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321
Genetic variation in the PTH pathway and bone phenotypes in elderly women: Evaluation of PTH, PTHLH, PTHR1 and PTHR2 genes
Genetic variation in the PTH pathway and bone phenotypes in elderly women: Evaluation of PTH, PTHLH, PTHR1 and PTHR2 genes
Tenne, M., | Elsevier Inc | 2008 ,
322
Jump starting skeletal health: A 4-year longitudinal study assessing the effects of jumping on skeletal development in pre and circum pubertal children
Jump starting skeletal health: A 4-year longitudinal study assessing the effects of jumping on skeletal development in pre and circum pubertal children
Gunter, K., | Elsevier Inc | 2008 ,
323
Effects of alendronate and pamidronate on cultured rat metatarsal bones: Failure to prevent dexamethasone-induced growth retardation
Effects of alendronate and pamidronate on cultured rat metatarsal bones: Failure to prevent dexamethasone-induced growth retardation
Heino, T. J., | Elsevier Inc | 2008 ,
324
Role of genetic background in determining phenotypic severity throughout postnatal development and at peak bone mass in Col1a2 deficient mice (oim)
Role of genetic background in determining phenotypic severity throughout postnatal development and at peak bone mass in Col1a2 deficient mice (oim)
Carleton, S. M., | Elsevier Inc | 2008 ,
325
High impact exercise is more beneficial than dietary calcium for building bone strength in the growing rat skeleton
High impact exercise is more beneficial than dietary calcium for building bone strength in the growing rat skeleton
Welch, J. M., | Elsevier Inc | 2008 ,
326
32 wk old C3H/HeJ mice actively respond to mechanical loading
32 wk old C3H/HeJ mice actively respond to mechanical loading
Poliachik, S. L., | Elsevier Inc | 2008 ,
327
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 ,
328
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 ,
329
Body composition and bone density in Canadian White and Aboriginal women: The First Nations Bone Health Study
Body composition and bone density in Canadian White and Aboriginal women: The First Nations Bone Health Study
Leslie, W. D., | Elsevier Inc | 2008 ,
330
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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