Zobrazeno 1 - 10
of 11
pro vyhledávání: '"L C, Quattrochi"'
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 29(8)
We examined the effects of several agents, including dietary flavonoids, on CYP1A1 expression utilizing a recently developed high-throughput screening system for assessing human cytochrome P450 (CYP) induction. HepG2 cells, stably integrated with reg
Autor:
L C, Quattrochi, P S, Guzelian
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 29(5)
Among the human liver cytochrome P450s (P450s), a family of microsomal hemoproteins responsible for catalyzing the oxidative metabolism of clinically used drugs and environmental chemicals, attention has been focused on CYP3A, a form that is the most
Publikováno v:
Molecular pharmacology. 50(1)
Interindividual variation in the spontaneous and in the glucocorticoid-or rifampicin-inducible expression of the CYP3A cytochromes P450, the dominant froms of this supergene family that catalyze the oxidation of numerous drugs and environmental chemi
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology. 73(6)
Although it has been known for more than three decades that administration of lipophilic chemicals, including phenobarbital, produces liver hypertrophy, proliferation of smooth endoplasmic reticulum, and induction of liver microsomal enzymes such as
Publikováno v:
The Journal of biological chemistry. 269(9)
The gene for cytochrome P4501A2 is constitutively expressed in the liver of vertebrates and shows induced expression when an organism is exposed to polycyclic aromatic hydrocarbons and halogenated hydrocarbons. To identify DNA elements regulating tra
Autor:
W, Tassaneeyakul, D J, Birkett, M E, Veronese, M E, McManus, R H, Tukey, L C, Quattrochi, H V, Gelboin, J O, Miners
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 265(1)
Kinetic and inhibitor studies using cDNA-expressed enzymes and human liver microsomes have characterized the specificity of a range of cytochrome P450 (CYP) 1A substrate and inhibitor probes towards the two isoforms comprising this subfamily. Express
Autor:
L C, Quattrochi, R H, Tukey
Publikováno v:
Molecular pharmacology. 43(4)
In the presence of halogenated and polycyclic aromatic hydrocarbons, the CYP1A1 gene is regulated through induction after ligand binding to the cytosolic Ah receptor (AhR). Ligand-dependent AhR activation leads to nuclear translocation and binding of
Publikováno v:
Cancer research. 50(11)
The human P-450 CYP1A1 gene and a P450IA2 complementary DNA have been expressed in Cos-1 cells and the expressed proteins were assayed for their capacity to metabolize the carcinogens 2-acetylaminofluorene (AAF), benzo(a)pyrene, 2-amino-3-methylimida
Autor:
M E, McManus, W M, Burgess, M E, Veronese, J S, Felton, M G, Knize, E G, Snyderwine, L C, Quattrochi, R H, Tukey
Publikováno v:
Progress in clinical and biological research.
Autor:
L C, Quattrochi, R H, Tukey
Publikováno v:
Molecular pharmacology. 36(1)
The regulation of the human cytochrome Cyp1A2 gene by 3-methylcholanthrene was studied through the transfection of 5'-flanking sequences into human cells. The Cyp1A2 promoter sequence and 3700 bases 5' to the cap site were linked to the procaryotic c