Karen M. Lyons
Affiliations: | Molec, Cell, & Dev Biology 0644 | University of California, Los Angeles, Los Angeles, CA |
Area:
Human Development, Evolution and Development BiologyGoogle:
"Karen Lyons"Children
Sign in to add trainee| Soyun E. Yi | grad student | 2000 | UCLA |
| Matthew E. Bahamonde | grad student | 2002 | UCLA |
| Byeong S. Yoon | grad student | 2005 | UCLA |
| Kelsey N. Retting | grad student | 2008 | UCLA |
| Bau-Lin Huang | grad student | 2009 | UCLA |
| Kristine D. Estrada | grad student | 2012 | UCLA |
| Faith L. Hall-Glenn | grad student | 2012 | UCLA |
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Publications
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| Qiao X, Wu X, Zhao Y, et al. (2023) Cell Transitions Contribute to Glucocorticoid-Induced Bone Loss. Cells. 12 |
| Liu NQ, Lin Y, Li L, et al. (2022) gp130/STAT3 signaling is required for homeostatic proliferation and anabolism in postnatal growth plate and articular chondrocytes. Communications Biology. 5: 64 |
| Deng P, Yuan Q, Cheng Y, et al. (2021) Loss of KDM4B exacerbates bone-fat imbalance and mesenchymal stromal cell exhaustion in skeletal aging. Cell Stem Cell |
| Zhao G, Kim EW, Jiang J, et al. (2020) CCN1/Cyr61 is required in osteoblasts for responsiveness to the anabolic activity of PTH. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research |
| Ohkawara B, Kobayakawa A, Kanbara S, et al. (2020) CTGF/CCN2 facilitates LRP4-mediated formation of the embryonic neuromuscular junction. Embo Reports. e48462 |
| Hsu GC, Marini S, Negri S, et al. (2020) Endogenous CCN family member WISP-1 inhibits trauma-induced heterotopic ossification. Jci Insight |
| Wang W, Rigueur D, Lyons KM. (2020) TGFβ as a gatekeeper of BMP action in the developing growth plate. Bone. 115439 |
| Lyons K, Katagiri T. (2020) Decision letter: Activin A forms a non-signaling complex with ACVR1 and type II Activin/BMP receptors via its finger 2 tip loop Elife |
| Lopez N, Rigueur D, Lyons K. (2020) Regenerative properties of the humerus bone in the absence of Stat3 The Faseb Journal. 34: 1-1 |
| Russell BE, Rigueur D, Weaver KN, et al. (2019) Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic features. Molecular Genetics & Genomic Medicine. 7: e969 |