Coupling Signals between the Osteoclast and Osteoblast: How are Messages Transmitted between These Temporary Visitors to the Bone Surface?

Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF.

Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1112 · Cited by 3,166 · cited 1×

Presidential Address: Discount Rates

Cochrane, J. H. (2011) · The Journal of Finance · doi:10.1111/j.1540-6261.2011.01671.x · Cited by 2,135

Mechanical Stimulation of Bone in Vivo Reduces Osteocyte Expression of Sost/Sclerostin

Robling, A. G., Niziolek, P. J., Baldridge, L. A., Condon, K. W., Allen, M. R., Alam, I., Mantila, S. M., Gluhak-Heinrich, J., Bellido, T. M., Harris, S. E., et al. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m705092200 · Cited by 1,350

TGF-β1–induced migration of bone mesenchymal stem cells couples bone resorption with formation

Tang, Y., Wu, X., Lei, W., Pang, L., Wan, C., Shi, Z., Zhao, L., Nagy, T. R., Peng, X., Hu, J., et al. (2009) · Nature Medicine · doi:10.1038/nm.1979 · Cited by 1,165

Bidirectional ephrinB2-EphB4 signaling controls bone homeostasis

Zhao, C., Irie, N., Takada, Y., Shimoda, K., Miyamoto, T., Nishiwaki, T., Suda, T., & Matsuo, K. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.05.012 · Cited by 777

Coupling the activities of bone formation and resorption: a multitude of signals within the basic multicellular unit

Sims, N. A., & Martin, T. J. (2014) · BoneKEy Reports · doi:10.1038/bonekey.2013.215 · Cited by 745

Osteoclast-derived activity in the coupling of bone formation to resorption

Martin, T. J., & Sims, N. A. (2005) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2004.12.004 · Cited by 661

Matrix IGF-1 maintains bone mass by activation of mTOR in mesenchymal stem cells

Xian, L., Wu, X., Pang, L., Lou, M., Rosen, C. J., Qiu, T., Crane, J., Frassica, F., Zhang, L., Rodriguez, J. P., et al. (2012) · Nature Medicine · doi:10.1038/nm.2793 · Cited by 631

Regulation of bone formation by osteoclasts involves Wnt/BMP signaling and the chemokine sphingosine-1-phosphate

Pederson, L., Ruan, M., Westendorf, J. J., Khosla, S., & Oursler, M. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805133106 · Cited by 556

Induction of Rapid Osteoblast Differentiation in Rat Bone Marrow Stromal Cell Cultures by Dexamethasone and BMP-2

Rickard, D. J., Sullivan, T. A., Shenker, B. J., Leboy, P. S., & Kazhdan, I. (1994) · Developmental Biology · doi:10.1006/dbio.1994.1022 · Cited by 537

Commentary: Concurrent administration of PTH and antiresorptives: Additive effects or DXA cosmetics

Eriksen, E. F., & Brown, J. P. (2016) · Bone · doi:10.1016/j.bone.2016.02.009 · Cited by 15

Exercise for optimizing bone health after hormone-induced increases in bone stiffness

Hughes, J. M., Guerriere, K. I., Popp, K. L., Castellani, C. M., & Pasiakos, S. M. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1219454 · Cited by 14

Osteoporosis under psychological stress: mechanisms and therapeutics

Xu, H., Liu, J.-X., Zhou, Z.-K., Zheng, C., Sui, B., Yuan, Y., Kong, L., Jin, Y. J., & Chen, J. (2024) · Life Medicine · doi:10.1093/lifemedi/lnae009 · Cited by 13

Toll-like receptor-2 induced inflammation causes local bone formation and activates canonical Wnt signaling

Henning, P., Kassem, A., Westerlund, A., Lundberg, P., Engdahl, C., Lionikaite, V., Wikström, P., Wu, J., Li, L., Lindholm, C., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1383113 · Cited by 12

High throughput, quantitative analysis of human osteoclast differentiation and activity

Diepenhorst, N. A., Nowell, C. J., Rueda, P., Henriksen, K., Pierce, T. L., Cook, A. E., Pastoureau, P., Sabatini, M., Charman, W. N., Christopoulos, A., et al. (2016) · Analytical Biochemistry · doi:10.1016/j.ab.2016.12.010 · Cited by 13

Evaluation of the effect of CaD on the bone structure and bone metabolic changes in senile osteoporosis rats based on MLP–ANN methods

Tang, X., Gao, Y., Chen, Y., Li, X., Yu, P., Ma, Z., & Liu, R. (2019) · Food & Function · doi:10.1039/c9fo01322a · Cited by 12

Roles of Slit Ligands and Their Roundabout (Robo) Family of Receptors in Bone Remodeling

Niimi, T. (2020) · Advances in experimental medicine and biology · doi:10.1007/5584_2020_586 · Cited by 11

Effects of Long-Term Odanacatib Treatment on Bone Gene Expression in Ovariectomized Adult Rhesus Monkeys: Differentiation From Alendronate

Muise, E. S., Podtelezhnikov, A. A., Pickarski, M., Loboda, A. P., Tan, Y., Hu, G., Thomspon, J. R., & Duong, L. T. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2752 · Cited by 12

Fermentation Improves the Preventive Effect of Soybean Against Bone Loss in Senescence‐Accelerated Mouse Prone 6

Nirmala, F. S., Lee, H.-J., Kim, J., Jung, C. H., Ha, T. Y., Jang, Y. J., & Ahn, J. (2019) · Journal of Food Science · doi:10.1111/1750-3841.14433 · Cited by 12

The protective role of Ephrin-B2/EphB4 signaling in osteogenic differentiation under inflammatory environment

Qu, F., Song, Y., Wu, Y., Huang, Y., Zhong, Q., Zhang, Y., Fan, Z., & Xu, C. H. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112505 · Cited by 11

An IGA-FEA model for flexoelectricity-induced healing of microcracks in cortical bone

Witt, C., Kaiser, T., & Menzel, A. (2024) · Computer Methods in Applied Mechanics and Engineering · doi:10.1016/j.cma.2024.116919 · Cited by 11

The osteoblast lineage

Sims, N. A., & Martin, T. J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00004-x · Cited by 11

Context-Dependent Skeletal Effects of Erythropoietin

Hiram‐Bab, S., Neumann, D., & Gabet, Y. (2017) · Vitamins and hormones · doi:10.1016/bs.vh.2017.02.003 · Cited by 11

Macrophages and osteoclasts: similarity and divergence between bone phagocytes

Halper, J., Dolfi, B., Ivanov, S., Madel, M., & Blin‐Wakkach, C. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1683872 · Cited by 12

Notch signaling inhibition protects against LPS mediated osteolysis

Goel, P. N., Egol, A. J., Moharrer, Y., Brandfield-Harvey, B., Ahn, J., & Ashley, J. W. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.05.166 · Cited by 10

The Metabolic Features of Osteoblasts: Implications for Multiple Myeloma (MM) Bone Disease

Lungu, O., Toscani, D., Burroughs-Garcia, J., & Giuliani, N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054893 · Cited by 10

Biomimetic polydopamine-laced hydroxyapatite collagen material orients osteoclast behavior to an anti-resorptive pattern without compromising osteoclasts’ coupling to osteoblasts

Wang, L., Wu, T., Hu, X., Liu, J., Wu, D., Miguez, P. A., Wright, J. T., Zhang, S., Chi, J., Tseng, H. C., et al. (2021) · Biomaterials Science · doi:10.1039/d1bm01119g · Cited by 11

Coupling of bone formation and resorption

Sims, N. A., & Martin, T. J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00010-5 · Cited by 11

Ablation of Discoidin Domain Receptor 1 Provokes an Osteopenic Phenotype by Regulating Osteoblast/Osteocyte Autophagy and Apoptosis

Chou, H., Lin, S., Chou, L.-Y., Ho, M., Chuang, S., Cheng, T., Kang, L., Lin, Y.-S., Wang, Y., Wei, C.-W., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10092173 · Cited by 9

The Impact of Culture Variables on a 3D Human In Vitro Bone Remodeling Model: A Design of Experiments Approach

de Wildt, B. W. M., Cuypers, L. A. B., Cramer, E. E. A., Wentzel, A. S., Ito, K., & Hofmann, S. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202301205 · Cited by 9

Basic Aspects of Osteoblast Function

Vrahnas, C., & Sims, N. A. (2020) · Contemporary Endocrinology · doi:10.1007/978-3-319-69287-6_1 · Cited by 10

Effects of hydroxyapatite gypsum puger scaffold applied to rat alveolar bone sockets on osteoclasts, osteoblasts and the trabecular bone area

Naini, A., Sudiana, I. K., Rubianto, M., Kresnoadi, U., & Latief, F. D. E. (2019) · Dental Journal (Majalah Kedokteran Gigi) · doi:10.20473/j.djmkg.v52.i1.p13-17 · Cited by 8

Nutraceuticals in osteoporosis prevention

Roseti, L., Borciani, G., Grassi, F., Desando, G., Gambari, L., & Grigolo, B. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1445955 · Cited by 12

A small molecular inhibitor of LRRK1 identified by homology modeling and virtual screening suppresses osteoclast function, but not osteoclast differentiation, in vitro

Si, M.-J., Zeng, C., Goodluck, H., Shen, S., Mohan, S., & Xing, W. (2019) · Aging · doi:10.18632/aging.101977 · Cited by 8

Bif‐1/Endophilin B1/SH3GLB1 regulates bone homeostasis

Touyama, K., Khan, M., Aoki, K., Matsuda, M., Hiura, F., Takakura, N., Matsubara, T., Harada, Y., Hirohashi, Y., Tamura, Y., et al. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.29193 · Cited by 8

Targeting osteoclast-derived DPP4 alleviates inflammation-mediated ectopic bone formation in ankylosing spondylitis

Lee, S. H., Lee, K. H., Kim, D. H., Jeon, C., Whangbo, M., Jo, H.-R., Youn, J., Lee, C., Choi, S. H., Park, Y., et al. (2025) · Arthritis Research & Therapy · doi:10.1186/s13075-025-03474-2 · Cited by 8

Molecularly Imprinted Polymers: Shaping the Future of Early-Stage Bone Loss Detection─A Review

Agnishwaran, B., Manivasagam, G., & Udduttula, A. (2024) · ACS Omega · doi:10.1021/acsomega.3c08977 · Cited by 7

Cellular Contributors to Bone Homeostasis

Rauner, M., Jähn, K., Hemmatian, H., Colditz, J., & Goettsch, C. (2020) · Contemporary cardiology · doi:10.1007/978-3-030-46725-8_16 · Cited by 6

Distinct Concentration-Dependent Molecular Pathways Regulate Bone Cell Responses to Cobalt and Chromium Exposure from Joint Replacement Prostheses

Shah, K. M., Dunning, M., Gartland, A., & Wilkinson, J. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105225 · Cited by 7

Pretreatment with Pamidronate Decreases Bone Formation but Increases Callus Bone Volume in a Rat Closed Fracture Model

Morse, A., McDonald, M. M., Mikulec, K., Schindeler, A., Munns, C. F., & Little, D. G. (2019) · Calcified Tissue International · doi:10.1007/s00223-019-00615-z · Cited by 7

Estrogen loss activates memory T-cells to compromise bone integrity through distinct cortical compartments in mice

Wu, D., Cline-Smith, A., Goering, D., Choudhary, A., Novack, D. V., & Aurora, R. (2025) · Journal of Bone and Mineral Research · doi:10.1093/jbmr/zjaf089 · Cited by 6

Activation of protein kinase C accelerates murine osteoclastogenesis partly via transactivation of RANK gene through functional AP-1 responsive element in RANK gene promoter

Kitazawa, R., Kinto-Shibahara, S., Haraguchi, R., Kohara, Y., & Kitazawa, S. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.05.144 · Cited by 6

Plasma Membrane Receptors Involved in the Binding and Response of Osteoclasts to Noncellular Components of the Bone

Karanth, D., Martin, M. L., & Holliday, L. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810097 · Cited by 7

EphrinB2 Signalling in Osteoblast Differentiation, Bone Formation and Endochondral Ossification

Vrahnas, C., & Sims, N. A. (2015) · Current Molecular Biology Reports · doi:10.1007/s40610-015-0024-0 · Cited by 6

Deficiency of sphingosine-1-phosphate receptor 3 does not affect the skeletal phenotype of mice lacking sphingosine-1-phosphate lyase

Heckt, T., Brylka, L., Neven, M., Amling, M., & Schinke, T. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219734 · Cited by 6

Giant Cell Tumor of Bone: Biology, Pathophysiology, and Histopathology in the Era of H3F3A

Carneiro, B. D., Brilhante, S. G., Faria, C., Fonseca, S., & Pozza, D. H. (2026) · Biomedicines · doi:10.3390/biomedicines14020449 · Cited by 5

Bone remodeling biology

Kahla, R. B., & Barkaoui, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-88467-9.00002-3 · Cited by 6

Integrating Endocrine and Paracrine Influences on Bone; Lessons From Parathyroid Hormone and Parathyroid Hormone-Related Protein

Martin, T. J., & Sims, N. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804182-6.00017-4 · Cited by 5

Apoptotic bodies in bone homeostasis and skeletal disease: biology and therapeutic implications

Xi, Y., Qu, Y., Zhang, Z. H., Xu, J., Luo, F., & Dou, C. (2026) · APOPTOSIS · doi:10.1007/s10495-026-02386-z · Cited by 4

Exploring Omega-3′s Impact on the Expression of Bone-Related Genes in Meagre (Argyrosomus regius)

Luján-Amoraga, L., Delgado-Martín, B., Lourenço‐Marques, C., Gavaia, P. J., Bravo, J., Bandarra, N. M., Domínguez, D., Izquierdo, M. S., Pousão‐Ferreira, P., & Ribeiro, L. (2023) · Biomolecules · doi:10.3390/biom14010056 · Cited by 4

Strategies for the Codelivery of Osteoclasts and Mesenchymal Stem Cells in 3D-Printable Osteochondral Scaffolds

Jabari, E., Choe, R. H., Kuzemchak, B. C., Venable-Croft, A., Choi, J. Y., McLoughlin, S. T., Packer, J. D., & Fisher, J. P. (2024) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2024.0162 · Cited by 4

Analysis of Myrmecodia Pendens in Bone Healing Process to Improve the Quality of Life: Literature Review

Epsilawati, L., Satari, M. H., & Azhari (2019) · IOP Conference Series Earth and Environmental Science · doi:10.1088/1755-1315/248/1/012052 · Cited by 4

Unraveling Jawbone Susceptibility: Distinctive Features Underlying Medication-Related Osteonecrosis

Paczona, B., Piffkò, J., & Janovszky, Á. (2026) · Dentistry Journal · doi:10.3390/dj14010018 · Cited by 3

The adiponectin agonist AdipoRon accelerates osteoporosis development in two different models and modulates adipocyte differentiation

Halper, J., Nicolas, S., Gilardi, F., Winkler, C., Materozzi, M., Schiffrin, M., Jouzeau, J., Blin‐Wakkach, C., Desvergne, B., Chabry, J., et al. (2025) · Bone · doi:10.1016/j.bone.2025.117628 · Cited by 3

Bifunctional Role of CrkL during Bone Remodeling

Kim, J. H., Kim, K., Kim, I., Seong, S., Kook, H. Y., Kim, K. K., Koh, J., & Kim, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137007 · Cited by 3

Cellular Senescence in Bone

Wang, D., & Wang, H. (2022) · Physiology · doi:10.5772/intechopen.101803 · Cited by 4

Secondary injury and pro-inflammatory macrophages increase osteophyte growth and fracture healing in canine atrophic nonunion.

Pan, J., Gao, Y., Pan, Z., Lu, K., Fan, J., Wang, C., Hao, Z., Li, Z., Wang, T., & Zhi, Y. (2022) · PubMed Central · Cited by 3

Nutraceutical Benefits for Bone Health: Role in Osteoporosis PreventionPreprint

Roseti, L., Borciani, G., Grassi, F., Desando, G., Gambari, L., & Grigolo, B. (2023) · Preprints.org · doi:10.20944/preprints202311.1546.v1 · Cited by 3

Neuro-osteo crosstalk: The sympathetic nervous system as a key driver of SCI-induced osteoporosis

Bryan, J. A., Jackson, W., Lemmens, N., & Hook, M. A. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115824 · Cited by 2

Treatment with 50 μM Sodium Fluoride Suppresses Aging-Induced Alveolar Bone Resorption in Mice

Oka, S., Li, X., Taguchi, C., Wang, C., Tewari, N., Arikawa, K., Liu, Y. F., & BHAWAL, U. K. (2021) · Journal of Hard Tissue Biology · doi:10.2485/jhtb.30.225 · Cited by 2

Association between rs12742784 polymorphism and hip fracture, bone mineral density, and EPHB2 mRNA expression levels in elderly Chinese women

Ruan, Z., Zhu, Y., Lin, Z., Long, H., Zhao, R., Sun, B., Cheng, L., & Zhao, S. (2019) · Climacteric · doi:10.1080/13697137.2019.1640195 · Cited by 2

The comparative Micro-CT analysis on trabecular bone density between hydroxyapatite gypsum puger scaffold application and bovine hydroxyapatite scaffold application

Naini, A. (2021) · Dental Journal (Majalah Kedokteran Gigi) · doi:10.20473/j.djmkg.v54.i1.p11-15 · Cited by 2

Citral promotes the cell proliferation, differentiation, and calcium mineralization in human osteoblast-like MG-63 cells

Mu, H., Pang, Y., Liu, L., Li, F., & Wang, J. (2021) · Pharmacognosy Magazine · doi:10.4103/pm.pm_242_20 · Cited by 2

Role of Interleukins on Physiological and Pathological Bone Resorption and Bone Formation: Effects by Cytokines in The IL-6 and IL-10 Families

Lerner, U. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11553-3 · Cited by 2

Glucocorticoid-induced osteoporosis in children: emerging vascular and molecular targets

Barik, S. K., & Crane, J. L. (2025) · Current Opinion in Pediatrics · doi:10.1097/mop.0000000000001476 · Cited by 2

The nervous system: innervations of the skeleton; bone homeostasis; and peripheral neuropathies (Baxter’s neuropathy, tarsal tunnel syndrome, and peroneal neuropathy)

Pierre-Jerome, C. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99352-4.00009-7 · Cited by 1

Bone Tumours - A Comprehensive Review of Selected Topics

Amarasekera, H. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.100923

Perspective Chapter: Breast-Tumor-Derived Bone Pre-Metastatic Disease – Interplay between Immune and Bone Cells within Bone Marrow Microenvironment

Monteiro, A. C., & Bonomo, A. C. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.107278 · Cited by 1

Tuning the biological performance of calcium phosphates through microstructural and chemical modifications

Díez-Escudero, A. (2017) · doi:10.5821/dissertation-2117-121021 · Cited by 1

Stem cell niches in bone and their roles in cancer metastasis

Holen, I., & Quayle, L. A. (2020) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2020.09.002

Modeling maintenance and repair: The matrix loaded

Suki, B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819716-5.00009-5

PTHR1 in Bone

Hénaff, C. L., & Partridge, N. C. (2022) · Wiley eBooks · doi:10.1002/9781119564782.ch20

The impact of culture variables on 3D human in vitro bone remodeling; a design of experiments approachPreprint

de Wildt, B. W. M., Cuypers, L. A. B., Cramer, E. E. A., Wentzel, A. S., Ito, K., & Hofmann, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.11.516134

Bone Remodeling – Clinical Evaluation

Nuti, R. (2023) · Endocrinology · doi:10.1007/978-3-030-19632-5_6-1 · Cited by 1

Bone remodeling

Narla, R. R., & Ott, S. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00034-0

The peripheral nervous system: peripheral neuropathies in the diabetic foot

Pierre-Jerome, C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13328-2.00022-2

A novel optimized silver nitrate staining method for visualizing the osteocyte lacuno-canalicular system

Wu, J., Xue, C., Li, Q., Wu, H., Zhang, J., Wang, C., Dai, W., & Wang, L. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1561576

Additional file 1 of LncRNA PTCSC3 is upregulated in osteoporosis and negatively regulates osteoblast apoptosis

Liu, X., Chen, M., Liu, Q., Li, G., Yang, P., & Zhang, G. (2022) · Figshare · doi:10.6084/m9.figshare.19373230

Integrating endocrine and paracrine influences on bone: lessons from parathyroid hormone and parathyroid hormone-related protein

Martin, T. J., & Sims, N. A. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-13683-2.00004-9

Effects of continuous and intermittent hypergravity on skeleton

Gnyubkin, V. (2015) · theses.fr (ABES) · doi:10.70675/2e978c63z66ebz4a68zb083za6c62d439b14 · Cited by 1

Two-dimentional complex modeling of bone and joint infections using agent-based simulation

Alsassa, S. (2019) · theses.fr (ABES) · doi:10.70675/5dde1efcza50dz454azb715z5fccb48fd646

Hypoxia and FGF-2 priming for bone tissue engineering : an in vitro and in vivo study

Novais, A. (2019) · theses.fr (ABES) · doi:10.70675/9259747ezadcez4488zbf3fz0f2e537f5dd9

Inhibition des jonctions gap dans l'hématopoïèse leucémique

Kouzi, F. (2018) · doi:10.70675/c8bd8bf4za13cz454bzb425ze6a9e1f6d731

Dosimetric characterization and evaluation of radiation-induced lesions after irradiation on interventional radiology condition

Guillou, M. (2023) · doi:10.70675/0e17b9d4z4ba3z4bb7zbcd1z01ac7eb0d22b

Synergistic effects of intermittent parathyroid hormone (1–34) and masticatory force for alveolar bone remodeling in the maxilla of dogs

Kim, M.-J., Moon, H.-J., Kyoung, D.-K., Kim, J.-Y., Kim, S.-H., & Kim, J.-W. (2026) · Journal of Stomatology Oral and Maxillofacial Surgery · doi:10.1016/j.jormas.2026.102850

Stage-dependent analysis of IL-6, TGF-β, osteocalcin, and sRANKL in the synovial fluid of dogs with osteoarthritis

Neumann, S., Diekmann, H., & Lauenstein-Bosse, S. (2026) · Scientific Reports · doi:10.1038/s41598-026-56559-6 · Cited by 1

Progress on novel compounds for the treatment of bone metabolism-related disorders: focus on osteoporosis and beyond

Song, Y., Zhang, R., Zhang, X., Wang, J., Chen, J., & Li, L. (2026) · Frontiers in Chemistry · doi:10.3389/fchem.2026.1861883

Osteoimmune microenvironmental failure in osteonecrosis of the femoral head: a necrosis-inflammation-repair loop and immune-editing-inspired framework for hip preservation

Zheng, H., Li, C., Xie, X. S., Yao, C., Ma, J., Chen, W., & Gao, X. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1891308

2′-O-Galloylhyperin attenuates osteoclastogenesis and estrogen-deficiency osteoporosis by targeting MLK3-mediated NF-κB signaling

He, G., Chen, R., Fang, Z., Fu, S., Wang, Y., Li, H., Hu, P., Bao, J., & Ran, J. (2026) · Biochemical Pharmacology · doi:10.1016/j.bcp.2026.118327

Heme Oxygenase-1 in Bone Remodeling: Molecular Mechanisms and Therapeutic Implications

Pattananandecha, T., Apichai, S., Saenjum, C., & Surh, Y. (2026) · Biomolecules · doi:10.3390/biom16091224

Effects of Withania somnifera root extract on sleep quality, body composition, and menopausal symptoms in postmenopausal women: a randomized, double-blind, placebo-controlled trial

Obhrai, S., Shenoy, S., & ARORA, M. (2026) · Menopause The Journal of The North American Menopause Society · doi:10.1097/gme.0000000000002894

Advances in 3D bioprinting of immunoregulatory biomaterials for bone regeneration

Xiaonan, W., & Zhang, A. (2026) · Materials Today Bio · doi:10.1016/j.mtbio.2026.103714

Glucocorticoid receptor regulates osteoblast differentiation in association with Map7d2 and Erk2 signaling

Kölbl, C., Eckert, A., Nungeß, S., Lee, S., Tuckermann, J. P., Ignatius, A. A., & Ahmad, M. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1967862

Osteoclasts Provide Coupling Signals to Osteoblast Lineage Cells Through Multiple Mechanisms

Sims, N. A., & Martin, T. J. (2020) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021119-034425 · Cited by 286

Molecular Mechanisms in Coupling of Bone Formation to Resorption

Martin, T. J., Gooi, J. H., & Sims, N. A. (2009) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukargeneexpr.v19.i1.40 · Cited by 167

New aspects of bone biology

de Vernejoul, M. C., & Marie, P. J. (2001) · doi:10.1093/oso/9780192632302.003.0001 · Cited by 1

Estrogens, Cytokines, and Bone Metabolism

Manolagas, S. C. (1994) · Springer eBooks · doi:10.1007/978-3-662-03043-1_6

Osteonal and hemi‐osteonal remodeling: The spatial and temporal framework for signal traffic in adult human bone

Parfitt, A. M. (1994) · Journal of Cellular Biochemistry · doi:10.1002/jcb.240550303 · Cited by 1,001