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Journal Abstract Search


359 related items for PubMed ID: 12766032

  • 1. Age-dependent iris abnormalities in collagen XVIII/endostatin deficient mice with similarities to human pigment dispersion syndrome.
    Marneros AG, Olsen BR.
    Invest Ophthalmol Vis Sci; 2003 Jun; 44(6):2367-72. PubMed ID: 12766032
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  • 3. Lack of type XVIII collagen results in anterior ocular defects.
    Ylikärppä R, Eklund L, Sormunen R, Kontiola AI, Utriainen A, Määttä M, Fukai N, Olsen BR, Pihlajaniemi T.
    FASEB J; 2003 Dec; 17(15):2257-9. PubMed ID: 14525950
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  • 6. Unilateral or asymmetric pseudoexfoliation syndrome? An ultrastructural study.
    Hammer T, Schlötzer-Schrehardt U, Naumann GO.
    Arch Ophthalmol; 2001 Jul; 119(7):1023-31. PubMed ID: 11448324
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  • 12. Localization of collagen XVIII and endostatin in the human eye.
    Ohlmann AV, Ohlmann A, Welge-Lüssen U, May CA.
    Curr Eye Res; 2005 Jan; 30(1):27-34. PubMed ID: 15875362
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  • 14. A histopathologic study of iris changes in pseudoexfoliation syndrome.
    Asano N, Schlötzer-Schrehardt U, Naumann GO.
    Ophthalmology; 1995 Sep; 102(9):1279-90. PubMed ID: 9097764
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  • 15. Localization of collagen XVIII and the endostatin portion of collagen XVIII in aged human control eyes and eyes with age-related macular degeneration.
    Bhutto IA, Kim SY, McLeod DS, Merges C, Fukai N, Olsen BR, Lutty GA.
    Invest Ophthalmol Vis Sci; 2004 May; 45(5):1544-52. PubMed ID: 15111613
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  • 16. Endostatin overexpression specifically in the lens and skin leads to cataract and ultrastructural alterations in basement membranes.
    Elamaa H, Sormunen R, Rehn M, Soininen R, Pihlajaniemi T.
    Am J Pathol; 2005 Jan; 166(1):221-9. PubMed ID: 15632014
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  • 17. Persistence of fetal vasculature in a patient with Knobloch syndrome: potential role for endostatin in fetal vascular remodeling of the eye.
    Duh EJ, Yao YG, Dagli M, Goldberg MF.
    Ophthalmology; 2004 Oct; 111(10):1885-8. PubMed ID: 15465551
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  • 18. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome.
    Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR.
    Am J Hum Genet; 2002 Dec; 71(6):1320-9. PubMed ID: 12415512
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  • 19. The exfoliation syndrome.
    Sugar HS, Harding C, Barsky D.
    Ann Ophthalmol; 1976 Oct; 8(10):1165-81. PubMed ID: 984637
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