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