Research history for keratinizing disorders at Department of Dermatology, Juntendo University School of Medicine
Author:
Affiliation:
1. Department of Dermatology, Juntendo University School of Medicine
Publisher
The Jutendo Medical Journal
Link
https://www.jstage.jst.go.jp/article/pjmj/52/1/52_45/_pdf
Reference44 articles.
1. 1) OgawaH, HattoriM, IshibashiY: Abnormal fibrous protein isolated from the stratum corneum of a patient with bullous congenital ichthyosiform erythroderma (BCIE). Arch Dermatol Res, 1979;266: 109-116.
2. 3) YoshiikeT, NegiM, ManabeM, et al: Fractionation and characterization of the human epidermal stratum corneum in keratinization disorders. J Dermatol, 1982;9: 243-251.
3. 4) BonifasJM, RothmanAL, EpsteinEH Jr.: Epidermolysis bullosa simplex: Evidence in two families for keratin gene abnormalities. Science, 1991;254: 1202-1205.
4. 5) VassarR, CoulombePA, DegensteinL, et al: Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease. Cell, 1991;64: 365-380.
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