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Volumn 131, Issue 3, 2011, Pages 561-564

Peeling skin syndrome: Genetic defects in late terminal differentiation of the epidermis

Author keywords

[No Author keywords available]

Indexed keywords

CORNEODESMOSIN; DESMOSINE; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; UNCLASSIFIED DRUG;

EID: 79951482804     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2010.434     Document Type: Note
Times cited : (20)

References (21)
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  • 4
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    • Skin shedding (keratolysis exfoliativa congenita): Report of a case
    • Fox H (1921) Skin shedding (keratolysis exfoliativa congenita): report of a case. Arch Dermatol Syph 3:202
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    • Fox, H.1
  • 5
    • 1842639321 scopus 로고    scopus 로고
    • A 4.2 kb upstream region of the human corneodesmosin gene directs site-specific expression in hair follicles and hyperkeratotic epidermis of transgenic mice
    • DOI 10.1111/j.0022-202X.2004.22306.x
    • Gallinaro H, Jonca N, Langbein L et al. (2004) A 4.2 upstream region of the human corneodesmosin gene directs site-specific expression in hair follicles and hyperkeratotic epidermis of transgenic mice. J Invest Dermatol 122:730-8 (Pubitemid 38471343)
    • (2004) Journal of Investigative Dermatology , vol.122 , Issue.3 , pp. 730-738
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  • 6
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    • Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5
    • DOI 10.1159/000084755
    • Geyer AS, Ratajczak P, Pol-Rodriguez M et al. (2005) Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5. Dermatology 210:308-14 (Pubitemid 40976738)
    • (2005) Dermatology , vol.210 , Issue.4 , pp. 308-314
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  • 8
    • 0042564615 scopus 로고    scopus 로고
    • Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population
    • DOI 10.1034/j.1600-0625.2003.00048.x
    • Holm SJ, Carlen LM, Mallbris L et al. (2003) Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population. Exp Dermatol 12:435-44 (Pubitemid 36992418)
    • (2003) Experimental Dermatology , vol.12 , Issue.4 , pp. 435-444
    • Holm, S.J.1    Carlen, L.M.2    Mallbris, L.3    Stahle-Backdahl, M.4    O'Brien, K.P.5
  • 9
    • 79951497066 scopus 로고    scopus 로고
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    • Israeli S, Zamir H, Sarig O et al. (2011) Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin. J Invest Dermatol 131:779-81
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  • 11
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    • A missense mutation in TGM5 causes acral peeling skin syndrome in a Tunisian family
    • Kharfi M, El Fekih N, Ammar D et al. (2009) A missense mutation in TGM5 causes acral peeling skin syndrome in a Tunisian family. J Invest Dermatol 129:2512-5
    • (2009) J Invest Dermatol , vol.129 , pp. 2512-2515
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  • 12
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  • 15
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.