Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation
骨骼祖细胞 LRP1 缺乏会导致严重且持续的骨骼缺陷,并伴有 Wnt 通路失调
期刊:Bone Research
影响因子:14.3
doi:10.1038/s41413-024-00393-x
Mohammad Alhashmi #, Abdulrahman M E Gremida #, Santosh K Maharana, Marco Antonaci, Amy Kerr, Shijian Fu, Sharna Lunn, David A Turner, Noor A Al-Maslamani, Ke Liu, Maria M Meschis, Hazel Sutherland, Peter Wilson, Peter Clegg, Grant N Wheeler, Robert J van 't Hof, George Bou-Gharios, Kazuhiro Yamamot
免疫
细胞生物学
其它细胞
Wnt/β-Catenin
Wnt5a