Integrative multi-omics analysis reveals novel idiopathic pulmonary fibrosis endotypes associated with disease progression (additional file 6)

Authors

Peifeng Ruan, Yale University
Jamie L. Todd, Duke University
Hongyu Zhao, Yale University
Yi Liu, Boehringer Ingelheim (United States)
Richard Vinisko, Boehringer Ingelheim (United States)
Julia F. Soellner, Boehringer Ingelheim (Germany)
Ramona Schmid, Boehringer Ingelheim (Germany)
Robert J. Kaner, Cornell University
Tracy R. Luckhardt, University of Alabama at Birmingham
Megan L. Neely, Duke University Hospital, Duke University
Imre Noth, University of Virginia
Mary Porteous, Hospital of the University of Pennsylvania
Rishi Raj, Stanford University
Zeenat Safdar, Houston Methodist
Mary E. Strek, University of Chicago
Christian Hesslinger, Boehringer Ingelheim (Germany)
Scott M. Palmer, Duke University
Thomas B. Leonard, Boehringer Ingelheim (United States)
Margaret L. Salisbury, Vanderbilt University Medical Center

Publication Date

6-22-2023

Abstract

Additional file 6: Table S8. Canonical pathways that were significantly enriched (FDR p-value < 0.05) for genes associated with down-regulated proteins.

Keywords

Medicine, Cell Biology, Genetics, FOS: Biological sciences, Molecular Biology, Pharmacology, Biotechnology, Cancer, Virology, Computational Biology

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