Хайлтын үр дүнгүүд - Anneke I. den Hollander
- 88-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Omics Biomarkers in Ophthalmology -н Susette Lauwen, Eiko K. de Jong, Dirk J. Lefeber, Anneke I. den Hollander
Хэвлэсэн 2017Revisão -
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Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290 -н Rob W.J. Collin, Anneke I. den Hollander, Saskia D. van der Velde-Visser, Jeannette Bennicelli, Jean Bennett, Frans P.M. Cremers
Хэвлэсэн 2012Artigo -
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A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium -н Eszter Emri, Elöd Körtvely, Sascha Dammeier, Franziska Klose, David Simpson, EYE-RISK Consortium Consortium, Anneke I. den Hollander, Marius Ueffing, Imre Lengyel
Хэвлэсэн 2020Artigo -
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Genomic Copy Number Variations of the Complement Component<i>C4B</i>Gene Are Associated With Chronic Central Serous Chorioretinopathy -н Myrte B. Breukink, Rosa L. Schellevis, Camiel J. F. Boon, Sascha Fauser, Carel B. Hoyng, Anneke I. den Hollander, Eiko K. de Jong
Хэвлэсэн 2015Artigo -
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A Homozygous Missense Mutation in the<i>IRBP</i>Gene (<i>RBP3</i>) Associated with Autosomal Recessive Retinitis Pigmentosa -н Anneke I. den Hollander, Terri L. McGee, Carmela Ziviello, Sandro Banfi, Thaddeus P. Dryja, Federico Gonzalez‐Fernandez, Debashis Ghosh, Eliot L. Berson
Хэвлэсэн 2009Artigo -
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Cell culture models to study retinal pigment epithelium-related pathogenesis in age-related macular degeneration -н Kapil Bharti, Anneke I. den Hollander, Aparna Lakkaraju, Debasish Sinha, David Williams, Silvia C. Finnemann, Catherine Bowes Rickman, Goldis Malek, Patricia A. D’Amore
Хэвлэсэн 2022Revisão -
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Genetic Variants and Systemic Complement Activation Levels Are Associated With Serum Lipoprotein Levels in Age-Related Macular Degeneration -н 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
Хэвлэсэн 2015Artigo -
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Implications of genetic variation in the complement system in age-related macular degeneration -н 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
Хэвлэсэн 2021Revisão -
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Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene -н 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
Хэвлэсэн 2008Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Genetics
Gene
Medicine
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