Endoglin and Activin Receptor-like Kinase 1 (Alk1) Modify Adrenomedullin Expression in an Organ-Specific Manner in Mice

SIMPLE SUMMARY: Hereditary hemorrhagic telangiectasia (HHT) is called a rare disease because it affects relatively few people. It is characterized by malformations in some blood vessels and usually results in profuse nose bleedings. In a recent article, we found that these patients have higher level...

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Detalles Bibliográficos
Autores principales: García-Sanmartín, Josune, Narro-Íñiguez, Judit, Rodríguez-Barbero, Alicia, Martínez, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945164/
https://www.ncbi.nlm.nih.gov/pubmed/35336733
http://dx.doi.org/10.3390/biology11030358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945164/
https://www.ncbi.nlm.nih.gov/pubmed/35336733
http://dx.doi.org/10.3390/biology11030358

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