- ►iovs.org TS Aleman, AV Cideciyan, A Sumaroka, EAM … - Investigative Ophthalmology & Visual Science, 2008 - ARVO RESULTS. Class A patients had only cone-mediated vision. The outer nuclear layer
(ONL) thinned with eccentricity and was not detectable within 3 to 4 mm of the
fovea. Scotomatous extracentral retina showed loss of ONL, thickening of ... Cited by 14 - Related articles - BL Direct - All 2 versions
- ►nih.gov AV Cideciyan, M Swider, TS Aleman, MI … - Journal of the Optical Society of America A, 2007 - opticsinfobase.org Received July 31, 2006; revised September 21, 2006; accepted September 26, 2006;
posted October 2, 2006 (Doc. ID 73260); published April 11, 2007 The health of
the retinal pigment epithelium (RPE) can be estimated with autofluorescence ... Cited by 13 - Related articles - BL Direct - All 29 versions
- ►iovs.org DA White, WW Hauswirth, S Kaushal, AS … - Investigative ophthalmology & visual science, 2007 - ARVO METHODS. Mice were bred to express the hT17M rhodopsin transgene in a line that
was hemizygous null for wild-type mouse rhodopsin (mrho +/– ), and the eyes of
transgenic mice and nontransgenic littermates were exposed for 2.5 minutes ... Cited by 8 - Related articles - BL Direct - All 4 versions
- ►iovs.org V Chrysostomou, J Stone, S Stowe, NL Barnett … - Investigative Ophthalmology & Visual Science, 2008 - ARVO METHODS. P23H-3 rats were raised in scotopic cyclic (12 hours of 5 lux, 12 hours
of dark) ambient light. At postnatal day 90 to 130, some were transferred to
photopic conditions (12 hours of 300 lux, 12 hours of dark) for 1 week and ... Cited by 6 - Related articles - BL Direct - All 3 versions
- ►cjb.net BM Tam, OL Moritz - Journal of Neuroscience, 2007 - neuro.cjb.net To elucidate the molecular mechanisms underlying the light-sensitive retinal
degeneration caused by the rhodopsin mutation P23H, which causes retinitis
pigmentosa (RP) in humans, we expressed Xenopus laevis, bovine, human, and ... Cited by 5 - Related articles - All 3 versions
JE Young, EM Kasperek, TM Vogt, A Lis, SC … - Genomics, 2007 - Elsevier Rhodopsin kinase (RK) is a conserved component of the light adaptation and
recovery pathways shared among rod and cone photoreceptors of a variety of
species. To gain insight into transcriptional mechanisms driving RK and ... Cited by 4 - Related articles - All 4 versions
K Valter, DK Kirk, J Stone - Advances in experimental medicine and biology, 2008 - Springer Reviewing, in 1999, the non-genetic factors that regulate retinal degeneration,
we (Stone et al., 1999) hypothesized that the loss of vision during degeneration
results only partly from photoreceptor death. Significant visual loss ... Cited by 2 - Related articles - BL Direct - All 4 versions
DG Telander, MD Anthony de Beus, KW Small - members.medscape.com Overview: Retinitis pigmentosa (RP) is a group of inherited disorders characterized
by progressive peripheral vision loss and night vision difficulties (nyctalopia ... Cited by 1 - Related articles - Cached - All 3 versions
EE Biswas-Fiss - Ocular Transporters in Ophthalmic Diseases and Drug …, 2008 - Springer The retina-specific ABC transporter, ABCR, has been implicated in a wide
spectrum of inherited macular degenerations including Stargardt disease (STGD),
fundus flavimacula- tus (FFM) and autosomal recessive cone-rod dystrophy, ... Related articles - All 2 versions
D Gu, WA Beltran, S Pearce-Kelling, Z Li, GM … - Investigative Ophthalmology & Visual Science, 2009 - ARVO METHODS. The dogs were dark adapted overnight, eyes dilated with mydriatics; the
right eye was light occluded and the fundus of the left eye photographed (
15–17 overlapping frames) with a fundus camera. For biochemical studies, ... Related articles - All 3 versions
