Results 1 to 10 of about 320 (132)
Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey [PDF]
20(S)-Hydroxyvitamin D3 (20(OH)D3) is an endogenous metabolite produced by the action of CYP11A1 on the side chain of vitamin D3 (D3). 20(OH)D3 can be further hydroxylated by CYP11A1, CYP27A1, CYP24A1 and/or CYP27B1 to several hydroxyderivatives. CYP11A1
, Adrian Fabisiak, Robert Tuckey
exaly +6 more sources
Localization and biosynthesis of 7-dehydrocholesterol in rat skin
By differential assay, the concentration of 7-dehydrocholesterol in the dead keratin layer, the epidermal mucosa, the sebaceous glands and associated appendages of the epidermis, and the dermis of rat skin was determined; 85% of the 7-dehydrocholesterol ...
J.L. Gaylor, Frances M. Sault
doaj +3 more sources
Metabolic engineering of Saccharomyces cerevisiae for 7-dehydrocholesterol overproduction [PDF]
Background 7-Dehydrocholesterol (7-DHC) has attracted increasing attentions due to its great medical value and the enlarging market demand of its ultraviolet-catalyzed product vitamin D3.
Xiao-Jing Guo +7 more
doaj +3 more sources
Regulating blood cholesterol (Chol) levels by pharmacotherapy has successfully improved cardiovascular health. There is growing interest in the role of Chol precursors in the treatment of diseases.
Phillip Wages +2 more
exaly +3 more sources
Effects of Psychotropic Medication on Somatic Sterol Biosynthesis of Adult Mice
Polypharmacy is commonly used to treat psychiatric disorders. These combinations often include drugs with sterol biosynthesis inhibiting side effects, including the antipsychotic aripiprazole (ARI), and antidepressant trazodone (TRZ).
Marta Balog +4 more
doaj +1 more source
Cholesterol is essential to human health, and its levels are tightly regulated by a balance of synthesis, uptake, and efflux. Cholesterol synthesis requires the actions of more than twenty enzymes to reach the final product, through two alternate ...
Winnie Luu +3 more
doaj +1 more source
The Smith-Lemli-Opitz syndrome (SLOS) is a congenital birth defect syndrome caused by a deficiency of 3β-hydroxysterol Δ7-reductase, the final enzyme in the cholesterol biosynthetic pathway.
Akira Honda +9 more
doaj +1 more source
Vulnerability of DHCR7+/− mutation carriers to aripiprazole and trazodone exposure
Smith-Lemli-Opitz syndrome is a recessive disorder caused by mutations in 7-dehydrocholesterol reductase (DHCR)7 with a heterozygous (HET) carrier frequency of 1–3%.
Zeljka Korade +8 more
doaj +1 more source
Tunneling in tocopherol-mediated peroxidation of 7-dehydrocholesterol [PDF]
We report here that H-atom tunneling facilitates the propagation step in the tocopherol-mediated peroxidation (TMP) of 7-dehydrocholesterol. This process likely becomes a major propagation pathway when radical intermediates are isolated in cellular organelles or lipid particles such as low-density lipoproteins.
H, Muchalski, L, Xu, N A, Porter
openaire +2 more sources
The impaired conversion of 7-dehydrocholesterol to cholesterol, as a result of a permanent inhibition of the activity of 7-dehydrocholesterol-delta 7-reductase, has been reported in the Smith-Lemli-Opitz (SLO) syndrome (1, 2).
C Wolf +6 more
doaj +1 more source

