Literature DB >> 7963675

Ultrastructural clues to genetic disorders of skin: the dermal-epidermal junction.

R A Eady1, J A McGrath, J R McMillan.   

Abstract

The candidate gene approach in tracking the underlying cause of a number of genetic skin disorders has proved remarkably effective over the past few years. Electron microscopy has had a unique role in identifying morphologic abnormalities of various fibers, fibrils, and filaments, and helping to localize biochemical constituents to these structures. Nowhere is this approach more strongly demonstrated than in its application to different forms of epidermolysis bullosa, of which two major forms, junctional and dystrophic epidermolysis bullosa, are caused by mutations of genes encoding structural proteins in the dermal-epidermal junction.

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Year:  1994        PMID: 7963675     DOI: 10.1111/1523-1747.ep12398895

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  8 in total

1.  IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa.

Authors:  J E Kuster; M H Guarnieri; J G Ault; L Flaherty; P J Swiatek
Journal:  Mamm Genome       Date:  1997-09       Impact factor: 2.957

2.  Morphology of the keratin filament network in palm and sole skin: evidence for site-dependent features based on stereological analysis.

Authors:  O Swensson; R A Eady
Journal:  Arch Dermatol Res       Date:  1996-02       Impact factor: 3.017

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.  Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

Authors:  J A McGrath; B Gatalica; K Li; M G Dunnill; J R McMillan; A M Christiano; R A Eady; J Uitto
Journal:  Am J Pathol       Date:  1996-06       Impact factor: 4.307

5.  End-stage renal disease secondary to IgA nephropathy in recessive dystrophic epidermolysis bullosa: a case report.

Authors:  Fabiana Tammaro; Raffaele Calabrese; Gabriella Aceto; Lucia Lospalluti; Lucrezia Garofalo; Ernesto Bonifazi; Tiziana Piccolo; Giovanni Pannarale; Rosa Penza
Journal:  Pediatr Nephrol       Date:  2007-10-23       Impact factor: 3.714

Review 6.  Inherited epidermolysis bullosa.

Authors:  Jo-David Fine
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

Review 7.  [What is new in 2010 for electron microscopy in surgical pathology?].

Authors:  Mireille Mari; Véronique Hofman; Catherine Butori; Marius Ilie; Sandra Lassalle; Pascal Grier; Dominique Sadoulet; Jean-Yves Scoazec; Paul Hofman
Journal:  Ann Pathol       Date:  2010-07-31       Impact factor: 0.407

Review 8.  Interplay between Cell-Surface Receptors and Extracellular Matrix in Skin.

Authors:  Svenja Kleiser; Alexander Nyström
Journal:  Biomolecules       Date:  2020-08-11
  8 in total

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