| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG0997-122A |
| P698 | PubMed publication ID | 9288113 |
| P2093 | author name string | R Allikmets | |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | photoreceptor protein | Q7187894 |
| P304 | page(s) | 122 | |
| P577 | publication date | 1997-09-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy | |
| P478 | volume | 17 |
| Q37091380 | A review of therapeutic prospects of non-viral gene therapy in the retinal pigment epithelium |
| Q90206579 | ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants |
| Q24301397 | ABCA5 resides in lysosomes, and ABCA5 knockout mice develop lysosomal disease-like symptoms |
| Q33541901 | Advances in imaging of Stargardt disease |
| Q31048292 | Age-related macular degeneration: epidemiology and optimal treatment |
| Q90748672 | Antioxidant Saffron and Central Retinal Function in ABCA4-Related Stargardt Macular Dystrophy |
| Q28084726 | Biology and therapy of inherited retinal degenerative disease: insights from mouse models |
| Q24651375 | Ceramide stimulates ABCA12 expression via peroxisome proliferator-activated receptor {delta} in human keratinocytes |
| Q28295779 | Chemistry of the retinoid (visual) cycle |
| Q33569372 | Complement modulation in the retinal pigment epithelium rescues photoreceptor degeneration in a mouse model of Stargardt disease |
| Q30500872 | Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease |
| Q33769321 | Decreased fixation stability of the preferred retinal location in juvenile macular degeneration. |
| Q34112207 | Deducing the pathogenic contribution of recessive ABCA4 alleles in an outbred population |
| Q89267042 | Disrupted cholesterol metabolism promotes age-related photoreceptor neurodegeneration |
| Q37591108 | Effective delivery of large genes to the retina by dual AAV vectors |
| Q94603167 | Exome sequencing analysis identifies novel homozygous mutation in ABCA4 in a Chinese family with Stargardt disease |
| Q58612184 | Expression of ABCA4 in the retinal pigment epithelium and its implications for Stargardt macular degeneration |
| Q50504065 | Foveal sparing in patients with Japanese Stargardt's disease and good visual acuity. |
| Q34234455 | Genetic basis of inherited macular dystrophies and implications for stem cell therapy. |
| Q43229069 | Genetics and ARMD. |
| Q92524765 | High-Resolution Adaptive Optics in Vivo Autofluorescence Imaging in Stargardt Disease |
| Q54981136 | High-throughput screening identifies kinase inhibitors that increase dual AAV vectors transduction in vitro and in mouse retina. |
| Q38265848 | Highly penetrant alleles in age-related macular degeneration |
| Q35484400 | Human organic anion transporting polypeptide 1A2 (OATP1A2) mediates cellular uptake of all-trans-retinol in human retinal pigmented epithelial cells |
| Q34701967 | Identification of a promoter for the human C1Q-tumor necrosis factor-related protein-5 gene associated with late-onset retinal degeneration |
| Q28361881 | Isomerization of 11-cis-retinoids to all-trans-retinoids in vitro and in vivo |
| Q28538229 | Molecular diagnosis of putative Stargardt disease by capture next generation sequencing |
| Q37273740 | Molecular pathology of age-related macular degeneration |
| Q64098583 | Multi-platform imaging in ABCA4-Associated Disease |
| Q36172144 | Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus |
| Q37264277 | Na+ coordination at the Na2 site of the Na+/I- symporter |
| Q37548619 | Novel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease |
| Q37235131 | Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family |
| Q93095010 | RETINAL FLECKS IN STARGARDT DISEASE REVEAL CHARACTERISTIC FLUORESCENCE LIFETIME TRANSITION OVER TIME |
| Q26796608 | STRA6: role in cellular retinol uptake and efflux |
| Q92636130 | Scavenging of Retinoid Cation Radicals by Urate, Trolox, and α-, β-, γ-, and δ-Tocopherols |
| Q41866189 | Stargardt disease: towards developing a model to predict phenotype. |
| Q33603580 | Synthesis and characterization of glycol chitosan DNA nanoparticles for retinal gene delivery |
| Q39158595 | The impact of the human genome project on complex disease |
| Q35676416 | The influence of genetics on response to treatment with ranibizumab (Lucentis) for age-related macular degeneration: the Lucentis Genotype Study (an American Ophthalmological Society thesis). |
| Q36405906 | The role of inflammation in the pathogenesis of age-related macular degeneration |
| Q64953637 | Variants in the ABCA4 gene in a Brazilian population with Stargardt disease. |
Search more.