ethylbenzene

keratin 14 ; Homo sapiens







8 Article(s)
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Title
Pub. Year
#Total Relationships
1 34680898 A Familial Form of Epidermolysis Bullosa Simplex Associated with a Pathogenic Variant in KRT5. 2021 Sep 25 1
2 30099737 An ex vivo RNA trans-splicing strategy to correct human generalized severe epidermolysis bullosa simplex. 2019 Jan 3
3 31772641 Known and novel mutations responsible for epidermolysis bullosa simplex cases in a Chinese population. 2019 Dec 3
4 28888469 Cut and Paste: Efficient Homology-Directed Repair of a Dominant Negative KRT14 Mutation via CRISPR/Cas9 Nickases. 2017 Nov 1 3
5 24981776 Novel KRT14 mutation causing epidermolysis bullosa simplex with variable phenotype. 2014 Sep 3
6 23528216 Imbalance of intermediate filament component keratin 14 contributes to increased stress signalling in epidermolysis bullosa simplex. 2013 Apr 4
7 21734713 A new case of keratin 14 functional knockout causes severe recessive EBS and questions the haploinsufficiency model of Naegeli-Franceschetti-Jadassohn syndrome. 2011 Oct 1
8 17617404 A mutation of keratin 18 within the coil 1A consensus motif causes widespread keratin aggregation but cell type-restricted lethality in mice. 2007 Aug 15 1