Author pages are created from data sourced from our academic publisher partnerships and public sources.
Share This Author
Enzymes of uracil catabolism in normal and neoplastic human tissues.
Dihydropyrimidinase, on the other hand, is highly active in all solid tumors studied but not in their normal counterparts; therefore, it is suggested that dihydropyrimide can serve as a good marker of tumorigenicity as well as a target for cancer chemotherapy of human solid tumors.
5-benzylacyclouridine and 5-benzyloxybenzylacyclouridine, potent inhibitors of uridine phosphorylase.
Structure-activity relationship of ligands of the pyrimidine nucleoside phosphorylases.
Pyrimidine acyclonucleosides, inhibitors of uridine phosphorylase.
Metabolism of adenosine analogues by Schistosoma mansoni and the effect of nucleoside transport inhibitors.
Combination therapy of schistosomiasis by tubercidin and nitrobenzylthioinosine 5'-monophosphate.
- M. H. el Kouni, D. Diop, S. Cha
- Biology, MedicineProceedings of the National Academy of Sciences…
- 1 November 1983
It is demonstrated that through combination therapy, highly selective toxicity against a parasite can be achieved and the effectiveness, simplicity, and practicality of host protection afforded by this method may yield a promising chemotherapeutic approach for the treatment of schistosomiasis and other parasitic diseases.
Combination effects of baicalein with antibiotics against oral pathogens.
Treatment of schistosomiasis by purine nucleoside analogues in combination with nucleoside transport inhibitors.
Enzymes of uridine 5'-monophosphate biosynthesis in Schistosoma mansoni.