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CYP4F22 gene

Known as: CYTOCHROME P450, FAMILY 4, SUBFAMILY F, POLYPEPTIDE 22, FLJ39501, cytochrome P450 family 4 subfamily F member 22 
 
National Institutes of Health

Papers overview

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2020
2020
Mutations in CYP4F22 cause autosomal recessive congenital ichthyosis (ARCI). However, less than 10% of all ARCI patients carry a… Expand
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Review
2018
Review
2018
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of rare disorders of keratinization characterized by… Expand
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2017
2017
Autosomal recessive congenital ichthyosis (ARCI) caused by mutations in CYP4F22 is very rare. CyP4F22, a protein of the… Expand
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2017
2017
 
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2015
2015
A skin permeability barrier is essential for terrestrial animals, and its impairment causes several cutaneous disorders such as… Expand
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2013
2013
[3] Negi M, Tsuboi R, Matsui T, Ogawa H. Isolation and characterization from Candida albicans: substrate specificity. J Invest… Expand
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2011
2011
BACKGROUND   Mutations in six genes have been identified in autosomal recessive congenital ichthyosis (ARCI). To date, few… Expand
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2011
2011
Cytochrome P450s are superfamily of heme proteins which generally monooxygenate hydrophobic compounds. The human cytochrome P450… Expand
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2010
2010
CYP4F22 and CYP4F8 are expressed in epidermis, and mutations of CYP4F22 are associated with lamellar ichthyosis. Epoxyalcohols… Expand
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2007
2007
Congenital recessive ichthyoses (CRI) form a remarkably heterogeneous group of diseases, resulting from mutations in at least… Expand
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