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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
8 To test how the beta4 protein regulates Na channel gating, we transfected beta4 into HEK (human embryonic kidney) cells
9 he gene encoding P. vivax dihydrofolate reductase (pvdhfr), we transfected blood specimens from Saimiri boliviensis monke
10 hematopoietic defects of FA patients, in the present study, we transfected BM cells from FA patients with hsa-miR-181c to
12 To determine the role of HNK-1 glycan, we transfected C6 glioma cells, which lack HNK-1 glycan expre
15 well as confirm the results obtained with 3-MA inhibition, we transfected cells with ATG5 small interfering RNA to block
16 on of both DNA templates.To identify the effector proteins, we transfected cells with biotinylated DNA encoding a nonvira
17 To determine the impact of STAT6 binding, we transfected cells with STAT6VT, a constitutively active ST
18 determine if these effects were caused by EGFR expression, we transfected Chinese hamster ovary (CHO) cells, which lack
21 om somatosensory or motor cortex of rats (layers 2/3 or 5), we transfected cortical neurons with DNA for a Kv2.1 pore mut
23 To test if this also occurs for neurofilaments in neurons, we transfected cultured rat cortical neurons with fluorescent
27 To analyse this interactions functionally, we transfected fibroblasts with non-replicating, non-translat
29 role of the holoenzyme in the control of synaptic strength, we transfected hippocampal neurons with constructs encoding f
31 To assess the pathogenicity of the identified mutations, we transfected human embryonic kidney 293 cells with plasmids
33 To corroborate the histochemical results we transfected living tadpole brain with a Xenopus TRbeta pro
34 these differentially abundant miRNAs on glucose metabolism, we transfected miR-20b-5p, a highly abundant exoRNA in patien
35 role of salivary gland miRNAs in POWV replication in-vitro, we transfected miRNA inhibitors into VeroE6 cells to profile
37 normal pumping function but is defective in Src regulation, we transfected Na/K-ATPase alpha1 knockdown PY-17 cells with
38 To determine the roles of core3 O-glycans, we transfected PC3 and LNCaP prostate cancer cells with beta3
39 combinant VACVs that express the cowpox full-length ATIp or we transfected plasmids encoding ATIp into cells infected wit
40 To map the LPS-regulated SerpinB2 promoter regions, we transfected reporter constructs driven by the approximatel
41 cytoplasm affected their translation during VSV infection, we transfected reporter mRNAs into cells at various times rel
42 pletion of the helicases and not due to off-target effects, we transfected rescue plasmids for each respective helicase.
43 To further define the mechanism of the microparasol, we transfected siRNA targeted against p150(Glued) into human
47 To characterize FCV binding to surface-expressed fJAM-A, we transfected truncated and chimeric forms of fJAM-A into a