M
Michael J. Marshall
Researcher at Robert Jones and Agnes Hunt Orthopaedic Hospital
Publications - 34
Citations - 1265
Michael J. Marshall is an academic researcher from Robert Jones and Agnes Hunt Orthopaedic Hospital. The author has contributed to research in topics: Osteoclast & Bone resorption. The author has an hindex of 19, co-authored 34 publications receiving 1196 citations.
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Journal ArticleDOI
Hsp70 release from peripheral blood mononuclear cells.
Claire Hunter-Lavin,Emma L. Davies,Maria M. F. V. G. Bacelar,Michael J. Marshall,Sarah M. Andrew,John H. H. Williams +5 more
TL;DR: The data suggest that Hsp70 is released from cells via a non-classical pathway, possibly involving lysosomal lipid rafts, and this release is not due to cellular damage.
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RANK, RANKL and osteoprotegerin in bone biology and disease
TL;DR: This review aims to bring the interested reader up to date with the latest news and views on the mechanisms controlling bone resorption in normal and pathological conditions.
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Effects of dissociated glucocorticoids on OPG and RANKL in osteoblastic cells.
TL;DR: It is demonstrated that deflazacort and the dissociated glucocorticoids are weak stimulators of the RANKL:OPG ratio compared to prednisolone, which means that these compounds have the potential to cause less bone loss than that seen with prednisolsone.
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Decreased osteogenesis, increased cell senescence and elevated Dickkopf-1 secretion in human fracture non union stromal cells
Stefan Bajada,Michael J. Marshall,Karina T. Wright,James B. Richardson,William E. B. Johnson +4 more
TL;DR: The results suggest that the development of fracture non union is linked with a localised reduced capacity of cells to undergo osteogenesis, which in turn is associated with increased cell senescence and Dkk-1 secretion.
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Osteoprotegerin ligand regulates osteoclast adherence to the bone surface in mouse calvaria.
TL;DR: Evidence is presented that the change in the adhesion of osteoclasts from the periosteum to the bone surface, resulting in osteoclast activation, is mediated by OPGL.