ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/006/SRR7169736/SRR7169736_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/004/SRR7169734/SRR7169734_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/003/SRR7169733/SRR7169733_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/007/SRR7169737/SRR7169737_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/004/SRR7169734/SRR7169734_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/005/SRR7169735/SRR7169735_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/005/SRR7169735/SRR7169735_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/006/SRR7169736/SRR7169736_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/003/SRR7169733/SRR7169733_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR716/007/SRR7169737/SRR7169737_2.fastq.gzprimaryOK200GenomicsShanghai Institute of Immunologyhttps://www.ebi.ac.uk/ena/browser/view/PRJNA471628Single NG2-glia with GFP fluorescence labeling from PDGFRαCreER mGFP mice was selected and aspirated into a glass pipette from hippocampal acute slices. In brief, cells were picked promptly by micromanipulation and immediately placed in lysis buffer. All NG2 glial cells were collected within 3 h after slice preparation. The selected NG2-glia were processed for single-cell RNA extraction and reverse transcription within 1 h and were subjected to RNA-sequencing.ENAfalseKir4.1 channels in NG2-glia play a role in development, potassium signaling, and ischemia-related myelin loss.2023-05-172018-05-19PRJNA471628