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Journal Abstract Search


375 related items for PubMed ID: 15857886

  • 1. Physiological role of collagen XVIII and endostatin.
    Marneros AG, Olsen BR.
    FASEB J; 2005 May; 19(7):716-28. PubMed ID: 15857886
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  • 2. The multiple functions of collagen XVIII in development and disease.
    Seppinen L, Pihlajaniemi T.
    Matrix Biol; 2011 Mar; 30(2):83-92. PubMed ID: 21163348
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  • 3. Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial function.
    Marneros AG, Keene DR, Hansen U, Fukai N, Moulton K, Goletz PL, Moiseyev G, Pawlyk BS, Halfter W, Dong S, Shibata M, Li T, Crouch RK, Bruckner P, Olsen BR.
    EMBO J; 2004 Jan 14; 23(1):89-99. PubMed ID: 14685281
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  • 7. Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin.
    Menzel O, Bekkeheien RC, Reymond A, Fukai N, Boye E, Kosztolanyi G, Aftimos S, Deutsch S, Scott HS, Olsen BR, Antonarakis SE, Guipponi M.
    Hum Mutat; 2004 Jan 14; 23(1):77-84. PubMed ID: 14695535
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  • 8. Non-heparan sulfate-binding interactions of endostatin/collagen XVIII in murine development.
    Rychkova N, Stahl S, Gaetzner S, Felbor U.
    Dev Dyn; 2005 Feb 14; 232(2):399-407. PubMed ID: 15614762
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  • 10. Lack of collagen XVIII/endostatin exacerbates immune-mediated glomerulonephritis.
    Hamano Y, Okude T, Shirai R, Sato I, Kimura R, Ogawa M, Ueda Y, Yokosuka O, Kalluri R, Ueda S.
    J Am Soc Nephrol; 2010 Sep 14; 21(9):1445-55. PubMed ID: 20616167
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  • 11. Lack of collagen XVIII accelerates cutaneous wound healing, while overexpression of its endostatin domain leads to delayed healing.
    Seppinen L, Sormunen R, Soini Y, Elamaa H, Heljasvaara R, Pihlajaniemi T.
    Matrix Biol; 2008 Jul 14; 27(6):535-46. PubMed ID: 18455382
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  • 12. The collagen type XVIII endostatin domain is co-localized with perlecan in basement membranes in vivo.
    Miosge N, Simniok T, Sprysch P, Herken R.
    J Histochem Cytochem; 2003 Mar 14; 51(3):285-96. PubMed ID: 12588956
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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 14; 111(10):1885-8. PubMed ID: 15465551
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  • 18. Mutations in collagen 18A1 and their relevance to the human phenotype.
    Passos-Bueno MR, Suzuki OT, Armelin-Correa LM, Sertié AL, Errera FI, Bagatini K, Kok F, Leite KR.
    An Acad Bras Cienc; 2006 Mar 14; 78(1):123-31. PubMed ID: 16532212
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  • 19. Lack of collagen XVIII/endostatin results in eye abnormalities.
    Fukai N, Eklund L, Marneros AG, Oh SP, Keene DR, Tamarkin L, Niemelä M, Ilves M, Li E, Pihlajaniemi T, Olsen BR.
    EMBO J; 2002 Apr 02; 21(7):1535-44. PubMed ID: 11927538
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  • 20. Collagen XVIII/endostatin is associated with the epithelial-mesenchymal transformation in the atrioventricular valves during cardiac development.
    Carvalhaes LS, Gervásio OL, Guatimosim C, Heljasvaara R, Sormunen R, Pihlajaniemi T, Kitten GT.
    Dev Dyn; 2006 Jan 02; 235(1):132-42. PubMed ID: 16170784
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