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Insulin mutations impair beta-cell development in a patient-derived iPSC model of neonatal diabetes
Insulin gene mutations are a leading cause of neonatal diabetes. They can lead to proinsulin misfolding and its retention in endoplasmic reticulum (ER). This results in increased ER-stress suggested to trigger beta-cell apoptosis. In humans, the mechanisms underlying beta-cell failure remain unclear...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | eLife |
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| Prif Awduron: | , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
eLife Sciences Publications, Ltd
2018
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6294552/ https://ncbi.nlm.nih.gov/pubmed/30412052 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.38519 |
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