Article
Investigation Diagnostic Gene Markers and Immune Infiltration in Idiopathic Pulmonary Fibrosis
2023-09-28
Abstract excerpt
<h4>Objective: </h4> Idiopathic pulmonary fibrosis (IPF) is a difficult to cure and low survival lung disease, and the pathogenesis has not been elucidated clearly. This study is to explore the potential hub genes in IPF and explore their role in the progression of IPF with immune cell infiltration, providing evidence support for potential diagnostic markers and targets of IPF. <h4>Method: </h4> Download the data...
Topics
Open a Topic to create a Post that cites this publication.
- Cardiovascular, Neuropeptides, and Oxidative Stress Research
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Medical Imaging and Pathology Studies
- Occupational and environmental lung diseases
- Pulmonary Hypertension Research and Treatments
- Renin-Angiotensin System Studies
- Sarcoidosis and Beryllium Toxicity Research
- Systemic Sclerosis and Related Diseases
Identifiers and source
- Literature Corpus work
- 678437c1-5eb5-539a-95f6-c8534cc4103e
- DOI
- 10.21203/rs.3.rs-3369276/v1
