Show source-provided references
1. Functional anatomy of the musculoskeletal system
2. An, Y.H., and Draughn, R.A. (2000). Basic composition and structure of bone. Mechanical Testing of Bone and the Bone-Implant Interface, CRC Press. [1st ed.].
10.1201/9781420073560 ↗3. Péoc’h, M. (2004). Normal histological architecture of tissue. Biomechanics and Biomaterials in Orthopedics, Springer.
10.1007/978-1-4471-3774-0_18 ↗4. An, Y.H., and Draughn, R.A. (2000). Tensile and Compression Testing of Bone. Mechanical Testing of Bone and the Bone-Implant Interface, CRC Press. [1st ed.].
10.1201/9781420073560 ↗9. Hierarchical Nature of Nanoscale Porosity in Bone Revealed by Positron Annihilation Lifetime Spectroscopy
10.1021/acsnano.0c07478 ↗17. Friedrich, J. (2009). Analyzing Interactions between Cells and Extracellular Matrix by Atomic Force Microscopy. [Ph.D. Thesis, Technischen Universität Dresden].
18. Gültekin, O. (2019). Computational Inelasticity of Fibrous Biological Tissues with a Focus on Viscoelasticity, Damage and Rupture, Verlag der Technischen Universität Graz.
19. Age-related changes in molecular organization of type I collagen in tendon as probed by polarized SHG and Raman microspectroscopy
10.1038/s41598-019-43636-2 ↗20. Bone: A story of breakthroughs, a promising future
21. Kutz, M. (2003). Bone mechanics. Standard Handbook of Biomedical Engineering & Design, McGraw-Hill. [1st ed.].
24. A finite element study evaluating the influence of mineralization distribution and content on the tensile mechanical response of mineralized collagen fibril networks
10.1016/j.jmbbm.2019.07.019 ↗25. Structure and mechanical quality of the collagen–mineral nano-composite in bone
10.1039/B402005G ↗30. Effect of material and structural factors on fracture behaviour of mineralised collagen microfibril using finite element simulation
10.1080/10255842.2014.883601 ↗33. Bone fracture toughness and strength correlate with collagen cross-link maturity in a dose-controlled lathyrism mouse model
10.1002/jbmr.2356 ↗34. Influence of cross-link structure, density and mechanical properties in the mesoscale deformation mechanisms of collagen fibrils
10.1016/j.jmbbm.2014.07.008 ↗37. A ductile-to-brittle transition in bone failure due to non-enzymatic collagen-crosslinks-A computational study
38. Age-related loss in bone toughness is explained by non-enzymatic glycation of collagen
44. Black, J., and Hastings, G. (2013). Cancellous bone. Handbook of Biomaterial Properties, Springer Science & Business Media.
45. Yoa, H. (2007). Mechanical Testing of Bone and Bone-Like Materials Using Image Correlation Strain Measurement Technique, Xi’an Jiaotong University.
46. Weld-Moore, R. (2018). The Use of Quantitative Ultrasound to Investigate Bone Strength in the Facial Skeleton, Trinity College.
47. In situ micropillar compression reveals superior strength and ductility but an absence of damage in lamellar bone
10.1038/nmat3959 ↗49. Arnett, T. (2015). Osteocytes—Human Bone, Bone Research Society.
50. Arnett, T., and Manzano, J. (2015). Osteoclast Resorption, Bone Research Society.
10.69645/ILWO1949 ↗51. Mackenzie, K. (2015). Osteocytes, Bone Research Society.
52. (2022, March 16). International Osteoporosis Foundation. Available online: https://www.osteoporosis.foundation/health-professionals/about-osteoporosis/bone-biology.
53. Bone remodelling in vitro: Where are we headed?—A review on the current understanding of physiological bone remodelling and inflammation and the strategies for testing biomaterials in vitro
10.1016/j.bone.2018.01.015 ↗56. Deformation strain is the main physical driver for skeletal precursors to undergo osteogenesis in earlier stages of osteogenic cell maturation
58. Numerical simulation of streaming potentials due to deformation-induced hierarchical flows in cortical bone
10.1115/1.1336796 ↗59. Poromicromechanics reveals that physiological bone strains induce osteocyte-stimulating lacunar pressure
10.1007/s10237-015-0704-y ↗60. In silico study of bone tissue regeneration in an idealised porous hydrogel scaffold using a mechano-regulation algorithm
10.1007/s10237-017-0941-3 ↗61. Mechanical Loading Disrupts Osteocyte Plasma Membranes Which Initiates Mechanosensation Events in Bone
10.1002/jor.23665 ↗62. Dendritic processes of osteocytes are mechanotransducers that induce the opening of hemichannels
10.1073/pnas.1009382107 ↗66. Lactation-induced changes in the volume of osteocyte lacunar-canalicular space alter mechanical properties in cortical bone tissue
10.1002/jbmr.3044 ↗68. Stress concentrations and bone microdamage: John Currey’s contributions to understanding the initiation and arrest of cracks in bone
10.1016/j.bone.2019.07.015 ↗74. Dutta, S.K., and Datta, D. (2008). Composition of musculoskeletal structures. Applied Orthopaedic Biomechanics, BI Publications Pvt Ltd.. [1st ed.].
78. Integrating molecular and cellular kinetics into a coupled continuum mechanobiological stimulus for bone reconstruction
10.1007/s00161-018-0726-7 ↗79. Mechanobiological osteocyte feedback drives mechanostat regulation of bone in a multiscale computational model
10.1007/s10237-019-01158-w ↗80. A numerical bone regeneration model incorporating angiogenesis, considering oxygen-induced secretion of vascular endothelial growth factor and vascular remodeling
10.1016/j.jbiomech.2021.110656 ↗85. Age-related changes in the tensile properties of cortical bone. The relative importance of changes in porosity, mineralization, and microstructure
10.2106/00004623-199308000-00009 ↗88. Winkelstein, B.A. (2013). Bone biomechanics. Orthopaedic Biomechanics, CRC Press.
10.1201/b13733 ↗89. Porteous, M., and Bäuerle, S. (2010). Techniques and Principles for the Operating Room, Georg Thieme Verlag.
10.1055/b-002-85510 ↗90. Dutta, S.K., and Datta, D. (2008). Long bone shape its mechanical significance. Applied Orthopaedic Biomechanics, BI Publications Pvt Ltd.. [1st ed.].
92. The biomechanics of human femurs in axial and torsional loading: Comparison of finite element analysis, human cadaveric femurs, and synthetic femurs
10.1115/1.2401178 ↗93. Hench, L.L., and Wilson, J. (1993). Introduction. An Introduction to Bioceramics, World Scientific.
10.1142/2028 ↗94. Cortical bone
95. Influence of the intramedullary nail preparation method on nail’s mechanical properties and degradation rate
10.1016/j.msec.2015.02.043 ↗97. Simulation of fracture healing in the tibia: Mechanoregulation of cell activity using a lattice modeling approach
10.1002/jor.21362 ↗98. Wang, X., Nyman, J.S., Dong, X., Leng, H., and Reyes, M. (2010). Fundamental Biomechanics in Bone Tissue Engineering, Morgan & Claypool.
10.1007/978-3-031-02579-2 ↗100. Drake, R.L., Vogl, A.W., and Mitchell, A.W.M. (2016). Gray’s Basic Anatomy, Elsevier Health Sciences. [2nd ed.].