Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of the Molecular Subgroups in Idiopathic Pulmonary Fibrosis by Gene Expression Profiles

4 Oct 2021

Abstract excerpt

Background. Idiopathic Pulmonary Fibrosis (IPF) is one of the most common idiopathic interstitial pneumonia, which can occur all over the world. The median survival time of patients is about 3-5 years, and the mortality is relatively high. Objective. To reveal the potential molecular characteristics of IPF and deepen the understanding of the molecular mechanism of IPF. In order to provide some guidance for the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bioinformatics and Genomic Networks
Share to Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Share to Lung Cancer Treatments and Mutations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34646338
DOI: 10.1155/2021/7922594

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of the Molecular Subgroups in Idiopathic Pulmonary Fibrosis by Gene Expression ProfilesPMID 34646338Read ↗

A Comprehensive Study on Molecular Characteristics and Clinical Prognosis of Immune- Related Genes in Idiopathic Pulmonary FibrosisSemantic proximity Read ↗

Identification of key genes associated with Idiopathic Pulmonary Fibrosis by combining multiple analytical methodsSemantic proximity Read ↗

An 8-ferroptosis-related genes signature from Bronchoalveolar Lavage Fluid for prognosis in patients with idiopathic pulmonary fibrosisSemantic proximity Read ↗

Integrative bioinformatics analyses reveal new molecular signatures and immune infiltration in chronic obstructive pulmonary disease: mediators of airflow limitationSemantic proximity Read ↗

Bioinformatic analysis of differentially expressed genes and pathways in idiopathic pulmonary fibrosisSemantic proximity Read ↗

Transcriptomics in idiopathic pulmonary fibrosis unveiled: a new perspective from differentially expressed genes to therapeutic targetsSemantic proximity Read ↗

Bioinformatic Analyses of Potential Key Genes in the Pathogenesis of Idiopathic Pulmonary FibrosisSemantic proximity Read ↗

Integrative analyses of genes associated with idiopathic pulmonary fibrosisSemantic proximity Read ↗

Using bioinformatics approach identifies key genes and pathways in idiopathic pulmonary fibrosisSemantic proximity Read ↗

A prognostic model of idiopathic pulmonary fibrosis was constructed based on macrophage-related genes and mitochondria-related genesSemantic proximity Read ↗

Study on potential differentially expressed genes in idiopathic pulmonary fibrosis by bioinformatics and next generation sequencing data analysisSemantic proximity Read ↗

Identification of Molecular Subtypes and Key Gene of Pulmonary Fibrosis Through Gene Expression ProfilesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.