Osteoclasts Provide Coupling Signals to Osteoblast Lineage Cells Through Multiple Mechanisms

Effect of Parathyroid Hormone (1-34) on Fractures and Bone Mineral Density in Postmenopausal Women with Osteoporosis

Neer, R. M., Arnaud, C. D., Zanchetta, J. R., Prince, R., Gaich, G. A., Reginster, J.-Y., Hodsman, A. B., Eriksen, E. F., Ish-Shalom, S., Genant, H. K., et al. (2001) · New England Journal of Medicine · doi:10.1056/nejm200105103441904 · Cited by 4,602

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

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Modulation of Osteoclast Differentiation and Function by the New Members of the Tumor Necrosis Factor Receptor and Ligand Families

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Classification, Functions, and Clinical Relevance of Extracellular Vesicles

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c-Fos: a Key Regulator of Osteoclast-Macrophage Lineage Determination and Bone Remodeling

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The Effects of Parathyroid Hormone and Alendronate Alone or in Combination in Postmenopausal Osteoporosis

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

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PDGF-BB secreted by preosteoclasts induces angiogenesis during coupling with osteogenesis

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Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate

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Soluble interleukin-6 receptor triggers osteoclast formation by interleukin 6.

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A novel stromal cell source of RANKL during sustained osteoclast activation in disuse osteoporosis

Gochi, K., Sumiya, E., Sakitani, N., Otsuka, Y., Muratani, M., Sawa, S., Ochi, H., Sawada, Y., Nakahama, K., & Shinohara, M. (2026) · The Journal of Physiology · doi:10.1113/jp289268 · Cited by 2

Implications of notoginsenoside R1 in osteoclastogenesis and bone remodeling via nitric oxide modulation

Chen, J., Chen, C.-C., Lin, W.-L., & Hsueh, T.-P. (2026) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-026-05264-y · Cited by 2

Beyond resorption-driven coupling: a multi-layered framework for osteoclast–osteoblast communication and its therapeutic consequences

Qiu, H., Liu, S., Jiang, Y., Lai, Y., Lin, Q., & Huang, A. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1821292 · Cited by 2

From Bone Marrow Reserve to Metastatic Niche: How Neutrophil-Lineage Cells Shape Skeletal Colonization

Hamza, F. N., Zhra, M., Holail, J., Alotab, S., Alshater, S., Al-Masud, A. A., & Mohammad, K. S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27135975 · Cited by 2

The potential of RANKL reverse signaling as a novel pharmacological target

Honma, M. (2023) · Folia Pharmacologica Japonica · doi:10.1254/fpj.22145 · Cited by 2

Flavonoids from Dalbergia cochinchinensis: Impact on osteoclastogenesis

Shao, F., Panahipour, L., & Gruber, R. (2022) · Journal of Dental Sciences · doi:10.1016/j.jds.2022.06.026 · Cited by 2

Mechanical load, sex hormones, and bone modeling

Windahl, S. H., & Lerner, U. H. (2015) · Wiley eBooks · doi:10.1002/9781118916148.ch6 · 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

Quantitative Multicolored Deep Imaging of Human Bones Reveals a Composite Osteo-Sinusoidal Niche for Mesenchymal Stromal CellsPreprint

Chu, N. T. L., Dregval, O. A., Chang, Y., Kryukov, E., Tian, X., Liu, X., Trompet, D., Zhang, M. S., Li, L., Li, Z., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.07.680053 · Cited by 2

Serine synthesis promotes bone degradation

Riddle, R. C., & Choquette, G. M. (2024) · Nature Metabolism · doi:10.1038/s42255-023-00949-x · Cited by 1

Spatiotemporal Characterization of Microstructure Morphology, Mechanical Properties and Bone Remodeling of Rat Tibia Under Uniaxial Compressive Overload Loading

Liu, Z., Gao, J., & Gong, H. (2024) · Annals of Biomedical Engineering · doi:10.1007/s10439-024-03531-y · Cited by 1

Discovery of Novel Antiosteoporosis Leads with Bone Resorption Inhibition and Anabolic Promotion through a Chemotype-Assembly Approach

Huang, D., Zhao, C., Li, R., Yao, N., Xu, J., & Gu, Q. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c00909 · Cited by 1

Conotoxins from sea snails as potential bone remodeling disruptors

Iduarte, B. I., Fournier, P. G. J., Galindo-Torres, P., Ventura-López, C., Licea-Navarro, A. F., Bernáldez-Sarabia, J., & Juárez, P. (2025) · JBMR Plus · doi:10.1093/jbmrpl/ziaf025 · Cited by 1

Formation of Membrane Domains via Actin Waves: A Fundamental Principle in the Generation of Dynamic Structures in Phagocytes

Takito, J., & Nonaka, N. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104759 · Cited by 1

Liquid biopsy in orthopedic trauma: exosomes as functional mediators and mechanistic indicators in post-traumatic complications

Gan, J., Zhong, S., Xie, J., & Zou, L. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1707928 · Cited by 1

Microstructure-tailored β-tricalcium phosphate scaffolds utilize degradation-guided osteoclast suppression to accelerate bone regeneration

Lu, Q., Zeng, F., Diao, J., Kuang, Y., Zhao, N., & Wang, Y. (2025) · Journal of Materials Chemistry B · doi:10.1039/d5tb01393c · Cited by 1

Determination of the binding affinity between osteoprotegerin (OPG) and receptor activator of nuclear factor-κB ligand (RANKL) utilizing Gaussia luciferase in living cells

Shibata, Y., Nishida‐Fukuda, H., Nakayama, H., Izumi, Y., Suzuki, R., Yokawa, S., Sato, T., Furuno, T., Matsubara, M., Miyazawa, K., et al. (2026) · Journal of Oral Biosciences · doi:10.1016/j.job.2025.100727 · Cited by 1

JAK1/STAT3 signalling in cortical bone development, growth and maintenance

Koh, N. Y. Y., Maes, C., & Sims, N. A. (2026) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2026.120129 · Cited by 1

Bone-seeking nanomaterials for rebalancing bone remodeling in osteoporosis

Wang, F., Liang, F., Zhou, X., Ding, Y., Wu, M., Li, N., Wang, F., & Yan, W. (2026) · International Journal of Pharmaceutics X · doi:10.1016/j.ijpx.2026.100578 · Cited by 1

Mitochondrial OXPHOS integrates immunometabolic cascade for bone regeneration via coupled ATP production and ROS homeostasis

Chen, J., He, P., Gu, J., Wu, J., Liu, Y., Lei, W., He, T., Zheng, L., de Bruijn, J. D., Yuan, H., et al. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104272 · Cited by 1

Functionalizing biomaterials for osseointegration – microRNAs at the crossroads of bone formation and immune modulation

Azari, M., Bella, E. D., & Wildemann, B. (2026) · Bone and Joint Research · doi:10.1302/2046-3758.157.bjr-2025-0576.r1 · Cited by 1

Stanniocalcin 1 at the nexus of calcium homeostasis, IGF signaling, and cancer immunity

Duan, C. (2026) · Endocrine Reviews · doi:10.1210/endrev/bnag026 · Cited by 1

Preventing osteoporotic bone loss in mice by promoting balanced bone remodeling through M-CSFRGD, a dual antagonist to c-FMS and αvβ3 receptors

Zur, Y., Katchkovsky, S., Itzhar, A., Abramovitch-Dahan, C.-V., Stepensky, D., Papo, N., & Levaot, N. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136821 · Cited by 1

High performance composites of bioactive glass fiber-reinforced degradable PCL- b -PLLA for load-bearing bone repair

Wang, Y., He, Z., Zhao, Q. B., Pan, Y., Zhang, Z., Pu, Y., Zhu, Y., & He, B. (2025) · New Journal of Chemistry · doi:10.1039/d5nj01300c · Cited by 1

Effect of melatonin on reparative regeneration of bone tissue in the jaw bones experiment

Shchetinin, E., Sirak, E. S., Афанасьева, Г. А., Petrosyan, G., Shchetinina, E. E., & Sirak, S. (2020) · Medical news of the North Caucasus · doi:10.14300/mnnc.2020.15135 · Cited by 1

Bone Metabolism

Kim, S., Macfarlane, E., Seibel, M. J., & Zhou, H. (2021) · Springer eBooks · doi:10.1007/978-3-030-57401-7_31 · Cited by 1

CD11B + CD36 + cells are bone anabolic macrophages that limit age-associated bone lossPreprint

Koroth, J., Karkache, I. Y., Vu, E. K., Mansky, K. C., & Bradley, E. W. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.13.612932 · Cited by 1

Epigenetics of Osteoporosis

Bischof, O., Ebert, R., Taipaleenmäki, H., Hesse, E., & Jakob, F. J. (2021) · Osteologie/Osteology · doi:10.1055/a-1527-4395

Editorial: Developmental Biology and Regulation of Osteoclasts

Gabet, Y., Neumann, D., Levaot, N., Elson, A., & Sims, N. A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.769320

Osteoclast-rich lesions of bone

Flanagan, A. M., Tirabosco, R., & Amary, F. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821666-8.00045-1

Efeito do alendronato, da dexametasona e da associação de ambos sobre a osteoclastogênese: um estudo in vitro

de Faria, L. P. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.23.2021.tde-27102021-123034

Sugar transporter Slc37a2 regulates bone metabolism via a dynamic tubular lysosomal network in osteoclastsPreprint

Ng, P. Y., Ribet, A. B. P., Guo, Q., Mullin, B. H., Tan, J., Landao‐Bassonga, E., Stephens, S., Chen, K., Abudulai, L. N., Bollen, M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.28.489831

Bone Metabolism

Kim, S., Macfarlane, E., Seibel, M. J., & Zhou, H. (2020) · Springer eBooks · doi:10.1007/978-3-030-21573-6_31-1

Engineering micro for repairing macro

Galván-Chacón, V. (2022) · doi:10.26481/dis.20220531vg

Muscle-Derived Extracellular Vesicles Improved Disuse-Induced Osteoporosis by Rebalancing Bone Formation and Bone ResorptionPreprint

Su, X., Huang, H., Liao, L., Xing, X., Ma, S., Xu, X., Tang, Q., Gao, X. Q., Yang, J., Li, M., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4158151

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

Metal-doped ceramic nanoparticles in bone therapeutics

Muthuraman, A. R., Siddartha, U. S. R., Kumar, R. A., & Moorthi, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85784-0.00020-0

Cellular Basis for Sequencing of Antiresorptive and Anabolic Therapies for Bone: Commentary on “Bone Remodeling and Modeling: Cellular Targets for Antiresorptive and Anabolic Treatments, Including Approaches Through the Parathyroid Hormone (PTH)/PTH-Related Protein Pathway”

Sims, N. A. (2023) · Neurospine · doi:10.14245/ns.2347242.621

Bone Remodeling – Clinical Evaluation

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

Calcium-sensing receptor

Vezzoli, G., Foligno, N. E., Maruca, K., & Mora, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00018-2

Inflammation and macrophage development

Izquierdo, E., Ardura, J. A., Gortázar, A. R., Alonso, V., Barker‐Tejeda, T. C., Pérez‐Gordo, M., & Escribese, M. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-821754-2.00006-0

Skeletal Physiology: Responses to Exercise and Training

Whitton, R. C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-7020-8370-9.00012-6

Odanacatib Coating Supports Osseointegration of Implants: A Preclinical Study

Sanches, N. D. S., Marchiolli, C. L., Cervantes, L. C. C., Stein, M. C. R. V., Berton, S. A., do Prado, E. L. L., Kampleitner, C., Souza, F. Á., Okamoto, R., Gruber, R., et al. (2025) · Clinical Oral Implants Research · doi:10.1111/clr.70038

Anabolic effects of Sost deficiency partially offset Opg deficiency–induced catabolism in cortical bone

Koide, M., Yamashita, T., Kobayashi, Y., Yasuda, H., Nakamura, M., & Udagawa, N. (2025) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-025-01653-4

Qingre Huoxue decoction and its active compound Quercetin modulate bone remodeling by inhibiting ATF4 hyperactivation to attenuate bone erosion in rheumatoid arthritis

Xia, C., Chang, T., Gong, X., Zhang, F., Peng, Q., Song, M., Yao, C., Tang, X., & Jiang, Q. (2025) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-025-06333-7 · Cited by 2

Interdisciplinarity of secondary osteons: relevance of bioarchaeological and palaeontological research in biomedical cortical bone histology studies

Miszkiewicz, J. J., Cooke, K. M., Reid, H. E., & Louys, J. (2025) · Bone Reports · doi:10.1016/j.bonr.2025.101893 · Cited by 1

Additional file 1 of RhoA promotes osteoclastogenesis and regulates bone remodeling through mTOR-NFATc1 signaling

Wang, J., Xu, C., Zhang, J., Bao, Y., Tang, Y., Lv, X., Ma, B., Wu, X., & Mao, G. (2023) · Figshare · doi:10.6084/m9.figshare.22621151

Additional file 1 of Young osteocyte-derived extracellular vesicles facilitate osteogenesis by transferring tropomyosin-1

Wang, Z.-X., Lin, X., Cao, J., Liu, Y.-W., Luo, Z.-W., Rao, S.-S., Wang, Q., Wang, Y.-Y., Chen, C.-Y., Zhu, G.-Q., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25698287

Bone health in children and adolescents: impact of risk factors and modern preventive strategies

Бекетова, Г. В., Sharikadze, O. V., Balatska, N. I., & Солдатова, О. В. (2025) · CHILD`S HEALTH · doi:10.22141/2224-0551.20.8.2025.1932

Research Progress on Urinary Calcium and Other Bone Turnover Markers in Osteoporotic Fractures

罗, 金. (2026) · Advances in Clinical Medicine · doi:10.12677/acm.2026.162428

An alkaline nanosized platelet vesicle-based hydrogel for the treatment of osteoporotic bone defects

Yang, K., Yang, Y., Chen, X., Chen, Y., Dai, Z., Wang, Z., Hu, L., Li, Y. H., Wang, Y., Wang, Y., et al. (2026) · Materials Today Bio · doi:10.1016/j.mtbio.2026.103000

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

Synthetic Novel Flavonoids SZQ-4 Suppress Osteoclastogenesis and Ameliorate Osteoporosis via Inhibiting Reactive Oxygen Species and Regulating SIRT3

Zhou, R., Zhang, Y. M., Li, B., Yi, M., Tu, J., Jiang, T., Jiang, H., Hu, C., Ping, Y., Wang, J., et al. (2026) · Antioxidants · doi:10.3390/antiox15040426

Role of the osteoclast in bone regeneration induced by mesenchymal stem cells and calcium phosphate biomaterials

Humbert, P. (2020) · theses.fr (ABES) · doi:10.70675/8e4fd827zbb15z43a0zb23ez3e157122f5fa

Arginine–Silicate–Inositol Promotes Femoral Fracture Healing in Rats

Demir, Ş., Şahin, K., Özercan, İ. H., Once, G., Key, S., & Gürger, M. (2026) · Biological Trace Element Research · doi:10.1007/s12011-026-05085-7

Regulatory role of CXCR4 signaling in the multipotency and hematopoiesis-supporting capacities of skeletal stromal/stem cells in the bone marrow

Nader, Z. A. (2023) · theses.fr (ABES) · doi:10.70675/6755936dzb0dez4040z8c07za7d8177d8f67

Role of osteoblast-lineage cells in the systemic control of breast cancer growth and metastasis

Sakr, L. H. D. (2023) · theses.fr (ABES) · doi:10.70675/179977d9z1e5dz4366z9f34z1c637ab6d71c

A three-dimensional dynamic in vitro bone remodeling model reveals multicellular effects of anti-osteoporotic agents

Cai, J., Han, Y.-X., Mo, Y.-Y., Wang, T., Shan, Y., Wu, H., Li, L., Bu, Y., Xiao, F., Jiang, H., et al. (2026) · Life Sciences · doi:10.1016/j.lfs.2026.124396

Lysosome-triggered nanotherapy packages osteoclast apoptotic bodies with pro-anabolic lipids to couple anti-resorption and bone formation

Chen, P., Chen, Z. Y., Zhang, Z. H., Yu, Q., Zhang, J., Qu, Y., Dai, Q., Tan, J., Luo, Y., Guo, S., et al. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108225

Understanding the osteoinductivity of calcium phosphate ceramics: From material factors to biological mechanisms

Xu, T., Zhuang, J., Lu, J., Xu, S., Zeb, S., Ren, Y., Chen, M., Yuan, C., & Duan, R. (2026) · Ceramics International · doi:10.1016/j.ceramint.2026.05.162

TRPV4-mediated mechanotransduction governs surface topography-induced bone formation via macrophage-osteoclast axis

Wu, J., Gu, J., He, P., Liu, Y., Chen, J., Yang, L., Lei, W., He, T., de Bruijn, J. D., Zheng, L., et al. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.177550

A Two-Criteria Remodelling Model for Loading-Dependent Morphological Adaptation of Individual Trabeculae

Liu, Z., Li, S., & Silberschmidt, V. V. (2026) · Biomechanics · doi:10.3390/biomechanics6020048

In Silico Discovery and Preliminary In Vitro Evaluation of a SETDB1-Related Candidate Compound Associated with Early Osteogenic Effects

Li, Z., Zhang, X., Chen, S., Meng, Q., Lv, Z., Niu, Z., Li, J. M., & Chen, X. (2026) · Future Pharmacology · doi:10.3390/futurepharmacol6020031

Perfluorocarbon nanodroplets are cytocompatible with osteoblast-lineage cells and modulate in vitro osteoclastogenesis differentially in normoxia and hypoxia

O’Brien, K., Knowles, H. J., Sloan, S. P., Rumney, R. M. H., Carugo, D., Stride, E., & Evans, N. D. (2026) · Scientific Reports · doi:10.1038/s41598-026-57136-7

Wnt-activated osteocyte-driven 3D-bioprinted scaffolds orchestrate bone remodeling, angiogenesis and innervation to accelerate critical bone defect repair

Liu, Y., Huang, J., Li, S., & Tu, X. (2026) · Regenerative Biomaterials · doi:10.1093/rb/rbag124

Myeloid-specific interferon regulatory factor 5 promotes bone formation via orchestration of osteoclast lineage-osteoblast coupling

Zhao, H., Sun, X., Zhou, S., Zj, C., Yang, J., Yu, J., Wang, Z., Tang, Y., Lin, C., Wang, L., et al. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113279

Effects of hyperglycemia on the bone microenvironment in diabetic osteoporosis

Li, B., Wei, W., Zhang, Y.-L., & Zhang, X.-X. (2026) · World Journal of Diabetes · doi:10.4239/wjd.121312

Enfermedades metabólicas óseas y fisiología básica del hueso

Millán, M. M., & Hernández, J. L. H. (2026) · Medicine - Programa de Formación Médica Continuada Acreditado · doi:10.1016/j.med.2026.07.001

Targeting macrophage-mediated TGF-β/BMP signaling in ankylosing spondylitis: from inflammation to pathological bone formation

Aierxiding, S., & Ren, Z. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1788883 · Cited by 1

Encoding Intermittent Parathyroid Hormone Signals in Stem Cell Exosomes Enables Targeted Repair of Osteoporotic Bone DefectsPreprint

Fang, J., Wu, Y., Jin, X., Wu, X., Xu, B., Shan, J., Nan, L., Liu, S., Nie, W., Liu, J., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-10428498/v1

Bone structure, growth, adaptation and repair

Metzger, C. E., & Allen, M. R. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-26739-0.00011-9

Unraveling the Multifaceted Roles of Tissue-Resident Macrophages: Focus on Bone Homeostasis and Regeneration

Feng, X., Wu, Q., Yan, Y., Yu, B., Zhu, Z., Qiao, Y., & Wei, J. (2026) · Stem Cell Reviews and Reports · doi:10.1007/s12015-026-11202-9

Immunomodulatory role of MINDIN in bone microenvironment under inflammatory conditions

Rodríguez, V. A., Álvarez‐Carrión, L., Romeo, M., Gutiérrez-Rojas, I., de Casasola-Rodríguez, G. G., & Rodríguez, J. A. A. (2026) · Revista de Osteoporosis y Metabolismo Mineral · doi:10.20960/revosteoporosmetabminer.00102

Chondroitin sulfate modulates gut microbiota to improve bone metabolism and reduce locomotion problems in yellow-feathered broilers

Xue, Y., Yu-yang, X., Yao, M., Peng, X.-J., Wang, F., Nan, S., Jing, W., Zhang, F., Liu, X., Liu, Z., et al. (2026) · Animal nutrition · doi:10.1016/j.aninu.2026.03.008

Disease-associated TNFRSF11B variants differentially disrupt osteoprotegerin secretion and function

Suzuki, R., Nishida‐Fukuda, H., Fukuda, S., Shibata, Y., Sato, T., Miyazawa, K., & Suzuki, T. (2026) · Bone · doi:10.1016/j.bone.2026.118046

Reframing Osteoblast Homeostasis as a Systemic Endocrine–Metabolic Node: Mechanisms, Inter‐Organ Crosstalk, and Translational Strategies

Li, Y., Chen, Z., Li, G., Ji, S., Yin, R., & Wang, S. (2026) · Comprehensive physiology · doi:10.1002/cph4.70242

Adynamic Bone Disease in Chronic Kidney Disease: From Parathyroid Hormone Suppression-Driven Remodeling Phenotype to Osteoanabolic Therapy

Lu, K., Hou, Y., Wu, C., Fang, T., Hung, K.-C., & Lu, C.-L. (2026) · American Journal of Nephrology · doi:10.1159/ajn/ablag003

Pyroptotic cell-derived factors promote osteoclast differentiationPreprint

Li, Y., Wang, C., 许灿新, Zou, W., Kaur, K., Rohatgi, R., Pokhrel, N. K., Rohatgi, R., Abu‐Amer, Y., & 许灿新 (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.03.748049

Virtual Screening and Molecular Dynamics Simulations Identifying Natural Product-Derived Cathepsin K Inhibitors as Potential Therapeutics for Osteoporosis

Tarathipayakul, T., Ravikumar, Y., Srichairatanakool, P., Khowsathit, J., & Srichairatanakool, S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27188258

Engineering high-fidelity bone organoids: Operational classification, multilineage crosstalk, biofabrication evidence, and translational validation

Huang, Y., Zhang, T., Chen, S., Zhou, H., Xu, H., Zhang, F., Li, L., & Lyu, F. (2026) · Materials Today Bio · doi:10.1016/j.mtbio.2026.103676

Fracture healing: from molecular and cellular mechanisms to therapeutic strategies

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