Cited by 795Bone Metabolism and DiseasesAlkaline Phosphatase Research StudiesBone and Dental Protein Studies

The DOI matches its Crossref record; 164 of the 165 references it cites were found in a registry or an index.

Buried alive: How osteoblasts become osteocytes

Open access

Franz‐Odendaal, Tamara A., Hall, Brian K., Witten, P. Eckhard·2006·Developmental Dynamics

DOI 10.1002/dvdy.20603

Open this paper in CoChat — free account Open PDF

Abstract

During osteogenesis, osteoblasts lay down osteoid and transform into osteocytes embedded in mineralized bone matrix. Despite the fact that osteocytes are the most abundant cellular component of bone, little is known about the process of osteoblast‐to‐osteocyte transformation. What is known is that osteoblasts undergo a number of changes during this transformation, yet retain their connections to preosteoblasts and osteocytes. This review explores the osteoblast‐to‐osteocyte transformation during intramembranous ossification from both morphological and molecular perspectives. We investigate how these data support five schemes that describe how an osteoblast could become entrapped in the bone matrix (in mammals) and suggest one of the five scenarios that best fits as a model. Those osteoblasts on the bone surface that are destined for burial and destined to become osteocytes slow down matrix production compared to neighbouring osteoblasts, which continue to produce bone matrix. That is, cells that continue to produce matrix actively bury cells producing less or no new bone matrix (passive burial). We summarize which morphological and molecular changes could be used as characters (or markers) to follow the transformation process. Developmental Dynamics 235:176–190, 2006. © 2005 Wiley‐Liss, Inc.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1002/dvdy.20603

Cites

164 of 164 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation.
Lacey, D. L., Timms, E., Tan, H.-L., Kelley, M. J., Dunstan, C. R., Burgess, T., Elliott, R., Colombero, A., Elliott, G., Scully, S., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81569-x · Cited by 5,439
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
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development
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
Birth and Death of Bone Cells: Basic Regulatory Mechanisms and Implications for the Pathogenesis and Treatment of Osteoporosis
Manolagas, S. C. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.2.0395 · Cited by 2,639
A Textbook of Histology
Bloom, W., & Fawcett, D. W. (1962) · Cited by 2,210
Handbuch der Mikroskopischen Anatomie des Menschen
Möllendorff, W. V., & Bargmann, W. (1958) · Springer eBooks · doi:10.1007/978-3-662-30619-2 · Cited by 1,515
Principles of Bone Biology
Compston, J. E. (1997) · Clinical Endocrinology · doi:10.1046/j.1365-2265.1997.2431019.x · Cited by 1,383
Birth and Death of Bone Cells: Basic Regulatory Mechanisms and Implications for the Pathogenesis and Treatment of Osteoporosis
Manolagas, S. C. (2000) · Endocrine Reviews · doi:10.1210/er.21.2.115 · Cited by 1,318
Identity of Osteoclastogenesis Inhibitory Factor (OCIF) and Osteoprotegerin (OPG): A Mechanism by which OPG/OCIF Inhibits Osteoclastogenesis in Vitro1
Yasuda, H., Shima, N., Nakagawa, N., Mochizuki, S.-I., Yano, K., Fujise, N., Sato, Y., Goto, M., Yamaguchi, K., Kuriyama, M., et al. (1998) · Endocrinology · doi:10.1210/endo.139.3.5837 · Cited by 1,201
The Osteoblast: A Sophisticated Fibroblast under Central Surveillance
Ducy, P. F., Schinke, T., & Karsenty, G. (2000) · Science · doi:10.1126/science.289.5484.1501 · Cited by 1,137

Flagged first, then by citations

Show all 165 references

1 of the 165 references couldn’t be matched to a known paper.

Research works printed but not linked: 20

10.1002/(SICI)1097-4644(1998)72:30/31 <73::AID-JCB11>3.0.CO;2-L · DOI
Bélanger LF, 1977, Histology
Beresford WA, 1993, Patterns of structural and systematic diversity, 9
Boyde A, 1980, Evidence against “osteocytic osteolysis.”, Metab Bone Dis Rel Res, 25, 239
10.1097/00003086-198304000-00036 · DOI
Delling G, 1992, Osteoporose
Gehron Robey P, 1993, Structural and molecular regulation of bone matrix proteins, J Bone Miner Res, 8, S2
Hall BK, 1990, Bonem, 494
Heersche JNM, 1990, Bone, 327
Holtrop ME, 1990, Bone, 1
Huysseune A, 1990, Carbohydrate histochemistry of mature chondroid bone in Astatotilapia elegans. (Teleostei: Cichlidae) with a comparison to acellular bone and cartilage, Ann Sci Natur Zool Paris, 13, 29
Kwiecinski GG, 1985, Bone remodelling and its regulation in Myotis lucifugus, Prog Zool, 30, 45
Meunier FJ, 1989, The acellularisation process in Osteichthyan bone, Fortschr Zool, 35, 443
Ørvig T, 1951, Histological studies of placoderms and fossil elasmobranches: I. The endoskeleton with remarks on the hard tissues of lower vertebrates in general, Arkin Zool, 2, 321
Parfitt AM, 1990, Bone, 351
Semba T, 1966, Observations on the fine structure of chick embryo osteocytes: effects of parathyroid extract, 569
Vickaryous MK, 2005, Fins and limbs
10.1210/en.136.6.2741 · DOI
Windle WF, 1976, Textbook of histology, 561
Witten PE, 2005, Fins and Limbs

Sorted by citations

Items 701–789 of 789

Involvement of osteocytes in cancer bone niche
Terpos, E., & Christoulas, D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-416721-6.00006-6
Faculty Opinions recommendation of Conditional mouse osteosarcoma, dependent on p53 loss and potentiated by loss of Rb, mimics the human disease.
Lessnick, S. L. (2008) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1116164.572151
Immunology of Osteoporosis
Kerschan‐Schindl, K., Nebot, E., & Pietschmann, P. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_153
Osteocytes
Bonewald, L. F. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-375098-3.50009-3
12. Additional Effect Of Soybean Waste Probiotic And Palm Kernel Fermented With Aspergillus Niger (Akbis Prob) On The Growth Of Boiler Bone
Nurliana, N., Tanjung, A., Sabri, M., Masyitah, D., Jalaluddin, M., & Rastina, R. (2019) · Jurnal medika Veterinaria · doi:10.21157/j.med.vet..v13i1.4116
References
(2015) · Elsevier eBooks · doi:10.1016/b978-0-12-416678-3.00059-8
Aspects of osteoporosis and fracture risk assessment in primary dental care: attitudes, willingness to pay and evaluation of an automated software
Gullberg, J. (2021) · doi:10.24834/isbn.9789178772018
Alkaline Phosphatase Activity Present in Serum Influences Osteogenic Differentiation CulturesPreprint
Ansari, S., Ito, K., & Hofmann, S. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3940870
Skeletal System
(2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-2002-0.00014-x
Bone Research Society 2015
(2015) · doi:10.3389/978-2-88919-659-3
Osteocyte
Akbarzadeh, J., & Godoy, C. (2021) · Springer eBooks · doi:10.1007/978-3-030-75750-2_1
Investigation of Factors Influencing the Prognosis in Prostate Cancer Patients with Isolated Bone Metastasis
Ebinç, S., Oruç, Z., Urakçı, Z., Ma, K., Küçüköner, M., & Işıkdoğan, A. (2022) · Bulletin of Urooncology · doi:10.4274/uob.galenos.2022.2022.1.4
Role of Nitric Oxide in Type 2 Diabetes-Induced Osteoporosis
Yousefzadeh, N., Jeddi, S., Kashfi, K., & Ghasemi, A. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079814122010011
Electroactive Environments for Mesenchymal Stem Cells Osteogenic Differentiation
Guillot-Ferriols, M. T. (2022) · doi:10.4995/thesis/10251/191003
Mechanosensitivity of osteocytes in their native matrix
Zhang, C. (2023) · doi:10.5463/thesis.189
Einfluss von Zoledronat und Denosumab auf humane Zellen der osteoblastären Linie aus dem Kieferknochen anhand osteogener Marker
Lautenbacher, F. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9917
Skeletal Resident Stem Cells
Martins-Santos, R., Kronemberger, G. S., Baptista, L. S., Taichman, R. S., Granjeiro, J. M., & Duarte, M. E. L. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-15289-4.00012-3 · Cited by 1
Atlas de histologia essencial
Bacchi, R. R., & Rodrigues, H. G. (2023) · doi:10.46551/978-65-86467-29-1
Vitamin D activity in osteoblasts and osteocytes
Anderson, P. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91386-7.00030-1
Lateral bone ridge expansion and internal tissue replacement for vertebral body growth in Pacific bluefin tuna Thunnus orientalis
Sakashita, M., Kondo, S., & Wada, N. (2023) · Journal of Morphology · doi:10.1002/jmor.21666
Integrating AI With Tissue Engineering
Malviya, R., Rajput, S., & Vaidya, M. (2024) · Wiley eBooks · doi:10.1002/9781394230914.ch2
Bone equilibria and disruptions
van Bosse, H. J. P. (2024) · Journal of the Pediatric Orthopaedic Society of North America · doi:10.1016/j.jposna.2024.100059
Direct and indirect regulation of SIX1+EYA transcriptional activity by PA2G4, MCRS1, and SOBP
Jourdeuil, K., Chukwuocha, K., Gafurova, J., Ben-Mayor, A., Moody, S. A., & Tavares, A. L. P. (2026) · Tissue and Cell · doi:10.1016/j.tice.2026.103790
Nanotechnology-based approaches for bone tissue engineering
Bonany, M. (2022) · doi:10.5821/dissertation-2117-413337
Bone cells: Osteoblast/osteoclast/osteocyte
Ucci, A., & Rucci, N. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00158-8
Contemporary Developmental Biology of the Cranio-Maxillofacial Hard Tissue: Histology
Azadi, A., Teimoori, M., & Khojasteh, A. (2025) · Springer eBooks · doi:10.1007/978-3-031-36962-9_308-1
Nano-Scale Peri-Lacunar Bone Formation and Implications for the Modulation of Whole Bone QualityPreprint
Ford, S., Tiedemann, K., Shapiro, R., Komarova, S. V., Jähn, K., & Zimmermann, E. A. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5277249
Adaptive Bone Remodelling
Gupta, S., Saviour, C. M., Pal, B., Chanda, S., & Mukherjee, K. (2025) · Springer eBooks · doi:10.1007/978-981-96-0586-6_9
Hydrogels for bone regeneration
Sreena, R., Ebinesh, S., Angel, S. S., & Nathanael, A. J. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-29260-6.00014-7
The Human Osteocyte Lacunocanalicular Network Structure in the Iliac Crest of Post-Menopausal Women Depends on Mineral Content But Not Individual AgePreprint
Jones, C., Blouin, S., Raguin, É., Weinkamer, R., Berzlanovich, A. M., Fratzl, P., & Hartmann, M. A. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5343824
A three-stage assembly program governing pancreatic, plasma, pituitary, and bone secretory cell differentiation: A strategy to augment protein delivery
Bidwell, J. P., Robling, A. G., & Wek, R. C. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110562
Deep-freezing and decontamination strategy for a large autologous bone graft with presentation of the osteogenic potential of resident osteoblasts
Zekušić, M., Skoko, M., Vukušić, K., Ledinski, M., Mihica, M. B., Blažević, D., Sosic, Z. A., Đura, M., Martinčić, J., Zimić, I. V., et al. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04839-9
Primary trabecular bone formation in vitro by the OmGFP66 osteogenic cell line: Multiscale symmetry breaking and characterization in 3D
Khurshid, B., Mousa, A., Dallas, S. L., Deering, J., Reznikov, N., & McKee, M. D. (2025) · Bone · doi:10.1016/j.bone.2025.117767 · Cited by 1
Additional file 1 of Osteoclasts differential-related prognostic biomarker for osteosarcoma based on single cell, bulk cell and gene expression datasets
Shao, H., Ge, M., Zhang, J., Zhao, T., & Zhang, S. (2022) · Figshare · doi:10.6084/m9.figshare.19381077
Additional file 3 of Inflammatory macrophages interrupt osteocyte maturation and mineralization via regulating the Notch signaling pathway
Wang, S., Xiao, L., Prasadam, I., Crawford, R., Zhou, Y., & Xiao, Y. (2022) · Figshare · doi:10.6084/m9.figshare.20933547
Additional file 2 of Inflammatory macrophages interrupt osteocyte maturation and mineralization via regulating the Notch signaling pathway
Wang, S., Xiao, L., Prasadam, I., Crawford, R., Zhou, Y., & Xiao, Y. (2022) · Figshare · doi:10.6084/m9.figshare.20933544
Additional file 1 of Inflammatory macrophages interrupt osteocyte maturation and mineralization via regulating the Notch signaling pathway
Wang, S., Xiao, L., Prasadam, I., Crawford, R., Zhou, Y., & Xiao, Y. (2022) · Figshare · doi:10.6084/m9.figshare.20933541
Additional file 4 of Inflammatory macrophages interrupt osteocyte maturation and mineralization via regulating the Notch signaling pathway
Wang, S., Xiao, L., Prasadam, I., Crawford, R., Zhou, Y., & Xiao, Y. (2022) · Figshare · doi:10.6084/m9.figshare.20933550
Additional file 5 of Inflammatory macrophages interrupt osteocyte maturation and mineralization via regulating the Notch signaling pathway
Wang, S., Xiao, L., Prasadam, I., Crawford, R., Zhou, Y., & Xiao, Y. (2022) · Figshare · doi:10.6084/m9.figshare.20933553
The role of maternal omega-3 supplementation in shaping offspring skeletal health
Chakraborty, A., Usharani, D., & Sharan, K. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-19116-9.00037-3
Sodium Butyrate Exacerbates Inflammation and Osteoblastic Dysfunction in Various Oral Cell Types Infected with Porphyromonas gingivalis
Song, Y. (2025) · Journal of dental hygiene science · doi:10.17135/jdhs.2025.25.4.389
Multiscale Structuring of Hydroxyapatite via Two‐Photon Lithography of Nanocomposites
Hambitzer, L., Hornbostel, J. M., Prediger, R., Kluck, S., Daub, M., Lee‐Thedieck, C., & Kotz, F. (2026) · Advanced Functional Materials · doi:10.1002/adfm.202517592
Mechano-adaptation and mechano-sensing in skeletal biology
Busse, B., & Zimmermann, E. A. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-13683-2.00017-7
Contrôle du métabolisme oxydatif des cellules leucémiques par le microenvironnement médullaire
Vignon, C. (2011) · theses.fr (ABES) · doi:10.70675/46c47371z1ee4z4069zb265z15a0300cc74f
Ostéoblastes et environnement physico-chimique : effets du contenu minéral matriciel et des micro-vibrations
Perrier, A. (2010) · doi:10.70675/75dcee23za4f6z414dzb338z2f66308a0517
Associations cellules souches mésenchymateuses et céramiques pour l'ingénierie tissulaire osseuse : intérêt du milieu cellulaire et de l'environnement tridimensionnel sur la différenciation ostéoblastique
Cordonnier, T. (2010) · theses.fr (ABES) · doi:10.70675/004f5db1z573dz4db8zae29z8311b99fd503
Imaging the bone cell network with nanoscale synchrotron computed tomography
Pacureanu, A. (2012) · doi:10.70675/8ff9918fz0074z4468z90f6z1d15659dc2e0
Impact de l'extinction génique de la sialoprotéine osseuse (BSP) sur la différenciation des ostéoblastes et l'ostéogenèse in vitro : développement et validation d'un bioréacteur pour la culture ostéoblastique en trois dimensions
Bouet, G. (2013) · theses.fr (ABES) · doi:10.70675/2f53f6f4z1c94z4120za098z6d42e41f66be
Contribution à l'étude de la variabilité des propriétés mécaniques de l'os cortical diaphysaire d'un os porteur (fémur) et non-porteur (humérus)
Bry, R. (2015) · theses.fr (ABES) · doi:10.70675/17b6d644z80f0z4beeza32ezafb68fe06909 · Cited by 2
Effects of continuous and intermittent hypergravity on skeleton
Gnyubkin, V. (2015) · theses.fr (ABES) · doi:10.70675/2e978c63z66ebz4a68zb083za6c62d439b14 · Cited by 1
Evaluation des modifications transcriptionnelles, phénotypiques et fonctionnelles des cellules souches mésenchymateuses dans les leucémies aiguës myéloblastiques de novo
Desbourdes, L. M. (2015) · theses.fr (ABES) · doi:10.70675/625718ecze05fz451fzb8baz7c7ee0ba1b6e
Evaluation des mécanismes d’action des cellules stromales mésenchymateuses pour l’optimisation de la régénération osseuse : impact des biomatériaux et de l’hétérogénéité des donneurs
Mebarki, M. (2016) · theses.fr (ABES) · doi:10.70675/734eb991ze5cdz4d25zbf87zf1307218492b
Rôle de la différenciation hypertrophique des chondrocytes dans le remodelage pathologique de la jonction ostéochondrale au cours de l'arthrose
van Eegher, S. (2017) · theses.fr (ABES) · doi:10.70675/4da13c46z57ccz423cz9ed9zef1cf5a6fd81
Expression et implication du système cholinergique dans l'arthrose
Courties, A. (2019) · theses.fr (ABES) · doi:10.70675/1aa2eec5z74d2z48b5zb03ez1741f09b3fa4
Two-dimentional complex modeling of bone and joint infections using agent-based simulation
Alsassa, S. (2019) · theses.fr (ABES) · doi:10.70675/5dde1efcza50dz454azb715z5fccb48fd646
In vitro evaluation of cell-material interactions on bioinert ceramics with novel surface modifications for enhanced osseointegration
Stanciuc, A. (2017) · doi:10.70675/4c0c1e5bz677fz4b29zb25azef064c7b4f05
Relations entre plusieurs critères d'évaluation de la sarcopénie et les paramètres osseux chez les jeunes adultes Libanais
Khawaja, A. (2019) · doi:10.70675/1d7b6248z94cfz4bfczbbb0z4f7217ee74ca
The clownfish Amphiprion ocellaris : a model species to study the metamorphosis of coral reef
Roux, N. (2019) · theses.fr (ABES) · doi:10.70675/df0ee706z135bz40b1zaac1zd8511c590fb4
Etude des effets anti-inflammatoires et anti-cancéreux de nouvelles molécules agrosourcées à motif pyridazinone
Moniot, A. (2020) · theses.fr (ABES) · doi:10.70675/9be60ae3z24c2z427fzbfcbzf7a9c8fa1f39
Hypoxia and FGF-2 priming for bone tissue engineering : an in vitro and in vivo study
Novais, A. (2019) · theses.fr (ABES) · doi:10.70675/9259747ezadcez4488zbf3fz0f2e537f5dd9
Impact de la mutation G380R du récepteur FGFR3 responsable de l’achondroplasie sur le métabolisme énergétique et évaluation de l’effet d’un traitement par sFGFR3
Saint-Laurent, C. (2018) · theses.fr (ABES) · doi:10.70675/4009375fzcda1z4b66z89d2z53f370c37d8b
Modélisation pathologique pour la neurofibromatose de Type 1 : développement d’un test d’étude et applications pour la découverte de molécules actives
Aubin, D. (2019) · theses.fr (ABES) · doi:10.70675/0ccbf38ezf523z491ezb79dz8d9c14dd63a4
Caractérisation phénotypique et fonctionnelle des cellules stromales mésenchymateuses natives de la moelle osseuse humaine adulte
Fiévet, L. (2020) · theses.fr (ABES) · doi:10.70675/bfdad3e7z4e0fz4fe4z8fd9z651c2fb3a39e
Cellules souches de la pulpe dentaire et matrice de collagène : une association au service de l’ingénierie tissulaire osseuse prévascularisée
Kichenbrand, C. (2020) · doi:10.70675/b5a3462az2e25z462czb74dz24053e2baeff
Rôle de mir-342-3p dans l'hétérogénéité fonctionnelle des ostéoclastes et implication dans l’arthrite auto-immune
Lozano, C. (2020) · theses.fr (ABES) · doi:10.70675/6e4ff659zc1bbz4b05z87f6zc4471e79ec4f
Structuration en 3D de phases cristal-liquides pour la formation biomimétique de tissus osseux
Bessot, E. (2020) · theses.fr (ABES) · doi:10.70675/c4c2086ez0d7az4934z8753z27438d7e42e4
Rôle des chondrocytes hypertrophiques dans le remodelage pathologique de la jonction ostéochondrale au cours de l'arthrose : implication du SDF-1 dans l'angiogenèse
Toillon, I. (2021) · theses.fr (ABES) · doi:10.70675/0521c11az1a2bz423az9521zad6dc6c2df87
Synthesis of bioactive surfaces for the control of stem cells differentiation
Prouvé, É. (2021) · theses.fr (ABES) · doi:10.70675/e6e40875z38c9z479ezb35fz53ede1161671
Etude du rôle du récepteur LPA1 dans l'ostéogénèse au cours de la croissance du squelette : implication dans l'acquisition de masse osseuse
Alioli, A. C. (2020) · theses.fr (ABES) · doi:10.70675/91ed89a7zfc2fz442fz8da8zad0726b68cdd
Effets de l'exercice physique sur le tissu osseux et sa vascularisation : comparaison entre différentes modalités de course
Wazzani, R. (2022) · theses.fr (ABES) · doi:10.70675/15a76c20z12d7z487azb896z09042b1bb02b
La matrice extracellulaire des adipocytes médullaires : caractérisation et impact sur l'ostéoblastogénèse et la minéralisation dans le contexte de l'ostéoporose
Entz, L. (2022) · theses.fr (ABES) · doi:10.70675/ea1297aez0e22z47fbzb5c5ze51ddd039f68
Déterminants de la perte osseuse au cours de déclins fonctionnels multiples ˸ pour une approche intégrée : Caractérisation des déterminants de perte osseuse chez l'insuffisant rénal et l'obèse opéré de chirurgie bariatrique
Cailleaux, P. (2022) · theses.fr (ABES) · doi:10.70675/c86911ecz3e22z449fzb988ze55d8c9e7ae8
Medullary adipocytes and age-related osteoporosis
Quacquarelli, F. (2023) · theses.fr (ABES) · doi:10.70675/534a5ef6z7c27z4540zbfffzf8da9fa46873
Multi-isotopic tracing of historical mining pollution in European environmental archives and their impact on the population
Heredia, C. (2024) · doi:10.70675/5e3f423fzee91z4f99z85acz72792ed6a230
Correlations Between Osteocytes and Bone Density in Bovine Bony Pelvic Floor: A Pilot Study
Nahkur, E., Torga, T., Andrianov, V., Arend, A., Kaart, T., & Aunapuu, M. (2026) · Anatomia Histologia Embryologia · doi:10.1111/ahe.70112
Intraosseous therapy: harnessing the potential of tissue regeneration and repair
Artamonov, M. Y., & Minenko, I. A. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1775823
Mechanical loading-induced bone formation is associated with increased blood velocity and vascular canal bone porosity, with localized vascular adaptation
DeVet, T., Moussa, M. S., Gonzalez, H., Zaslansky, P., Chalifour, L. E., Komarova, S. V., & Willie, B. M. (2026) · Journal of Bone and Mineral Research · doi:10.1093/jbmr/zjag076
Comparative Effects of Escherichia coli vs. Porphyromonas gingivalis Lipopolysaccharides on Osteogenic Differentiation and the Expression of lncRNAs in Periodontal Ligament Stem Cells
Suciu, T.-S., Bran, S., Berindan‐Neagoe, I., Ráduly, L., Zănoagă, O., Budișan, L., Nutu, A. M., Şoriţău, O., Strilciuc, Ș., Leucuta, D., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27115006
The “osteostat”: a theory of bone mechanosensing and setpoint adaptation based on osteocytesPreprint
Pauchard, Y., & Buenzli, P. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.23.734120 · Cited by 1
The role and therapeutic potential of vitamins in fracture healing
Yu, Q., Yu, G., Dong, H., Wang, C., Guan, M., Shi, B., & Li, Z. (2026) · Nutrition Journal · doi:10.1186/s12937-026-01360-4
Bioprinted bonoid-on-a-chip model for studying drug effects on human osteocyte differentiation
Scheinpflug, J., Höfer, C. T., Steinfath, M., Thomas, A., Schmerbeck, S. S., John, T., Schneider, M. R., Schönfelder, G., Schulze, F., & Barenys, M. (2026) · Biofabrication · doi:10.1088/1758-5090/ae7ed2
Bone cells, roles and functions
Dollas, N., Kennedy, O. D., Majeska, R. J., & Schaffler, M. B. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-26739-0.00014-4
High-resolution mapping of osteoblast metabolism and bone matrix turnover in vivo
Chen, K., Guo, J., Chen, X., Chen, B., Qiu, H., Yang, H., Guagliardo, P. R., Hu, S., Bui, C., Chandrasekaran, K. N., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2533109123
Sustainable Valorization of Biogenic Waste for Bone Repair and Regeneration: A Comprehensive Review of Eggshell and Aquatic Biomaterials
Waqar, S., Ahmed, T. A. E., & Hincke, M. T. (2026) · Journal of Functional Biomaterials · doi:10.3390/jfb17080417
Bioinspired Approaches for Dental Implants
Bano, N. Z., Alam, B. F., Khan, M., Alkhalifa, F. B. H., Ali, S., & Khan, A. S. (2026) · Royal Society of Chemistry eBooks · doi:10.1039/9781837677443-00119
Do osteohistology, microanatomy or life history traits show patterns linked to neotenic lifestyles in extant Caudata and the Permian temnospondyl Apateon?
Klein, N., Konietzko‐Meier, D., Schoch, R. R., & Griebeler, E. M. (2026) · BMC Ecology and Evolution · doi:10.1186/s12862-026-02577-x
Microgravity-Induced Uncoupling of Bone Remodelling: Roles of Impaired Mechanosensing and Osteoimmune Regulation
Mo, L., Luo, Y., Huang, K., Li, X., Yang, J., Li, J., Lv, S., Quan, H., Lei, Y., Chen, H., et al. (2026) · Advanced Orthopaedics · doi:10.1016/j.advop.2026.10.004
Induction and Patterning of Neural Crest Cells in the Developing Mouse Embryo: Roles for Gcnf and Hhat
Dennis, J. F. (2008)
Experimentelle Untersuchung zur Alveolarkammaugmentation mit Trikalziumphosphat-Hydroxylapatit-Komposit eingebettet in eine Poloxamermatrix
Köwing, M. (2015) · doi:10.53846/goediss-4958

Authors: Franz‐Odendaal, T. A., Hall, B. K., & Witten, P. E.
Affiliations: Dalhousie University (CA)
Corresponding author: Franz‐Odendaal, Tamara A.
Witten, P. Eckhard
ORCID: Franz‐Odendaal, Tamara A.
Hall, Brian K.
Witten, P. Eckhard
Venue: Developmental Dynamics
Publisher: Wiley
Published: 2005-10-28
Volume: 235
Issue: 1
Pages: 176-190
ISSN: 1058-8388 (ISSN-L)
1097-0177
DOI: 10.1002/dvdy.20603
OpenAlex: W2032394856
Cited by: 795
References: 165
Citations by year: 2026: 25 · 2025: 29 · 2024: 30 · 2023: 48 · 2022: 41 · 2021: 68 · 2020: 55 · 2019: 58 · 2018: 38 · 2017: 53 · 2016: 38 · 2015: 45 · 2014: 33 · 2013: 48 · 2012: 41
FWCI: 1.56
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Developmental Dynamics (publishedVersion)
PubMed (publishedVersion)
Ghent University Academic Bibliography (Ghent University) (publishedVersion)
Ghent University Academic Bibliography (Ghent University) (submittedVersion)
Funders: Deutsche Forschungsgemeinschaft
Natural Sciences and Engineering Research Council of Canada
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Alkaline Phosphatase Research Studies
Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Bone and Dental Protein Studies
Keywords: osteocytes, osteoblasts, intramembranous ossification, bone formation, bone matrix mineralization, osteoblast markers
MeSH terms: Animals, Bone and Bones, Cell Differentiation, Humans, Models, Biological, Osteoblasts, Osteocytes, Osteogenesis

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Buried alive: How osteoblasts become osteocytes

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks