The Potential Role of MiRs-139-5p and -454-3p in Endoglin-Knockdown-Induced Angiogenic Dysfunction in HUVECs

Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disease characterized by aberrant angiogenesis and vascular malformations. Mutations in the transforming growth factor beta co-receptor, endoglin (ENG), account for approximately half of known HHT cases and cause abnormal angiogenic activ...

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Detalles Bibliográficos
Autores principales: Cannavicci, Anthony, Zhang, Qiuwang, Kutryk, Michael J. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003543/
https://www.ncbi.nlm.nih.gov/pubmed/36902347
http://dx.doi.org/10.3390/ijms24054916

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003543/
https://www.ncbi.nlm.nih.gov/pubmed/36902347
http://dx.doi.org/10.3390/ijms24054916

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