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Skeletal Biology Laboratory, Center for Healthy Aging Research, Biostatistics, School of Biological and Population Health Sciences
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Skeletal Biology Laboratory, Center for Healthy Aging Research, Biostatistics, School of Biological and Population Health Sciences
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dual-energy X-ray absorptiometry (DXA), microcomputed tomography (μCT), and histomorphometry. Tibiae were removed, cleaned of soft tissue, frozen in liquid nitrogen, and stored at −80 °C for mRNA isolation and gene expression analysis. Serum chemistry
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(Instron Corp., Norwood, MA, USA). Based on the recorded load deformation curves, the biomechanical parameters were calculated from raw files produced by Bluehill 2 software, version 2.6 (Instron) with custom-made Excel macros. Bone histomorphometry
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. Histomorphometry Calcein and demeclocycline were injected intraperitoneally at 20mg/kg of body weight at respectively 9 days and 2 days prior to killing the mice at 16 weeks of age. Tibiae were fixed for 48 h in 10% buffered formalin and stored in 70% ethanol
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reconstruction following established guidelines ( Bouxsein et al. 2010 ). Histomorphometry and measurement of mechanical strength For the measure of dynamic bone parameters, mice were injected (i.p.) with 100 µL of calcein (50 mg/kg) 8 and 1 day before
Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK
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, West Sussex, UK). A 100 N loading cell was used with the span fixed at 10 mm and the cross-head was lowered at 1 mm/min to determine the load to failure and maximum stiffness and deflection of tibiae ( Huesa et al. 2011 ). Bone histomorphometry
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Departments of Pharmacology, Orthodontics, Transcriptome Research Group, Department of Developmental Biology of Hard Tissue, Department of Molecular Pharmacology, School of Dental Medicine, Tsurumi University, 2‐1‐3 Tsurumi, Tsurumi‐ku, Yokohama 230-8501, Japan
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Departments of Pharmacology, Orthodontics, Transcriptome Research Group, Department of Developmental Biology of Hard Tissue, Department of Molecular Pharmacology, School of Dental Medicine, Tsurumi University, 2‐1‐3 Tsurumi, Tsurumi‐ku, Yokohama 230-8501, Japan
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( n =4), and 1 mM DC ( n =4) for 5 min at room temperature, and put back into their sockets. At certain time points, tissues were fixed and subjected to bone histomorphometry and immunohistochemistry (see below). Bone histomorphometry Animals in the
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Department of Veterinary Basic Sciences, INSERM, CNRS, Université Paris Decartes, INSERM, Department of Endocrinology, Royal Veterinary College, Royal College Street, London NW1 0TU, UK
Department of Veterinary Basic Sciences, INSERM, CNRS, Université Paris Decartes, INSERM, Department of Endocrinology, Royal Veterinary College, Royal College Street, London NW1 0TU, UK
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tibiae were harvested from these mice for micro-CT (studies 1, 2 and 3) and bone histomorphometric analyses (study 1) respectively. Femora were collected for western blot and RT-PCR analyses. Histomorphometry analysis of tibia Right tibia from sham
Center for Healthy Aging Research, Oregon State University, Corvallis, Oregon, USA
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Center for Healthy Aging Research, Oregon State University, Corvallis, Oregon, USA
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epiphysis and in lumbar vertebra included cancellous bone volume fraction (bone volume/tissue volume, %), trabecular thickness (µm), trabecular number (/mm), and trabecular separation (µm). Histomorphometry Distal femora were dehydrated in a graded
UMR‐1132 Inserm, Université Paris Diderot, Hôpital Lariboisière, 2 Rue Ambroise Paré, 75475 Paris Cedex 10, France
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UMR‐1132 Inserm, Université Paris Diderot, Hôpital Lariboisière, 2 Rue Ambroise Paré, 75475 Paris Cedex 10, France
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UMR‐1132 Inserm, Université Paris Diderot, Hôpital Lariboisière, 2 Rue Ambroise Paré, 75475 Paris Cedex 10, France
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UMR‐1132 Inserm, Université Paris Diderot, Hôpital Lariboisière, 2 Rue Ambroise Paré, 75475 Paris Cedex 10, France
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UMR‐1132 Inserm, Université Paris Diderot, Hôpital Lariboisière, 2 Rue Ambroise Paré, 75475 Paris Cedex 10, France
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, by ELISA (R&D Systems, Lille, France). Bone microarchitecture and histomorphometry The animals were killed and, lumbar vertebrae and right femurs (distal metaphysis) were obtained for analysis of micro- and macro-structures. The bones were scanned
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,25-Dihydroxyvitamin D3 modulates glucocorticoid-induced alteration in serum bone Gla protein and bone histomorphometry. Endocrinology 120 531 –536. Karsdal MA , Larsen L, Engsig MT, Lou H, Ferreras M, Lochter A, Delaisse JM & Foged NT