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Journal Abstract Search

376 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. 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 14; 44(6):2367-72. PubMed ID: 12766032
    [Abstract] [Full Text] [Related]

  • 5. Endogenous endostatin inhibits choroidal neovascularization.
    Marneros AG, She H, Zambarakji H, Hashizume H, Connolly EJ, Kim I, Gragoudas ES, Miller JW, Olsen BR.
    FASEB J; 2007 Dec 14; 21(14):3809-18. PubMed ID: 17526870
    [Abstract] [Full Text] [Related]

  • 6. Abnormal maturation of the retinal vasculature in type XVIII collagen/endostatin deficient mice and changes in retinal glial cells due to lack of collagen types XV and XVIII.
    Hurskainen M, Eklund L, Hägg PO, Fruttiger M, Sormunen R, Ilves M, Pihlajaniemi T.
    FASEB J; 2005 Sep 14; 19(11):1564-6. PubMed ID: 15976268
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 9. Increased angiogenic response in aortic explants of collagen XVIII/endostatin-null mice.
    Li Q, Olsen BR.
    Am J Pathol; 2004 Aug 14; 165(2):415-24. PubMed ID: 15277216
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. Endostatin affects osteoblast behavior in vitro, but collagen XVIII/endostatin is not essential for skeletal development in vivo.
    Sipola A, Seppinen L, Pihlajaniemi T, Tuukkanen J.
    Calcif Tissue Int; 2009 Nov 14; 85(5):412-20. PubMed ID: 19763371
    [Abstract] [Full Text] [Related]

  • 14. 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 14; 17(15):2257-9. PubMed ID: 14525950
    [Abstract] [Full Text] [Related]

  • 15. Structurally altered basement membranes and hydrocephalus in a type XVIII collagen deficient mouse line.
    Utriainen A, Sormunen R, Kettunen M, Carvalhaes LS, Sajanti E, Eklund L, Kauppinen R, Kitten GT, Pihlajaniemi T.
    Hum Mol Genet; 2004 Sep 15; 13(18):2089-99. PubMed ID: 15254016
    [Abstract] [Full Text] [Related]

  • 16. Collagen XVIII in tissue homeostasis and dysregulation - Lessons learned from model organisms and human patients.
    Heljasvaara R, Aikio M, Ruotsalainen H, Pihlajaniemi T.
    Matrix Biol; 2017 Jan 15; 57-58():55-75. PubMed ID: 27746220
    [Abstract] [Full Text] [Related]

  • 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 15; 111(10):1885-8. PubMed ID: 15465551
    [Abstract] [Full Text] [Related]

  • 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 15; 78(1):123-31. PubMed ID: 16532212
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

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