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/geo/query/acc.cgi?acc=GSE247889
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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. Jawbone cells isolated from mouse maxilar and madibular with collagenase/EDTA digestion and analyzed using scRNAseq
创建时间：
2023-12-01
