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Journal Abstract Search

205 related items for PubMed ID: 16882192

  • 1. A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda.
    Muslumanoglu MH, Saracoglu N, Cilingir O, Basmaci T, Urer S, Sabuncu I, Demir S, Bademci G, Artan S.
    Br J Dermatol; 2006 Aug; 155(2):467-9. PubMed ID: 16882192
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Pseudodominant inheritance with the G86R mutation in the ARS gene in Mal de Meleda.
    Chao SC, Huang CY, Lai FJ, Yang MH.
    Int J Dermatol; 2006 Dec; 45(12):1456-8. PubMed ID: 17184264
    [No Abstract] [Full Text] [Related]

  • 4. A recurrent mutation in the ARS (component B) gene encoding SLURP-1 in Turkish families with mal de Meleda: evidence of a founder effect.
    Hu G, Yildirim M, Baysal V, Yerebakan O, Yilmaz E, Inaloz HS, Martinez-Mir A, Christiano AM, Celebi JT.
    J Invest Dermatol; 2003 Jun; 120(6):967-9. PubMed ID: 12787122
    [Abstract] [Full Text] [Related]

  • 5. Gene Symbol: ars. Disease: Mal de Meleda.
    Abdelhak S, Charfeddine C, Mokni M, Mousli RB, Elkares R, Bouchlaka C, Boubaker S, Ghedamsi S, Baccouche D, Osman AB, Dellagi K.
    Hum Genet; 2004 May; 114(6):609. PubMed ID: 15176391
    [No Abstract] [Full Text] [Related]

  • 6. Mal de Meleda without mutations in the ARS coding sequence.
    van Steensel MA, van Geel MV, Steijlen PM.
    Eur J Dermatol; 2002 May; 12(2):129-32. PubMed ID: 11872406
    [Abstract] [Full Text] [Related]

  • 7. Identification of recurrent mutations in the ARS (component B) gene encoding SLURP-1 in two families with mal de Meleda.
    Ward KM, Yerebakan O, Yilmaz E, Celebi JT.
    J Invest Dermatol; 2003 Jan; 120(1):96-8. PubMed ID: 12535203
    [Abstract] [Full Text] [Related]

  • 8. ARS Component B: structural characterization, tissue expression and regulation of the gene and protein (SLURP-1) associated with Mal de Meleda.
    Mastrangeli R, Donini S, Kelton CA, He C, Bressan A, Milazzo F, Ciolli V, Borrelli F, Martelli F, Biffoni M, Serlupi-Crescenzi O, Serani S, Micangeli E, El Tayar N, Vaccaro R, Renda T, Lisciani R, Rossi M, Papoian R.
    Eur J Dermatol; 2003 Jan; 13(6):560-70. PubMed ID: 14721776
    [Abstract] [Full Text] [Related]

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  • 11. A novel homozygous missense mutation in SLURP1 causing Mal de Meleda with an atypical phenotype.
    Gruber R, Hennies HC, Romani N, Schmuth M.
    Arch Dermatol; 2011 Jun; 147(6):748-50. PubMed ID: 21690549
    [No Abstract] [Full Text] [Related]

  • 12. 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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  • 14. Compound heterozygosity for ARS component B mutations in a Dutch patient with mal de Meleda.
    Nellen RG, van Geel M, Steijlen PM, van Steensel MA.
    Br J Dermatol; 2009 Apr; 160(4):878-80. PubMed ID: 19120323
    [No Abstract] [Full Text] [Related]

  • 15. Mal de Meleda with homozygous mutation p.G86R in SLURP-1.
    Jia WX, Zhang YY, Wu YD, Li WR, Cheng P, Bu WB, Li CR.
    Int J Dermatol; 2020 Jun; 59(6):751-754. PubMed ID: 32048728
    [No Abstract] [Full Text] [Related]

  • 16. A novel mutation in SLURP1 in patients with mal de Meleda from the Indian subcontinent.
    Nellen RG, Claessens T, Subramaniam R, Betkerur J, Prashanth A, Steijlen PM, van Geel M.
    J Dermatol Sci; 2015 Oct; 80(1):76-8. PubMed ID: 26254200
    [No Abstract] [Full Text] [Related]

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  • 18. Mutations in the gene encoding SLURP-1 in Mal de Meleda.
    Fischer J, Bouadjar B, Heilig R, Huber M, Lefèvre C, Jobard F, Macari F, Bakija-Konsuo A, Ait-Belkacem F, Weissenbach J, Lathrop M, Hohl D, Prud'homme JF.
    Hum Mol Genet; 2001 Apr 01; 10(8):875-80. PubMed ID: 11285253
    [Abstract] [Full Text] [Related]

  • 19. [Meleda-type palmo-plantar keratoderma is caused by mutations in the gene coding the SLURP protein].
    Dereure O.
    Ann Dermatol Venereol; 2004 Feb 01; 131(2):224. PubMed ID: 15026760
    [No Abstract] [Full Text] [Related]

  • 20. 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 01; 56(11):1161-1168. PubMed ID: 29023701
    [Abstract] [Full Text] [Related]

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