1. Boudker, Olga 美国 Weill Cornell Medicine 2022美国科学院院士 Structural basis of pH-dependent activation in a CLC transporter
2. 孙宝国 中国 北京工商大学 中国工程院院士 The potential benefits and mechanisms of protein nutritional intervention on bone health improvement
3. 朱立国 中国 中国中医科学院 2023中国工程院院士 Exploring the Relationship of Bone Turnover Markers and Bone Mineral Density in Community-Dwelling P..
4. 张学 中国 哈尔滨医科大学 中国工程院院士 Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta
5. Mattison, Donald R. 美国 University of South Carolina 2000美国医学院院士 Thiazolidinedione drugs in the treatment of type 2 diabetes mellitus: past, present and future
6. 陈子江 中国 山东大学 中国科学院院士 A FKBP5 mutation is associated with Paget's disease of bone and enhances osteoclastogenesis
7. Davey Smith, George 英国 University of Bristol 2008美国医学院院士 Mutations in Known Monogenic High Bone Mass Loci Only Explain a Small Proportion of High Bone Mass C..
8. Amagai, Masayuki 日本 Keio University 2016美国医学院院士 Pathological characterization of pachydermia in pachydermoperiostosis
9. Amagai, Masayuki 日本 Keio University 2016美国医学院院士 The complete type of pachydermoperiostosis: A novel nonsense mutation p.E141* of the SLC02A1 gene
10. Amagai, Masayuki 日本 Keio University 2016美国医学院院士 The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603*in a female pa..
11. Lee, Brendan 美国 Baylor College of Medicine 2013美国医学院院士 Recessive Osteogenesis Imperfecta Due to Mutations in CRTAP, LEPRE1 and PPIB
12. Gluckman, Peter D. 新西兰 University of Auckland 2004美国医学院院士 Associations Between Ethnicity, Body Composition, and Bone Mineral Density in a Southeast Asian Popu..
13. 宁光 中国 上海交通大学医学院 中国工程院院士 An Independent Positive Relationship Between the Serum Total Osteocalcin Level and Fat-Free Mass in ..
14. Amagai, Masayuki 日本 Keio University 2016美国医学院院士 Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype..
15. Gluckman, Peter D. 新西兰 University of Auckland 2004美国医学院院士 Transcriptome Changes Affecting Hedgehog and Cytokine Signalling in the Umbilical Cord: Implications..
16. Da-Tian Bau 中国 中国医药大学 Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia I..
17. Stuart J,Warden 美国 Indiana University Autosomal Dominant Osteopetrosis (ADO) Caused by a Missense Variant in the TCIRG1 Gene
18. Michael J,Econs 美国 Indiana University Autosomal Dominant Osteopetrosis (ADO) Caused by a Missense Variant in the TCIRG1 Gene
19. Kenji,Izuhara 日本 SAGA Medicine School Mechanisms of tissue degeneration mediated by periostin in spinal degenerative diseases and their im..
20. Mosca, Marta 意大利 University of Pisa LRP5 high bone mass (Worth-type autosomal dominant endosteal hyperostosis): case report and historic..