Molecular and functional characterization of the BMPR2 gene in Pulmonary Arterial Hypertension
Abstract Pulmonary arterial hypertension is a progressive disease that causes the obstruction of precapillary pulmonary arteries and a sustained increase in pulmonary vascular resistance. The aim was to analyze functionally the variants found in the BMPR2 gene and to establish a genotype-phenotype c...
Guardado en:
Autores principales: | Guillermo Pousada, Vincenzo Lupo, Sheila Cástro-Sánchez, María Álvarez-Satta, Ana Sánchez-Monteagudo, Adolfo Baloira, Carmen Espinós, Diana Valverde |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/6b58ee7f72ba4e7fbad01dfe022de748 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Deficiency of Axl aggravates pulmonary arterial hypertension via BMPR2
por: Tatyana Novoyatleva, et al.
Publicado: (2021) -
The role of TGF-β or BMPR2 signaling pathway-related miRNA in pulmonary arterial hypertension and systemic sclerosis
por: Bei Xu, et al.
Publicado: (2021) -
Liver abnormalities in pulmonary arterial hypertension
por: Nils P. Nickel, et al.
Publicado: (2021) -
Systemic arterial properties in pulmonary hypertension
por: Randi Goodman, et al.
Publicado: (2021) -
Pulmonary artery dissection in long standing idiopathic pulmonary arterial hypertension: A case report
por: Luis Regalado, BS, MSc, et al.
Publicado: (2022)