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M J Calverley

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Endocrinology|December 6, 1997
The vitamin D analog, KH1060, is rapidly degraded both in vivo and in vitro via several pathways: principal metabolites generated retain significant biological activityF J Dilworth, G R Williams, A M Kissmeyer, et al.
The Journal of Biological Chemistry|July 14, 1995
Different mechanisms of hydroxylation site selection by liver and kidney cytochrome P450 species (CYP27 and CYP24) involved in vitamin D metabolismF J Dilworth, I Scott, A Green, et al.
Biochemical Pharmacology|March 21, 1997
Metabolism of the vitamin D analog EB1089 by cultured human cells: redirection of hydroxylation site to distal carbons of the side-chainV N Shankar, F J Dilworth, H L Makin, et al.
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Showing results (21-30 of 23) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 23 results.
Endocrinology|December 6, 1997
The vitamin D analog, KH1060, is rapidly degraded both in vivo and in vitro via several pathways: principal metabolites generated retain significant biological activityF J Dilworth, G R Williams, A M Kissmeyer, et al.
The Journal of Biological Chemistry|July 14, 1995
Different mechanisms of hydroxylation site selection by liver and kidney cytochrome P450 species (CYP27 and CYP24) involved in vitamin D metabolismF J Dilworth, I Scott, A Green, et al.
Biochemical Pharmacology|March 21, 1997
Metabolism of the vitamin D analog EB1089 by cultured human cells: redirection of hydroxylation site to distal carbons of the side-chainV N Shankar, F J Dilworth, H L Makin, et al.
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