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Journal Abstract Search

457 related items for PubMed ID: 7532198

  • 1. Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.
    Navsaria HA, Swensson O, Ratnavel RC, Shamsher M, McLean WH, Lane EB, Griffiths D, Eady RA, Leigh IM.
    J Invest Dermatol; 1995 Mar; 104(3):425-9. PubMed ID: 7532198
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  • 3. R162W mutation of keratin 9 in a family with autosomal dominant palmoplantar keratoderma with unique histologic features.
    Mayuzumi N, Shigihara T, Ikeda S, Ogawa H.
    J Investig Dermatol Symp Proc; 1999 Sep; 4(2):150-2. PubMed ID: 10536990
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  • 6. Identification of the keratin K9 R162W mutation in patients of Italian origin with epidermolytic palmoplantar keratoderma.
    Terrinoni A, Cocuroccia B, Gubinelli E, Zambruno G, Candi E, Melino G, Girolomoni G.
    Eur J Dermatol; 2004 Sep; 14(6):375-8. PubMed ID: 15564199
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  • 7. Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
    Shamsher MK, Navsaria HA, Stevens HP, Ratnavel RC, Purkis PE, Kelsell DP, McLean WH, Cook LJ, Griffiths WA, Gschmeissner S.
    Hum Mol Genet; 1995 Oct; 4(10):1875-81. PubMed ID: 8595410
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  • 9. De novo mutation of keratin 9 gene in two Taiwanese patients with epidermolytic palmoplantar keratoderma.
    Yang MH, Lee JY, Lin JH, Chao SC.
    J Formos Med Assoc; 2003 Jul; 102(7):492-6. PubMed ID: 14517588
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  • 11. 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
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  • 14. Palmoplantar keratoderma with tonotubular keratin.
    Wevers A, Kuhn A, Mahrle G.
    J Am Acad Dermatol; 1991 Apr; 24(4):638-42. PubMed ID: 1709652
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  • 16. 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; 40(4):215-6. PubMed ID: 10570560
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  • 17. Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).
    Reis A, Hennies HC, Langbein L, Digweed M, Mischke D, Drechsler M, Schröck E, Royer-Pokora B, Franke WW, Sperling K.
    Nat Genet; 1994 Feb; 6(2):174-9. PubMed ID: 7512862
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  • 18. Keratin 9 gene mutations in five Korean families with epidermolytic palmoplantar keratoderma.
    Lee JH, Ahn KS, Lee CH, Youn SJ, Kim JW, Lee DY, Lee ES, Steinert PM, Yang JM.
    Exp Dermatol; 2003 Dec; 12(6):876-81. PubMed ID: 14675368
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  • 20. Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis.
    Virtanen M, Smith SK, Gedde-Dahl T, Vahlquist A, Bowden PE.
    J Invest Dermatol; 2003 Nov; 121(5):1013-20. PubMed ID: 14708600
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