The orphan nuclear hormone ERRb regulates rod photoreceptor development and survival
Onishi A, Peng G-H, Chen J, Lee DA, Alexis, U, Poth E, de Melo J, Chen S, and Blackshaw S. Proc Natl Acad Sci USA 2010 107:11579-84.
The inherited blindness associated protein, AIPL1, interacts with the cell-cycle regulator protein, NUB1
Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Blackshaw S, Fukuda-Kamitani T, Daiger SP, Craft C, Kamitani T, Sohocki MM. Hum Mol Genet 2002 11:2723-33.
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
Browne SJ, Sullivan LS, Blanton SH, Cepko CL, Blackshaw S, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. Hum Mol Genet 2002 11:559-568.
Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes
Blackshaw S, Fraioli RE, Furukawa T, Cepko CL. Cell 2001 107:579-89.
Heme oxygenase-2 acts to prevent neuronal death in brain cultures and following transient cerebral ischemia
Dore S, Goto S, Sampei K, Blackshaw S, Hester LD, Ingi T, Sawa A, Traystman RJ, Koehler RC, Snyder SH. Neuroscience 2000 99:587-92.
Type 3 inositol 1,4,5-triphosphate receptor modulates cell death
Blackshaw S, Sawa A, Snyder SH, Khan A. FASEB J 2000 14:1375-1379.
Mutations in a new photoreceptor-pineal gene on 17p cause Leber’s congenital amaurosis
Sohocki M M, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, BhattacharyaSS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. Nat Genet 2000 24:79
Heme oxygenase-2 is neuroprotective in focal cerebral ischemia
Dore S, Sampi K, Goto S, Alkayed NJ, Blackshaw S, Gallagher M, Traysman RJ, Hurn PD, Guastella D, Koehler RC, Snyder SH. Mol Med 1999; 5:656-663.22.