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1 -4 increases 15-LOX-1 protein levels through pretranslational actions.
2 te that eIF4E-mediated rescue is governed by pretranslational and translational activation of bcl-x a
3                            The mechanism was pretranslational, as adenosine receptor stimulation caus
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)
7             The induction is mediated at the pretranslational level and involves activating the TIMP-
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
14 n renal CYP2J5 expression are regulated at a pretranslational level.
15 ply that this regulation occurs in part at a pretranslational level.
16 n CYP2C11 and CYP2E1 expression occur at the pretranslational level.
17 ll types and its actions are mediated at the pretranslational level.
18 regulation of GnRH at both the secretory and pretranslational levels.
19                                              Pretranslational mechanism mediated NF-kappaB activation
20 oform thus appears to result from an altered pretranslational mechanism of PRPS1 expression.
21 imit Hsp70 expression by transcriptional and pretranslational mechanisms, perhaps to avoid the potent
22  whereas MAT2A-encoded protein increased via pretranslational mechanisms.
23 progression machinery in the nucleolus, in a pretranslational mode of pathogenesis.
24 m memory (LTM) by describing a novel form of pretranslational processing required for LTM, which reli
25     In this study, we investigated NF-kappaB pretranslational regulation by performing a series of da
26  protein synthesis inhibitors, implicating a pretranslational role for transcription in origin specif
27 f the level of IEMT activity is exerted at a pretranslational step.
28 trations of LPS and a slower, NO-independent pretranslational suppression occurring at low concentrat
29 -tRNA(Asn), are formed in many bacteria by a pretranslational tRNA-dependent amidation of the mischar