ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Bone Organoids: A Novel Tool for Modeling and Managing Skeletal Disorders in Diabetes.
Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Decades of research have revealed the profound impact of diabetes on skeletal health, yet the biological basis of diabetic bone fragility remains incompletely understood, and no existing in vitro or animal model has faithfully recapitulated these disease phenotypes. Organoid technologies are emerging as powerful tools for investigating human biology, modeling disease, and developing novel therapies. While organoids for many tissue types have been developed and continue to advance rapidly due to a growing regulatory shift toward human-relevant in vitro models, bone organoids remain underrepresented, with only a few models described to date. Bone organoids can be generated using cell-based self-assembly or scaffold-based guided approaches, each capable of reconstructing key features of native bone, including its multicellular composition, coordinated remodeling processes, and hierarchical extracellular matrix organization. In this review, we examine progress toward bone organoid development within the broader landscape of soft-tissue organoid innovation and then use diabetes-associated skeletal disorders as a representative case study to highlight the unmet needs and illustrate how next-generation bone organoids could advance the modeling and management of these complex diseases.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.