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CYP4F22 encodes a member of the cytochrome P450 superfamily of enzymes. Zusätzlich bieten wir Ihnen CYP4F22 Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 14 products:
Human Polyclonal CYP4F22 Primary Antibody für WB - ABIN949833
Sasaki, Akiyama, Yanagi, Sakai, Miyamura, Sato, Shimizu: CYP4F22 is highly expressed at the site and timing of onset of keratinization during skin development. in Journal of dermatological science 2012
patients carrying one or two truncating CYP4F22 mutations affecting the SBRs tend to develop collodion membrane at birth
We report two cases of Congenital Ichthyosiform Erythroderma showing homozygous mutations in the gene CYP4F22.
description of CYP4F22 mutations from a Japanese collodion baby with lamellar ichthyosis (zeige LBR Antikörper) [case report]
Letter: CYP4F22 is highly expressed at the site and timing of onset of keratinization during skin development.
REVIEW: genetic analyses have identified a wide spectrum of mutations in the CYP4V2gene from patients suffering from Bietti's crystalline corneoretinal dystrophy, and mutations in theCYP4F22 gene have been linked to lamellar ichthyosis (zeige LBR Antikörper)
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is part of a cluster of cytochrome P450 genes on chromosome 19 and encodes an enzyme thought to play a role in the 12(R)-lipoxygenase pathway. Mutations in this gene are the cause of ichthyosis lamellar type 3.
cytochrome P450 4F22
, cytochrome P450, family 2, subfamily E, polypeptide 2 homolog
, cytochrome P450, family 4, subfamily F, polypeptide 22