Epidermolysis bullosa - a group of skin diseases with different causes but commonalities in gene expression

Experimental Dermatology

Volumn 21, Issue 7, 2012, Pages 526-530

  Knaup, Julia ^a   Verwanger, Thomas ^a   Gruber, Christina ^b   Ziegler, Verena ^a   Bauer, Johann W ^b   Krammer, Barbara ^a  

^a UNIVERSITY OF SALZBURG   (Austria)

^b PARACELSUS MEDICAL UNIVERSITY   (Austria)

Author keywords

Comparative gene expression; Epidermolysis bullosa; Epidermolysis bullosa simplex; Generalized benign epidermolysis bullosa; Recessive dystrophic epidermolysis bullosa; Type XVI collagen

Indexed keywords

COLLAGEN TYPE 16; FATTY ACID; FIBRONECTIN; GLYCEROL; LOW DENSITY LIPOPROTEIN RECEPTOR; MESSENGER RNA; RIBOSOME PROTEIN;

APOPTOSIS; ARTICLE; CELL MIGRATION; CONTROLLED STUDY; ENERGY CONSERVATION; EPIDERMOLYSIS BULLOSA; GENE EXPRESSION; GENE EXPRESSION PROFILING; PROTEIN DEGRADATION; RECEPTOR UPREGULATION;

CELL CYCLE PROTEINS; CELLS, CULTURED; COLLAGEN; DOWN-REGULATION; EPIDERMOLYSIS BULLOSA DYSTROPHICA; EPIDERMOLYSIS BULLOSA SIMPLEX; EPIDERMOLYSIS BULLOSA, JUNCTIONAL; FIBRONECTINS; GENE EXPRESSION; HUMANS; KERATINOCYTES; MUSCULAR DYSTROPHIES; MUTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; REAL-TIME POLYMERASE CHAIN REACTION; RECEPTORS, LDL; RIBOSOMAL PROTEINS; RNA, MESSENGER; UP-REGULATION;

EID: 84863100208     PISSN: 09066705     EISSN: 16000625     Source Type: Journal    
DOI: 10.1111/j.1600-0625.2012.01519.x     Document Type: Article

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