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Journal Abstract Search

150 related items for PubMed ID: 27864007

  • 1. Six generations of epidermolytic palmoplantar keratoderma, associated with a KRT9 R163W mutation.
    Wang P, Kang XJ, Tang XH, Liu JY, Li WZ, Wang WJ, Liang SN, Feng YY, Ding Y, Chen WJ.
    Cancer Genet; 2016 Nov; 209(11):515-524. PubMed ID: 27864007
    [Abstract] [Full Text] [Related]

  • 2. 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 Nov; 46(5):1919-1929. PubMed ID: 29719290
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  • 3. 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
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  • 4. 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 Jul; 30(3):354-8. PubMed ID: 23278372
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
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  • 9. 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 15; 287():104971. PubMed ID: 37467889
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  • 12. A novel mutation within the 2B rod domain of keratin 9 in a Chinese pedigree with epidermolytic palmoplantar keratoderma combined with knuckle pads and camptodactyly.
    Du ZF, Wei W, Wang YF, Chen XL, Chen CY, Liu WT, Lu JJ, Mao LG, Xu CM, Fang H, Zhang XN.
    Eur J Dermatol; 2011 Sep 15; 21(5):675-9. PubMed ID: 21715251
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  • 15. [Mutation analysis and prenatal diagnosis of keratin 9 gene in a large Chinese family with epidermolytic palmoplantar keratoderma].
    Liu N, Shi H, Kong X, Wu Q, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb 15; 31(1):48-51. PubMed ID: 24510562
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  • 17. [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 15; 29(3):280-3. PubMed ID: 22678789
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  • 19. Missense mutation of keratin 9 (c.487C>T (p.R163W) in southern Chinese patients with epidermolytic palmoplantar keratoderma.
    Xu CM, Chen XL, Chen CY, Zhang XN.
    Eur J Dermatol; 2009 Jun 15; 19(3):265-6. PubMed ID: 19223272
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