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1 ic, high-mobility group-like nuclear protein prothymosin alpha (ProT(alpha)) and the transcriptional
2 his study, we investigate how BETT regulates prothymosin alpha (ProT), a nuclear protein previously s
3 have shown the strong anti-HIV-1 activity of prothymosin alpha (ProTalpha) derived from CD8(+) T cell
4 ve shown that EBNA3C interacts with p300 and prothymosin alpha (ProTalpha) in EBV-infected cells and
6 critical for immortalization interacts with prothymosin alpha (ProTalpha), a cellular protein previo
8 t mRNAs complexing with HuR is that encoding prothymosin alpha (ProTalpha), an inhibitor of the apopt
12 ecently, Vega et al. proposed that exogenous prothymosin alpha can specifically increase the phosphor
14 r laboratory has recently shown that primate prothymosin alpha contains stoichiometric amounts of pho
16 dride showed that: 1) phosphate recovered on prothymosin alpha decreased 8-fold when lysates were tre
17 protein, and a histidine-tagged recombinant prothymosin alpha expressed either in bacteria or in COS
18 mine the half-life of the acyl phosphates on prothymosin alpha in vivo by pulse-labeling HeLa cells w
23 The ability of cells to phosphorylate old prothymosin alpha molecules was established by demonstra
24 curves of metabolically labeled native [32P]prothymosin alpha or a [32P]histidine-tagged variant res
26 hemistry for one of the identified proteins, prothymosin alpha, demonstrated prominent nuclear staini
27 n, and sonication) and three preparations of prothymosin alpha, one of which was purified by gentle m
33 ity purification we recently discovered that prothymosin-alpha (ProTalpha), a small highly acidic pro
34 in zero, mitogen-activated protein kinase 3, prothymosin beta 4, and brain lipid-binding protein.
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