Pages that link to "Q42016265"

The following pages link to The formation and reduction of the 14,15-double bond in cholesterol biosynthesis (Q42016265):

Displaying 13 items.

• Chemical and enzymic studies on the characterization of intermediates during the removal of the 14α-methyl group in cholesterol biosynthesis. The use of 32-functionalized lanostane derivatives (Q28316968) (← links)
• The mechanism of C-4 demethylation during cholesterol biosynthesis (Q28323548) (← links)
• Physiological Effects of an Antimycotic Azasterol on Cultures of Saccharomyces cerevisiae (Q34984111) (← links)
• The 14α—demethylation of lanosterol by a reconstituted cytochrome P-450 system from yeast microsomes (Q39648480) (← links)
• A novel olefinic rearrangement. The enzymic conversion of cholesta-7,9-dien-3 -ol into cholesta-8,14-dien-3 -ol. (Q41819474) (← links)
• Is a Schiff base involved in the mechanism of the delta4-3-oxo steroid 5alpha- or 5beta-reductases from mammalian liver? (Q42176255) (← links)
• The pathway for the conversion of dihydroagnosterol into cholesterol in rat liver (Q42548181) (← links)
• The metabolic sequence by which some 4,4-dimethyl sterols are converted into cholesterol (Q42585874) (← links)
• The effect of carbon monoxide on the nature of the accumulated 4,4-dimethyl sterol precursors of cholesterol during its biosynthesis from (2-14C)mevalonic acid in vitro (Q42923498) (← links)
• Studies on the mechanism and regulation of C-4 demethylation in cholesterol biosynthesis. The role of adenosine 3':5'-cyclic monophosphate (Q42924230) (← links)
• The biosynthesis of cholesta-8,14-dien-3β-ol by Chang human liver cells (Q42924452) (← links)
• The substrate activation in some pyridine nucleotide linked enzymic reactions. The conversion of desmosterol into cholesterol. (Q53920657) (← links)
• The Biosynthesis of Ergosterol (Q104838366) (← links)