Human iPSCs as Model Systems for BMP-Related Rare Diseases
Disturbances in bone morphogenetic protein (BMP) signalling contribute to onset and development of a number of rare genetic diseases, including Fibrodysplasia ossificans progressiva (FOP), Pulmonary arterial hypertension (PAH), and Hereditary haemorrhagic telangiectasia (HHT). After decades of anima...
| Glavni autori: | , |
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| Format: | Članak |
| Jezik: | English |
| Izdano: |
MDPI AG
2023-09-01
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| Serija: | Cells |
| Teme: | |
| Online pristup: | https://www.mdpi.com/2073-4409/12/17/2200 |