Idiopathic pulmonary fibrosis is associated with endothelial to mesenchymal transition.

American journal of respiratory cell and molecular biology ·Vol. 43 ·No. 2 ·2010-08-00 ·Pages 129-30

Nataraj D, Ernst A, Kalluri R

Abstract

暂无摘要

MeSH Terms

Animals Bone Marrow Cells/cytology Cytoskeleton/metabolism Disease Progression Endothelium/pathology Fibroblasts/pathology Fibrosis Gene Expression Regulation Humans Mesoderm/pathology Models, Biological Pulmonary Fibrosis/physiopathology Signal Transduction Stem Cells/cytology Transforming Growth Factor beta/metabolism ras Proteins/metabolism

Chemicals

Transforming Growth Factor beta ras Proteins

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Nataraj Dilip

Ernst Armin

Kalluri Raghu

Article Info

Journal

American journal of respiratory cell and molecular biology

Abbr.

Am J Respir Cell Mol Biol

ISSN

1535-4989

DOI

10.1165/rcmb.2010-0044ED

Published

2010-08-00

Pages

129-30

Language

English

Region

United States

NLM ID

8917225

Subset

Grants

NIDDK NIH HHS · R01 DK055001 · United States

Corrections

CommentOn

PMID: 19767450

External Links

PubMed source DOI: 10.1165/rcmb.2010-0044ED View journal details

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Idiopathic pulmonary fibrosis is associated with endothelial to mesenchymal transition.

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