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Journal Abstract Search

125 related items for PubMed ID: 24510562

  • 1. [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; 31(1):48-51. PubMed ID: 24510562
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. 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 Jun; 46(5):1919-1929. PubMed ID: 29719290
    [Abstract] [Full Text] [Related]

  • 5. KRT9 gene mutation as a reliable indicator in the prenatal molecular diagnosis of epidermolytic palmoplantar keratoderma.
    Ke HP, Jiang HL, Lv YS, Huang YZ, Liu RR, Chen XL, Du ZF, Luo YQ, Xu CM, Fan QH, Zhang XN.
    Gene; 2014 Aug 01; 546(1):124-8. PubMed ID: 24862219
    [Abstract] [Full Text] [Related]

  • 6. Identification of the keratin 9 (KRT9) N161S mutation in a Chinese kindred with epidermolytic palmoplantar keratoderma.
    Feng W, Han W, Man X, Jiang M, Bian C, Wang G, Li X, Yi D, Li J.
    Eur J Dermatol; 2008 Aug 01; 18(4):387-90. PubMed ID: 18573708
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 209(11):515-524. PubMed ID: 27864007
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 7(7):e00703. PubMed ID: 31074163
    [Abstract] [Full Text] [Related]

  • 9. Keratin-9 gene mutation in epidermolytic palmoplantar keratoderma combined with knuckle pads in a large Chinese family.
    Li M, Yang LJ, Hua HK, Zhu XH, Dai XY.
    Clin Exp Dermatol; 2009 Jan 01; 34(1):26-8. PubMed ID: 17362238
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of epidermolytic palmoplantar keratoderma caused by c.T470C (p.M157T) of the keratin 9 gene in a Chinese kindred.
    Chen XL, Xu CM, Cai SR, Chen CY, Zhang XN.
    Prenat Diagn; 2009 Sep 01; 29(9):911-3. PubMed ID: 19548225
    [No 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 01; 295(4):604-9. PubMed ID: 22262370
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 7(11):e977. PubMed ID: 31525823
    [Abstract] [Full Text] [Related]

  • 13. 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 07; 13(4):8089-93. PubMed ID: 25299193
    [Abstract] [Full Text] [Related]

  • 14. 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 Oct 07; 21(5):675-9. PubMed ID: 21715251
    [Abstract] [Full Text] [Related]

  • 15. [Mutation analysis of the keratin 9 gene in a pedigree with diffuse epidermolytic plamoplantar keratoderma].
    Li M, Zhang GL, Zhai JX, Wei L, Zhu XH, Dai XY, Yang LJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug 07; 25(4):387-9. PubMed ID: 18683133
    [Abstract] [Full Text] [Related]

  • 16. [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 07; 29(3):301-5. PubMed ID: 17369150
    [Abstract] [Full Text] [Related]

  • 17. 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 Mar 07; 30(3):354-8. PubMed ID: 23278372
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. An in-frame 18 bp deletion in linker domain L1 of KRT9 identified in a Japanese patient with epidermolytic palmoplantar keratoderma.
    Omi M, Takeichi T, Chiba T, Asano Y, Muro Y, Akiyama M.
    J Dermatol; 2023 Nov 15; 50(11):e370-e372. PubMed ID: 37401035
    [No Abstract] [Full Text] [Related]

  • 20. Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9.
    Fuchs-Telem D, Padalon-Brauch G, Sarig O, Sprecher E.
    Clin Exp Dermatol; 2013 Mar 15; 38(2):189-92: quiz 192. PubMed ID: 23397986
    [Abstract] [Full Text] [Related]

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