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 unprocessed IAPP, pro-IAPP, polypeptides can cross-react.
2 ularly interesting to check whether they can cross-react.
5 hey were conventional MHC-restricted T cells cross-reacting against CD1d-alpha-galactosylceramide.
7 all IgE-mediated food allergies is caused by cross-reacting allergenic structures shared by inhalants
9 rgen positivity; (2) sIgE to two or more non-cross-reacting allergens; (3) sIgE to cross-reacting all
10 re non-cross-reacting allergens; (3) sIgE to cross-reacting allergens; and (4) sIgE to components pot
12 h one serotype generates antibodies that may cross-react and enhance infection with other serotypes i
17 an autoimmune disorder based on findings of cross-reacting antibodies between neuronal structures an
26 a paucity of monoclonal antibodies that can cross-react between the glycoproteins of different ebola
28 solated from younger donors born after 1968, cross-reacted between H7 and H3 haemagglutinins in bindi
31 ed (1)B1 state followed by rapid intersystem crossing, reacts directly with water to form H2SO3 in th
32 nce suggests that GPCRs exist as monomers or cross-react forming dimers and higher-ordered oligomers.
35 s encoded by the deleted genes which did not cross-react in vaccinated or in uninfected guinea pigs.
36 ests suggested that some argan allergens can cross-react in vitro with hazelnut allergens, including
40 is a sequential IgE response to distinct non-cross-reacting molecules from the same allergenic source
43 of S1 and RBD antibodies is specific, which cross-reacts neither with other antibodies such as RBD,
44 h angiotensin-converting enzyme 2 (ACE2) and cross-reacting neutralizing antibody were found to be co
45 es; however, antisera to several DBL domains cross-reacted on parasite isolates that had polymorphic
47 to activate self-tolerant T cells capable of cross-reacting on self-peptide-MHC in vivo represents an
48 ccurred on day 10; none was induced with non-cross-reacting or without Ag; nonatopic PBMC did not res
51 plex with pyro-Glu3-Abeta peptide and with a cross-reacting peptide from Ror2 have been determined at
52 synthesized and accumulated three anti-EF-Tu cross-reacting polypeptides of similar molecular mass bu
53 ntaneously arising pathogenic human TSHR Abs cross-react poorly with the mouse TSHR and do not cause
54 expressed in Ad5-vectored vaccines and have cross-reacting potential with non-Ad5 adenoviral vectors
55 sts allow the discrimination of genuine from cross-reacting sensitization and the selection of the ri
57 type 6C, a recently recognized serotype that cross-reacts serologically with serotype 6A, was investi
58 onal PCV13 serotypes 1, 6A, 7F, and 19A; the cross-reacting serotype 6C; and the common PCV7 serotype
60 the five nonvaccine M peptides that did not cross-react shared high sequence identity (>=50%) with t
66 cially those selected by CD154, additionally cross-react to different Aspergillus and Mucorales speci
73 It has been reported recently that UAE can cross react with Nedd8 to enable its passage through the
77 ure COVID-19 neutralizing antibodies without cross reacting with patient specimens with other viral,
79 putative anti-HspB5 Abs from 23 MS patients cross-react with 7 other members of the human small Hsp
80 has a structural motif that elicits Abs that cross-react with a cellular Ag present on retrovirus par
81 f aquaporin-4, exhibit Th17 polarization and cross-react with a homologous sequence of a Clostridium
82 iral immunity, a single TCR ideally needs to cross-react with a multitude of pathogenic epitopes.
83 expressed on the B. subtilis spore surface, cross-react with a number of seemingly unrelated protein
84 nst Schistosoma mansoni egg antigens (SmSEA) cross-react with allergens in natural rubber latex, pean
85 gous immunity, when microbe-specific T cells cross-react with allogeneic Ag and mediate graft rejecti
88 were predicted to elicit antisera that would cross-react with an additional 15 nonvaccine M types of
89 isease, and the degree to which these assays cross-react with antibodies against related coronaviruse
92 y provides evidence that antigen testing may cross-react with at least one additional non-jejuni and
93 nlike the FilmArray RP, the Aries BA did not cross-react with B. bronchiseptica in our study, althoug
94 r the major birch pollen allergen frequently cross-react with Bet v 1 homologous food proteins, for e
95 est neutralizing antibodies, which appear to cross-react with both gB and gD, and (ii) enhanced the n
96 ditionally, anti-B. miyamotoi antibodies can cross-react with C6 antigen testing for B. burgdorferi,
97 duction, and anti-zebra finch CBG antibodies cross-react with CBGs in other birds, extending opportun
98 re screened for peptides that simultaneously cross-react with CD patient antibodies present in two se
99 lay high levels of somatic hypermutation and cross-react with circulating HCoVs, suggesting recall of
100 ange on many cancerous cell lines and do not cross-react with cisplatin in A2780/DDP cell lines.
102 ) specific to S. prolificans, which does not cross-react with closely related fungi in the Pseudalles
106 , the ZIKV E-dimer-induced response does not cross-react with DENV or induce ADE of DENV infection.
111 that most of the anti-E-cadherin antibodies cross-react with Dsg1, whereas others may represent inde
115 o found that CD8(+) T cells generally do not cross-react with epitopes in the four seasonal coronavir
116 solates recovered from pigs at fairs did not cross-react with ferret antisera produced against the hu
117 odies to the lipo-oligosaccharide (LOS) that cross-react with gangliosides at peripheral nerves causi
118 a broad enough humoral response in humans to cross-react with genetically diverse parasite population
120 1 peptide-specific T-cell lines that did not cross-react with H1 or H3 influenza virus HA peptides we
121 ned the ability of the HA1.7 T-cell clone to cross-react with HA(306-318) presented by multiple MHC-I
122 930 swine H1N1 influenza strain, but did not cross-react with HAs of more contemporary human influenz
125 d autoreactive CD4(+) T cell clones that can cross-react with HLA-DR-derived self-peptides (HLA-DR-SP
126 infection induces the production of Abs that cross-react with host neuronal proteins, and these anti-
127 s against DENV nonstructural protein 1 (NS1) cross-react with human endothelial cells and cause NF-ka
130 -double-stranded DNA (dsDNA) antibodies that cross-react with inherent renal antigens, ii) the impact
131 ansient receptor potential (TRP) channels to cross-react with intracellular Ca(2)(+) release channels
133 roposed that preformed memory T cells, which cross-react with low avidity to epitopes presented in su
138 of a single T cell antigen receptor (TCR) to cross-react with multiple antigens allows the finite num
142 biotechnological use as enzymes that do not cross-react with nontarget substrates (i.e. as bio-ortho
146 ately, they often elicit T cells that do not cross-react with or that have low affinity for the tumor
151 ific anti-mouse FcgammaRIIB mAbs that do not cross-react with other FcRs, allowing us to study the po
152 y concern that elicited antibodies (Abs) may cross-react with other flaviviruses that share a similar
153 However, these ZIKV neutralizing antibodies cross-react with other flaviviruses, which may aggravate
155 finity upon light stimulation, it should not cross-react with other molecules in the cell, and it sho
156 whether T cells induced by one viral species cross-react with other related flaviviruses has not been
157 ral infections, mitochondrial components can cross-react with pathogen sensors and invoke inflammatio
158 ally recognize 1-pHis or 3-pHis; they do not cross-react with phosphotyrosine or the other pHis isome
159 ults indicate that TCZ and siltuximab do not cross-react with pig IL-6R and pig IL-6, respectively.
161 Here we describe antigenic molecules that cross-react with rabbit anti-S. mansoni IgG antibodies i
162 induce Bet v 1-specific IgG4 antibodies that cross-react with related food allergens and inhibit IgE
163 lls elicited by a circulating H1N1 strain to cross-react with related sequences found in an avian H5N
164 ognate receptor is RXFP1, it is also able to cross-react with RXFP2, the native receptor for a relate
166 CoV monoclonal antibodies for its ability to cross-react with SARS-CoV-2, has been examined for its a
169 However, B1 cell-associated antibodies often cross-react with self-antigens, which leads to autoimmun
170 for peptide epitopes derived from pathogens cross-react with self-epitopes, leading to autoimmune ti
171 xpressed by C. jejuni induce antibodies that cross-react with self-glycolipids in peripheral nerves,
172 es with host peptides stimulate T cells that cross-react with self-peptides, thereby initiating and/o
175 for the major birch pollen allergen Bet v 1 cross-react with structurally related food allergens, su
177 f the aggressive, stereotyped subset 7P that cross-react with the BCRs of several CLL patients in sub
178 However, the anti-ZIKV E antibodies can cross-react with the E protein of the related dengue vir
179 1 epitope and the antibodies to that epitope cross-react with the four serotypes 6A, 6B, 6C, and 19A
181 bination of human monoclonal antibodies that cross-react with the glycoproteins of all four clades of
182 y antagonize each receptor paralogue and yet cross-react with the human and mouse sequences, enabling
183 s other than M. intracellulare were found to cross-react with the M. intracellulare probe in the assa
184 will elicit T cell responses that completely cross-react with the native epitope, maximizing protecti
188 have studied lupus AAbs that bind dsDNA and cross-react with the NR2A and NR2B subunits of the NMDA
191 nal TIV induces neutralizing antibodies that cross-react with the reconstructed 1918 pandemic virus i
192 rn of ZIKV vaccines inducing antibodies that cross-react with the related dengue virus (DENV), we des
193 iscovered mAbs MPE8 and 25P13, both of which cross-react with the respiratory syncytial virus (RSV) F
196 howed that antibodies generated against MP-4 cross-react with the whole venom and provide protection
197 gainst their engineered promoters and do not cross-react with the wild-type promoter, thus ensuring o
204 eactive T cells involved in CeD pathogenesis cross-react with ubiquitous bacterial peptides, thereby
207 agglutination inhibition assays, 12 antisera cross-reacted with >/=14 of 20 H10 viruses, and 7 viruse
208 it antisera against this recombinant vaccine cross-reacted with 10 of the 15 nonvaccine M peptides.
210 uenza H5 virus that elicited antibodies that cross-reacted with a broad range of H5 viruses, includin
212 mmercial antibody against shrimp tropomyosin cross-reacted with a protein of similar size in Antarcti
213 Borrelia turicatae-seroreactive samples cross-reacted with a whole-cell indirect fluorescent ant
214 us nucleoprotein (NP) dominated and strongly cross-reacted with A(H1N1)pdm09 NP (P < 0.001) in partic
220 ity-purified antibodies to the human peptide cross-reacted with citrullinated recombinant P gingivali
221 ntisera from dk/Hok/69 ca-vaccinated ferrets cross-reacted with clade 2.3.4.4 and 2.2.1 viruses but n
222 ognized MHC class II ligands exclusively, or cross-reacted with classical and nonclassical MHC class
223 rity (82%) of the ileum anti-gp41 antibodies cross-reacted with commensal bacteria, and of those, 43%
224 te these antibodies and have shown that they cross-reacted with comparable nanomolar avidity with bot
225 NS1-specific IgG in naive individuals, which cross-reacted with DENV-1, -3, and -4 NS1 to varying ext
226 nti-M. pneumoniae antibodies (p < 0.001) and cross-reacted with different M. pneumoniae strains.
227 rologic analyses showed that the 93 isolates cross-reacted with each other to different extents.
228 T cell populations reactive with one epitope cross-reacted with either of several other epitopes enco
234 f gp41-reactive antibodies isolated from RMs cross-reacted with host antigens, including autologous i
235 in-induced anti-human-PF4/heparin antibodies cross-reacted with human PF4/nucleic acid and PF4/aptame
236 703- and IAV-PA224-specific responses, which cross-reacted with LCMV-GP34 and LCMV-GP276, respectivel
238 rom Uroderma bilobatum, the tent-making bat, cross-reacted with monoclonal antibodies against the HBV
240 rtain atabecestat and DIAT-responsive clones cross-reacted with N-acetyl DIAT; however, no cross-reac
241 against a deamidated proinsulin peptide, but cross-reacted with native proinsulin peptide upon restim
243 colleagues show that heparin-PF4 antibodies cross-reacted with nucleic acid (NA)-PF4 complexes and i
244 s demonstrated that melioidosis patient sera cross-reacted with OPSs of other Burkholderia species.
245 mmunogenic B. pseudomallei FliC epitope also cross-reacted with orthologous FliC sequences from Burkh
249 ntibodies (human IgG4 homolog) that strongly cross-reacted with recombinant DSG1; these IgG1 antibodi
250 ll, approximately 43% of the agents selected cross-reacted with RyR1-mediated and/or RyR1-independent
251 cytes transfected with all three bat viruses cross-reacted with sera against the HBV core protein, co
256 e had elevated levels of IgA antibodies that cross-reacted with the gram-negative enteric bacterial p
258 titer, high-avidity antibody responses which cross-reacted with the immobilized peptide sequence comp
263 No single virus elicited antibodies that cross-reacted with viruses from all three animal sources
265 readth for pre-fusion F-specific antibodies, cross-reacting with F proteins from both RSV subgroups A
273 IgE sensitization to food allergens not cross-reacting with pollens is rare and more evenly dist
274 e most common foods containing allergens not cross-reacting with pollens were sesame, shrimp and haze
275 lonal antibodies were identified by ELISA as cross-reacting with the GPs of all 5 Ebolavirus species.
276 ents with autoimmune diseases inhibit IKr by cross-reacting with the HERG channel likely at the pore
277 response that neutralizes native ST without cross-reacting with the human endogenous guanylate cycla
278 he entire carbohydrate motif of GD2 but also cross-reacts with a 105 kDa glycoprotein expressed by GD
280 The orangutan C1-specific KIR reacts or cross-reacts with all four polymorphic epitopes (C1, C2,
281 in a Swedish cat-sensitized population that cross-reacts with Can f 1, and may contribute to symptom
285 inds with high affinity to human PECAM-1 and cross-reacts with its counterpart in rats and other anim
289 hemolytic anemia, and the causative auto-IgM cross-reacts with naive T cells despite the lack of glyc
290 insight into how an insulin-reactive T cell cross-reacts with pathogen-derived antigens by focusing
294 from the female gastrourinary tract in 2006, cross-reacts with serogrouping kits for group B Streptoc
295 so, the globulin fraction of chickpea likely cross-reacts with the allergenic proteins of pea and len
297 onse to the self-antigen desmoglein 1 (Dsg1) cross-reacts with the LJM11 sand fly salivary gland Ag.
298 Mycobacterium tuberculosis complex, the NTM cross-reacts with the M. tuberculosis complex nucleic ac
299 hese antibodies, present in 40% of patients, cross-reacts with the NR2A and NR2B subunits of the N-me
300 t vaccinees induced CD8 and CD4 T cells that cross-reacted within the DENV serocomplex but were consi