Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis
Author:
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0625.2003.00021.x/fullpdf
Reference41 articles.
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2. Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis;Rothnagel;Science,1992
3. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation;Irvine;Br J Dermatol,1999
4. Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis;Anton-Lamprecht;J Invest Dermatol,1983
5. Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma);Ishida-Yamamoto;J Invest Dermatol,1992
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