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Journal Abstract Search

374 related items for PubMed ID: 24604124

  • 1. Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda.
    Zhao L, Vahlquist A, Virtanen M, Wennerstrand L, Lind LK, Lundström A, Hellström Pigg M.
    Acta Derm Venereol; 2014 Nov; 94(6):707-10. PubMed ID: 24604124
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  • 2. SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene.
    Bergqvist C, Kadara H, Hamie L, Nemer G, Safi R, Karouni M, Marrouche N, Abbas O, Hasbani DJ, Kibbi AG, Nassar D, Shimomura Y, Kurban M.
    Int J Dermatol; 2018 Feb; 57(2):162-170. PubMed ID: 29231248
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  • 3. Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates.
    Eckl KM, Stevens HP, Lestringant GG, Westenberger-Treumann M, Traupe H, Hinz B, Frossard PM, Stadler R, Leigh IM, Nürnberg P, Reis A, Hennies HC.
    Hum Genet; 2003 Jan; 112(1):50-6. PubMed ID: 12483299
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  • 6. Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda.
    Radiono S, Pramono ZAD, Oh GGK, Surana U, Widiyani S, Danarti R.
    Int J Dermatol; 2017 Nov; 56(11):1161-1168. PubMed ID: 29023701
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  • 7. Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous.
    Taylor JA, Bondavalli D, Monif M, Yap LM, Winship I.
    Australas J Dermatol; 2016 Feb; 57(1):e11-3. PubMed ID: 25557416
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  • 8. Abnormal keratinization and cutaneous inflammation in Mal de Meleda.
    Kudo M, Ishiura N, Tamura-Nakano M, Shimizu T, Kamata M, Akasaka E, Nakano H, Okuma Y, Tada Y, Okochi H, Tamaki T.
    J Dermatol; 2020 May; 47(5):554-558. PubMed ID: 32157724
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  • 9. A novel homozygous mutation disrupting the initiation codon in the SLURP1 gene underlies mal de Meleda in a consanguineous family.
    Shah K, Nasir A, Irfanullah, Shahzad S, Khan S, Ahmad W.
    Clin Exp Dermatol; 2016 Aug; 41(6):675-679. PubMed ID: 29226984
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  • 16. SLURP1 is a late marker of epidermal differentiation and is absent in Mal de Meleda.
    Favre B, Plantard L, Aeschbach L, Brakch N, Christen-Zaech S, de Viragh PA, Sergeant A, Huber M, Hohl D.
    J Invest Dermatol; 2007 Feb; 127(2):301-8. PubMed ID: 17008884
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  • 20. "Nagashima-type" keratosis as a novel entity in the palmoplantar keratoderma category.
    Kabashima K, Sakabe J, Yamada Y, Tokura Y.
    Arch Dermatol; 2008 Mar; 144(3):375-9. PubMed ID: 18347294
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