6 results for author:"Grassi M.A." in Literature citations
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| Fas ligand-Fas signaling participates in light-induced apoptotic death in photoreceptor cells. Chang Q., Peter M.E., Grassi M.A. Invest. Ophthalmol. Vis. Sci. 53:3703-3716(2012) · Mapped (6) |
| Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs. Zhao C., Bellur D.L., Lu S., Zhao F., Grassi M.A., Bowne S.J., Sullivan L.S., Daiger S.P., Chen L.J., Pang C.P. et al. Am. J. Hum. Genet. 85:617-627(2009) · UniProtKB (1) · Mapped (10) |
| Mitochondrial variant G4132A is associated with familial non-arteritic anterior ischemic optic neuropathy in one large pedigree. Fingert J.H., Grassi M.A., Janutka J.C., East J.S., Howard J.G., Sheffield V.C., Jacobson D.M., Hayreh S.S., Stone E.M. Ophthalmic Genet. 28:1-7(2007) · Mapped (2) |
| Complement factor H polymorphism p.Tyr402His and cuticular Drusen. Grassi M.A., Folk J.C., Scheetz T.E., Taylor C.M., Sheffield V.C., Stone E.M. Arch. Ophthalmol. 125:93-97(2007) · Mapped (5) |
| Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His. Grassi M.A., Fingert J.H., Scheetz T.E., Roos B.R., Ritch R., West S.K., Kawase K., Shire A.M., Mullins R.F., Stone E.M. Hum. Mutat. 27:921-925(2006) · Mapped (5) |
| A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD). Sokal I., Dupps W.J., Grassi M.A., Brown J. Jr., Affatigato L.M., Roychowdhury N., Yang L., Filipek S., Palczewski K., Stone E.M. et al. Invest. Ophthalmol. Vis. Sci. 46:1124-1132(2005) · UniProtKB (1) · Mapped (2) |