Partially disturbed lamellar granule secretion in mild congenital ichthyosiform erythroderma with ALOX12B mutations

British Journal of Dermatology

Volumn 163, Issue 1, 2010, Pages 201-204

  Akiyama, M ^a   Sakai, K ^a   Yanagi, T ^a   Tabata, N ^b   Yamada, M ^b   Shimizu, H ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b Sendai Red Cross Hospital   (Japan)

Author keywords

ichthyosis; keratinization; lipid; lipoxygenase; LOX

Indexed keywords

ARACHIDONATE 12 LIPOXYGENASE; ARGININE; PYROXYLIN; WHITE PETROLATUM;

ALLELE; ALOX12B GENE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CELL DIFFERENTIATION; CELLULAR DISTRIBUTION; CLINICAL FEATURE; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; CONTROLLED STUDY; DNA ISOLATION; ECTROPION; EDEMA; ELECTRON MICROSCOPY; ENZYME ACTIVITY; EPIDERMIS; ERYTHRODERMA; EXON; FOOT; FOOT SOLE; GENE; GENE AMPLIFICATION; HAND; HAND PALM; HETEROZYGOTE; HUMAN; HYPERKERATOSIS; IMMUNOFLUORESCENCE; IMMUNOREACTIVITY; JAPANESE; KERATINOCYTE; LAMELLAR BODY; MALE; MISSENSE MUTATION; NEWBORN; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; OCCLUSIVE DRESSING; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SKIN BIOPSY; SKIN FISSURE; STRATUM CORNEUM;

ARACHIDONATE 12-LIPOXYGENASE; CYTOPLASMIC GRANULES; HUMANS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; INFANT, NEWBORN; LIPOXYGENASE; MALE; MUTATION;

EID: 77953965844     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2010.09745.x     Document Type: Article

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