Loricrin and human skin diseases: Molecular basis of ioricrin keratodermas

Histology and Histopathology

Volumn 13, Issue 3, 1998, Pages 819-826

  Ishida Yamamoto, A ^a  

^a ASAHIKAWA MEDICAL COLLEGE   (Japan)

Author keywords

Cornified cell envelope; Inherited skin diseases; Keratinocytes; Progressive symmetric erythrokeratoderma; Vohwinkel's syndrome

Indexed keywords

LORICRIN;

AMINO TERMINAL SEQUENCE; CARBOXY TERMINAL SEQUENCE; CROSS LINKING; ELECTRON MICROSCOPY; EPIDERMIS; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GRANULAR CELL; HUMAN; HUMAN CELL; HUMAN TISSUE; KERATINOCYTE; KERATODERMA; REVIEW; SKIN DISEASE; TISSUE DISTRIBUTION;

ANIMALS; DISEASE PROGRESSION; GENE EXPRESSION REGULATION; HUMANS; KERATOSIS; MEMBRANE PROTEINS; MUTATION;

EID: 0031850973     PISSN: 02133911     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (1)

1. Akiyama M., Smith L.T., Yoneda K., Kim S.-Y., Holbrook K.A. and Shimizu H. (1997). Expression of transglutaminase 1 (TG1) and cornified cell envelope (CCE) proteins during human epidermal development. J. Invest. Dermatol. 108, 598.