A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype
Author:
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Reference15 articles.
1. Ultrastructure of Blister Formation in Epidermolysis Bullosa Hereditaria: V. Epidermolysis Bullosa Simplex Localisata Type Weber-Cockayne
2. Epidermolysis Bullosa Herpetiformis Dowling-Meara
3. Abnormal organization of keratin intermediate filaments in cultured keratinocytes of epidermolysis bullosa simplex
4. Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease
5. Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities
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1. A de novo mutation in KRT5 in a crossbred calf with epidermolysis bullosa simplex;Journal of Veterinary Internal Medicine;2020-11
2. KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family;Journal of Investigative Dermatology;2016-09
3. Gene expression analysis of an epidermolysis bullosa simplex Dowling-Meara cell line by subtractive hybridization: recapitulation of cellular differentiation, migration and wound healing;Experimental Dermatology;2011-12-14
4. Gene Therapy for Keratin Genodermatoses: Striving Forward but Obstacles Persist;Journal of Investigative Dermatology;2011-07
5. Keratin gene mutations in disorders of human skin and its appendages;Archives of Biochemistry and Biophysics;2011-04
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