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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
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
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
17 ile in functional assays of transactivation (tyrosine aminotransferase, TAT, and glutamine synthetase
20 sphoenolpyruvate carboxykinase, transferrin, tyrosine aminotransferase) were reduced by 50 to 70%, in
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