Title : Evidence for a functional genetic polymorphism of the human retinoic acid-metabolizing enzyme CYP26A1, an enzyme that may be involved in spina bifida.

Pub. Date : 2006 Jun

PMID : 16933217






3 Functional Relationships(s)
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1 BACKGROUND: CYP26A1, together with CYP26B1 and CYP26C1, are key enzymes of all-trans retinoic acid (RA) inactivation and their specific and restricted expression in developing embryos participate in the fine tuning RA levels. Tretinoin cytochrome P450 family 26 subfamily A member 1 Homo sapiens
2 BACKGROUND: CYP26A1, together with CYP26B1 and CYP26C1, are key enzymes of all-trans retinoic acid (RA) inactivation and their specific and restricted expression in developing embryos participate in the fine tuning RA levels. Tretinoin cytochrome P450 family 26 subfamily A member 1 Homo sapiens
3 BACKGROUND: CYP26A1, together with CYP26B1 and CYP26C1, are key enzymes of all-trans retinoic acid (RA) inactivation and their specific and restricted expression in developing embryos participate in the fine tuning RA levels. Tretinoin cytochrome P450 family 26 subfamily A member 1 Homo sapiens