Expression levels of fibrosis and inflammatory markers in cultured... | Download Scientific Diagram
Diagnosis and management of idiopathic pulmonary fibrosis: French practical guidelines | European Respiratory Society
Matrix regulation of idiopathic pulmonary fibrosis: the role of enzymes | Fibrogenesis & Tissue Repair | Full Text
Idiopathic Pulmonary Fibrosis | NEJM
JCI - Fra-2–expressing macrophages promote lung fibrosis
Vitamin D suppresses bleomycin-induced pulmonary fibrosis by targeting the local renin–angiotensin system in the lung | Scientific Reports
Reprogramming of profibrotic macrophages for treatment of bleomycin‐induced pulmonary fibrosis | EMBO Molecular Medicine
Time for a change: is idiopathic pulmonary fibrosis still idiopathic and only fibrotic? - The Lancet Respiratory Medicine
Genetic Risk Factors for Idiopathic Pulmonary Fibrosis: Insights into | JIR
Administration of aloperine attenuated lung fibrosis after BLM... | Download Scientific Diagram
Frontiers | Quantification of Lung Fibrosis in IPF-Like Mouse Model and Pharmacological Response to Treatment by Micro-Computed Tomography
Sulforaphane prevents bleomycin‑induced pulmonary fibrosis in mice by inhibiting oxidative stress via nuclear factor erythroid 2‑related factor‑2 activation
Blockade of IL-6 Trans Signaling Attenuates Pulmonary Fibrosis | The Journal of Immunology
IJMS | Free Full-Text | Idiopathic Pulmonary Fibrosis: Pathogenesis and the Emerging Role of Long Non-Coding RNAs | HTML
Recent Advances in Molecular Diagnosis of Pulmonary Fibrosis for Precision Medicine | ACS Pharmacology & Translational Science
Unifying mechanism for different fibrotic diseases | PNAS
IJMS | Free Full-Text | Idiopathic Pulmonary Fibrosis: Pathogenesis and the Emerging Role of Long Non-Coding RNAs | HTML
Targeting Runt-Related Transcription Factor 1 Prevents Pulmonary Fibrosis and Reduces Expression of Severe Acute Respiratory Syndrome Coronavirus 2 Host Mediators - The American Journal of Pathology
Frontiers | Dissecting the Role of Mesenchymal Stem Cells in Idiopathic Pulmonary Fibrosis: Cause or Solution
Fibroblasts and their responses to chronic injury in pulmonary fibrosis - ScienceDirect
![Differential Lysotracker Uptake Defines Two Populations of Distal Epithelial Cells in Idiopathic Pulmonary Fibrosis[v1] | Preprints](https://www.preprints.org/img/dyn_abstract_figures/2021/11/1272817178e65d48c7849464c391563d/preprints-52023-graphical.v1(1).jpg "Differential Lysotracker Uptake Defines Two Populations of Distal Epithelial Cells in Idiopathic Pulmonary Fibrosis[v1] | Preprints")
Differential Lysotracker Uptake Defines Two Populations of Distal Epithelial Cells in Idiopathic Pulmonary Fibrosis[v1] | Preprints
MicroRNAs in idiopathic pulmonary fibrosis: involvement in pathogenesis and potential use in diagnosis and therapeutics - ScienceDirect
Idiopathic pulmonary fibrosis: Are any of the morphological-molecular markers useful in clinical management? | Semantic Scholar
The histone methyltransferase DOT1L is a new epigenetic regulator of pulmonary fibrosis | Cell Death & Disease
Genetic Risk Factors for Idiopathic Pulmonary Fibrosis: Insights into | JIR
