About
Research
Overview
Dr. Kaminski’s team main ambition is to uncover the mechanisms, and thus have a significant impact on the management of advanced lung diseases with a specific focus on IPF, a chronic progressive interstitial lung disease that is currently incurable. To study these mechanisms Dr. Kaminski’s team applies systems biology approaches that incorporate a combination of traditional molecular biology methods, high-throughput genomic technologies such as transcript level profiling (single cell RNA sequencing and epigenomic profiling ) , genome scale analyses of gene variants, advanced bioinformatics approaches and targeted proteomic approaches. These studies have led to shifts in the perception of pulmonary fibrosis, the realization that aberrant activation of developmental pathways is at the core of lung fibrosis, the discovery of the role of microRNAs in IPF, the identification and validation of novel prognostic biomarkers in the bloodstream, as well many additional insights.
Mechanisms of pulmonary fibrosis and other chronic lung diseases
- Understanding and identifying the genetic and molecular networks that determine the lung phenotype using high throughput high resolution genomic and proteomic technologies.
- Role of miRNA in advanced lung disease (IPF, Emphysema).
- Role of other non-coding RNAs (lincRNAs) in advanced lung disease
- The IPF Cell Atlas (www.IPFCellAtlas.com)
- The Normal Aging Lung Cell Atlas
- The Pulmonary Fibrosis Connectome
- Epigenomics of chronic lung disease.
- Using AI to Integrate clinical, biological, genomic and proteomic data to identify new molecular phenotypes of disease.
New molecular targets in Pulmonary Fibrosis
- The role and regulation of microRNAs (let-7, mir-33, mir-29) in human pulmonary fibrosis and development of microRNA inhibitors and agonist for therapeutic interventions
- The role of large non-coding RNAs in pulmonary fibrosis
- Role of GPR87 in Pulmonary fibrosis
- The role of thyroid hormone signaling in epithelial cell protection in fibrosis
- Origin and role of Aberrant Basaloid Cells
- Novel lung resident cell specific therapeutic approaches in pulmonary fibrosis
Biomarker Discovery and Validation in chronic and progressive lung disease
- Approaches to the development of liquid biopsy in human pulmonary fibrosis and other interstitial lung disease
- Immune cells in interstitial lung diseaes
- Peripheral blood protein markers in lung fibrosis
- Genetic predictors of outcome in lung fibrosis
- Peripheral blood gene expression changes and disease progression
Medical Research Interests
Public Health Interests
Academic Achievements & Community Involvement
Clinical Care
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News & Links
Media
- Dr. Kaminski Receiving the Helmholtz International Award from Dr. Eickelberg in Munich, June 2013
How Lungs Age
Scientists created a cellular atlas of the lungs to pinpoint cells especially vulnerable to aging. They could be targeted to prevent acute and chronic lung diseases.
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Get In Touch
Contacts
Pulmonary, Critical Care & Sleep Medicine
300 Cedar Street, TAC-441 South, PO Box 208057
New Haven, CT 06520-8057
United States
Administrative Support
Locations
The Anlyan Center
Academic Office
300 Cedar Street, Ste S441D
New Haven, CT 06519
Appointments
203.737.4612Patient Care Locations
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