Cilia-like Structures and Polycystin-1 in Osteoblasts/Osteocytes and Associated Abnormalities in Skeletogenesis and Runx2 Expression

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

Nauli, S. M., Alenghat, F. J., Luo, Y., Williams, E., Vassilev, P., Li, X., Elia, A. E. H., Lu, W., Brown, E. M., Quinn, S. J., et al. (2003) · Nature Genetics · doi:10.1038/ng1076 · Cited by 2,057

The Polycystic Kidney Disease Proteins, Polycystin-1, Polycystin-2, Polaris, and Cystin, Are Co-Localized in Renal Cilia

Yoder, B. K., Hou, X., & Guay-Woodford, L. M. (2002) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000029587.47950.25 · Cited by 935

Polycystic Kidney Disease

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Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

Hanaoka, K., Qian, F., Boletta, A., Bhunia, A. K., Piontek, K., Tsiokas, L., Sukhatme, V. P., Guggino, W. B., & Germino, G. G. (2000) · Nature · doi:10.1038/35050128 · Cited by 822

ATF4 Is a Substrate of RSK2 and an Essential Regulator of Osteoblast Biology

Yang, X., Matsuda, K., Bialek, P., Jacquot, S., Masuoka, H. C., Schinke, T., Li, L., Brancorsini, S., Sassone‐Corsi, P., Townes, T. M., et al. (2004) · Cell · doi:10.1016/s0092-8674(04)00344-7 · Cited by 822

Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease

Lin, F., Hiesberger, T., Cordes, K. R., Sinclair, A. M., Goldstein, L. S. B., Somlo, S., & Igarashi, P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0836980100 · Cited by 602

PDGFRαα Signaling Is Regulated through the Primary Cilium in Fibroblasts

Schneider, L., Clement, C. A., Teilmann, S. C., Pazour, G. J., Hoffmann, E. K., Satir, P., & Christensen, S. T. (2005) · Current Biology · doi:10.1016/j.cub.2005.09.012 · Cited by 592

Regulation of the osteoblast‐specific transcription factor, Runx2: Responsiveness to multiple signal transduction pathways

Franceschi, R. T., & Xiao, G. (2003) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10369 · Cited by 540

Mechanotransduction and strain amplification in osteocyte cell processes

Han, Y., Cowin, S. C., Schaffler, M. B., & Weinbaum, S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407429101 · Cited by 495

Molecular pathways mediating mechanical signaling in bone

Rubin, J. E., Rubin, C. T., & Jacobs, C. R. (2005) · Gene · doi:10.1016/j.gene.2005.10.028 · Cited by 481

Mechanical signals as a non-invasive means to influence mesenchymal stem cell fate, promoting bone and suppressing the fat phenotype

Luu, Y. K., Pessin, J. E., Judex, S., Rubin, J. E., & Rubin, C. T. (2009) · IBMS BoneKEy · doi:10.1138/20090371 · Cited by 41

Heterogeneity in The Mechanical Properties of Integrins Determines Mechanotransduction Dynamics in Bone Osteoblasts

Shuaib, A., Motan, D., Bhattacharya, P., McNabb, A., Skerry, T. M., & Lacroix, D. (2019) · Scientific Reports · doi:10.1038/s41598-019-47958-z · Cited by 40

Role of TGF-β in a Mouse Model of High Turnover Renal Osteodystrophy

Liu, S., Song, W., Boulanger, J., Tang, W., Sabbagh, Y., Kelley, B., Gotschall, R. R., Ryan, S., Phillips, L. A., Malley, K., et al. (2013) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2120 · Cited by 35

Cilia Ift protein and motor -related bone diseases and mouse models

Yang, S. (2015) · Frontiers in bioscience · doi:10.2741/4323 · Cited by 37

Calcium-mediated mechanisms of cystic expansion

Abdul-Majeed, S., & Nauli, S. M. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.09.016 · Cited by 36

Role of the polycystins as mechanosensors of extracellular stiffness

Nigro, E. A., & Boletta, A. (2021) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00545.2020 · Cited by 35

Runx2 and Polycystins in Bone Mechanotransduction: Challenges for Therapeutic Opportunities

Gargalionis, A. N., Adamopoulos, C., Vottis, C. T., Papavassiliou, A. G., & Basdra, E. K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105291 · Cited by 36

Mechanotransduction

Tschumperlin, D. J. (2011) · Comprehensive physiology · doi:10.1002/cphy.c100016 · Cited by 46

A distinct bone phenotype in ADPKD patients with end-stage renal disease

Evenepoel, P., Claes, K. J., Cavalier, E., Meijers, B. K. I., Stenvinkel, P., Behets, G. J. S., Jankowska, M., D’Haese, P. C., & Bammens, B. (2019) · Kidney International · doi:10.1016/j.kint.2018.09.018 · Cited by 34

The osteocyte: the underestimated conductor of the bone orchestra

BONUCCI, E. (2009) · RENDICONTI LINCEI · doi:10.1007/s12210-009-0051-y · Cited by 33

The mechanosensory and mechanotransductive processes mediated by ion channels and the impact on bone metabolism: A systematic review

Zhang, K., Liu, X., Wang, L., Liu, Z., Yi, Q., Geng, B., Chen, X., Yu, D., & Xia, Y. (2021) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2021.109020 · Cited by 34

Role for Primary Cilia as Flow Detectors in the Cardiovascular System

der Heiden, K. V., Egorova, A. D., Poelmann, R. E., Wentzel, J. J., & Hierck, B. P. (2011) · International review of cytology · doi:10.1016/b978-0-12-386037-8.00004-1 · Cited by 31

Downregulation of PKD1 by shRNA results in defective osteogenic differentiation via cAMP/PKA pathway in human MG‐63 cells

Qiu, N., Zhou, H., & Xiao, Z. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23426 · Cited by 30

Sensing a Sensor: Identifying the Mechanosensory Function of Primary Cilia

Prasad, R. M., Jin, X., & Nauli, S. M. (2014) · Biosensors · doi:10.3390/bios4010047 · Cited by 29

Development of beak polymorphism in the African seedcracker, Pyrenestes ostrinus

Clabaut, C., Herrel, A., Sanger, T. J., Smith, T. B., & Abzhanov, A. (2009) · Evolution & Development · doi:10.1111/j.1525-142x.2009.00371.x · Cited by 29

Bone as a Material

McNamara, L. M. (2011) · Elsevier eBooks · doi:10.1016/b978-0-08-055294-1.00068-4 · Cited by 31

Advancing our understanding of osteocyte cell biology

Guo, D., & Bonewald, L. F. (2009) · Therapeutic Advances in Musculoskeletal Disease · doi:10.1177/1759720x09341484 · Cited by 27

The Primary Cilium of Connective Tissue Cells: Imaging by Multiphoton Microscopy

Donnelly, E. L., Williams, R. M., & Farnum, C. E. (2008) · The Anatomical Record · doi:10.1002/ar.20665 · Cited by 29

Cellular Complexity at the Interface: Challenges in Enthesis Tissue Engineering

Calejo, I., Costa‐Almeida, R., & Gomes, M. E. (2019) · Advances in experimental medicine and biology · doi:10.1007/5584_2018_307 · Cited by 26

The Osteocyte

Klein‐Nulend, J., & Bonewald, L. F. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-373884-4.00028-8 · Cited by 26

Ciliary signaling in stem cells in health and disease: Hedgehog pathway and beyond

Shimada, I. S., & Kato, Y. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.04.011 · Cited by 24

Osteocytes: Mechanosensors of Bone and Orchestrators of Mechanical Adaptation

Klein‐Nulend, J., & Bakker, A. D. (2007) · Clinical Reviews in Bone and Mineral Metabolism · doi:10.1007/s12018-008-9014-6 · Cited by 25

Bone mechanobiology in health and disease

Verbruggen, S. W., & McNamara, L. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812952-4.00006-4 · Cited by 24

Osteocytes are not only mechanoreceptive cells

Rochefort, G. Y., & Benhamou, C.-L. (2013) · International Journal for Numerical Methods in Biomedical Engineering · doi:10.1002/cnm.2561 · Cited by 26

Scl-Ab reverts pro-osteoclastogenic signalling and resorption in estrogen deficient osteocytes

Allison, H., Holdsworth, G., & McNamara, L. M. (2020) · BMC Molecular and Cell Biology · doi:10.1186/s12860-020-00322-w · Cited by 24

From bone abnormalities to mineral metabolism dysregulation in autosomal dominant polycystic kidney disease

Mekahli, D., & Bacchetta, J. (2013) · Pediatric Nephrology · doi:10.1007/s00467-012-2384-5 · Cited by 23

A cut above (and below): Protein cleavage in the regulation of polycystin trafficking and signaling

Padovano, V., Mistry, K., Merrick, D., Gresko, N., & Caplan, M. J. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109634 · Cited by 21

Inducible expression of Runx2 results in multiorgan abnormalities in mice

He, N., Xiao, Z., Yin, T., Stubbs, J. R., Li, L., & Quarles, L. D. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22968 · Cited by 20

Mechanical protein polycystin-1 directly regulates osteoclastogenesis and bone resorption

Huang, M., Zhou, J., Li, X., Liu, R., Jiang, Y., Chen, K., Jiao, Y., Yin, X., Liu, L., Sun, Y., et al. (2024) · 中国科学通报：英文版 · doi:10.1016/j.scib.2024.04.044 · Cited by 20

Evidence for Bone and Mineral Metabolism Alterations in Children With Autosomal Dominant Polycystic Kidney Disease

Rechter, S. D., Bacchetta, J., Godefroid, N., Dubourg, L. D., Cochat, P., Maquet, J., Raes, A. M., Schepper, J. D., Vermeersch, P., Dyck, M. V., et al. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-01157 · Cited by 20

Epigenetic regulation of Tbx18 gene expression during endochondral bone formation

Haraguchi, R., Kitazawa, R., & Kitazawa, S. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-2028-0 · Cited by 19

Ciliary Signalling and Mechanotransduction in the Pathophysiology of Craniosynostosis

Tiberio, F., Parolini, O., & Lattanzi, W. (2021) · Genes · doi:10.3390/genes12071073 · Cited by 19

Hypertension in Autosomal Dominant Polycystic Kidney Disease: A Clinical and Basic Science Perspective.

Ratnam, S., & Nauli, S. M. (2010) · PubMed · Cited by 19

Conditional Mesenchymal Disruption of Pkd1 Results in Osteopenia and Polycystic Kidney Disease

Qiu, N., Xiao, Z., Cao, L., David, V., & Quarles, L. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046038 · Cited by 19

Continuous hydrostatic pressure induces differentiation phenomena in chondrocytes mediated by changes in polycystins, SOX9, and RUNX2

Karamesinis, K., Spyropoulou, A., Dalagiorgou, G., Katsianou, M. A., Nokhbehsaim, M., Beisel-Memmert, S., Deschner, J., Vastardis, H., & Piperi, C. (2016) · Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie · doi:10.1007/s00056-016-0061-1 · Cited by 18

Ciliary Rootlet Coiled-Coil 2 (crocc2)Is Associated with Evolutionary Divergence and Plasticity of Cichlid Jaw Shape

Gilbert, M. C., Tetrault, E. R., Packard, M. C., Navon, D., & Albertson, R. C. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab071 · Cited by 20

Serum Alkaline Phosphatase Reflects Post-Fontan Hemodynamics in Children

Chin, A. J., Stephens, P., Goldmuntz, E., & Leonard, M. B. (2008) · Pediatric Cardiology · doi:10.1007/s00246-008-9292-2 · Cited by 18

Polycystin 2 is involved in the nitric oxide production in responding to oscillating fluid shear in MLO-Y4 cells

Xu, H., Guan, Y., Wu, J., Zhang, J., Duan, J., An, L., & Shang, P. (2013) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2013.11.018 · Cited by 18

Primary cilia in skeletal development and disease

Quadri, N., & Upadhyai, P. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113751 · Cited by 19

Genetic interactions between polycystin-1 and Wwtr1 in osteoblasts define a novel mechanosensing mechanism regulating bone formation in mice

Xiao, Z., Cao, L., Smith, M. D., Li, H., Li, W., Smith, J. C., & Quarles, L. D. (2023) · Bone Research · doi:10.1038/s41413-023-00295-4 · Cited by 17

Primary cilia in hard tissue development and diseases

Li, S., Zhang, H., & Sun, Y. (2021) · Frontiers of Medicine · doi:10.1007/s11684-021-0829-6 · Cited by 15

RUNX2 mutations in Chinese patients with cleidocranial dysplasia

Li, Y., Pan, W., Xu, W., He, N., Chen, X., Liu, H., Quarles, L. D., Zhou, H., & Xiao, Z. (2009) · Mutagenesis · doi:10.1093/mutage/gep025 · Cited by 16

Characterisation of transcription factor profiles in polycystic kidney disease (PKD): identification and validation of STAT3 and RUNX1 in the injury/repair response and PKD progression

Formica, C., Malas, T. B., Balog, J., Verburg, L., Hoen, P. A. C. ’., & Peters, D. J. M. (2019) · Journal of Molecular Medicine · doi:10.1007/s00109-019-01852-3 · Cited by 15

2.10 Bone as a Material ☆

McNamara, L. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803581-8.10127-4 · Cited by 18

The role of transient receptor potential polycystin channels in bone diseases

Katsianou, M. A., Skondra, F. G., Gargalionis, A. N., Piperi, C., & Basdra, E. K. (2018) · Annals of Translational Medicine · doi:10.21037/atm.2018.04.10 · Cited by 14

Cellular and Molecular Mechanotransduction in Bone

Chen, J. C., Castillo, A. B., & Jacobs, C. R. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415853-5.00020-0 · Cited by 17

The factory, the antenna and the scaffold: the three-way interplay between the Golgi, cilium and extracellular matrix underlying tissue function

Stevenson, N. L. (2023) · Biology Open · doi:10.1242/bio.059719 · Cited by 14

Autosomal Dominant Polycystic Kidney Disease: Extrarenal Involvement

Righini, M., Mancini, R., Busutti, M., & Buscaroli, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052554 · Cited by 14

The Pyrophosphate Transporter ANKH is Expressed in Kidney and Bone Cells and Colocalises to the Primary Cilium/Basal Body Complex

Carr, G., Moochhala, S. H., Eley, L., Vandewalle, A., Simmons, N. L., & Sayer, J. A. (2009) · Cellular Physiology and Biochemistry · doi:10.1159/000257515 · Cited by 15

Recent Progress in Osteocyte Research

Pajevic, P. D. (2013) · Endocrinology and Metabolism · doi:10.3803/enm.2013.28.4.255 · Cited by 16

Primary cilia mediate mechanosensing in bone cells by a calcium-independent mechanism

Clarke, B. L. (2008) · Yearbook of Endocrinology · doi:10.1016/s0084-3741(08)79085-1 · Cited by 14

Ultrastructural evidence for telocytes in equine tendon

Bartolomé, M. J. L., Cantarero, I., Sánchez-Cano, A. I., Rodellar, C., & Junquera, C. (2020) · Journal of Anatomy · doi:10.1111/joa.13335 · Cited by 14

Putative Receptors for Gravity Sensing in Mammalian Cells: The Effects of Microgravity

Aventaggiato, M., Barreca, F., Vernucci, E., Bizzarri, M., Ferretti, E., Russo, M. A., & Tafani, M. (2020) · Applied Sciences · doi:10.3390/app10062028 · Cited by 12

Primary Cilia are Mechanosensory Organelles in Vestibular Tissues

Nauli, S. M., Haymour, H. S., AbouAlaiwi, W. A., Lo, S. T., & Nauli, A. M. (2010) · Springer eBooks · doi:10.1007/978-90-481-9881-8_14 · Cited by 13

Effects of vascular endothelial growth factor (VEGF-A) and endostatin on bone

Sipola, A. (2009) · Cited by 12

Chapter 4. Osteocytes

Bonewald, L. F. (2008) · Primer on the metabolic bone diseases and disorders of mineral metabolism · doi:10.1002/9780470623992.ch4 · Cited by 12

New and Old Osteocytic Cell Lines and 3D Models

Pajevic, P. D. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00613-3 · Cited by 11

Postnatal Bone Growth: Growth Plate Biology, Bone Formation, and Remodeling

Maes, C., & Kronenberg, H. M. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-382040-2.10004-8 · Cited by 12

Post-natal bone physiology

El-Farrash, R. A., Ali, R. H., & Barakat, N. M. (2019) · Seminars in Fetal and Neonatal Medicine · doi:10.1016/j.siny.2019.101077 · Cited by 12

Primary Cilia-Mediated Mechanotransduction in Bone

Lee, K. L., Hoey, D. A., & Jacobs, C. R. (2010) · Clinical Reviews in Bone and Mineral Metabolism · doi:10.1007/s12018-010-9078-y · Cited by 11

The osteocyte

Klein‐Nulend, J., & Bonewald, L. F. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00006-3 · Cited by 11

Cellular and molecular mechanotransduction in bone

Castillo, A. B., Chen, J. C., & Jacobs, C. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813073-5.00014-9 · Cited by 12

Osteocyte Biology

Bonewald, L. F. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415853-5.00010-8 · Cited by 14

The BMP antagonist Noggin is produced by osteoblasts in response to the presence of prostate cancer cells

Alshaibi, H. F., Ahmed, F., Buckle, C., Fowles, A., Awlia, J., Cecchini, M. G., & Eaton, C. L. (2017) · Biotechnology and Applied Biochemistry · doi:10.1002/bab.1619 · Cited by 10

Thm2 interacts with paralog, Thm1, and sensitizes to Hedgehog signaling in postnatal skeletogenesis

Allard, B. A., Wang, W., Pottorf, T. S., Mumtaz, H., Hufft‐Martinez, B. M., Wang, H. H., Silva, L. M., Jacobs, D. T., Wang, J., Bumann, E. E., et al. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03806-w · Cited by 9

Mechanisms of exercise effects on bone quantity and quality

Patel, V. S., Judex, S., Rubin, J. E., & Rubin, C. T. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00076-2 · Cited by 10

Osteocytes

Bonewald, L. F. (2013) · Primer on the metabolic bone diseases and disorders of mineral metabolism · doi:10.1002/9781118453926.ch4 · Cited by 10

Mechanical effects in aging of the musculoskeletal system: Molecular signaling and spatial scale alterations

Zhang, Z., Cao, F., Liang, D., Pan, M., Lu, W. W., Lyu, H., Xie, Y., Zhang, L., & Tang, P. (2025) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2025.04.018 · Cited by 10

Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiation

Upadhyai, P., Guleria, V. S., & Udupa, P. (2020) · PeerJ · doi:10.7717/peerj.9799 · Cited by 11

Characterization of Primary Cilia in Osteoblasts Isolated From Patients With ADPKD and CKD

Pereira, R. C., Gitomer, B. Y., Chonchol, M., Harris, P. C., Noche, K. J., Salusky, I. B., & Albrecht, L. V. (2021) · JBMR Plus · doi:10.1002/jbm4.10464 · Cited by 10

Severe skeletal abnormalities caused by defects in retrograde intraflagellar transport dyneins

Schmidts, M., & Mitchison, H. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809470-9.00015-1 · Cited by 9

The biological basis of treating jaw discrepancies: An interplay of mechanical forces and skeletal configuration

Karamesinis, K., & Basdra, E. K. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.02.007 · Cited by 9

Osteocytes

Bonewald, L. F. (2008) · Elsevier eBooks · doi:10.1016/b978-012370544-0.50010-0 · Cited by 9

The role of primary cilia in mechanical transmission of osteocyte based on a 3D finite element model

Han, Z., Ding, D., Fan, Y., Wu, X., Yang, X. Y., & Sun, L. (2023) · Medicine in Novel Technology and Devices · doi:10.1016/j.medntd.2023.100275 · Cited by 8

Patterns of Trophic Evolution: Integration and Modularity of the Cichlid Skull

Hu, Y., & Albertson, R. C. (2021) · Springer eBooks · doi:10.1007/978-94-024-2080-7_20 · Cited by 8

Bone health in autosomal dominant polycystic kidney disease (ADPKD) patients after kidney transplantation

Zubidat, D., Hanna, C., Randhawa, A. K., Smith, B. H., Chedid, M., Kaidbay, D.-H. N., Nardelli, L., Mkhaimer, Y. G., Neal, R. M., Madsen, C. D., et al. (2023) · Bone Reports · doi:10.1016/j.bonr.2023.101655 · Cited by 8

Mechanobiology of Primary Cilia

Kwon, R. Y., Hoey, D. A., & Jacobs, C. R. (2010) · Studies in mechanobiology, tissue engineering and biomaterials · doi:10.1007/8415_2010_28 · Cited by 8

Nonvascular transport distraction osteogenesis in bone formation and regeneration. Is it an accidental phenomenon?

Guo, P., Zeng, J., & Zhou, N. (2014) · Journal of Cranio-Maxillofacial Surgery · doi:10.1016/j.jcms.2014.10.004 · Cited by 8

Real-time vascular mechanosensation through ex vivo artery perfusion

Prasad, R. M., Jin, X., AbouAlaiwi, W. A., & Nauli, S. M. (2014) · Biological Procedures Online · doi:10.1186/1480-9222-16-6 · Cited by 8

An Unusually Prolonged Case of FGF23-mediated Hypophosphatemia Secondary to Ferric Carboxymaltose Use

Arora, I., Kaprove, A., Perrone, R. D., & Ceglia, L. (2023) · JCEM Case Reports · doi:10.1210/jcemcr/luad117 · Cited by 7

Mechanisms of Exercise Effects on Bone Quantity and Quality

Judex, S., Rubin, J. E., & Rubin, C. T. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-373884-4.00088-4 · Cited by 7

Osteoblast Biology

van Leeuwen, J. P. T. M., van der Eerden, B. C. J., van de Peppel, J., Stein, G. S., & Lian, J. B. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415853-5.00009-1 · Cited by 7

Osteocyte Mechanosensation and Transduction

Bonewald, L. F. (2010) · Springer eBooks · doi:10.1007/978-4-431-89757-6_10 · Cited by 6

Animal Models of Bone Disease-B

McGee‐Lawrence, M. E., Secreto, F. J., & Syed, F. A. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415894-8.00017-8 · Cited by 8

WNT Signaling in Skeletal Homeostasis and Diseases

Gori, F., & Baron, R. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415853-5.00018-2 · Cited by 6

New pathogenic insights inform therapeutic target development for renal osteodystrophy

Hruska, K. A., & Mahjoub, M. R. (2019) · Kidney International · doi:10.1016/j.kint.2018.10.026 · Cited by 6

Bone remodeling biology

Kahla, R. B., & Barkaoui, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-88467-9.00002-3 · Cited by 6

Tolvaptan treatment is associated with altered mineral metabolism parameters and increased bone mineral density in ADPKD patients

Bargagli, M., Vetsch, A., Anderegg, M. A., Dhayat, N. A., Huynh‐Do, U., Faller, N., Vogt, B., Ferraro, P. M., & Fuster, D. G. (2022) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfac298 · Cited by 5

Recent advances in primary cilia in bone metabolism

Lian, F., Li, H., Ma, Y., Zhou, R., & Wu, W. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1259650 · Cited by 5

Role of osteocytes in the adaptation of bone to mechanical loading

Bakker, A. D., & Klein‐Nulend, J. (2008) · Future Rheumatology · doi:10.2217/17460816.3.6.571 · Cited by 5

A novel role for primary cilia in airway remodeling

Trempus, C. S., Song, W., Lazrak, A., Yu, Z., Creighton, J. R., Young, B. M., Heise, R. L., Yu, Y. R., Ingram, J. L., Tighe, R. M., et al. (2017) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00284.2016 · Cited by 5

Osteoblast Biology

Lian, J. B., & Stein, G. S. (2008) · Elsevier eBooks · doi:10.1016/b978-012370544-0.50008-2 · Cited by 5

Cells Involved in Mechanotransduction Including Mesenchymal Stem Cells

Zuckerman, P. C., Liu, C., & Castillo, A. B. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11209-7 · Cited by 5

Osteocytes

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