Association between MUC5B and TERT polymorphisms and different interstitial lung disease phenotypes

scientific article published on 17 December 2013

Association between MUC5B and TERT polymorphisms and different interstitial lung disease phenotypes is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.TRSL.2013.12.006
P932PMC publication ID4074379
P698PubMed publication ID24434656
P5875ResearchGate publication ID259769982

P50authorYava Jones-HallQ92528058
P2093author name stringChong Li
Min Zhang
Rongrong Wei
Wanqing Liu
Jamie L Myers
Imre Noth
P2860cites workIdiopathic pulmonary fibrosis--a sticky businessQ83910473
MUC5B promoter polymorphism and pulmonary fibrosisQ84550972
???Q28215495
A mutation in the surfactant protein C gene associated with familial interstitial lung diseaseQ28201394
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosisQ28943334
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association studyQ28943525
A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosisQ29417118
Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease. NHLBI/WHO Global Initiative for Chronic Obstructive Lung Disease (GOLD) Workshop summaryQ29614692
Telomerase mutations in families with idiopathic pulmonary fibrosisQ29615671
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer.Q30374030
Clinical advances in the diagnosis and therapy of the interstitial lung diseasesQ33214781
Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutationsQ33587591
Structure and function of the polymeric mucins in airways mucus.Q34686458
A variant in the promoter of MUC5B and idiopathic pulmonary fibrosisQ35083039
Idiopathic pulmonary fibrosis: update on genetic discoveriesQ35092480
Distinctive epidermal growth factor receptor/extracellular regulated kinase-independent and -dependent signaling pathways in the induction of airway mucin 5B and mucin 5AC expression by phorbol 12-myristate 13-acetateQ35570361
Adult-onset pulmonary fibrosis caused by mutations in telomeraseQ35759839
A common MUC5B promoter polymorphism and pulmonary fibrosis.Q36048530
Genetic factors in pulmonary fibrotic disordersQ36694852
MUC5B promoter polymorphism and interstitial lung abnormalitiesQ37105760
Identification of seven loci affecting mean telomere length and their association with diseaseQ37735420
Epithelial mucin stores are increased in the large airways of smokers with airflow obstructionQ42502620
Idiopathic pulmonary fibrosis: a disorder of epithelial cell dysfunctionQ42740080
Global Initiative for Chronic Obstructive Lung Diseases (GOLD)Q74763638
P433issue5
P921main subjectinterstitial lung diseaseQ1153419
P304page(s)494-502
P577publication date2013-12-17
P1433published inTranslational ResearchQ15761127
P1476titleAssociation between MUC5B and TERT polymorphisms and different interstitial lung disease phenotypes
P478volume163

Reverse relations

cites work (P2860)
Q38450487A meta-analysis examining the association between the MUC5B rs35705950 T/G polymorphism and susceptibility to idiopathic pulmonary fibrosis
Q37149994Association Between the MUC5B Promoter Polymorphism rs35705950 and Idiopathic Pulmonary Fibrosis: A Meta-analysis and Trial Sequential Analysis in Caucasian and Asian Populations
Q37081313Association Study for 26 Candidate Loci in Idiopathic Pulmonary Fibrosis Patients from Four European Populations
Q91605838Association between FCGR2A rs1801274 and MUC5B rs35705950 variations and pneumonia susceptibility
Q37094624CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism
Q36119163Epigenetics in lung fibrosis: from pathobiology to treatment perspective
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Q30388977Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia
Q37563857IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER.
Q93091814Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways
Q38821078Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways
Q35786160Incorporating genetics into the identification and treatment of Idiopathic Pulmonary Fibrosis
Q47239342Insights from human genetic studies of lung and organ fibrosis
Q26998459Is there still hope for single therapies: how do we set up experimental systems to efficiently test combination therapies?
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Q38269057Promising new treatment targets in patients with fibrosing lung disorders
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