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Journal Abstract Search

182 related items for PubMed ID: 12838553

  • 21. A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.
    He XH, Zhang XN, Mao W, Chen HP, Xu LR, Chen H, He XL, Le YP.
    Br J Dermatol; 2004 Apr; 150(4):647-51. PubMed ID: 15099359
    [Abstract] [Full Text] [Related]

  • 22. 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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  • 26. Mutations in the 1A domain of keratin 9 in patients with epidermolytic palmoplantar keratoderma.
    Rothnagel JA, Wojcik S, Liefer KM, Dominey AM, Huber M, Hohl D, Roop DR.
    J Invest Dermatol; 1995 Mar 15; 104(3):430-3. PubMed ID: 7532199
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  • 28. Knuckle pads, in an epidermal palmoplantar keratoderma patient with Keratin 9 R163W transgrediens expression.
    Codispoti A, Colombo E, Zocchi L, Serra V, Pertusi G, Leigheb G, Tiberio R, Bornacina G, Zuccoli R, Ramponi A, Campione E, Melino G, Terrinoni A.
    Eur J Dermatol; 2009 Mar 15; 19(2):114-8. PubMed ID: 19106041
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  • 29. A novel keratin 9 gene mutation (Met156Arg) in a Japanese patient with epidermolytic palmoplantar keratoderma.
    Shimazu K, Tsunemi Y, Hattori N, Saeki H, Komine M, Adachi M, Tamaki K.
    Int J Dermatol; 2006 Sep 15; 45(9):1128-30. PubMed ID: 16961539
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  • 30. Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography.
    Rugg EL, Common JE, Wilgoss A, Stevens HP, Buchan J, Leigh IM, Kelsell DP.
    Br J Dermatol; 2002 Jun 15; 146(6):952-7. PubMed ID: 12072061
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  • 31. Epidermolytic palmoplantar keratoderma in a Hispanic kindred resulting from a mutation in the keratin 9 gene.
    Warmuth I, Cserhalmi-Friedman PB, Schneiderman P, Grossman ME, Christiano AM.
    Clin Exp Dermatol; 2000 May 15; 25(3):244-6. PubMed ID: 10844507
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  • 32. A case of spontaneous mutation in the keratin 9 gene associated with epidermolytic palmoplantar keratoderma.
    Morgan VA, Byron K, Paiman L, Varigos GA.
    Australas J Dermatol; 1999 Nov 15; 40(4):215-6. PubMed ID: 10570560
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  • 34. Keratin 9 mutations in the coil 1A region in epidermolytic palmoplantar keratoderma.
    Szalai S, Szalai C, Becker K, Török E.
    Pediatr Dermatol; 1999 Nov 15; 16(6):430-5. PubMed ID: 10632938
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  • 35. Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity.
    Kelsell DP, Stevens HP, Ratnavel R, Bryant SP, Bishop DT, Leigh IM, Spurr NK.
    Hum Mol Genet; 1995 Jun 15; 4(6):1021-5. PubMed ID: 7544664
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  • 37. An insertion-deletion mutation in keratin 9 in three Chinese families with epidermolytic palmoplantar keratoderma.
    Zhang XN, He XH, Lai Z, Yin WG, Le YP, Guo JM, Mao W, He XL, Li JC.
    Br J Dermatol; 2005 Apr 15; 152(4):804-6. PubMed ID: 15840121
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  • 38. Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosis.
    Bonifas JM, Matsumura K, Chen MA, Berth-Jones J, Hutchison PE, Zloczower M, Fritsch PO, Epstein EH.
    J Invest Dermatol; 1994 Oct 15; 103(4):474-7. PubMed ID: 7523529
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