7-Dehydrocholesterol: Difference between revisions
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<noinclude> | <noinclude>Cholecalciferol is formed in the skin from 7-dehydrocholesterol with the help of UV radiation . Cholecalciferol is gradually hydroxylated in the liver and kidneys to 1,25-dihydrocholecalciferol − calcitriol (the most effective form of vitamin D ). | ||
== Links == | |||
== | === related articles === | ||
=== | * [[Ultrafialové záření (biofyzika)|Ultraviolet radiation (biophysics)]] | ||
* [[Ultrafialové záření (biofyzika)]] | * [[1,25-dihydrocholekalciferol|1,25-dihydrocholecalciferol]] | ||
* [[1,25-dihydrocholekalciferol]] | * [[25-hydroxycholekalciferol|25-Hydroxycholecalciferol]] | ||
* [[25-hydroxycholekalciferol]] | |||
=== | === References === | ||
* {{Citace | * {{Citace | ||
|typ = kniha | |typ = kniha | ||
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|isbn = 80-7319-013-3 | |isbn = 80-7319-013-3 | ||
}} | }} | ||
** MURRAY, Robert K.. ''Harper's Biochemistry. ''2nd edition. Jinočany: H&H, 1998. <nowiki>ISBN 80-7319-013-3</nowiki> . | |||
</noinclude> | </noinclude> | ||
[[Kategorie:Biochemie]] | [[Kategorie:Biochemie]] | ||
Revision as of 13:57, 21 December 2022
Cholecalciferol is formed in the skin from 7-dehydrocholesterol with the help of UV radiation . Cholecalciferol is gradually hydroxylated in the liver and kidneys to 1,25-dihydrocholecalciferol − calcitriol (the most effective form of vitamin D ).
Links
References
-
- MURRAY, Robert K.. Harper's Biochemistry. 2nd edition. Jinočany: H&H, 1998. ISBN 80-7319-013-3 .
