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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
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
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
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
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
26 rformance of high complexity methods such as Enzyme-Linked Immunosorbent Assay (ELISA) and Chemilumin
28 F-1alpha in GCF and serum were quantified by enzyme-linked immunosorbent assay (ELISA) and reported a
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
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
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
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
53 etecting Plasmodium antigen in a fluorescent enzyme-linked immunosorbent assay (ELISA) using a fluore
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
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
72 functional neutralizing antibodies), and the enzyme-linked immunosorbent assay (ELISA), which measure
94 ed by a commercial SARS-CoV-2 total antibody enzyme-linked immunosorbent assay (ELISA, Wantai Biologi
98 asma samples collected in 211 patients using enzyme-linked immunosorbent assay (Tac/Sir = 104, Tac/Mt
101 InBios ZIKV Detect 2.0 IgM antibody capture enzyme-linked immunosorbent assay (ZIKV 2.0 MAC-ELISA; I
103 IKV antibodies using a ZIKV immunoglobulin G enzyme-linked immunosorbent assay and a virus neutraliza
105 l outgrowth was measured by the standard p24 enzyme-linked immunosorbent assay and an ultrasensitive
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
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
116 e compared findings of 2 orthogonal methods, enzyme-linked immunosorbent assay and mass spectrometry,
118 e also measured fecal pancreatic elastase by enzyme-linked immunosorbent assay and performed quantita
120 sponses were higher with higher dose (day 29 enzyme-linked immunosorbent assay anti-S-2P antibody geo
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
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
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.
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.
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
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
148 erotonin release assay, and immunoglobulin G enzyme-linked immunosorbent assay positive) and serotoni
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
154 healthy controls (CON, n = 14), we utilized enzyme-linked immunosorbent assay to measure NFL and pro
156 more, we analyzed galectin-9 serum levels by enzyme-linked immunosorbent assay using serum samples fr
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
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
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
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
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
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
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
254 molecule 1 [VCAM-1]) were measured by using enzyme-linked immunosorbent assays at 1 day, 2 weeks, an
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
261 t antigens of Bexsero, and Western blots and enzyme-linked immunosorbent assays were used to assess t
263 as performed with the use of protein arrays, enzyme-linked immunosorbent assays, and Western blot ana
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
276 2Delta30 and used them in a gamma interferon enzyme-linked immunosorbent spot assay to interrogate CD
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
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
290 s of Candida-specific T-cell responses using enzyme-linked immunospot assays revealed higher numbers
292 flow cytometry for cell surface markers and enzyme-linked immunospot methods to assess the subset di
294 parameters, cell-mediated immunogenicity by enzyme-linked immunospot, functional neutralizing antibo
298 We have developed a single-tube Transposase Enzyme Linked Long-read Sequencing (TELL-seq) technology
300 diversity of ADAR isoforms, key RNA editing enzymes linked with the innate immune system and viral i