国际皮肤性病学杂志    2006 32 (3): 185-187   ISSN: 2096-5540  CN: 32-1880/R  

表皮分化复合物和皮肤病
陈小英, 郑捷
上海交通大学医学院附属瑞金医院皮肤科 200025
收稿日期 2005-09-09  修回日期 null  网络版发布日期 null
参考文献  [1] Eckert RL,Broome AM,Ruse M,et al.S100 proteins in the epidermis.J Invest Dermatol,2004,123:23-33.
[2] Marshall D,Hardman MJ,Nield KM,et al.Differentially expressed late constituents of the epidermal cornified envelope.Proc Natl Acad Sci U S A,2001,98:13031-13036.
[3] Marenholz I,Zirra M,Fischer DF,et al.Identification of human epidermal differentiation complex (EDC)-encoded genes by subtractive hybridization of entire YACs to a gridded keratinocyte cDNA library.Genome Res,.2001,11:341-355.
[4] Huber M,Siegenthaler G,Mirancea N,et al.Isolation and characterization of human repetin,a member of the fused gene family of the epidermal differentiation complex.J Invest Dermatol,2005,124:998-1007.
[5] Contzler R,Favre B,Huber M,et al.Cornulin,a new member of the "fused gene" family,is expressed during epidermal differentiation.J Invest Dermatol,2005,124:990-997.
[6] Wolf R,Mirmohammadsadegh A,Walz M,et al.Molecular cloning and characterization of alternatively spliced mRNA isoforms from psoriatic skin encoding a novel member of the S100 family.FASEB J,2003,17:1969-1971.
[7] Ishida-Yamamoto A.Loricrin keratoderma:a novel disease entity characterized by nuclear accumulation of mutant loricrin.J Dermatol Sci,2003,31:3-8.
[8] Takahashi H,Ishida-Yamamoto A,Kishi A,et al.Loricrin gene mutation in a Japanese patient of Vohwinkel's syndrome.J Dermatol Sci,1999,19:44-47.
[9] O'Driscoll J,Muston GC,McGrath JA,et al.A recurrent mutation in the loricrin gene underlies the ichthyotic variant of Vohwinkel syndrome.Clin Exp Dermatol,2002,27:243-246.
[10] Matsumoto K,Muto M,Seki S,et al.Loricrin keratoderma:a cause of congenital ichthyosiform erythroderma and collodion baby.Br J Dermatol,2001,145:657-660.
[11] Ishida-Yamamoto A,McGrath JA,Lam H,et al.The molecular pathology of progressive symmetric erythrokeratoderma:a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope.Am J Hum Genet,1997,61:581-589.
[12] Suga Y,Jarnik M,Attar PS,et al.Transgenic mice expressing a mutant form of loricrin reveal the molecular basis of the skin diseases,Vohwinkel syndrome and progressive symmetric erythrokeratoderma.J Cell Biol,2000,151:401-412.
[13] Schmuth M,Fluhr JW,Crumrine DC,et al.Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis).J Invest Dermatol,2004,122:909-922.
[14] Schon MP,Ruzicka T.Psoriasis:the plot thickens.Nat Immunol,2001,2:91.
[15] Zheng J,Jin S,Shi R.Confirmation of PSORS psoriasis susceptibility loci in a Chinese population.Arch Dermatol Res,2003,295:14-18.
[16] Capon F,Semprini S,Chimenti S,et al.Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21.J Invest Dermatol,2001,116:728-730.
[17] Semprini S,Capon F,Bovolenta S,et al.Genomic structure,promoter characterisation and mutational analysis of the S100A7 gene:exclusion of a candidate for familial psoriasis susceptibility.Hum Genet,1999,104:130-134.
[18] Giardina E,Capon F,De Rosa MC,et al.Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus.Ann Hum Genet,2004,68 (Pt 6):639-645.
[19] Sugiura H,Ebise H,Tazawa T,et al.Large-scale DNA microarray analysis of atopic skin lesions shows overexpression of an epidermal differentiation gene cluster in the alternative pathway and lack of protective gene expression in the cornified envelope.Br J Dermatol,2005,152:146-149.
[20] Tobin DJ.Characterization of hair follicle antigens targeted by the anti-hair follicle immune response.J Investig Dermatol Symp Proc,2003,8:176-181.
[21] Ribe A,McNutt NS.S100A protein expression in the distinction between lentigo maligna and pigmented actinic keratosis.Am J Dermatopathol,2003,25:93-99.
[22] Alowami S,Qing G,Emberley E,et al.Psoriasin (S100A7) expression is altered during skin tumorigenesis.BMC Dermatol,2003,3:1.

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