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Journal Abstract Search

267 related items for PubMed ID: 29231248

  • 1. 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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  • 2. 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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  • 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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  • 4. 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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  • 5. 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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  • 6. 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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  • 7. Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families.
    Akbar A, Prince C, Payne C, Fasham J, Ahmad W, Baple EL, Crosby AH, Harlalka GV, Gul A.
    BMC Med Genet; 2019 Aug 23; 20(1):145. PubMed ID: 31443639
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  • 8. SLURP1 mutation-impaired T-cell activation in a family with mal de Meleda.
    Tjiu JW, Lin PJ, Wu WH, Cheng YP, Chiu HC, Thong HY, Chiang BL, Yang WS, Jee SH.
    Br J Dermatol; 2011 Jan 23; 164(1):47-53. PubMed ID: 20854438
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  • 12. Pain Hypersensitivity in SLURP1 and SLURP2 Knock-out Mouse Models of Hereditary Palmoplantar Keratoderma.
    Weinberg RL, Kim S, Pang Z, Awad S, Hanback T, Pan B, Bettin L, Chang D, Polydefkis MJ, Qu L, Caterina MJ.
    J Neurosci; 2024 Jul 10; 44(28):. PubMed ID: 38866482
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  • 13. 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 10; 47(5):554-558. PubMed ID: 32157724
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  • 15. Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families.
    Wajid M, Kurban M, Shimomura Y, Christiano AM.
    J Dermatol Sci; 2009 Oct 10; 56(1):27-32. PubMed ID: 19692209
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  • 16. A hypomorphic Egfr allele does not ameliorate the palmoplantar keratoderma caused by SLURP1 deficiency.
    Allan CM, Tran D, Tu Y, Heizer PJ, Young LC, Fong LG, Beigneux AP, Young SG.
    Exp Dermatol; 2017 Nov 10; 26(11):1134-1136. PubMed ID: 28418591
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  • 20. Amelanotic melanoma arising in an area of SLURP-1 mutated Mal de Meleda.
    Arousse A, Mokni S, H'mida Ben Brahim D, Bdioui A, Aounallah A, Gammoudi R, Saidi W, Boussofara L, Ghariani N, Denguezli M, Belajouza C, Nouira R.
    Int J Dermatol; 2019 Aug 10; 58(8):966-968. PubMed ID: 30246339
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