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H Milam

Showing results (81-90 of 104) with videos related to

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American Journal of Ophthalmology|March 1, 2005
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15F Yesim K Demirci, Nisha Gupta, Amy L Radak, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.
Experimental Eye Research|October 22, 2002
Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15Gustavo D Aguirre, Beverly M Yashar, Sinoj K John, et al.
Glia|December 31, 1997
Cellular retinaldehyde-binding protein is expressed by oligodendrocytes in optic nerve and brainJ C Saari, J Huang, D E Possin, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2Bo Chang, Mark S Dacey, Norm L Hawes, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR geneS G Jacobson, M Buraczynska, A H Milam, et al.
Experimental Eye Research|February 1, 1995
Evidence of retinoid metabolism within cells of inner retinaJ C Saari, J Huang, M A Asson-Batres, et al.
The Journal of Biological Chemistry|July 31, 2001
Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptorsP K Swain, D Hicks, A J Mears, et al.
Investigative Ophthalmology & Visual Science|February 26, 2003
Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3Artur V Cideciyan, Samuel G Jacobson, Nisha Gupta, et al.
Molecular Vision|July 5, 2001
Localization of pigment epithelium derived factor (PEDF) in developing and adult human ocular tissuesP C Karakousis, S K John, K C Behling, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
American Journal of Ophthalmology|March 1, 2005
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15F Yesim K Demirci, Nisha Gupta, Amy L Radak, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.
Experimental Eye Research|October 22, 2002
Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15Gustavo D Aguirre, Beverly M Yashar, Sinoj K John, et al.
Glia|December 31, 1997
Cellular retinaldehyde-binding protein is expressed by oligodendrocytes in optic nerve and brainJ C Saari, J Huang, D E Possin, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2Bo Chang, Mark S Dacey, Norm L Hawes, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR geneS G Jacobson, M Buraczynska, A H Milam, et al.
Experimental Eye Research|February 1, 1995
Evidence of retinoid metabolism within cells of inner retinaJ C Saari, J Huang, M A Asson-Batres, et al.
The Journal of Biological Chemistry|July 31, 2001
Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptorsP K Swain, D Hicks, A J Mears, et al.
Investigative Ophthalmology & Visual Science|February 26, 2003
Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3Artur V Cideciyan, Samuel G Jacobson, Nisha Gupta, et al.
Molecular Vision|July 5, 2001
Localization of pigment epithelium derived factor (PEDF) in developing and adult human ocular tissuesP C Karakousis, S K John, K C Behling, et al.
Pageof 11