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

Endogenous Bone Regeneration Is Dependent Upon a Dynamic Oxygen Event

Sammarco, M. C., Simkin, J., Fassler, D., Cammack, A. J., Wilson, A. C., Meter, K. V., & Muneoka, K. (2014) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2261 · Cited by 44

Osteostimulatory effect of biocomposite scaffold containing phytomolecule diosmin by Integrin/FAK/ERK signaling pathway in mouse mesenchymal stem cells

Chandran, S. V., Vairamani, M., & Selvamurugan, N. (2019) · Scientific Reports · doi:10.1038/s41598-019-48429-1 · Cited by 44

The Impairment of MAGMAS Function in Human Is Responsible for a Severe Skeletal Dysplasia

Mehawej, C., Delahodde, A., Legeai‐Mallet, L., Delague, V., Kaci, N., Desvignes, J., Kibar, Z., Capo‐Chichi, J., Chouery, É., Münnich, A., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004311 · Cited by 44

Coordinated transcriptional regulation of bone homeostasis by Ebf1 and Zfp521 in both mesenchymal and hematopoietic lineages

Kiviranta, R., Yamana, K., Saito, H., Ho, D. K., Laine, J., Tarkkonen, K. M., Nieminen-Pihala, V., Hesse, E., Correa, D., Määttä, J. A., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20121187 · Cited by 44

Bone Turnover Markers as a New Predicting Factor for Nonunion After Spinal Fusion Surgery

Inose, H., Yamada, T., Mulati, M., Hirai, T., Ushio, S., Yoshii, T., Kato, T., Kawabata, S., & Okawa, A. (2016) · Spine · doi:10.1097/brs.0000000000001995 · Cited by 44

Evolution and functional significance of derived sternal ossification patterns in ornithothoracine birds

O'Connor, J. K., Zheng, X., Sullivan, C., Chuong, C., Wang, X. ‐., Li, A., Wang, Y., Zhang, X. ‐., & Zhou, Z. ‐. (2015) · Journal of Evolutionary Biology · doi:10.1111/jeb.12675 · Cited by 43

Epiphyseal bone formation occurs via thyroid hormone regulation of chondrocyte to osteoblast transdifferentiation

Aghajanian, P., Xing, W., Cheng, S., & Mohan, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-11050-1 · Cited by 47

Novel insights into parathyroid hormone: report of The Parathyroid Day in Chronic Kidney Disease

Ureña, P., Vervloet, M. G., Mazzaferro, S., Oury, F., Brandenburg, V. M., Bover, J., Cavalier, E., Cohen-Solal, M. E., Covic, A. C., Drüeke, T. B., et al. (2018) · Clinical Kidney Journal · doi:10.1093/ckj/sfy061 · Cited by 42

Impaired mesenchymal stem cell differentiation and osteoclastogenesis in mice deficient for Igf2-P2 transcripts

Hardouin, S., Guo, R., Roméo, P., Nagy, A., & Aubin, J. E. (2010) · Development · doi:10.1242/dev.054916 · Cited by 42

Osterix acetylation at K307 and K312 enhances its transcriptional activity and is required for osteoblast differentiation

Lü, J., Qu, S., Yao, B., Xu, Y., Jin, Y., Shi, K., Shui, Y., Pan, S., Chen, L., & Ma, C. (2016) · Oncotarget · doi:10.18632/oncotarget.9650 · Cited by 41

New Genetic Diagnoses of Short Stature Provide Insights into Local Regulation of Childhood Growth

de Andrade, A. C., Jee, Y. H., & Nilsson, O. (2017) · Hormone Research in Paediatrics · doi:10.1159/000455850 · Cited by 41

An Optimized Method to Generate Human Active Osteoclasts From Peripheral Blood Monocytes

Abdallah, D., Jourdain, M., Braux, J., Guillaume, C., Gangloff, S. C., Jacquot, J. P., & Velard, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00632 · Cited by 41

Regulation of Breast Cancer-Induced Osteoclastogenesis by MacroH2A1.2 Involving EZH2-Mediated H3K27me3

Kim, J., Shin, Y., Lee, S., Kim, M., Punj, V., Lu, J. F., Shin, H., Kim, K., Ulmer, T. S., Koh, J., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.020 · Cited by 43

Lactobacillus‐ fermented milk products attenuate bone loss in an experimental rat model of ovariectomy‐induced post‐menopausal primary osteoporosis

Lee, C. S., Kim, J.-Y., Kim, B. K., Lee, I. O., Park, N. H., & Kim, S. H. (2020) · Journal of Applied Microbiology · doi:10.1111/jam.14852 · Cited by 41

Pathogenesis and treatment of spine disease in the mucopolysaccharidoses

Peck, S. H., Casal, M. L., Malhotra, N. R., Ficicioglu, C. H., & Smith, L. J. (2016) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2016.06.002 · Cited by 40

Prenatal exposure to environmental factors and congenital limb defects

Alexander, P. G., Clark, K. L., & Tuan, R. S. (2016) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21140 · Cited by 40

Mesenchymal Stem Cells and Tissue Repair

Coutu, D. L., François, M., & Galipeau, J. (2011) · Humana Press eBooks · doi:10.1007/978-1-61779-471-1_4 · Cited by 40

RECENT RESEARCH ON THE GROWTH PLATE: Advances in fibroblast growth factor signaling in growth plate development and disorders

Xie, Y., Zhou, S., Chen, H., Du, X., & Chen, L. (2014) · Journal of Molecular Endocrinology · doi:10.1530/jme-14-0012 · Cited by 40

Class I PI-3-Kinase Signaling Is Critical for Bone Formation Through Regulation of SMAD1 Activity in Osteoblasts

Gámez, B., Rodríguez-Carballo, E., Graupera, M., Rosa, J. L., & Ventura, F. (2016) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2819 · Cited by 39

Bone Size and Quality Regulation: Concerted Actions of mTOR in Mesenchymal Stromal Cells and Osteoclasts

Wu, H., Wu, Z., Li, P., Cong, Q., Chen, R., Xu, W., Biswas, S., Liu, H., Xia, X., Li, S., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.04.005 · Cited by 39

In-vivo imaging of the fracture healing in medaka revealed two types of osteoclasts before and after the callus formation by osteoblasts

Takeyama, K., Chatani, M., Takano, Y., & Kudō, A. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.08.007 · Cited by 39

Histone demethylase JMJD3 is required for osteoblast differentiation in mice

Zhang, F., Xu, L., Xu, L., Xu, Q., Karsenty, G., & Chen, C. D. (2015) · Scientific Reports · doi:10.1038/srep13418 · Cited by 38

Zinc finger protein 521, a new player in bone formation

Hesse, E., Kiviranta, R., Wu, M., Saito, H., Yamana, K., Correa, D., Atfi, A., & Baron, R. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05347.x · Cited by 38

Bone Health and Associated Metabolic Complications in Neuromuscular Diseases

Joyce, N. C., Hache, L. P., & Clemens, P. R. (2012) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2012.08.005 · Cited by 41

Minireview: Nuclear Receptor Regulation of Osteoclast and Bone Remodeling

Jin, Z., Li, X., & Wan, Y. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1316 · Cited by 38

Artificial cartilage bio-matrix formed of hyaluronic acid and Mg2+-polyphosphate

Wang, X., Ackermann, M., Tolba, E., Neufurth, M., Wurm, F. R., Feng, Q., Wang, S., Schröder, H. C., & Müller, W. (2016) · European Cells and Materials · doi:10.22203/ecm.v032a18 · Cited by 37

mTORC1 Activation in Osteoclasts Prevents Bone Loss in a Mouse Model of Osteoporosis

Hiraiwa, M., Ozaki, K., Yamada, T., Iezaki, T., Park, G., Fukasawa, K., Horie, T., Kamada, H., Tokumura, K., Motono, M., et al. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00684 · Cited by 37

Initiation of Early Osteoblast Differentiation Events through the Direct Transcriptional Regulation of Msx2 by FOXC1

Mirzayans, F., Lavy, R., Penner-Chea, J., & Berry, F. B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049095 · Cited by 36

IL-1β promotes osteoclastogenesis by increasing the expression of IGF2 and chemokines in non-osteoclastic cells

Otsuka, Y., Kondo, T., Aoki, H., Goto, Y., Kawaguchi, Y., Waguri‐Nagaya, Y., Miyazawa, K., Goto, S., & Aoyama, M. (2022) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2022.10.007 · Cited by 36

The short-chain fatty acid receptors Gpr41/43 regulate bone mass by promoting adipogenic differentiation of mesenchymal stem cells

Behler-Janbeck, F., Baranowsky, A., Yorgan, T. A., Jaeckstein, M. Y., Worthmann, A., Fuh, M. M., Gunasekaran, K., Tiegs, G., Amling, M., Schinke, T., et al. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1392418 · Cited by 37

Daily intake of β-cryptoxanthin prevents bone loss by preferential disturbance of osteoclastic activation in ovariectomized mice

Ozaki, K., Okamoto, M., Fukasawa, K., Iezaki, T., Onishi, Y., Yoneda, Y., Sugiura, M., & Hinoi, E. (2015) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2015.08.003 · Cited by 36

Core Binding Factor β Plays a Critical Role During Chondrocyte Differentiation

Park, N. R., Lim, K., Han, M. S., Che, X., Park, C. Y., Kim, J., Taniuchi, I., Bae, S., & Choi, J. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25068 · Cited by 36

miR-383 negatively regulates osteoblastic differentiation of bone marrow mesenchymal stem cells in rats by targeting Satb2

Tang, J., Zhang, Z., Jin, X., & Shi, H. (2018) · Bone · doi:10.1016/j.bone.2018.06.010 · Cited by 36

Chondroitin sulfate-E mediates estrogen-induced osteoanabolism

Koike, T., Mikami, T., Shida, M., Habuchi, O., & Kitagawa, H. (2015) · Scientific Reports · doi:10.1038/srep08994 · Cited by 36

Gene Expression Responses to Mechanical Stimulation of Mesenchymal Stem Cells Seeded on Calcium Phosphate Cement

Gharibi, B., Cama, G., Capurro, M., Thompson, I. D., Deb, S., Silvio, L. D., & Hughes, F. J. (2013) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0623 · Cited by 37

To BMP or not to BMP during vertebrate limb bud development

Pignatti, E., Zeller, R., & Zúñiga, A. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.04.004 · Cited by 35

Environmental factors unveil dormant developmental capacities in multipotent progenitors of the trunk neural crest

Coelho‐Aguiar, J. M., Douarin, N. M. L., & Dupin, É. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.09.030 · Cited by 35

Growth plate stress distribution implications during bone development: A simple framework computational approach

Guevara, J., Moncayo, M. A., Vaca‐González, J. J., Gutiérrez, M. L., Barrera, L. A., & Garzón–Alvarado, D. A. (2014) · Computer Methods and Programs in Biomedicine · doi:10.1016/j.cmpb.2014.10.007 · Cited by 35

The L-type amino acid transporter LAT1 inhibits osteoclastogenesis and maintains bone homeostasis through the mTORC1 pathway

Ozaki, K., Yamada, T., Horie, T., Ishizaki, A., Hiraiwa, M., Iezaki, T., Park, G., Fukasawa, K., Kamada, H., Tokumura, K., et al. (2019) · Science Signaling · doi:10.1126/scisignal.aaw3921 · Cited by 35

Oxygen-Generating Biomaterials for Translational Bone Regenerative Engineering

Hosseini, F. S., Abedini, A. A., Chen, F., Whitfield, T., Ude, C. C., & Laurencin, C. T. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c20715 · Cited by 35

Findings of metabolic bone disease in infants with unexplained fractures in contested child abuse investigations: a case series of 75 infants

Miller, M. E., Stolfi, A., & Ayoub, D. (2019) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem-2019-0093 · Cited by 34

Evolutionarily Conserved, Growth Plate Zone-Specific Regulation of the Matrilin-1 Promoter: L-Sox5/Sox6 and Nfi Factors Bound near TATA Finely Tune Activation by Sox9

Nagy, A., Kénesi, E., Rentsendorj, O., Molnár, A., Szénási, T., Sinkó, I., Zvara, Á., Oommen, S. T., Barta, E., Puskás, L. G., et al. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00019-10 · Cited by 34

Osteocrin, a peptide secreted from the heart and other tissues, contributes to cranial osteogenesis and chondrogenesis in zebrafish

Chiba, A., Watanabe‐Takano, H., Terai, K., Fukui, H., Miyazaki, T., Uemura, M., Hashimoto, H., Hibi, M., Fukuhara, S., & Mochizuki, N. (2016) · Development · doi:10.1242/dev.143354 · Cited by 34

Pharmacologic Calcitriol Inhibits Osteoclast Lineage Commitment via the BMP-Smad1 and IκB-NF-κB Pathways

Li, A., Cong, Q., Xia, X., Leong, W. F., Yeh, J., Miao, D., Mishina, Y. M., Liu, H., & Li, B. (2017) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3146 · Cited by 38

Uncarboxylated osteocalcin inhibits high glucose-induced ROS production and stimulates osteoblastic differentiation by preventing the activation of PI3K/Akt in MC3T3-E1 cells

Liu, J., & Yang, J. (2015) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2015.2412 · Cited by 33

Potential Involvement of Twist2 and Erk in the Regulation of Osteoblastogenesis by HB-EGF-EGFR Signaling

Nakamura, T., Toita, H., Yoshimoto, A., Nishimura, D., Takagi, T., Ogawa, T., Takeya, T., & Ishida‐Kitagawa, N. (2010) · Cell Structure and Function · doi:10.1247/csf.10001 · Cited by 33

Serotonin Inhibits Osteoblast Differentiation and Bone Regeneration in Rats

Nam, S., Lee, J. C., Kim, H. J., Park, J., Lee, J., Suh, J., Um, H., Kim, J., Lee, Y., & Kim, Y. (2015) · Journal of Periodontology · doi:10.1902/jop.2015.150302 · Cited by 33

ATF3 controls proliferation of osteoclast precursor and bone remodeling

Fukasawa, K., Park, G., Iezaki, T., Horie, T., Kanayama, T., Ozaki, K., Onishi, Y., Takahata, Y., Yoneda, Y., Takarada, T., et al. (2016) · Scientific Reports · doi:10.1038/srep30918 · Cited by 33

Octacalcium phosphate collagen composite stimulates the expression and activity of osteogenic factors to promote bone regeneration

Kouketsu, A., Matsui, K., Kawai, T., Ezoe, Y., Yanagisawa, T., Yasuda, A., Takahashi, T., & Kamakura, S. (2019) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2969 · Cited by 33

Boning up on glypicans—opportunities for new insights into bone biology

Dwivedi, P. P., Lam, N. N., & Powell, B. C. (2013) · Cell Biochemistry and Function · doi:10.1002/cbf.2939 · Cited by 34

The role of CDK8 in mesenchymal stem cells in controlling osteoclastogenesis and bone homeostasis

Yamada, T., Fukasawa, K., Horie, T., Kadota, T., Lyu, J., Tokumura, K., Ochiai, S., Iwahashi, S., Suzuki, A., Park, G., et al. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.06.001 · Cited by 32

ER Stress During the Pubertal Growth Spurt Results in Impaired Long-Bone Growth in Chondrocyte-Specific ERp57 Knockout Mice

Linz, A., Knieper, Y., Gronau, T., Hansen, U. J., Aszódi, A., Garbi, N., Hämmerling, G. J., Pap, T., Brückner, P., & Dreier, R. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2484 · Cited by 32

The p38α MAPK Function in Osteoprecursors Is Required for Bone Formation and Bone Homeostasis in Adult Mice

Rodríguez-Carballo, E., Gámez, B., Sedó-Cabezón, L., Sánchez‐Feutrie, M., Antonio Zorzano, A., Manzanares‐Céspedes, M. C., Rosa, J. L., & Ventura, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102032 · Cited by 33

Emerging Targets in Osteoporosis Disease Modification

Allen, J. G., Fotsch, C. H., & Babij, P. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm9018756 · Cited by 32

What do we know about bone morphogenetic proteins and osteochondroprogenitors in inflammatory conditions?

Lukač, N., Katavić, V., Novak, S., Šućur, A., Filipović, M., Kalajzić, I., Grčević, D., & Kovačić, N. (2020) · Bone · doi:10.1016/j.bone.2020.115403 · Cited by 32

Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone

Nookaew, I., Xiong, J., Onal, M., Bustamante-Gomez, C., Wanchai, V., Fu, Q., Kim, H., Almeida, M., & O’Brien, C. A. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107158 · Cited by 34

BMP signaling and skeletal development in fibrodysplasia ossificans progressiva ( FOP )

Towler, O. W., & Shore, E. M. (2021) · Developmental Dynamics · doi:10.1002/dvdy.387 · Cited by 31

1,25(OH)2D3 Alters Growth Plate Maturation and Bone Architecture in Young Rats with Normal Renal Function

Idelevich, A., Kerschnitzki, M., Shahar, R., & Ornan, E. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020772 · Cited by 31

Stromal Cell-Derived Factor 1 Regulates the Actin Organization of Chondrocytes and Chondrocyte Hypertrophy

Murata, K., Kitaori, T., Oishi, S., Watanabe, N., Yoshitomi, H., Tanida, S., Ishikawa, M., Kasahara, T., Shibuya, H., Fujii, N., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037163 · Cited by 31

Foxc1 Expression in Early Osteogenic Differentiation Is Regulated by BMP4‐SMAD Activity

Hopkins, A., Mirzayans, F., & Berry, F. B. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25464 · Cited by 31

Hypoxia-inducible factor-2α mediates senescence-associated intrinsic mechanisms of age-related bone loss

Lee, S. Y., Park, K. H., Lee, G., Kim, S., Song, W., Kwon, S., Koh, J., Huh, Y. H., & Ryu, J. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00594-y · Cited by 32

Protein tyrosine phosphatases in skeletal development and diseases

Yang, H., Wang, L., Shigley, C., & Yang, W. (2022) · Bone Research · doi:10.1038/s41413-021-00181-x · Cited by 32

LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice

Geister, K. A., Brinkmeier, M. L., Cheung, L., Wendt, J., Oatley, M. J., Burgess, D. L., Kozloff, K. M., Cavalcoli, J. D., Oatley, J. M., & Camper, S. A. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005569 · Cited by 31

Myristoleic acid inhibits osteoclast formation and bone resorption by suppressing the RANKL activation of Src and Pyk2

Kwon, J., Jin, W. J., Kim, B.-J., Kim, H., & Lee, Z. H. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.10.053 · Cited by 31

Re-engineering Development to Instruct Tissue Regeneration

Tonnarelli, B., Centola, M., Barbero, A., Zeller, R., & Martín, I. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-391498-9.00005-x · Cited by 30

The MAPK Erk5 is necessary for proper skeletogenesis involving a Smurf-Smad-Sox9 molecular axis

Iezaki, T., Fukasawa, K., Horie, T., Park, G., Robinson, S. T., Nakaya, M., Fujita, H., Onishi, Y., Ozaki, K., Kanayama, T., et al. (2018) · Development · doi:10.1242/dev.164004 · Cited by 30

Cell proliferation controls body size growth, tentacle morphogenesis, and regeneration in hydrozoan jellyfish Cladonema pacificum

Fujita, S., Kuranaga, E., & Nakajima, Y.-I. (2019) · PeerJ · doi:10.7717/peerj.7579 · Cited by 29

Limonoid Triterpene, Obacunone Increases Runt-Related Transcription Factor 2 to Promote Osteoblast Differentiation and Function

Park, K.-R., Kim, S., Cho, M., & Yun, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052483 · Cited by 29

Effects of polyphenols and their metabolites on age-related diseases

Chouari, Z., Lounis, W., Ghzaiel, I., Kessas, K., Zarrouk, A., Ksila, M., Ghrairi, T., Latruffe, N., Masmoudi‐Kouki, O., Midaoui, A. E., et al. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115674 · Cited by 30

The Transcriptional Modulator Interferon-Related Developmental Regulator 1 in Osteoblasts Suppresses Bone Formation and Promotes Bone Resorption

Iezaki, T., Onishi, Y., Ozaki, K., Fukasawa, K., Takahata, Y., Nakamura, Y., Fujikawa, K., Takarada, T., Yoneda, Y., Yamashita, Y., et al. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2720 · Cited by 29

The transcription factor RUNX2 regulates receptor tyrosine kinase expression in melanoma

Boregowda, R. K., Medina, D. J., Markert, E. K., Bryan, M. A., Chen, W., Chen, S., Rabkin, A., Vido, M. J., Gunderson, S., Chekmareva, M. A., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8822 · Cited by 31

Ontogenetic and Genetic Influences on Bone’s Responsiveness to Mechanical Signals

Wallace, I. J., Demes, B., & Judex, S. (2017) · Cambridge University Press eBooks · doi:10.1017/9781316388907.011 · Cited by 28

MACF1 promotes osteoblast differentiation by sequestering repressors in cytoplasm

Hu, L., Yin, C., Chen, D., Wu, Z., Liang, S., Zhang, Y., Huang, Z., Liu, S., Xu, X., Chen, Z., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-021-00744-9 · Cited by 28

DLX5 promotes Col10a1 expression and chondrocyte hypertrophy and is involved in osteoarthritis progression

Chen, J., Chen, F., Wu, X., Bian, H., Chen, C., Zhang, X., Hei, R., XiaotongYang, Yuan, H., Wang, Q., et al. (2023) · Genes & Diseases · doi:10.1016/j.gendis.2022.12.016 · Cited by 28

Instruction of mesenchymal cell fate by the transcription factor C/EBPβ

Smink, J. J., & Leutz, A. (2012) · Gene · doi:10.1016/j.gene.2012.01.043 · Cited by 29

Exposure to a PBDE/OH-BDE mixture alters juvenile zebrafish (Danio rerio) development

Macaulay, L. J., Chernick, M., Chen, A., Hinton, D. E., Bailey, J. M., Kullman, S. W., Levin, E. D., & Stapleton, H. M. (2016) · Environmental Toxicology and Chemistry · doi:10.1002/etc.3535 · Cited by 29

Transcriptional Modulator Ifrd1 Regulates Osteoclast Differentiation through Enhancing the NF-κB/NFATc1 Pathway

Iezaki, T., Fukasawa, K., Park, G., Horie, T., Kanayama, T., Ozaki, K., Onishi, Y., Takahata, Y., Nakamura, Y., Takarada, T., et al. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.01075-15 · Cited by 29

Fetal Mineral Homeostasis

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Mst1/2 Kinases Modulate Glucose Uptake for Osteoblast Differentiation and Bone Formation

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