The identification of Ogfrl1 expressing cells in jawbone tissue
收藏NIAID Data Ecosystem2026-05-01 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP472183
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资源简介：
Human data demonstrates loss of function mutations of OGFRL1 are a cause of autosomal recessive forms of cherubism. However, the gene function of OGFRL1 is unknown. We performed scRNAseq to investigate the cell types expressing Ogfrl1 in jawbone tissue. Overall design: Jawbone cells isolated from mouse maxilar and madibular with collagenase/EDTA digestion and analyzed using scRNAseq
创建时间：
2023-12-01
