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1 sidues 18-21 (nuclear magnetic resonance and epitope mapping).
2 nd WbGST by in silico analysis and by linear epitope mapping.
3 st time oxidative labeling has been used for epitope mapping.
4 attering, and inhibitory monoclonal antibody epitope mapping.
5  PA were identified by using tetramer-guided epitope mapping.
6 ins of other BoNT subtypes and serotypes for epitope mapping.
7  of responses to synthetic IA-2 peptides and epitope mapping.
8 people were re-obtained for AMA and relative epitope mapping.
9 ative SK, which was consistent with previous epitope mapping.
10 ries provide a rapid alternative for surface epitope mapping.
11  algorithms, allowing structure-based immune epitope mapping.
12 y using ELISA, Western blotting, and peptide epitope mapping.
13 in accordance with the results obtained from epitope mapping.
14 G1 peptides were synthesized for IgA and IgG epitope mapping.
15               Using the novel HDXMEM for NMR epitope mapping allowed identification of the first stru
16 IRPalpha.D1 binding to CD47 was confirmed by epitope mapping analyses of anti-SIRP Abs.
17                  In this report, we describe epitope mapping analysis of SERCA2a in A/J mice that lea
18                                   A detailed epitope mapping analysis of three of these rhesus antibo
19 q-IgG and -IgM interactions were used in the epitope mapping analysis.
20 ear B-cell epitope, as determined by peptide epitope mapping analysis.
21                              Tetramer-guided epitope mapping and Ag-specific class II tetramers were
22 human hybridoma technology were used for IgE epitope mapping and analysis of epitopes associated with
23                                              Epitope mapping and binding assays indicated that both L
24 env) were analyzed using a peptide array for epitope mapping and by a peptide enzyme-linked immunosor
25 ormed multiomic single-cell gene expression, epitope mapping and chromatin accessibility profiling in
26                            Using solid-phase epitope mapping and confirmatory assays, we identified s
27                            T-cell responses, epitope mapping and cross-reactivity to profilins (Phl p
28                                              Epitope mapping and cryo-electron microscopy defined two
29                                              Epitope mapping and database searches revealed the prese
30                                              Epitope mapping and functional studies performed with 17
31                                              Epitope mapping and genetic studies revealed that the an
32  structural biology technology combined with epitope mapping and increased metagenomic sequencing.
33                                         Fine epitope mapping and inhibitory immunoassays allowed the
34                                By performing epitope mapping and library screenings, we identified am
35                             A combination of epitope mapping and ligation-based PCR methods identifie
36                          Monoclonal antibody epitope mapping and serologic inhibition studies using C
37                                              Epitope mapping and single-cell RNA sequencing revealed
38 ationally designed using "in-silico" insulin epitope mapping and synthesized by solid phase polymeris
39 ope for RV-A16 and RV-A39 by tetramer-guided epitope mapping and the ability for RV-A16-specific Th1
40                                          STD epitope mapping and trNOESY bioactive conformation analy
41 d multiple approaches including mutagenesis, epitope mapping, and comparisons to primate MCP to make
42 sorbent assay, Western blotting, solid-phase epitope mapping, and competition assays.
43 e personalized allergy diagnostic, allergens epitope mapping, and cross-reactivity studies.
44                                      Titers, epitope mapping, and isotypes of the Abeta42-specific an
45           Using longitudinal neutralization, epitope mapping, and sequence data from 14 participants,
46 een 26D1 and H16.V5 was shown using pairwise epitope mapping, and their binding difference is demonst
47 in-ligand interactions and is widely used in epitope mapping, antibody engineering and screening for
48  We studied NKp46D2 by using a peptide-based epitope mapping approach and identified an NKp46D2-deriv
49                            A tetramer-guided epitope mapping approach was used to identify HLA-restri
50                          The tetramer-guided epitope mapping approach was used to identify IGRP-speci
51  using an alanine scanning mutagenesis-based epitope mapping approach.
52 a manner entirely different from traditional epitope mapping approaches.
53      The Fab-Fc complex half-life screen and epitope mapping are potentially useful tools in the scre
54 embrane proteins, structure elucidation, and epitope mapping are showcased.
55 s therapeutics underscores the importance of epitope mapping as an essential step in characterizing a
56                Using a yeast surface display epitope mapping assay and neutralization escape mutant,
57 ells were determined by a novel CD154 T cell epitope mapping assay.
58           Based on glycosidase digestion and epitope mapping, band 0.03 was hypothesized to represent
59                                    In silico epitope mapping based on the patients' HLA-I alleles ind
60 erization by selection of escape mutants and epitope mapping by flow cytometry analysis of site-direc
61                                      Further epitope mapping by functional group modification establi
62                                              Epitope mapping by phage display analysis indicated that
63                                              Epitope mapping by phage display revealed that both inhi
64  norovirus strains involved in cell binding, epitope mapping by phage display was performed with an M
65                                              Epitope mapping by real-time surface plasmon resonance s
66 development of the novel method differential epitope mapping by STD NMR (DEEP-STD NMR) for identifyin
67       We used an approach of protein surface epitope mapping by synthetic peptides to analyze the sur
68                However, very few methods for epitope mapping can tolerate the complexity of a pAb sam
69                                          Our epitope mapping data indicate that the organization of Z
70                         This data along with epitope mapping data of anti rHuEPO monoclonals was used
71 s is a simple yet rational strategy based on epitope mapping data to develop a genetically modified h
72 ce constraints, are generated from available epitope mapping data.
73                                              Epitope mapping demonstrated increased targeting of cons
74                                              Epitope mapping demonstrated sites on the Na-ASP-2 molec
75   Harnessing data from previous experimental epitope mapping efforts of several class I fusion protei
76               Electron microscopy polyclonal epitope mapping (EMPEM) revealed that reoH2HA (group 1)
77                                              Epitope mapping enabled the identification of MHC/T cell
78                        Functional assays and epitope mapping established that potently inhibitory ant
79                                              Epitope mapping experiments demonstrate that the CREB.CB
80                Antibody binding patterns and epitope mapping experiments identified differences in E1
81                                              Epitope mapping experiments showed that positive control
82 een used to detect KLK4-specific peptides in epitope mapping experiments.
83                                              Epitope-mapping experiments indicated that Wnt1 class-sp
84                                              Epitope mapping for one of the MAbs, which recognizes a
85                           We first conducted epitope mapping for pairing nanobodies and then prepared
86  different truncated forms of MARCO, allowed epitope mapping for the PLK-1 Ab to MARCO domain V betwe
87                                     Although epitope mapping has identified residues on the human pap
88      The complexity and importance of T cell epitope mapping have motivated the development of comput
89                                              Epitope mapping identified the N-terminal domain of FH a
90                                              Epitope mapping identified two IgE-binding antigenic reg
91 etween mAbs that were not predicted by prior epitope mapping, identifying 3 distinct neutralization c
92 ven though other investigators have reported epitope mapping in the H5 HA, much of this information p
93 ssfully tested by many workers in fine scale epitope mapping, in protein folding studies, and in diss
94                                         Fine epitope mapping, in which an array of overlapping 13-mer
95 e used a hybrid method approach for antibody epitope mapping, including single-particle cryo-electron
96                                              Epitope mapping indicated MAb 1C3 recognized a region of
97                                              Epitope mapping indicated that a putative nuclear locali
98                                     In-depth epitope mapping indicated that anti-PLIN1 autoantibodies
99                                              Epitope mapping indicated that the anti-C2b mAb 3A3.3, w
100                                              Epitope mapping indicates that a potent LAG3 antagonist
101                                     Antibody epitope mapping is a key step in understanding antibody-
102                                              Epitope mapping is a technique employed to define the re
103                             Antigen-antibody epitope mapping is essential for understanding binding m
104                                              Epitope mapping localized the epitope of 3F3A and a comm
105                                          For epitope mapping, Mal d 1-specific T-cell lines were stim
106 fluidic electron microscopy-based polyclonal epitope mapping (mEM), which combines microfluidics with
107 opes were determined using a high-throughput epitope mapping method.
108                                  Traditional epitope mapping methods are laborious, time-intensive, a
109 bactericidal mAb 12C1 was studied by various epitope mapping methods.
110                              Proteomic-based epitope mapping of 11B9/61 monoclonal antibody revealed
111                                              Epitope mapping of 12 monoclonal antibodies (MAbs) direc
112                                              Epitope mapping of 125-2H using human-mouse IL-18 chimer
113                                              Epitope mapping of 42F and 43F by binding to linear pept
114 t the humanization, affinity maturation, and epitope mapping of 8H9 based on structure determination,
115                                              Epitope mapping of a bactericidal anti-GNA33 mAb using o
116 We sought to clone, express, and perform IgA epitope mapping of a CD-specific wheat antigen and to st
117 meric interspecies and homologue muteins and epitope mapping of a monoclonal antibody (MoAb) to the h
118 e of tumor cell lines and subsequent peptide epitope mapping of a NKp30 blocking antibody, we have id
119                                              Epitope mapping of Ab-binding reactivity revealed prefer
120 esion molecule-1 (ICAM-1) binding assays and epitope mapping of activation-sensitive antibodies using
121  demonstrating the potential use of detailed epitope mapping of Ags for staging of the infection, and
122                                              Epitope mapping of all potential IgE epitopes on the sur
123 onfirmed as critical for collagen binding by epitope mapping of an inhibitory phage antibody against
124                        In the present study, epitope mapping of antagonistic anti-gamma(c) monoclonal
125                                              Epitope mapping of anti-ADAMTS13 immunoglobulin G from p
126 ate the basis for this cross-neutralization, epitope mapping of anti-E1E2 antibodies present within a
127                                              Epitope mapping of anti-PfRh4 monoclonal antibodies iden
128                                              Epitope mapping of antibodies (Abs) is crucial for under
129 ants transfected into cells and by anti-PAR1 epitope mapping of APC-treated endothelial cells.
130                                       T cell epitope mapping of Art v 6 revealed that it contains onl
131 reviously discovered via phage display-based epitope mapping of autoantibodies in patients.
132                                          IgE epitope mapping of Bla g 5 revealed that 2 linear N-term
133                       The identification and epitope mapping of broadly neutralizing anti-human immun
134                                              Epitope mapping of diverse F1 and F2 monoclonal antibodi
135                                         Fine epitope mapping of DRalphabeta1*0401-and DRalphabeta1*04
136                                     Antibody epitope mapping of endogenous dystrophin indicated prote
137  surface antigen (HBsAg) was investigated by epitope mapping of four anti-HBsAg monoclonal antibodies
138 es involved in Ab binding provided the first epitope mapping of hIgE mAbs to an allergen.
139  expression system, lambda foo, was used for epitope mapping of human galectin-3.
140                                              Epitope mapping of human monoclonal antibodies (HMAbs) t
141                                              Epitope mapping of IgA anti-PDC-E2 antibodies indicated
142                                              Epitope mapping of IgG autoantibodies against kinectin r
143 ta on more than 900 peptides used for B-cell epitope mapping of immunodominant proteins of Chlamydia
144 ed peptide microarray approach, coupled with epitope mapping of known autoantigens, to identify and c
145                                              Epitope mapping of LipC identified 6 immunodominant epit
146                        Here, high-throughput epitope mapping of local GC B cells is used to identify
147 am facilitates single-cell immune profiling, epitope mapping of monoclonal antibodies and mosaic prot
148     We report a facile methodology for rapid epitope mapping of neutralizing antibodies (NAbs) agains
149 s characteristic of flavivirus envelopes and epitope mapping of neutralizing antibodies onto the stru
150 investigated by using monoclonal antibodies, epitope mapping of P66 of Borrelia burgdorferi, and DNA
151 ic techniques can provide a new approach for epitope mapping of polysaccharide-binding Abs and sugges
152 pplications such as protein footprinting and epitope mapping of proteins (and their complexes) in gen
153                                              Epitope mapping of PTRP delineated 4 peptides that can i
154 mining relative proteinase K sensitivity and epitope mapping of representative cases from each codon
155           Our approach involved a systematic epitope mapping of responses to myelin proteolipid prote
156                                              Epitope mapping of sera from CAEV-infected goats localiz
157       The use of a glycan microarray allowed epitope mapping of several monoclonal antibodies (mAbs)
158                                              Epitope mapping of SG/19 revealed that Thr(82) in the be
159                                     Thorough epitope mapping of such metastable conformations is diff
160             As expected, monoclonal antibody epitope mapping of the lipid-free and lipid-bound 10F6 a
161                                              Epitope mapping of the neutralizing mAbs via escape muta
162                                              Epitope mapping of the neutralizing monoclonal antibodie
163                                              Epitope mapping of the putative CD44 binding site was pe
164                                     Results: Epitope mapping of the scFv binding site revealed a line
165                                              Epitope mapping of the three CXCR4 i-bodies AM3-114, AM4
166                                         Fine epitope mapping of therapeutically relevant monoclonal a
167                                   Functional epitope mapping of these mAbs and small animal prophylax
168                                              Epitope mapping of these MAbs demonstrates how some E2/E
169                                        Crude epitope mapping of TpN17 and TpN37 showed that multiple
170 arrays were generated to enable the detailed epitope mapping of two monoclonal antibodies known to re
171                                     Antibody epitope mapping of untensioned microfibrils revealed the
172 n of the bicistronic nature of CYP27 mRNA by epitope mapping of uORF1 suggests that translation of CY
173                                     Antibody epitope mapping of viral proteins plays a vital role in
174 te, we used random peptide phage display and epitope mapping of VL Len using wild-type and alanine-mu
175                                     Previous epitope-mapping of autoantibodies (AutoAbs) from prostat
176 l diversity observed within HLA-I restricted epitopes, mapping of 609 experimentally validated epitop
177 h 1, 2, 3, 6, 7, and 8 using tetramer-guided epitope mapping on cell lines, followed by ex vivo valid
178                                              Epitope mapping on the target proteins provides key info
179       This study is the first to demonstrate epitope mapping on the three-dimensional structure of th
180 or further characterization, such as minimal epitope mapping or identification of MHC restriction, wi
181 mal sequence diversity is essential, such as epitope mapping or novel receptor identification, combin
182                                              Epitope mapping performed by screening a random peptide
183                                              Epitope mapping performed by selecting and sequencing an
184 were validated using a suite of experimental epitope mapping protocols, including cross-linking mass
185     However, accurate K(D) determination and epitope mapping requires a long series of experiments at
186                                     M4008_N1 epitope mapping revealed a glycan-independent V3 epitope
187                                              Epitope mapping revealed an AMA pattern of reactivity to
188                                              Epitope mapping revealed contact residues for CBH-2 and
189                                         Fine epitope mapping revealed differences in antibody specifi
190         Further characterization by antibody epitope mapping revealed differences in the qualitative
191                                              Epitope mapping revealed eight continuous epitopes acces
192            In the symptomatic mice, antibody epitope mapping revealed enrichment of C-terminal trunca
193                                 T and B cell epitope mapping revealed major and minor T and B cell ep
194  with other Ebolavirus species, and detailed epitope mapping revealed overlapping target epitopes wit
195 s that share a conserved central region, and epitope mapping revealed T-cell epitopes in this region.
196                               In this study, epitope mapping revealed that 25F10 interacts at site II
197                                              Epitope mapping revealed that Aw3.18 detects a change in
198                                              Epitope mapping revealed that mAb 2G9 recognizes the C t
199                                              Epitope mapping revealed that the humoral anti-EBNA-1 re
200                                              Epitope mapping revealed that the two classes of CARs bi
201                                              Epitope mapping revealed that they recognize few distinc
202                                              Epitope mapping revealed the presence of overlapping but
203                                              Epitope mapping revealed two epitope supersites on the g
204                                              Epitope mapping reveals that cleavage of the pro-piece o
205                         Moreover, a detailed epitope mapping reveals that the conformational epitopes
206 ges over a 12-18-mo period in response to an epitope-mapping series of 265 12-mer peptides of myelin
207 y-antigen interactions by using the Antibody Epitope Mapping server (AbEMap).
208 ast, researchers typically choose for B-cell epitope mapping short peptide antigens in antibody bindi
209                                              Epitope mapping showed that 14 of the 16 patients with t
210                                              Epitope mapping showed that CK6 and CK8 bound between re
211                                       B-cell epitope mapping showed that compared to sera from experi
212                                              Epitope mapping showed that mAb-1E7 recognized the (75)N
213                                Linear B cell epitope mapping showed that serum antibodies recognized
214 ent nanobodies were identified, and detailed epitope mapping showed that these bind to distinct, nono
215                                              Epitope mapping showed that this collection of nineteen
216                                       T cell epitope mapping strategies increasingly rely on algorith
217                            Using the PepScan epitope mapping strategy, a library of 179 potential pep
218                      We also devised a rapid epitope-mapping strategy, which relies on crosslinking m
219 d by competitive mAbs, (3) confirms previous epitope mapping studies and (4) has the potential to ide
220          Such predictions guide experimental epitope mapping studies and enable computational analysi
221                                              Epitope mapping studies demonstrated the complex nature
222                                              Epitope mapping studies identified antibodies specific f
223                                              Epitope mapping studies identified that both T-1A5 and C
224   Alanine scanning-based shotgun mutagenesis epitope mapping studies revealed diverse patterns of fin
225                                              Epitope mapping studies revealed that both the cellular
226                                              Epitope mapping studies revealed that the two MAbs were
227                                              Epitope mapping studies revealed that ZIKV-117 recognize
228                                              Epitope mapping studies revealed the presence of HLA cla
229                                              Epitope mapping studies showed that Ab responses in mice
230 data are consistent with results of previous epitope mapping studies showing that Mabs 25D2 and 35F2
231                                              Epitope mapping studies using competition analysis showe
232                                       T cell epitope mapping studies using IFN-gamma ELISPOT was perf
233                                Comprehensive epitope mapping studies with 166 E protein DIII-LR varia
234 s (MAbs) against the toxin and used them for epitope mapping studies.
235 founding artifacts when IgM Abs are used for epitope mapping studies.
236 otein in the virion, which supports previous epitope mapping studies.
237                                              Epitope-mapping studies did not identify a single, major
238               We have taken advantage of our epitope-mapping studies of the E2 components of PDC, BCO
239                                              Epitope-mapping studies revealed that these hydrophilic
240                                              Epitope-mapping studies using neutralization escape muta
241 proteins were employed to perform monoclonal epitope-mapping studies with three LPS-blocking Abs that
242 ponse against this virus, we performed a CTL epitope mapping study of JCV VP1 major capsid protein by
243                                    A binding epitope mapping study on clone 1121 and one of the paren
244                                        In an epitope mapping study using biotinylated peptides, all t
245                                              Epitope mapping suggested that the antibody bound to TNF
246                                              Epitope mapping suggests that all these mAbs recognize c
247 e multichannel pipet form a highly efficient epitope mapping system.
248 he structural topography of IpaD, the Geysen epitope-mapping system was used to identify epitopes rec
249 eviously developed method, intact transition epitope mapping-targeted high-energy rupture of extracte
250    Collectively, these data show that linear epitope mapping techniques provide useful but incomplete
251  have now been identified using a variety of epitope mapping techniques, including fragmentation by t
252  and assess the potential of the most common epitope mapping techniques, we generated a series of mAb
253  nine residues long and is more efficient in epitope mapping than random peptide libraries.
254 munoassay, where it was demonstrated through epitope mapping that mAb 11-1F4 recognizes a conformatio
255                                              Epitope mapping the specific residues of an antibody/ant
256                            Combined with the epitope mapping, these results indicate portions of the
257  been implicated by mutagenesis and antibody epitope mapping to play a key role in gp120 association.
258 combinatorial phage display-based approach ("epitope mapping") to select peptides binding to the orig
259 e advantages of the server compared to other epitope-mapping tools, its limitations and potential are
260                                       T cell epitope mapping unveiled a 13-residue sequence conserved
261 perform simultaneous antibody sequencing and epitope mapping using a combination of single particle c
262                                              Epitope mapping using a comprehensive shotgun mutagenesi
263                                              Epitope mapping using activation-sensitive antibodies su
264                The method is based on binary epitope mapping using anti-peptide antibodies.
265     To localize the epitopes, we carried out epitope mapping using chimeras between hLAG3 and mouse L
266                                              Epitope mapping using hydrogen-deuterium exchange mass s
267                                              Epitope mapping using limited proteolysis, reversed phas
268  antibody sequencing, the ability to perform epitope mapping using only the sequence of the antibody
269 ntibodies were analyzed by immunoblot and by epitope mapping using phage display.
270                                              Epitope mapping using solution nuclear magnetic resonanc
271                                              Epitope mapping using surface plasmon resonance in a BIA
272                                              Epitope mapping, using a phage display peptide library,
273  Analyses of the functional consequences and epitope mapping, using both fluid phase and solid phase
274 fied by peptide/MHC class II tetramer-guided epitope mapping, validated by direct ex vivo enumeration
275                              High-resolution epitope mapping was accomplished through hydrogen deuter
276                            In such a manner, epitope mapping was applied to the complex interactions
277                                              Epitope mapping was performed by IFN-gamma ELISpot scree
278                                              Epitope mapping was performed by pepscan analysis, site-
279                                              Epitope mapping was performed by sequencing of antibody-
280 pseudotyped lentiviral vectors, and antibody epitope mapping was performed with a peptide array.
281 diction, in vivo immunogenicity testing, and epitope mapping was used to identify candidates for FSP
282                                        Using epitope mapping, we discovered mouse monoclonal antibodi
283 respective formulation solutions and antigen epitope mapping were also evaluated.
284 08 of human PrP and have characterized it by epitope mapping, Western immunoblot analysis, and immuno
285 is widely used for monoclonal antibody (mAb) epitope mapping, which aids in the development of therap
286                                     Detailed epitope mapping will provide the information needed for
287                                 In addition, epitope mapping with a phage-displayed random peptide li
288                                              Epitope mapping with Ca2+-dependent monoclonal antibodie
289                                     Based on epitope mapping with huntingtin-specific antibodies, we
290                                              Epitope mapping with mammalian and bacterially expressed
291                                       B-cell epitope mapping with overlapping peptides, and cross-inh
292 s with alternative protein constructs and by epitope mapping with peptides covering the identified re
293     In this study, we combined comprehensive epitope mapping with sequence conservation analyses to i
294 -cell epitopes bind antibodies poorly; thus, epitope mapping with short peptide antigens falsely clas
295                                              Epitope mapping with synthetic peptides and electrophili
296                                              Epitope mapping with synthetic peptides revealed that MA
297                                              Epitope mapping with this monoclonal antibody identifies
298 mologs of known sequence were used to refine epitope mapping, with some epitopes ultimately confirmed
299 e inoculated with wild-type Ad recognized an epitope mapping within E1B.
300                                              Epitope mapping, X-ray crystallography, and cryo-electro

 
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