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

Osteogenic potential of dental and oral derived stem cells in bone tissue engineering among animal models: An update

Berbéri, A., Fayyad‐Kazan, M., Ayoub, S., Assaf, R. B., Sabbagh, J., Ghassibe‐Sabbagh, M., & Badran, B. M. (2021) · Tissue and Cell · doi:10.1016/j.tice.2021.101515 · Cited by 14

Biological Mechanisms of Paeonoside in the Differentiation of Pre-Osteoblasts and the Formation of Mineralized Nodules

Park, K.-R., Lee, J. Y., Cho, M., Hong, J. T., & Yun, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136899 · Cited by 14

Hypomorphic and dominant-negative impact of truncated SOX9 dysregulates Hedgehog–Wnt signaling, causing campomelia

Au, T. Y. K., Yip, R. K. H., Wynn, S. L., Tan, T. Y., Fu, X., Geng, Y., Szeto, I. Y. Y., Niu, B., Yip, K. Y.-L., Cheung, M. C. H., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2208623119 · Cited by 15

Leader genes in osteogenesis: a theoretical study

Orlando, B., Giacomelli, L., Ricci, M., Barone, A. A., & Covani, U. (2012) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2012.07.010 · Cited by 14

Bone Micro-CT Assessments in an Orchidectomised Rat Model Supplemented withEurycoma longifolia

Ramli, R. B., Khamis, M. F., & Shuid, A. N. (2012) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2012/501858 · Cited by 15

Identification of a Novel Transcription Factor Required for Osteogenic Differentiation of Mesenchymal Stem Cells

Querques, F., D'Agostino, A. G., Cozzolino, C., Cozzuto, L., Lombardo, B., Leggiero, E., Ruosi, C., & Pastore, L. (2019) · Stem Cells and Development · doi:10.1089/scd.2018.0152 · Cited by 14

Hypertrophic Chondrocytes Have a Limited Capacity to Cope with Increases in Endoplasmic Reticulum Stress without Triggering the Unfolded Protein Response

Kung, L. H. W., Rajpar, M. H., Briggs, M. D., & Boot-Handford, R. (2012) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155412458436 · Cited by 13

Extracellular Vesicle-Mediated Bone Remodeling and Bone Metastasis: Implications in Prostate Cancer

Patil, K., & Soekmadji, C. (2021) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-030-67171-6_12 · Cited by 14

Paeonolide as a Novel Regulator of Core-Binding Factor Subunit Alpha-1 in Bone-Forming Cells

Park, K., Lee, J. Y., Cho, M., Hong, J. T., & Yun, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094924 · Cited by 13

Ectopic Expression of SOX9 in Osteoblasts Alters Bone Mechanical Properties

Liang, B., Cotter, M. M., Chen, D., Hernandez, C. J., & Zhou, G. D. (2011) · Calcified Tissue International · doi:10.1007/s00223-011-9550-9 · Cited by 13

The transcription factor early B‐cell factor 1 regulates bone formation in an osteoblast‐nonautonomous manner

Zee, T., Boller, S., Győry, I., Makinistoglu, M. P., Tuckermann, J. P., Grosschedl, R., & Karsenty, G. (2013) · FEBS Letters · doi:10.1016/j.febslet.2013.01.049 · Cited by 13

Skeletal Toxicity of Coplanar Polychlorinated Biphenyl Congener 126 in the Rat Is Aryl Hydrocarbon Receptor Dependent

Williams, A. E., Watt, J. D., Robertson, L. W., Gadupudi, G. S., Osborn, M. L., Soares, M. J., Iqbal, K., Pedersen, K. B., Shankar, K., Littleton, S., et al. (2020) · Toxicological Sciences · doi:10.1093/toxsci/kfaa030 · Cited by 13

Mice Carrying a Ubiquitous R235W Mutation of Wnt1 Display a Bone-Specific Phenotype

Yorgan, T. A., Rolvien, T., Stürznickel, J., Vollersen, N., Lange, F., Zhao, W., Baranowsky, A., Rosenthal, L., Hermans-Borgmeyer, I., Sharaf, A. L., et al. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4043 · Cited by 13

Dlx genes and the maintenance of bone homeostasis and skeletal integrity

Levi, G., & Gitton, Y. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.94 · Cited by 13

Pathogenic variants in GNPTAB and GNPTG encoding distinct subunits of GlcNAc-1-phosphotransferase differentially impact bone resorption in patients with mucolipidosis type II and III

Lorenzo, G. D., Westermann, L. M., Yorgan, T. A., Stürznickel, J., Ludwig, N. F., Ammer, L. S., Baranowsky, A., Ahmadi, S., Pourbarkhordariesfandabadi, E., Breyer, S. R., et al. (2021) · Genetics in Medicine · doi:10.1038/s41436-021-01285-9 · Cited by 12

The Role of Genes and Development in the Evolution of the Primate Hand

Rolian, C. (2016) · Developments in primatology · doi:10.1007/978-1-4939-3646-5_5 · Cited by 13

Erythropoietin Receptor (EPOR) Signaling in the Osteoclast Lineage Contributes to EPO-Induced Bone Loss in Mice

Awida, Z., Hiram‐Bab, S., Bachar, A., Saed, H., Zyc, D., Gorodov, A., Ben‐Califa, N., Omari, S., Omar, J., Younis, L., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231912051 · Cited by 13

Death Receptor 3 (TNFRSF25) Increases Mineral Apposition by Osteoblasts and Region Specific New Bone Formation in the Axial Skeleton of Male DBA/1 Mice

Collins, F. L., Williams, J. O., Bloom, A. C., Stone, M. D., Choy, E., Wang, E. C. Y., & Williams, A. S. (2015) · Journal of Immunology Research · doi:10.1155/2015/901679 · Cited by 12

The Sox2 high mobility group transcription factor inhibits mature osteoblast function in transgenic mice

Holmes, G., Bromage, T. G., & Basilico, C. (2011) · Bone · doi:10.1016/j.bone.2011.06.008 · Cited by 12

Appearance of cell-adhesion factor in osteoblast proliferation and differentiation of apatite coating titanium by blast coating method

Umeda, H., Mano, T., Harada, K., Ferdous, T., & Ueyama, Y. (2017) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-017-5913-8 · Cited by 12

Functional protein materials: beyond elastomeric and structural proteins

Carter, N. A., & Grove, T. Ž. (2019) · Polymer Chemistry · doi:10.1039/c9py00337a · Cited by 12

Treatment of myeloma bone disease: When, how often, and for how long?

Gundesen, M. T., Schjesvold, F. H., & Lund, T. (2025) · Journal of bone oncology · doi:10.1016/j.jbo.2025.100680 · Cited by 12

Insights from dietary supplementation with zinc and strontium on the skeleton of zebrafish,Danio rerio(Hamilton, 1822) larvae: From morphological analysis to osteogenic markers

Roberto, V. P., Martins, G., Pereira, A. C., Rodrigues, S., Grenha, A., Pinto, W., Cancela, M. L., Dias, J. P., & Gavaia, P. J. (2018) · Journal of Applied Ichthyology · doi:10.1111/jai.13664 · Cited by 11

Implications of Altered Endosome and Lysosome Biology in Space Environments

Johnson, I. R. D., Nguyen, C. T., Wise, P. M., & Grimm, D. G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218205 · Cited by 11

Study on the Role of MicroRNA-214 in the Rehabilitation of Cartilage in Mice with Exercise-Induced Traumatic Osteoarthritis

Cao, H., Zhou, X., Li, H., Wang, M., Wu, W., & Zou, J. (2022) · Current Issues in Molecular Biology · doi:10.3390/cimb44090281 · Cited by 11

Hmgb1 can facilitate activation of the matrilin-1 gene promoter by Sox9 and L-Sox5/Sox6 in early steps of chondrogenesis

Szénási, T., Kénesi, E., Nagy, A., Molnár, A., Bálint, B. L., Zvara, Á., Csabai, Z., Deák, F., Boros-Oláh, B., Mátés, L., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.07.004 · Cited by 11

Twist1-Haploinsufficiency Selectively Enhances the Osteoskeletal Capacity of Mesoderm-Derived Parietal Bone Through Downregulation of Fgf23

Quarto, N., Shailendra, S., Meyer, N. P., Menon, S., Renda, A., & Longaker, M. T. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01426 · Cited by 11

Morphological changes of physeal cartilage and secondary ossification centres in the developing femur of the house mouse (Mus musculus): A micro‐CT based study

Moncayo‐Donoso, M., Guevara, J., Márquez-Flórez, K. M., Fontanilla, M. R., Barrera, L. A., & Garzón–Alvarado, D. A. (2018) · Anatomia Histologia Embryologia · doi:10.1111/ahe.12417 · Cited by 11

Rocaglamide-A Potentiates Osteoblast Differentiation by Inhibiting NF-κB Signaling

Li, A., Yang, L., Geng, X., Peng, X., Tan, L., Deng, Y., & Dong, Y. (2015) · Molecules and Cells · doi:10.14348/molcells.2015.2353 · Cited by 11

Purinergic signalling-evoked intracellular Ca2+ concentration changes in the regulation of chondrogenesis and skeletal muscle formation

Matta, C., Fodor, J., Csernoch, L. J., & Zákány, R. (2016) · Cell Calcium · doi:10.1016/j.ceca.2016.01.006 · Cited by 11

Biology of Bone and Cartilage

Boyce, B. F., Zuscik, M. J., & Xing, L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804182-6.00011-3 · Cited by 14

L’os, un organe pas si inerte…

Oury, J., & Oury, F. (2018) · médecine/sciences · doi:10.1051/medsci/20183401014 · Cited by 11

Osteochondrogenesis by TGF-β3, BMP-2 and noggin growth factor combinations in an ex vivo muscle tissue model: Temporal function changes affecting tissue morphogenesis

Liu, H., Müller, P. E., Aszódi, A., & Klar, R. M. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1140118 · Cited by 10

Distinct differences between calvarial and long bone osteocytes in cell morphologies, gene expression and aging responses

Gao, M., Zhu, B., Fan, J., Gao, Y., Xue, F., Li, G., Hubbard, A., Gao, X., Sun, J., Jing, L., et al. (2023) · FEBS Journal · doi:10.1111/febs.16797 · Cited by 10

RhoA Promotes Synovial Proliferation and Bone Erosion in Rheumatoid Arthritis through Wnt/PCP Pathway

Chen, N., Diao, C., Huang, X. H., Tan, W., Chen, Y.-B., Qian, X.-Y., Gao, J., & Zhao, D. (2023) · Mediators of Inflammation · doi:10.1155/2023/5057009 · Cited by 11

Point mutations in an epigenetic factor lead to multiple types of bone tumors: role of H3.3 histone variant in bone development and disease

Kato, S., Ishii, T., & Kouzmenko, A. (2015) · BoneKEy Reports · doi:10.1038/bonekey.2015.84 · Cited by 10

Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype ofPrkar1a+/−mice

Liu, S., Saloustros, E. S., Mertz, E. L., Tsang, K., Starost, M. F., Salpea, P., Faucz, F. R., Szarek, E., Nesterova, M., Leikin, S., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv320 · Cited by 10

Immobilization Osteoporosis

Bauman, W. A., & Cardozo, C. P. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415853-5.00047-9 · Cited by 11

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

Nishitani, K., Bello‐Irizarry, S. N., Bentley, K. L. D. M., Daiss, J. L., & Schwarz, E. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800571-2.00016-5 · Cited by 10

YY2 Promotes Osteoblast Differentiation by Upregulating Osterix Transcriptional Activity

Piao, M., Lee, S. H., Kim, M. J., Kim, H. S., & Lee, K. Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084303 · Cited by 9

RUNX2 Reverses p53-Induced Chemotherapy Resistance in Gastric Cancer

Huang, Y., Liang, L., Zhao, Y.-X., Yao, B., Zhang, R., Song, L., & Zhang, Z. (2023) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s394393 · Cited by 9

Concentric-mineralized hybrid silk-based scaffolds for bone tissue engineering in vitro models

Bosio, V. E., Rybner, C., & Kaplan, D. L. (2023) · Journal of Materials Chemistry B · doi:10.1039/d3tb00717k · Cited by 9

Gene expression supports a single origin of horns and antlers in hoofed mammals

Calamari, Z. T., & Flynn, J. J. (2024) · Communications Biology · doi:10.1038/s42003-024-06134-4 · Cited by 9

Possible Modulation of Process Extension by N-Methyl-D-aspartate Receptor Expressed in Osteocytic MLO-Y4 Cells

Fujita, H., Hinoi, E., Nakatani, E., Yamamoto, T. M., Takarada, T., & Yoneda, Y. (2012) · Journal of Pharmacological Sciences · doi:10.1254/jphs.12068sc · Cited by 9

Emergence of the osteo-epigenome in bone biology

Kato, S., Inoue, K., & Youn, M. (2010) · IBMS BoneKEy · doi:10.1138/20100464 · Cited by 9

Glutamate signaling in non-neuronal tissues

Hinoi, E., & Yoneda, Y. (2012) · Folia Pharmacologica Japonica · doi:10.1254/fpj.139.165 · Cited by 9

Histone Mutations and Bone Cancers

Taylor, E. L., & Westendorf, J. J. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-8104-5_4 · Cited by 9

Vitamin K alleviates bone calcium loss caused by Salmonella Enteritidis through carboxylation of osteocalcin

Liu, Y., Mosenthin, R., Zhao, L., Zhang, J., Ji, C., & Ma, Q. (2021) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-021-00604-z · Cited by 9

An innovative immunotherapeutic strategy for rheumatoid arthritis: Selectively suppressing angiogenesis and osteoclast differentiation by fully human antibody targeting thymocyte antigen-1

Hu, X., Li, M., Zhang, Y. L., Sang, K., Zhang, Y., Li, W., Liu, B., Wan, L., Du, B., Qian, J., et al. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113490 · Cited by 9

A thermosensitive chitosan/corn starch/β-glycerol phosphate hydrogel containing TGF-β1 promotes differentiation of MSCs into chondrocyte-like cells

Faikrua, A., Wittaya‐areekul, S., Oonkhanond, B., & Viyoch, J. (2014) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-014-0030-y · Cited by 9

Cellular automata model for human articular chondrocytes migration, proliferation and cell death: An in vitro validation

Vaca‐González, J. J., Gutiérrez, M. L., Guevara, J., & Garzón–Alvarado, D. A. (2016) · In Silico Biology · doi:10.3233/isb-150466 · Cited by 9

Management of hard tissue abnormalities and digital orthopaedics using additive manufacturing techniques

Das, M., Alam, R., Das, M., Biswal, B., Samal, B. P., Patnaik, A., Panda, S. K., Owuor, P. S., Patra, P., & Tiwary, C. S. (2022) · Oxford Open Materials Science · doi:10.1093/oxfmat/itac009 · Cited by 8

NFIB–MLL1 complex is required for the stemness and Dlx5-dependent osteogenic differentiation of C3H10T1/2 mesenchymal stem cells

Choi, J. H., & Lee, H. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105193 · Cited by 8

Mef2c regulates bone mass through Sost-dependent and -independent mechanisms

Morfin, C., Sebastian, A., Wilson, S. P., Amiri, B., Murugesh, D. K., Hum, N. R., Christiansen, B., & Loots, G. G. (2023) · Bone · doi:10.1016/j.bone.2023.116976 · Cited by 8

Serine Metabolism Regulates the Replicative Senescence of Human Dental Pulp Cells through Histone Methylation

Zhou, S., Cui, J., & Shi, Y. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46040179 · Cited by 8

Gliotoxin potentiates osteoblast differentiation by inhibiting nuclear factor-κB signaling

Wang, G., ZHANG, X., Yu, B., & REN, K. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.3524 · Cited by 8

A comparative genomic database of skeletogenesis genes: from fish to mammals

Nie, C., Zhang, N.-A., Chen, Y., Chen, Z., Wang, G., Li, Q., & Gao, Z. (2021) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2021.100796 · Cited by 8

The Potential of Probiotics as a Therapy for Osteoporosis

Collins, F. L., Rios‐Arce, N. D., Schepper, J. D., Parameswaran, N., & McCabe, L. R. (2018) · ASM Press eBooks · doi:10.1128/9781555819705.ch9 · Cited by 9

Surfactin suppresses osteoclastogenesis via the NF-κB signaling pathway, promotes osteogenic differentiation in vitro, and inhibits oestrogen deficiency-induced bone loss in vivo

Kuang, Z., Yang, X., Cao, Z., Li, Y., Hu, J., Hong, X., Li, B., Wu, C., Qi, Q., Liu, X., et al. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109884 · Cited by 8

A Histological Study of Postnatal Development of Clavicle Articular Ends

Calixto, L. F., Penagos, R., Jaramillo, L., Guitierrez, M. L., & Garzón–Alvarado, D. A. (2015) · Universitas Scientiarum · doi:10.11144/javeriana.sc20-3.ahso · Cited by 8

Integumentary, Skeletal, and Muscular Systems

Carlson, B. M. (2009) · Elsevier eBooks · doi:10.1016/b978-0-323-05385-3.50013-1 · Cited by 8

Radiation alters osteoclastogenesis by regulating the cytoskeleton and lytic enzymes in RAW 264.7 cells and mouse bone marrow-derived macrophages

Tong, L., Wang, Y., Wang, J., He, F., Zhai, J., Bai, J., & Zhu, G. (2020) · International Journal of Radiation Biology · doi:10.1080/09553002.2020.1798542 · Cited by 8

The Non-Erythropoietic EPO Analogue Cibinetide Inhibits Osteoclastogenesis In Vitro and Increases Bone Mineral Density in Mice

Awida, Z., Bachar, A., Saed, H., Gorodov, A., Ben‐Califa, N., Ibrahim, M., Kolomansky, A., Iden, J. A., Visacovsky, L. G., Liron, T., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010055 · Cited by 7

Benign and low-grade cartilaginous tumors: an update on differential diagnosis

Savci-Heijink, C. D., Cleven, A. H. G., & Bovée, J. V. M. G. (2022) · Diagnostic histopathology · doi:10.1016/j.mpdhp.2022.09.001 · Cited by 7

Screening of SNP Loci Related to Leg Length Trait in Leizhou Goats Based on Whole-Genome Resequencing

Liu, J., Dong, S., Lv, J., Li, Y., Sun, B., Guo, Y., Deng, M., Liu, D., & Liu, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212450 · Cited by 7

Searching for additional endocrine functions of the skeleton: genetic approaches and implications for therapeutics

Wei, J., Flaherty, S. E., & Karsenty, G. (2015) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.2015.1058152 · Cited by 7

Spine Metastases in Immunocompromised Mice after Intracardiac Injection of MDA-MB-231-SCP2 Breast Cancer Cells

Brylka, L., Jähn, K., Baranowsky, A., Neven, M., Horn, M., Yorgan, T. A., Wikman, H., Werner, S., Lübke, A. M., Amling, M., et al. (2022) · Cancers · doi:10.3390/cancers14030556 · Cited by 7

Developmental Pathways in CAVD

Elaine, E., & Katherine, E. (2013) · InTech eBooks · doi:10.5772/54356 · Cited by 8

A report from Fukushima: an assessment of bone health in an area affected by the Fukushima nuclear plant incident

Ishii, T., Itô, K., Kato, S., Tsubokura, M., Ochi, S., Iwamoto, Y., & Saito, Y. (2013) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-013-0482-5 · Cited by 7

Fetal Control of Calcium and Phosphate Homeostasis – Lessons from Mouse Models

Kovács, C. S. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-387829-8.00014-7 · Cited by 7

Characterization of mesenchymal stem cells in mucolipidosis type II (I-cell disease)

Köse, S., Aerts‐Kaya, F., Kuşkonmaz, B., & Uçkan, D. (2019) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-1902-20 · Cited by 7

Osteogenesis Imperfecta

Marini, J. C., & Rajpar, M. H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-387829-8.00017-2 · Cited by 7

Growth Plate Pathology in the Mucopolysaccharidosis Type VI Rat Model—An Experimental and Computational Approach

Guevara, J., Frohbergh, M. E., Castro-Abril, H. A., Vaca‐González, J. J., Barrera, L. A., Garzón–Alvarado, D. A., Schuchman, E. H., & Simonaro, C. M. (2020) · Diagnostics · doi:10.3390/diagnostics10060360 · Cited by 7

Age Estimation from Clavicle by Histomorphometry Method: A Review

Mahakkanukrauh, P. (2017) · Medicine & health · doi:10.17576/mh.2017.1201.02 · Cited by 7

Heparanase: A Potential Therapeutic Target in Sarcomas

Cassinelli, G., & Lanzi, C. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-34521-1_15 · Cited by 7

Temporal TGF-β Supergene Family Signalling Cues Modulating Tissue Morphogenesis: Chondrogenesis within a Muscle Tissue Model?

Xiong, F., Hausdorf, J., Niethammer, T. R., Jansson, V. A., & Klar, R. M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144863 · Cited by 7

Tinkering with Growth Plates

Rolian, C. (2015) · Wiley eBooks · doi:10.1002/9781118524756.ch7 · Cited by 7

The Role of Osteoporosis in Total Hip Arthroplasty Periprosthetic Fractures and Current Management Strategies: a Review

Bauer, J., Duero, J., & Lindsay, A. D. (2025) · Current Osteoporosis Reports · doi:10.1007/s11914-025-00922-5 · Cited by 6

The relationship between second-to-fourth digit ratio (2D:4D), muscle strength and body composition to bone mineral density in young women

Arazi, H., & Eghbali, E. (2019) · Kinesiology · doi:10.26582/k.51.2.8 · Cited by 6

Genes and elements involved in the regulation of the nervous system and growth affect the development of spinal deformity in Cyprinus carpio

Bagi, Z., Balog, K., Tóth, B., Fehér, M., Bársony, P., Baranyai, E., Harangi, S., Ashrafzadeh, M. R., Hegedűs, B., Stündl, L., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0266447 · Cited by 6

Evolutionary trends in the emergence of skeletal cell types

Damatac, A. M., Koska, S., Ullrich, K. K., Domazet‐Lošo, T., Klimovich, A. V., & Kaucká, M. (2025) · Evolution Letters · doi:10.1101/2024.09.26.615131 · Cited by 6

A QUANTITATIVE AND QUALITATIVE GROWTH PLATE DESCRIPTION — A SIMPLE FRAMEWORK FOR CHONDROCYTES COLUMNAR ARRANGEMENT EVALUATION

Guevara, J., Castro-Abril, H. A., Barrera, L. A., & Garzón–Alvarado, D. A. (2015) · Journal of Mechanics in Medicine and Biology · doi:10.1142/s0219519416500548 · Cited by 6

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Cellular Plasticity in Musculoskeletal Development, Regeneration, and Disease

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Analysis of the Effect of Human Type I Collagen-Derived Peptide on Bone Regenerative Capacity and Comparison with Various Collagen Materials In Vivo

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Prospects of circadian clock in joint cartilage development

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