Cargando…
Role for miR-204 in human pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) is characterized by enhanced proliferation and reduced apoptosis of pulmonary artery smooth muscle cells (PASMCs). Because microRNAs have been recently implicated in the regulation of cell proliferation and apoptosis, we hypothesized that these regulatory molecu...
Autores principales: | Courboulin, Audrey, Paulin, Roxane, Giguère, Nellie J., Saksouk, Nehmé, Perreault, Tanya, Meloche, Jolyane, Paquet, Eric R., Biardel, Sabrina, Provencher, Steeve, Côté, Jacques, Simard, Martin J., Bonnet, Sébastien |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058572/ https://www.ncbi.nlm.nih.gov/pubmed/21321078 http://dx.doi.org/10.1084/jem.20101812 |
Ejemplares similares
-
DNA Damage and Pulmonary Hypertension
por: Ranchoux, Benoît, et al.
Publicado: (2016) -
Krüppel-like Factor 5 contributes to pulmonary artery smooth muscle proliferation and resistance to apoptosis in human pulmonary arterial hypertension
por: Courboulin, Audrey, et al.
Publicado: (2011) -
Signal transduction in the development of pulmonary arterial hypertension
por: Malenfant, Simon, et al.
Publicado: (2013) -
STAT3 signaling in pulmonary arterial hypertension
por: Paulin, Roxane, et al.
Publicado: (2012) -
Critical Role for the Advanced Glycation End‐Products Receptor in Pulmonary Arterial Hypertension Etiology
por: Meloche, Jolyane, et al.
Publicado: (2013)