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1 erase on this variant generated mutants with tyrosine aminotransferase activities better than those p
3 cat)/K(m)(Phe) and had as much as 11% of the tyrosine aminotransferase activity of WT E.coli TATase.
4 d) expression of mRNA for hepatocyte markers tyrosine aminotransferase and alpha-1 antitrypsin, but t
6 viously described regulatory elements in the tyrosine aminotransferase and transferrin receptor promo
7 encoding phosphoenolpyruvate carboxykinase, tyrosine aminotransferase, and insulin-like growth facto
9 reduced PEPCK, GLUT2, glucose-6-phosphatase, tyrosine aminotransferase, CRP, and hGx reporter gene ex
11 rs (GRs): a 21-base pair sequence of the rat tyrosine aminotransferase gene called a glucocorticoid m
12 orticoid modulatory element (GME) of the rat tyrosine aminotransferase gene is the only cis-acting el
13 Our findings uncover a critical role for tyrosine aminotransferase in the oxidative stress respon
14 monstrated by elucidating the time-course of tyrosine aminotransferase induction in the liver of rats
15 onversion of aspartate aminotransferase into tyrosine aminotransferase is demonstrated and compared t
16 successfully used to model published data on tyrosine aminotransferase pharmacodynamics.Conclusions:
17 ygenase, endothelin receptor A, haptoglobin, tyrosine aminotransferase, phosphoribosylpyrophosphate s
18 enzymes in the tyrosine degradation pathway (tyrosine aminotransferase (TAT) and 4-hydroxyphenylpyruv
21 ile in functional assays of transactivation (tyrosine aminotransferase, TAT, and glutamine synthetase
24 that the Caenorhabditis elegans ortholog of tyrosine aminotransferase (TATN-1)-the first enzyme invo
25 sphoenolpyruvate carboxykinase, transferrin, tyrosine aminotransferase) were reduced by 50 to 70%, in