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

Single-Cell Transcriptomic Analysis Reveals the Cellular Heterogeneity of Mesenchymal Stem Cells

Zhang, C., Han, X., Liu, J., Chen, L., Lei, Y., Chen, K., Si, J., Wang, T.-Y., Zhou, H. F., Zhao, X., et al. (2022) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2022.01.005 · Cited by 89

Regulation of lysosome biogenesis and functions in osteoclasts

Lacombe, J., Karsenty, G., & Ferron, M. (2013) · Cell Cycle · doi:10.4161/cc.25825 · Cited by 92

Advances in Skeletal Dysplasia Genetics

Geister, K. A., & Camper, S. A. (2015) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-090314-045904 · Cited by 87

Biophysical Stimuli: A Review of Electrical and Mechanical Stimulation in Hyaline Cartilage

Vaca‐González, J. J., Guevara, J., Moncayo, M. A., Castro-Abril, H. A., Hata, Y., & Garzón–Alvarado, D. A. (2017) · Cartilage · doi:10.1177/1947603517730637 · Cited by 86

Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways

Rolfe, R. A., Nowlan, N. C., Kenny, E. M., Cormican, P., Morris, D. W., Prendergast, P. J., Kelly, D. J., & Murphy, P. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-48 · Cited by 88

Osteoblast dysfunctions in bone diseases: from cellular and molecular mechanisms to therapeutic strategies

Marie, P. J. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1801-2 · Cited by 86

p38α MAPK regulates proliferation and differentiation of osteoclast progenitors and bone remodeling in an aging-dependent manner

Cong, Q., Jia, H., Li, P., Qiu, S., Yeh, J., Wang, Y., Zhang, Z., Ao, J., Li, B., & Liu, H. (2017) · Scientific Reports · doi:10.1038/srep45964 · Cited by 85

Osteomodulin positively regulates osteogenesis through interaction with BMP2

Lin, W.-Z., Zhu, X., Gao, L., Mao, M., Gao, D., & Huang, Z. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03404-5 · Cited by 83

Neighbor of Brca1 gene (Nbr1) functions as a negative regulator of postnatal osteoblastic bone formation and p38 MAPK activity

Whitehouse, C. A., Waters, S., Marchbank, K., Horner, A. A., McGowan, N. W. A., Jovanovic, J. V., Xavier, G. M., Kashima, T. G., Cobourne, M. T., Richards, G. O., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913058107 · Cited by 83

Positive regulation of osteoclastic differentiation by growth differentiation factor 15 upregulated in osteocytic cells under hypoxia

Hinoi, E., Ochi, H., Takarada, T., Nakatani, E., Iezaki, T., Nakajima, H., Fujita, H., Takahata, Y., Hidano, S., Kobayashi, T., et al. (2011) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1538 · Cited by 84

GCN5 modulates osteogenic differentiation of periodontal ligament stem cells through DKK1 acetylation in inflammatory microenvironment

Li, B., Sun, J., Dong, Z., Xue, P., He, X., Liao, L., Yuan, L., & Jin, Y. J. (2016) · Scientific Reports · doi:10.1038/srep26542 · Cited by 81

Sphingolipid metabolism and its role in the skeletal tissues

Khavandgar, Z., & Murshed, M. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1778-x · Cited by 79

Hox11 genes are required for regional patterning and integration of muscle, tendon and bone

Swinehart, I. T., Schlientz, A. J., Quintanilla, C. A., Mortlock, D. P., & Wellik, D. M. (2013) · Development · doi:10.1242/dev.096693 · Cited by 79

The transcription factor Foxc1 is necessary for Ihh–Gli2-regulated endochondral ossification

Yoshida, M., Hata, K., Takashima, R., Ono, K., Nakamura, E., Takahata, Y., Murakami, T., Iseki, S., Takano‐Yamamoto, T., Nishimura, R., et al. (2015) · Nature Communications · doi:10.1038/ncomms7653 · Cited by 79

Stromal cell-derived factor-1 enhances distraction osteogenesis-mediated skeletal tissue regeneration through the recruitment of endothelial precursors

Fujio, M., Yamamoto, A., Ando, Y., Shohara, R., Kinoshita, K., Kaneko, T., Hibi, H., & Ueda, M. (2011) · Bone · doi:10.1016/j.bone.2011.06.024 · Cited by 79

JMJD3 promotes chondrocyte proliferation and hypertrophy during endochondral bone formation in mice

Zhang, F., Xu, L., Xu, L., Xu, Q., Li, D., Yang, Y., Karsenty, G., & Chen, C. D. (2015) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjv003 · Cited by 77

Extrinsic Mechanisms Involved in Age-Related Defective Bone Formation

Marie, P. J., & Kassem, M. S. (2011) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2010-2113 · Cited by 78

Intracellular Accumulation of Advanced Glycation End Products Induces Osteoblast Apoptosis Via Endoplasmic Reticulum Stress

Suzuki, R., Fujiwara, Y., Saito, M., Arakawa, S., Shirakawa, J., Yamanaka, M., Komohara, Y., Marumo, K., & Nagai, R. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4053 · Cited by 75

Modeling human skeletal development using human pluripotent stem cells

Lamandé, S. R., Ng, E. S., Cameron, T. L., Kung, L. H. W., Sampurno, L., Rowley, L., Lilianty, J., Patria, Y. N., Stenta, T., Hanssen, E. G., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2211510120 · Cited by 75

Chaperoning osteogenesis: new protein-folding disease paradigms

Makareeva, E., Aviles, N. A., & Leikin, S. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.11.007 · Cited by 75

Thymidine phosphorylase exerts complex effects on bone resorption and formation in myeloma

Liu, H., Liu, Z., Du, J., He, J., Lin, P., Amini, B., Starbuck, M. W., Novane, N., Shah, J. J., Davis, R. E., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad8949 · Cited by 74

Periosteal Tissue Engineering: Current Developments and Perspectives

Lou, Y., Wang, H., Ye, G., Li, Y., Liu, C., Yu, M., & Ying, B. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202100215 · Cited by 75

Glutamine Metabolism Is Essential for Stemness of Bone Marrow Mesenchymal Stem Cells and Bone Homeostasis

Zhou, T., Yang, Y., Chen, Q., & Xie, L. (2019) · Stem Cells International · doi:10.1155/2019/8928934 · Cited by 73

Chondrocyte-Specific RUNX2 Overexpression Accelerates Post-traumatic Osteoarthritis Progression in Adult Mice

Catheline, S. E., Hoak, D., Chang, M., Ketz, J. P., Hilton, M. J., Zuscik, M. J., & Jonason, J. H. (2019) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3737 · Cited by 73

Hierarchical Micro-Nano Topography Promotes Cell Adhesion and Osteogenic Differentiation via Integrin α2-PI3K-AKT Signaling Axis

Zheng, H., Tian, Y., Gao, Q., Yu, Y., Xia, X., Feng, Z., Dong, F., Wu, X., & Sui, L. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00463 · Cited by 74

Osteoimmunological insights into the pathogenesis of ankylosing spondylitis

Liu, L., Yuan, Y. J., Zhang, S., Xu, J., & Zou, J. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30313 · Cited by 73

The chondrocytic journey in endochondral bone growth and skeletal dysplasia

Tsang, K. Y., Tsang, S. W., Chan, D. T.-M., & Cheah, K. S. E. (2014) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21060 · Cited by 73

Regulation of Long Bone Growth in Vertebrates; It Is Time to Catch Up

Roselló‐Díez, A., & Joyner, A. L. (2015) · Endocrine Reviews · doi:10.1210/er.2015-1048 · Cited by 78

Histone deacetylase 3 supports endochondral bone formation by controlling cytokine signaling and matrix remodeling

Shull, L. C., Bradley, E. W., McGee‐Lawrence, M. E., Weivoda, M. M., Poston, D., Dudakovic, A., Xu, M., Tchkonia, T., Kirkland, J. L., van Wijnen, A. J., et al. (2016) · Science Signaling · doi:10.1126/scisignal.aaf3273 · Cited by 73

Hox Genes and Limb Musculoskeletal Development

Pineault, K. M., & Wellik, D. M. (2014) · Current Osteoporosis Reports · doi:10.1007/s11914-014-0241-0 · Cited by 72

Distinct Functions of Sox2 Control Self-Renewal and Differentiation in the Osteoblast Lineage

Seo, E., Basu-Roy, U., Zavadil, J., Basilico, C., & Mansukhani, A. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05798-11 · Cited by 75

Osteocalcin: an osteoblast-derived polypeptide hormone that modulates whole body energy metabolism

Brennan-Speranza, T. C., & Conigrave, A. D. (2015) · Calcified Tissue International · doi:10.1007/s00223-014-9931-y · Cited by 71

miRNA expression profile during osteogenic differentiation of human adipose‐derived stem cells

Zhang, Z., Zhang, H., Kang, Y. Q., Sheng, P., Ma, Y., Yang, Z., Zhang, Z., Fu, M., He, A., & Liao, W. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23418 · Cited by 70

Chondrocyte-specific ablation of Osterix leads to impaired endochondral ossification

Oh, J.-H., Park, S., Crombrugghe, B. D., & Kim, J. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.064 · Cited by 70

An Overview of the Metabolic Functions of Osteocalcin

Wei, J., & Karsenty, G. (2015) · Current Osteoporosis Reports · doi:10.1007/s11914-015-0267-y · Cited by 69

Syringic acid, a phenolic acid, promotes osteoblast differentiation by stimulation of Runx2 expression and targeting of Smad7 by miR-21 in mouse mesenchymal stem cells

Balasubramanian, A., Balagangadharan, K., & Selvamurugan, N. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0449-3 · Cited by 69

Integrin signaling in skeletal development and function

Docheva, D., Popov, C., Alberton, P., & Aszódi, A. (2014) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21059 · Cited by 68

Spatiotemporal Immunomodulation Using Biomimetic Scaffold Promotes Endochondral Ossification‐Mediated Bone Healing

Liu, Y., Yang, Z., Wang, L., Sun, L., Kim, B. Y. S., Jiang, W., Yuan, Y., & Liu, C. (2021) · Advanced Science · doi:10.1002/advs.202100143 · Cited by 66

Mouse limb skeletal growth and synovial joint development are coordinately enhanced by Kartogenin

Decker, R. S., Koyama, E., Enomoto‐Iwamoto, M., Maye, P. F., Rowe, D. W., Zhu, S., Schultz, P. G., & Pacifici, M. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.09.011 · Cited by 66

Magnesium Attenuates Phosphate-Induced Deregulation of a MicroRNA Signature and Prevents Modulation of Smad1 and Osterix during the Course of Vascular Calcification

Louvet, L., Metzinger, L., Büchel, J., Steppan, S., & Massy, Z. A. (2016) · BioMed Research International · doi:10.1155/2016/7419524 · Cited by 66

Allen's Rule Revisited: Temperature Influences Bone Elongation During a Critical Period of Postnatal Development

Serrat, M. A. (2013) · The Anatomical Record · doi:10.1002/ar.22763 · Cited by 65

Osteoclast fusion is initiated by a small subset of RANKL-stimulated monocyte progenitors, which can fuse to RANKL-unstimulated progenitors

Levaot, N., Ottolenghi, A., Mann, M., Ram, G. G., Kam, Z., & Geiger, B. (2015) · Bone · doi:10.1016/j.bone.2015.05.021 · Cited by 68

Glypican-6 promotes the growth of developing long bones by stimulating Hedgehog signaling

Capurro, M., Izumikawa, T., Suarez, P., Shi, W., Cydzik, M., Kaneiwa, T., Gariépy, J., Bonafé, L., & Filmus, J. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201605119 · Cited by 67

Tcf12, A Member of Basic Helix-Loop-Helix Transcription Factors, Mediates Bone Marrow Mesenchymal Stem Cell Osteogenic Differentiation In Vitro and In Vivo

Yi, S., Yu, M., Yang, S., Miron, R. J., & Zhang, Y. (2016) · Stem Cells · doi:10.1002/stem.2491 · Cited by 64

Estrogen receptors in breast and bone: from virtue of remodeling to vileness of metastasis

Bado, I., Gugala, Z., Fuqua, S. A. W., & Zhang, X. (2017) · Oncogene · doi:10.1038/onc.2017.94 · Cited by 65

The balance of tissue repair and remodeling in chronic arthritis

Lories, R. J. U. (2011) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2011.156 · Cited by 64

Role of C-type natriuretic peptide signalling in maintaining cartilage and bone function

Peake, N., Hobbs, A. J., Pingguan‐Murphy, B., Salter, D. M., Berenbaum, F., & Chowdhury, T. T. (2014) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2014.07.018 · Cited by 63

A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type

Geister, K. A., Brinkmeier, M. L., Hsieh, M., Faust, S. M., Karolyi, I. J., Perosky, J. E., Kozloff, K. M., Conti, M., & Camper, S. A. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds432 · Cited by 63

Controlling hypoxia-inducible factor-2α is critical for maintaining bone homeostasis in mice

Lee, S. Y., Park, K. H., Yu, H.-G., Kook, E., Song, W., Lee, G., Koh, J., Shin, H., Choi, J., Huh, Y. H., et al. (2019) · Bone Research · doi:10.1038/s41413-019-0054-y · Cited by 63

Semaphorin 3A

Xu, R. (2013) · Cell Adhesion & Migration · doi:10.4161/cam.27752 · Cited by 63

p53 inhibits SP7/Osterix activity in the transcriptional program of osteoblast differentiation

Artigas, N., Gámez, B., Cubillos‐Rojas, M., Sánchez‐de‐Diego, C., Valer, J. A., Pons, G., Rosa, J. L., & Ventura, F. (2017) · Cell Death and Differentiation · doi:10.1038/cdd.2017.113 · Cited by 62

Extracellular miR-574-5p Induces Osteoclast Differentiation via TLR 7/8 in Rheumatoid Arthritis

Hegewald, A. B., Breitwieser, K., Ottinger, S. M., Mobarrez, F., Korotkova, M., Réthi, B., Jakobsson, P., Catrina, A. I., Wähämaa, H., & Saul, M. J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.585282 · Cited by 62

Osteogenic differentiation cues of the bone morphogenetic protein-9 (BMP-9) and its recent advances in bone tissue regeneration

Bharadwaz, A., & Jayasuriya, A. C. (2020) · Materials Science and Engineering C · doi:10.1016/j.msec.2020.111748 · Cited by 63

Bone metabolism in the fetus and neonate

Kovács, C. S. (2013) · Pediatric Nephrology · doi:10.1007/s00467-013-2461-4 · Cited by 62

Kif7 promotes hedgehog signaling in growth plate chondrocytes by restricting the inhibitory function of Sufu

Hsu, S.-H. C., Zhang, X., Yu, C., Li, Z. J., Wunder, J. S., Hui, C., & Alman, B. A. (2011) · Development · doi:10.1242/dev.069492 · Cited by 61

The unfolded protein response in skeletal development and homeostasis

Horiuchi, K., Tohmonda, T., & Morioka, H. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2178-1 · Cited by 62

HDAC4 integrates PTH and sympathetic signaling in osteoblasts

Obri, A., Makinistoglu, M. P., Zhang, H., & Karsenty, G. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201403138 · Cited by 60

Signaling pathways effecting crosstalk between cartilage and adjacent tissues

Maes, C. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.05.007 · Cited by 61

Systems Genetic Analysis of Osteoblast-Lineage Cells

Calabrese, G. M., Bennett, B. J., Orozco, L. D., Kang, H. M., Eskin, E., Dombret, C., Backer, O. D., Lusis, A. J., & Farber, C. R. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003150 · Cited by 59

MiR‐144‐3p regulates osteogenic differentiation and proliferation of murine mesenchymal stem cells by specifically targeting Smad4

Huang, C. X., Geng, J., Wei, X., Zhang, R., & Jiang, S. (2016) · FEBS Letters · doi:10.1002/1873-3468.12112 · Cited by 58

Transcriptional regulation of bone formation

Kim, J.-E. (2010) · Frontiers in Bioscience-Scholar · doi:10.2741/s138 · Cited by 57

BMP growth factor signaling in a biomechanical context

Kopf, J., Paarmann, P., Hiepen, C., Horbelt, D., & Knaus, P. I. (2013) · BioFactors · doi:10.1002/biof.1137 · Cited by 65

IL-3 promotes osteoblast differentiation and bone formation in human mesenchymal stem cells

Barhanpurkar, A. P., Gupta, N., Srivastava, R. K., Tomar, G. B., Naik, S. P., Joshi, S. R., Pote, S. T., Mishra, G. C., & Wani, M. R. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.074 · Cited by 55

Chondrocytic Atf4 regulates osteoblast differentiation and function via Ihh

Wang, W., Lian, N., Ma, Y., Li, L., Gallant, R., Elefteriou, F., & Yang, X. (2011) · Development · doi:10.1242/dev.069575 · Cited by 54

Loss of Osteoblast Runx3 Produces Severe Congenital Osteopenia

Bauer, O., Sharir, A., Kimura, A., Hantisteanu, S., Takeda, S., & Groner, Y. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.01106-14 · Cited by 54

NFATC1 promotes epicardium-derived cell invasion into myocardium

Combs, M. D., Braitsch, C. M., Lange, A. W., James, J. F., & Yutzey, K. E. (2011) · Development · doi:10.1242/dev.060996 · Cited by 56

Impact of RUNX2 on drug-resistant human pancreatic cancer cells with p53 mutations

Ozaki, T., Yu, M., Yin, D., Sun, D., Zhu, Y., Bu, Y., & Sang, M. (2018) · BMC Cancer · doi:10.1186/s12885-018-4217-9 · Cited by 57

Hypoxia-inducible factor 2α is a negative regulator of osteoblastogenesis and bone mass accrual

Merceron, C., Ranganathan, K., Wang, E. Y., Tata, Z., Makkapati, S., Khan, M. P., Mangiavini, L., Yao, Q., Castellini, L., Lévi, B., et al. (2019) · Bone Research · doi:10.1038/s41413-019-0045-z · Cited by 54

MicroRNA‐145 regulates osteoblastic differentiation by targeting the transcription factor Cbfb

Fukuda, T., Ochi, H., Sunamura, S., Haiden, A., Bando, W., Inose, H., Okawa, A., Asou, Y., & Takeda, S. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.09.024 · Cited by 53

The Multifaceted Osteoclast; Far and Beyond Bone Resorption

Drissi, H., & Sanjay, A. (2016) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25560 · Cited by 55

IRX3 and IRX5 Inhibit Adipogenic Differentiation of Hypertrophic Chondrocytes and Promote Osteogenesis

Tan, Z., Kong, M., Wen, S., Tsang, K. Y., Niu, B., Hartmann, C., Chan, D., Hui, C.-C., & Cheah, K. S. E. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4132 · Cited by 52

ATF3 deficiency in chondrocytes alleviates osteoarthritis development

Iezaki, T., Ozaki, K., Fukasawa, K., Inoue, M., Kitajima, S., Muneta, T., Takeda, S., Fujita, H., Onishi, Y., Horie, T., et al. (2016) · The Journal of Pathology · doi:10.1002/path.4739 · Cited by 52

Parathyroid Hormone-Like Hormone is a Poor Prognosis Marker of Head and Neck Cancer and Promotes Cell Growth via RUNX2 Regulation

Chang, W., Lin, Y., Su, C., Peng, H., Chang, Y., Hsiao, J., Chen, C., Chang, J., Shieh, Y., Hsiao, M., et al. (2017) · Scientific Reports · doi:10.1038/srep41131 · Cited by 52

Osteoporosis and autophagy: What is the relationship?

Florencio‐Silva, R., Sasso, G. R. D. S., Simões, M. D. J., Simões, R. S., Baracat, M. C. P., Sasso‐Cerri, E., & Cerri, P. S. (2017) · Revista da Associação Médica Brasileira · doi:10.1590/1806-9282.63.02.173 · Cited by 53

Plastin 3 influences bone homeostasis through regulation of osteoclast activity

Neugebauer, J., Heilig, J., Hosseinibarkooie, S., Ross, B. C., Mendoza-Ferreira, N., Nolte, F., Peters, M., Hölker, I., Hupperich, K., Tschanz, T., et al. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy318 · Cited by 54

3D Hybrid Nanofiber Aerogels Combining with Nanoparticles Made of a Biocleavable and Targeting Polycation and MiR‐26a for Bone Repair

Li, R., Wang, H., John, J. V., Song, H., Teusink, M. J., & Xie, J. (2020) · Advanced Functional Materials · doi:10.1002/adfm.202005531 · Cited by 52

Bone Development in the Fetus and Neonate: Role of the Calciotropic Hormones

Kovács, C. S. (2011) · Current Osteoporosis Reports · doi:10.1007/s11914-011-0073-0 · Cited by 51

Thiazolidinediones on PPAR γ : The Roles in Bone Remodeling

Wei, W., & Wan, Y. (2011) · PPAR Research · doi:10.1155/2011/867180 · Cited by 51

Extracellular Matrix and Developing Growth Plate

Myllyharju, J. (2014) · Current Osteoporosis Reports · doi:10.1007/s11914-014-0232-1 · Cited by 52

Ubiquitin-Dependent Regulation of Stem Cell Biology

Werner, A. A., Manford, A. G., & Rapé, M. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.04.002 · Cited by 52

Compensatory regulation of the Snai1 and Snai2 genes during chondrogenesis

Chen, Y., & Gridley, T. (2013) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1871 · Cited by 50

Growth differentiation factor 11 is a protective factor for osteoblastogenesis by targeting PPARgamma

Zhang, Y., Shao, J., Wang, Z., Yang, T., Liu, S., Liu, Y., Fan, X., & Ye, W. (2014) · Gene · doi:10.1016/j.gene.2014.12.039 · Cited by 51

Endochondral ossification and the evolution of limb proportions

Rolian, C. (2020) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.373 · Cited by 49

Lipid Metabolism in Cartilage Development, Degeneration, and Regeneration

Su, Z., Zong, Z., Deng, J., Huang, J., Liu, G., Wei, B., Cui, L., Li, G., Zhong, H., & Lin, S. (2022) · Nutrients · doi:10.3390/nu14193984 · Cited by 51

Employing the Biology of Successful Fracture Repair to Heal Critical Size Bone Defects

Cameron, J. A., Milner, D. J., Lee, J., Cheng, J., Fang, N. X., & Jasiuk, I. (2012) · Current topics in microbiology and immunology · doi:10.1007/82_2012_291 · Cited by 48

Interferon-γ is a master checkpoint regulator of cytokine-induced differentiation

Zha, Z., Bucher, F., Nejatfard, A., Zheng, T., Zhang, H., Yea, K., & Lerner, R. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1706915114 · Cited by 48

Opposite Spectrum of Activity of Canonical Wnt Signaling in the Osteogenic Context of Undifferentiated and Differentiated Mesenchymal Cells: Implications for Tissue Engineering

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Expression of osteoblastic and osteoclastic genes during spontaneous regeneration and autotransplantation of goldfish scale: A new tool to study intramembranous bone regeneration

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The WTX Tumor Suppressor Regulates Mesenchymal Progenitor Cell Fate Specification

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Endoplasmic Reticulum Stress in Arterial Smooth Muscle Cells: A Novel Regulator of Vascular Disease

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Circulating miRNAs as diagnostic biomarkers for adolescent idiopathic scoliosis

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The long noncoding RNA Crnde regulates osteoblast proliferation through the Wnt/β-catenin signaling pathway in mice

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The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development

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Semi-automatic grading system in histologic and immunohistochemistry analysis to evaluate in vitro chondrogenesis

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Evidences for a New Role of miR-214 in Chondrogenesis

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On the evolutionary relationship between chondrocytes and osteoblasts

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Skeletal energy homeostasis: a paradigm of endocrine discovery

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Mineral and bone physiology in the foetus, preterm and full-term neonates

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Adult chondrogenesis and spontaneous cartilage repair in the skate, Leucoraja erinacea

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Development of a subset of forelimb muscles and their attachment sites requires the ulnar-mammary syndrome gene Tbx3

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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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Molecular control of osteo-chondroprogenitors formation

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