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6 ew cell numbers resulted from impaired proliferation, which we confirmed both in vivo and in vitro.
7 py crossing points for a year (7,102 canopy camera nights), we confirmed bridge use by 25 mammal species from 12 families
10 s Selaginella moellendorffii Using de novo transcriptomics, we confirmed expression of five transcripts in S. moellendorf
13 g the fluorescent-dye conjugate, [S14R, W50Pra(Bodipy)]Ts1, we confirmed its binding to Nav1.4 through Lanthanide-based R
16 s following blocking of different inhibitory receptors, and we confirmed our results in a Friend virus retroviral model o
20 e plasmon resonance and leakage assays with model vesicles, we confirmed that Ctn(15-34) binds to and disrupts lipid memb
21 the essentiality of GAPDH1 in intracellular replication but we confirmed that glycolysis is not strictly essential.
25 Using a recombinant virus derived from the JFH1 strain, we confirmed that plasma-derived and recombinant lipoprotein(
26 imaging of calcium transients from cultured pupal neurons, we confirmed that Ral does not participate in SOCE, but acts
32 ain further mechanistic insights into this phenomenon, here we confirmed that the plasma membrane-localized transporter (
36 ion of mutants) are candidate hypo-competition alleles, and we confirmed the hypo-competition phenotype for four of these
38 criptome-guided approach on gene ontology and tox-pathways, we confirmed the novel approach effective for exploring tox-p
41 When we extended the study to 3 months of quiescence, we confirmed the replication-independent mutational spectrum
42 sferases was highly specific for stilbenoid substrates, and we confirmed their subcellular location in the plastid by flu
46 ecancers/cancers compared to higher levels in the controls; we confirmed this in cancers from around the world.
49 tional behavior of the full-length GluK2/K5 receptor, which we confirmed via electrophysiological recordings.
50 cies-specific adaptation to low phosphate conditions, which we confirmed with growth experiments.
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