Cargando…
Lung Fibroblasts from Patients with Idiopathic Pulmonary Fibrosis Exhibit Genome-Wide Differences in DNA Methylation Compared to Fibroblasts from Nonfibrotic Lung
Excessive fibroproliferation is a central hallmark of idiopathic pulmonary fibrosis (IPF), a chronic, progressive disorder that results in impaired gas exchange and respiratory failure. Fibroblasts are the key effector cells in IPF, and aberrant expression of multiple genes contributes to their exce...
Autores principales: | Huang, Steven K., Scruggs, Anne M., McEachin, Richard C., White, Eric S., Peters-Golden, Marc |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162578/ https://www.ncbi.nlm.nih.gov/pubmed/25215577 http://dx.doi.org/10.1371/journal.pone.0107055 |
Ejemplares similares
-
Iron deposition and increased alveolar septal capillary density in nonfibrotic lung tissue are associated with pulmonary hypertension in idiopathic pulmonary fibrosis
por: Kim, Kyung-Hee, et al.
Publicado: (2010) -
Invadosome Formation by Lung Fibroblasts in Idiopathic Pulmonary Fibrosis
por: Lebel, Mégane, et al.
Publicado: (2022) -
Histone modifications are responsible for decreased Fas expression and apoptosis resistance in fibrotic lung fibroblasts
por: Huang, S K, et al.
Publicado: (2013) -
Effect of Hypoxia in the Transcriptomic Profile of Lung Fibroblasts from Idiopathic Pulmonary Fibrosis
por: Romero, Yair, et al.
Publicado: (2022) -
Altered intercellular communication in lung fibroblast cultures from patients with idiopathic pulmonary fibrosis
por: Trovato-Salinaro, Angela, et al.
Publicado: (2006)