Full-thickness human skin models for congenital ichthyosis and related keratinization disorders

Journal of Investigative Dermatology

Volumn 131, Issue 9, 2011, Pages 1938-1942

  Eckl, Katja Martina ^a   Alef, Thomas ^a,b   Torres, Serena ^a   Hennies, Hans Christian ^a,b  

^a UNIVERSITY OF COLOGNE   (Germany)

^b UNIVERSITY OF COLOGNE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BETA1 INTEGRIN; COLLAGEN TYPE 4; SMALL INTERFERING RNA; TRANSFORMING GROWTH FACTOR BETA1;

AUTOSOMAL RECESSIVE CONGENITAL ICHTHYOSIS; AUTOSOMAL RECESSIVE DISORDER; BASEMENT MEMBRANE; CELL DIFFERENTIATION; CELL ISOLATION; CELL PROLIFERATION; FIBROBLAST CULTURE; FULL THICKNESS HUMAN SKIN; GENE EXPRESSION; GENE MUTATION; HISTOPATHOLOGY; HOUSEKEEPING GENE; HUMAN; ICHTHYOSIS; INFORMED CONSENT; KERATINIZATION; KERATINIZATION DISORDER; KERATINOCYTE; LETTER; MODEL; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEFICIENCY; RNA ISOLATION; SKIN; SKIN BIOPSY; SKIN DISEASE; SKIN FIBROBLAST; STRATUM CORNEUM; TISSUE CULTURE;

EID: 80051785898     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2011.126     Document Type: Letter

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