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1 atenation of DNA through the induction of an enzyme-linked double-strand break (DSB) in one DNA molec
2  month 4 including BKPyV-specific T cells by enzyme-linked immune absorbent spot (ELISPOT) at month 3
3 es of presenting cells by flow cytometry and enzyme-linked immune absorbent spot (ELISPOT) in freshly
4                     We used interferon-gamma enzyme-linked immune absorbent spot analyses on peripher
5 Month 4, including BKPyV-specific T cells by enzyme-linked immune absorbent spot at Month 3 and cidof
6 , video capsule endoscopy enteropathy score, enzyme-linked immune absorbent spot, gut-homing CD8 T ce
7 l analysis with HLA-DQ2-gluten tetramers and enzyme-linked immune absorbent spot, gut-homing CD8 T ce
8 C), purified and the quality was assessed by enzyme linked immuno sorbet assay.
9 yet, or rely on high-costing methods such as Enzyme-Linked Immuno-Sorbent Assay (ELISA), High-Perform
10 e identified by serological assays including enzyme-linked immunoassay (EIA), complement fixation (CF
11 transcription polymerase chain reaction, and enzyme-linked immunoassay.
12 days postinjury, and serum was collected for enzyme-linked immunoassays to quantify peripheral HMGB1.
13 itivity (100 pg/ml) in comparison to optical enzyme-linked immunosorbant assay (1 ng/ml) and previous
14 cimen, and subsequent immunofluorescence and enzyme-linked immunosorbant assays identified preservati
15 ercial COVID-19 antibody tests, including an enzyme linked immunosorbent assay (ELISA) and a Luminex-
16 dvance over the state of the art method, the enzyme linked immunosorbent assay (ELISA) used in clinic
17 fection stage rely on Gram stains, cultures, Enzyme linked immunosorbent assay (ELISA), polymerase ch
18 y, we established and used multiple indirect Enzyme Linked Immunosorbent Assay (ELISA)-based serologi
19 tions (PCR), lateral flow devices (LFID) and enzyme linked immunosorbent assays (ELISA) are being ada
20 IgG antibodies and PGI and PGII levels using enzyme linked immunosorbent assays.
21 by luciferase immunoprecipitation (LIPS) and enzyme-linked immunosorbent (ELISA) immunoassays.
22  this work, we describe an electronics-based Enzyme-Linked ImmunoSorbent Assay (eELISA), using a Lab-
23 etermine the diagnostic performance of a CRP enzyme-linked immunosorbent assay (ELISA) (Eurolyser) in
24 uantified the levels of tropomyosin by using enzyme-linked immunosorbent assay (ELISA) among raw and
25                   In immunohistochemical and enzyme-linked immunosorbent assay (ELISA) analyses of ti
26 rformance of high complexity methods such as Enzyme-Linked Immunosorbent Assay (ELISA) and Chemilumin
27              Results of whole-bacterial-cell enzyme-linked immunosorbent assay (ELISA) and flow cytom
28 F-1alpha in GCF and serum were quantified by enzyme-linked immunosorbent assay (ELISA) and reported a
29                          The second assay is enzyme-linked immunosorbent assay (ELISA) based and can
30 ecificity comparable or better than standard enzyme-linked immunosorbent assay (ELISA) directly from
31 anti-EBOV-specific IgM and IgG antibodies by enzyme-linked immunosorbent assay (ELISA) for 126 study
32      Here, we developed a sensitive sandwich enzyme-linked immunosorbent assay (ELISA) for PEG by tet
33  near million-fold improvement over standard enzyme-linked immunosorbent assay (ELISA) for protein de
34 ffusion (SRID), we report a new quantitative enzyme-linked immunosorbent assay (ELISA) for seasonal t
35     Then, we applied it in an ultrasensitive enzyme-linked immunosorbent assay (ELISA) for the detect
36 dapted a commercially available, serum-based enzyme-linked immunosorbent assay (ELISA) for use with s
37                                     ZEBOV-GP enzyme-linked immunosorbent assay (ELISA) geometric mean
38                                              Enzyme-linked immunosorbent assay (ELISA) is a widely us
39                                              Enzyme-linked immunosorbent assay (ELISA) is a widely us
40                                          The enzyme-linked immunosorbent assay (ELISA) is commonly us
41                                              Enzyme-linked immunosorbent assay (ELISA) is the gold st
42 ficult to quantify using currently available enzyme-linked immunosorbent assay (ELISA) kits and, ther
43  lower than those obtained with conventional enzyme-linked immunosorbent assay (ELISA) methodologies
44 osen for validation through a CXCL12 protein enzyme-linked immunosorbent assay (ELISA) on patient ser
45          We assessed cytokine production via enzyme-linked immunosorbent assay (ELISA) or V-Plex, and
46                                  Competitive enzyme-linked immunosorbent assay (ELISA) studies showed
47                                    Moreover, enzyme-linked immunosorbent assay (ELISA) tests were neg
48 formed using serological techniques like the enzyme-linked immunosorbent assay (ELISA) to detect anti
49 h focused on the pathway toward a recognized enzyme-linked immunosorbent assay (ELISA) to determine s
50 ative to the natural enzyme in a traditional enzyme-linked immunosorbent assay (ELISA) to establish a
51 of adding the Toxoplasma gondii IgA antibody enzyme-linked immunosorbent assay (ELISA) to the serolog
52 ses with IgG titers reaching several million enzyme-linked immunosorbent assay (ELISA) units.
53 etecting Plasmodium antigen in a fluorescent enzyme-linked immunosorbent assay (ELISA) using a fluore
54               We evaluated these antigens by enzyme-linked immunosorbent assay (ELISA) using sera fro
55 prototype biosensor was compared to standard enzyme-linked immunosorbent assay (ELISA) using unstimul
56 has sensitivity superior to that of the Zeus enzyme-linked immunosorbent assay (ELISA) VZV IgG assay
57                                         This enzyme-linked immunosorbent assay (ELISA) was based on s
58                                      A novel enzyme-linked immunosorbent assay (ELISA) was developed
59        Chlamydia trachomatis elementary body enzyme-linked immunosorbent assay (ELISA) was used to in
60 umps, measles, and rubella determined by IgG enzyme-linked immunosorbent assay (ELISA) were 93, 93, a
61 um samples, as well as 44 serum samples from enzyme-linked immunosorbent assay (ELISA) West Nile- and
62 va of OSCC patients from healthy subjects by enzyme-linked immunosorbent assay (ELISA) with sensitivi
63 sively among the following 4 patient groups: enzyme-linked immunosorbent assay (ELISA)+/serotonin-rel
64 , osmotic shock increased cBIN1 detection by enzyme-linked immunosorbent assay (ELISA), and cBIN1 lev
65 identified IBV-M41 receptor was confirmed by enzyme-linked immunosorbent assay (ELISA), demonstrating
66     APP metabolite levels were determined by enzyme-linked immunosorbent assay (ELISA), for Human Abe
67 age matrix-related proteins were assessed by enzyme-linked immunosorbent assay (ELISA), histology, an
68 romatography-Mass Spectrometry (UPLC-MS) and Enzyme-Linked Immunosorbent Assay (ELISA), including hig
69  overall HCP levels are usually monitored by enzyme-linked immunosorbent assay (ELISA), liquid chroma
70 mania research diagnostics utilized included enzyme-linked immunosorbent assay (ELISA), rk39 test str
71                                        Using enzyme-linked immunosorbent assay (ELISA), we obtain ser
72 functional neutralizing antibodies), and the enzyme-linked immunosorbent assay (ELISA), which measure
73                  Here, we developed a simple enzyme-linked immunosorbent assay (ELISA)-based assay th
74 covery method, which was further compared to enzyme-linked immunosorbent assay (ELISA).
75  a conventional detection method, such as an enzyme-linked immunosorbent assay (ELISA).
76 a3 (C6Malpha3) and employed in a competitive enzyme-linked immunosorbent assay (ELISA).
77 inst serum samples, compared to conventional enzyme-linked immunosorbent assay (ELISA).
78 nd sera for SARS-CoV-2 antibodies testing by enzyme-linked immunosorbent assay (ELISA).
79    HBGA phenotype was determined by salivary enzyme-linked immunosorbent assay (ELISA).
80 to Pf circumsporozoite protein (PfCSP) using enzyme-linked immunosorbent assay (ELISA).
81 d in NOD/ShiLtJ using metabololipidomics and enzyme-linked immunosorbent assay (ELISA).
82      PCLS function was quantified by albumin enzyme-linked immunosorbent assay (ELISA).
83 use as serodiagnostic antigen in an indirect enzyme-linked immunosorbent assay (ELISA).
84 (42)) of P. vivax and P. falciparum using an enzyme-linked immunosorbent assay (ELISA).
85   Cytokine levels were assayed via multiplex enzyme-linked immunosorbent assay (ELISA).
86 imab-TNF complexes and ADAs were measured by enzyme-linked immunosorbent assay (ELISA).
87 cloprid concentrations were determined by an enzyme-linked immunosorbent assay (ELISA).
88 ion sensitivity is as good as or better than enzyme-linked immunosorbent assay (ELISA).
89 d and analyzed for NE using a single-analyte enzyme-linked immunosorbent assay (ELISA).
90  mAb-EspB-B7 and validated it by competitive enzyme-linked immunosorbent assay (ELISA).
91 ) participants (n=297), we measured apo M by Enzyme-Linked ImmunoSorbent Assay (ELISA).
92 tensin II) in the plasma were measured by an enzyme-linked immunosorbent assay (ELISA).
93 pecific antibodies were measured by means of enzyme-linked immunosorbent assay (ELISA).
94 ed by a commercial SARS-CoV-2 total antibody enzyme-linked immunosorbent assay (ELISA, Wantai Biologi
95           Using these antibodies, a sandwich enzyme-linked immunosorbent assay (LAM-ELISA) was develo
96 dard immunoglobulin M (IgM) antibody-capture enzyme-linked immunosorbent assay (MAC-ELISA).
97 olymerase chain reaction (messenger RNA) and enzyme-linked immunosorbent assay (protein).
98 asma samples collected in 211 patients using enzyme-linked immunosorbent assay (Tac/Sir = 104, Tac/Mt
99 eceptor (CD206) and tumor necrosis factor by enzyme-linked immunosorbent assay (test cohort).
100                                A VP2-peptide enzyme-linked immunosorbent assay (VP2-ELISA) was optimi
101  InBios ZIKV Detect 2.0 IgM antibody capture enzyme-linked immunosorbent assay (ZIKV 2.0 MAC-ELISA; I
102 ety; and IgG anti-spike protein response (in enzyme-linked immunosorbent assay [ELISA] units).
103 IKV antibodies using a ZIKV immunoglobulin G enzyme-linked immunosorbent assay and a virus neutraliza
104                         Several methods like enzyme-linked immunosorbent assay and affinity chromatog
105 l outgrowth was measured by the standard p24 enzyme-linked immunosorbent assay and an ultrasensitive
106           We measured levels of S100A8-A9 by enzyme-linked immunosorbent assay and analyzed fecal mic
107 and 7 were assayed for IL-1beta and IL-10 by enzyme-linked immunosorbent assay and compared using the
108 urnetii immunoreactive proteins validated by enzyme-linked immunosorbent assay and demonstrate the ef
109 mage, neurofilament light chain (NfL), using enzyme-linked immunosorbent assay and electrochemilumine
110 yze a semi-homogeneous bead-based electronic enzyme-linked immunosorbent assay and find that experime
111 mouse serum, we developed a highly sensitive enzyme-linked immunosorbent assay and found that HN3-ABD
112                We measured levels of IFNL by enzyme-linked immunosorbent assay and immunohistochemist
113 vels were further confirmed by Western blot, enzyme-linked immunosorbent assay and immunohistochemist
114 re screened by MERS-CoV nucleocapsid protein enzyme-linked immunosorbent assay and indirect immunoflu
115 repair, and growth factors with immunoassay (enzyme-linked immunosorbent assay and Luminex).
116 e compared findings of 2 orthogonal methods, enzyme-linked immunosorbent assay and mass spectrometry,
117                                              Enzyme-linked immunosorbent assay and microsphere-based
118 e also measured fecal pancreatic elastase by enzyme-linked immunosorbent assay and performed quantita
119                 Prospective determination of enzyme-linked immunosorbent assay anti-RBD IgG titer fac
120 sponses were higher with higher dose (day 29 enzyme-linked immunosorbent assay anti-S-2P antibody geo
121 mmunoglobulin G titers were quantified using enzyme-linked immunosorbent assay at 4.5 years.
122 ng highly sensitive double antibody sandwich enzyme-linked immunosorbent assay at baseline and 2 week
123  NiV antibodies using a comparative indirect enzyme-linked immunosorbent assay based on the recombina
124 oglobulin G titers were measured by means of enzyme-linked immunosorbent assay before and 1 month aft
125                            Using an indirect enzyme-linked immunosorbent assay for all 5 muscarinic r
126 Serum samples were also screened by means of enzyme-linked immunosorbent assay for antibodies reactiv
127 nase assay performed for cell damage, and an enzyme-linked immunosorbent assay for cytokine expressio
128     Sixty-five patients with BP underwent an enzyme-linked immunosorbent assay for IgE antibodies aga
129 ents with a total of 197 specimens tested by enzyme-linked immunosorbent assay for IgM, IgG, and IgA
130  and demonstrated a high correlation with an enzyme-linked immunosorbent assay for sample detection i
131              Here, we describe a serological enzyme-linked immunosorbent assay for the screening and
132  fluopyram were developed in two alternative enzyme-linked immunosorbent assay formats, using homolog
133 ry examination phase were processed using an enzyme-linked immunosorbent assay from a single batch.
134             Its performance is comparable to enzyme-linked immunosorbent assay from the studies on cl
135                 GAP-43 was measured using an enzyme-linked immunosorbent assay in 105 MS patients (73
136 pithelial cells were investigated by PCR and enzyme-linked immunosorbent assay in an in vitro diabete
137  IgA, and IgG) to these antigens by means of enzyme-linked immunosorbent assay in patients with suspe
138 roup box 1 protein levels were analyzed with enzyme-linked immunosorbent assay in repeated samples.
139             If antiplatelet factor 4/heparin enzyme-linked immunosorbent assay is used to consider im
140 althy individuals was highly correlated with enzyme-linked immunosorbent assay measurements; moreover
141 mated in peri-implant crevicular fluid using enzyme-linked immunosorbent assay method and assessed wi
142 ere independently validated using Luminex or enzyme-linked immunosorbent assay methods.
143 G-Abs) were first detected by immunoblot and enzyme-linked immunosorbent assay nearly 30 years ago, b
144 objective was to evaluate the application of enzyme-linked immunosorbent assay optical density thresh
145 rm a sensitivity and specificity analysis of enzyme-linked immunosorbent assay optical density thresh
146 tudy was to evaluate the applicability of an enzyme-linked immunosorbent assay optical density thresh
147           These proteins were immobilized on enzyme-linked immunosorbent assay plates in their native
148 erotonin release assay, and immunoglobulin G enzyme-linked immunosorbent assay positive) and serotoni
149                                              Enzyme-linked immunosorbent assay revealed that the form
150 chain reaction (RT-PCR) and immunoglobulin M enzyme-linked immunosorbent assay testing to detect ZIKV
151 alizing antibody [PRNT80 titers, 40-640] and enzyme-linked immunosorbent assay titers) after the boos
152                              We developed an enzyme-linked immunosorbent assay to measure anti-DENV N
153                                   We used an enzyme-linked immunosorbent assay to measure levels of s
154  healthy controls (CON, n = 14), we utilized enzyme-linked immunosorbent assay to measure NFL and pro
155                By co-immunoprecipitation and enzyme-linked immunosorbent assay using recombinant prot
156 more, we analyzed galectin-9 serum levels by enzyme-linked immunosorbent assay using serum samples fr
157                                  An in-house enzyme-linked immunosorbent assay utilizing recombinant
158                                              Enzyme-linked immunosorbent assay was used to assess lev
159                                              Enzyme-linked immunosorbent assay was used to determine
160                                              Enzyme-linked immunosorbent assay was used to determine
161 ction antibody titer (measured by inhibition enzyme-linked immunosorbent assay) and dengue severity,
162 10 was measured in serum samples by means of enzyme-linked immunosorbent assay, and coronary atherosc
163 IBS-D had increased levels of PGE2, based on enzyme-linked immunosorbent assay, and COX2 messenger RN
164 mmaRI binding via surface plasmon resonance, enzyme-linked immunosorbent assay, and flow cytometry.
165  factors were analyzed using immunostaining, enzyme-linked immunosorbent assay, and heparanase procoa
166 on factors were analyzed via immunostaining, enzyme-linked immunosorbent assay, and heparanase procoa
167 mRNA extraction, real-time quantitative PCR, enzyme-linked immunosorbent assay, and immunohistochemic
168 um samples were analyzed by gliadin antibody enzyme-linked immunosorbent assay, and intestinal tissue
169     DBS sample CRP measurements were made by enzyme-linked immunosorbent assay, and venepuncture samp
170     PE-PilA was found to bind vitronectin by enzyme-linked immunosorbent assay, as isolated PE does.
171 raphy, gas chromatography-mass spectrometry, enzyme-linked immunosorbent assay, capillary electrophor
172 T cell effector functions were determined by enzyme-linked immunosorbent assay, carboxyfluorescein su
173  fluorescence-activated cell sorting (FACS), enzyme-linked immunosorbent assay, immunofluorescence (I
174 s-reactivity to VAR2CSA was characterized by enzyme-linked immunosorbent assay, immunofluorescence as
175 rse-transcription polymerase chain reaction, enzyme-linked immunosorbent assay, immunofluorescence, a
176                                        Using enzyme-linked immunosorbent assay, immunohistochemistry,
177 e characterization of monoclonal antibodies (enzyme-linked immunosorbent assay, or "ELISA"), to small
178 ice were analyzed using HEV antigen-specific enzyme-linked immunosorbent assay, reverse transcription
179 roduction was measured using flow cytometry, enzyme-linked immunosorbent assay, RNA in situ hybridiza
180 ding age, sex, antiplatelet factor 4/heparin enzyme-linked immunosorbent assay, serotonin release ass
181 onal and monoclonal antibodies by inhibition enzyme-linked immunosorbent assay, surface plasmon reson
182 tients were tested with the immunoglobulin G enzyme-linked immunosorbent assay, the serotonin release
183 he presence of anti-Cas9 antibodies using an enzyme-linked immunosorbent assay, we detected antibodie
184 rum anti-CFA/I total antibodies, detected by enzyme-linked immunosorbent assay, were the best predict
185 les, in various immunoassay formats, such as enzyme-linked immunosorbent assay, Western blot, and lat
186          Conventional techniques such as the enzyme-linked immunosorbent assay, Western Blot, and mas
187 rming a paper-based HIV-1 p24 capsid protein enzyme-linked immunosorbent assay, which achieved a reco
188 itory capacity were also explored through an enzyme-linked immunosorbent assay-based measurement of n
189 plied the CID system to a sensitive sandwich enzyme-linked immunosorbent assay-like assay of cannabid
190 ry, real-time polymerase chain reaction, and enzyme-linked immunosorbent assay.
191 asured in cell culture supernatants using an enzyme-linked immunosorbent assay.
192 and 180 were assessed via flow cytometry and enzyme-linked immunosorbent assay.
193 sed by hemagglutination inhibition assay and enzyme-linked immunosorbent assay.
194 i-vaccine antibody titers were quantified by enzyme-linked immunosorbent assay.
195 glutination assay and a Competitive Indirect Enzyme-linked immunosorbent assay.
196 parum circumsporozoite protein (PfCSP) using enzyme-linked immunosorbent assay.
197 ns of PvMSP3alpha, were measured by means of enzyme-linked immunosorbent assay.
198 ts hospitalized with CAP were measured using enzyme-linked immunosorbent assay.
199 arvested to evaluate cytokine profiles using Enzyme-Linked Immunosorbent Assay.
200 oglobulin M (IgM) and immunoglobulin G (IgG) enzyme-linked immunosorbent assay.
201 ated dUTP nick-end labeling and DNA fragment enzyme-linked immunosorbent assay.
202 s measured using a virus-like particle-based enzyme-linked immunosorbent assay.
203 ogens was determined in an in vitro model by enzyme-linked immunosorbent assay.
204 PS-specific antibodies were determined using enzyme-linked immunosorbent assay.
205 D, PAD2, and MMP-8 levels were determined by enzyme-linked immunosorbent assay.
206 nd the HRP2 concentration was measured by an enzyme-linked immunosorbent assay.
207 nalyzed for anti-PEG-ASP immunoglobulin G by enzyme-linked immunosorbent assay.
208 ere analyzed using multiplex immunoassay and enzyme-linked immunosorbent assay.
209 oproteinase-2 (MMP-2) were measured using an enzyme-linked immunosorbent assay.
210          Melatonin levels were determined by enzyme-linked immunosorbent assay.
211  VEGF, and TNF-alpha levels were measured by enzyme-linked immunosorbent assay.
212 ntibodies by Crithidia luciliae staining and enzyme-linked immunosorbent assay.
213    Serum PRO-C3 was assessed by competitive, enzyme-linked immunosorbent assay.
214 mples) when combined with the IgG anti-BP180 enzyme-linked immunosorbent assay.
215 nd chemokines using a 17-plex Luminex kit or enzyme-linked immunosorbent assay.
216  interleukin 22 in serum from 28 patients by enzyme-linked immunosorbent assay.
217  IL-1beta, and calprotectin were analyzed by enzyme-linked immunosorbent assay.
218 mens with a 62-cytokine multiplex bead-based enzyme-linked immunosorbent assay.
219 The PC- and gB-specific ABs were assessed by enzyme-linked immunosorbent assay.
220 ied using a broadly reactive, genus-specific enzyme-linked immunosorbent assay.
221 ibody titer >=10 AU/mL using a drug-tolerant enzyme-linked immunosorbent assay.
222 istochemistry, western-blotting, and also by enzyme-linked immunosorbent assay.
223 S-CoV-2 spike protein were detected by using enzyme-linked immunosorbent assay.
224  soluble FAS ligand (sFASL) were measured by enzyme-linked immunosorbent assay.
225 s had positive antiplatelet factor 4/heparin enzyme-linked immunosorbent assay; 10 patients were iden
226 sm or Alzheimer's disease were quantified by enzyme-linked immunosorbent assays (ELISA) or theoretica
227                                    Plasmonic enzyme-linked immunosorbent assays (ELISA) using the loc
228 ed Enpp1 and Impdh2, which were validated by enzyme-linked immunosorbent assays (ELISA).
229 tactin (PRN) were evaluated using commercial enzyme-linked immunosorbent assays (ELISA).
230 derived Lb8E and Lb6H, and evaluated both in enzyme-linked immunosorbent assays (ELISA).
231                                        Three enzyme-linked immunosorbent assays (ELISAs) (Hemagen, Or
232 sitivities and specificities of 4 commercial enzyme-linked immunosorbent assays (ELISAs) and 2 rapid
233 able SARS-CoV-2 detection tests and in-house enzyme-linked immunosorbent assays (ELISAs) and correlat
234  bound to heparin and chondroitin sulfate in enzyme-linked immunosorbent assays (ELISAs) and depended
235                  We reported previously that enzyme-linked immunosorbent assays (ELISAs) based on the
236                                              Enzyme-linked immunosorbent assays (ELISAs) for BP180 an
237                    GST pulldown and indirect enzyme-linked immunosorbent assays (ELISAs) further conf
238 niae serum antibody detection via commercial enzyme-linked immunosorbent assays (ELISAs) is widely us
239 activities to a panel of class 5 adhesins in enzyme-linked immunosorbent assays (ELISAs) revealed sev
240 and compared to three commercially available enzyme-linked immunosorbent assays (ELISAs) targeting th
241                                  IgG1 or IgG enzyme-linked immunosorbent assays (ELISAs) with rK39 or
242            Instead, using immunoblotting and enzyme-linked immunosorbent assays (ELISAs), we found th
243 lis somatic antigens ("crude antigen") using enzyme-linked immunosorbent assays (ELISAs).
244 raction with soluble dimeric FcgammaRIIIa in enzyme-linked immunosorbent assays (ELISAs).
245  obtained using quantitative, single-plexed, enzyme-linked immunosorbent assays (ELISAs).
246 of autoimmune diseases routinely detected by enzyme-linked immunosorbent assays (ELISAs).
247 phic factor (GDNF) were analysed by specific enzyme-linked immunosorbent assays (ELISAs).
248 he full use of double nanobodies in sandwich enzyme-linked immunosorbent assays (ELISAs).
249 ralization, and immunoglobulin A (IgA) and G enzyme-linked immunosorbent assays (ELISAs); NPW specime
250 brane antigen (FAMA) assays and glycoprotein enzyme-linked immunosorbent assays (gpELISAs) were used
251 rse transcription-PCR (rRT-PCR), IgM capture enzyme-linked immunosorbent assays (IgM-ELISAs), and inh
252                                              Enzyme-linked immunosorbent assays against whole bacteri
253                                              Enzyme-linked immunosorbent assays are currently the mos
254  molecule 1 [VCAM-1]) were measured by using enzyme-linked immunosorbent assays at 1 day, 2 weeks, an
255                                              Enzyme-linked immunosorbent assays determined highly sig
256 , PCR, or culture or positive results by two enzyme-linked immunosorbent assays for cases presenting
257      Enzyme immunoassay determined LTB4, and enzyme-linked immunosorbent assays quantified tumor necr
258  flow assays (LFAs) and two laboratory-based enzyme-linked immunosorbent assays to detect anti-SARS-C
259                            We also performed enzyme-linked immunosorbent assays using a recombinant w
260                                      Capture enzyme-linked immunosorbent assays using specific rabbit
261 t antigens of Bexsero, and Western blots and enzyme-linked immunosorbent assays were used to assess t
262                                  Comparative enzyme-linked immunosorbent assays with monoclonal antib
263 as performed with the use of protein arrays, enzyme-linked immunosorbent assays, and Western blot ana
264                                        Using enzyme-linked immunosorbent assays, levels of antibody r
265 n quantitative polymerase chain reaction and enzyme-linked immunosorbent assays, respectively.
266 ed by techniques based on flow cytometry and enzyme-linked immunosorbent assays.
267  response to rATG was analyzed via multiplex enzyme-linked immunosorbent assays.
268 popolysaccharide (Pg-LPS) stimulation, using enzyme-linked immunosorbent assays.
269 1) were serially measured using quantitative enzyme-linked immunosorbent assays.
270 evicular fluid (GCF) of all participants via enzyme-linked immunosorbent assays.
271 aging, immunoblot, and functional assays and enzyme-linked immunosorbent assays.
272 tactin (PRN) were evaluated using commercial enzyme-linked immunosorbent assays.
273    We evaluated a CMV-specific peptide-based enzyme-linked immunosorbent spot (ELISPOT) assay to dete
274 d, Ag-specific interleukin-4 (IL-4) T-helper enzyme-linked immunosorbent spot (ELISpot) assays of the
275                                  In cultured enzyme-linked immunosorbent spot (ELISpot) assays, indiv
276 2Delta30 and used them in a gamma interferon enzyme-linked immunosorbent spot assay to interrogate CD
277 ation was assessed using an interferon gamma enzyme-linked immunosorbent spot assay.
278  means of lateral-flow rapid test as well as enzyme-linked-immunosorbent-assay (ELISA).
279 cific IgM antibody-secreting cells (ASCs) by enzyme-linked immunospot (ELISpot) assay allowed for dif
280 common cold coronaviruses.METHODSWe used the enzyme-linked immunospot (ELISPOT) assay to characterize
281 rferon gamma (IFN-gamma) production using an enzyme-linked immunospot (ELISPOT) CMV assay (T-SPOT.CMV
282 y (CMV-CMI) as determined by a peptide-based enzyme-linked immunospot (ELISPOT) CMV assay may identif
283                                 By contrast, enzyme-linked immunospot (ELISPOT), flow cytometry, time
284 of 32 HDV-infected patients were analyzed by enzyme-linked immunospot analysis and intracellular cyto
285 lobulin M antibody-secreting cells (ASCs) by enzyme-linked immunospot assay allowed for differentiati
286  T-cell responses were analyzed using T-cell enzyme-linked immunospot assay before convalescent plasm
287       Mycoplasma pneumoniae ASCs measured by enzyme-linked immunospot assay were assessed alongside M
288 e assessed using an ex-vivo interferon-gamma enzyme-linked immunospot assay.
289 ses were assessed using an ex-vivo IFN-gamma enzyme-linked immunospot assay.
290 s of Candida-specific T-cell responses using enzyme-linked immunospot assays revealed higher numbers
291 d mononuclear cells using flow cytometry and enzyme-linked immunospot assays.
292  flow cytometry for cell surface markers and enzyme-linked immunospot methods to assess the subset di
293                  We previously introduced an enzyme-linked immunospot spot (ELISpot)-based assay to m
294  parameters, cell-mediated immunogenicity by enzyme-linked immunospot, functional neutralizing antibo
295                                              Enzyme-linked immunospots, cytotoxicity assays as well a
296                                              Enzyme-linked lectin assay was used to screen PS-SGCL ag
297                 Secretion was measured by an enzyme-linked lectin assay, change in intracellular [Ca(
298  We have developed a single-tube Transposase Enzyme Linked Long-read Sequencing (TELL-seq) technology
299                   In this work, a duplex PCR-Enzyme Linked Oligonucleotide Assay (ELONA) is reported
300  diversity of ADAR isoforms, key RNA editing enzymes linked with the innate immune system and viral i

 
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