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2 te that eIF4E-mediated rescue is governed by pretranslational and translational activation of bcl-x a
4 Decreases in both mRNA and protein suggest pretranslational control of SERCA1 expression, whereas t
5 ting that this form of the disorder involves pretranslational dysregulation of PRPS1 expression and m
6 concordantly lower in fetal cortex, whereas pretranslational expression of PTTG binding factor (PBF)
8 he expression of bTREK-1 in AZF cells at the pretranslational level by a cAMP-dependent mechanism tha
9 channel whose expression is inhibited at the pretranslational level by ACTH and 8-pcpt-cAMP by a mech
10 apical bile acid transporter is induced at a pretranslational level by free or taurine-conjugated cho
11 e rat is regulated, at least in part, at the pretranslational level in some tissues, and (c) DII is l
12 es in skeletal muscle gene expression at the pretranslational level that cannot be explained by inact
13 The induction of both enzymes occurs at the pretranslational level, is the consequence of enhanced g
21 imit Hsp70 expression by transcriptional and pretranslational mechanisms, perhaps to avoid the potent
24 In this study, we investigated NF-kappaB pretranslational regulation by performing a series of da
25 protein synthesis inhibitors, implicating a pretranslational role for transcription in origin specif
27 trations of LPS and a slower, NO-independent pretranslational suppression occurring at low concentrat
28 -tRNA(Asn), are formed in many bacteria by a pretranslational tRNA-dependent amidation of the mischar
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