Last Updated: 09/26/2026
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Found 7 publications
Skeletal diseases caused by mutations in PTH1R show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTOR.
Journal: Frontiers in cell and developmental biology
Published: June 07, 2022
4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: December 30, 2020
Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia.
Journal: EBioMedicine
Published: July 28, 2020
Dominant-negative SOX9 mutations in campomelic dysplasia.
Journal: Human mutation
Published: April 12, 2019
The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling.
Journal: Science translational medicine
Published: April 19, 2018
Numerical simulations of odorant detection by biologically inspired sensor arrays.
Journal: Bioinspiration & biomimetics
Published: December 14, 2011
Showing 1-7 of 7
Last Updated: 09/26/2026