolites on farnesoid X recepto
255 dynamics simulation of model tripeptides and sulfated protein complexes, potentials of mean force for
256  is essentially unknown how the formation of sulfated protein-binding domains in HS can be regulated
257 only a small fraction of the total predicted sulfated proteins has been identified to date.
258 imilar procedures can be applied to identify sulfated proteins in yeast and human proteome microarray
259 es around tyrosines of both sulfated and non-sulfated proteins to differentiate them.
260     Among the 4256 E. coli K12 proteins, 875 sulfated proteins were identified using antisulfotyrosin
261 curring amyloid deposits are associated with sulfated proteoglycans and other factors.
262             Heparan and chondroitin/dermatan sulfated proteoglycans have a wide range of roles in cel
263 potential for interactions with membranes or sulfated proteoglycans is lacking and it is possible tha
264 nd infection via Ca(2+)-dependent binding to sulfated proteoglycans on intestinal epithelial cells.
265 re was significantly less total collagen and sulfated proteoglycans present in the type VI collagen-d
266 rter that promotes a ventral accumulation of sulfated proteoglycans, which is required for ventral PM
267 XIa), we screened a library of 26 synthetic, sulfated quinazolin-4(3H)-ones (QAOs) resulting in the i
268               Here we found that a synthetic sulfated RaxX derivative comprising 13 residues (RaxX13-
269 terminal amino acids, including the tyrosine-sulfated region) when the soluble tyrosine-sulfated pept
270 -O sulphate group from glucosamine in highly sulfated regions of HS chains.
271  remove 6-O-sulfate groups within the highly sulfated regions on HS.
272 S from NMuMG cells contained frequent highly sulfated regions, whereas the non-bound material demonst
273 as the non-bound material demonstrated fewer sulfated regions.
274 tic cleavage of the glycoside bond between 3-sulfated rhamnose and uronic acid according to a beta-el
275 of disaccharide building blocks comprising 3-sulfated rhamnose linked to d-glucuronic acid (GlcUA), l
276 s that preferentially bind anionic residues (sulfated rhamnose, glucuronic/iduronic acid).
277 tween amino acids of viral glycoproteins and sulfated saccharides on the GAG chain.
278                            HS is composed of sulfated saccharides that are biosynthesized through a c
279 We used an mAb and/or a multimeric synthetic sulfated sialoglycan ligand recognizing Siglec-8 in comb
280 s positively charged molecules on the highly sulfated side chains of aggrecan.
281                                   Third, the sulfated SK (sSK) and sSK-related peptides were more pot
282 designed a group of novel exosite-2-directed sulfated, small, allosteric inhibitors of thrombin.
283 arin showed marginal competition with highly sulfated SPGG variants but robust competition with less
284                           Maps to a panel of sulfated steroid odorants identified tightly juxtaposed
285 based PXR antagonists inspired by the marine sulfated steroids solomonsterol A and B as natural leads
286 ich range from small, volatile molecules and sulfated steroids to large families of proteins.
287                            Using mixtures of sulfated steroids, key constituents of urine, we found t
288 rder of hydrophilicity, with the more highly sulfated structures eluting first.
289 in two serotypes suggesting a propensity for sulfated-sugar binding.
290 sponses as intact heparin, (ii) that a fully sulfated tetrasaccharide isolated from bacterial heparin
291 f the Delta-2S-iduronate to expose the fully sulfated trisaccharide (GlcNS(6S)-IdoUA(2S)-GlcNS(6S)) d
292 l efficacy of PG9 and RSH is the presence of sulfated tyrosine residues in their antigen-binding regi
293 eptides in the PSY (plant peptide containing sulfated tyrosine) family.
294 sess this, we synthesized SbO4L based on the sulfated tyrosine-containing sequence of GPIbalpha.
295  second variable loop (V2) of gp120 contains sulfated tyrosines (Tys173 and Tys177) that in the CD4-u
296 rm, further confirming the importance of the sulfated tyrosines for function.
297 d variable loop (V3), functionally mimicking sulfated tyrosines in CCR5 and anti-coreceptor-binding-s
298 GG variants but robust competition with less sulfated variants.
299 t Cp*ZrBz2 /ZrS (Cp*=Me5 C5 , Bz=benzyl, ZrS=sulfated zirconia) catalyzes the single-face/all-cis hyd
300 complexes are chemisorbed on Bronsted acidic sulfated ZrO2 (ZrS), sulfated Al2O3 (AlS), and ZrO2-WO3

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