Notch signaling maintains bone marrow mesenchymal progenitors by suppressing osteoblast differentiation

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

Generalized lacZ expression with the ROSA26 Cre reporter strain

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Bone Marrow Stromal Stem Cells: Nature, Biology, and Potential Applications

Bianco, P., Riminucci, M., Gronthos, S., & Robey, P. G. (2001) · Stem Cells · doi:10.1634/stemcells.19-3-180 · Cited by 1,944

Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain

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Reaching a Genetic and Molecular Understanding of Skeletal Development

Karsenty, G., & Wagner, E. F. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00157-0 · Cited by 1,611

Mutations in NOTCH1 cause aortic valve disease

Garg, V., Muth, A. N., Ransom, J. F., Schluterman, M. K., Barnes, R., King, I. N., Grossfeld, P. D., & Srivastava, D. (2005) · Nature · doi:10.1038/nature03940 · Cited by 1,509

HES and HERP families: Multiple effectors of the notch signaling pathway

Iso, T., Kedes, L., & Hamamori, Y. (2003) · Journal of Cellular Physiology · doi:10.1002/jcp.10208 · Cited by 1,259

Stromal Stem Cells: Marrow‐Derived Osteogenic Precursors

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Notch signaling is essential for vascular morphogenesis in micePreprint

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Expression of Cre recombinase in the developing mouse limb bud driven by a Prxl enhancer

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

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

The impact of neuronal Notch-1/JNK pathway on intracerebral hemorrhage-induced neuronal injury of rat model

Chen, M., Sun, J. F., Lü, C., Chen, X., Ba, H., Lin, Q., Cai, J., & Dai, J. (2016) · Oncotarget · doi:10.18632/oncotarget.12094 · Cited by 15

The implication of the notch signaling pathway in biphasic calcium phosphate ceramic‐induced ectopic bone formation: A preliminary experiment

Guo, X., Jiang, H., Zong, X., Du, L., Zhao, J., Zhang, D., Song, G., & Jin, X. (2020) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36878 · Cited by 15

Bone morphogenetic protein 9 (BMP9) directly induces Notch effector molecule Hes1 through the SMAD signaling pathway in osteoblasts

Seong, C., Chiba, N., Kusuyama, J., Amir, M. S., Eiraku, N., Yamashita, S., Ohnishi, T., Nakamura, N., & Matsuguchi, T. (2020) · FEBS Letters · doi:10.1002/1873-3468.14016 · Cited by 15

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

Goel, D., & Vohora, D. (2020) · Bone · doi:10.1016/j.bone.2020.115807 · Cited by 15

Transgenic mouse strains for conditional gene deletion during skeletal development

VanKoevering, K. K., & Williams, B. O. (2008) · IBMS BoneKEy · doi:10.1138/20080312 · Cited by 15

Effects of Sex and Notch Signaling on the Osteocyte Cell Pool

CANALIS, E. M., Schilling, L., & Zanotti, S. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25433 · Cited by 15

Tumor-supportive and Osteoclastogenic Changes Induced by Breast Cancer-derived Factors Are Reversed by Inhibition of γ-Secretase

Fong, J. E., Nihouannen, D. L., & Komarova, S. V. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.114496 · Cited by 15

Genomic variants within chromosome 14q32.32 regulate bone mass through MARK3 signaling in osteoblasts

Zhang, Q., Mesner, L. D., Calabrese, G. M., Dirckx, N., Zhu, L., Verardo, A., Yang, Q., Tower, R. J., Monier‐Faugere, M., Farber, C. R., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci142580 · Cited by 14

Systematic dissection of coordinated stromal remodeling identifies Sox10+ glial cells as a therapeutic target in myelofibrosis

Sarkaria, S. M., Zhou, J., Bao, S., Zhao, W., Fang, Y., Que, J., Bhagat, G., Zhang, C., & Ding, L. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.05.002 · Cited by 14

Human skin neural crest progenitor cells are susceptible to BRAFV600E-induced transformation

Kumar, S., Dai, J., Li, S., Yang, R., Yu, H., Nathanson, K. L., Liu, S., Zhou, H., Guo, J., & Xu, X. (2013) · Oncogene · doi:10.1038/onc.2012.642 · Cited by 14

SMAD4 contributes to chondrocyte and osteocyte development

Pakravan, K., Razmara, E., Hussen, B. M., Sattarikia, F., Sadeghizadeh, M., & Babashah, S. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17080 · Cited by 14

Alteration of Notch signaling and functionality of adipose tissue derived mesenchymal stem cells in heart failure

Fortini, C., Cesselli, D., Beltrami, A. P., Bergamin, N., Caragnano, A., Moretti, L., Cecaro, F., Aquila, G., Rizzo, P., Riberti, C., et al. (2014) · International Journal of Cardiology · doi:10.1016/j.ijcard.2014.03.173 · Cited by 14

Notch signaling: a novel regulating differentiation mechanism of human umbilical cord blood-derived mesenchymal stem cells into insulin-producing cells in vitro

Hu, Y., Wu, D., Gao, F., Li, G., & Zhang, X. (2010) · Chinese Medical Journal · doi:10.3760/cma.j.issn.0366-6999.2010.05.019 · Cited by 14

Magnesium: An old player revisited in the context of CKD-MBD

de Mier, M. V. P.-R., Rodelo‐Haad, C., Díaz‐Tocados, J. M., Muñoz-Castañeda, J. R., & Rodríguez, M. (2019) · Clinica Chimica Acta · doi:10.1016/j.cca.2019.11.037 · Cited by 14

The soluble form of BMPRIB is a novel therapeutic candidate for treating bone related disorders

Yamawaki, K., Kondo, Y., Okada, T., Oshima, T., Kakitani, M., & Tomizuka, K. (2016) · Scientific Reports · doi:10.1038/srep18849 · Cited by 14

Signal Transduction Cascades Controlling Osteoblast Differentiation

de Gorter, D. J. J., & ten Dijke, P. (2013) · Wiley eBooks · doi:10.1002/9781118453926.ch2 · Cited by 14

Disruption of cell-cell contact-mediated notch signaling via hydrogel encapsulation reduces mesenchymal stem cell chondrogenic potential

Chen, A. X., Hoffman, M. D., Chen, C. S., Shubin, A. D., Reynolds, D. S., & Benoit, D. S. W. (2014) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.35383 · Cited by 13

Contextual Regulation of Skeletal Physiology by Notch Signaling

Youngstrom, D. W., & Hankenson, K. D. (2019) · Current Osteoporosis Reports · doi:10.1007/s11914-019-00516-y · Cited by 13

The Skeleton of Lateral Meningocele Syndrome

CANALIS, E. M. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2020.620334 · Cited by 13

The multifunctional role of Notch signaling in multiple myeloma

Sabol, H. M., & Delgado‐Calle, J. (2021) · Journal of Cancer Metastasis and Treatment · doi:10.20517/2394-4722.2021.35 · Cited by 13

3D printing of osteocytic Dll4 integrated with PCL for cell fate determination towards osteoblasts in vitro

Wang, P., Wang, X., Wang, B., Li, X., Xie, Z., Chen, J., Honjo, T., & Tu, X. (2022) · Bio-Design and Manufacturing · doi:10.1007/s42242-022-00196-1 · Cited by 13

NOTCH2 sensitizes the chondrocyte to the inflammatory response of tumor necrosis factor α

CANALIS, E. M., Yu, J., Singh, V., Mocarska, M., & Schilling, L. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105372 · Cited by 13

Carfilzomib promotes the osteogenic differentiation potential of mesenchymal stem cells derived from myeloma patients by inhibiting notch1 activity in vitro

Li, Y., Li, J., Zhuang, W., Wang, Q., Ge, X., Zhang, X., Chen, P., Fu, J., & Li, B.-Z. (2014) · Leukemia Research · doi:10.1016/j.leukres.2014.05.022 · Cited by 13

Osteocytes Produces RANKL Via Wnt-TGFβ Signaling Axis for Osteoclastogenesis

Liu, Y., Zhao, L., Li, M., Gong, W., Wang, X., Cheng, Y., Zhang, Y., Wang, P., Luo, Y., Zhang, Y., et al. (2025) · International Journal of Biological Sciences · doi:10.7150/ijbs.117481 · Cited by 12

DLX5 regulates the osteogenic differentiation of spinal ligaments cells derived from ossification of the posterior longitudinal ligament patients via NOTCH signaling

Tang, T., Zhu, Z., He, Z., Wang, F., Chen, H., Liu, S., Zhan, M., Wang, J., Tian, W., Chen, D., et al. (2023) · JOR Spine · doi:10.1002/jsp2.1247 · Cited by 12

Lack of ADAM15 in mice is associated with increased osteoblast function and bone mass

Marzia, M., Guaiquil, V. H., Horne, W. C., Blobel, C., Baron, R., & Chiusaroli, R. (2011) · Biological Chemistry · doi:10.1515/bc.2011.080 · Cited by 13

Overexpression of Notch Signaling Induces Hyperosteogeny in Zebrafish

Liang, S., Chen, J., Tsai, J.-J., Lai, Y., & Hsiao, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153613 · Cited by 12

Enhanced Osteogenic Differentiation of Pluripotent Stem Cells via γ-Secretase Inhibition

Helmi, S. A., Rohani, L., Zaher, A. R., Hawary, Y. M. E., & Rancourt, D. E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105215 · Cited by 12

miRNA‐34c Suppresses Osteosarcoma Progression In Vivo by Targeting Notch and E2F

Bae, Y., Zeng, H., Chen, Y., Ketkar, S., Munivez, E. M., Yu, Z., Gannon, F. H., & Lee, B. (2022) · JBMR Plus · doi:10.1002/jbm4.10623 · Cited by 12

Glycolipid toxicity induces osteogenic dysfunction via the TLR4/S100B pathway

Liang, B., Shen, X., Lan, C., Lin, Y., Li, C., Zhong, S., & Yan, S. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.107792 · Cited by 12

Regulatory Pathways Governing Odonto/Osteogenic Differentiation in Dental Pulp Stem Cells

Kornsuthisopon, C., Nowwarote, N., Srisuwan, T., Dissanayaka, W. L., & Osathanon, T. (2025) · International Endodontic Journal · doi:10.1111/iej.70069 · Cited by 11

Role of Notch Signaling in the Physiological Patterning of Posterofrontal and Sagittal Cranial Sutures

Liu, X., Zhang, C., Jing, J., Peng, W., Zhu, S., & Zou, S. (2017) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000003721 · Cited by 11

Activated B Lymphocyte Inhibited the Osteoblastogenesis of Bone Mesenchymal Stem Cells by Notch Signaling

Pan, M., Hong, W., Yao, Y., Gao, X., Zhou, Y., Fu, G., Li, Y., Guo, Q., Rao, X., Tang, P., et al. (2019) · Stem Cells International · doi:10.1155/2019/8150123 · Cited by 11

Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor

Kuang, Y., Pyo, A., Eafergan, N., Cain, B., Gutzwiller, L. M., Axelrod, O., Gagliani, E. K., Weirauch, M. T., Kopan, R., Kovall, R. A., et al. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009039 · Cited by 11

Enhanced osteogenic differentiation of rat bone marrow mesenchymal stem cells on titanium substrates by inhibiting Notch3

Wang, H., Jiang, Z., Zhang, J., Xie, Z., Wang, Y., & Yang, G. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.03.012 · Cited by 11

Activation of Notch3 in osteoblasts/osteocytes causes compartment-specific changes in bone remodeling

CANALIS, E. M., Zanotti, S., Schilling, L., Eller, T., & Yu, J. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100583 · Cited by 11

Notch2 Blockade Mitigates Methotrexate Chemotherapy-Induced Bone Loss and Marrow Adiposity

Peymanfar, Y., Su, Y., & Xian, C. J. (2022) · Cells · doi:10.3390/cells11091521 · 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

Unraveling the molecular landscape of osteoarthritis: A comprehensive review focused on the role of non-coding RNAs

Shakeri, M., Aminian, A., Mokhtari, K., Bahaeddini, M. R., Tabrizian, P., Farahani, N., Nabavi, N., & Hashemi, M. (2024) · Pathology - Research and Practice · doi:10.1016/j.prp.2024.155446 · Cited by 10

Pathophysiology of bone remodelling cycle: Role of immune system and lipids

Parolini, C. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.116844 · Cited by 10

Vascular Calcification: Mechanisms, Models, and Therapies

Zhu, W., Yang, S., Chen, Z., Yang, X., Liang, Z., & Chen, Y. (2026) · iNew Medicine · doi:10.1002/inm3.70035 · Cited by 10

The role and clinical implications of the endosteal niche and osteoblasts in regulating leukemia

Azizidoost, S., Vijay, V., Cogle, C. R., Khodadi, E., & Saki, N. (2017) · Clinical & Translational Oncology · doi:10.1007/s12094-017-1642-1 · Cited by 10

Icariin: A Potential Alternative Against Osteoporosis

Long, L., Wang, X., Yang, L., Guo, S., Wang, C., Dai, W., Lin, B., Xie, M., Xu, H., & Li, S. (2022) · Natural Product Communications · doi:10.1177/1934578x221134881 · Cited by 10

Glucose metabolism in skeletal cells

Long, F. (2022) · Bone Reports · doi:10.1016/j.bonr.2022.101640 · Cited by 10

Notch-RBPJ Pathway for the Differentiation of Bone Marrow Mesenchymal Stem Cells in Femoral Head Necrosis

Liu, K., Ge, H., Liu, C., Jiang, Y., Yu, Y., & Zhou, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076295 · Cited by 10

Deletion of RBPJK in Mesenchymal Stem Cells Enhances Osteogenic Activity by Up-Regulation of BMP Signaling

Shang, X., Luo, Z., Wang, X., Jaeblon, T., Marymont, J. V., & Dong, Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135971 · Cited by 10

Constitutive Activation of Gli2 Impairs Bone Formation in Postnatal Growing Mice

Joeng, K. S., & Long, F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055134 · Cited by 10

Hairy and Enhancer of Split‐Related With YRPW Motif‐Like (HeyL) Is Dispensable for Bone Remodeling in Mice

CANALIS, E. M., & Zanotti, S. (2016) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25859 · Cited by 10

Mathematical modelling of interacting mechanisms for hypoxia mediated cell cycle commitment for mesenchymal stromal cells

Zhang, B., Ye, H., & Yang, A. (2018) · BMC Systems Biology · doi:10.1186/s12918-018-0560-3 · Cited by 10

Osteogenesis of Adipose-Derived Stem Cells

Cai, X., Su, X., Guo, L., Wang, J., & Li, Y. (2012) · InTech eBooks · doi:10.5772/34025 · Cited by 10

In vitro culture and differentiation of osteoblasts from human umbilical cord blood

Toai, T. C., Thao, H. D., Thao, N. P., Gargiulo, C., Ngoc, P. K., Vân, P. H., & Strong, D. M. (2009) · Cell and Tissue Banking · doi:10.1007/s10561-009-9141-4 · Cited by 10

Notch in the Niche

Gering, M., & Patient, R. K. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.03.016 · Cited by 10

The Notch signaling pathway in regulating bone and cartilage homeostasis: novel insights into the pathogenesis and therapeutics of osteoarthritis

Wang, H., Li, M., Wang, X., Han, J., & Zhang, X. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02584-3 · Cited by 9

Notch signalling in alveolar bone development and regeneration: A critical regulator for osteoblasts to osteocytes transitioning

Cai, D., Shao, J., & Xiao, Y. (2026) · Dental Research · doi:10.1016/j.dtrs.2026.100025 · Cited by 9

Transcriptional responses of skeletal stem/progenitor cells to hindlimb unloading and recovery correlate with localized but not systemic multi-systems impacts

Booker, C. N., Haga, C. L., Boregowda, S. V., Strivelli, J., & Phinney, D. G. (2021) · npj Microgravity · doi:10.1038/s41526-021-00178-0 · Cited by 9

PIEZO1 activity promotes stemness in mesenchymal stem cells under shear stress and enhances protection of leukemia cells

Sharma, A. K., Bhattacharyya, J., Sukumar, P., & Jaganathan, B. G. (2025) · Scientific Reports · doi:10.1038/s41598-025-09549-z · Cited by 8

Interaction between Notch signaling pathway and bioactive compounds and its intervention on cancer

Nie, R., Wang, H., Wang, S., Luo, H.-M., Chen, C., Jing, Z.-H., & Li, P. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1647661 · Cited by 8

Oral manifestations of Alagille syndrome

Bonnet, A., Greset, V., & Davit‐Béal, T. (2020) · BMJ Case Reports · doi:10.1136/bcr-2020-234689 · Cited by 8

FoxO3 Regulates Mouse Bone Mesenchymal Stem Cell Fate and Bone–Fat Balance During Skeletal Aging

Yu, W., Tong, M.-J., Wu, G., Ma, T.-L., Cai, C., Wang, L., Zhang, Y., Gu, J.-L., & Yan, Z.-Q. (2024) · Stem Cells and Development · doi:10.1089/scd.2024.0055 · Cited by 8

Molecular and cellular regulation of intramembranous and endochondral bone formation during embryogenesis

Hartmann, C., & Yang, Y. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00001-4 · Cited by 8

Aus alt mach neu

Beckmann, R., Tohidnezhad, M., Lichte, P., Wruck, C. J., Jahr, H., Pape, H., & Pufe, T. (2014) · Der Orthopäde · doi:10.1007/s00132-013-2160-7 · Cited by 9

Patient-derived xenografts and in vitro model show rationale for imatinib mesylate repurposing in HEY1-NCoA2-driven mesenchymal chondrosarcoma

Tepeš, P. Š., Segovia, D., Jevtic, S., Ramirez, D. C., Lyons, S. K., & Sordella, R. (2021) · Laboratory Investigation · doi:10.1038/s41374-021-00704-4 · Cited by 8

Enrichment and Correlation Analysis of Serum miRNAs in Comorbidity Between Arnold-Chiari and Tourette Syndrome Contribute to Clarify Their Molecular Bases

Mirabella, F., Gulisano, M., Capelli, M., Lauretta, G., Cirnigliaro, M., Palmucci, S., Stella, M., Barbagallo, D., Pietro, C. D., Purrello, M., et al. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.608355 · Cited by 7

Distinct and redundant roles for zebrafish her genes during mineralization and craniofacial patterning

Stenzel, A., Mumme‐Monheit, A., Sucharov, J., Walker, M. B., Mitchell, J. M., Appel, B., & Nichols, J. T. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1033843 · Cited by 7

Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy

Kaimari, S., Kamalakar, A., & Goudy, S. L. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1217211 · Cited by 7

Liraglutide Ameliorates Renal Endothelial Dysfunction in Diabetic Rats Through the Inhibition of the Dll4/Notch2 Pathway

Li, Y., Chen, Y., Zhang, H., Chen, W., & Pan, Y. (2024) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s492252 · Cited by 8

Notch Coordinates Periodontal Ligament Maturation through Regulating Lamin A

Denes, B. J., Bolton, C., Illsley, C. S., Kok, W. L., Walker, J. V., Poetsch, A., Tredwin, C. J., Kiliaridis, S., & Hu, B. (2019) · Journal of Dental Research · doi:10.1177/0022034519871448 · Cited by 7

4-Amino-2-trifluoromethyl-phenyl retinate induced differentiation of human myelodysplastic syndromes SKM-1 cell lines by up-regulating DDX23

Wang, C., Wang, K., Li, S., Song, S., Du, Y. Z., Niu, R., Qian, X., Peng, X., & Chen, F. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109736 · Cited by 7

Low-dose radiation-induced SUMOylation of NICD1 negatively regulates osteogenic differentiation in BMSCs

Zhou, L., Huang, C., HuangFu, C., Shen, P., Hu, Y., Wang, N., Li, G., Deng, H., Xia, T., Zhou, Y., et al. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116655 · Cited by 7

Developmental Pathways in CAVD

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

One-Bone Forearm Procedure for Hajdu–Cheney Syndrome: A Case Report

Bachoura, A., Jacoby, S. M., & Osterman, A. L. (2013) · Hand · doi:10.1007/s11552-013-9542-5 · Cited by 7

Cellular and Molecular Basis of Osteoblastic and Vascular Niches in the Processes of Hematopoiesis and Bone Remodeling (A Short Review of Modern Views)

Yurova, K. A., Хазиахматова, О. Г., Мелащенко, Е. С., Malashchenko, V. V., Shunkin, E. O., Shupletsova, V. V., Ivanov, P. A., Хлусов, И. А., & Litvinova, L. S. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190329153626 · Cited by 7

Notch signaling is involved in Fgf23 upregulation in osteocytes

Tamamura, Y., Sakamoto, K., Katsube, K., & Yamaguchi, A. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.08.038 · Cited by 7

Skeletal stem cells

Robey, P. G., & Riminucci, M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00002-6 · Cited by 7

Methotrexate treatment suppresses osteoblastic differentiation by inducing Notch2 signaling and blockade of Notch2 rescues osteogenesis by preserving Wnt/β‐catenin signaling

Peymanfar, Y., Su, Y., Hassanshahi, M., & Xian, C. J. (2021) · Journal of Orthopaedic Research® · doi:10.1002/jor.25253 · Cited by 7

Osteogenic differentiation of mouse mesenchymal progenitor cell, Kusa-A1 is promoted by mammalian transcriptional repressor Rbpj

Wang, S., Kawashima, N., Sakamoto, K., Katsube, K., Umezawa, A., & Suda, H. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.07.133 · Cited by 7

Biology of Bone and Cartilage

Boyce, B. F., Zuscik, M. J., & Xing, L. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-387829-8.00001-9 · Cited by 8

Nemo‐Like Kinase Regulates Postnatal Skeletal Homeostasis

Canalis, E., Kranz, L., & Zanotti, S. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24625 · Cited by 7

Indoxyl Sulfate Inhibits Osteogenesis in Bone Marrow Mesenchymal Stem Cells through the AhR/Hes1 Pathway

Hsieh, C., Chang, L.-H., Wang, Y., Li, W.-T., Chang, J., Chen, C., & Ho, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168770 · Cited by 6

EGFL7 Promotes Osteoblast Differentiation of Human Bone Mesenchymal Stem Cells Partly Via Downregulation of Notch Signaling

Zhang, W., Bai, J., Li, L., Zhang, Y., Hang, K., Wang, Y., Wang, Z., Ye, C., & Xue, D. (2022) · Stem Cell Reviews and Reports · doi:10.1007/s12015-022-10503-z · Cited by 6

Linoleic acid blunts early osteoblast differentiation and impairs oxidative phosphorylation in vitro

Nesbeth, P.-D. C., Ziegler, T. R., Tripathi, A. K., Dabeer, S., Weiss, D., Li, H., Smith, M. R., Jones, D. P., Maner-Smith, K. M., Tu, C., et al. (2024) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2024.102617 · Cited by 6

Microenvironmental Control of Disc Cell Function: Influence of Hypoxia and Osmotic Pressure

Risbud, M. V., & Shapiro, I. M. (2013) · Springer eBooks · doi:10.1007/978-3-7091-1535-0_6 · Cited by 7

Osteoporosis Genes Identified by Genome-Wide Association Studies

Rivadeneira, F., & Uitterlinden, A. G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804182-6.00022-8 · Cited by 6

Immune and Inflammatory Pathways are Involved in Inherent Bone Marrow Ossification

Gurkan, U. A., Golden, R. J., Kishore, V., Riley, C. P., Adamec, J., & Akkuş, O. (2012) · Clinical Orthopaedics and Related Research · doi:10.1007/s11999-012-2459-4 · Cited by 6

Signaling in Osteoblast Differentiation

Hayashi, M., Ono, T., & Nakashima, T. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11182-1 · Cited by 7

Prenatal Bone Development

Long, F. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-382040-2.10003-6 · Cited by 5

Mesenchymal Stem Cells as Regulators of the Bone Marrow and Bone Components

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