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...

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Detalles Bibliográficos
Autores principales: Sánchez-Duffhues, Gonzalo, Hiepen, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487005/
https://www.ncbi.nlm.nih.gov/pubmed/37681932
http://dx.doi.org/10.3390/cells12172200

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487005/
https://www.ncbi.nlm.nih.gov/pubmed/37681932
http://dx.doi.org/10.3390/cells12172200

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