These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
167 related articles for article (PubMed ID: 15254016)
1. 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; 13(18):2089-99. PubMed ID: 15254016 [TBL] [Abstract][Full Text] [Related]
2. Physiological role of collagen XVIII and endostatin. Marneros AG; Olsen BR FASEB J; 2005 May; 19(7):716-28. PubMed ID: 15857886 [TBL] [Abstract][Full Text] [Related]
3. 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 [TBL] [Abstract][Full Text] [Related]
4. 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; 27(6):535-46. PubMed ID: 18455382 [TBL] [Abstract][Full Text] [Related]
5. 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; 235(1):132-42. PubMed ID: 16170784 [TBL] [Abstract][Full Text] [Related]
6. 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 [TBL] [Abstract][Full Text] [Related]
7. Collagen XVIII modulation is altered during progression of oral dysplasia and carcinoma. Väänänen A; Ylipalosaari M; Parikka M; Kainulainen T; Rehn M; Heljasvaara R; Tjäderhane L; Salo T J Oral Pathol Med; 2007 Jan; 36(1):35-42. PubMed ID: 17181740 [TBL] [Abstract][Full Text] [Related]
8. 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; 19(11):1564-6. PubMed ID: 15976268 [TBL] [Abstract][Full Text] [Related]
9. 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 [TBL] [Abstract][Full Text] [Related]
10. Expression pattern of collagen XVIII and its cleavage product, the angiogenesis inhibitor endostatin, at the fetal-maternal interface. Pollheimer J; Bauer S; Huber A; Husslein P; Aplin JD; Knöfler M Placenta; 2004 Nov; 25(10):770-9. PubMed ID: 15451191 [TBL] [Abstract][Full Text] [Related]
11. 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; 21(9):1445-55. PubMed ID: 20616167 [TBL] [Abstract][Full Text] [Related]
14. Non-heparan sulfate-binding interactions of endostatin/collagen XVIII in murine development. Rychkova N; Stahl S; Gaetzner S; Felbor U Dev Dyn; 2005 Feb; 232(2):399-407. PubMed ID: 15614762 [TBL] [Abstract][Full Text] [Related]
15. 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; 23(1):77-84. PubMed ID: 14695535 [TBL] [Abstract][Full Text] [Related]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. Hydrocephalus-3, a murine mutant: I. Alterations in fine structure of choroid plexus and ependyma. Lawson RF; Raimondi AJ Surg Neurol; 1973 Mar; 1(2):115-28. PubMed ID: 4772794 [No Abstract] [Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]
19. Novel pathogenic mutations and skin biopsy analysis in Knobloch syndrome. Suzuki O; Kague E; Bagatini K; Tu H; Heljasvaara R; Carvalhaes L; Gava E; de Oliveira G; Godoi P; Oliva G; Kitten G; Pihlajaniemi T; Passos-Bueno MR Mol Vis; 2009; 15():801-9. PubMed ID: 19390655 [TBL] [Abstract][Full Text] [Related]
20. Increased angiogenic response in aortic explants of collagen XVIII/endostatin-null mice. Li Q; Olsen BR Am J Pathol; 2004 Aug; 165(2):415-24. PubMed ID: 15277216 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]