Murine models of sickle cell disease and beta-thalassemia demonstrate pulmonary hypertension with distinctive features

Sickle cell anemia and β-thalassemia intermedia are very different genetically determined hemoglobinopathies predisposing to pulmonary hypertension. The etiologies responsible for the associated development of pulmonary hypertension in both diseases are multi-factorial with extensive mechanistic con...

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Detalles Bibliográficos
Autores principales: Buehler, Paul W., Swindle, Delaney, Pak, David I., Fini, Mehdi A., Hassell, Kathryn, Nuss, Rachelle, Wilkerson, Rebecca B., D’Alessandro, Angelo, Irwin, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579334/
https://www.ncbi.nlm.nih.gov/pubmed/34777785
http://dx.doi.org/10.1177/20458940211055996

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579334/
https://www.ncbi.nlm.nih.gov/pubmed/34777785
http://dx.doi.org/10.1177/20458940211055996

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