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Toshiyuki Yoneda

Researcher at Osaka University

Publications -  239
Citations -  20124

Toshiyuki Yoneda is an academic researcher from Osaka University. The author has contributed to research in topics: Bone resorption & Bone metastasis. The author has an hindex of 79, co-authored 233 publications receiving 18736 citations. Previous affiliations of Toshiyuki Yoneda include Indiana University – Purdue University Indianapolis & National Institutes of Health.

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Bisphosphonates promote apoptosis in murine osteoclasts in vitro and in vivo

TL;DR: Osteoclast apoptosis may be a major mechanism whereby bisphosphonates reduce osteoclast numbers and activity, and induction of apoptosis could be a therapeutic goal for new antiosteoclast drugs.
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Evidence for a causal role of parathyroid hormone-related protein in the pathogenesis of human breast cancer-mediated osteolysis.

TL;DR: Results indicate that tumor-produced PTHrP can cause local bone destruction in breast cancer metastatic to bone, even in the absence of hypercalcemia or increased circulating plasma concentrations of P THrP.
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Requirement of pp60c-src expression for osteoclasts to form ruffled borders and resorb bone in mice

TL;DR: Results indicate that osteoclasts appear in the absence of pp60c-src, but that pp60 c-src expression is required for mature osteoclast to form ruffled borders and resorb bone.
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BMP2 Regulates Osterix through Msx2 and Runx2 during Osteoblast Differentiation

TL;DR: Osterix is regulated via both Runx2-dependent and -independent mechanisms, and that Osterix controls osteoblast differentiation, at least in part, by regulating the expression of genes not controlled by Runx 2.
Journal Article

Bisphosphonate Risedronate Reduces Metastatic Human Breast Cancer Burden in Bone in Nude Mice

TL;DR: It is demonstrated that risedronate decreases metastatic MDA-231 breast cancer burden selectively in bone, as well as suppresses progression of established osteolytic lesions and prevents the development of new osteolytics lesions; thus, the data suggest that inhibition of osteoclastic bone resorption may be a useful adjunctive therapy for the treatment of cancers that have colonized in bone.