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Related Concept Videos

EPS and iPS Cells in Disease Research01:21

EPS and iPS Cells in Disease Research

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Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...
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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
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Related Experiment Video

Updated: Sep 18, 2025

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
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Modeling CF Patient-Specific Responses to CFTR Modulators Using Human Induced Pluripotent Stem Cells

Kayshani R Kanagarajah1, Ming Jia Michael Wu2, Timothy Lam2

  • 1The Hospital for Sick Children, Toronto, Canada.

American Journal of Respiratory and Critical Care Medicine
|June 23, 2025
PubMed
Summary

No abstract available in PubMed .

Keywords:
CFTR modulatorsDisease modelingGene-corrected isogenic controlsInduced pluripotent stem cellsPrecision medicine

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