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1 ying an MSG gene lacking the UCS expressed a nonglycosylated 130-kDa protein.
2 ycosylated 91-kDa subunit, gp91(phox), and a nonglycosylated 22-kDa subunit, p22(phox).
3 ain protein detected on Western blots as the nonglycosylated 27-kDa form, with overexpression of this
4 e mutant forms of FR-beta were identified as nonglycosylated (29.3 kDa) or glycosylated polypeptides
5                                    CD20 is a nonglycosylated 33 to 37 kD phosphoprotein involved in B
6                           AgSF2 represents a nonglycosylated 40-kDa protein that has novel internal a
7                                          The nonglycosylated 44-kDa P2X(4) receptor was resistant to
8      In this study, we investigated a unique nonglycosylated active fragment of hepatocyte growth fac
9  that the enhanced epimerization relative to nonglycosylated amino acids is due to a combination of f
10 MR structural characterizations of refolded, nonglycosylated amino-terminal fragments, and another pa
11 ) GalNAc(alpha-->)Thr10 contulakin-G and its nonglycosylated analog were prepared using an Fmoc (9-fl
12 n carcinomas as a combination of both 27-kDa nonglycosylated and 28-kDa glycosylated mature two-chain
13 to determine the solution structures of both nonglycosylated and fucosylated FVII EGF-1 in the presen
14 of the properties of binding of IL-7 to both nonglycosylated and glycosylated forms of the IL-7Ralpha
15 halpy and entropy changes of IL-7 binding to nonglycosylated and glycosylated IL-7Ralpha.
16 44, whereas intracellular LOXL2 (~75-kDa) is nonglycosylated and N-terminally processed, and is prima
17 ecombinant glycosylated full-length Ags, and nonglycosylated and truncated Ags recognized by 4E10 usi
18 ut homology to mammalian sequences labeled a nonglycosylated approximately 41-kDa protein (spx1) on W
19 e capacity of recombinant, histidine-tagged, nonglycosylated BclA (rBclA) given with adjuvant to prot
20                                          Two nonglycosylated BiP substrates, NS-1kappa light chain an
21               To investigate the disposal of nonglycosylated BiP substrates, we used a nonsecreted ka
22 coproteins > neoglycoproteins based on BSA > nonglycosylated BSA >> free sugars.
23 ate that enhanced binding of 3-6-fold over a nonglycosylated CBM is achieved by the addition of a sin
24 increasing it up to 140-fold relative to the nonglycosylated CBM.
25                                      Because nonglycosylated channels appear to pass through the secr
26 using purified collagen type I, type IV, and nonglycosylated, commercially available recombinant SLRP
27 ble entropy changes and smaller unfavorable (nonglycosylated complex) and favorable (glycosylated com
28  N- or C-terminal activities relative to the nonglycosylated control peptides.
29 ented N-linked glycosylation, resulting in a nonglycosylated core protein devoid of ATP and ADP hydro
30 of COX-2 protein, which is distinct from the nonglycosylated COX-2 protein generated in the presence
31 e in the E2P form in complex with bufalin (a nonglycosylated CTS with a six-membered lactone) and dig
32 ions (a) a newly synthesized, highly mobile, nonglycosylated, cytosolic receptor that is depleted by
33                           Highly methylated, nonglycosylated derivatives of the flavonoid myricetin f
34 re stimulated with peptides representing the nonglycosylated domain of G protein.
35 1A domain (GA733 type 2 motif), and a unique nonglycosylated domain without cysteines (GA733 type 3 m
36                                      It is a nonglycosylated envelope protein that is regulated as a
37 1 (HSV-1) UL20 gene encodes a 222-amino-acid nonglycosylated envelope protein which forms a complex w
38 hybridomas specific for the glycosylated and nonglycosylated epitope CII(259-273) were developed.
39 osylated EPO had a 20-fold slower k(on) than nonglycosylated EPO, indicating that the core carbohydra
40 ed for ubiquitination or degradation of this nonglycosylated ERAD substrate.
41 the present report, folding comparisons of a nonglycosylated erythropoietin (EPO) mutant are made wit
42                                              Nonglycosylated erythropoietin bearing acetamidomethyl p
43 HSV-1 infectivity.IMPORTANCE HSV-1 UL20 is a nonglycosylated essential envelope protein that is highl
44 show that glycosylated ETSHR-gp, but not the nonglycosylated ETSHR protein, can react with autoantibo
45                   Earlier, we identified two nonglycosylated exofacial regions of erythrocyte band 3
46                                          Two nonglycosylated exofacial regions of human band 3 in the
47  in bacterial biofilm formation, whereas the nonglycosylated Fap1 peptide mediates bacterial initial
48 IL-8 release from A549 cells stimulated with nonglycosylated flagellar preparations (having less then
49                   When the inhibitor and its nonglycosylated form (SmCI N23A mutant) were overproduce
50  newly synthesized Aaop1 is converted to the nonglycosylated form and deposited in the rhabdomeres.
51 elevated concentrations of AVP (100 nM), the nonglycosylated form desensitized to the same extent as
52 wever, the delta Cj1496c mutant expressing a nonglycosylated form of Cj1496c exhibited levels of inva
53 ivity was observed in strains expressing the nonglycosylated form of EmaA.
54         The ability of TgI4.4 to recognize a nonglycosylated form of gI suggests that HSV-1 recogniti
55 deficiency virus (HIV)-1 gp120 and env2-3, a nonglycosylated form of gp120.
56 PDGFRalpha did exhibit binding activity to a nonglycosylated form of PDGFRalpha.
57 ingently regulated than is processing of the nonglycosylated form of the same epitope.
58 uired more extensive processing than did the nonglycosylated form of the same epitope.
59 es: a slow migrating glycosylated form and a nonglycosylated form.
60   The proteins are found in glycosylated and nonglycosylated forms in infected cells.
61                        Both glycosylated and nonglycosylated forms of Drm exhibit identical distribut
62 ons bearing combinations of glycosylated and nonglycosylated forms of prM and E could infect mammalia
63  in the steady-state levels of the mono- and nonglycosylated forms of PrP in the brain.
64 V2) from potato (Solanum tuberosum) than its nonglycosylated forms.
65                          Here we report that nonglycosylated full-length and C-terminal truncated amy
66             The in vitro fucosylation of the nonglycosylated FVII EGF-1 was achieved by using O-fucos
67                                              Nonglycosylated G protein also interacted with CNX, but
68                        If, however, unfolded nonglycosylated G protein was the starting material, ref
69                               A structure of nonglycosylated G(C) reveals an extended conformation th
70 cific hydrophobic amino acid residues on the nonglycosylated GFCC'C" face of CEACAM1 N-terminal domai
71 ein, with high affinity, but it did not bind nonglycosylated gp120 or BSA.
72                         It was found to be a nonglycosylated heterodimeric protein, belonging to the
73 eta glycosylation inhibition revealed 30-47% nonglycosylated hFSHbeta associated with four of six hFS
74                                              Nonglycosylated HIV envelope protein was not associated
75                            We also show that nonglycosylated HIV-1(SF-2) gp120 or sodium metaperiodat
76 ation by tunicamycin treatment resulted in a nonglycosylated hOAT4, which was unable to target to the
77 bles into homo and hetero complexes with its nonglycosylated homologue, Rom-1, to maintain the integr
78 covalent homo- and hetero-tetramers with its nonglycosylated homologue, Rom-1.
79 centration of tunicamycin yielded completely nonglycosylated hPTH/PTHrP receptor (approximately 60 kD
80                                          The nonglycosylated hPTH/PTHrP receptor remains fully functi
81 gh molecular weight (approximately 190 kDa), nonglycosylated hUG-binding protein, readily detectable
82 ycosylated, indicating that glycosylated and nonglycosylated human calreticulin have indistinguishabl
83                Production of two recombinant nonglycosylated human serum transferrins (hTF-NG), conta
84 eir sensitivities to neighboring proline and nonglycosylated hydroxyamino acid residues, from which a
85 fter ATG5 knockdown, while expression of the nonglycosylated IE62 tegument protein was unchanged.
86 y size is sufficient to accommodate a single nonglycosylated Ig domain such as the CD3epsilon ectodom
87                               High levels of nonglycosylated IgA were found in patients with Wiskott-
88         The results suggest that the unbound nonglycosylated IL-7Ralpha samples an extensive conforma
89 (1) approximately 10(2) M(-1) s(-1)) for the nonglycosylated interaction to a "diffusion-controlled"
90 d here suggests that the decreased number of nonglycosylated K(2P)3.1 channels on the cell surface ma
91                                          The nonglycosylated Kv1.2 protein had a similar protein half
92                      It is a non-ATP-binding nonglycosylated ligand-regulated molecular chaperone of
93 phate (Man-6-P) modified proteins as well as nonglycosylated ligands.
94  and decreased cellulose interaction for the nonglycosylated linker.
95 7/IL-24 signal peptide linked to the mutated nonglycosylated mda-7/IL-24 gene retained the ability to
96                         Vaccination with the nonglycosylated, milk-derived MSP1(42) successfully prot
97 tant thyroglobulin, whereas degradation of a nonglycosylated misfolded secretory protein substrate ap
98 expressed MUC1 have not been successful when nonglycosylated MUC1 sequences were used for vaccination
99 s studies have localized these properties to nonglycosylated mucin domains, and we have recently show
100 ype vesicular stomatitis virus G protein and nonglycosylated mutant forms in the presence of microsom
101                 In serial propagation with a nonglycosylated mutant PrP(C) substrate, the dominant Pr
102 allergens of Phl p 4 were expressed, and the nonglycosylated mutant was crystallized.
103 rsor of asialoglycoprotein receptor H2a, its nonglycosylated mutant, makes use of calnexin, EDEM1, an
104  trioxacarcins appear to be derivatives of a nonglycosylated natural product known as DC-45-A2.
105 lecular mass (approximately 90-110 kDa) than nonglycosylated NIS (approximately 50 kDa).
106 ilar affinities; however, the double mutant, nonglycosylated NK1R showed only half the B(max) of the
107 sing a variety of antibodies, reveal a novel nonglycosylated nucleoporin, Nup84, that is tightly asso
108 e ON from E. coli and mammalian cell-derived nonglycosylated ON bind identically to type V collagen a
109 the peptide backbone specific for either the nonglycosylated or the glycosylated peptide.
110 gococci by a novel target recognition of two nonglycosylated outer membrane proteins, Opa and PorB.
111 ced at the cell surface, indicating that the nonglycosylated P2X2 receptors are retained inside the c
112 tion of a collagen triple helix, whereas the nonglycosylated peptide does not.
113                                              Nonglycosylated peptide fragments were susceptible to co
114 ated vaccine gave CTLs which recognized only nonglycosylated peptide.
115 e reactive with antibody than the synthetic (nonglycosylated) peptide, and periodate treatment of the
116 al sequences of many of the glycosylated and nonglycosylated peptides combined with published informa
117                                              Nonglycosylated peptides incidentally collected in the s
118  the column and separated from the remaining nonglycosylated peptides present in the digest.
119                      Further quantitation of nonglycosylated peptides revealed that sialylation is in
120 copeptides from mixtures of glycosylated and nonglycosylated peptides, sequence both glycan and pepti
121 CTLs, which recognized both glycosylated and nonglycosylated peptides, whereas a similar nonglycosyla
122 ctural similarities between glycosylated and nonglycosylated peptides.
123 cosylation sites on-resin after synthesis of nonglycosylated peptides.
124                             Furthermore, the nonglycosylated phytocyanin-like domain from GhPLA1, whi
125 rmed that the expression of glycosylated and nonglycosylated polypeptides occurred in appropriate sub
126 hydroceramide, sphingosine, only ceramide, a nonglycosylated precursor metabolite unable to bind to G
127           The retrotranslocation kinetics of nonglycosylated pro-alpha factor were not significantly
128 o antagonizes the proteasomal degradation of nonglycosylated pro-alpha factor, a postulated nonubiqui
129  HF were incubated with or without exogenous nonglycosylated proBNP1-108 tagged with 6 C-terminal His
130 major component is the 37-kDa, palmitylated, nonglycosylated product of the F13L gene.
131         Furthermore, only low amounts of the nonglycosylated products of the GPEET and EP2 genes were
132  had no effect on the rate of secretion of a nonglycosylated protein (human growth hormone [hGH]) tha
133 ted GLAST increased with maturation, whereas nonglycosylated protein decreased in abundance postnatal
134  We also find that OS-9 binds to a misfolded nonglycosylated protein destined for ERAD, but not to th
135                            The native 17-kDa nonglycosylated protein inhibits both human and guinea p
136             Cell-free translation produced a nonglycosylated protein migrating at 29 kDa.
137 vel beta(2)-microglobulin-independent 37-kDa nonglycosylated protein on intestinal epithelia.
138 ted in activated T cells and gives rise to a nonglycosylated protein that resides in the cytosol.
139 his study, we showed that this intracellular nonglycosylated protein was as effective as wild-type MD
140 Sf9 system, homogeneous, crystallizable, and nonglycosylated protein was expressed after mutagenizing
141 h structure by 3.1 kcal/mol, relative to the nonglycosylated protein.
142  its dimeric form, and Epl1 is produced as a nonglycosylated protein.
143                       Here, we studied three nonglycosylated proteins and analyzed their use of known
144 somal inhibition induced accumulation of the nonglycosylated proteins and ERAD machinery in the endop
145  Calreticulin also inhibits precipitation of nonglycosylated proteins and thus contains generic prote
146                   Mechanisms of targeting of nonglycosylated proteins are less clear.
147 t a shared ERAD pathway for glycosylated and nonglycosylated proteins composed of luminal lectin mach
148  measurements indicate that glycosylated and nonglycosylated proteins induce "open" and "closed" P-do
149 how that calreticulin binds glycosylated and nonglycosylated proteins with similar affinities but dis
150 regation and degradation of glycosylated and nonglycosylated proteins, and antibodies under various c
151                The primary membrane contains nonglycosylated proteins, appears as crescents in the cy
152 side of its mannosidase-like domain with the nonglycosylated proteins.
153 virtually identical with those observed with nonglycosylated pseudocathepsin D.
154                       Using glycosylated and nonglycosylated purified flagellin and a cell reporter s
155 asigin, it was demonstrated that the native, nonglycosylated rBSG protein forms dimers in solution.
156 he band representing the photo-cross-linked, nonglycosylated receptor (obtained from the tunicamycin-
157 n enter the (a) "nuclear pathway," where the nonglycosylated receptor is extruded from the pre-Golgi
158 y for human IL-7 300-fold versus that of the nonglycosylated receptor through an allosteric mechanism
159 roduced on expression in transfected cells a nonglycosylated receptor with ligand binding affinity an
160                             In contrast, the nonglycosylated receptor, in which all four glycosylatio
161 photoaffinity cross-link specifically to the nonglycosylated receptor.
162                                          The nonglycosylated receptors displayed normal function and
163 rescence revealed that the expression of the nonglycosylated receptors produced by either tunicamycin
164 lse-positive test results up to 2 kUA/L with nonglycosylated recombinant allergens in patients with h
165                                 Two forms of nonglycosylated recombinant alpha2AP were expressed, iso
166                                            A nonglycosylated recombinant ETSHR protein expressed earl
167                                      Because nonglycosylated recombinant FGF-5 does not appear to be
168                          The production of a nonglycosylated recombinant form of Amb a 11 in Escheric
169                    Natively glycosylated and nonglycosylated recombinant forms, lenograstim and filgr
170                             Glycosylated and nonglycosylated recombinant Phl p 4 showed identical inh
171 M but only weakly inhibiting hydrolysis of a nonglycosylated recombinant protein substrate.
172 ly, these were all confined to two conserved nonglycosylated regions toward the carboxyl terminus of
173                        NinaA associates with nonglycosylated Rh1(N20I); therefore, retention of nongl
174 thesized, glycosylated rhodopsin from mature nonglycosylated rhodopsin to characterize the fate of Aa
175 cosylated Rh1(N20I); therefore, retention of nonglycosylated rhodopsin within the ER is not due to th
176 levated concentration of ERManI, whereas the nonglycosylated secretory glycoprotein albumin was not a
177 tional high sensitivities to the presence of nonglycosylated Ser/Thr residues.
178 imultaneous analysis of the glycosylated and nonglycosylated species, we interrogate the hormone bios
179 omomultimers reside in core-glycosylated and nonglycosylated states.
180  culture medium ( approximately 40 mg/L), no nonglycosylated sTFR could be produced, suggesting that
181 of a glycosylated subunit, gp91(phox), and a nonglycosylated subunit, p22(phox).
182 is consistent with a failure of less stable, nonglycosylated subunits to replenish surface compartmen
183 nged in the mutant, suggesting that residual nonglycosylated surface hNETs execute a key step in the
184 ne regions that are related to transporters, nonglycosylated SVOP and highly glycosylated SV2, sugges
185 nt gp36 reduced the antibody reactivity, and nonglycosylated synthetic peptide repeat units from E. c
186 fic B*3501-restricted CTL clone recognized a nonglycosylated, synthetic nonamer representing the mini
187 -restricted, env peptide is identical with a nonglycosylated, synthetic nonamer.
188 to be active at 10-fold lower doses than the nonglycosylated Thr10 contulakin-G analog.
189 e binding affinities of contulakin-G and the nonglycosylated Thr10 contulakin-G for a number of neuro
190                  The binding affinity of the nonglycosylated Thr10 contulakin-G was approximately an
191               However, both contulakin-G and nonglycosylated Thr10 contulakin-G were found to be pote
192 dly, Grp170 also promotes degradation of the nonglycosylated transthyretin (TTR) D18G misfolded clien
193 -type NIS activity, including the completely nonglycosylated triple mutant.
194                     The expressed protein is nonglycosylated, unlike the protein isolated from the or
195                                          The nonglycosylated UT-A1 showed reduced localization in lip
196                                Wild-type and nonglycosylated V2R yielded tritium signals at 45-55 and
197  nonglycosylated peptides, whereas a similar nonglycosylated vaccine gave CTLs which recognized only
198 Mn(II), Mn(III), and Mn(IV)) and producing a nonglycosylated variant for detailed biochemical and spe
199 enovirus vector expressing a nonsecreted and nonglycosylated version of MDA-7/IL-24 protein was gener
200 urthermore, the glycosylation content (i.e., nonglycosylated vs glycosylated, sialylated vs desialyla
201  from saliva of various races and genders is nonglycosylated with the same molecular weight of 55,881
202 257Y, presumed to be toxic to the cells, and nonglycosylated WT opsin obtained by growth in the prese
203 ith tunicamycin, consistent with the size of nonglycosylated Xenopus laevis alphaENaC.
204 tivity assay conditions, we demonstrate that nonglycosylated XXT2 lacking its cytosolic amino-termina
205 glycosylated COS7-expressed receptor and the nonglycosylated yeast-produced receptor.

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