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Journal of Neuroscience Research|October 15, 1993
Retinal morphology and visual pigment levels in 6- and 12-month-old rhesus monkeys fed a taurine-free human infant formulaH Imaki, S G Jacobson, C M Kemp, et al.Experimental Eye Research|October 1, 1987
Rhodopsin topography and rod-mediated function in cats with the retinal degeneration of taurine deficiencyS G Jacobson, C M Kemp, F X Borruat, et al.Ophthalmic Genetics|March 1, 1996
Analysis of phosducin as a candidate gene for retinopathiesF Ara-Iwata, S G Jacobson, J D Gass, et al.Documenta Ophthalmologica. Advances in Ophthalmology|January 18, 2024
ISCEV and IPS guideline for the full-field stimulus test (FST)J K Jolly, J R Grigg, A M McKendrick, et al.Investigative Ophthalmology & Visual Science|January 1, 1993
Autoantibodies against retinal bipolar cells in cutaneous melanoma-associated retinopathyA H Milam, J C Saari, S G Jacobson, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1992
Ultrastructure of connecting cilia in different forms of retinitis pigmentosaS D Barrong, M H Chaitin, S J Fliesler, et al.Human Molecular Genetics|August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6pJ A Knowles, Y Shugart, P Banerjee, et al.Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.Genomics|November 1, 1995
Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosaM Danciger, J Blaney, Y Q Gao, et al.Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.Pageof 13