官方服务：
资源简介：
Investigate subretinal microglia and RPE cell by RNA-seq
应用场景：
创建时间：
2025-12-31
相关数据集
Identification of the retinoschisin-binding site on the retinal Na/K-ATPase
X-linked juvenile retinoschisis (XLRS) is a hereditary retinal dystrophy, caused by mutations in the RS1 gene which encodes the secreted protein retinoschisin. In recent years, several molecules have
NIAID Data Ecosystem50
scRNAseq comparison of iPSC-derived retinal organoids from Control and LCA7 patients
To comprehensively capture changes in retinal transcriptome for the LCA7 organoids compared to control, we performed single cell RNA-sequencing (scRNAseq) using the 10X Genomics platform. Retinal orga
NIAID Data Ecosystem30
Crystal Structure of the human Retinitis Pigmentosa protein 2 (RP2)
Crystal Structure of the human Retinitis Pigmentosa protein 2 (RP2) Descriptor: SULFATE ION, XRP2 PROTEIN Authors: Kuhnel, K, Veltel, S, Schlichting, I, Wittinghofer, A. Deposit date: 2005-07-24 Relea
Protein Data Bank Japan2024-05-08 更新20
Additional file 4: of RNAseq analysis of hippocampal microglia after kainic acid-induced seizures
Table S3. List of all identifed molecular function GO terms. (XLSX 23 kb)
Figshare2018-06-21 更新40
MicroRNA profiling of mouse wild type (C57) retina and a retina from a mouse model of retinitis pigmentosa (Pro347Ser)
MicroRNA profiling of mouse wild type (C57) retina and a retina from a mouse model of retinitis pigmentosa (Pro347Ser)
ChEBI2007-11-22 更新20
