Search Results - Anneke I. den Hollander
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Omics Biomarkers in Ophthalmology by Susette Lauwen, Eiko K. de Jong, Dirk J. Lefeber, Anneke I. den Hollander
Published 2017Revisão -
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A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium by Eszter Emri, Elöd Körtvely, Sascha Dammeier, Franziska Klose, David Simpson, EYE-RISK Consortium Consortium, Anneke I. den Hollander, Marius Ueffing, Imre Lengyel
Published 2020Artigo -
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Genomic Copy Number Variations of the Complement Component<i>C4B</i>Gene Are Associated With Chronic Central Serous Chorioretinopathy by Myrte B. Breukink, Rosa L. Schellevis, Camiel J. F. Boon, Sascha Fauser, Carel B. Hoyng, Anneke I. den Hollander, Eiko K. de Jong
Published 2015Artigo -
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A Homozygous Missense Mutation in the<i>IRBP</i>Gene (<i>RBP3</i>) Associated with Autosomal Recessive Retinitis Pigmentosa by Anneke I. den Hollander, Terri L. McGee, Carmela Ziviello, Sandro Banfi, Thaddeus P. Dryja, Federico Gonzalez‐Fernandez, Debashis Ghosh, Eliot L. Berson
Published 2009Artigo -
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Cell culture models to study retinal pigment epithelium-related pathogenesis in age-related macular degeneration by Kapil Bharti, Anneke I. den Hollander, Aparna Lakkaraju, Debasish Sinha, David Williams, Silvia C. Finnemann, Catherine Bowes Rickman, Goldis Malek, Patricia A. D’Amore
Published 2022Revisão -
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Genetic Variants and Systemic Complement Activation Levels Are Associated With Serum Lipoprotein Levels in Age-Related Macular Degeneration by Constantin C. Paun, Lebriz Ersoy, Tina Schick, J.M.M. Groenewoud, Yara Lechanteur, Sascha Fauser, Carel B. Hoyng, Eiko K. de Jong, Anneke I. den Hollander
Published 2015Artigo -
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Implications of genetic variation in the complement system in age-related macular degeneration by Sarah de Jong, Giuliana Gagliardi, Alejandro Garanto, Anita de Breuk, Yara Lechanteur, Suresh Katti, Lambert P. van den Heuvel, Elena B. Volokhina, Anneke I. den Hollander
Published 2021Revisão -
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Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene by Camiel J.F. Boon, B. Jeroen Klevering, Carel B. Hoyng, Marijke N. Zonneveld-Vrieling, Sander B. Nabuurs, Ellen A.W. Blokland, Frans P.M. Cremers, Anneke I. den Hollander
Published 2008Artigo
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Biology
Genetics
Gene
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Ophthalmology
Macular degeneration
Phenotype
Retinal
Internal medicine
Mutation
Retinitis pigmentosa
Genotype
Biochemistry
Single-nucleotide polymorphism
Pathology
Retinal degeneration
Allele
Neuroscience
Bioinformatics
Complement system
Disease
Retina
Retinal pigment epithelium
Cell biology
Immunology
Missense mutation
Antibody
Factor H
Genome-wide association study
Cilium