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A functional bias towards compression has also been observed for bone, but with the formation of microcracks in the region under greatest tension.
In our study, cells grown in standard media showed spindle-shaped and flattened cells and had the ability to continuously divide, as has been observed for bone marrow stroma and tissue-specific MSCs from other species [ 39, 40].
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No associations were observed for bone fractures.
No significant differences were observed for bone volume or BMD.
An effect for artery only was observed for bone morphogenetic protein 3 (BMpotassiumssium voltage-gated channel, Isk-related famembermember 1 (KCNE1), angiotensin II receptor, type 1 (AGTR1), G protein-coupled receptor, family C, group 5, member C (GPRC5C), formin homology 2 domain containing 3 (FHOD3), and proproteinconvertase subtilisin/kexin type 5 (PCSK5) for both methods.
Furthermore, significantly larger colonies of CFU-Fs were observed for bone-marrow-derived primary cells cultured on 1% (wt/v) gelatin-coated matrix).
Dose response relationships have been observed for lung, liver and bone cancers, for most solid tumours and for cerebrovascular and ischemic heart diseases [ 4, 5, 11, 12] in Mayak workers.
Crestal bone remodeling has been observed for either internal and external, or conical and butt joint connections.
Neither inflammatory symptom nor heterotopic bone formation of the right TMJ has been observed for 1 year.
Significant force x repetition interaction effects were observed for each bone morphological attribute and serum biomarker of bone turnover analyzed at 12 weeks of task performance.
After 48 weeks, significantly greater changes from baseline were observed for all bone markers in subjects receiving TDF/FTC/EFV, indicating more active bone turnover when compared to changes seen in subjects receiving DTG + ABC/3TC.
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