il[J]. Lancet 1996; 348: 1357-9. [5]Carr SF, Pappe E, Wu JC. Characterization of human type I and type II IMP dehydrogenase[J]. J Biol Chem 1993; 268: 27286-90.
[6]Langman LT, LeGatt DF, Yarscoff RW. Pharmacodynamic assessment of mycophenolic acid-induced immunosuppression by measuring IMP dehydrogenase activity[J]. Clin Chem 1995; 41: 295-9.
[7]Langman LJ, Shapiro AMJ, Lakey JRT. Pharmacodynamic assessment of MPA-induced immunosuppression by measurement of IMP dehydrogenase activity in a canine model[J]. transplantation 1996; 61: 87-92.
[8]Franklin TJ, Morris WP. Pharmacodynamics of the inhibition of GTP synthesis in vitro by mycophenolic acid[J]. Adv Enzyme Regul 1994; 34:107-17.
[9]Nage SE, Andersson JP, Andersson UG. Effect of mycophenolate mofetil on cytokine production inhibition of superantigen-induced cytokines[J]. immunopharmacology 1993; 26: 11-20.
[10]Bullingham R, Monroe S, Nicholls A. Pharmacokinetics and bioavailability of mycophenolate mofetil in healthy subjects after single-dose oral and intravenous administration[J]. J Clin Pharmacol 1996; 36: 315-24.
[11]Sugioka N, Chen SH, Hayashida K. Stability and pharmacokinetic studies of a new immunosuppressant mycophenolate mofetil (RS-61443) in rats[J]. biopharm Drug Dispos 1995; 16: 591-601.
[12]Sollinger HW, Deierhoi MH, Belzer FO. RS-61443-a phase I clinical trial and pilot rescue study[J]. Transplantation 1992; 53: 428-32.
[13]European Mycophenolate mofetil Cooperative Study Group. Placebo controlled study of mycophenolate mofetil combined with cyclosporin and corticosteroids for prevention of acute rejection[J]. Lancet 1
995; 345:1321-5. [14]Sollinger HW, US Renal Transplant Mycophenolate mofetil Study Group. mycophenolate mofetil for the prevention of acute rejection in primary cadaveric renal allograft recipients[J]. Transplantation 1995; 60: 225-32.
[15]The Tricontinental Mycophenolate mofetil Renal Tra
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