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Results: 1-19 |
Results: 19
Gene therapy restores vision in a canine model of childhood blindness
Authors: Acland, GM Aguirre, GD Ray, J Zhang, Q Aleman, TS Cideciyan, AV Pearce-Kelling, SE Anand, V Zeng, Y Maguire, AM Jacobson, SG Hauswirth, WW Bennett, J
Citation: Gm. Acland et al., Gene therapy restores vision in a canine model of childhood blindness, NAT GENET, 28(1), 2001, pp. 92-95
Melatonin delays photoreceptor degeneration in the rds/rds mouse
Authors: Liang, FQ Aleman, TS Yang, ZX Cideciyan, AV Jacobson, SG Bennett, J
Citation: Fq. Liang et al., Melatonin delays photoreceptor degeneration in the rds/rds mouse, NEUROREPORT, 12(5), 2001, pp. 1011-1014
Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndrome
Authors: Aleman, TS Duncan, JL Bieber, ML de Castro, E Marks, DA Gardner, LM Steinberg, JD Cideciyan, AV Maguire, MG Jacobson, SG
Citation: Ts. Aleman et al., Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndrome, INV OPHTH V, 42(8), 2001, pp. 1873-1881
Phenotypic marker for early disease detection in dominant late-onset retinal degeneration
Authors: Jacobson, SG Cideciyan, AV Wright, E Wright, AF
Citation: Sg. Jacobson et al., Phenotypic marker for early disease detection in dominant late-onset retinal degeneration, INV OPHTH V, 42(8), 2001, pp. 1882-1890
Augmented rod bipolar cell function in partial receptor loss: an ERG studyin P23H rhodopsin transgenic and aging normal rats
Authors: Aleman, TS LaVail, MM Montemayor, R Ying, GS Maguire, MM Laties, AM Jacobson, SG Cideciyan, AV
Citation: Ts. Aleman et al., Augmented rod bipolar cell function in partial receptor loss: an ERG studyin P23H rhodopsin transgenic and aging normal rats, VISION RES, 41(21), 2001, pp. 2779-2797
A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophy
Authors: Poehner, WJ Fossarello, M Rapoport, AL Aleman, TS Cideciyan, AV Jacobson, SG Wright, AF Danciger, M Farber, DB
Citation: Wj. Poehner et al., A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophy, MOL VIS, 6(24), 2000, pp. 192-198
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
Authors: Haider, NB Jacobson, SG Cideciyan, AV Swiderski, R Streb, LM Searby, C Beck, G Hockey, R Hanna, DB Gorman, S Duhl, D Carmi, R Bennett, J Weleber, RG Fishman, GA Wright, AF Stone, EM Sheffield, VC
Citation: Nb. Haider et al., Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate, NAT GENET, 24(2), 2000, pp. 127-131
Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man
Authors: Cideciyan, AV Haeseleer, F Fariss, RN Aleman, TS Jang, GF Verlinde, CLMJ Marmor, MF Jacobson, SG Palczewski, K
Citation: Av. Cideciyan et al., Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man, VIS NEUROSC, 17(5), 2000, pp. 667-678
Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration
Authors: Milam, AH Curcio, CA Cideciyan, AV Saxena, S John, SK Kruth, HS Malek, G Heckenlively, JR Weleber, RG Jacobson, SG
Citation: Ah. Milam et al., Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration, OPHTHALMOL, 107(12), 2000, pp. 2256-2266
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa
Authors: Jacobson, SG Cideciyan, AV Iannaccone, A Weleber, RG Fishman, GA Maguire, AM Affatigato, LM Bennett, J Pierce, EA Danciger, M Farber, DB Stone, EM
Citation: Sg. Jacobson et al., Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa, INV OPHTH V, 41(7), 2000, pp. 1898-1908
Psychophysical evidence for rod vulnerability in age-related macular degeneration
Authors: Owsley, C Jackson, GR Cideciyan, AV Huang, YJ Fine, SL Ho, AC Maguire, MG Lolley, V Jacobson, SG
Citation: C. Owsley et al., Psychophysical evidence for rod vulnerability in age-related macular degeneration, INV OPHTH V, 41(1), 2000, pp. 267-273
In vivo assessment of photoreceptor function in human diseases caused by photoreceptor-specific gene mutations
Authors: Cideciyan, AV
Citation: Av. Cideciyan, In vivo assessment of photoreceptor function in human diseases caused by photoreceptor-specific gene mutations, METH ENZYM, 316, 2000, pp. 611-626
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness
Authors: Van Hooser, JP Aleman, TS He, YG Cideciyan, AV Kuksa, V Pittler, SJ Stone, EM Jacobson, SG Palczewski, K
Citation: Jp. Van Hooser et al., Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness, P NAS US, 97(15), 2000, pp. 8623-8628
Optical coherence tomography (OCT) abnormalities in rhodopsin mutant transgenic swine with retinal degeneration
Authors: Huang, YJ Cideciyan, AV Aleman, TS Banin, E Huang, JC Syed, NA Petters, RM Wong, F Milam, AH Jacobson, SG
Citation: Yj. Huang et al., Optical coherence tomography (OCT) abnormalities in rhodopsin mutant transgenic swine with retinal degeneration, EXP EYE RES, 70(2), 2000, pp. 247-251
Pitfalls in homozygosity mapping
Authors: Miano, MG Jacobson, SG Carothers, A Hanson, I Teague, P Lovell, J Cideciyan, AV Haider, N Stone, EM Sheffield, VC Wright, AF
Citation: Mg. Miano et al., Pitfalls in homozygosity mapping, AM J HU GEN, 67(5), 2000, pp. 1348-1351
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus
Authors: Guillonneau, X Piriev, NI Danciger, M Kozak, CA Cideciyan, AV Jacobson, SG Farber, DB
Citation: X. Guillonneau et al., A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus, HUM MOL GEN, 8(8), 1999, pp. 1541-1546
Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development
Authors: Banin, E Cideciyan, AV Aleman, TS Petters, RM Wong, F Milam, AH Jacobson, SG
Citation: E. Banin et al., Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development, NEURON, 23(3), 1999, pp. 549-557
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration
Authors: Lewis, CA Batlle, IR Batlle, KGR Banerjee, P Cideciyan, AV Huang, JC Aleman, TS Huang, YJ Ott, J Gilliam, TC Knowles, JA Jacobson, SG
Citation: Ca. Lewis et al., Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration, INV OPHTH V, 40(9), 1999, pp. 2106-2114
Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina
Authors: Bennett, J Maguire, AM Cideciyan, AV Schnell, M Glover, E Anand, V Aleman, TS Chirmule, N Gupta, AR Huang, YJ Gao, GP Nyberg, WC Tazelaar, J Hughes, J Wilson, JM Jacobson, SG
Citation: J. Bennett et al., Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina, P NAS US, 96(17), 1999, pp. 9920-9925
Risultati: 1-19 |