Heterologous expression of human cDNAs in the yeast Saccharomyces cerevisiae represents an attractive alternative source of human enzymes and allows metabolic studies to be performed without the need of human tissue. Here we report on the functional expression of human microsomal epoxide hydrolase (hmEH) and cytochrome P450 1A1 and 1A2 in yeast. Microsomal fractions of corresponding yeast strains exhibited enzyme specific activities which allowed the characterization of the heterologous enzymes. The use of these microsomes enabled us to study drug interactions on the respective enzymes with pharmacologically relevant drugs such as carbamazepine epoxide, valpromide and ketoconazole
AbstractRat liver microsomal cytochrome P-450d was abundantly expressed in the yeast Saccharomyces c...
The metabolism and genotoxicity of the carcinogenic mycotoxin, aflatoxin B1 (AFB), was studied in th...
Heterologous expression systems can be utilized to great advantage in the study of cytochrome P450 e...
A cDNA of human microsomal epoxide hydrolase (hmEH) was constitutively and inducibly expressed in Sa...
A cDNA of human cytochrome P450IA1 was expressed in yeast Saccharomyces cerevisiae on a multicopy pl...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
Cytochrome P450s (CYPs) hold a balance in studying pharmacokinetics, toxico-kinetics, drug metabolis...
Heterologous expression systems can be utilized to great advantage in the study of cytochrome P450 (...
A 1.57kb BamH1 fragment containing a full-length human debrisoquine 4-hydroxylase cytochrome P450 (C...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
High drug attrition rates due to toxicity, the controversy of experimental animal usage, and the EU ...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
AbstractRat liver microsomal cytochrome P-450d was abundantly expressed in the yeast Saccharomyces c...
AbstractRat liver microsomal cytochrome P-450d was abundantly expressed in the yeast Saccharomyces c...
The metabolism and genotoxicity of the carcinogenic mycotoxin, aflatoxin B1 (AFB), was studied in th...
Heterologous expression systems can be utilized to great advantage in the study of cytochrome P450 e...
A cDNA of human microsomal epoxide hydrolase (hmEH) was constitutively and inducibly expressed in Sa...
A cDNA of human cytochrome P450IA1 was expressed in yeast Saccharomyces cerevisiae on a multicopy pl...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
Cytochrome P450s (CYPs) hold a balance in studying pharmacokinetics, toxico-kinetics, drug metabolis...
Heterologous expression systems can be utilized to great advantage in the study of cytochrome P450 (...
A 1.57kb BamH1 fragment containing a full-length human debrisoquine 4-hydroxylase cytochrome P450 (C...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
High drug attrition rates due to toxicity, the controversy of experimental animal usage, and the EU ...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
Yeast Saccharomyces cerevisiae strains have been constructed that co-express cDNAs coding for the hu...
AbstractRat liver microsomal cytochrome P-450d was abundantly expressed in the yeast Saccharomyces c...
AbstractRat liver microsomal cytochrome P-450d was abundantly expressed in the yeast Saccharomyces c...
The metabolism and genotoxicity of the carcinogenic mycotoxin, aflatoxin B1 (AFB), was studied in th...
Heterologous expression systems can be utilized to great advantage in the study of cytochrome P450 e...