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Meghan E. McGee-Lawrence

Researcher at Georgia Regents University

Publications -  94
Citations -  3214

Meghan E. McGee-Lawrence is an academic researcher from Georgia Regents University. The author has contributed to research in topics: Osteoblast & Bone marrow. The author has an hindex of 29, co-authored 85 publications receiving 2565 citations. Previous affiliations of Meghan E. McGee-Lawrence include Michigan Technological University & Mayo Clinic.

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Update on Wnt signaling in bone cell biology and bone disease

TL;DR: Recent advances and discrepancies in how Wnt/Lrp5 signaling regulates osteoblasts and osteocytes are reviewed, new players are introduced, and emerging areas such as the role of Wnt signaling in osteoclastogenesis are discussed.
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Fatty Infiltration of Skeletal Muscle: Mechanisms and Comparisons with Bone Marrow Adiposity.

TL;DR: In this paper, the authors investigated the factors leading to accumulation of intra-and intermuscular fat (myosteatosis) in skeletal muscle and bone and found that increases in intramuscular fat are associated with disuse, altered leptin signaling, sex steroid deficiency, and glucocorticoid treatment, factors that are also implicated in bone marrow adipogenesis.
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Epigenetic Control of Skeletal Development by the Histone Methyltransferase Ezh2

TL;DR: The expression profiles of a large cohort of epigenetic regulators during osteogenic differentiation of human mesenchymal cells derived from the stromal vascular fraction of adipose tissue (AMSCs) show that the polycomb group protein EZH2 (enhancer of zeste homolog 2) is down-regulated during osteoblastic differentiation of AMSCs, and the epigenetic activity of EZh2 expression declines during terminal osteoblast differentiation and matrix production.
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Histone Deacetylases in Bone Development and Skeletal Disorders.

TL;DR: The general properties of Hdacs/Sirts and the research that has revealed their essential functions in bone forming cells and bone resorbing osteoclasts are summarized and the utility of this knowledge for orthopedic applications and bone tissue engineering is offered.
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Sclerostin alters serum vitamin D metabolite and fibroblast growth factor 23 concentrations and the urinary excretion of calcium.

TL;DR: The data show that sclerostin not only alters bone mineralization, but also influences mineral metabolism by altering concentrations of hormones that regulate mineral accretion.