Cargando…
Artificial neural network identified the significant genes to distinguish Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease that causes irreversible damage to lung tissue characterized by excessive deposition of extracellular matrix (ECM) and remodeling of lung parenchyma. The current diagnosis of IPF is complex and usually completed by a mult...
Autores principales: | Li, Zhongzheng, Wang, Shenghui, Zhao, Huabin, Yan, Peishuo, Yuan, Hongmei, Zhao, Mengxia, Wan, Ruyan, Yu, Guoying, Wang, Lan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867697/ https://www.ncbi.nlm.nih.gov/pubmed/36681777 http://dx.doi.org/10.1038/s41598-023-28536-w |
Ejemplares similares
-
Single-Cell RNA Sequencing Provides New Insights into Therapeutic Roles of Thyroid Hormone in Idiopathic Pulmonary Fibrosis
por: Wang, Lan, et al.
Publicado: (2023) -
Inhibition of MAD2L1 Mediates Pulmonary Fibrosis through Impairment of Mitochondrial Function and Induction of Cell Senescence
por: Wang, Lan, et al.
Publicado: (2022) -
ADRB2 inhibition combined with antioxidant treatment alleviates lung fibrosis by attenuating TGFβ/SMAD signaling in lung fibroblasts
por: Wan, Ruyan, et al.
Publicado: (2023) -
Identification ferroptosis-related hub genes and diagnostic model in Alzheimer’s disease
por: Zhao, Huabin, et al.
Publicado: (2023) -
Injured Endothelial Cell: A Risk Factor for Pulmonary Fibrosis
por: Zhao, Weiming, et al.
Publicado: (2023)