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Structural consequences of BMPR2 kinase domain mutations causing pulmonary arterial hypertension

Bone morphogenetic proteins (BMPs) are secreted ligands of the transforming growth factor-β (TGF-β) family that control embryonic patterning, as well as tissue development and homeostasis. Loss of function mutations in the type II BMP receptor BMPR2 are the leading cause of pulmonary arterial hypert...

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Dettagli Bibliografici
Pubblicato in:Sci Rep
Autori principali: Chaikuad, Apirat, Thangaratnarajah, Chancievan, von Delft, Frank, Bullock, Alex N.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6892941/
https://ncbi.nlm.nih.gov/pubmed/31797984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-54830-7
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