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The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6
Open accessAbstract
To examine whether the transcription factor Sox9 has an essential role during the sequential steps of chondrocyte differentiation, we have used the Cre/ loxP recombination system to generate mouse embryos in which either Sox9 is missing from undifferentiated mesenchymal cells of limb buds or the Sox9 gene is inactivated after chondrogenic mesenchymal condensations. Inactivation of Sox9 in limb buds before mesenchymal condensations resulted in a complete absence of both cartilage and bone, but markers for the different axes of limb development showed a normal pattern of expression. Apoptotic domains within the developing limbs were expanded, suggesting that Sox9 suppresses apoptosis. Expression of Sox5 and Sox6 , two other Sox genes involved in chondrogenesis, was no longer detected. Moreover, expression of Runx2 , a transcription factor needed for osteoblast differentiation, was also abolished. Embryos, in which Sox9 was deleted after mesenchymal condensations, exhibited a severe generalized chondrodysplasia, similar to that in Sox5 ; Sox6 double-null mutant mice. Most cells were arrested as condensed mesenchymal cells and did not undergo overt differentiation into chondrocytes. Furthermore, chondrocyte proliferation was severely inhibited and joint formation was defective. Although Indian hedgehog , Patched1 , parathyroid hormone-related peptide ( Pthrp ), and Pth/Pthrp receptor were expressed, their expression was down-regulated. Our experiments further suggested that Sox9 is also needed to prevent conversion of proliferating chondrocytes into hypertrophic chondrocytes. We conclude that Sox9 is required during sequential steps of the chondrocyte differentiation pathway.
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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
Regulation of Rate of Cartilage Differentiation by Indian Hedgehog and PTH-Related Protein
Vortkamp, A., Lee, K., Lanske, B., Segre, G. V., Kronenberg, H. M., & Tabin, C. J. (1996) · Science · doi:10.1126/science.273.5275.613 · Cited by 1,999
Sox9 is required for cartilage formation
Bi, W., Deng, J. M., Zhang, Z., Behringer, R. R., & Crombrugghe, B. D. (1999) · Nature Genetics · doi:10.1038/8792 · Cited by 1,760
St‐Jacques, B., Hammerschmidt, M., & McMahon, A. P. (1999) · Genes & Development · doi:10.1101/gad.13.16.2072 · Cited by 1,742
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
Foster, J. W., Dominguez-Steglich, M., Guioli, S., Kwok, C., Weller, P., Stevanović, M., Weissenbach, J., Mansour, S., Young, I., Goodfellow, P., et al. (1994) · Nature · doi:10.1038/372525a0 · Cited by 1,602
Wagner, T., Wirth, J., Meyer, J., Zabel, B., Held, M., Zimmer, J., Pasantes, J., Bricarelli, F. D., Keutel, J., Hustert, E., et al. (1994) · Cell · doi:10.1016/0092-8674(94)90041-8 · Cited by 1,592
Deletion of a DNA Polymerase β Gene Segment in T Cells Using Cell Type-Specific Gene Targeting
Gu, H., Marth, J. D., Orban, P. C., Mossmann, H., & Rajewsky, K. (1994) · Science · doi:10.1126/science.8016642 · Cited by 1,397
PTH/PTHrP Receptor in Early Development and Indian Hedgehog—Regulated Bone Growth
Lanske, B., Karaplis, A. C., Lee, K., Luz, A., Vortkamp, A., Pirro, A. E., Karperien, M., Defize, L. H. K., Ho, C., Mulligan, R. C., et al. (1996) · Science · doi:10.1126/science.273.5275.663 · Cited by 1,325
Schwenk, F., Baron, U., & Rajewsky, K. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.24.5080 · Cited by 1,289
Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene.Preprint
Karaplis, A. C., Luz, A., Glowacki, J., Bronson, R. T., Tybulewicz, V. L. J., Kronenberg, H. M., & Mulligan, R. C. (1994) · Genes & Development · doi:10.1101/gad.8.3.277 · Cited by 1,151
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- Hogan B. Beddington R. Costantini F. Lucy E. (1994) Manipulating the mouse embryo. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY), 2nd Edition.
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Sorted by citations
Items 401–500 of 1,002
Epigenetic Switch between SOX2 and SOX9 Regulates Cancer Cell Plasticity
Lin, S., Chou, Y., Jiang, S. S., Chang, J.-L., Chung, C.-H., Kao, Y.-R., Chang, I., & Wu, C.-W. (2016) · Cancer Research · doi:10.1158/0008-5472.can-15-3178 · Cited by 73
Kawasaki, Y., Kugimiya, F., Chikuda, H., Kamekura, S., Ikeda, T., Kawamura, N., Saito, T., Shinoda, Y., Higashikawa, A., Yano, F., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci35243 · Cited by 73
EPO Promotes Bone Repair through Enhanced Cartilaginous Callus Formation and Angiogenesis
Lin, W., Zhang, F., He, Q., Tsang, W. P., Lu, L., Li, Q., Wu, Z., Qiu, G., Zhou, G., & Wan, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102010 · Cited by 76
Yao, B., Wang, Q. K., Liu, C.-F., Bhattaram, P., Li, W., Mead, T. J., Crish, J. F., & Lefebvre, V. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv426 · Cited by 73
Amano, K., Densmore, M., Nishimura, R., & Lanske, B. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.570507 · Cited by 73
Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia
Egunsola, A. T., Bae, Y., Jiang, M., Liu, D. S., Chen, Y., Bertin, T., Chen, S., Lu, J. T., Nevarez, L., Magal, N., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90193 · Cited by 73
SOX9: A genomic view of tissue specific expression and action.
Symon, A., & Harley, V. (2017) · International Journal of Biochemistry and Cell Biology · doi:10.1016/j.biocel.2017.03.005 · Cited by 72
Sox9 positive periosteal cells in fracture repair of the adult mammalian long bone
He, X., Bougioukli, S., Ortega, B., Arevalo, E., Lieberman, J. R., & McMahon, A. P. (2017) · Bone · doi:10.1016/j.bone.2017.06.008 · Cited by 73
Shibata, S., Suda, N., Suzuki, S., Fukuoka, H., & Yamashita, Y. (2006) · Journal of Anatomy · doi:10.1111/j.1469-7580.2006.00525.x · Cited by 72
Neven, E., Persy, V. P., Dauwe, S. E. H., Schutter, T. M. D., Broe, M. E. D., & D’Haese, P. C. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.204834 · Cited by 72
Uchimura, T., Hollander, J. M., Nakamura, D. S., Liu, Z., Rosen, C. J., Georgakoudi, I., & Zeng, L. (2017) · Development · doi:10.1242/dev.155598 · Cited by 72
Provot, S., & Schipani, E. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1402.076 · Cited by 72
Bone regulatory factors NFATc1 and Osterix in human calcific aortic valves
Alexopoulos, A., Bravou, V., Peroukides, S., Kaklamanis, L., Varakis, J. N., Alexopoulos, D., & Papadaki, H. H. (2008) · International Journal of Cardiology · doi:10.1016/j.ijcard.2008.10.014 · Cited by 75
A critical evaluation of specific aspects of joint development
Pitsillides, A. A., & Ashhurst, D. E. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21654 · Cited by 71
Arginine methyltransferase CARM1/PRMT4 regulates endochondral ossification
Ito, T., Yadav, N., Lee, J. H., Furumatsu, T., Yamashita, S., Yoshida, K., Taniguchi, N., Hashimoto, M., Tsuchiya, M., Ozaki, T., et al. (2009) · BMC Developmental Biology · doi:10.1186/1471-213x-9-47 · Cited by 71
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
Kushwaha, P., Khedgikar, V., Gautam, J., Dixit, P., Chillara, R., Verma, A., Thakur, R. K., Mishra, D. P., Singh, D. R., Maurya, R., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.350 · Cited by 70
What Is New in the miRNA World Regarding Osteosarcoma and Chondrosarcoma?
Palmini, G., Marini, F., & Brandi, M. L. (2017) · Molecules · doi:10.3390/molecules22030417 · Cited by 70
Tsiapalis, D., & Zeugolis, D. I. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.120943 · Cited by 72
Sox9 is required for invagination of the otic placode in mice
Barrionuevo, F. J., Naumann, A., Bagheri‐Fam, S., Speth, V., Taketo, M. M., Scherer, G., & Neubüser, A. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.02.011 · Cited by 70
Gao, Y., Jheon, A. H., Nourkeyhani, H., Kobayashi, H., & Ganss, B. (2004) · Gene · doi:10.1016/j.gene.2004.05.026 · Cited by 70
p53 Loss Increases the Osteogenic Differentiation of Bone Marrow Stromal Cells
He, Y., de Castro, L. F., Shin, M. H., Dubois, W., Yang, H. H., Jiang, S., Mishra, P. J., Ren, L., Gou, H., Lal, A., et al. (2014) · Stem Cells · doi:10.1002/stem.1925 · Cited by 72
Hattori, T., Eberspaecher, H., Lu, J., Zhang, R., Nishida, T., Kahyo, T., Yasuda, H., & Crombrugghe, B. D. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m511330200 · Cited by 70
Regulatory mechanisms for the development of growth plate cartilage
Michigami, T. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1346-9 · Cited by 69
Carlson, H. L., Quinn, J. J., Yang, Y. W., Thornburg, C. K., Chang, H. Y., & Stadler, H. S. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005680 · Cited by 68
Stem Cell Determinant SOX9 Promotes Lineage Plasticity and Progression in Basal-like Breast Cancer
Christin, J. R., Wang, C., Chung, C., Liu, Y., Dravis, C., Tang, W., Oktay, M. H., Wahl, G. M., & Guo, W. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107742 · Cited by 69
Extracellular matrix genes as hypoxia-inducible targets
Myllyharju, J., & Schipani, E. (2009) · Cell and Tissue Research · doi:10.1007/s00441-009-0841-7 · Cited by 72
Scleraxis and E47 cooperatively regulate the Sox9-dependent transcription
Furumatsu, T., Shukunami, C., Amemiya-Kudo, M., Shimano, H., & Ozaki, T. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.10.003 · Cited by 69
A reevaluation of X-irradiation-induced phocomelia and proximodistal limb patterning
Galloway, J. L., Delgado, I., Ros, M. A., & Tabin, C. J. (2009) · Nature · doi:10.1038/nature08117 · Cited by 69
Lin, S., Tzeng, B., Lee, K., Smith, R. J., Campbell, K. P., & Chen, C. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323112111 · Cited by 73
Schock, E. N., & LaBonne, C. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.606889 · Cited by 72
Matsumoto, S., Hayashi, M., Suzuki, Y., Suzuki, N., Maeno, M., & Ogiso, B. (2012) · Journal of Endodontics · doi:10.1016/j.joen.2012.10.006 · Cited by 68
Sparc (Osteonectin) functions in morphogenesis of the pharyngeal skeleton and inner ear
Rotllant, J., Liu, D., Yan, Y.-L., Postlethwait, J. H., Westerfield, M., & Du, S. (2008) · Matrix Biology · doi:10.1016/j.matbio.2008.03.001 · Cited by 68
Takigawa, Y., Hata, K., Muramatsu, S., Amano, K., Ono, K., Wakabayashi, M., Matsuda, A., Takada, K., Nishimura, R., & Yoneda, T. (2010) · Journal of Cell Science · doi:10.1242/jcs.071373 · Cited by 68
SOXC proteins amplify canonical WNT signaling to secure nonchondrocytic fates in skeletogenesis
Bhattaram, P., Penzo‐Méndez, A., Kato, K. H., Bandyopadhyay, K., Gadi, A., Taketo, M. M., & Lefebvre, V. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201405098 · Cited by 68
Introduction to the state-of-the-art 3D bioprinting methods, design, and applications in orthopedics
Semba, J. A., Mieloch, A. A., & Rybka, J. D. (2019) · Bioprinting · doi:10.1016/j.bprint.2019.e00070 · Cited by 70
Bala, P., Rennhack, J. P., Aitymbayev, D., Morris, C. X., Moyer, S. M., Duronio, G. N., Doan, K. T., Li, Z., Liang, X., Hornick, J. L., et al. (2023) · Science Advances · doi:10.1126/sciadv.adf0927 · Cited by 70
Pan, Y., Liu, Z., Shen, J., & Kopan, R. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.08.037 · Cited by 67
Lavery, R., Lardenois, A., Jian-Motamedi, F., Pauper, E., Gregoire, E. P., Vigier, C., Moreilhon, C., Primig, M., & Chaboissier, M. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.03.029 · Cited by 67
Self-citationAssembly, maturation, and degradation of the supraspinatus enthesis
Jensen, P. T., Lambertsen, K. L., & Frich, L. H. (2018) · Journal of Shoulder and Elbow Surgery · doi:10.1016/j.jse.2017.10.030 · Cited by 68
Genetic Causes of Craniosynostosis: An Update
Goos, J. A. C., & Mathijssen, I. M. J. (2018) · Molecular Syndromology · doi:10.1159/000492266 · Cited by 68
Growth plate skeletal stem cells and their transition from cartilage to bone
Matsushita, Y., Ono, W., & Ono, N. (2020) · Bone · doi:10.1016/j.bone.2020.115359 · Cited by 66
Cartilage regeneration using biodegradable oxidized alginate/hyaluronate hydrogels
Park, H., & Lee, K. Y. (2014) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.35126 · Cited by 66
Sox9 is critical for suppression of neurogenesis but not initiation of gliogenesis in the cerebellum
Vong, K. I., Leung, C. K. Y., Behringer, R. R., & Kwan, K. M. (2015) · Molecular Brain · doi:10.1186/s13041-015-0115-0 · Cited by 63
Models of global gene expression define major domains of cell type and tissue identity
Hutchins, A. P., Yang, Z., Li, Y., He, F., Fu, X., Wang, X., Li, D., Liu, K., He, J., Wang, Y., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx054 · Cited by 63
Gene expression and digit homology in the chicken embryo wing
Welten, M. C. M., Verbeek, F. J., Meijer, A. H., & Richardson, M. K. (2005) · Evolution & Development · doi:10.1111/j.1525-142x.2005.05003.x · Cited by 66
The cartilage matrisome in adolescent idiopathic scoliosis
Wise, C. A., Sepich, D. S., Ushiki, A., Khanshour, A. M., Kidane, Y. H., Makki, N., Gurnett, C. A., Gray, R. S., Rios, J. J., Ahituv, N., et al. (2020) · Bone Research · doi:10.1038/s41413-020-0089-0 · Cited by 63
Dysregulated overexpression of Sox9 induces fibroblast activation in pulmonary fibrosis
Gajjala, P. R., Kasam, R. K., Soundararajan, D., Sinner, D. I., Huang, S. K., Jegga, A. G., & Madala, S. K. (2021) · JCI Insight · doi:10.1172/jci.insight.152503 · Cited by 65
Mechanical feedback defines organizing centers to drive digit emergence
Parada, C., Banavar, S. P., Khalilian, P., Rigaud, S. U., Michaut, A., Liu, Y., Joshy, D. M., Campàs, O., & Gros, J. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.03.004 · Cited by 65
Stem Cell-Laden Hydrogel-Based 3D Bioprinting for Bone and Cartilage Tissue Engineering
Yang, Z., Yi, P., Liu, Z., Zhang, W., Mei, L., Feng, C., Tu, C., & Li, Z. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.865770 · Cited by 67
Cell biological and physicochemical aspects of arterial calcification
Neven, E., Schutter, T. M. D., Broe, M. E. D., & D’Haese, P. C. (2011) · Kidney International · doi:10.1038/ki.2011.59 · Cited by 65
Konishi, E., Nakashima, Y., Iwasa, Y., Nakao, R., & Yanagisawa, A. (2009) · Human Pathology · doi:10.1016/j.humpath.2009.07.014 · Cited by 65
Soung, D. Y., Talebian, L., Matheny, C., Guzzo, R. M., Speck, M. E., Lieberman, J. R., Speck, N. A., & Drissi, H. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1601 · Cited by 65
Morphological and molecular characterization of developing vertebral fusions using a teleost model
Ytteborg, E., Torgersen, J. S., Bæverfjord, G., & Takle, H. (2010) · BMC Physiology · doi:10.1186/1472-6793-10-13 · Cited by 65
SOX9 modulates the expression of key transcription factors required for heart valve development
Garside, V. C., Cullum, R., Alder, O., Lu, D. Y., Vander Werff, R., Bilenky, M., Zhao, Y., Jones, S. J. M., Marra, M. A., Underhill, T. M., et al. (2015) · Development · doi:10.1242/dev.125252 · Cited by 65
Baird, D. A., Evans, D. S., Kamanu, F., Gregory, J. S., Saunders, F. R., Giuraniuc, C. V., Barr, R. J., Aspden, R. M., Jenkins, D., Kiel, D. P., et al. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3605 · Cited by 62
L-type voltage-gated Ca 2+ channel Ca V 1.2 regulates chondrogenesis during limb development
Atsuta, Y., Tomizawa, R. R., Levin, M. G., & Tabin, C. J. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1908981116 · Cited by 65
Kurakazu, I., Akasaki, Y., Hayashida, M., Tsushima, H., Goto, N., Sueishi, T., Toya, M., Kuwahara, M., Okazaki, K., Duffy, T., et al. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.009409 · Cited by 64
Assessing skeletal maturity by using blood spot insulin-like growth factor I (IGF-I) testing
Masoud, M. I., Masoud, I., Kent, R., Gowharji, N., & Cohen, L. E. (2008) · American Journal of Orthodontics and Dentofacial Orthopedics · doi:10.1016/j.ajodo.2006.09.063 · Cited by 64
Transcriptional induction of SOX9 by NF-κB family member RelA in chondrogenic cells
Ushita, M., Saito, T., Ikeda, T., Yano, F., Higashikawa, A., Ogata, N., Chung, U., Nakamura, K., & Kawaguchi, H. (2009) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2009.02.003 · Cited by 64
Ihh and Runx2/Runx3 Signaling Interact to Coordinate Early Chondrogenesis: A Mouse Model
Kim, E., Cho, S. W., Shin, J.-O., Lee, M.-J., Kim, K.-S., & Jung, H.-S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055296 · Cited by 64
SOX9 is targeted for proteasomal degradation by the E3 ligase FBW7 in response to DNA damage
Hong, X., Liu, W., Song, R., Shah, J. J., Feng, X., Tsang, C. K., Morgan, K. M., Bunting, S. F., Inuzuka, H., Zheng, X., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw748 · Cited by 64
Fox proteins are modular competency factors for facial cartilage and tooth specification
Xu, P., Balczerski, B., Ciozda, A., Louie, K., Oralová, V., Huysseune, A., & Crump, J. G. (2018) · Development · doi:10.1242/dev.165498 · Cited by 64
To, K., Zhang, B., Romain, K. A., Mak, C. C. H., & Khan, W. S. (2019) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2019.00314 · Cited by 64
Cartilage formation in growth plate and arteries: from physiology to pathology
Magne, D., Julien, M., Vinatier, C. S., Merhi, F., Weiss, P., & Guicheux, J. (2005) · BioEssays · doi:10.1002/bies.20254 · Cited by 64
Sox6 regulation of cardiac myocyte development
Cohen‐Barak, O. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg807 · Cited by 64
Fujimaki, R., Toyama, Y., Hozumi, N., & Tezuka, K. (2006) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-005-0671-y · Cited by 64
Zhao, J., Patel, J., Kaur, S., Sim, S.-L., Wong, H. Y., Styke, C., Hogan, I., Kahler, S., Hamilton, H., Wadlow, R., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22717-9 · Cited by 63
Hojo, H., Ohba, S., Taniguchi, K., Shirai, M., Yano, F., Saito, T., Ikeda, T., Nakajima, K., Komiyama, Y., Nakagata, N., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.409342 · Cited by 63
The genetic program for cartilage development has deep homology within Bilateria
Tarazona, O. A., Slota, L. A., Lopez, D. H., Zhang, G., & Cohn, M. J. (2016) · Nature · doi:10.1038/nature17398 · Cited by 62
Marchetto, A., Ohmura, S., Orth, M. F., Knott, M. M. L., Colombo, M. V., Arrigoni, C., Bardinet, V., Saucier, D., Wehweck, F. S., Li, J., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16244-2 · Cited by 64
Dieterle, M. P., Husari, A., Rolauffs, B., Steinberg, T., & Tomakidi, P. (2021) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2021.16 · Cited by 62
Comparison of Tendon Development Versus Tendon Healing and Regeneration
He, P., Ruan, D., Huang, Z., Wang, C., Xu, Y., Cai, H., Liu, H., Fei, Y., Heng, B. C., Chen, W., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.821667 · Cited by 66
Pellet culture elicits superior chondrogenic redifferentiation than alginate‐based systems
Bernstein, P., Dong, M., Corbeil, D., Gelinsky, M., Günther, K., & Fickert, S. (2009) · Biotechnology Progress · doi:10.1002/btpr.186 · Cited by 62
MicroRNAs and post-transcriptional regulation of skeletal development
Gámez, B., Rodríguez-Carballo, E., & Ventura, F. (2014) · Journal of Molecular Endocrinology · doi:10.1530/jme-13-0294 · Cited by 63
miR-190 enhances endocrine therapy sensitivity by regulating SOX9 expression in breast cancer
Yu, Y., Yin, W., Yu, Z.-H., Zhou, Y., Chi, J.-R., Ge, J., & Cao, X. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-019-1039-9 · Cited by 63
Akiyama, H., Kamitani, T., Yang, X.-J., Kandyil, R. M., Bridgewater, L. C., Fellous, M., Mori–Akiyama, Y., & deCrombrugghe, B. (2004) · Matrix Biology · doi:10.1016/j.matbio.2004.10.002 · Cited by 62
Self-citationSchmidt, K., Hughes, C., Chudek, J. A., Goodyear, S. R., Aspden, R. M., Talbot, R., Gundersen, T. E., Blomhoff, R., Henderson, C., Wolf, C. R., et al. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01638-08 · Cited by 61
Fang, F., Xiao, Y., Zelzer, E., Leong, K. W., & Thomopoulos, S. (2022) · Cell stem cell · doi:10.1016/j.stem.2022.11.007 · Cited by 63
Makita, N., Suzuki, M., Asami, S., Takahata, R., Kohzaki, D., Kobayashi, S., Hakamazuka, T., & Hozumi, N. (2008) · Gene · doi:10.1016/j.gene.2007.12.025 · Cited by 60
Sato, S., Kimura, A., Ozdemir, J., Asou, Y., Miyazaki, M., Jinno, T., Ae, K., Liu, X., Osaki, M., Takeuchi, Y., et al. (2008) · Arthritis & Rheumatism · doi:10.1002/art.23805 · Cited by 61
Establishment of smooth muscle and cartilage juxtaposition in the developing mouse upper airways
Hines, E. A., Jones, M.-K. N., Verheyden, J. M., Harvey, J. F., & Sun, X. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313223110 · Cited by 61
AP-1 family members act with Sox9 to promote chondrocyte hypertrophy
He, X., Ohba, S., Hojo, H., & McMahon, A. P. (2016) · Development · doi:10.1242/dev.134502 · Cited by 61
MiR-133b targets Sox9 to control pathogenesis and metastasis of breast cancer
Wang, Q., Zhou, C.-X., Zhan, M., Tang, J., Wang, C.-L., Ma, C.-N., He, M., Chen, G., He, J., & Zhao, Q. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0715-6 · Cited by 60
Hoz, L., Romo, E., Zeichner‐David, M., Sanz, M., Núñez, J., Gaitán-Cepeda, L. A., Mercado, G., & Arzate, H. (2011) · Cell Biology International · doi:10.1042/cbi20110168 · Cited by 60
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
Tan, Z., Niu, B., Tsang, K. Y., Melhado, I. G., Ohba, S., He, X., Huang, Y., Wang, C., McMahon, A. P., Jauch, R., et al. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007346 · Cited by 66
Overview of Skeletal Development
Kobayashi, T., & Kronenberg, H. M. (2014) · Methods in molecular biology · doi:10.1007/978-1-62703-989-5_1 · Cited by 61
Vaes, B. L. T., Ducy, P. F., Sijbers, A. M., Hendriks, J. M. A., van Someren, E. P., de Jong, N. G., van den Heuvel, E. R., Olijve, W., van Zoelen, E. J. J., & Dechering, K. J. (2006) · Bone · doi:10.1016/j.bone.2006.04.024 · Cited by 60
Transcriptional networks controlling stromal cell differentiation
Rauch, A., & Mandrup, S. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00357-7 · Cited by 57
Chuah, Y. J., Zhang, Y., Wu, Y., Menon, N. V., Goh, G. H., Lee, A. C., Chan, V., Zhang, Y., & Kang, Y. (2015) · Acta Biomaterialia · doi:10.1016/j.actbio.2015.05.023 · Cited by 58
Horiuchi, K., Kimura, T., Miyamoto, T. K., Miyamoto, K., Akiyama, H., Takaishi, H., Morioka, H., Nakamura, T., Okada, Y., Blobel, C., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802491 · Cited by 60
Self-citationEffects of compressive force on the differentiation of pluripotent mesenchymal cells
Yanagisawa, M., Suzuki, N., Mitsui, N., Koyama, Y., Otsuka, K., & Shimizu, N. (2007) · Life Sciences · doi:10.1016/j.lfs.2007.06.004 · Cited by 59
Growth and differentiation of a long bone in limb development, repair and regeneration
Egawa, S., Miura, S., Yokoyama, H., Endo, T., & Tamura, K. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12136 · Cited by 59
Arid5a cooperates with Sox9 to stimulate chondrocyte-specific transcription
Amano, K., Hata, K., Muramatsu, S., Wakabayashi, M., Takigawa, Y., Ono, K., Nakanishi, M., Takashima, R., Kogo, M., Matsuda, A., et al. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-07-0566 · Cited by 59
Molecular mechanisms of the cartilage-specific microRNA-140 in osteoarthritis
Zhang, R., Ma, J., & Yao, J. (2013) · Inflammation Research · doi:10.1007/s00011-013-0654-8 · Cited by 59
SOX9: a useful marker for pancreatic ductal lineage of pancreatic neoplasms
Shroff, S. G., Rashid, A., Wang, H., Katz, M. H. G., Abbruzzese, J. L., Fleming, J. B., & Wang, H. (2013) · Human Pathology · doi:10.1016/j.humpath.2013.10.008 · Cited by 59
Stöckl, S., Bauer, R. J., Bosserhoff, A., Göttl, C., Grifka, J. K., & Grässel, S. (2013) · Journal of Cell Science · doi:10.1242/jcs.124305 · Cited by 58
Airik, R., Trowe, M., Foik, A. B., Farin, H. F., Petry, M., Schuster-Gossler, K., Schweizer, M., Scherer, G., Kist, R., & Kispert, A. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq426 · Cited by 59
Vijayakumar, S., Kraus, P., Sun, W., Hu, T. X., Lim, S. L., Prabhakar, S., & Lufkin, T. (2016) · Biology Open · doi:10.1242/bio.023218 · Cited by 56
Metadata
- Authors
- Akiyama, H., Chaboissier, M.-C., Martin, J. F., Schedl, A., & de Crombrugghe, B.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2002-11-01
- Volume
- 16
- Issue
- 21
- Pages
- 2813-2828
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC187468
- OpenAlex
- W2150134228
- Semantic Scholar
- e65963187a4e29b254fc91c0e5fb771b639a3d8d
- Cited by
- 1,721
- References
- 47
- Citations by year
- 2026: 52 · 2025: 47 · 2024: 54 · 2023: 73 · 2022: 83 · 2021: 92 · 2020: 98 · 2019: 81 · 2018: 79 · 2017: 82 · 2016: 79 · 2015: 82 · 2014: 89 · 2013: 89 · 2012: 81
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- March of Dimes Foundation
- Volkswagen Foundation
- National Institutes of Health (CA-16 672, AR42919)
- National Cancer Institute (CA-16672, P30CA016672)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (P01AR042919)
- National Institute of Dental and Craniofacial Research (R01DE013509, R29DE012324)
- Topics
- Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone Tumor Diagnosis and Treatments
- Keywords
- SOX9, chondrogenic differentiation, chondrogenesis, SOX5, SOX6, Runx2, chondrodysplasia, mesenchymal condensation, apoptosis, Indian hedgehog, Patched1, parathyroid hormone-related protein, chondrocyte hypertrophy, joint formation, limb development, osteogenic differentiation, Cre-loxP conditional knockout
- MeSH terms
- Animals, Cell Differentiation, Cell Division, DNA-Binding Proteins, High Mobility Group Proteins, Mutation, Nuclear Proteins, Transcription Factors, Signal Transduction, Gene Expression Regulation, Developmental, Chondrocytes, Mice, SOXD Transcription Factors, SOX9 Transcription Factor
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