Zobrazeno 1 - 10
of 15
pro vyhledávání: '"W. J. O'reilly"'
Autor:
S. W. Homans, W. J. O'reilly, Peter J. F. Henderson, Paul J. R. Spooner, Anthony Watts, Nicholas G. Rutherford
The weak binding of sugar substrates fails to induce any quantifiable physical changes in the L-fucose-H+ symport protein, FucP, from Escherichia coli, and this protein lacks any strongly binding ligands for competitive binding assays. Access to subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be5fd14b9c5eef31635b041eae62d657
https://ora.ox.ac.uk/objects/uuid:172676df-e815-473e-acc9-2ba1415bd02f
https://ora.ox.ac.uk/objects/uuid:172676df-e815-473e-acc9-2ba1415bd02f
Publikováno v:
Clinical Pharmacokinetics. 4:310-319
The pharmacokinetics of N1-acetylsulphamethoxazole and N4-acetylsulphamethoxazole in man are described. N1-Acetylsulphamethoxazole is deacetylated to sulphamethoxazole and acetylated to N4-acetylsulphamethoxazole. N4-Acetylsulphamethoxazole is excret
Publikováno v:
Clinical Pharmacokinetics. 5:274-294
The pharmacokinetics of sulphamethizole, sulphamethoxazole, sulphadiazine, sulphapyridine and sulphadimidine have been studied in man. Renal clearance values of the metabolite N4-acetylsulphonamide are 6 to 20 times higher than those of the correspon
Autor:
B. G. Priestly, W. J. O'reilly
Publikováno v:
Journal of Pharmacy and Pharmacology. 18:41-45
The kinetics of biliary excretion of four dyes, amaranth, geranine, lissamine and dechlorolissamine have been examined in the rat. The protein binding of each dye to blood and liver in vitro was examined, and a correlation found between excretion rat
Publikováno v:
British Journal of Pharmacology. 43:167-179
Summary 1 A one-compartment pharmacokinetic model was developed in which a drug underwent two successive metabolical reactions (for example, metabolism followed by conjugation) and free drug and both metabolites were excreted. 2 Techniques were descr
Publikováno v:
Medical Journal of Australia. 2:590-592
In children, the blood level of phenytoin was found to be significantly higher when 100 mg capsules rather than 100 mg tablets were administered. When, on the other hand, 30 mg capsules and tablets were compared; the situation was reversed; tablets p
Autor:
Lloyd Sansom, Roy G. Beran, Philip E. Stanley, C. J. Doecke, W. J. O'Reilly, Graham J. Schapel, Phillip A. Reece, R. H. C. Rischbieth
Publikováno v:
European journal of clinical pharmacology. 17(1)
Pharmacokinetic analysis of the plasma valproic acid concentration-time course, following a single oral dose (600 mg) of sodium valproate, was performed in 20 epileptic patients as an aid to the prediction of a proper chronic dosage regimen. A simple
Autor:
W. J. O’Reilly
Publikováno v:
Volume 1A: General.
Continuing worldwide escalation of fuel prices has provided the impetus for the design and manufacture of power conversion equipment of higher efficiency. A high-effectiveness regenerator design, based on adaptions of the criteria used in the aerospa
Publikováno v:
The Medical journal of Australia. 2(15)
A cross-over study was conducted to compare the plasma phenytoin levels produced by different phenytoin preparations available in Australia. The preparations were found not to be equivalent, a liquid suspension product producing higher levels compare
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 201(3)
Rats, with and without bile duct ligation (BDL), were injected with hexobarbital (i.p. and i.v.) and blood concentrations measured as a function of time. Analysis of these curves using a single-compartment model showed that BDL altered hexobarbital p