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1 The effect of cAMP on Fe(II) and 5hmC was confirmed by adenylate cyclase activators, phosphodiester
4 for both reduced-dose and partial-breast radiotherapy, and was confirmed by the test against the critical HR being more
5 pase-3, indicating the onset of apoptosis of LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-me
6 moting the localization of excitons in the shell domain, as was confirmed by ultrafast transient absorption and emission
7 association of lipid rafts with HCV-induced autophagosomes was confirmed by Western blotting, immunofluorescence microsc
8 eaved transcripts of miRNA-targeted ARFs in C. roseus cells was confirmed by Poly(A) Polymerase-Mediated Rapid Amplificat
12 ortho or para position of the phenol structure of THC-COOH was confirmed by detection of monochlorinated byproduct fragm
13 Efficient lineage-specific differentiation was confirmed by uniform NCAM1 and myosin heavy chain express
16 presence of both AgNPs and dissolved silver in the extracts was confirmed by single particle (SP)-ICPMS analysis.
18 The basophil-targeting effect of ibrutinib was confirmed by demonstrating that IgE-dependent histamine r
19 esting that ETS1 is involved in regulating CDKN2A This idea was confirmed by RNAi-mediated suppression or genetic deletio
23 ence of mixing between isotopically distinct Cd end-members was confirmed by a Bayesian modeling approach.
25 The predictive ability of the models was confirmed by an external validation procedure with an ind
27 Binding of PHR1 and PHL1 factors to P1BS was confirmed by Y1H, electrophoretic mobility assay and chro
33 T was considered true-positive if the positive primary site was confirmed by histology or follow-up imaging.
34 rmore, the exact biological function of these binding sites was confirmed by site-directed mutagenesis.
35 The release of these nanoparticles into the solution was confirmed by monitoring their catalytically amplified col
38 t significant target expression in tumor, lung, and stomach was confirmed by immunohistochemistry.
39 EXLB8 expression in response to the aforementioned stresses was confirmed by qRT-PCR analysis in distinct Arachis genotyp
46 The model fits the observed GPP well (R(2) = 0.79), which was confirmed by other model performance checks that compared
47 5 of gestation, implicating early pregnancy factors, which was confirmed by reduced expression of BAT markers in progest
48 ting to the interaction between ATP5alpha and FANCD2, which was confirmed by protein docking analysis.
49 of substantial amount of lycopene in soluble fraction which was confirmed by the appearance of lycopene crystals when obs
50 suggested an interaction with the endocytic pathway, which was confirmed by direct measurement of fluid-phase endocytosi
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