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Article

Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis.

Human genetics - 1 Nov 2003

Selman Moises, Lin Hung-Mo, Montaño Martha, Jenkins Audrey L, Estrada Andrea, Lin Zhenwu, Wang Guirong, DiAngelo Susan L, Guo Xiaoxuan, Umstead Todd M, Lang C Max, Pardo Annie, Phelps David S, Floros Joanna

Abstract excerpt

Derangement in pulmonary surfactant or its components and alveolar collapse are common findings in idiopathic pulmonary fibrosis (IPF). Surfactant proteins play important roles in innate host defense and normal function of the lung. We examined associations between IPF and genetic polymorphic var...

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Share to Genetic Predisposition to Disease
Share to Polymorphism, Single Nucleotide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pulmonary Fibrosis

Share to Pulmonary Surfactant-Associated Protein A

Share to Pulmonary Surfactant-Associated Protein B

Share to Pulmonary Surfactant-Associated Protein C

Share to Pulmonary Surfactant-Associated Protein D

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Source

Identifiers

PMID: 13680361
DOI: 10.1007/s00439-003-1015-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-13680361-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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