OtherArticle
The glucuronidation of δ4-3-keto C19- and C21- hydroxy-steroids by human liver microsomal and recombinant UDP-glucuronosyltransferases (UGT): 6α- and 21- hydroxyprogesterone are selective substrates for UGT2B7
Kushari Bowalgaha, D Elliot, Peter MacKenzie, Kathleen Knights and John Miners
Drug Metabolism and Disposition December 6, 2006, DOI: https://doi.org/10.1124/dmd.106.013052
Kushari Bowalgaha
D Elliot
Peter MacKenzie
Kathleen Knights
Jump to comment:
No eLetters have been published for this article.
In this issue
OtherArticle
The glucuronidation of δ4-3-keto C19- and C21- hydroxy-steroids by human liver microsomal and recombinant UDP-glucuronosyltransferases (UGT): 6α- and 21- hydroxyprogesterone are selective substrates for UGT2B7
Kushari Bowalgaha, D Elliot, Peter MacKenzie, Kathleen Knights and John Miners
Drug Metabolism and Disposition December 6, 2006, DOI: https://doi.org/10.1124/dmd.106.013052
OtherArticle
The glucuronidation of δ4-3-keto C19- and C21- hydroxy-steroids by human liver microsomal and recombinant UDP-glucuronosyltransferases (UGT): 6α- and 21- hydroxyprogesterone are selective substrates for UGT2B7
Kushari Bowalgaha, D Elliot, Peter MacKenzie, Kathleen Knights and John Miners
Drug Metabolism and Disposition December 6, 2006, DOI: https://doi.org/10.1124/dmd.106.013052
Jump to section
Related Articles
Cited By...
More in this TOC Section
Similar Articles
Advertisement