Marneros AG - Search Results

1

Endogenous endostatin inhibits choroidal neovascularization.

Marneros AG, She H, Zambarakji H, Hashizume H, Connolly EJ, Kim I, Gragoudas ES, Miller JW, Olsen BR. Marneros AG, et al. FASEB J. 2007 Dec;21(14):3809-18. doi: 10.1096/fj.07-8422com. Epub 2007 May 25. FASEB J. 2007. PMID: 17526870

2

Age-dependent iris abnormalities in collagen XVIII/endostatin deficient mice with similarities to human pigment dispersion syndrome.

Marneros AG, Olsen BR. Marneros AG, et al. Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2367-72. doi: 10.1167/iovs.02-1180. Invest Ophthalmol Vis Sci. 2003. PMID: 12766032

3

Physiological role of collagen XVIII and endostatin.

Marneros AG, Olsen BR. Marneros AG, et al. FASEB J. 2005 May;19(7):716-28. doi: 10.1096/fj.04-2134rev. FASEB J. 2005. PMID: 15857886 Review.

4

The role of collagen-derived proteolytic fragments in angiogenesis.

Marneros AG, Olsen BR. Marneros AG, et al. Matrix Biol. 2001 Sep;20(5-6):337-45. doi: 10.1016/s0945-053x(01)00151-2. Matrix Biol. 2001. PMID: 11566268 Review.

5

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. Fukai N, et al. Among authors: marneros ag. EMBO J. 2002 Apr 2;21(7):1535-44. doi: 10.1093/emboj/21.7.1535. EMBO J. 2002. PMID: 11927538 Free PMC article.

6

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. Marneros AG, et al. EMBO J. 2004 Jan 14;23(1):89-99. doi: 10.1038/sj.emboj.7600014. Epub 2003 Dec 11. EMBO J. 2004. PMID: 14685281 Free PMC article.

7

Vascular endothelial growth factor expression in the retinal pigment epithelium is essential for choriocapillaris development and visual function.

Marneros AG, Fan J, Yokoyama Y, Gerber HP, Ferrara N, Crouch RK, Olsen BR. Marneros AG, et al. Am J Pathol. 2005 Nov;167(5):1451-9. doi: 10.1016/S0002-9440(10)61231-X. Am J Pathol. 2005. PMID: 16251428 Free PMC article.

8

Genome scans provide evidence for keloid susceptibility loci on chromosomes 2q23 and 7p11.

Marneros AG, Norris JE, Watanabe S, Reichenberger E, Olsen BR. Marneros AG, et al. J Invest Dermatol. 2004 May;122(5):1126-32. doi: 10.1111/j.0022-202X.2004.22327.x. J Invest Dermatol. 2004. PMID: 15140214 Free article.

9

Clinical genetics of familial keloids.

Marneros AG, Norris JE, Olsen BR, Reichenberger E. Marneros AG, et al. Arch Dermatol. 2001 Nov;137(11):1429-34. doi: 10.1001/archderm.137.11.1429. Arch Dermatol. 2001. PMID: 11708945

10

Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome.

Marneros AG, Mehenni H, Reichenberger E, Antonarakis SE, Krieg T, Olsen BR. Marneros AG, et al. Cytogenet Cell Genet. 2001;92(3-4):213-6. doi: 10.1159/000056905. Cytogenet Cell Genet. 2001. PMID: 11435690

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