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441
Low-density lipoprotein receptor-related protein 5 (LRP5) variation in fracture prone children
Low-density lipoprotein receptor-related protein 5 (LRP5) variation in fracture prone children
Saarinen, A., | Elsevier Inc | 2010 ,
442
Characterization of circulating osteoblast lineage cells in humans
Characterization of circulating osteoblast lineage cells in humans
Eghbali-Fatourechi, G. Z., | Elsevier Inc | 2008 ,
443
Calcitonin induces podosome disassembly and detachment of osteoclasts by modulating Pyk2 and Src activities
Calcitonin induces podosome disassembly and detachment of osteoclasts by modulating Pyk2 and Src activities
Shyu, J. F., | Elsevier Inc | 2008 ,
444
Lithium use and the risk of fractures
Lithium use and the risk of fractures
Wilting, I., | Elsevier Inc | 2008 ,
445
A single zoledronic acid infusion reduces bone resorption markers more rapidly than weekly oral alendronate in postmenopausal women with low bone mineral density
A single zoledronic acid infusion reduces bone resorption markers more rapidly than weekly oral alendronate in postmenopausal women with low bone mineral density
Saag, K., | Elsevier Inc | 2008 ,
446
Prediction of bone mineral density with dental radiographs
Prediction of bone mineral density with dental radiographs
Geraets, W. G., | Elsevier Inc | 2008 ,
447
Pelvic body composition measurements by quantitative computed tomography: Association with recent hip fracture
Pelvic body composition measurements by quantitative computed tomography: Association with recent hip fracture
Lang, T., | Elsevier Inc | 2008 ,
448
Activation of extracellular-signal regulated kinase (ERK1/2) by fluid shear is Ca2+- and ATP-dependent in MC3T3-E1 osteoblasts
Activation of extracellular-signal regulated kinase (ERK1/2) by fluid shear is Ca2+- and ATP-dependent in MC3T3-E1 osteoblasts
Liu, D., | Elsevier Inc | 2008 ,
449
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
Yin, L., | Elsevier Inc | 2008 ,
450
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study
Langdahl, B. L., | Elsevier Inc | 2008 ,
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