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Nutritional risk factors for age-related macular degeneration.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Nutritional Risk Factors for Age-Related Macular Degeneration.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/413150
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- Publication type:
- Article
Characterization of XAGE-1b, a short major transcript of cancer/testis-associated gene XAGE-1, induced in melanoma metastasis.
- Published in:
- International Journal of Cancer, 2002, v. 97, n. 2, p. 195, doi. 10.1002/ijc.1584
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- Publication type:
- Article
A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium.
- Published in:
- Nutrients, 2020, v. 12, n. 10, p. 3051, doi. 10.3390/nu12103051
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- Publication type:
- Article
Exploring the Use of Molecular Biomarkers for Precision Medicine in Age-Related Macular Degeneration.
- Published in:
- Molecular Diagnosis & Therapy, 2018, v. 22, n. 3, p. 315, doi. 10.1007/s40291-018-0332-1
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- Publication type:
- Article
Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndrome.
- Published in:
- Neurogenetics, 2016, v. 17, n. 1, p. 17, doi. 10.1007/s10048-015-0462-0
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- Publication type:
- Article
Exome sequencing in patients with chronic central serous chorioretinopathy.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-43152-3
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- Publication type:
- Article
Genetic risk score has added value over initial clinical grading stage in predicting disease progression in age-related macular degeneration.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-43144-3
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- Publication type:
- Article
Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 1, p. 230, doi. 10.1093/hmg/ddu441
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- Publication type:
- Article
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 22, p. 6081, doi. 10.1093/hmg/ddu307
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- Publication type:
- Article
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3174, doi. 10.1093/hmg/ddt169
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- Publication type:
- Article
Non-syndromic retinal ciliopathies: translating gene discovery into therapy.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. R1, p. R111, doi. 10.1093/hmg/dds298
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- Publication type:
- Article
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 9, p. 1559, doi. 10.1093/hmg/ddl079
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- Publication type:
- Article
Towards understanding CRUMBS function in retinal dystrophies.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 2, p. r235, doi. 10.1093/hmg/ddl195
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- Publication type:
- Article
Towards understanding CRUMBS function in retinal dystrophies.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R235, doi. 10.1093/hmg/ddl195
- By:
- Publication type:
- Article
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 24, p. 3865, doi. 10.1093/hmg/ddi411
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- Publication type:
- Article
Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 2, p. 255, doi. 10.1093/hmg/ddi023
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- Publication type:
- Article
Comparing half-dose photodynamic therapy with high-density subthreshold micropulse laser treatment in patients with chronic central serous chorioretinopathy (the PLACE trial): study protocol for a randomized controlled trial.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Regulation of ABCA1 by AMD-Associated Genetic Variants and Hypoxia in iPSC-RPE.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 6, p. 3194, doi. 10.3390/ijms23063194
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- Publication type:
- Article
Variants in the <italic>PRPF8</italic> Gene are Associated with Glaucoma.
- Published in:
- Molecular Neurobiology, 2018, v. 55, n. 5, p. 4504, doi. 10.1007/s12035-017-0673-5
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- Publication type:
- Article
Identification of <italic>TP53BP2</italic> as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family.
- Published in:
- Molecular Neurobiology, 2018, v. 55, n. 2, p. 1387, doi. 10.1007/s12035-017-0403-z
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- Publication type:
- Article
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 2, p. 155, doi. 10.1038/sj.ejhg.5200942
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- Publication type:
- Article
Imaging diabetic retinal disease: clinical imaging requirements.
- Published in:
- Acta Ophthalmologica (1755375X), 2022, v. 100, n. 7, p. 752, doi. 10.1111/aos.15110
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- Publication type:
- Article
The use of eplerenone in therapy-resistant chronic central serous chorioretinopathy.
- Published in:
- Acta Ophthalmologica (1755375X), 2014, v. 92, n. 6, p. e488, doi. 10.1111/aos.12392
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- Publication type:
- Article
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.
- Published in:
- Nature Genetics, 2015, v. 47, n. 7, p. 757, doi. 10.1038/ng.3319
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- Publication type:
- Article
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis.
- Published in:
- Nature Genetics, 2010, v. 42, n. 2, p. 175, doi. 10.1038/ng.519
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- Publication type:
- Article
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
- Published in:
- Nature Genetics, 2009, v. 41, n. 6, p. 739, doi. 10.1038/ng.366
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- Publication type:
- Article
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 7, p. 889, doi. 10.1038/ng2066
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- Publication type:
- Article
Analysis of hemopexin plasma levels in patients with age-related macular degeneration.
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- Molecular Vision, 2022, v. 28, p. 536
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- Publication type:
- Article
Genetic and environmental risk factors for reticular pseudodrusen in the EUGENDA study.
- Published in:
- Molecular Vision, 2021, v. 27, p. 757
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- Publication type:
- Article
Genetic and environmental risk factors for extramacular drusen.
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- Molecular Vision, 2020, v. 26, p. 661
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- Publication type:
- Article
Geographic distribution of rare variants associated with agerelated macular degeneration.
- Published in:
- Molecular Vision, 2018, v. 24, p. 75
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- Publication type:
- Article
Identification of an Amino Acid Motif in HLA–DRβ1 That Distinguishes Uveitis in Patients With Juvenile Idiopathic Arthritis.
- Published in:
- Arthritis & Rheumatology, 2018, v. 70, n. 7, p. 1155, doi. 10.1002/art.40484
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- Publication type:
- Article
Major Predictive Factors for Progression of Early to Late Age-Related Macular Degeneration.
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- Ophthalmologica, 2020, v. 243, n. 6, p. 444, doi. 10.1159/000507196
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- Publication type:
- Article
Corrigendum to “Nutritional Risk Factors for Age-Related Macular Degeneration”.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/7589328
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- Publication type:
- Article
A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290.
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- Genes, 2017, v. 8, n. 8, p. 208, doi. 10.3390/genes8080208
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- Publication type:
- Article
The Molecular Basis of Retinal Dystrophies in Pakistan.
- Published in:
- Genes, 2014, v. 5, n. 1, p. 176, doi. 10.3390/genes5010176
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- Publication type:
- Article
Alteration of retinal layers in healthy subjects over 60 years of age until nonagenarians.
- Published in:
- Clinical Ophthalmology, 2017, v. 11, p. 1499, doi. 10.2147/OPTH.S137223
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- Publication type:
- Article
Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes.
- Published in:
- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0608-2
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- Publication type:
- Article
Common and rare variants in patients with early onset drusen maculopathy.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 5, p. 414, doi. 10.1111/cge.14212
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- Publication type:
- Article
Genetic screening for macular dystrophies in patients clinically diagnosed with dry age‐related macular degeneration.
- Published in:
- Clinical Genetics, 2018, v. 94, n. 6, p. 569, doi. 10.1111/cge.13447
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- Publication type:
- Article
Chronic central serous chorioretinopathy: long-term follow-up and vision-related quality of life.
- Published in:
- Clinical Ophthalmology, 2017, v. 11, p. 39, doi. 10.2147/OPTH.S115685
- By:
- Publication type:
- Article
Zinc Supplementation Inhibits Complement Activation in Age-Related Macular Degeneration.
- Published in:
- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0112682
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- Publication type:
- Article
Association of a Polymorphism in the <i>BIRC6</i> Gene with Pseudoexfoliative Glaucoma.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105023
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- Publication type:
- Article
Analysis of Rare Variants in the <i>C3</i> Gene in Patients with Age-Related Macular Degeneration.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094165
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- Publication type:
- Article
Impact of the Common Genetic Associations of Age-Related Macular Degeneration upon Systemic Complement Component C3d Levels.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0093459
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- Publication type:
- Article
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0051622
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- Publication type:
- Article
The p53 Codon 72 PRO/PRO Genotype May Be Associated with Initial Central Visual Field Defects in Caucasians with Primary Open Angle Glaucoma.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045613
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- Publication type:
- Article
Melanoregulin, Product of the dsu Locus, Links the BLOC-Pathway and Oa1 in Organelle Biogenesis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0042446
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- Publication type:
- Article
Expression of Wild-Type Rp1 Protein in Rp1 Knock-in Mice Rescues the Retinal Degeneration Phenotype.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043251
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- Publication type:
- Article