| 1 |
32113649 | Ichthyosis with confetti caused by new and recurrent mutations in KRT10 associated with varying degrees of keratin 10 mis-localization. | 2020 Apr |
5 |
| 2 |
26581228 | Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. | 2016 May |
1 |
| 3 |
20804491 | Induction of p38, tumour necrosis factor-α and RANTES by mechanical stretching of keratinocytes expressing mutant keratin 10R156H. | 2011 Jan |
1 |
| 4 |
21811984 | [Mutation analysis of KRT10 gene in a patient with bullous congenital ichthyosiform erythroderma]. | 2011 Aug |
1 |
| 5 |
17683385 | R156C mutation of keratin 10 causes mild form of epidermolytic hyperkeratosis. | 2007 Aug |
1 |
| 6 |
11204523 | Recurrent R156H mutation of KRT10 in a Japanese family with bullous congenital ichthyosiform erythroderma. | 2000 Jul |
1 |
| 7 |
10098704 | Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis. | 1999 Feb |
2 |
| 8 |
9742571 | Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis. | 1998 Aug |
1 |
| 9 |
9833037 | Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma. | 1998 Nov |
1 |
| 10 |
9184002 | A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis. | 1997 Mar |
4 |
| 11 |
7512983 | Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity. | 1994 Apr |
1 |
| 12 |
1381287 | The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes. | 1992 Sep 4 |
2 |