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See Latest ArticlesLoss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
Human Molecular Genetics, 09/24/09
Narooie–Nejad M et al. – The p.Tyr1793fsX55 mutation affects an amino acid close to the C–terminal of the encoded protein. Subsequently, LTBP2 expression was shown in human eyes, including the trabecular meshwork and ciliary processes that are thought to be relevant to the etiology of PCG.
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MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma
Molecular Vision, 11/09/09
IL-33 shifts macrophage polarization, promoting resistance against Pseudomonas aeruginosa keratitis
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Understanding ischemic retinopathies: emerging concepts from oxygen-induced retinopathy
Documenta Ophthalmologica, 11/03/09
Today in Glaucoma...keeping you current
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Central Corneal Thickness During Treatment With Travoprost 0.004% in Glaucoma Patients
Journal of Ocular Pharmacology and Therapeutics, 11/02/09
Natural History of Open-Angle Glaucoma
Ophthalmology, 10/28/09
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