Satish K. Madala

Dual targeting of MEK and PI3K pathways attenuates established and progressive pulmonary fibrosis.

Cardiac metabolic pathways affected in the mouse model of barth syndrome.

Fibrocytes Regulate Wilms Tumor 1-Positive Cell Accumulation in Severe Fibrotic Lung Disease.

p70 ribosomal S6 kinase regulates subpleural fibrosis following transforming growth factor-α expression in the lung.

IL-31-Driven Skin Remodeling Involves Epidermal Cell Proliferation and Thickening That Lead to Impaired Skin-Barrier Function.

Hsp90 regulation of fibroblast activation in pulmonary fibrosis.

Unsupervised gene expression analyses identify IPF-severity correlated signatures, associated genes and biomarkers.

Subacute TGFβ expression drives inflammation, goblet cell hyperplasia, and pulmonary function abnormalities in mice with effects dependent on CFTR function.

Wilms' tumor 1 drives fibroproliferation and myofibroblast transformation in severe fibrotic lung disease.

New therapeutics based on emerging concepts in pulmonary fibrosis.

Longitudinal free-breathing MRI measurement of murine lung physiology in a progressive model of lung fibrosis.

Dysregulation of Mesenchymal Cell Survival Pathways in Severe Fibrotic Lung Disease: The Effect of Nintedanib Therapy.

Heat shock protein 70 is a positive regulator of airway inflammation and goblet cell hyperplasia in a mouse model of allergic airway inflammation.

Subacute TGFβ Exposure Drives Airway Hyperresponsiveness in Cystic Fibrosis Mice through the PI3K Pathway.

Fibrocyte accumulation in the lungs of cystic fibrosis patients.

Inhibition of Aurora Kinase B attenuates fibroblast activation and pulmonary fibrosis.

Pan-transcriptome-based candidate therapeutic discovery for idiopathic pulmonary fibrosis.

Notch3: A New Culprit in Fibrotic Lung Disease.

The Protective Effects of IL-31RA Deficiency During Bleomycin-Induced Pulmonary Fibrosis.

Dysregulated overexpression of Sox9 induces fibroblast activation in pulmonary fibrosis.

ASK1ng to Delay the Progression of Pulmonary Fibrosis.

Consensus Gene Co-Expression Network Analysis Identifies Novel Genes Associated with Severity of Fibrotic Lung Disease.

Lung Fibrosis Finds an Unsung Hero in Neuropeptide Y.

Wnt signaling regulates ion channel expression to promote smooth muscle and cartilage formation in developing mouse trachea.

Wilms Tumor 1-Driven Fibroblast Activation and Subpleural Thickening in Idiopathic Pulmonary Fibrosis.

Interleukin 31 receptor alpha augments muscarinic acetylcholine receptor 3-driven calcium signaling and airway hyperresponsiveness in asthma.

Searching for an Animal Model with Clinical Features of Scleroderma.

Wnt signaling regulates ion channel expression to promote smooth muscle and cartilage formation in developing mouse trachea.

Pulmonary fibroelastosis - A review.

Nε-Carboxymethyl-Lysine Modification of Extracellular Matrix Proteins Augments Fibroblast Activation.

Interleukin 31 receptor α promotes smooth muscle cell contraction and airway hyperresponsiveness in asthma.

SEMA3B inhibits TGFβ-induced extracellular matrix protein production and its reduced levels are associated with a decline in lung function in IPF.

Emerging Concepts in Cytokine Regulation of Airway Remodeling in Asthma.