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Journal Abstract Search

468 related items for PubMed ID: 10367729

  • 1. Mutation analysis and molecular genetics of epidermolysis bullosa.
    Pulkkinen L, Uitto J.
    Matrix Biol; 1999 Feb; 18(1):29-42. PubMed ID: 10367729
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  • 5. Ultrastructural findings in epidermolysis bullosa.
    Smith LT.
    Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
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  • 7. Molecular basis of the dystrophic and junctional forms of epidermolysis bullosa: mutations in the type VII collagen and kalinin (laminin 5) genes.
    Uitto J, Pulkkinen L, Christiano AM.
    J Invest Dermatol; 1994 Nov; 103(5 Suppl):39S-46S. PubMed ID: 7963683
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  • 9. Molecular basis of dystrophic epidermolysis bullosa: mutations in the type VII collagen gene (COL7A1).
    Järvikallio A, Pulkkinen L, Uitto J.
    Hum Mutat; 1997 Nov; 10(5):338-47. PubMed ID: 9375848
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  • 10. Genetic abnormalities and clinical classification of epidermolysis bullosa.
    Mitsuhashi Y, Hashimoto I.
    Arch Dermatol Res; 2003 Apr; 295 Suppl 1():S29-33. PubMed ID: 12677430
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  • 12. Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity.
    Uitto J, Pulkkinen L, McLean WH.
    Mol Med Today; 1997 Oct; 3(10):457-65. PubMed ID: 9358473
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  • 13. Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zone.
    Has C, Nyström A, Saeidian AH, Bruckner-Tuderman L, Uitto J.
    Matrix Biol; 2018 Oct; 71-72():313-329. PubMed ID: 29627521
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  • 18. Molecular pathology of the basement membrane zone in heritable blistering diseases:: The paradigm of epidermolysis bullosa.
    Uitto J, Has C, Vahidnezhad H, Youssefian L, Bruckner-Tuderman L.
    Matrix Biol; 2017 Jan; 57-58():76-85. PubMed ID: 27496350
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  • 20. The molecular basis for inherited bullous diseases.
    Korge BP, Krieg T.
    J Mol Med (Berl); 1996 Feb; 74(2):59-70. PubMed ID: 8820401
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