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Skeletal abnormalities caused by a Connexin43R239Q mutation in a mouse model for autosomal recessive craniometaphyseal dysplasia 年/期:2025/2被引:0 下载:0 | |
Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation 年/期:2025/2被引:0 下载:0 | |
Nuclear farnesoid X receptor protects against bone loss by driving osteoblast differentiation through stabilizing RUNX2 年/期:2025/2被引:0 下载:0 | |
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CCN2 mediates fibroblast-macrophage interaction in knee arthrofibrosis based on single-cell RNA-seq analysis 年/期:2025/2被引:0 下载:0 | |
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