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Journal Abstract Search

162 related items for PubMed ID: 25557416

  • 21.
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  • 23. 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
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  • 27. Heterogeneity in the properties of mutant secreted lymphocyte antigen 6/urokinase receptor-related protein 1 (SLURP1) in Mal de Meleda.
    Adeyo O, Oberer M, Ploug M, Fong LG, Young SG, Beigneux AP.
    Br J Dermatol; 2015 Oct; 173(4):1066-9. PubMed ID: 25919322
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  • 29. Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.
    Marrakchi S, Audebert S, Bouadjar B, Has C, Lefèvre C, Munro C, Cure S, Jobard F, Morlot S, Hohl D, Prud'homme JF, Zahaf A, Turki H, Fischer J.
    J Invest Dermatol; 2003 Mar; 120(3):351-5. PubMed ID: 12603845
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  • 31. 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; 164(1):47-53. PubMed ID: 20854438
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  • 34. Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region.
    Charfeddine C, Mokni M, Kassar S, Zribi H, Bouchlaka C, Boubaker S, Rebai A, Ben Osman A, Abdelhak S.
    J Hum Genet; 2006 Jan; 51(10):841-845. PubMed ID: 16865292
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  • 35. Reply to Nellen et al's comment on the classification of clinical/genetic variants of Mal de Meleda.
    Zhao L, Vahlquist A, Virtanen M, Wennerstrand L, Lind LK, Lundström A, Pigg MH.
    Acta Derm Venereol; 2015 Nov; 95(8):1034-5. PubMed ID: 26844309
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  • 36. Palmoplantar Keratoderma in Slurp2-Deficient Mice.
    Allan CM, Procaccia S, Tran D, Tu Y, Barnes RH, Larsson M, Allan BB, Young LC, Hong C, Tontonoz P, Fong LG, Young SG, Beigneux AP.
    J Invest Dermatol; 2016 Feb; 136(2):436-443. PubMed ID: 26967477
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  • 37. A novel missense mutation in the gene encoding SLURP-1 in patients with Mal de Meleda from northern Tunisia.
    Charfeddine C, Mokni M, Ben Mousli R, Elkares R, Bouchlaka C, Boubaker S, Ghedamsi S, Baccouche D, Ben Osman A, Dellagi K, Abdelhak S.
    Br J Dermatol; 2003 Dec; 149(6):1108-15. PubMed ID: 14674887
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  • 38. A novel mutation in SLURP1 in patients with Mal de Meleda from Turkey.
    İmren IG, Ertürk S, Çetin GO, Kaçar N.
    Int J Dermatol; 2024 Sep; 63(9):1263-1266. PubMed ID: 38647179
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  • 39. Nagashima-type palmoplantar keratosis in a Chinese Han population.
    Zhang J, Zhang G, Ni C, Cheng R, Liang J, Li M, Yao Z.
    Mol Med Rep; 2016 Nov; 14(5):4049-4054. PubMed ID: 27666198
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  • 40. [Meleda-type palmo-plantar keratoderma is caused by mutations in the gene coding the SLURP protein].
    Dereure O.
    Ann Dermatol Venereol; 2004 Feb; 131(2):224. PubMed ID: 15026760
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