Organoids as tools for fundamental discovery and translation-a Keystone Symposia report.

dc.contributor.author

Cable, Jennifer

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Lutolf, Matthias P

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Fu, Jianping

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Park, Sunghee Estelle

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Apostolou, Athanasia

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Chen, Shuibing

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Song, Cheng Jack

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Spence, Jason R

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Liberali, Prisca

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Lancaster, Madeline

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Meier, Anna B

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Pek, Nicole Min Qian

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Wells, James M

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Capeling, Meghan M

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Uzquiano, Ana

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Musah, Samira

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Huch, Meritxell

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Gouti, Mina

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Hombrink, Pleun

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Quadrato, Giorgia

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Urenda, Jean-Paul

dc.date.accessioned

2024-12-29T06:47:56Z

dc.date.available

2024-12-29T06:47:56Z

dc.date.issued

2022-12

dc.description.abstract

Complex three-dimensional in vitro organ-like models, or organoids, offer a unique biological tool with distinct advantages over two-dimensional cell culture systems, which can be too simplistic, and animal models, which can be too complex and may fail to recapitulate human physiology and pathology. Significant progress has been made in driving stem cells to differentiate into different organoid types, though several challenges remain. For example, many organoid models suffer from high heterogeneity, and it can be difficult to fully incorporate the complexity of in vivo tissue and organ development to faithfully reproduce human biology. Successfully addressing such limitations would increase the viability of organoids as models for drug development and preclinical testing. On April 3-6, 2022, experts in organoid development and biology convened at the Keystone Symposium "Organoids as Tools for Fundamental Discovery and Translation" to discuss recent advances and insights from this relatively new model system into human development and disease.

dc.identifier.issn

0077-8923

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1749-6632

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https://hdl.handle.net/10161/31828

dc.language

eng

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Wiley

dc.relation.ispartof

Annals of the New York Academy of Sciences

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10.1111/nyas.14874

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

Organoids

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Stem Cells

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Animals

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Humans

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Models, Animal

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Models, Biological

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Organoids as tools for fundamental discovery and translation-a Keystone Symposia report.

dc.type

Journal article

pubs.begin-page

196

pubs.end-page

208

pubs.issue

1

pubs.organisational-group

Duke

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Pratt School of Engineering

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School of Medicine

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Cell Biology

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Biomedical Engineering

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Medicine

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Medicine, Nephrology

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Duke Cancer Institute

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Duke Regeneration Center

pubs.publication-status

Published

pubs.volume

1518

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