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Results:
1-12
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Results: 12
Authors:
Al Safarjalani, ON
Zhou, XJ
Naguib, FNM
Shi, JX
Schinazi, RF
el Kouni, MH
Citation: On. Al Safarjalani et al., Enhancement of the bioavailability of oral uridine by coadministration of 5-(phenylthio) acyclouridine, a uridine phosphorylase inhibitor: implications for uridine rescue regimens in chemotherapy, CANC CHEMOT, 48(5), 2001, pp. 389-397
Authors:
Al Safarjalani, ON
Zhou, XJ
Naguib, FNM
Goudgaon, NM
Schinazi, RF
el Kouni, MH
Citation: On. Al Safarjalani et al., Modulation of the pharmacokinetics of endogenous plasma uridine by 5-(phenylthio) acyclouridine, a uridine phosphorylase inhibitor: implications for chemotherapy, CANC CHEMOT, 48(2), 2001, pp. 145-150
Authors:
Ashour, OM
Naguib, FNM
Goudgaon, NM
Schinazi, RF
el Kouni, MH
Citation: Om. Ashour et al., Effect of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on plasma concentration of uridine released from 2 ',3 ',5 '-tri-O-acetyluridine, a prodrug of uridine: relevance to uridine rescue in chemotherapy, CANC CHEMOT, 46(3), 2000, pp. 235-240
Authors:
Ashour, OM
Al Safarjalani, ON
Naguib, FNM
Goudgaon, NM
Schinazi, RF
el Kouni, MH
Citation: Om. Ashour et al., Modulation of plasma uridine concentration by 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase: relevance to chemotherapy, CANC CHEMOT, 45(5), 2000, pp. 351-361
Authors:
el Kouni, MH
Goudgaon, NM
Rafeeq, M
Al Safarjalani, ON
Schinazi, RF
Naguib, FNM
Citation: Mh. El Kouni et al., 5-phenylthioacyclouridine: A potent and specific inhibitor of uridine phosphorylase, BIOCH PHARM, 60(6), 2000, pp. 851-856
Authors:
Ashour, OM
Naguib, FNM
Goudgaon, NM
Schinazi, RF
el Kouni, MH
Citation: Om. Ashour et al., Effect of administration of 5-(phenylselenenyl)acyclouridine, an inhibitorof uridine phosphorylase, on the anti-tumor efficacy of 5-fluoro-2 '-deoxyuridine against murine colon tumor C26-10, BIOCH PHARM, 60(5), 2000, pp. 687-692
Authors:
Ashour, OM
Naguib, FNM
Panzica, RP
Al Safarjalani, ON
el Kouni, MH
Citation: Om. Ashour et al., Modulation of 5-fluorouracil host toxicity by 5-(benzyloxybenzyl)barbituric acid acyclonucleoside, a uridine phosphorylase inhibitor, and 2 ',3 ',5 '-tri-O-acetyluridine, a prodrug of uridine, BIOCH PHARM, 60(3), 2000, pp. 427-431
Authors:
Guerin, DJ
Mazeas, D
Musale, MS
Naguib, FNM
Al Safarjalani, ON
el Kouni, MH
Panzica, RP
Citation: Dj. Guerin et al., Uridine phosphorylase inhibitors: Chemical modification of benzyloxybenzyl-barbituric acid and its effects on UrdPase inhibition, BIOORG MED, 9(11), 1999, pp. 1477-1480
Authors:
Sullivan, WJ
Chiang, CW
Wilson, CM
Naguib, FNM
el Kouni, MH
Donald, RGK
Roos, DS
Citation: Wj. Sullivan et al., Insertional tagging of at least two loci associated with resistance to adenine arabinoside in Toxoplasma gondii, and cloning of the adenosine kinase locus, MOL BIOCH P, 103(1), 1999, pp. 1-14
Authors:
el Kouni, MH
Guarcello, V
al Safarjalani, ON
Naguib, FNM
Citation: Mh. El Kouni et al., Metabolism and selective toxicity of 6-nitrobenzylthioinosine in Toxoplasma gondii, ANTIM AG CH, 43(10), 1999, pp. 2437-2443
Authors:
Chiang, CW
Carter, N
Sullivan, WJ
Donald, RGK
Roos, DS
Naguib, FNM
el Kouni, MH
Ullman, B
Wilson, CM
Citation: Cw. Chiang et al., The adenosine transporter of Toxoplasma gondii - Identification by insertional mutagenesis, cloning, and recombinant expression, J BIOL CHEM, 274(49), 1999, pp. 35255-35261
Authors:
Javaid, ZZ
el Kouni, MH
Iltzsch, MH
Citation: Zz. Javaid et al., Pyrimidine nucleobase ligands of orotate phosphoribosyltransferase from Toxoplasma gondii, BIOCH PHARM, 58(9), 1999, pp. 1457-1466
Risultati:
1-12
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