The cell biology of bone metabolism

Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation.

Lacey, D. L., Timms, E., Tan, H.-L., Kelley, M. J., Dunstan, C. R., Burgess, T., Elliott, R., Colombero, A., Elliott, G., Scully, S., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81569-x · Cited by 5,439

The Wnt Signaling Pathway in Development and Disease

Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325

Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation

Ducy, P., Zhang, R., Geoffroy, V., Ridall, A. L., & Karsenty, G. (1997) · Cell · doi:10.1016/s0092-8674(00)80257-3 · Cited by 4,246

Targeted Disruption of Results in a Complete Lack of Bone Formation owing to Maturational Arrest of Osteoblasts

Komori, T., Yagi, H., Nomura, S., Yamaguchi, A., Sasaki, K., Deguchi, K., Shimizu, Y., Bronson, R. T., Gao, Y.-H., Inada, M., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80258-5 · Cited by 4,244

Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL

Yasuda, H., Shima, N., Nakagawa, N., Yamaguchi, K., Kinosaki, M., Mochizuki, S.-I., Tomoyasu, A., Yano, K., Goto, M., Murakami, A., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.3597 · Cited by 4,224

Novel Regulators of Bone Formation: Molecular Clones and Activities

Wozney, J. M., Rosen, V., Celeste, A. J., Mitsock, L. M., Whitters, M. J., Kriz, R., Hewick, R. M., & Wang, E. A. (1988) · Science · doi:10.1126/science.3201241 · Cited by 3,874

The Novel Zinc Finger-Containing Transcription Factor Osterix Is Required for Osteoblast Differentiation and Bone Formation

Nakashima, K., Zhou, X., Kunkel, G., Zhang, Z., Deng, J. M., Behringer, R. R., & de Crombrugghe, B. (2002) · Cell · doi:10.1016/s0092-8674(01)00622-5 · Cited by 3,608

Functional interaction of β-catenin with the transcription factor LEF-1

Behrens, J., von Kries, J. P., Kühl, M., Bruhn, L., Wedlich, D., Grosschedl, R., & Birchmeier, W. (1996) · Nature · doi:10.1038/382638a0 · Cited by 2,912

Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development

Otto, F., Thornell, A., Crompton, T., Denzel, A., Gilmour, K. C., Rosewell, I. R., Stamp, G., Beddington, R. S. P., Mundlos, S., Olsen, B. R., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80259-7 · Cited by 2,813

Induction and Activation of the Transcription Factor NFATc1 (NFAT2) Integrate RANKL Signaling in Terminal Differentiation of Osteoclasts

Takayanagi, H., Kim, S., Koga, T., Nishina, H., Isshiki, M., Yoshida, H., Saiura, A., Isobe, M., Yokochi, T., Inoue, J.-I., et al. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00369-6 · Cited by 2,701

Bisphosphonate conjugation enhances the bone-specificity of NELL-1-based systemic therapy for spaceflight-induced bone loss in mice

Ha, P., Kwak, J. H., Zhang, Y., Shi, J., Tran, L., Liu, T. P., Pan, H.-C., Lee, S., Kim, J. K., Chen, E., et al. (2023) · npj Microgravity · doi:10.1038/s41526-023-00319-7 · Cited by 21

Roles of IL-11 in the regulation of bone metabolism

Han, Y., Gao, H., Gan, X., Liu, J., Bao, C., & He, C. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1290130 · Cited by 24

The decisive early phase of biomaterial-induced bone regeneration

Dang, Y., Zhang, Y., Luo, G., Li, D., Ma, Y., Xiao, Y., Xiao, L., & Wang, X. (2024) · Applied Materials Today · doi:10.1016/j.apmt.2024.102236 · Cited by 25

Paracrine-mediated osteoclastogenesis by the osteosarcoma MG63 cell line: is RANKL/RANK signalling really important?

Costa‐Rodrigues, J., Teixeira, C. A., & Fernandes, M. H. (2011) · Clinical & Experimental Metastasis · doi:10.1007/s10585-011-9387-7 · Cited by 24

Pharmacophysiology of bone and spinal fusion

Kalb, S., Mahan, M. A., Elhadi, A. M., Dru, A. B., Eales, J., Lemos, M., & Theodore, N. (2013) · The Spine Journal · doi:10.1016/j.spinee.2013.06.005 · Cited by 22

Heme Oxygenase-1 Is a Pivotal Modulator of Bone Turnover and Remodeling: Molecular Implications for Prostate Cancer Bone Metastasis

Anselmino, N., Starbuck, M. W., Labanca, E., Cotignola, J., Navone, N. M., Gueron, G., Zenclussen, A. C., & Vazquez, E. S. (2019) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7879 · Cited by 24

Changes in the mRNA expression of osteoblast‐related genes in response to β3‐adrenergic agonist in UMR106 cells

Nuntapornsak, A., Wongdee, K., Thongbunchoo, J., Krishnamra, N., & Charoenphandhu, N. (2009) · Cell Biochemistry and Function · doi:10.1002/cbf.1617 · Cited by 22

Pyk2 deficiency potentiates osteoblast differentiation and mineralizing activity in response to estrogen or raloxifene

Posritong, S., Hong, J. M., Eleniste, P. P., McIntyre, P. W., Wu, J. L., Himes, E. R., Patel, V., Kacena, M. A., & Bruzzaniti, A. (2018) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2018.02.005 · Cited by 21

Circulating MicroRNA Expression, Vitamin D, and Hypercortisolism as Predictors of Osteoporosis in Elderly Postmenopausal Women

Al‐Rawaf, H. A., Alghadir, A. H., & Gabr, S. A. (2021) · Disease Markers · doi:10.1155/2021/3719919 · Cited by 21

Hypoxia-inducible factor 1α enhances RANKL-induced osteoclast differentiation by upregulating the MAPK pathway

Wang, D., Liu, L., Qu, Z., Zhang, B., Gao, X., Huang, W., Feng, M., Gong, Y., Kong, L., Wang, Y., et al. (2022) · Annals of Translational Medicine · doi:10.21037/atm-22-4603 · Cited by 21

The Antimicrobial and Anti-Biofilm Effects of Hypericum perforatum Oil on Common Pathogens of Periodontitis: An In Vitro Study

Bagheri, R., Bohlouli, S., Dizaj, S. M., Shahi, S., Memar, M. Y., & Salatin, S. (2022) · Clinics and Practice · doi:10.3390/clinpract12060104 · Cited by 21

Hypoxia‐Inducible Factor‐2α Signaling in the Skeletal System

Mendoza, S. V., Genetos, D. C., & Yellowley, C. E. (2023) · JBMR Plus · doi:10.1002/jbm4.10733 · Cited by 25

Bisphosphonates

Iannitti, T., Rosini, S., Lodi, D., Frediani, B., Rottigni, V., & Palmieri, B. (2012) · American Journal of Therapeutics · doi:10.1097/mjt.0b013e318247148f · Cited by 21

Circulating miRNAs: A New Opportunity in Bone Fragility

Donati, S., Ciuffi, S., Palmini, G., & Brandi, M. L. (2020) · Biomolecules · doi:10.3390/biom10060927 · Cited by 21

BMP-2 Enhances Osteogenic Differentiation of Human Adipose-Derived and Dental Pulp Stem Cells in 2D and 3D In Vitro Models

Martín-Iglesias, S., Milián, L., Sancho‐Tello, M., Salvador-Clavell, R., de Llano, J. J. M., Cardá, C., & Mata, M. (2022) · Stem Cells International · doi:10.1155/2022/4910399 · Cited by 20

Vitamin K2 Improves Osteogenic Differentiation by Inhibiting STAT1 via the Bcl-6 and IL-6/JAK in C3H10 T1/2 Clone 8 Cells

Wang, H., Li, L., Zhang, N., & Ma, Y. (2022) · Nutrients · doi:10.3390/nu14142934 · Cited by 20

Suppression of mast cell activity contributes to the osteoprotective effect of an herbal formula containing Herba Epimedii, Fructus Ligustri Lucidi and Fructus Psoraleae

Chan, B. C.-L., Lee, H. Y., Siu, W. S., Yip, K. H., Ko, C., Lau, C. B., Leung, P. C., & Lau, H. Y. A. (2013) · Journal of Pharmacy and Pharmacology · doi:10.1111/jphp.12166 · Cited by 20

Heparanase in primary human osteoblasts

Smith, P. N., Freeman, C. G., Yu, D., Chen, M., Gatenby, P. A., Parish, C. R., & Li, R. (2010) · Journal of Orthopaedic Research® · doi:10.1002/jor.21138 · Cited by 20

Tailoring the in vitro characteristics of poly(vinyl alcohol)-nanohydroxyapatite composite scaffolds for bone tissue engineering

Kaur, T., Thirugnanam, A., & Pramanik, K. (2016) · Journal of Polymer Engineering · doi:10.1515/polyeng-2015-0252 · Cited by 20

Oral administration of melatonin contained in drinking water increased bone strength in naturally aged mice

Igarashi-Migitaka, J., Seki, A., Ikegame, M., Honda, M., Sekiguchi, T., Mishima, H., Shimizu, N., Matsubara, H., Srivastav, A. K., Hirayama, J., et al. (2020) · Acta Histochemica · doi:10.1016/j.acthis.2020.151596 · Cited by 20

The phytochemical plumbagin reciprocally modulates osteoblasts and osteoclasts

Yadav, A. M., Bagade, M. M., Ghumnani, S., Raman, S., Saha, B., Kubatzky, K. F., & Ashma, R. (2021) · Biological Chemistry · doi:10.1515/hsz-2021-0290 · Cited by 20

Influence of fiber architecture and growth factor formulation on osteoblastic differentiation of mesenchymal stem cells in coacervate-coated electrospun fibrous scaffolds

Kim, S. J., Lee, J., Hwang, M. P., Wang, Y., & Kim, K. (2019) · Journal of Industrial and Engineering Chemistry · doi:10.1016/j.jiec.2019.06.044 · Cited by 19

Local delivery of gaseous signaling molecules for orthopedic disease therapy

Sun, J., Wang, W., Hu, X., Zhang, X., Zhu, C., Hu, J., & Ma, R. (2023) · Journal of Nanobiotechnology · doi:10.1186/s12951-023-01813-6 · Cited by 18

mTOR Signaling Pathway in Bone Diseases Associated with Hyperglycemia

Wang, S., Wang, J., Wang, S., Tao, R., Yi, J., Chen, M., & Zhao, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119198 · Cited by 21

Phosphate glass fibers facilitate proliferation and osteogenesis through Runx2 transcription in murine osteoblastic cells

Lin, X., Chen, Q., Xiao, Y., Gao, Y., Ahmed, I., Li, M., Li, H., Zhang, K., Qiu, W., Liu, X., et al. (2019) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36818 · Cited by 19

Human mast cells induce osteoclastogenesis through cell surface RANKL

Ng, C. W., Chan, B. C.-L., Ko, C., Tam, I. Y. S., Sam, S. W., Lau, C. B., Leung, P. C., & Lau, H. Y. A. (2022) · Inflammation Research · doi:10.1007/s00011-022-01608-9 · Cited by 19

Pyroptosis mediates osteoporosis via the inflammation immune microenvironment

Chen, T., Jin, L., Li, J., & Liu, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1371463 · Cited by 18

The complex relationship between vitamin D and kidney stones: balance, risks, and prevention strategies

Zhang, F., & Li, W. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1435403 · Cited by 19

Skeletal muscle-derived exosomes prevent osteoporosis by promoting osteogenesis

Xing, Z., Guo, L., Li, S., Huang, W., Su, J., Chen, X., Li, Y., & Zhang, J. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123079 · Cited by 20

Bone remodeling and regulating biomarkers in women at the time of breast cancer diagnosis

Yao, S., Zhang, Y., Tang, L., Roh, J. M., Laurent, C. A., Hong, C., Hahn, T., Lo, J. C.-M., Ambrosone, C. B., Kushi, L. H., et al. (2016) · Breast Cancer Research and Treatment · doi:10.1007/s10549-016-4068-5 · Cited by 18

Nanohybrid composed of graphene oxide functionalized with sodium hyaluronate accelerates bone healing in the tibia of rats

Dantas, P. C. D. L., Martins‐Júnior, P. A., Coutinho, D. C. O., Andrade, V. B., Valverde, T. M., Ávila, É. D. S., de Almeida, T. C. S., Queiroz‐Junior, C. M., de Sá, M. A., de Goes, A. M., et al. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.111961 · Cited by 18

Lactoferrin Is a Potential Activator of the Vitamin D Receptor in Its Regulation of Osteogenic Activities in C57BL/6J Mice and MC3T3-E1 Cells

Li, Y., Huang, J., Wang, J., Ma, M., Lu, Y., Wang, R., & Guo, H. (2021) · Journal of Nutrition · doi:10.1093/jn/nxab105 · Cited by 18

The Impact of Sedentary Lifestyle, High-fat Diet, Tobacco Smoke, and Alcohol Intake on the Hematopoietic Stem Cell Niches

Kaastrup, K., & Grønbæk, K. (2021) · HemaSphere · doi:10.1097/hs9.0000000000000615 · Cited by 18

Does the serum level of vitamin D affect marginal bone loss around dental implants?

Tabrizi, R., Mohajerani, H., Jafari, S., & Tümer, M. K. (2021) · International Journal of Oral and Maxillofacial Surgery · doi:10.1016/j.ijom.2021.11.006 · Cited by 18

Bone as a source of organism vitality and regeneration

Mackiewicz, Z., Niklińska, W., Kowalewska, J., & Chyczewski, L. (2012) · Folia Histochemica et Cytobiologica · doi:10.5603/fhc.2011.0079 · Cited by 19

miR-134-5p inhibits osteoclastogenesis through a novel miR-134-5p/Itgb1/MAPK pathway

Huang, M., Wang, Y., Wang, Z., Qin, Q., Zhang, H., Liu, S., Cui, J., Zhang, Y., Jiang, X., & Xu, L. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102116 · Cited by 17

Anti-Osteoporosis Effects of the Fruit of Sea Buckthorn (Hippophae rhamnoides) through Promotion of Osteogenic Differentiation in Ovariectomized Mice

Park, K. H., Hong, J.-H., Kim, S., Kim, S., Kim, J., & Park, K. (2022) · Nutrients · doi:10.3390/nu14173604 · Cited by 17

Oxytocin effects on osteoblastic differentiation of Bone Marrow Mesenchymal Stem Cells from adult and aging female Wistar rats

dos Santos, L. F., Singulani, M. P., Stringhetta-Garcia, C. T., Oliveira, S. H. P., Chaves-Neto, A. H., & Dornelles, R. C. M. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.09.023 · Cited by 17

CUEDC2 controls osteoblast differentiation and bone formation via SOCS3–STAT3 pathway

Kim, J.-W., Oh, S., Lee, M. N., Song, J. H., Jeong, B., Yang, J.-W., Piao, X., Zang, Y., Ryu, J., & Koh, J. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2562-5 · Cited by 17

The ionic substituted octacalcium phosphate for biomedical applications: A new pathway to follow?

Ressler, A., Ivanišević, I., Žužić, A., & Somers, N. (2021) · Ceramics International · doi:10.1016/j.ceramint.2021.12.126 · Cited by 17

In Vitro Models of Bone Marrow Remodelling and Immune Dysfunction in Space: Present State and Future Directions

Sarkar, R., & Pampaloni, F. (2022) · Biomedicines · doi:10.3390/biomedicines10040766 · Cited by 17

The Molecular Biological Approach in Paleopathology

Gosman, J. H. (2011) · Wiley eBooks · doi:10.1002/9781444345940.ch5 · Cited by 18

The Effects and Mechanisms of Low-Intensity Pulsed Ultrasound on Bone Remodeling: From Laboratory to Clinic

Zong, B., Sun, W., Cai, C., & Shang, P. (2025) · Biomolecules · doi:10.3390/biom15101351 · Cited by 19

Mycobacterium tuberculosis Induced Osteoblast Dysregulation Involved in Bone Destruction in Spinal Tuberculosis

Ma, W., Jin, W., He, X., Sun, Y., Yin, H., Wang, Z., & Shi, S. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.780272 · Cited by 17

Osteoporosis: From Bone Biology to Individual Treatment Decision

Gonçalves, M. J., Rodrigues, A. M., Canhão, H. M., & Fonseca, J. E. (2013) · Acta Médica Portuguesa · doi:10.20344/amp.4271 · Cited by 16

Monocyte chemoattractant protein-1 modulates invasion and apoptosis of PC-3M prostate cancer cells via regulating expression of VEGF, MMP9 and caspase-3.

Shi, C., Yu, C.-H., Zhang, Y., Zhao, D., Chang, X.-H., & Wang, W. (2011) · PubMed · Cited by 16

Fundamentals of Human Bone and Dental Biology

Lynnerup, N., & Klaus, H. D. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-809738-0.00004-1 · Cited by 19

Humanin suppresses receptor activator of nuclear factor-κB ligand-induced osteoclast differentiation via AMP-activated protein kinase activation

Kang, N., Kim, K. W., & Shin, D. M. (2019) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2019.23.5.411 · Cited by 16

Bone physiology and therapeutics in chronic critical illness

Via, M. A., Gallagher, E. J., & Mechanick, J. I. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05807.x · Cited by 16

Evolution of the parathyroid hormone family and skeletal formation pathways

Danks, J. A., D’Souza, D. G., Gunn, H. J., Milley, K. M., & Richardson, S. J. (2010) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2010.10.023 · Cited by 17

Osteogenic differentiation of bone marrow mesenchymal stem cells of ovariectomized and non-ovariectomized female rats with thyroid dysfunction

Boeloni, J. N., Ocarino, N. M., Silva, J. F., Corrêa, C. R., Bertollo, C. M., Hell, R. C. R., Pereira, M. M., Goes, A. M., & Serákides, R. (2012) · Pathology - Research and Practice · doi:10.1016/j.prp.2012.10.004 · Cited by 16

Growth factor-mediated augmentation of long bones: evaluation of a BMP-7 loaded thermoresponsive hydrogel in a murine femoral intramedullary injection model

Neuerburg, C., Mittlmeier, L. M., Keppler, A. M., Westphal, I., Glass, A. S., Saller, M. M., Herlyn, P. K. E., Richter, H., Böcker, W., Schieker, M., et al. (2019) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-019-1315-6 · Cited by 19

Amino acid metabolism in primary bone sarcomas

Jiménez, J. A., Lawlor, E. R., & Lyssiotis, C. A. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1001318 · Cited by 15

Bone formation ability of Gli1+ cells in the periodontal ligament after tooth extraction

Fujii, S., Takebe, H., Mizoguchi, T., Nakamura, H., Shimo, T., & Hosoya, A. (2023) · Bone · doi:10.1016/j.bone.2023.116786 · Cited by 16

Exploring the Impact of Catechins on Bone Metabolism: A Comprehensive Review of Current Research and Future Directions

German, Í. J. S., Barbalho, S. M., Andreo, J. C., Zutin, T. L. M., Laurindo, L. F., Rodrigues, V. D., Araújo, A. C., Guiguer, É. L., Direito, R., Pomini, K. T., et al. (2024) · Metabolites · doi:10.3390/metabo14100560 · Cited by 15

Bisphosphonates and Cancer: A Relationship Beyond the Antiresorptive Effects

Teixeira, S., Branco, L. C., Fernandes, M. H., & Costa‐Rodrigues, J. (2019) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557519666190424163044 · Cited by 18

The dual face of parathyroid hormone and prostaglandins in the osteoimmune system

Agas, D., Marchetti, L., Capitani, M., & Sabbieti, M. G. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00290.2013 · Cited by 16

The Emerging Role of the Mitochondrial Respiratory Chain in Skeletal Aging

Tao, H., Zhu, P., Xia, W., Chu, M., Chen, K., Wang, Q., Gu, Y., Lu, X., Bai, J., & Geng, D. (2023) · Aging and Disease · doi:10.14336/ad.2023.0924 · Cited by 15

The association between body roundness index and osteoporosis in American adults: analysis from NHANES dataset

Zhang, X., Liang, J., Luo, H., Zhang, H., Xiang, J., Lianjin, G., & Zhu, X. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1461540 · Cited by 16

Complex Effect of Hydroxyapatite Nanoparticles on the Differentiation and Functional Activity of Human Pre-Osteoclastic Cells

Costa‐Rodrigues, J., Silva, A., Santos, C. F., Almeida, M. M., Costa, M. E. V., & Fernandes, M. H. (2014) · Journal of Biomedical Nanotechnology · doi:10.1166/jbn.2014.1873 · Cited by 14

Vessel stiffness, calcification and osteoporosis. Common pathogenetic components

Skripnikova, I. A., Абирова, Э. С., Арсланалиевна, А. Н., & Kosmatova, O. V. (2018) · CARDIOVASCULAR THERAPY AND PREVENTION · doi:10.15829/1728-8800-2018-4-95-102 · Cited by 14

Alveolar bone healing in mice genetically selected in the maximum (AIRmax) or minimum (AIRmin) inflammatory reaction

Colavite, P. M., Vieira, A. E., Repeke, C. E. P., Linhari, R. P. D. A., Andrade, R. G. C. S. D., Borrego, A., Franco, M. D., Trombone, A. P. F., & Garlet, G. P. (2018) · Cytokine · doi:10.1016/j.cyto.2018.11.027 · Cited by 14

Bone markers

Konukoğlu, D. (2019) · International journal of medical biochemistry/International journal of medical biochemistry : · doi:10.14744/ijmb.2019.60362 · Cited by 19

Water Extract of Piper longum Linn Ameliorates Ovariectomy-Induced Bone Loss by Inhibiting Osteoclast Differentiation

Gu, D. R., Yang, H. J., Kim, S. C., Hwang, Y., & Ha, H. (2022) · Nutrients · doi:10.3390/nu14173667 · Cited by 14

Differential characteristics of bone quality and bone turnover biochemical markers in patients with hip Fragility Fractures and Hip Osteoarthritis: results of a clinical pilot study

Resmini, G., Migliaccio, S., Carbonare, L. D., Sala, U., Brama, M., Fornari, R., Maggi, S., Siviero, P., Malavolta, N., & Iolascon, G. (2011) · Aging Clinical and Experimental Research · doi:10.1007/bf03351075 · Cited by 14

Regeneration of bone marrow after tibial ablation in immunocompromised rats is age dependent

Fisher, M., Hyzy, S. L., Guldberg, R. E., Schwartz, Z., & Boyan, B. D. (2009) · Bone · doi:10.1016/j.bone.2009.09.029 · Cited by 14

In Vitro Osteogenesis Study of Shell Nacre Cement with Older and Young Donor Bone Marrow Mesenchymal Stem/Stromal Cells

Wilson, B. J., Owston, H. E., Iqbal, N., Giannoudis, P. V., McGonagle, D., Pandit, H. G., Pampadykandathil, L. P., Jones, E., & Ganguly, P. (2024) · Bioengineering · doi:10.3390/bioengineering11020143 · Cited by 13

Association Between Sleep Duration and Low Bone Mineral Density and Osteoporosis: A Systematic Review and Meta-analysis

Tian, J., Zhang, J., Ding, L., & Qi, X. (2024) · Calcified Tissue International · doi:10.1007/s00223-024-01319-9 · Cited by 13

The Impact of Fermented Dairy Products and Probiotics on Bone Health Improvement

Bashir, H. H., Hasnain, M. A., Abbas, A., Lee, J.-H., & Moon, G. (2025) · Food Science of Animal Resources · doi:10.5851/kosfa.2025.e7 · Cited by 14

Osteoporosis and People with Down Syndrome: A Preliminary Descriptive Examination of the Intellectual Disability Supplement to the Irish Longitudinal Study on Ageing Wave 1 Results

Burke, E. A., Carroll, R. E., O’Dwyer, M., Walsh, J. B., McCallion, P., & McCarron, M. (2018) · Health · doi:10.4236/health.2018.109095 · Cited by 13

Crosstalk between dihydroceramides produced by Porphyromonas gingivalis and host lysosomal cathepsin B in the promotion of osteoclastogenesis

Duarte, C., Yamada, C., Garcia, C., Akkaoui, J., Ho, A., Nichols, F., & Movila, A. (2022) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17299 · Cited by 14

FTY720 administration results in a M2 associated immunoregulatory effect that positively influences the outcome of alveolar bone repair outcome in mice

Tabanêz, A. P., Azevedo, M. D. C. S., Melchiades, J. L., Fonseca, A. C., Francisconi, C. F., Colavite, P. M., Biguetti, C. C., Rodini, C. O., Trombone, A. P. F., & Garlet, G. P. (2022) · Bone · doi:10.1016/j.bone.2022.116506 · Cited by 13

Repercussion of nonsteroidal anti-inflammatory drugs on the gene expression of human osteoblasts

Melguizo‐Rodríguez, L., Costela-Ruiz, V. J., Manzano‐Moreno, F. J., Montes, R. I., Ramos‐Torrecillas, J., García‐Martínez, O., & Ruíz, C. (2018) · PeerJ · doi:10.7717/peerj.5415 · Cited by 13

Evaluation of selected bone metabolism markers in rheumatoid arthritis patients.

Matuszewska, A., & Szechiński, J. (2013) · PubMed · Cited by 13

From bone homeostasis to skeletal metastasis and osteosarcoma: Insights into osteoclast and osteoblast roles in bone remodelling and cancer

Kottmann, V., Nienhaus, M., Drees, P., Gercek, E., & Ritz, U. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189551 · Cited by 14

Conjugated linoleic acid and glucosamine supplements may prevent bone loss in aging by regulating the RANKL/RANK/OPG pathway

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