Title : Multidrug resistance 1 genotype and disposition of budesonide in early primary biliary cirrhosis.

Pub. Date : 2006 Apr

PMID : 16584389






6 Functional Relationships(s)
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Protein Name
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1 Multidrug resistance 1 genotype and disposition of budesonide in early primary biliary cirrhosis. Budesonide ATP binding cassette subfamily B member 1 Homo sapiens
2 BACKGROUND: Budesonide, which is a dual substrate of P-glycoprotein, the product of the multidrug resistance 1 (MDR1) gene, and cytochrome P450 3A (CYP3A) has been proposed for treatment of early primary biliary cirrhosis (PBC). Budesonide ATP binding cassette subfamily B member 1 Homo sapiens
3 BACKGROUND: Budesonide, which is a dual substrate of P-glycoprotein, the product of the multidrug resistance 1 (MDR1) gene, and cytochrome P450 3A (CYP3A) has been proposed for treatment of early primary biliary cirrhosis (PBC). Budesonide ATP binding cassette subfamily B member 1 Homo sapiens
4 BACKGROUND: Budesonide, which is a dual substrate of P-glycoprotein, the product of the multidrug resistance 1 (MDR1) gene, and cytochrome P450 3A (CYP3A) has been proposed for treatment of early primary biliary cirrhosis (PBC). Budesonide ATP binding cassette subfamily B member 1 Homo sapiens
5 We tested the hypothesis that MDR1 gene polymorphisms affect absorption of oral budesonide. Budesonide ATP binding cassette subfamily B member 1 Homo sapiens
6 RESULTS: In MDR1 2,677 GG and 3,435 CC genotypes, absorption and elimination of budesonide were not significantly different from those in corresponding homozygous variants. Budesonide ATP binding cassette subfamily B member 1 Homo sapiens