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1 e bridging, which was hardly observed when C-mannosylated.
2 ure CPO are partially (40-50%) or completely mannosylated.
3 tococcus neoformans are dependent on heavily mannosylated Ags termed mannoproteins.
4 e findings point to the potential utility of mannosylated albumin nanoparticles in delivering TGFbeta
5                                              Mannosylated albumin nanoparticles incorporating TGFbeta
6                                We engineered mannosylated albumin nanoparticles, which were found to
7 paired Pneumocystis carinii phagocytosis and mannosylated albumin uptake.
8 or extracellular matrix protein binding to O-mannosylated alpha-dystroglycan that is lacking in secon
9 ducts, glycosides, and amino acids were beta-mannosylated and beta-rhamnosylated successfully using a
10 in folding and stability, we analyzed both C-mannosylated and non-C-mannosylated thrombospondin type
11               In this report, functionalized mannosylated aniline polymer (manno-PANI) was investigat
12   Cryptococcal mannoproteins (MP) are highly mannosylated antigens which elicit T-cell responses in i
13 LD to generate glycopeptides mimicking viral mannosylated antigens, glucosylated species and precurso
14 -lipid IVA, functions as an acceptor, but is mannosylated at less than 1% the rate of Kdo2-lipid IVA.
15 d reveal that the WSXWS motif of IL-21R is C-mannosylated at the first tryptophan.
16 bset of IgM(+) FL samples, displaying highly mannosylated BCR, efficiently bound dendritic cell-speci
17 n/activation molecules, were able to take up mannosylated bovine serum albumin more efficiently than
18 sfer was inhibited by the addition of excess mannosylated bovine serum albumin to the culture medium
19 at was found to endocytose rhodamine-labeled mannosylated BSA (rMBSA), though the receptor was not in
20 l aspartic proteinase inhibitor pepstatin to mannosylated BSA via a cleavable disulfide linker.
21 ositol residue methylated are recognized and mannosylated by the GPI biosynthetic pathways of Trypano
22 Compared to the non-mannosylated nanomotors, mannosylated c-CLEnM exhibited enhanced motion and highe
23 e to cyanovirin's ability to bridge gp120 to mannosylated cell surface proteins.
24          Mycobacterium tuberculosis contains mannosylated cell wall components which are important in
25 ecal depletion of CD206(+) macrophages using mannosylated clodronate liposomes promoted sustained pai
26 g microglia by intrathecal administration of mannosylated clodronate liposomes reduced the capacity o
27                         Herein, we introduce mannosylated compartmentalized cross-linked enzyme-drive
28         We report that static quenching of a mannosylated conjugated polymer (sugar-PPE) by Concanava
29  Our results further define the functional O-mannosylated glycan structure and indicate that B4GAT1 i
30                                 Upon binding mannosylated glycans, FimH, an adhesin in E. coli, under
31 automated solid-phase peptide syntheses of C-mannosylated glycopeptides, which we used to map the epi
32  A and LC-MS analysis, we identified a novel mannosylated glycoprotein phosphoribosyltransferase, enc
33 ll is composed of an outer layer enriched in mannosylated glycoproteins (mannan) and an inner layer e
34              FimH, the type 1 adhesin, binds mannosylated glycoproteins on the surface of human and m
35 tip of bacterial type 1 pili, interacts with mannosylated glycoproteins on the urothelial mucosa.
36 anthamoeba trophozoites bind specifically to mannosylated glycoproteins upregulated on the surfaces o
37 modification without nonspecific labeling of mannosylated glycoproteins.
38 possible regulated degradation pathway for O-mannosylated glycoproteins.
39  appendages that carry adhesins specific for mannosylated glycoproteins.
40            Inositol deacylation of the fully mannosylated GPI intermediate allows further processing,
41                Inositol acylation of the non-mannosylated GPI intermediate D-GlcNalpha1-6-D-myo-inosi
42 The subsequent inositol deacylation of fully mannosylated GPI intermediates is inhibited by both phen
43  characterization of novel inositol-acylated mannosylated GPI intermediates.
44  biosynthesis, we found that the assembly of mannosylated GPI species was impaired when purified ER p
45 in the conversion of GlcN-PI to H5 (a singly mannosylated GPI structure containing one phosphoethanol
46  appendages that carry adhesins specific for mannosylated host glycoconjugates.
47    We recently developed a polythiolated and mannosylated human serum albumin (SH-Man-HSA), a nano-an
48                       We have now identified mannosylated IgM at the surface of primary lymphoma cell
49 duced a DC-SIGN-dependent adhesion of highly mannosylated IgM(+) FL B cells and triggered BCR-associa
50 of the mannose receptor (MR) or DC-SIGN bind mannosylated Igs in vitro and bind to FL cells, signalin
51 fic steric hindrance, leading to exposure of mannosylated immunoglobulin (Ig) to the microenvironment
52              We demonstrate that Mid2 is not mannosylated in a pmt2 mutant and that this modification
53 there must be additional proteins that are O-mannosylated in the mammalian brain.
54 ha-PI(C8) and GlcNalpha-acyl-PI(C8) could be mannosylated in vitro, but mannosylation of the latter w
55 pendent on mannose receptors, as competitive mannosylated inhibitors and calcium chelators each inter
56 irst verified synthesis of Carmo-HrTH-I, a C-mannosylated insect hormone.
57 ed here identify key novel inositol-acylated mannosylated intermediates, allowing the formulation of
58 ic absorbance biosensor (P-FAB) strategy for mannosylated LAM (Man-LAM or Mtb LAM) detection down to
59                      In contrast, terminally mannosylated LAM (ManLAM) binds the macrophage mannose r
60                              Both terminally mannosylated LAM isolated from Mtb and LAM lacking the t
61                      In contrast, terminally mannosylated LAM isolated from Mycobacterium bovis BCG f
62 antibodies enhanced FimH-mediated binding to mannosylated ligands and increased by severalfold bacter
63 onstrate an extended ligand binding site for mannosylated ligands and the significant contribution of
64 e to assess macrophage receptor activity for mannosylated ligands in vivo.
65 r binding of the N-terminal lectin domain to mannosylated ligands on host cells.
66 mans supernatants to stimulate X5A3 and (ii) mannosylated ligands to competitively inhibit this stimu
67 6-phosphate receptor (IGF-IIR) with IGFs and mannosylated ligands was analyzed in real time.
68 m tuberculosis cell-wall glycolipids such as mannosylated lipoarabinomannan (ManLAM) can inhibit muri
69               Recent work has indicated that mannosylated lipoarabinomannan (ManLAM) isolated from My
70 oglycan (LPG) and Mycobacterium tuberculosis mannosylated lipoarabinomannan (ManLAM), modulate essent
71                            Another important mannosylated lipoglycan on the M. tuberculosis surface i
72 nctional PMM involved in the biosynthesis of mannosylated lipoglycans that participate in the associa
73 ated with intra-LC or intra-central amygdala mannosylated liposomes containing clodronate (m-CLD; 0 o
74 hages are depleted with either unmodified or mannosylated liposomes encapsulating dichloromethylene d
75 y suggest that a subset of the presumptively mannosylated M. leprae glycoproteins act as ligands for
76 The recent expansion of well-characterized O-mannosylated mammalian proteins beyond the archetypical
77  injury; (2) Polyman2, the newly synthesized mannosylated molecule selected for its binding to MBL, i
78                                              Mannosylated molecules on the Mycobacterium tuberculosis
79 rotein and the first complete structure of a mannosylated mycobacterial protein, and establishes the
80   The results provide support that alpha-1,2-mannosylated N-glycans present on cancer cell membrane p
81                          Compared to the non-mannosylated nanomotors, mannosylated c-CLEnM exhibited
82 NC5A contain WxxWxxWxxC motifs that can be C-mannosylated on all tryptophans.
83 through the plasma membrane and are highly O-mannosylated on their extracellular domains.
84        The glycoprotein GC was mainly highly mannosylated on tick cell-derived viral progeny.
85 NT1-only site is sufficient to convert the O-mannosylated peptide to a substrate for POMGNT2.
86 2L-A enabled specific enrichment of C- and O-mannosylated peptides and might have superior properties
87 ides, we applied BC2L-A affinity to enrich C-mannosylated peptides from complex samples of tryptic di
88      Mass spectrometry (MS) easily detects C-mannosylated peptides from purified proteins but not fro
89 emonstrate that POMGNT1 is promiscuous for O-mannosylated peptides, whereas POMGNT2 displays signific
90 cation but was until now not available for C-mannosylated peptides.
91 lity, this lectin is able to retain C- and O-mannosylated peptides.
92 ibe the design, synthesis, and evaluation of mannosylated phenylalanine grafted chitosan (Man-CS-Phe)
93  summary, we show that a novel mycobacterial mannosylated phosphoribosyltransferase acts as a virulen
94 enrichment strategy to identify accumulating mannosylated plasma glycoproteins linked to the absence
95  structural configuration for cell uptake of mannosylated poly(ethylene glycol)-conjugate type NCs wa
96            Complexes were formed between the mannosylated polylysine and oligonucleotides and added t
97 consisting of an irrelevant plasmid bound to mannosylated polylysine or the expression plasmid bound
98 pression can be achieved using the antisense mannosylated polylysine system.
99 synthetic molecular conjugate, consisting of mannosylated polylysine that exploits endocytosis via th
100 elivery, a molecular conjugate consisting of mannosylated polylysine that exploits endocytosis via th
101 M-A), lipoarabinomannan (Cg-LAM) and a multi-mannosylated polymer (Cg-LM-B) based on a 1,2-di-O-C(16)
102 ssembling (40-50 nm micelles), pH-sensitive, mannosylated polymeric peptide delivery platform that ta
103 roteolysis during sepsis are proportional to mannosylated protein accumulation in the blood.
104 glycoprotein epithelial (E)-cadherin as an O-mannosylated protein and establish a functional link bet
105 ation sites, and it is possible that it is a mannosylated protein like the major polar tube protein (
106 ave shown that Acanthamoeba interacts with a mannosylated protein on corneal epithelial cells and sti
107  also reflected in their binding to selected mannosylated proteins and in their ability to promote se
108 e of over two hundred circulating endogenous mannosylated proteins in healthy mice at steady state, i
109           FimH-mediated cellular adhesion to mannosylated proteins is critical in the ability of urop
110 that facilitates adhesion of trophozoites to mannosylated proteins on corneal epithelial cells.
111   We show that contact lens wear upregulates mannosylated proteins on the corneal epithelium, stimula
112 ults suggest that binding of trophozoites to mannosylated proteins on the corneal surface induces A.
113 thamoeba keratitis is profoundly affected by mannosylated proteins on the ocular surface, which stimu
114 g tropism and bound equally to all cells and mannosylated proteins tested.
115                    Assignment of circulating mannosylated proteins to curated biological and pathogen
116  1 (MR), which functions to clear endogenous mannosylated proteins, a principle used to endow insulin
117 ia pastoris, resulting in unglycosylated and mannosylated proteins, respectively.
118  uroepithelial cells and for various soluble mannosylated proteins.
119 ng to acute urinary tract infection, yet the mannosylated receptor for type 1 pili on the squamous ep
120 o form IBCs even though it bound normally to mannosylated receptors in the urothelium.
121 ause urinary tract infections by adhering to mannosylated receptors on the human urothelium via the c
122                                              Mannosylated scFv also bound to DC-SIGN on the surface o
123                                              Mannosylated scFv bound specifically to the lectin domai
124 per enzyme to prevent the vast majority of O-mannosylated sites on proteins from becoming modified wi
125 de, with little labeling in the more complex mannosylated sphingolipids, whereas disruption of ELO2 r
126 Langerhans cells, would recognize the highly mannosylated structures in pathogenic Mycobacterium spp.
127 to HIV-1 virions via the abundant and highly mannosylated sugar moieties of HIV-1 envelope glycoprote
128  HIV-1, Mycobacterium tuberculosis expresses mannosylated surface structures and exploits C-type lect
129          As simulated cells progress along a mannosylated surface under flow, the fimbriae bend and b
130                FimH is able to interact with mannosylated surface via a shear-enhanced catch bond mec
131 udy the length of time that E. coli pause on mannosylated surfaces and report a double exponential de
132 low type 1 fimbriated bacteria to move along mannosylated surfaces under relatively low flow conditio
133 n, FimH, mediates shear-dependent binding to mannosylated surfaces via force-enhanced allosteric catc
134 ia, such as Escherichia coli when binding to mannosylated surfaces via the adhesive protein FimH, adh
135 y, we analyzed both C-mannosylated and non-C-mannosylated thrombospondin type 1 repeats (TSRs) of net
136 proof of concept that LIT with synthetically mannosylated tolerogens provides a rapid, safe, and effe
137                               Replacement of mannosylated Trp residues in TSR1 with either Ala or Phe
138 ns emanating from GPC3 (N241 in human) and C-mannosylated tryptophans of the Unc5D thrombospondin-lik
139 erium tuberculosis (M.tb) envelope is highly mannosylated with phosphatidyl-myo-inositol mannosides (

 
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