Keratin K6c Mutations Cause Focal Palmoplantar Keratoderma-Reference-Cited by-同舟云学术

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Keratin K6c Mutations Cause Focal Palmoplantar Keratoderma

Published:2010-02 Issue:2 Volume:130 Page:425-429
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Wilson Neil J.,Messenger Andrew G.,Leachman Sancy A.,O'Toole Edel A.,Lane E Birgitte,Irwin McLean W.H.,Smith Frances J.D.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference26 articles.

1. Mutation of a type II keratin gene (K6a) in pachyonychia congenita;Bowden;Nat Genet,1995

2. Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene;Corden;Exp Eye Res,2000

3. The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assembly;Herrmann;J Mol Biol,2000

4. Palmoplantar keratodermas;Itin;Clin Dermatol,2005

5. Disorders of keratinization;Judge,2004

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1. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19

2. A novel heterozygous frameshift mutation in the KRT6A gene responsible for an uncommon phenotype of pachyonychia congenita: One case report and review of literature;Heliyon;2024-03

3. Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders;Journal of Proteomics;2023-09

4. Pachyonychia Congenita: Clinical Features and Future Treatments;KEIO J MED;2023

5. Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma;British Journal of Dermatology;2023-05-20

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