Search Results - "Stet, E H"
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6-Mercaptopurine: cytotoxicity and biochemical pharmacology in human malignant T-lymphoblasts
Published in Biochemical pharmacology (06-04-1993)“…The effects of prolonged exposure to 2 and 10 microM 6-mercaptopurine (6MP) in the human lymphoblastic T-cell line MOLT-4 were studied with respect to…”
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The importance of methylthio-IMP for methylmercaptopurine ribonucleoside (Me-MPR) cytotoxicity in Molt F4 human malignant T-lymphoblasts
Published in Biochimica et biophysica acta (30-04-1993)“…The importance of methyl-thioIMP (Me-tIMP) formation for methylmercaptopurine ribonucleoside (Me-MPR) cytotoxicity was studied in Molt F4 cells. Cytotoxicity…”
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Decrease in S-adenosylmethionine synthesis by 6-mercaptopurine and methylmercaptopurine ribonucleoside in Molt F4 human malignant lymphoblasts
Published in Biochemical journal (15-11-1994)“…6-Mercaptopurine (6-MP) and methylmercaptopurine ribonucleoside (Me-MPR) are purine anti-metabolites which are both metabolized to methylthio-IMP (Me-tIMP), a…”
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A biochemical basis for synergism of 6-mercaptopurine and mycophenolic acid in Molt F4, a human malignant T-lymphoblastic cell line
Published in Biochimica et biophysica acta (22-01-1993)“…6-Mercaptopurine (6MP) cytotoxicity was studied in Molt F4 cells, a T-cell acute lymphoblastic leukemia (ALL) cell line. The effects on cytotoxicity were…”
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Thiopurine treatment in childhood leukemia. Metabolic aspects and sensitivity
Published in Advances in experimental medicine and biology (1998)Get more information
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Reversal of methylmercaptopurine ribonucleoside cytotoxicity by purine ribonucleosides and adenine
Published in Biochemical pharmacology (06-01-1995)“…6-Methylmercaptopurine ribonucleoside-5′-phosphate (MeSPuRMP), the sole metabolite of 6-methylmercaptopurine ribonucleoside (MeSPuRib), is a strong inhibitor…”
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Reversal of 6-mercaptopurine and 6-methylmercaptopurine ribonucleoside cytotoxicity by amidoimidazole carboxamide ribonucleoside in Molt F4 human malignant T-lymphoblasts
Published in Biochemical pharmacology (03-08-1993)“…Cytotoxicity of 6-mercaptopurine (6MP) and 6-methylmercaptopurine ribonucleoside (Me-MPR) was studied in Molt F4 human malignant lymphoblasts. Both drugs are…”
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Cell-kinetics and biochemical pharmacology of methotrexate and 6-mercaptopurine in human malignant T-lymphoblasts
Published in Klinische Pädiatrie (01-07-1992)“…The cell-kinetics and biochemical pharmacology of simultaneous and sequential combination treatment with 0.02 microM methotrexate (MTX) and 2 microM…”
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Inhibition of IMP dehydrogenase by mycophenolic acid in Molt F4 human malignant lymphoblasts
Published in Annals of clinical biochemistry (01-03-1994)“…The effects of inhibition of inosine monophosphate dehydrogenase (IMPDH), the rate-limiting enzyme in guanine nucleotide de novo synthesis, on cell growth,…”
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The IMP dehydrogenase inhibitor mycophenolic acid antagonizes the CTP synthetase inhibitor 3-deazauridine in MOLT-3 human leukemia cells: A central role for phosphoribosyl pyrophosphate
Published in Biochemical pharmacology (28-09-1995)“…Mycophenolic acid, an inhibitor of the enzyme IMP dehydrogenase, antagonizes the CTP synthetase inhibitor 3-deazauridine in its anti-proliferative effects on…”
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6-Mercaptopurine metabolism in two leukemic cell lines
Published in Advances in experimental medicine and biology (1991)Get more information
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