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Bone Morphogenetic Proteins (BMPs) are a group of signaling molecules that belongs to the Transforming Growth Factor-β (TGF-β) superfamily of proteins. Initially discovered for their ability to induce bone formation, BMPs are now known to play crucial roles in all organ systems. BMPs are important in embryogenesis and development, and also in maintenance of adult tissue homeostasis. Mouse knockout models of various components of the BMP signaling pathway result in embryonic lethality or marked defects, highlighting the essential functions of BMPs. In this review, we first outline the basic aspects of BMP signaling and then focus on genetically manipulated mouse knockout models that have helped elucidate the role of BMPs in development. A significant portion of this review is devoted to the prominent human pathologies associated with dysregulated BMP signaling.

Publication history
Copyright
Acknowledgements

Publication history

Received: 11 July 2014
Accepted: 15 July 2014
Published: 27 July 2014
Issue date: September 2014

Copyright

© 2014, Chongqing Medical University. All rights reserved.

Acknowledgements

The reported work was in part supported by research grants from the National Institutes of Health (AR50142 and AR054381 to RCH and HHL). RW, JG, and OI were recipients of the Pritzker Summer Research Fellowship funded through a NIH T-35 training grant (NIDDK). AH was a recipient of the Urban Leadership Fellowship from Miami University.

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