8 Article(s)Download |
PMID | 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 |