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1                             Disease-specific COMP fragments were isolated by affinity chromatography of synovial fluids f
2                                               LRP1 partners were isolated by affinity purification and characterized by m
3                      Human bronchial epithelial cells (BEC) were isolated by bronchoscopy from bronchial biopsies of heal
4                                 Rat pancreatic acinar cells were isolated by collagenase digestion and [Ca(2+)]i was meas
5        Bacterial members of the adult C. elegans microbiota were isolated by culture and identified using 16S rRNA gene s
6                                                The products were isolated by decantation of the solvent or by recrystalli
7                                                  Mouse BMCs were isolated by density-gradient centrifugation.
8                                                Released EVs were isolated by differential ultracentrifugation.
9 group was a 2-methylnaphthyl, thermally stable atropisomers were isolated by enantioselective HPLC and their absolute con
10 and noninfarcted neonatal (P1) and adult (P56) mouse hearts were isolated by enzymatic dissociation and fluorescence-acti
11  morphogenetic protein 4-induced cardiovascular progenitors were isolated by FACS for expression of vascular endothelial
12                                  Putative EpiSC populations were isolated by FACS sorting.
13 inal center (GC), early GC (eGC), and memory tonsil B cells were isolated by FACS, and their capacities for IL-4 and anti
14                                           Mononuclear cells were isolated by ficoll separation and cell surface staining
15                           Stable alpha-boryl ester products were isolated by flash chromatography in all cases except for
16                                    For 5 samples, CTCs also were isolated by flow cytometry and based on CD45 depletion.
17 in microglia (resting or activated with lipopolysaccharide) were isolated by flow cytometry and cocultured with neonatal
18       Cells were isolated from the tissue samples, and APCs were isolated by flow cytometry.
19 Wnt1-Cre mice were dissected and the 6 populations of cells were isolated by flow cytometry.
20             In vitro HIV-GFP infected and noninfected Tregs were isolated by flow-based cell-sorting to investigate Treg
21                          Six different populations of cells were isolated by fluorescence-activated cell sorting from dis
22                             The tear protein-FODE complexes were isolated by gel filtration and ion exchange chromatograp
23                                   Oligosaccharide fractions were isolated by high resolution size-exclusion chromatograph
24 rmation of the Prato monoaduct, two different diastereomers were isolated by HPLC (4, 5) whose absolute configurations we
25  cells expressing cell-surface NGFR protein (CD271, p75NTR) were isolated by immunoaffinity adsorption, and cultured as a
26                                               Uptake routes were isolated by introducing earthworms with sealed and unsea
27                    Viral subclones representing these forms were isolated by limiting dilution assays, and each replicate
28 corn, grapeseed, hazelnut, olive, peanut and sunflower oils were isolated by means of alkaline hydrolysis followed by sil
29                             Circulating ILC2s and TH2 cells were isolated by means of fluorescence-activated cell sorting
30                                                       ILC2s were isolated by means of fluorescence-activated cell sorting
31                                                The analytes were isolated by means of liquid-liquid extraction, including
32                                           Complexes 1 and 2 were isolated by photolysis of the corresponding side-bound d
33  defined number of glucose moieties attached to the protein were isolated by quadrupol and fragmented in the ICR cell by
34                                          Thus, the products were isolated by simple extractions, avoiding the use of chro
35         The aroma constituents of Kangra orthodox black tea were isolated by simultaneous distillation extraction (SDE),
36                                      The volatile compounds were isolated by simultaneous steam distillation-solvent extr
37                                                        CTCs were isolated by size using a filtration-based device and the
38                   The NUCB1-stabilized prefibrillar species were isolated by size-exclusion chromatography and analyzed b
39               Free and glycosidically-bound aroma compounds were isolated by solid phase extraction (SPE) to later be ana
40 f curuba fruit (Passiflora mollissima (Kunth) L. H. Bailey) were isolated by solvent assisted flavour evaporation (SAFE).
41 e volatile compounds of lulo fruit (Solanum quitoense Lam.) were isolated by solvent extraction followed by solvent-assis
42 tile components of raw, dry roasted and oil roasted almonds were isolated by solvent extraction/solvent-assisted flavor e
43                          In arils-only juices, 41 compounds were isolated by SPME, including 17 of the consensus volatile
44                          In this study, terminase complexes were isolated by tandem-affinity purification (TAP) using rec
45                               Cytomegalovirus-specific CTLs were isolated by the IFN-gamma secretion assay (gamma-catch)
46  (TEA)]r H2 O where p, q, r=[2,3,8] for 1 and [4,1,4] for 2 were isolated by the reaction of tungstate(VI) and vanadium(V
47                      Congenic normal mdr2 (+/+) hepatocytes were isolated by two-step collagenase perfusion and transplan
48              PMPs, generated from purified human platelets, were isolated by ultracentrifugation and labeled with biotin
49 an HDL from healthy and CAD subjects, as well as mouse HDL, were isolated by ultracentrifugation.
50                          Mice were sacrificed and plasma MP were isolated by ultracentrifugation.

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