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1 erase on this variant generated mutants with tyrosine aminotransferase activities better than those p
2 cat)/K(m)(Phe) and had as much as 11% of the tyrosine aminotransferase activity of WT E.coli TATase.
3 d) expression of mRNA for hepatocyte markers tyrosine aminotransferase and alpha-1 antitrypsin, but t
4 ssion of mature liver-specific genes such as tyrosine aminotransferase and apolipoproteins.
5 viously described regulatory elements in the tyrosine aminotransferase and transferrin receptor promo
6  encoding phosphoenolpyruvate carboxykinase, tyrosine aminotransferase, and insulin-like growth facto
7 reduced PEPCK, GLUT2, glucose-6-phosphatase, tyrosine aminotransferase, CRP, and hGx reporter gene ex
8  specificity of eAATase into that of E. coli tyrosine aminotransferase (eTATase).
9 rs (GRs): a 21-base pair sequence of the rat tyrosine aminotransferase gene called a glucocorticoid m
10 orticoid modulatory element (GME) of the rat tyrosine aminotransferase gene is the only cis-acting el
11 monstrated by elucidating the time-course of tyrosine aminotransferase induction in the liver of rats
12 onversion of aspartate aminotransferase into tyrosine aminotransferase is demonstrated and compared t
13 successfully used to model published data on tyrosine aminotransferase pharmacodynamics.Conclusions:
14 ygenase, endothelin receptor A, haptoglobin, tyrosine aminotransferase, phosphoribosylpyrophosphate s
15 otein coupled receptor 5-positive (Lgr5) and Tyrosine aminotransferase (TAT).
16 oxylase (TH), and tyrosine is catabolized by tyrosine aminotransferase (TAT).
17 ile in functional assays of transactivation (tyrosine aminotransferase, TAT, and glutamine synthetase
18      Aspartate aminotransferase (AATase) and tyrosine aminotransferase (TATase) are Escherichia coli
19      A continuous assay for Escherichia coli tyrosine aminotransferase (TATase) that employs Lactobac
20 sphoenolpyruvate carboxykinase, transferrin, tyrosine aminotransferase) were reduced by 50 to 70%, in

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