Zobrazeno 1 - 10
of 40
pro vyhledávání: '"J L, Falk"'
Autor:
M. S. Lee, Sue Atherton-Fessler, Laura L. Parker, K. I. Swenson, Helen Piwnica-Worms, S. Ogg, J. L. Falk
Publikováno v:
The EMBO Journal. 10:1255-1263
The regulation of p34cdc2 was investigated by overproducing p34cdc2, cyclin (A and B) and the wee1+ gene product (p107wee1) using a baculoviral expression system. p34cdc2 formed a functional complex with both cyclins as judged by co-precipitation, ph
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 295(2)
Despite wide use of cumulative-dosing procedures to evaluate dose-response relations, limited attention has been paid to investigating drug concentration-effect relations. We first characterized the pharmacokinetic (PK) parameters for i.v. (2 mg/kg)
Publikováno v:
Experimental and clinical psychopharmacology. 7(1)
Performance in rats (Rattus norvegicus) was measured on a differential reinforcement of low-rate schedule (DRL 45-s) in 1.5-hr sessions after 2 mg/kg intravenous (i.v.) or 10-20 mg/kg intraperitoneal (i.p.) cocaine administration, with each dose give
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 288(2)
We investigated dose-response cocaine pharmacokinetic and metabolite profiles in a within-subject design after intravenous bolus cocaine administration (1-4 mg/kg) in rats under a food-limited regimen. Cocaine was rapidly distributed (T1/2beta = 1.09
Autor:
J L, Falk
Publikováno v:
NIDA research monograph. 169
Autor:
J L, Falk
Publikováno v:
The Journal of the Florida Medical Association. 84(9)
Publikováno v:
The Journal of the Florida Medical Association. 84(9)
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 281(3)
To investigate the interaction between alprazolam and caffeine, performance on a differential reinforcement of low-rate behavior schedule and the respective pharmacokinetics (PK) were explored in concurrent studies. Alprazolam PK was not altered by c
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 278(3)
Rats were adapted to a water-deprivation regimen that allowed daily 1-hr drinking sessions of a single fluid, either 1.5% NaCl solution or water. Oral, presession, acute doses of triazolam (0.05-1.6 mg/kg) or alprazolam (0.4-6.4 mg/kg) produced dose-