ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
about
Candidate genes of idiopathic pulmonary fibrosis: current evidence and researchPersonalized medicine: applying 'omics' to lung fibrosisMolecular biomarkers in idiopathic pulmonary fibrosisEvolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genesAn official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and managementELMO domains, evolutionary and functional characterization of a novel GTPase-activating protein (GAP) domain for Arf protein family GTPasesA testis-specific regulator of complex and hybrid N-glycan synthesis.Deletion of 4q28.3-31.23 in the background of multiple malformations with pulmonary hypertension.Genetic predisposition to respiratory diseases: infiltrative lung diseases.Positional cloning reveals strain-dependent expression of Trim16 to alter susceptibility to bleomycin-induced pulmonary fibrosis in mice.Familial Interstitial Pneumonia (FIP).Regulation of myofibroblast differentiation by miR-424 during epithelial-to-mesenchymal transition.Genetics in pulmonary fibrosis--familial cases provide clues to the pathogenesis of idiopathic pulmonary fibrosis.Genetics of Interstitial Lung Disease: Vol de Nuit (Night Flight).ELMOD2 is anchored to lipid droplets by palmitoylation and regulates adipocyte triglyceride lipase recruitment.Smoking and idiopathic pulmonary fibrosisEcogenomics of respiratory diseases of public health significanceMicroRNAs as potential targets for progressive pulmonary fibrosisIntegrating genomic and clinical medicine: searching for susceptibility genes in complex lung diseasesGenetic analysis of sporadic and familial interstitial pneumoniaEpidemiology of idiopathic pulmonary fibrosis.Determinants of initiation and progression of idiopathic pulmonary fibrosis.Idiopathic pulmonary fibrosis-an epidemiological and pathological review.Viral infection and aging as cofactors for the development of pulmonary fibrosis.The genetic and environmental causes of pulmonary fibrosis.Biomarkers in idiopathic pulmonary fibrosis.Genetic background of idiopathic pulmonary fibrosis.Pathogenesis of idiopathic pulmonary fibrosis and its clinical implications.Facts and promises on lung biomarkers in interstitial lung diseases.The genetic basis of idiopathic pulmonary fibrosisGTPase-activating protein Elmod2 is essential for meiotic progression in mouse oocytes.
P2860
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P2860
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@ast
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@en
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@nl
type
label
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@ast
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@en
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@nl
prefLabel
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@ast
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@en
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@nl
P2093
P2860
P50
P356
P1476
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
@en
P2093
Kaisa Salmenkivi
Marko Rehn
Myriam Peyrard-Janvid
Paivi Lahermo
Pentti Tukiainen
Tarja Laitinen
Ulla Hodgson
Vesa Ollikainen
Vuokko Kinnula
P2860
P304
P356
10.1086/504639
P407
P577
2006-05-09T00:00:00Z