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Regulation of osteoblast differentiation Barendsz-van der Horst, Geertje

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Regulation of osteoblast differentiation Barendsz-van der Horst, Geertje

Citation

Barendsz-van der Horst, G. (2005, November 3). Regulation of osteoblast

differentiation. Retrieved from https://hdl.handle.net/1887/4974

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoralthesis in the Institutional Repository of the University of Leiden

Downloaded from: https://hdl.handle.net/1887/4974

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Contents

Contents

General Introduction

Differentiation of murine pre-osteoblastic KS483 cells depends on autocrine bone morphogenetic protein signaling during all phases of osteoblast formation

Hedgehog stimulates only osteoblastic differentiation of undifferentiated KS483 cells

Fast generation of stable cell lines to study gene function during mesenchymal differentiation using gene overexpression or RNA silencing

Downregulation of Wnt signaling by increased expression of Dkk-1 and –2 is a pre-requisite for late stage osteoblast differentiation of KS483 cells

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License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden Downloaded.

Printing of this thesis was financially supported by the Netherlands Organization of Scientific Research (NWO) and the Dutch Society of Calcium and Bone

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden. Downloaded

In addition, PTHrP might affect the expression or posttranslational modification of the transcription factors RunX2 or osx (respectively arrows 5 and 6 for RunX2 and 7 an 8 for

The presence of BMP signaling pathway components during all phases of differentiation, the specific induction of BMP-8a mRNA during the mineralization phase, and

Addition of recombinant human sonic hedgehog (rhSHh) potently increased osteoblastic differentiation of KS483 cells dose-dependently as determined by a modest increase in ALP

To study the effect of Wnt signaling on more mature stages of osteoblast differentiation, we examined the effects of Wnt/β-catenin signaling on bone nodule formation and

In contrast, treatment of undifferentiated KS483 cells with hPTHrP (1-34) for 72 hours prevented the increase in RunX2 mRNA and protein expression normally observed