|
Bidinost, Carla; Hernandez, Natalie; Edward, Deepak P et al. (2006) Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humans. Invest Ophthalmol Vis Sci 47:1486-90
|
|
Doshi, Manali; Marcus, Craig; Bejjani, Bassem A et al. (2006) Immunolocalization of CYP1B1 in normal, human, fetal and adult eyes. Exp Eye Res 82:24-32
|
|
Edward, Deepak; Al Rajhi, Ali; Lewis, Richard Alan et al. (2004) Molecular basis of Peters anomaly in Saudi Arabia. Ophthalmic Genet 25:257-70
|
|
Curry, Stacey M; Daou, Aline G; Hermanns, Pia et al. (2004) Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador. Ophthalmic Genet 25:3-9
|
|
Katsanis, Nicholas; Worley, Kim C; Gonzalez, Guillermo et al. (2002) A computational/functional genomics approach for the enrichment of the retinal transcriptome and the identification of positional candidate retinopathy genes. Proc Natl Acad Sci U S A 99:14326-31
|
|
Bejjani, Bassem A; Xu, Li; Armstrong, Dawna et al. (2002) Expression patterns of cytochrome P4501B1 (Cyp1b1) in FVB/N mouse eyes. Exp Eye Res 75:249-57
|
|
Shroyer, N F; Lewis, R A; Yatsenko, A N et al. (2001) Null missense ABCR (ABCA4) mutations in a family with stargardt disease and retinitis pigmentosa. Invest Ophthalmol Vis Sci 42:2757-61
|
|
Katsanis, N; Worley, K C; Lupski, J R (2001) An evaluation of the draft human genome sequence. Nat Genet 29:88-91
|
|
Shroyer, N F; Lewis, R A; Yatsenko, A N et al. (2001) Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration. Hum Mol Genet 10:2671-8
|
|
Katsanis, N; Venable, S; Smith, J R et al. (2000) Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13. Hum Genet 106:66-72
|
Showing the most recent 10 out of 14 publications
