Genetic Control of Bone Formation

Notch Signaling: Cell Fate Control and Signal Integration in Development

Artavanis-Tsakonas, S., Rand, M. D., & Lake, R. J. (1999) · Science · doi:10.1126/science.284.5415.770 · Cited by 5,909

Wnt/β-Catenin Signaling in Development and Disease

Clevers, H. (2006) · Cell · doi:10.1016/j.cell.2006.10.018 · Cited by 5,568

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

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

An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress

Harding, H. P., Zhang, Y., Zeng, H., Novoa, I., Lu, P. D., Calfon, M. A., Sadri, N., Yun, C., Popko, B., Paules, R. S., et al. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00105-9 · Cited by 3,336

Hedgehog signaling in animal development: paradigms and principlesPreprint

Ingham, P. W., & McMahon, A. P. (2001) · Genes & Development · doi:10.1101/gad.938601 · Cited by 3,025

AP-1 function and regulation

Karin, M., Liu, Z.-G., & Zandi, E. (1997) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(97)80068-3 · Cited by 2,904

Developmental regulation of the growth plate

Kronenberg, H. M. (2003) · Nature · doi:10.1038/nature01657 · Cited by 2,859

Effects of dietary calcium to available phosphorus ratios on bone metabolism and osteoclast activity of the OPG /RANK/RANKL signalling pathway in piglets

Zhao, L., Li, M., & Sun, H. (2019) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.13115 · Cited by 26

Advances in Collagen/Hydroxyapatite Composite Materials

Ficai, A., Andronescu, E., Voicu, G., & Ficai, D. (2011) · InTech eBooks · doi:10.5772/13707 · Cited by 24

Salidroside accelerates fracture healing through cell-autonomous and non-autonomous effects on osteoblasts

Guo, X. Q., Qi, L., Yang, J., Wang, Y., Wang, C., Li, Z. M., Li, L., Qu, Y., Wang, D., & Han, Z. M. (2016) · Cell and Tissue Research · doi:10.1007/s00441-016-2535-2 · Cited by 24

Reverse engineering development: Crosstalk opportunities between developmental biology and tissue engineering

Marcucio, R., Qin, L., Alsberg, E., & Boerckel, J. D. (2017) · Journal of Orthopaedic Research® · doi:10.1002/jor.23636 · Cited by 24

Propofol attenuates osteoclastogenesis by lowering RANKL/OPG ratio in mouse osteoblasts

Lee, D.-W., Kwon, J.-Y., Kim, H.-K., Lee, H. J., Kim, E., Kim, H. J., Kim, H. J., & Lee, H.-B. (2018) · International Journal of Medical Sciences · doi:10.7150/ijms.22713 · Cited by 25

Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1

Palagano, E., Zuccarini, G., Prontera, P., Borgatti, R., Stangoni, G., Elisei, S., Mantero, S., Menale, C., Forlino, A., Uva, P., et al. (2018) · Bone · doi:10.1016/j.bone.2018.06.013 · Cited by 24

Long bone development requires a threshold of Hox function

González‐Martín, C., Mallo, M., & Ros, M. A. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.06.004 · Cited by 23

CCN1 Regulates Chondrocyte Maturation and Cartilage Development

Zhang, Y., Sheu, T., Hoak, D., Shen, J., Hilton, M. J., Zuscik, M. J., Jonason, J. H., & O’Keefe, R. J. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2712 · Cited by 23

Possible Involvement of Glutamatergic Signaling Machineries in Pathophysiology of Rheumatoid Arthritis

Hinoi, E., & Yoneda, Y. (2011) · Journal of Pharmacological Sciences · doi:10.1254/jphs.11r03cr · Cited by 23

Growth factor progranulin blocks tumor necrosis factor-α-mediated inhibition of osteoblast differentiation

Wang, N., Zhang, J., & Yang, J. (2016) · Genetics and Molecular Research · doi:10.4238/gmr.15038126 · Cited by 23

Bre Enhances Osteoblastic Differentiation by Promoting the Mdm2-Mediated Degradation of p53

Jin, F., Wang, Y., Wang, X., Wu, Y., Wang, X., Liu, Q., Zhu, Y., Liu, E., Fan, J., & Wang, Y. (2017) · Stem Cells · doi:10.1002/stem.2620 · Cited by 23

E3-ubiquitin ligase NEDD4 enhances bone formation by removing TGFβ1-induced pSMAD1 in immature osteoblast

Jeon, S., Lee, J., Kim, D. W., & Cho, J. (2018) · Bone · doi:10.1016/j.bone.2018.08.012 · Cited by 23

Effects of PIN on Osteoblast Differentiation and Matrix Mineralization through Runt-Related Transcription Factor

Park, K., Kim, S., Cho, M., Kang, S. W., & Yun, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249579 · Cited by 23

BMP signaling-driven osteogenesis is critically dependent on Prdx-1 expression-mediated maintenance of chondrocyte prehypetrophy

Kumar, Y., Biswas, T., Thacker, G., Kanaujiya, J. K., Kumar, S., Shukla, A., Khan, K., Sanyal, S., Chattopadhyay, N., Bandyopadhyay, A., et al. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.02.016 · Cited by 22

Effects of the amide alkaloid piperyline on apoptosis, autophagy, and differentiation of pre-osteoblasts

Park, K.-R., Leem, H. H., Cho, M., Kang, S. W., & Yun, H. (2020) · Phytomedicine · doi:10.1016/j.phymed.2020.153347 · 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

A Phytochemical Constituent, (E)-Methyl-Cinnamate Isolated from Alpinia katsumadai Hayata Suppresses Cell Survival, Migration, and Differentiation in Pre-Osteoblasts

Park, K., Lee, H., Cho, M., & Yun, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103700 · Cited by 22

Investigation for GSK3β expression in diabetic osteoporosis and negative osteogenic effects of GSK3β on bone marrow mesenchymal stem cells under a high glucose microenvironment

Chen, Y., Chen, L., Huang, R., Yang, W., Chen, S., Lin, K., & Liu, J. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.11.010 · Cited by 22

PlexinA2 mediates osteoblast differentiation via regulation of Runx2

Oh, J.-E., Kim, H. J., Kim, W.-S., Lee, Z. H., Ryoo, H.-M., Hwang, S. J., Lee, Y., & Kim, H.-H. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1471 · Cited by 21

Understanding the initiation, delivery and processing of bone cancer pain from the peripheral to the central nervous system

Yang, L., Liu, B., Shang, Z., Xu, L., & Yao, M. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109641 · Cited by 21

FAD104, a Regulatory Factor of Adipogenesis, Acts as a Novel Regulator of Calvarial Bone Formation

Kishimoto, K., Nishizuka, M., Katoh, D., Kato, A., Osada, S., & Imagawa, M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.452961 · Cited by 21

Reduced chondrocyte proliferation, earlier cell cycle exit and increased apoptosis in neuronal nitric oxide synthase-deficient mice

Yan, Q., Feng, Q., & Beier, F. (2011) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2011.11.014 · Cited by 21

miRNAs in Bone Development

Papaioannou, G. (2015) · Current Genomics · doi:10.2174/1389202916666150817202425 · Cited by 21

Mouse genome-wide association and systems genetics identifies Lhfp as a regulator of bone mass

Mesner, L. D., Calabrese, G. M., Al-Barghouthi, B. M., Gatti, D. M., Sundberg, J. P., Churchill, G. A., Godfrey, D. A., Ackert‐Bicknell, C. L., & Farber, C. R. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008123 · Cited by 22

Collagen XIII-derived ectodomain regulates bone angiogenesis and intracortical remodeling

Koivunen, J. T., Kemppainen, A. V., Finnilä, M., Keski‐Filppula, R., Härönen, H., Tu, H., Pellikka, H., Heikkinen, A., Kylmäoja, E., Sormunen, R. T., et al. (2019) · Matrix Biology · doi:10.1016/j.matbio.2019.06.005 · Cited by 21

The Inducible Nitric Oxide Synthase Pathway Promotes Osteoclastogenesis under Hypoxic Culture Conditions

Kondo, T., Otsuka, Y., Aoki, H., Goto, Y., Kawaguchi, Y., Waguri‐Nagaya, Y., Miyazawa, K., Goto, S., & Aoyama, M. (2021) · American Journal Of Pathology · doi:10.1016/j.ajpath.2021.08.014 · Cited by 21

Profilin1 Regulates Sternum Development and Endochondral Bone Formation

Miyajima, D., Hayata, T., Suzuki, T., Hemmi, H., Nakamoto, T., Notomi, T., Amagasa, T., Böttcher, R. T., Costell, M., Fässler, R., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.329938 · Cited by 21

Exercise mitigates the stunting effect of cold temperature on limb elongation in mice by increasing solute delivery to the growth plate

Serrat, M. A., Williams, R. M., & Farnum, C. E. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01022.2010 · Cited by 21

MMP14 cleaves PTH1R in the chondrocyte-derived osteoblast lineage, curbing signaling intensity for proper bone anabolism

Chu, T. L., Chen, P., Yu, A. X., Kong, M., Tan, Z., Tsang, K. Y., Zhou, Z., & Cheah, K. S. E. (2023) · eLife · doi:10.7554/elife.82142 · Cited by 20

Multigenic Delineation of Lower Jaw Deformity in Triploid Atlantic Salmon (Salmo salar L.)

Amoroso, G., Ventura, T., Cobcroft, J. M., Adams, M. B., Elizur, A., & Carter, C. G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168454 · Cited by 20

The hedgehog target Vlk genetically interacts with Gli3 to regulate chondrocyte differentiation during mouse long bone development

Probst, S., Zeller, R., & Zúñiga, A. (2013) · Differentiation · doi:10.1016/j.diff.2013.03.002 · Cited by 20

Obacunone, a Promising Phytochemical Triterpenoid: Research Progress on Its Pharmacological Activity and Mechanism

Zhou, Y., Gu, J., Li, J., Zhang, H., Wang, M., Li, Y., Wang, T., Wang, J., & Shi, R. (2024) · Molecules · doi:10.3390/molecules29081791 · Cited by 19

Single-cell transcriptomics identifies chondrocyte differentiation dynamics in vivo and in vitro

Lawrence, J. E. G., Woods Jon, S., Roberts, K., Sumanaweera, D., Balogh, P., Li, T., Predeus, A. V., He, P., Polański, K., Prigmore, E., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.06.031 · Cited by 19

Biological Effects of β-Glucans on Osteoclastogenesis

Ariyoshi, W., Hara, S., Koga, A., Nagai‐Yoshioka, Y., & Yamasaki, R. (2021) · Molecules · doi:10.3390/molecules26071982 · Cited by 20

Sfrp4 and the Biology of Cortical Bone

Chen, R., Baron, R., & Gori, F. (2022) · Current Osteoporosis Reports · doi:10.1007/s11914-022-00727-w · Cited by 19

Anatomy, molecular structures, and hyaluronic acid – Gelatin injectable hydrogels as a therapeutic alternative for hyaline cartilage recovery: A review

Vaca‐González, J. J., Culma, J. J. S., Nova, L. M. H., & Garzón–Alvarado, D. A. (2023) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbm.b.35261 · Cited by 19

Inter-dependent tissue growth and Turing patterning in a model for long bone development

Tanaka, S., & Iber, D. (2013) · Physical Biology · doi:10.1088/1478-3975/10/5/056009 · Cited by 19

Skeletal Site-specific Changes in Bone Mass in a Genetic Mouse Model for Human 15q11-13 Duplication Seen in Autism

Lewis, K. E., Sharan, K., Takumi, T., & Yadav, V. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-09921-8 · Cited by 20

ER stress regulates alkaline phosphatase gene expression in vascular smooth muscle cells via an ATF4-dependent mechanism

Furmanik, M., & Shanahan, C. M. (2018) · BMC Research Notes · doi:10.1186/s13104-018-3582-4 · Cited by 19

Molecular profiling of failed endochondral ossification in mucopolysaccharidosis VII

Peck, S. H., Tobias, J. W., Shore, E. M., Malhotra, N. R., Haskins, M. E., Casal, M. L., & Smith, L. J. (2019) · Bone · doi:10.1016/j.bone.2019.115042 · Cited by 19

Mechanical and molecular parameters that influence the tendon differentiation potential of C3H10T1/2 cells in 2D- and 3D-culture systems

Gaut, L., Bonnin, M.-A., Blavet, C., Cacciapuoti, I., Orpel, M., Mericskay, M., & Duprez, D. (2020) · Biology Open · doi:10.1242/bio.047928 · Cited by 19

TGFβ as a gatekeeper of BMP action in the developing growth plate

Wang, W., Rigueur, D., & Lyons, K. M. (2020) · Bone · doi:10.1016/j.bone.2020.115439 · Cited by 19

Phosphorylation‐dependent osterix degradation negatively regulates osteoblast differentiation

Hoshikawa, S., Shimizu, K., Watahiki, A., Chiba, M., Saito, K., Wei, W., Fukumoto, S., & Inuzuka, H. (2020) · The FASEB Journal · doi:10.1096/fj.202001340r · Cited by 19

SPRY4 acts as an indicator of osteoarthritis severity and regulates chondrocyte hypertrophy and ECM protease expression

Park, S., Arai, Y., Bello, A. B., Park, H., Kim, D., Park, K., & Lee, S. (2021) · npj Regenerative Medicine · doi:10.1038/s41536-021-00165-9 · Cited by 19

Disruption of the mouseSlc39a14gene encoding zinc transporter ZIP 14 is associated with decreased bone mass, likely caused by enhanced bone resorption

Sasaki, S., Tsukamoto, M., Saito, M., Hojyo, S., Fukada, T., Takami, M., & Furuichi, T. (2018) · FEBS Open Bio · doi:10.1002/2211-5463.12399 · Cited by 19

Conditional ablation of MAPK7 expression in chondrocytes impairs endochondral bone formation in limbs and adaptation of chondrocytes to hypoxia

Yang, X., Zhong, D., Gao, W., Liao, Z., Chen, Y., Zhang, S., Zhou, H., Su, P., & Xu, C. (2020) · Cell & Bioscience · doi:10.1186/s13578-020-00462-8 · Cited by 18

Emerging therapeutic strategies targeting bone signaling pathways in periodontitis

Valverde, A. M., George, A., Nares, S., & Naqvi, A. R. (2024) · Journal of Periodontal Research · doi:10.1111/jre.13326 · Cited by 18

Co-stimulation with piezoelectric PVDF films and low intensity pulsed ultrasound enhances osteogenic differentiation

Tandon, B., Cosme, J. R. A., Xue, R., Srirussamee, K., Aguilar-Tadeo, J. A., Ballestrem, C., Blaker, J. J., & Cartmell, S. H. (2025) · Biomaterials Advances · doi:10.1016/j.bioadv.2025.214283 · Cited by 18

Endoplasmic reticulum stress in chondrodysplasias caused by mutations in collagen types II and X

Gawron, K. (2016) · Cell Stress and Chaperones · doi:10.1007/s12192-016-0719-z · Cited by 19

Loss of cyclin-dependent kinase 1 impairs bone formation, but does not affect the bone-anabolic effects of parathyroid hormone

Takahashi, A., Mulati, M., Saito, M., Numata, H., Kobayashi, Y., Ochi, H., Sato, S., Kaldis, P., Okawa, A., & Inose, H. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.004834 · Cited by 18

Long lasting inhibition of Mdm2-p53 interaction potentiates mesenchymal stem cell differentiation into osteoblasts

Daniele, S., Giacomelli, C., Pietrobono, D., Barresi, E., Piccarducci, R., Pietra, V. L., Taliani, S., Settimo, F. D., Marinelli, L., Novellino, E., et al. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.01.012 · Cited by 18

ScxLin cells directly form a subset of chondrocytes in temporomandibular joint that are sharply increased in Dmp1-null mice

Ma, C., Jing, Y., Li, H., Wang, K., Wang, Z., Xu, C., Sun, X., Kaji, D. A., Han, X., Huang, A. H., et al. (2020) · Bone · doi:10.1016/j.bone.2020.115687 · Cited by 18

Os odontoideum in identical twins: Comparative gene expression analysis

Traynelis, V., Straus, D., & Xu, S. (2014) · Surgical Neurology International · doi:10.4103/2152-7806.129259 · Cited by 18

RSK2 protects mice against TNF-induced bone loss

Böhm, C., Derer, A., Axmann, R., Hillienhoff, U., Zaiss, M. M., Luther, J., Zech, C., Stock, M., Scholtysek, C., Engelke, K., et al. (2012) · Journal of Cell Science · doi:10.1242/jcs.096008 · Cited by 18

Insulin-like growth factor 2 promotes osteoclastogenesis increasing inflammatory cytokine levels under hypoxia

Kondo, T., Aoki, H., Otsuka, Y., Kawaguchi, Y., Waguri‐Nagaya, Y., & Aoyama, M. (2022) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2022.03.007 · Cited by 17

Biology and therapeutic potential of mesenchymal stem cell extracellular vesicles in axial spondyloarthritis

Tavasolian, F., & Inman, R. D. (2023) · Communications Biology · doi:10.1038/s42003-023-04743-z · Cited by 17

The Atlantic Salmon (Salmo salar) Vertebra and Cellular Pathways to Vertebral Deformities

Ytteborg, E., Torgersen, J. S., Bæverfjord, G., & Takle, H. (2012) · InTech eBooks · doi:10.5772/30750 · Cited by 17

Apc bridges Wnt/β-catenin and BMP signaling during osteoblast differentiation of KS483 cells

Miclea, R. L., van der Horst, G., Robanus-Maandag, E. C., Löwik, C. W. G. M., Oostdijk, W., Wit, J. M., & Karperien, M. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.03.007 · Cited by 17

RCANs regulate the convergent roles of NFATc1 in bone homeostasis

Kim, J. H., Kim, K., Kim, I., Seong, S., Jeong, B., Nam, K. I., Kim, K. K., Molkentin, J. D., & Kim, N. (2016) · Scientific Reports · doi:10.1038/srep38526 · Cited by 17

Changes in acetyl-CoA mediate Sik3-induced maturation of chondrocytes in endochondral bone formation

Kosai, A., Horike, N., Takei, Y., Yamashita, A., Fujita, K., Kamatani, T., & Tsumaki, N. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.06.139 · Cited by 17

Downregulation of lncRNA XIST promotes proliferation and differentiation, limits apoptosis of osteoblasts through regulating miR-203-3p/ZFPM2 axis

Niu, S., Feng, X., & Jia, H. (2020) · Connective Tissue Research · doi:10.1080/03008207.2020.1752200 · Cited by 17

Stimulation of Osteoclast Formation by Oncostatin M and the Role of WNT16 as a Negative Feedback Regulator

de Souza, P. C., Henning, P., & Lerner, U. H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063287 · Cited by 17

The Role of BMP Signaling and NF-κB Signaling on Osteoblastic Differentiation, Cancer Development, and Vascular Diseases—Is the Activation of NF-κB a Friend or Foe of BMP Function?

Jimi, E. (2015) · Vitamins and hormones · doi:10.1016/bs.vh.2015.05.002 · Cited by 17

The transcription factor paired box-5 promotes osteoblastogenesis through direct induction of Osterix and Osteocalcin

Hinoi, E., Nakatani, E., Yamamoto, T. M., Iezaki, T., Takahata, Y., Fujita, H., Ishiura, R., Takamori, M., & Yoneda, Y. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1708 · Cited by 17

The Beneficial Effects of Bisphosphonate-enoxacin on Cortical Bone Mass and Strength in Ovariectomized Rats

Liu, X., Qu, X., Nie, T., Zhai, Z., Li, H., Ouyang, Z., Qin, A., Zhang, S., Zhang, S., Fan, Q., et al. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00355 · Cited by 17

Regulation of terminal hypertrophic chondrocyte differentiation in Prmt5 mutant mice modeling infantile idiopathic scoliosis

Liu, Z., Ramachandran, J., Vokes, S. A., & Gray, R. S. (2019) · Disease Models & Mechanisms · doi:10.1242/dmm.041251 · Cited by 17

Impact of Different Cell Types on the Osteogenic Differentiation Process of Mesenchymal Stem Cells

Wang, Z., Ren, L., Li, Z., Qingyuan, Q., Wang, H., Huang, X., & Ma, D. (2025) · Stem Cells International · doi:10.1155/sci/5551222 · Cited by 17

Zuogui Pills alleviate iron overload-induced osteoporosis by attenuating ROS-mediated osteoblast apoptosis via the PI3K-AKT pathway and mitigating mitochondrial damage

Lin, Y., He, Q., Chen, B., Li, Z., Chen, C., Deng, W., Li, H., Yang, J., Mai, B., Zhang, Z., et al. (2025) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2025.119455 · Cited by 16

A computational model of clavicle bone formation: A mechano-biochemical hypothesis

Garzón–Alvarado, D. A., Gutiérrez, M. L., & Calixto, L. F. (2014) · Bone · doi:10.1016/j.bone.2014.01.007 · Cited by 16

Quantification of Osteoclasts in Culture, Powered by Machine Learning

Cohen-Karlik, E., Awida, Z., Bergman, A., Eshed, S., Nestor, O., Kadashev, M., Yosef, S. B., Saed, H., Mansour, Y., Globerson, A., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.674710 · Cited by 16

Effects of Scoparone on differentiation, adhesion, migration, autophagy and mineralization through the osteogenic signalling pathways

Park, K., Kim, B., Lee, J. Y., Moon, H., Kwon, I. K., & Yun, H. (2022) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17476 · Cited by 16

Molecular basis of imprinting disorders affecting chromosome 14: lessons from murine models

Howard, M. C., & Charalambous, M. (2015) · Reproduction · doi:10.1530/rep-14-0660 · Cited by 16

Stk11 (Lkb1) deletion in the osteoblast lineage leads to high bone turnover, increased trabecular bone density and cortical porosity

Lai, L. P., Lotinun, S., Bouxsein, M., Baron, R., & McMahon, A. P. (2014) · Bone · doi:10.1016/j.bone.2014.09.010 · Cited by 16

Characterization of Adipose-Derived Mesenchymal Stem Cell Combinations for Vascularized Bone Engineering

Valenzuela, C. D., Allori, A. C., Reformat, D. D., Sailon, A. M., Allen, R. J., Davidson, E. H., Alikhani, M., Bromage, T. G., Ricci, J. L., & Warren, S. M. (2013) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0323 · Cited by 16

Associations between FGF21, osteonectin and bone turnover markers in type 2 diabetic patients with albuminuria

Xu, L., Niu, M., Yu, W., Xia, W., Gong, F., & Wang, O. (2016) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2016.11.012 · Cited by 16

Osteogenic and osteoclastogenic potential of jaw bone‐derived cells—A case study

Ruppeka‐Rupeika, E., Hogervorst, J. M. A., Wouters, F., Schoenmaker, T., Forouzanfar, T., & de Vries, T. J. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26690 · Cited by 16

Single-cell RNA sequencing analysis of the temporomandibular joint condyle in 3 and 4-month-old human embryos

Zhu, Q., Tan, M., Wang, C., Chen, Y., Wang, C., Zhang, J., Gu, Y., Guo, Y., Han, J., Li, L., et al. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-01069-5 · Cited by 15

The Impact of NLRP3 Inflammasome on Osteoblasts and Osteogenic Differentiation: A Literature Review

Yang, Z., Xu, J., Kang, T., Chen, X., & Zhou, C. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s457927 · Cited by 15

Tumor necrosis factor stimulates osteoclastogenesis from human bone marrow cells under hypoxic conditions

Nomura, T., Aoyama, M., Waguri‐Nagaya, Y., Goto, Y., Suzuki, M., Miyazawa, K., Asai, K., & Goto, S. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.11.020 · Cited by 15

Role of TGFβ Signaling in Maternal Ethanol-Induced Fetal Articular Cartilage Dysplasia and Adult Onset of Osteoarthritis in Male Rats

Ni, Q., Lu, K., Li, J., Tan, Y., Qin, J., Magdalou, J., Chen, L., & Wang, H. (2018) · Toxicological Sciences · doi:10.1093/toxsci/kfy080 · Cited by 15

Schlafen2 mutation in mice causes an osteopetrotic phenotype due to a decrease in the number of osteoclast progenitors

Omar, I., Ram, G. G., Rahat, D., Tabach, Y., Berger, M., & Levaot, N. (2018) · Scientific Reports · doi:10.1038/s41598-018-31428-z · Cited by 15

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TMARg, a Novel Anthraquinone Isolated from Rubia cordifolia Nakai, Increases Osteogenesis and Mineralization through BMP2 and β-Catenin Signaling

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Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice

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Liver X receptors and skeleton: Current state-of-knowledge

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Ziyuglycoside I Upregulates RUNX2 through ERK1/2 in Promoting Osteoblast Differentiation and Bone Mineralization

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La osteocalcina: de marcador de formación ósea a hormona; y el hueso, un órgano endocrino

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Mustn1 is essential for craniofacial chondrogenesis during Xenopus development

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Computational and mathematical models of chondrogenesis in vertebrate limbs

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Pathway-based association analysis of two genome-wide screening data identifies rheumatoid arthritis-related pathways

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The Expanding Life and Functions of Osteogenic Cells: From Simple Bone-Making Cells to Multifunctional Cells and Beyond

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Mechanobiological modeling of endochondral ossification: an experimental and computational analysis

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AdipoRon promotes diabetic fracture repair through endochondral ossification-based bone repair by enhancing survival and differentiation of chondrocytes

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Osteocalcin: A Protein Hormone Connecting Metabolism, Bone and Testis Function

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The Role of the Immune System and Bone Cells in Acute and Chronic Osteomyelitis

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Capacitively coupled electrical stimulation of rat chondroepiphysis explants: A histomorphometric analysis

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Come together over me: Cells that form the dermatocranium and chondrocranium in mice

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Intestinal Microbiota and Bone Health: The Role of Prebiotics, Probiotics, and Diet

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The Development and Evolution of Cartilage

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Treatment with synthetic glucocorticoid impairs bone metabolism, as revealed by in vivo imaging of osteoblasts and osteoclasts in medaka fish

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Biology of Bone and Cartilage

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The Molecular Genetics of Bone Formation

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Osteoblast biology: developmental origin and interactive nature of osteoblasts

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