Literature DB >> 1375393

Molecular genetics of epidermolysis bullosa.

E H Epstein1.   

Abstract

Blisters following minor trauma characterize epidermolysis bullosa, a group of hereditary diseases of the skin. In the simplex type, epidermal basal cells are fragile, and mutations of genes encoding keratin intermediate filament proteins underlie that fragility. In the dystrophic types, the causative mutation appears to be in the gene encoding type VII collagen, which is the major component of anchoring fibrils. These recent findings afford solid evidence that at least one function of the cytoskeletal intermediate filament network is the provision of mechanical stability and that anchoring fibrils indeed do anchor the epidermis to the underlying dermis.

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Year:  1992        PMID: 1375393     DOI: 10.1126/science.1375393

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  19 in total

Review 1.  Keratin gene mutations in human skin disease.

Authors:  H P Stevens; M H Rustin
Journal:  Postgrad Med J       Date:  1994-11       Impact factor: 2.401

2.  Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosa.

Authors:  B Gatalica; L Pulkkinen; K Li; K Kuokkanen; M Ryynänen; J A McGrath; J Uitto
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

3.  Transdermal Delivery of Functional Collagen Via Polyvinylpyrrolidone Microneedles.

Authors:  Wenchao Sun; Mohammed Inayathullah; Martin A C Manoukian; Andrey V Malkovskiy; Sathish Manickam; M Peter Marinkovich; Alfred T Lane; Lobat Tayebi; Alexander M Seifalian; Jayakumar Rajadas
Journal:  Ann Biomed Eng       Date:  2015-06-12       Impact factor: 3.934

Review 4.  Cultivation of human keratinocyte stem cells: current and future clinical applications.

Authors:  G Pellegrini; S Bondanza; L Guerra; M De Luca
Journal:  Med Biol Eng Comput       Date:  1998-11       Impact factor: 2.602

5.  Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosa.

Authors:  A Hovnanian; L Hilal; C Blanchet-Bardon; Y de Prost; A M Christiano; J Uitto; M Goossens
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

6.  Dominant dystrophic epidermolysis bullosa: identification of a Gly-->Ser substitution in the triple-helical domain of type VII collagen.

Authors:  A M Christiano; M Ryynänen; J Uitto
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

7.  Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis.

Authors:  C C Chipev; J M Yang; J J DiGiovanna; P M Steinert; L Marekov; J G Compton; S J Bale
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

Review 8.  Twelve hour anaesthesia in a patient with epidermolysis bullosa.

Authors:  A E Yonker-Sell; L A Connolly
Journal:  Can J Anaesth       Date:  1995-08       Impact factor: 5.063

9.  Truncated desmin in PtK2 cells induces desmin-vimentin-cytokeratin coprecipitation, involution of intermediate filament networks, and nuclear fragmentation: a model for many degenerative diseases.

Authors:  K R Yu; T Hijikata; Z X Lin; H L Sweeney; S W Englander; H Holtzer
Journal:  Proc Natl Acad Sci U S A       Date:  1994-03-29       Impact factor: 11.205

10.  Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster.

Authors:  L Pulkkinen; A M Christiano; R G Knowlton; J Uitto
Journal:  J Clin Invest       Date:  1993-01       Impact factor: 14.808

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