Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

FAM13A polymorphism as a prognostic factor in patients with idiopathic pulmonary fibrosis.

Respiratory medicine - 1 Feb 2017

Hirano Chihiro, Ohshimo Shinichiro, Horimasu Yasushi, Iwamoto Hiroshi, Fujitaka Kazunori, Hamada Hironobu, Hattori Noboru, Shime Nobuaki, Bonella Francesco, Guzman Josune, Costabel Ulrich, Kohno Nobuoki

Abstract excerpt

BACKGROUND: Family with sequence similarity 13, member A (FAM13A) variants have been associated with susceptibility to chronic lung diseases. A recent genome-wide association study has shown an association between a polymorphism in FAM13A rs2609255 and idiopathic interstitial pneumonias in a Caucasian population. However, the relationship between rs2609255 polymorphism and prognosis in idiopathic interstitial...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Acute Disease
Share to Aged
Share to Case-Control Studies
Share to Gene Frequency
Share to GTPase-Activating Proteins
Share to Idiopathic Pulmonary Fibrosis
Share to Kaplan-Meier Estimate
Share to Prognosis

Source

Identifiers

PMID: 28137485
DOI: 10.1016/j.rmed.2016.12.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FAM13A polymorphism as a prognostic factor in patients with idiopathic pulmonary fibrosis.PMID 28137485Read ↗

Identification of FAM13A gene associated with the ratio of FEV1 to FVC in Korean population by genome-wide association studies including gene-environment interactions.Semantic proximity Read ↗

Association of FAM13A polymorphisms with COPD and COPD-related phenotypes in Han Chinese.Semantic proximity Read ↗

Association of lung function genes with chronic obstructive pulmonary disease.Semantic proximity Read ↗

Association between MUC5B polymorphism and susceptibility and severity of idiopathic pulmonary fibrosis.Semantic proximity Read ↗

Variants in FAM13A are associated with chronic obstructive pulmonary disease.Semantic proximity Read ↗

Loss of family with sequence similarity 13, member A exacerbates pulmonary hypertension through accelerating endothelial-to-mesenchymal transitionSemantic proximity Read ↗

The rs2609255 polymorphism in the FAM13A gene is reproducibly associated with silicosis susceptibility in a Chinese population.Semantic proximity Read ↗

Potential clinical utility of MUC5B und TOLLIP single nucleotide polymorphisms (SNPs) in the management of patients with IPFSemantic proximity Read ↗

Potential clinical utility of MUC5B und TOLLIP single nucleotide polymorphisms (SNPs) in the management of patients with IPF.Semantic proximity Read ↗

MUC5B rs35705950 and its association with survival in Brazilian patients with idiopathic pulmonary fibrosis: A longitudinal cohort study.Semantic proximity Read ↗

MUC5B rs35705950 minor allele associates with older age and better survival in idiopathic pulmonary fibrosis.Semantic proximity Read ↗

FAM13A is a modifier gene of cystic fibrosis lung phenotype regulating rhoa activity, actin cytoskeleton dynamics and epithelial-mesenchymal transition.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.