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Journal Abstract Search

188 related items for PubMed ID: 15953088

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  • 2. Novel mutations of TGM1 in a child with congenital ichthyosiform erythroderma.
    Akiyama M, Takizawa Y, Kokaji T, Shimizu H.
    Br J Dermatol; 2001 Feb; 144(2):401-7. PubMed ID: 11251583
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  • 5. The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis.
    Akiyama M, Sawamura D, Shimizu H.
    Clin Exp Dermatol; 2003 May; 28(3):235-40. PubMed ID: 12780701
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  • 6. Epidermal transglutaminase in the ichthyoses.
    van Hooijdonk CA, Steijlen PM, Bergers M, Mier PD, Traupe H, Happle R.
    Acta Derm Venereol; 1991 May; 71(2):173-5. PubMed ID: 1675533
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  • 9. Knocking-in the R142C mutation in transglutaminase 1 disrupts the stratum corneum barrier and postnatal survival of mice.
    Nakagawa N, Yamamoto M, Imai Y, Sakaguchi Y, Takizawa T, Ohta N, Yagi N, Hatta I, Hitomi K, Takizawa T, Takeda J, Tsuda T, Matsuki M, Yamanishi K.
    J Dermatol Sci; 2012 Mar; 65(3):196-206. PubMed ID: 22258055
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  • 12. Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis.
    Laiho E, Niemi KM, Ignatius J, Kere J, Palotie A, Saarialho-Kere U.
    Eur J Hum Genet; 1999 Sep; 7(6):625-32. PubMed ID: 10482949
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  • 13. New mutations in the transglutaminase 1 gene in three families with lamellar ichthyosis.
    Cao X, Lin Z, Yang H, Bu D, Tu P, Chen L, Wu H, Yang Y.
    Clin Exp Dermatol; 2009 Dec; 34(8):904-9. PubMed ID: 19486042
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  • 14. Formation of cornified cell envelope in human hair follicle development.
    Akiyama M, Matsuo I, Shimizu H.
    Br J Dermatol; 2002 Jun; 146(6):968-76. PubMed ID: 12072064
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  • 16. Identification of two novel nonsense mutations in the transglutaminase 1 gene in a Hungarian patient with congenital ichthyosiform erythroderma.
    Becker K, Csikós M, Sárdy M, Szalai ZS, Horváth A, Kárpáti S.
    Exp Dermatol; 2003 Jun; 12(3):324-9. PubMed ID: 12823447
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