Systemic inflammatory and gut microbiota responses to fracture in young and middle-aged mice
Author:
Funder
National Institute on Aging
Publisher
Springer Science and Business Media LLC
Subject
Geriatrics and Gerontology,Aging
Link
https://link.springer.com/content/pdf/10.1007/s11357-023-00963-7.pdf
Reference76 articles.
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2. Naik AA, Xie C, Zuscik MJ, Kingsley P, Schwarz EM, Awad H, Guldberg R, Drissi H, Puzas JE, Boyce B, Zhang X, O’Keefe RJ. Reduced COX-2 expression in aged mice is associated with impaired fracture healing. J Bone Miner Res. 2009;24(2):251–64.
3. Lu C, Miclau T, Hu D, Hansen E, Tsui K, Puttlitz C, Marcucio RS. Cellular basis for age-related changes in fracture repair. J Orthop Res. 2005;23(6):1300–7.
4. He B, Zhang Z-K, Liu J, He Y-X, Tang T, Li J, Guo B-S, Lu A-P, Zhang B-T, Zhang G. Bioinformatics and microarray analysis of miRNAs in aged female mice model implied new molecular mechanisms for impaired fracture healing. Int J Mol Sci. 2016;17(8):1260.
5. Stolzing A, Jones E, McGonagle D, Scutt A. Age-related changes in human bone marrow-derived mesenchymal stem cells: consequences for cell therapies. Mech Ageing Dev. 2008;129(3):163–73.
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