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Volumn 127, Issue 6, 2007, Pages 1282-1284

Filaggrin's fuller figure: A glimpse into the genetic architecture of atopic dermatitis

Author keywords

[No Author keywords available]

Indexed keywords

ATOPIC DERMATITIS; ECZEMA; EXON; FILAGGRIN GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENE STRUCTURE; GENETIC SUSCEPTIBILITY; HISTOLOGY; HUMAN; ICHTHYOSIS VULGARIS; INTRON; NONSENSE MUTATION; PRIORITY JOURNAL; REVIEW; RISK FACTOR; STATISTICAL SIGNIFICANCE;

EID: 34248530680     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5700876     Document Type: Note
Times cited : (110)

References (11)
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    • Giardina E, Sinibaldi C, Chini L, Moschese V, Marulli G, Provini A et al. (2006) Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21. Hum Hered 61:229-36
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  • 5
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    • Fleshing out filaggrin phenotypes
    • Irvine AD (2007) Fleshing out filaggrin phenotypes. J Invest Dermatol 127:504-7
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    • Irvine, A.D.1
  • 6
    • 34247579998 scopus 로고    scopus 로고
    • Filaggrin mutations in children with severe atopic dermatitis
    • published online 15 February, doi:10.1038/sj.jid.5700739
    • Morar N, Cookson WO, Harper JI, Moffatt MF. Filaggrin mutations in children with severe atopic dermatitis. J Invest Dermatol, published online 15 February 2007; doi:10.1038/sj.jid.5700739
    • (2007) J Invest Dermatol
    • Morar, N.1    Cookson, W.O.2    Harper, J.I.3    Moffatt, M.F.4
  • 7
    • 33846820433 scopus 로고    scopus 로고
    • Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis
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    • Nomura, T.1    Sandilands, A.2    Akiyama, M.3    Liao, H.4    Evans, A.T.5    Sakai, K.6
  • 8
    • 33645399288 scopus 로고    scopus 로고
    • Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis
    • Palmer CNA, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP et al. (2006) Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet 38:441-6
    • (2006) Nat Genet , vol.38 , pp. 441-446
    • Palmer, C.N.A.1    Irvine, A.D.2    Terron-Kwiatkowski, A.3    Zhao, Y.4    Liao, H.5    Lee, S.P.6
  • 9
    • 33746129175 scopus 로고    scopus 로고
    • Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis
    • Sandilands A, O'Regan GM, Liao H, Zhao Y, Terron-Kwiatkowski A, Watson RM et al. (2006) Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis. J Invest Dermatol 126:1770-5
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    • Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
    • published online 8 April, doi:10.1038/ng2020
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    • (2007) Nat Genet
    • Sandilands, A.1    Terron-Kwiatkowski, A.2    Hull, P.R.3    O'Regan, G.M.4    Clayton, T.H.5    Watson, R.M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.