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1 synthase), Sk2 (sphingosine kinase) and Ras (IMP dehydrogenase).
2 elieved by single amino acid replacements in IMP dehydrogenase.
3 ave been prepared as potential inhibitors of IMP dehydrogenase.
4 the most potent cofactor type inhibitors of IMP dehydrogenase.
5 nthosine 5'-monophosphate (XMP) catalyzed by IMP dehydrogenase.
6 d as inhibitors of the two isoforms of human IMP-dehydrogenase.
12 nery render yeast sensitive to inhibitors of IMP dehydrogenase and defective in inducing transcriptio
13 synthesis pathways-inosine-5'-monophosphate (IMP) dehydrogenase and cytosine triphosphate (CTP) synth
18 osyltransferase (DRTase, encoded by bb0426), IMP dehydrogenase (GuaB) and GMP synthase (GuaA) catalys
19 o key enzymes in purine salvage pathways are IMP dehydrogenase (GuaB) and GMP synthase (GuaA), encode
21 n cells unable to convert IMP to XMP or AMP (IMP dehydrogenase, guaB; adenylosuccinate synthetase, pu
22 ve-site sequence of At IMPDH conforms to the IMP dehydrogenase/guanosine monophosphate reductase moti
23 e conformation of IMP bound to human type II IMP dehydrogenase has been determined by two-dimensional
24 of ribavirin, suggesting that inhibition of IMP dehydrogenase (IMPDH) and reduction of intracellular
42 Mycophenolic acid (MPA), an inhibitor of IMP-dehydrogenase (IMPDH), is used worldwide in transpla
44 inhibits aldolase and inosine monophosphate (IMP) dehydrogenase in a concentration-dependent manner.
45 stemin protein degradation in tumor cells by IMP dehydrogenase inhibition or by other small molecules
46 ld temperature, nutrient limitation, and the IMP dehydrogenase inhibitor mycophenolic acid (MPA).
47 tive secretory vacuoles, we hypothesize that IMP dehydrogenase inhibitors induce androgen-independent
49 itor of the de novo purine synthetic enzyme, IMP dehydrogenase, leads to the rapid disappearance of n
51 ds with extensive sequence similarity to the IMP dehydrogenases of Saccharomyces cerevisiae and vario
53 phenolic acid (MPA), a specific inhibitor of IMP dehydrogenases, per ml, whereas transformants hostin
54 ar motor switch protein and the guaB-encoded IMP dehydrogenase) were noninfectious, whereas four clon