Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: Trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition-Reference-Cited by-同舟云学术

Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: Trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition

Published:2009-03 Issue:3 Volume:53 Page:198-206
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Chamcheu Jean Christopher,Lorié Elizabeth Pavez,Akgul Baki,Bannbers Elin,Virtanen Marie,Gammon Luke,Moustakas Aristidis,Navsaria Harshad,Vahlquist Anders,Törmä Hans

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference38 articles.

1. The keratins and their disorders;Rugg;Am J Med Genet C: Semin Med Genet,2004

2. Keratins and skin disorders;Lane;J Pathol,2004

3. Modulation of keratin intermediate filament assembly by single amino acid exchanges in the consensus sequence at the C-terminal end of the rod domain;Hatzfeld;J Cell Sci,1991

4. The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on diagnosis and classification of EB;Fine;J Am Acad Dermatol,2008

5. Epidermolysis bullosa simplex (Dowling–Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14;Ishida-Yamamoto;J Invest Dermatol,1991

Cited by 34 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Human-Induced Pluripotent Stem Cell‒Derived Keratinocytes, a Useful Model to Identify and Explore the Pathological Phenotype of Epidermolysis Bullosa Simplex;Journal of Investigative Dermatology;2022-10

2. Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9;The CRISPR Journal;2022-08-01

3. Cell and Tissue Nanomechanics: From Early Development to Carcinogenesis;Biomedicines;2022-02-01

4. Damaged Keratin Filament Network Caused by KRT5 Mutations in Localized Recessive Epidermolysis Bullosa Simplex;Frontiers in Genetics;2021-11-29

5. Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis bullosa simplex with cardiomyopathy;Human Molecular Genetics;2021-11-05