Showing results 1 to 5 of 5
Title | Author(s) | Issue Date | Views | |
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Activating the unfolded protein response in osteocytes causes hyperostosis consistent with craniodiaphyseal dysplasia Journal:Human Molecular Genetics | 2017 | |||
Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestations Journal:Orphanet Journal of Rare Diseases | 2022 | 2 | ||
Regulation and Role of Transcription Factors in Osteogenesis Journal:International Journal of Molecular Sciences | 2021 | |||
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients Journal:Orphanet Journal of Rare Diseases | 20-Sep-2023 | |||
Single cell analyses of human intervertebral discs implicate HOPX as a regulator of homeostasis Proceeding/Conference:SBMS Research Day, School of Biomedical Sciences, The University of Hong Kong | 2018 | 67 |