Evidence map›Paper›PMID 37126720›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Modeling human skeletal development using human pluripotent stem cells.

Shireen R Lamandé, Elizabeth S Ng, Trevor L Cameron, Louise H W Kung, Lisa Sampurno, Lynn Rowley, Jinia Lilianty, Yudha Nur Patria, Tayla Stenta, Eric Hanssen and 6 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
16.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
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  8. Bridging skeletal stem cell diversity and human skeletal modeling.Journal of bone and mineral metabolism · 2026
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  19. Utilization of Stem Cells in Medicine: A Narrative Review.International journal of molecular sciences · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 2 countries.

Shireen R LamandéMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0003-2938-2711
Elizabeth S NgMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Trevor L CameronMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0002-3348-8562
Louise H W KungMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0002-1959-7009
Lisa SampurnoMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Lynn RowleyMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-8395-9708
Jinia LiliantyMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-8333-9744
Yudha Nur PatriaMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0002-4802-2685
Tayla StentaMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0003-4794-030X
Eric HanssenIan Holmes Imaging Center and Department of Biochemistry and Pharmacology, Bio21 Institute, University of Melbourne, Parkville, VIC 3010, Australia.ORCID 0000-0002-4064-1844
Katrina M BellMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Ritika SaxenaMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-5412-2255
Kathryn S StokDepartment of Biomedical Engineering, University of Melbourne, Parkville, VIC 3010, Australia.
Edouard G StanleyMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0002-6389-3665
Andrew G ElefantyMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-6448-8314
John F BatemanMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-8542-0730
The University of Melbourne · AUMurdoch Children's Research Institute · AUUniversitas Gadjah Mada · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondrocytes and osteoblasts differentiated from induced pluripotent stem cells (iPSCs) will provide insights into skeletal development and genetic skeletal disorders and will generate cells for regenerative medicine applications. Here, we describe a method that directs iPSC-derived sclerotome to chondroprogenitors in 3D pellet culture then to articular chondrocytes or, alternatively, along the growth plate cartilage pathway to become hypertrophic chondrocytes that can transition to osteoblasts. Osteogenic organoids deposit and mineralize a collagen I extracellular matrix (ECM), mirroring in vivo endochondral bone formation. We have identified gene expression signatures at key developmental stages including chondrocyte maturation, hypertrophy, and transition to osteoblasts and show that this system can be used to model genetic cartilage and bone disorders.

Indexed as

CartilageInduced Pluripotent Stem CellsCell DifferentiationChondrocytesHumansOsteoblastsbonecartilagegenetic skeletal disorderiPSC

Identifiers

PMID37126720
PMCPMC10175848
OpenAlexW4367626138

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.