戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 l has three of the main components but lacks mannoprotein.
2 neoformans lysate, and purified cryptococcal mannoprotein.
3 t multiple mannose receptors on DC recognize mannoprotein.
4  (CD209) was determined to have affinity for mannoprotein.
5 ponents of the N-linked glycans of cell wall mannoprotein.
6 ivo is beta(1-->3)glucan, beta(1-->6)glucan, mannoprotein.
7 tifies critical roles for fungal mannans and mannoproteins.
8 nly elicited by structurally unique C. auris mannoproteins.
9 yeast protein extracts (YPE), cell walls and mannoproteins.
10  are substrates in the biosynthesis of these mannoproteins.
11 h lacked terminal N-acetylglucosamine in its mannoproteins.
12 e that could remove N-acetylglucosamine from mannoproteins.
13 f substrates involved in the biosynthesis of mannoproteins.
14  species and composed of polysaccharides and mannoproteins.
15 ributed to physicochemical interactions with mannoproteins.
16 dependent on heavily mannosylated Ags termed mannoproteins.
17 particular epithelial cells and to aggregate mannoproteins.
18 hought to be comprised, at least in part, of mannoproteins.
19 tracellular changes arising from the loss of mannoproteins.
20 l in an och1 mutant that does not synthesize mannoproteins.
21 lacked terminal N-acetylglucosamine in their mannoproteins.
22 3, corresponded to the high concentration of mannoproteins, 2-phenyl ethanol and tyrosol.
23 rich in arabinose and galactose (39-54%) and mannoproteins (38-55%) were the major PS in the base win
24 ronoxylomannan (GXM), galactoxylomannan, and mannoprotein, affect expression of molecules on the surf
25 ally studied after isolating its components (mannoproteins, alpha1,3-glucan, beta1,3-glucan, and a br
26 es the complete structure of a mycobacterial mannoprotein and the first complete structure of a manno
27 and previous findings on the linkage between mannoproteins and beta(1-->6)-glucan, it is concluded th
28 in the incorporation of label into cell wall mannoproteins and beta(1-->6)glucan was observed.
29 accharides, with different behaviors between mannoproteins and beta-glucans.
30  cross-linking between beta-1,6-glycosylated mannoproteins and chitin.
31 Candida, but recently specific antibodies to mannoproteins and hsp90 have been shown to be protective
32 ance of cell wall integrity and retention of mannoproteins and known cryptococcal virulence factors i
33 itation steps, and clear distinction between mannoproteins and other wine polysaccharides.
34                                              Mannoproteins and polysaccharides rich in arabinose and
35 t analysis (PCA) results, being stronger for mannoproteins and rhamnogalacturonan-II (RG-II), but onl
36 ompounds), with the functional groups of the mannoproteins and the free amino acids of the surface of
37 reased the release of total polysaccharides, mannoproteins and total monosaccharides in the wines, an
38                                            A mannoprotein antigen, MP98, that stimulated one of the h
39 ->3)-glucan, beta(1-->6)-glucan, chitin, and mannoprotein are linked together.
40                                              Mannoproteins are major antigens driving T cell response
41    The mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cere
42        Mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cere
43    The mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cere
44                                           As mannoproteins are the primary components recognized by a
45  CWP1 and CWP2, the genes encoding the major mannoproteins, are down-regulated, suggesting that there
46 y is expected to broaden the applications of mannoproteins as value-added ingredients.
47 ucan is linked to both beta(1-->3)glucan and mannoprotein, as well as occasionally to chitin.
48 rium tuberculosis; however, the mechanism of mannoprotein assembly remains unclear.
49  the appropriate method for the formation of mannoproteins-based emulsions.
50 rine DC rapidly captured fluorescent-labeled mannoprotein by a mannose receptor-mediated process.
51 at is dependent upon the efficient uptake of mannoprotein by mannose receptors.
52                            Several cell wall mannoproteins can bind to immobilized osmotin, suggestin
53  order to evaluate the possible influence of mannoprotein characteristics in the interaction with fla
54 ryptococcal transcript for the extracellular mannoprotein Cig1 is highly regulated by iron and abunda
55                    Mitogen- and cryptococcal mannoprotein (CMP)-activated (CD25+CD134+) CD4+ T cells
56                                              Mannoprotein colocalized intracellularly with CD206 and
57 nthesis, it may participate in production of mannoprotein components of the capsule.
58                           Differences in the mannoprotein composition of C. albicans A9 and four spon
59 us of C. albicans, we compared the cell wall mannoprotein content and composition between C. albicans
60 DS and with the significant reduction in the mannoprotein content of mutants compared with the wild-t
61                       However, monitoring of mannoprotein content of wine during these processes, or
62 have been developed in order to increase the mannoprotein content of wine.
63                                        Thus, mannoproteins could be an effective alternative for prot
64                           Additionally, some mannoproteins decreased the browning potential.
65  the absence of serum, galactoxylomannan and mannoprotein did not affect L-selectin, TNF receptor, CD
66     Treating yeast cells to remove cell wall mannoprotein did not reduce SP-D binding, and SP-D faile
67 zed the wines; however, some arabic gums and mannoproteins do not stabilized the wines.
68 tion led to aggregation, while addition of a mannoprotein-enriched fraction exhibited a protective ef
69                                 The obtained mannoprotein extracts showed important differences in th
70       The results obtained indicate that the mannoprotein extracts were able to precipitate flavanols
71                          In this work, three mannoprotein extracts were obtained from T. delbrueckii
72 teristics in the interaction with flavanols, mannoprotein-flavanol interactions were studied by HPLC-
73  or wine polyphenols or tannins and a YPE, a mannoprotein fraction and a beta-glucan were monitored b
74 otein, hexose, and phosphate contents of the mannoprotein fraction did not differ significantly among
75 tablished based upon the capacity of (i) the mannoprotein fraction of C. neoformans supernatants to s
76                                The cell wall mannoproteins from hydrophilic and hydrophobic cells of
77                                  The DAN/TIR mannoprotein genes of Saccharomyces cerevisiae (DAN1, DA
78  is a complex structure consisting mainly of mannoproteins, glucan, and chitin.
79                              The presence of mannoproteins, glucans, non-pectic polysaccharides, and
80                        Thus, a C. neoformans mannoprotein has been characterized that stimulates T ce
81                  Thus, a second cryptococcal mannoprotein has been identified which stimulates T-cell
82 omyces cerevisiae strain EKD13 overproducing mannoproteins has been used to obtain Albarino white win
83 es but affects color stability in red wines, mannoproteins have a variable effectiveness depending on
84 e yeasts, particularly high molecular weight mannoproteins, have a protective effect against haze for
85 mouse bladder epithelial cells and a soluble mannoprotein, horseradish peroxidase, was contained with
86 e systemically screened all 49 predicted GPI-mannoproteins in Cryptococcus neoformans for enhanced ho
87      The DAN/TIR genes encode nine cell wall mannoproteins in Saccharomyces cerevisiae which are expr
88   Here, we found increased levels of exposed mannoproteins in ZNF2(oe) cells.
89 phatidylinositol anchor formation, prevented mannoprotein incorporation, whereas the beta(1-->3)-beta
90  a diffused cell wall with loss of the outer mannoprotein layer as compared with the WT cells.
91  aberrant cell wall structure with a reduced mannoprotein layer.
92                             Candida albicans mannoprotein (MAN) administered intravenously to mice st
93 mannan (GXM), galactoxylomannan (GalXM), and mannoprotein (MP), to interact with CD18 on human PMN.
94  After adsorption, no antibodies specific to mannoprotein (MP)-rich extracts or secretions were detec
95 ined in the presence and absence of isolated mannoproteins (MP) and arabinogalactans (AG) from WPM.
96                                 Cryptococcal mannoproteins (MP) are highly mannosylated antigens whic
97              Soluble Cryptococcus neoformans mannoproteins (MP) have emerged as promising vaccine can
98 he average molecular weight of smaller PRAG, mannoproteins (MP) or mannans.
99 ility of mannan to protein ratio of purified mannoproteins (MP), isolated from yeast cell walls upon
100 lin A affinity chromatography into adherent (mannoprotein [MP]) and nonadherent (flowthrough [FT]) fr
101 tatin nonaketide synthase [LNS], a cell wall mannoprotein [MP1], and a gene fragment of the cytochrom
102   The impact of the polysaccharide moiety of mannoproteins (MPs) on the color and astringency of red
103           In addition to the above defect in mannoproteins, mutant cells were also deficient in the b
104                                              Mannoprotein N-glycosyl phosphorylation appeared as the
105                                          The mannoprotein nature of MP88 was established based upon t
106 ch encodes a putative adhesin-like cell wall mannoprotein of C. albicans and radD, an arginine-inhibi
107  monoclonal antibody C7, a mAb directed to a mannoprotein of Candida albicans, significantly reduced
108 nts demonstrated that DC captured sufficient mannoprotein over 2 h to account for 50% of total stimul
109 o hyphae of a strain deficient in the fungal mannoprotein, Pra1.
110 tent of wine during these processes, or even mannoprotein quantification in the final wines, is an an
111 , we report a simple and accurate method for mannoprotein quantification in wines.
112 nd Mox2, and an activation factor, Mox4 (for mannoprotein regulation by oxygen).
113                                              Mannoproteins released by yeast cells throughout the win
114                                              Mannoproteins-rich extracts from sequential fermentation
115                                              Mannoproteins showed similar or lower solubility than ma
116 f Saccharomyces cerevisiae encode homologous mannoproteins, some of which are essential for anaerobic
117 ells, and macrophages were used to stimulate mannoprotein-specific T cells.
118 were assessed following ex vivo cryptococcal mannoprotein stimulation, using 13-color flow-cytometry.
119                                 However, the mannoprotein structural features that promote polyphenol
120 cell wall is enriched in highly glycosylated mannoproteins that are implicated in many aspects of the
121  potentially useful to produce wines rich in mannoproteins that have distinctive characteristics comp
122 individual oligomannosyl residues in Candida mannoprotein, the major antigenic determinant located on
123                                              Mannoproteins, the third major component of the cell wal
124  transfer protein 1, essential for anchoring mannoproteins to fungal cell wall, critical for host inv
125        By confocal microscopy, intracellular mannoprotein trafficked to an endo-lysosomal compartment
126  together with prior work demonstrating that mannoprotein was captured by the macrophage mannose rece
127 ork presented, the innate immune response to mannoprotein was determined.
128 annosylation, an immunoreactive cryptococcal mannoprotein was expressed recombinantly in E. coli and
129 lomannan (GXM), but not galactoxylomannan or mannoprotein, was found to cause loss of L-selectin from
130 ind suitable alternatives, eleven commercial mannoproteins were chemically characterized concerning t
131 h-MW Agrimos(R)-MP1 and YCW-b-MP1' contained mannoproteins with a mannan to protein ratio of 3.5 and
132 atile esters, dimethyl sulfide, glycerol and mannoproteins with harvest date.
133 f the cell wall is comprised of glycosylated mannoproteins with the majority of these post-translatio
134                                              Mannoprotein, with a protein moiety about 100 kDa in app

 
Page Top