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1 runcated AhRs were also subjected to limited trypsinization.
2 arated from epithelial cells by differential trypsinization.
3  degree of spreading of cells replated after trypsinization.
4 r removal of the drug and further passage by trypsinization.
5 the sialylated region of glycophorin by mild trypsinization.
6 ric shells of cells were harvested by serial trypsinization.
7  in astrocytes, which was prevented by light trypsinization.
8 isease linked mutants A30P and A53T, by mild trypsinization (0.1%, 30 s) of Ltk(-) cotransfected cell
9 observed extensive RNA degradation following trypsinization, a routine procedure used to dissociate a
10 CAM-1 expression was demonstrated by surface trypsinization and fractionation.
11                                              Trypsinization and immunoprecipitation studies with Golg
12                                              Trypsinization and sequence analysis of the 66-kDa rabbi
13                                              Trypsinization and several alternative procedures were u
14  Ric-8A-depleted RRL were not protected from trypsinization and therefore not folded correctly.
15    Beginning with intact spheroids, a serial trypsinization and trituration procedure was used to iso
16                         Even after extensive trypsinization, and anti-peptide antibody recognizing an
17 n and spreading, detachment and signaling by trypsinization, and signaling through either epidermal g
18  followed by intercellular disassociation by trypsinization, as a model for epidermal injury.
19 ment characteristic of the TGN; or (ii) mild trypsinization at neutral pH, resulted in the activation
20  vitro by different external stimuli such as trypsinization, cell density, and serum concentration.
21                                 We show that trypsinization decreases glycan fluctuations, demonstrat
22 ls, where DAT activity is not downregulated, trypsinization did not induce any changes.
23 ed receptor-2 activating peptides or through trypsinization, elevates cAMP in keratinocytes.
24 er, when the labeled enzyme was subjected to trypsinization, followed by sequencing of the labeled pe
25 ne disruption by depletion of cholesterol or trypsinization halts B(2)R internalization, invasion, an
26 bitors of protein secretion and abolished by trypsinization, indicating that the active substance inc
27                                         Mild trypsinization induced sensitivity of chromosome elastic
28                                    Prolonged trypsinization not only entirely removes the outer capsi
29                                       Serial trypsinization of glioblastoma specimens yielded cells w
30 rotomer (Ibp) bound to the cell surface, but trypsinization of Ibp was necessary for docking of the A
31                                         Mild trypsinization of intact PRBCs of P. falciparum strains
32 this report, we characterized the effects of trypsinization of Pgp on its ATPase function.
33 from that of the native fragment obtained by trypsinization of plasma fibronectin.
34 by secondary structure in the protein, since trypsinization of reduced and carboxymethylated RF-hsp 7
35                   These results suggest that trypsinization of rotavirus particles triggers a rearran
36 posed loop in the GII.3 NoVs facilitates the trypsinization of the capsid protein in the assembled fo
37 stinguished by their resistance to extensive trypsinization of the cell surface.
38 ssociated with the cells following extensive trypsinization of the cell surface.
39                                              Trypsinization of the confluent cells and replating them
40  remain within the membrane domain following trypsinization of the intact gastric H,K-ATPase in the p
41  steroid binding domain generated by partial trypsinization of the rat uterine ER, we demonstrate tha
42                                              Trypsinization of the resultant virus-like particles yie
43                                              Trypsinization of treated RPE cells results in the relea
44 LP-mediated fusion activity was dependent on trypsinization of VP4, and the strain-specific phenotype
45 s, viral protein 4 (VP4) and VP7, and on the trypsinization of VP4.
46 has the advantage of reducing the effects of trypsinization on measurements of adhesion, and therefor
47 aded when cell-cell contact was disturbed by trypsinization or EDTA release.
48                                            A trypsinization peptide (3647u) containing 5 leucine repe
49 nin and Fibronectin was also affected by the trypsinization process but not by the reduced temperatur
50            Our data show that after 5 min of trypsinization, projection-like spikes made of VP7 (35 k
51                                        GLUT1 trypsinization released full-length transmembrane helix
52                                              Trypsinization resulted in a complete degradation of RNA
53           Cell enumeration after washing and trypsinization revealed firm protein-based cell attachme
54                                 Cell-surface trypsinization revealed that more than half of mature mM
55 ts are distinct from those obtained from the trypsinization studies performed earlier on the NV (GI)
56                                    Following trypsinization, the intracellular accumulation of both e
57 din-based affinity purification and on-resin trypsinization, the resulting peptide mixture is subject
58 tress fibers were fewer and shorter, and the trypsinization time needed for cells to round up was red
59 gel to increase virus contact time, and mild trypsinization to increase virus penetration.