Literature DB >> 1705413

Epidermolysis bullosa simplex (Koebner) is a keratin disorder. Ultrastructural and immunohistochemical study.

M Ito1, C Okuda, N Shimizu, T Tazawa, Y Sato.   

Abstract

A skin biopsy specimen was obtained from a 1-month-old female with epidermolysis bullosa simplex (Koebner). Histologically, an intraepidermal separation was seen and considered to be formed by cytolysis of the epidermal basal cells. Ultrastructurally, the basal cells were lacking in cytoplasmic tonofilaments, and the initial change of the cytolysis seemed to be cleavages of the cytoplasm. Immunohistochemically, a basal cell keratin was expressed in a suprabasal cell layer but not in the basal cell layer, and a panepithelial keratin was not detected in the basal cell layer. These findings suggest that keratin production of the epidermal cells may be delayed, resulting in a weakness of the basal cells against minor trauma to the skin.

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Year:  1991        PMID: 1705413

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  10 in total

1.  Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.

Authors:  M Ryynänen; J Ryynänen; S Sollberg; R V Iozzo; R G Knowlton; J Uitto
Journal:  J Clin Invest       Date:  1992-03       Impact factor: 14.808

2.  Mapping of epidermolysis bullosa simplex mutation to chromosome 12.

Authors:  M Ryynänen; R G Knowlton; J Uitto
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

Review 3.  Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology.

Authors:  R A Eady; M G Dunnill
Journal:  Arch Dermatol Res       Date:  1994       Impact factor: 3.017

4.  Linkage of epidermolysis bullosa simplex to keratin gene loci.

Authors:  K E McKenna; A E Hughes; E A Bingham; N C Nevin
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

Review 5.  Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility.

Authors:  Pierre A Coulombe; Michelle L Kerns; Elaine Fuchs
Journal:  J Clin Invest       Date:  2009-07-01       Impact factor: 14.808

6.  Epidermolysis bullosa simplex: expression of gelatinase activity in cultured human skin fibroblasts.

Authors:  J O Winberg; T Gedde-Dahl
Journal:  Biochem Genet       Date:  1992-08       Impact factor: 1.890

Review 7.  Defining keratin protein function in skin epithelia: epidermolysis bullosa simplex and its aftermath.

Authors:  Pierre A Coulombe; Chang-Hun Lee
Journal:  J Invest Dermatol       Date:  2012-01-26       Impact factor: 8.551

8.  A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseases.

Authors:  P A Coulombe; M E Hutton; R Vassar; E Fuchs
Journal:  J Cell Biol       Date:  1991-12       Impact factor: 10.539

Review 9.  Discovery of keratin function and role in genetic diseases: the year that 1991 was.

Authors:  Pierre A Coulombe
Journal:  Mol Biol Cell       Date:  2016-09-15       Impact factor: 4.138

10.  Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.

Authors:  K Takahashi; J Folmer; P A Coulombe
Journal:  J Cell Biol       Date:  1994-10       Impact factor: 10.539

  10 in total

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