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Andrea I. Alford

Researcher at University of Michigan

Publications -  22
Citations -  796

Andrea I. Alford is an academic researcher from University of Michigan. The author has contributed to research in topics: Mesenchymal stem cell & Osteoblast. The author has an hindex of 10, co-authored 20 publications receiving 659 citations.

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Matricellular proteins: Extracellular modulators of bone development, remodeling, and regeneration

TL;DR: It is clear that although matricellular proteins are not required for bone development and function, the proteins act to modulate post-natal bone structure in response to aging, ovariectomy, mechanical loading, and bone regeneration.
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Extracellular matrix networks in bone remodeling.

TL;DR: This comprehensive review will focus on how networks of ECM proteins function to regulate osteoclast- and osteoblast-mediated bone remodeling and the clinical significance of these networks on normal bone and as they relate to pathologies of bone mass and geometry will be considered.
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Adults with Cerebral Palsy have Higher Prevalence of Fracture Compared with Adults Without Cerebral Palsy Independent of Osteoporosis and Cardiometabolic Diseases.

TL;DR: It is suggested that young and middle‐aged adults with CP have an elevated prevalence of all‐cause fracture compared with adults without CP, which was present even after accounting for cardiometabolic diseases and osteoporosis.
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Comparison of Uncultured Marrow Mononuclear Cells and Culture-Expanded Mesenchymal Stem Cells in 3D Collagen-Chitosan Microbeads for Orthopedic Tissue Engineering

TL;DR: This study demonstrates the microbead-based approach to culturing and delivering cells for tissue regeneration, and suggests that fresh BMMC may be an alternative to using culture-expanded MSC for bone tissue engineering.
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Masquelet's induced membrane technique: Review of current concepts and future directions.

TL;DR: Masquelet's induced membrane technique (MIMT) is a relatively new, two-stage surgical procedure to reconstruct segmental bone defects as discussed by the authors, which has shown great promise to revolutionize critical-sized bone defect repair and has several advantages over its alternative, distraction osteogenesis (DO).