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1 ll line Jurkat were separated by centrifugal elutriation.
2 tially growing cells isolated by centrifugal elutriation.
3 cell fractions were separated by centrifugal elutriation.
4 /F3 cell cycle fractions were prepared using elutriation.
5 ntaining regimens (53%), T-cell depletion by elutriation (42%), and others (2%).
6 riched from a rat gastric cell suspension by elutriation, a density-gradient fractionation, and a 48-
7                             A combination of elutriation and chemical lysis was used to deplete PBSC
8 cellular populations purified by counterflow elutriation and lectin panning, was validated by real-ti
9                               Countercurrent elutriation and magnetic bead selection were used to rap
10                                  Here we use elutriation and single-cell flow cytometry to analyze mi
11 ee independent methods: alpha factor arrest, elutriation, and arrest of a cdc15 temperature-sensitive
12 nd pronase digestion followed by centrifugal elutriation, and cell-associated H2O2 was determined by
13 -specificity antibodies, Campath antibodies, elutriation, and lectins.
14 efficient in small newborn cells obtained by elutriation, and this lowered phosphorylation correlates
15 l cycle with distinct temporal profiles post-elutriation, as exemplified by the observation of the ma
16  was fractionated by counterflow centrifugal elutriation (CCE), a differential binding to SBA among t
17  of these tissues by counterflow centrifugal elutriation (CCE).
18 fferent synchronization methods: centrifugal elutriation, cdc10 temperature-shift and release, and st
19 man myeloid leukemia cells using centrifugal elutriation combined with mass spectrometry-based proteo
20 y centrifugation with or without centrifugal elutriation, confirmed by vitamin A autofluorescence and
21 ified to 85% homogeneity by a combination of elutriation, density gradient centrifugation, and 48-hou
22 subpopulations were separated by centrifugal elutriation; each exhibited a unique rhodamine 123 fluor
23                                          The elutriation experiment, possibly being the least perturb
24  An examination of cycling cells enriched by elutriation for distinct phases of the cell cycle reveal
25 nce throughout the cell cycle by centrifugal elutriation, in the presence or absence of Cdh1.
26    Cell cycle studies using centrifugal cell elutriation indicated that the binding activity was sign
27 inct phases of the cell cycle by centrifugal elutriation, labeled cells with 5-ethynyl-2'-deoxyuridin
28 o delay cells in G2, counterflow centrifugal elutriation of cells into different phases of the cell c
29                            Using centrifugal elutriation of several human cell lines, we demonstrate
30                   To overcome the problem of elutriation of the original powdered material, the synth
31 such as the CAMPATH-1 monoclonal antibody or elutriation (P =.009).
32 report an optimised centrifugal counter-flow elutriation protocol for the rapid and direct isolation
33 t remove both T and B cells (alemtuzumab and elutriation, RR = 3.1; P = .025) compared with other met
34 show consistent patterns of phasing, but the elutriation synchrony results demonstrate a different pa
35 y perturbed' cell cycle by using centrifugal elutriation to differentially enrich distinct cell cycle
36                    Here, we used centrifugal elutriation to enrich for mouse ESCs at sequential stage
37 leukapheresis and countercurrent centrifugal elutriation to obtain myeloid origin mononuclear cell (M
38 To address this question we used centrifugal elutriation to separate hepatocytes by cell density.
39 elial cells purified by enzyme digestion and elutriation were evaluated for vacuolation in a blinded
40 scriptome of young and old cells isolated by elutriation, which allows isolation of biochemical quant

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