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PUBMED FOR HANDHELDS

Journal Abstract Search


319 related items for PubMed ID: 33253203

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  • 6. Runx2 deletion in hypertrophic chondrocytes impairs osteoclast mediated bone resorption.
    Rashid H, Smith CM, Convers V, Clark K, Javed A.
    Bone; 2024 Apr; 181():117014. PubMed ID: 38218304
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  • 8. Targeting Runx2 expression in hypertrophic chondrocytes impairs endochondral ossification during early skeletal development.
    Ding M, Lu Y, Abbassi S, Li F, Li X, Song Y, Geoffroy V, Im HJ, Zheng Q.
    J Cell Physiol; 2012 Oct; 227(10):3446-56. PubMed ID: 22223437
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  • 10. Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development.
    Chen W, Ma J, Zhu G, Jules J, Wu M, McConnell M, Tian F, Paulson C, Zhou X, Wang L, Li YP.
    Proc Natl Acad Sci U S A; 2014 Jun 10; 111(23):8482-7. PubMed ID: 24850862
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  • 13. Bone morphogenetic protein rescues the lack of secondary cartilage in Runx2-deficient mice.
    Fukuoka H, Shibata S, Suda N, Yamashita Y, Komori T.
    J Anat; 2007 Jul 10; 211(1):8-15. PubMed ID: 17555546
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  • 14. Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes.
    Hu DP, Ferro F, Yang F, Taylor AJ, Chang W, Miclau T, Marcucio RS, Bahney CS.
    Development; 2017 Jan 15; 144(2):221-234. PubMed ID: 28096214
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  • 16. Runx2, an inducer of osteoblast and chondrocyte differentiation.
    Komori T.
    Histochem Cell Biol; 2018 Apr 15; 149(4):313-323. PubMed ID: 29356961
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  • 18. Persistent Sox9 expression in hypertrophic chondrocytes suppresses transdifferentiation into osteoblasts.
    Lui JC, Yue S, Lee A, Kikani B, Temnycky A, Barnes KM, Baron J.
    Bone; 2019 Aug 15; 125():169-177. PubMed ID: 31121357
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