These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
208 related articles for article (PubMed ID: 23962810)
1. Keratin 9 is required for the structural integrity and terminal differentiation of the palmoplantar epidermis. Fu DJ; Thomson C; Lunny DP; Dopping-Hepenstal PJ; McGrath JA; Smith FJD; Irwin McLean WH; Leslie Pedrioli DM J Invest Dermatol; 2014 Mar; 134(3):754-763. PubMed ID: 23962810 [TBL] [Abstract][Full Text] [Related]
2. Mutations in the keratin 9 gene in Pakistani families with epidermolytic palmoplantar keratoderma. Shimomura Y; Wajid M; Weiser J; Kraemer L; Christiano AM Clin Exp Dermatol; 2010 Oct; 35(7):759-64. PubMed ID: 19874353 [TBL] [Abstract][Full Text] [Related]
3. Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders. Li P; Qi J; Zhong Y; Ding A; Xiao H J Proteomics; 2023 Sep; 287():104971. PubMed ID: 37467889 [TBL] [Abstract][Full Text] [Related]
4. Altered keratinocyte differentiation is an early driver of keratin mutation-based palmoplantar keratoderma. Zieman AG; Poll BG; Ma J; Coulombe PA Hum Mol Genet; 2019 Jul; 28(13):2255-2270. PubMed ID: 31220272 [TBL] [Abstract][Full Text] [Related]
5. [Pathological features and gene mutation analysis in two pedigrees of diffuse palmoplantar keratoderma]. Yin XZ; Zhang BR; Ding MP; Zhang H; Xia K; Hu ZM Yi Chuan; 2007 Mar; 29(3):301-5. PubMed ID: 17369150 [TBL] [Abstract][Full Text] [Related]
6. Keratins K2 and K10 are essential for the epidermal integrity of plantar skin. Fischer H; Langbein L; Reichelt J; Buchberger M; Tschachler E; Eckhart L J Dermatol Sci; 2016 Jan; 81(1):10-6. PubMed ID: 26603179 [TBL] [Abstract][Full Text] [Related]
7. Generic and personalized RNAi-based therapeutics for a dominant-negative epidermal fragility disorder. Leslie Pedrioli DM; Fu DJ; Gonzalez-Gonzalez E; Contag CH; Kaspar RL; Smith FJ; McLean WH J Invest Dermatol; 2012 Jun; 132(6):1627-35. PubMed ID: 22402445 [TBL] [Abstract][Full Text] [Related]
8. Analysis of the KRT9 gene in a Mexican family with epidermolytic palmoplantar keratoderma. Lopez-Valdez J; Rivera-Vega MR; Gonzalez-Huerta LM; Cazarin J; Cuevas-Covarrubias S Pediatr Dermatol; 2013; 30(3):354-8. PubMed ID: 23278372 [TBL] [Abstract][Full Text] [Related]
9. Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma. Xiao H; Guo Y; Yi J; Xia H; Xu H; Yuan L; Hu P; Yang Z; He Z; Lu H; Deng H Cell Physiol Biochem; 2018; 46(5):1919-1929. PubMed ID: 29719290 [TBL] [Abstract][Full Text] [Related]
10. [Present status of the molecular genetics in epidermolytic palmoplantar keratoderma]. Zhang XN; Mao W; He XH; Lai Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):372-5. PubMed ID: 15300637 [TBL] [Abstract][Full Text] [Related]
11. The most common mutation of KRT9, c.C487T (p.R163W), in epidermolytic palmoplantar keratoderma in two large Chinese pedigrees. Liu WT; Ke HP; Zhao Y; Chen XL; Lu JJ; Du ZF; Yu D; Zhang XN Anat Rec (Hoboken); 2012 Apr; 295(4):604-9. PubMed ID: 22262370 [TBL] [Abstract][Full Text] [Related]
13. A novel mutation of KRT9 gene in a Chinese Han pedigree with epidermolytic palmoplantar keratoderma. Chen N; Sun J; Song Y; Wei X; Shi Y; Zhang L J Cosmet Dermatol; 2017 Sep; 16(3):402-406. PubMed ID: 27726289 [TBL] [Abstract][Full Text] [Related]
14. Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review. Liu X; Qiu C; He R; Zhang Y; Zhao Y Mol Genet Genomic Med; 2019 Nov; 7(11):e977. PubMed ID: 31525823 [TBL] [Abstract][Full Text] [Related]
15. Human keratin diseases: hereditary fragility of specific epithelial tissues. Corden LD; McLean WH Exp Dermatol; 1996 Dec; 5(6):297-307. PubMed ID: 9028791 [TBL] [Abstract][Full Text] [Related]
16. Targeting the palm: a leap forward toward treatment of keratin disorders. Roth W; Hatzfeld M; Magin TM J Invest Dermatol; 2012 Jun; 132(6):1541-2. PubMed ID: 22584502 [TBL] [Abstract][Full Text] [Related]
17. Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motif. Coleman CM; Munro CS; Smith FJ; Uitto J; McLean WH Br J Dermatol; 1999 Mar; 140(3):486-90. PubMed ID: 10233272 [TBL] [Abstract][Full Text] [Related]
18. [Mutation analysis of keratin 9 gene in a family with epidermolytic palmoplantar keratoderma]. Li YL; Li NN; Wang YP; Li MR; Dai L; Deng Y; Liu Z; Mu DZ; Zhu J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun; 29(3):280-3. PubMed ID: 22678789 [TBL] [Abstract][Full Text] [Related]
19. Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9. Guo Y; Shi M; Tan ZP; Shi XL Genet Mol Res; 2014 Oct; 13(4):8089-93. PubMed ID: 25299193 [TBL] [Abstract][Full Text] [Related]
20. Exome sequencing identifies a KRT9 pathogenic variant in a Chinese pedigree with epidermolytic palmoplantar keratoderma. Li C; Chen P; Sun S; Zeng K; Liang J; Wang Q; Zhang S; Xu M; Li Z; Zhang X Mol Genet Genomic Med; 2019 Jul; 7(7):e00703. PubMed ID: 31074163 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]