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Article

ADAM33 gene polymorphisms are associated with the risk of idiopathic pulmonary fibrosis.

Lung - 1 Aug 2014

Uh Soo-Taek, Jang An-Soo, Park Sung-Woo, Park Jong-Sook, Min Chang-Gi, Kim Yong Hoon, Park Byung-Lae, Shin Hyoung Doo, Kim Dong Soon, Park Choon-Sik

Abstract excerpt

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is characterized by progressive dyspnea and worsening lung function due to remodeling of the lung, including epithelial mesenchymal transition. ADAM33 is a disintegrin and metalloprotease domain-containing protein, which may be related to lung fibrosis by exerting angiogenesis and remodeling of the lung. Thus, we evaluated the association of single-nucleotide...

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Source

Identifiers

PMID: 24728305
DOI: 10.1007/s00408-014-9578-5

Genes

ADAM33
MAF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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