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Journal Abstract Search

184 related items for PubMed ID: 3115194

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  • 3. Abnormal formation of collagen cross-links in skin fibroblasts cultured from patients with Ehlers-Danlos syndrome type VI.
    Pasquali M, Still MJ, Vales T, Rosen RI, Evinger JD, Dembure PP, Longo N, Elsas LJ.
    Proc Assoc Am Physicians; 1997 Jan; 109(1):33-41. PubMed ID: 9010914
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  • 4. Collagen synthesis by cultured skin fibroblasts from siblings with hydroxylysine-deficient collagen.
    Quinn RS, Krane SM.
    Biochim Biophys Acta; 1979 Jul 18; 585(4):589-98. PubMed ID: 465542
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  • 5. Ehlers-Danlos syndrome type VI: collagen type specificity of defective lysyl hydroxylation in various tissues.
    Ihme A, Krieg T, Nerlich A, Feldmann U, Rauterberg J, Glanville RW, Edel G, Müller PK.
    J Invest Dermatol; 1984 Sep 18; 83(3):161-5. PubMed ID: 6432919
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  • 6. Ascorbate regulation of collagen biosynthesis in Ehlers-Danlos syndrome, type VI.
    Dembure PP, Janko AR, Priest JH, Elsas LJ.
    Metabolism; 1987 Jul 18; 36(7):687-91. PubMed ID: 3110540
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  • 8. Ehlers-Danlos syndrome. A variant characterized by the deficiency of pro alpha 2 chain of type I procollagen.
    Sasaki T, Arai K, Ono M, Yamaguchi T, Furuta S, Nagai Y.
    Arch Dermatol; 1987 Jan 18; 123(1):76-9. PubMed ID: 3800425
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  • 9. Biochemical characterization of variants of the Ehlers-Danlos syndrome type VI.
    Ihme A, Risteli L, Krieg T, Risteli J, Feldmann U, Kruse K, Müller PK.
    Eur J Clin Invest; 1983 Aug 18; 13(4):357-62. PubMed ID: 6413223
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  • 10. Adenoviral gene transfer restores lysyl hydroxylase activity in type VI Ehlers-Danlos syndrome.
    Rauma T, Kumpumäki S, Anderson R, Davidson BL, Ruotsalainen H, Myllylä R, Hautala T.
    J Invest Dermatol; 2001 Apr 18; 116(4):602-5. PubMed ID: 11286629
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  • 11. Preferential hydroxylation of type IV collagen by lysyl hydroxylase from Ehlers-Danlos syndrome type VI fibroblasts.
    Risteli L, Risteli J, Ihme A, Krieg T, Müller PK.
    Biochem Biophys Res Commun; 1980 Oct 31; 96(4):1778-84. PubMed ID: 6778480
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  • 13. Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene.
    Walker LC, Teebi AS, Marini JC, De Paepe A, Malfait F, Atsawasuwan P, Yamauchi M, Yeowell HN.
    Mol Genet Metab; 2004 Dec 31; 83(4):312-21. PubMed ID: 15589118
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  • 15. Low levels of serum type III procollagen aminoterminal propeptide confirmed type III collagen deficiency in patients without typical clinical symptoms of Ehlers-Danlos type IV.
    Dyne KM, Zanaboni G, Annoni G, De Agostini MP, Cetta G.
    Eur J Clin Invest; 1989 Aug 31; 19(4):362-6. PubMed ID: 2506053
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  • 16. Biochemical and immunological studies of fibroblasts derived from a patient with Ehlers-Danlos syndrome type IV. Demonstrate reduced type III collagen synthesis.
    Aumailley M, Krieg T, Dessau W, Müller PK, Timpl R, Bricaud H.
    Arch Dermatol Res; 1980 Aug 31; 269(2):169-77. PubMed ID: 7458408
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  • 18. Patients with Ehlers-Danlos syndrome type IV lack type III collagen.
    Pope FM, Martin GR, Lichtenstein JR, Penttinen R, Gerson B, Rowe DW, McKusick VA.
    Proc Natl Acad Sci U S A; 1975 Apr 31; 72(4):1314-6. PubMed ID: 1055406
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  • 19. Inheritance of Ehlers-Danlos type IV syndrome.
    Pope FM, Martin GR, McKusick VA.
    J Med Genet; 1977 Jun 31; 14(3):200-4. PubMed ID: 881711
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