| 1 | CYP26C1, FFDD4
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| Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1.
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| Slavotinek AM, Mehrotra P, Nazarenko I, Tang PL, Lao R, Cameron D, Li B, Chu C, Chou C, Marqueling AL, Yahyavi M, Cordoro K, Frieden I, Glaser T, Prescott T, Morren MA, Devriendt K, Kwok PY, Petkovich M, Desnick RJ.
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| Hum Mol Genet um Mol Genet. 2012 Nov 21. [Epub ahead of print]
2012
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| 2 | CYP26A1, CYP26C1
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| Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes.
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| Meire F, Delpierre I, Brachet C, Roulez F, Van Nechel C, Depasse F, Christophe C, Menten B, De Baere E.
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| Mol Vis. 17:2072- 2011
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| 3 | CYP26A1,CYP26C1
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| CYP26A1 and CYP26C1 cooperatively regulate anterior-posterior patterning of the developing brain and the production of migratory cranial neural crest cells in the mouse.
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| Uehara M, Yashiro K, Mamiya S, Nishino J, Chambon P, Dolle P, Sakai Y.
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| Dev Biol 302(2):399-411. Epub 2006 Sep 30. 2007
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| 4 | CYP26A1, CYP26B1, CYP26C1
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| Evidence for a functional genetic polymorphism of the human retinoic acid-metabolizing enzyme CYP26A1, an enzyme that may be involved in spina bifida.
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| Rat E, Billaut-Laden I, Allorge D, Lo-Guidice JM, Tellier M, Cauffiez C, Jonckheere N, van Seuningen I, Lhermitte M, Romano A, Guéant JL, Broly F.
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| Birth Defects Res A Clin Mol Teratol 76(6):491-8.
2006
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| 5 | CYP26A1, CYP26C1
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| A novel human cytochrome P450, CYP26C1, involved in metabolism of 9-cis and all-trans isomers of retinoic acid.
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| Taimi M, Helvig C, Wisniewski J, Ramshaw H, White J, Amad M, Korczak B, Petkovich M.
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| J Biol Chem 279(1):77-85. Epub 2003 Oct 07. 2004
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| 6 | CYP26A1,CYP26C1
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| CYP26A1 and CYP26C1 cooperate in degrading retinoic acid within the equatorial retina during later eye development.
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| Sakai Y, Luo T, McCaffery P, Hamada H, Drager UC.
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| Dev Biol 276(1):143-57. 2004
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