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Missed that important publication? With an explosion in scientific literature on advanced in vitro methods, it's becoming increasingly difficult to keep up.

We select, analyze, and summarize key research findings, distilling them into structured summaries for easy and time-saving exploration of in vitro use cases.​

Our curated database showcases context of use, opening up new research avenues.

Human-based methods

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Number of results

64

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Heart Organoids

CELL TYPE

Human iPSC line

CONTEXT OF USE

The ability of human heart organoids to recapitulate the pathophysiological features of pregestational diabetes-induced congenital heart disease| including higher frequence of arrhythmic events| reduction in beating frequency| and cardiomyocyte hypertrophy.

REFERENCE

Kostina A| Lewis-Israeli YR| Abdelhamid M| et al. ER stress and lipid imbalance drive diabetic embryonic cardiomyopathy in an organoid model of human heart development. Stem Cell Reports| Volume 19| Issue 3| P317-330| March 12| 2024. doi:10.1016/j.stemcr.2024.01.003

YEAR

2024

LINK

METHOD

Human Multi-Chamber Cardioids

CELL TYPE

Human iPSC line. Human PSC lines.

CONTEXT OF USE

The ability of the human cardioid platform to recapitulate the development of all major embryonic heart compartments (right and left ventricles| atria| outflow tract| atrioventricular canal) and to model the effects of internal and external factors (mutations| drugs) on congenital heart disease pathogenesis.
Related pathologies: Congentital heart disease.
Potential applications: Mechanistic studies; Target identification; Drug testing.

REFERENCE

Schmidt C| Deyett A| Ilmer T| et al. Multi-chamber cardioids unravel human heart development and cardiac defects. Cell| Volume 186| Issue 25| p5587-5605.e27| December 07| 2023. doi: 10.1016/j.cell.2023.10.030

YEAR

2023

LINK

METHOD

Microvascularised Cardiac Spheroids-on-a-Chip

CELL TYPE

Human iPSC. Human primary cells.

CONTEXT OF USE

The ability of the microvascularized cardiac spheroid-on-chip model to produce perfusable and functional cardiac spheroids| enhancing their physiological relevance for cardiotoxicity testing.

REFERENCE

Di Cio S| Marhuenda E| Haddrick M| Gautrot JE. Vascularised cardiac spheroids-on-a-chip for testing the toxicity of therapeutics. Scientific Reports. 2024;14(1):3370. doi:10.1038/s41598-024-53678-w

YEAR

2024

LINK

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