Characterization of Hailey-Hailey Disease-mutants in presence and absence of wild type SPCA1 using Saccharomyces cerevisiae as model organism
Author:
Funder
Lundbeckfonden
Novo Nordisk
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-48866-y.pdf
Reference103 articles.
1. Sudbrak, R. et al. Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump. Hum. Mol. Genet. 9, 1131–1140 (2000).
2. Hu, Z. et al. Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease. Nat. Genet. 24, 61–65 (2000).
3. Ficociello, G. et al. Glutathione S-transferase -subunit as a phenotypic suppressor of pmr1Delta strain, the Kluyveromyces lactis model for Hailey-Hailey disease. Biochim. Biophys. Acta 1863, 2650–2657 (2016).
4. Biolcati, G. et al. Efficacy of the melanocortin analogue Nle4-D-Phe7-alpha-melanocyte-stimulating hormone in the treatment of patients with Hailey-Hailey disease. Clin. Exp. Dermatol. 39, 168–175 (2014).
5. Cialfi, S. et al. The loss of ATP2C1 impairs the DNA damage response and induces altered skin homeostasis: Consequences for epidermal biology in Hailey-Hailey disease. Sci. Rep. 6, 31567 (2016).
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