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2 s involved in ePi induction of osteopontin gene expression, we transfected a series of osteopontin promoter-luciferase co
3 whether this mutation could change the enzyme specificity, we transfected a teratocarcinoma cell line (2102Ep) with vect
9 To test how the beta4 protein regulates Na channel gating, we transfected beta4 into HEK (human embryonic kidney) cells
10 he gene encoding P. vivax dihydrofolate reductase (pvdhfr), we transfected blood specimens from Saimiri boliviensis monke
11 hematopoietic defects of FA patients, in the present study, we transfected BM cells from FA patients with hsa-miR-181c to
13 To determine the role of HNK-1 glycan, we transfected C6 glioma cells, which lack HNK-1 glycan expre
16 well as confirm the results obtained with 3-MA inhibition, we transfected cells with ATG5 small interfering RNA to block
17 on of both DNA templates.To identify the effector proteins, we transfected cells with biotinylated DNA encoding a nonvira
18 To determine the impact of STAT6 binding, we transfected cells with STAT6VT, a constitutively active ST
19 determine if these effects were caused by EGFR expression, we transfected Chinese hamster ovary (CHO) cells, which lack
20 om somatosensory or motor cortex of rats (layers 2/3 or 5), we transfected cortical neurons with DNA for a Kv2.1 pore mut
22 To test if this also occurs for neurofilaments in neurons, we transfected cultured rat cortical neurons with fluorescent
26 To analyse this interactions functionally, we transfected fibroblasts with non-replicating, non-translat
27 To demonstrate the necessity of the 2w sequence, we transfected hair cells with PMCA2 containing different var
30 role of the holoenzyme in the control of synaptic strength, we transfected hippocampal neurons with constructs encoding f
32 To assess the pathogenicity of the identified mutations, we transfected human embryonic kidney 293 cells with plasmids
34 To corroborate the histochemical results we transfected living tadpole brain with a Xenopus TRbeta pro
37 normal pumping function but is defective in Src regulation, we transfected Na/K-ATPase alpha1 knockdown PY-17 cells with
39 To determine the roles of core3 O-glycans, we transfected PC3 and LNCaP prostate cancer cells with beta3
40 combinant VACVs that express the cowpox full-length ATIp or we transfected plasmids encoding ATIp into cells infected wit
41 To map the LPS-regulated SerpinB2 promoter regions, we transfected reporter constructs driven by the approximatel
42 cytoplasm affected their translation during VSV infection, we transfected reporter mRNAs into cells at various times rel
43 pletion of the helicases and not due to off-target effects, we transfected rescue plasmids for each respective helicase.
44 To further define the mechanism of the microparasol, we transfected siRNA targeted against p150(Glued) into human
48 To characterize FCV binding to surface-expressed fJAM-A, we transfected truncated and chimeric forms of fJAM-A into a
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