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Retinal organoids differentiated form UiPSC of normal person and UiPSC containing OPA1 mutation
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创建时间：
2023-08-01
相关数据集
Electrophysiological characterization of photoreceptor-like cells in human inducible pluripotent stem cell-derived retinal organoids during in vitro maturation.
Retinal organoids (ROs) derived from human inducible pluripotent stem cells (hiPSCs) exhibit considerable therapeutic potential. However, current quality control of ROs during in vitro differentiation
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Single cell RNA-seq of CRX+ cells obtained at day 90 of retinal organoid differentiation. Single cell RNA-seq of CRX+ cells obtained at day 90 of retinal organoid differentiation
Death of photoreceptors and/or Retinal Pigment Epithelium (RPE) cells is a common cause of age related and inherited retinal dystrophies, thus their replenishment from renewable stem cell sources is a
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Annotation of a human retina organoid before and after imputation
Two Seurat-objects which include the unimputed and DCA-imputed retina organoid data sets, published by Kim et al. , stored in RDS-format.
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Spatial and temporal development of Müller glial cells in hiPSC-derived retinal organoids facilitating the cell enrichment and transcriptome analysis
Müller glial cells (MGs) play important roles in human retina during physiological and pathological conditions. However, there are still many obstacles to obtain large numbers of human MGs in vitro s
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Unveiling the Cellular and Molecular Mechanisms of Diabetic Retinopathy with Human Retinal Organoids
Diabetic retinopathy (DR) is a leading cause of vision impairment worldwide, driven by chronic hyperglycaemia and its complex metabolic consequences. While animal models have been widely used to study
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