Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

scientific journal article

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis is …
instance of (P31):
meta-analysisQ815382
scholarly articleQ13442814

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P6179Dimensions Publication ID1040356735
P356DOI10.1038/NG.2609
P3181OpenCitations bibliographic resource ID981548
P932PMC publication ID3677861
P698PubMed publication ID23583980
P5875ResearchGate publication ID236180697

P50authorMark LathropQ6768494
Moisés SelmanQ87622005
Annie Pardo CemoQ87622008
Yoichiro KamataniQ88032943
Tasha E FingerlinQ89288019
Kevin F GibsonQ124694079
Janet TalbertQ125264091
Steve GroshongQ125264382
Diana ZelenikaQ30248012
Naftali KaminskiQ41048454
Miriam F MoffattQ56959224
P2093author name stringDavid A. Schwartz
Dong Soon Kim
Karl Kossen
David Lynch
Keith Smith
Yingze Zhang
Anna L. Peljto
Athol U. Wells
Barry J. Make
Brent S. Pedersen
Cheryl R. Markin
Christine Kim Garcia
David McKean
Dinesha S. Walek
Elissa Murphy
Elizabeth A. Regan
Gregory P. Cosgrove
Gunnar Gudmundsson
Harold R. Collard
Helgi J. Isaksson
James D. Crapo
James E. Loyd
Jerry J. Daniel
Joy D. Cogan
Kenneth B. Beckman
Kevin K. Brown
Lisa H. Lancaster
Mark P. Steele
Marvin I. Schwarz
Megan S. Devine
Paul J. Wolters
Philip L. Molyneaux
Raven N. Kidd
Roland M. du Bois
Scott D. Seiwert
Toby M. Maher
Weiming Zhang
Wendi R. Mason
Williamson Z. Bradford
P2860cites workUsual interstitial pneumonia in an adolescent with ABCA3 mutationsQ81643537
Spi-1/PU.1 oncoprotein affects splicing decisions in a promoter binding-dependent mannerQ83337192
Idiopathic pulmonary fibrosis--a sticky businessQ83910473
Idiopathic pulmonary fibrosis: new evidence and an improved standard of care in 2012Q84819949
A flexible and accurate genotype imputation method for the next generation of genome-wide association studiesQ21129496
Population structure and eigenanalysisQ21145248
Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratodermaQ22008664
alphaT-catenin: a novel tissue-specific beta-catenin-binding protein mediating strong cell-cell adhesionQ24291766
Hedgehog signaling pathway and gastric cancerQ24293156
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathyQ24300083
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other lociQ24306903
Genotype imputation with thousands of genomesQ24633967
The desmosomeQ24656653
Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiencyQ28140124
Compound heterozygosity for non-sense and mis-sense mutations in desmoplakin underlies skin fragility/woolly hair syndromeQ28200853
DP8 and DP9 have extra-enzymatic roles in cell adhesion, migration and apoptosisQ28240199
Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trialQ28250518
Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathyQ28274829
Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosisQ28283421
A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous systemQ28511734
A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosisQ29417118
A new multipoint method for genome-wide association studies by imputation of genotypesQ29547209
GCTA: a tool for genome-wide complex trait analysisQ29547216
METAL: fast and efficient meta-analysis of genomewide association scansQ29547217
LocusZoom: regional visualization of genome-wide association scan resultsQ29614868
Genotype imputation for genome-wide association studiesQ29614880
Rare variants create synthetic genome-wide associationsQ29614955
Telomerase mutations in families with idiopathic pulmonary fibrosisQ29615671
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer.Q30374030
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.Q30427183
???Q28215495
Epithelial endoplasmic reticulum stress and apoptosis in sporadic idiopathic pulmonary fibrosisQ30484036
Idiopathic pulmonary fibrosis: aberrant recapitulation of developmental programs?Q30841647
Structural haplotypes and recent evolution of the human 17q21.31 regionQ33608188
Variants in FAM13A are associated with chronic obstructive pulmonary diseaseQ33687879
Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biologyQ33927045
Inhibition of Wnt/beta-catenin/CREB binding protein (CBP) signaling reverses pulmonary fibrosisQ34069594
Genetic epidemiology of COPD (COPDGene) study designQ34074731
A linear complexity phasing method for thousands of genomesQ34237936
ABCA3 gene mutations in newborns with fatal surfactant deficiencyQ34308818
ABCA3 mutations associated with pediatric interstitial lung diseaseQ34455684
A variant in the promoter of MUC5B and idiopathic pulmonary fibrosisQ35083039
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPFQ35536294
Aberrant Wnt/beta-catenin pathway activation in idiopathic pulmonary fibrosisQ35749152
Adult-onset pulmonary fibrosis caused by mutations in telomeraseQ35759839
A common MUC5B promoter polymorphism and pulmonary fibrosis.Q36048530
Structural diversity and African origin of the 17q21.31 inversion polymorphismQ36129488
Clinical and pathologic features of familial interstitial pneumoniaQ36234581
Respiratory tract mucin genes and mucin glycoproteins in health and diseaseQ36350071
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humansQ36435865
Short telomeres are a risk factor for idiopathic pulmonary fibrosisQ36861819
Novel homozygous mutation in DSP causing skin fragility-woolly hair syndrome: report of a large family and review of the desmoplakin-related phenotypesQ37782390
Synthetic associations in the context of genome-wide association scan signalsQ37784094
Pathobiology of pulmonary fibrosisQ37972597
Desmoplakin acts as a tumor suppressor by inhibition of the Wnt/β-catenin signaling pathway in human lung cancer.Q39315240
Fibroblast activation protein: a serine protease expressed at the remodeling interface in idiopathic pulmonary fibrosisQ40334332
Genome-wide efficient mixed-model analysis for association studiesQ41961596
An immunohistochemical study of architectural remodeling and connective tissue synthesis in pulmonary fibrosisQ42496001
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindredQ42675595
Resistance to farnesyltransferase inhibitors in Bcr/Abl-positive lymphoblastic leukemia by increased expression of a novel ABC transporter homolog ATP11aQ42742534
Investigation of the fine structure of European populations with applications to disease association studiesQ44199896
Improved whole-chromosome phasing for disease and population genetic studiesQ44584387
Exposure to commonly prescribed drugs and the etiology of cryptogenic fibrosing alveolitis: a case-control study.Q50900397
Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort.Q54418482
Idiopathic Pulmonary FibrosisQ56804123
P4510describes a project that usesgenome-wide association studyQ1098876
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectpulmonary fibrosisQ32446
genome-wide association studyQ1098876
susceptibility locusQ62091149
P304page(s)613–620
P577publication date2013-06-01
P1433published inNature GeneticsQ976454
P1476titleGenome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
P478volume45

Reverse relations

cites work (P2860)
Q4103439813th ERS Lung Science Conference. The most important take home messages: News from the Underground
Q37213583A Chronic Obstructive Pulmonary Disease Susceptibility Gene, FAM13A, Regulates Protein Stability of β-Catenin
Q42228778A Dataset of 26 Candidate Gene and Pro-Inflammatory Cytokine Variants for Association Studies in Idiopathic Pulmonary Fibrosis: Frequency Distribution in Normal Czech Population
Q43062900A Phenome-Wide Association Study Identifies a Novel Asthma Risk Locus Near TERC.
Q58714376A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family
Q35826595A comparison of visual and quantitative methods to identify interstitial lung abnormalities
Q43178545A first glimpse at the early origins of idiopathic pulmonary fibrosis
Q42704966A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese
Q37652005A genome-wide association study yields five novel thyroid cancer risk loci
Q35177444A genome-wide pleiotropy scan for prostate cancer risk
Q42378561A global perspective of lung transplantation: Part 1 - Recipient selection and choice of procedure
Q30578066A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant
Q38450487A meta-analysis examining the association between the MUC5B rs35705950 T/G polymorphism and susceptibility to idiopathic pulmonary fibrosis
Q64063038A novel germline mutation of the gene in familial interstitial pneumonia
Q27014138A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung disease
Q47563113AJRCCM: 100-Year Anniversary. Progress in Interstitial Lung Disease
Q38846300Alveolar epithelial disintegrity in pulmonary fibrosis.
Q39014952An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
Q47213836An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study.
Q33734193Analysis of Microarray-Identified Genes and MicroRNAs Associated with Idiopathic Pulmonary Fibrosis
Q35819457Analysis of heat shock protein 70 gene polymorphisms Mexican patients with idiopathic pulmonary fibrosis
Q89067942Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study
Q50077754Another building in the IPF Manhattan plot skyline.
Q64916149Application of Isobaric Tags for Relative and Absolute Quantification (iTRAQ) Coupled with Two-Dimensional Liquid Chromatography/Tandem Mass Spectrometry in Quantitative Proteomic Analysis for Discovery of Serum Biomarkers for Idiopathic Pulmonary F
Q90051408Assessing thyroid cancer risk using polygenic risk scores
Q30253080Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study
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
Q41437838Association between MUC5B and TERT polymorphisms and different interstitial lung disease phenotypes
Q36464726Association between MUC5B polymorphism and susceptibility and severity of idiopathic pulmonary fibrosis
Q90654792Association between Telomere-Related Polymorphisms and the Risk of IPF and COPD as a Precursor Lesion of Lung Cancer: Findings from the Fukuoka Tobacco-Related Lung Disease (FOLD) Registry
Q28291143Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis
Q53286287Association of lung function genes with chronic obstructive pulmonary disease.
Q92483181Autophagy inhibition-mediated epithelial-mesenchymal transition augments local myofibroblast differentiation in pulmonary fibrosis
Q36105254BARD1 mediates TGF-β signaling in pulmonary fibrosis.
Q38833878Basal cells of the human airways acquire mesenchymal traits in idiopathic pulmonary fibrosis and in culture
Q64262272Bioinformatic analysis of next‑generation sequencing data to identify dysregulated genes in fibroblasts of idiopathic pulmonary fibrosis
Q37094624CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism
Q35041517CT scan findings of probable usual interstitial pneumonitis have a high predictive value for histologic usual interstitial pneumonitis
Q26777324Candidate genes for COPD: current evidence and research
Q26764812Candidate genes of idiopathic pulmonary fibrosis: current evidence and research
Q38399493Characteristic patterns in the fibrotic lung. Comparing idiopathic pulmonary fibrosis with chronic lung allograft dysfunction
Q35942991Cigarette Smoke Enhances the Expression of Profibrotic Molecules in Alveolar Epithelial Cells.
Q54213046Clinical Genetics in Interstitial Lung Disease.
Q89344465Collagen biomarkers and subclinical interstitial lung disease: The Multi-Ethnic Study of Atherosclerosis
Q47655004Comparative RNA-Seq transcriptome analysis on silica induced pulmonary inflammation and fibrosis in mice silicosis model
Q26864326Complex genetics of pulmonary diseases: lessons from genome-wide association studies and next-generation sequencing
Q93216677Conditional deletion of Nedd4-2 in lung epithelial cells causes progressive pulmonary fibrosis in adult mice
Q36802305Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models
Q92510114Cross-Cancer Pleiotropic Associations with Lung Cancer Risk in African Americans
Q92029835DSP variants may be associated with longitudinal change in quantitative emphysema
Q36916067Desmoplakin Variants Are Associated with Idiopathic Pulmonary Fibrosis
Q47102579Divergent roles for Clusterin in Lung Injury and Repair.
Q41025473Effect of Muc5b promoter polymorphism on disease predisposition and survival in idiopathic interstitial pneumonias
Q34060344Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation.
Q26849378Efficacy and safety of pirfenidone for idiopathic pulmonary fibrosis
Q44825417Embracing complex diseases. The case for an idiopathic pulmonary fibrosis biorepository
Q47239127Emerging roles of CST in maintaining genome stability and human disease.
Q47913152Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease
Q55332823Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease.
Q50044127Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease.
Q37359126Epidemiology of idiopathic pulmonary fibrosis
Q33600748Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study
Q38346940Epigenetics in idiopathic pulmonary fibrosis
Q36119163Epigenetics in lung fibrosis: from pathobiology to treatment perspective
Q38205635Epigenetics of idiopathic pulmonary fibrosis
Q66476273Epigenome-wide association study for 28-day survival of acute respiratory distress syndrome
Q92003078Etiology, Risk Factors, and Biomarkers in Systemic Sclerosis with Interstitial Lung Disease
Q35554660Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening
Q35153490Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease.
Q34678023Familial Interstitial Pneumonia (FIP).
Q90606561Familial pulmonary fibrosis: a world without frontiers
Q51760494Fibrosis: Lessons from OMICS analyses of the human lung.
Q37564540Fibrotic microenvironment promotes the metastatic seeding of tumor cells via activating the fibronectin 1/secreted phosphoprotein 1-integrin signaling.
Q37698325Future directions in idiopathic pulmonary fibrosis research. An NHLBI workshop report
Q48037972Genetic Evaluation and Testing of Patients and Families with Idiopathic Pulmonary Fibrosis
Q37400152Genetic architecture of human fibrotic diseases: disease risk and disease progression
Q38210815Genetic determinants of pulmonary fibrosis: evolving concepts
Q30274832Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
Q104287299Genetic mechanisms of critical illness in Covid-19
Q104439908Genetic mechanisms of critical illness in Covid-19
Q28243802Genetic susceptibility and pulmonary fibrosis
Q36481348Genetic susceptibility loci of idiopathic interstitial pneumonia do not represent risk for systemic sclerosis: a case control study in Caucasian patients
Q40897444Genetic variant near TERC influencing the risk of gliomas with older age at diagnosis in a Chinese population
Q46125322Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
Q34479395Genetics and early detection in idiopathic pulmonary fibrosis
Q42367959Genetics in Idiopathic Pulmonary Fibrosis Pathogenesis, Prognosis, and Treatment
Q35649228Genetics of Interstitial Lung Disease: Vol de Nuit (Night Flight).
Q35239965Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy course
Q92148453Genome-Wide Association Studies in Idiopathic Pulmonary Fibrosis: Bridging the Gap between Sequence and Consequence
Q30252379Genome-wide association study of subclinical interstitial lung disease in MESA.
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.
Q41247286Identification of candidate protective variants for common diseases and evaluation of their protective potential
Q55238602Identification of periplakin as a major regulator of lung injury and repair in mice.
Q57170607Idiopathic Pulmonary Fibrosis (IPF): An Overview
Q93091814Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways
Q64274792Idiopathic Pulmonary Fibrosis and Lung Cancer: Mechanisms and Molecular Targets
Q38821078Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways
Q60496317Idiopathic Pulmonary Fibrosis: Epidemiology, Natural History, Phenotypes
Q87721963Idiopathic pulmonary fibrosis
Q89691744Idiopathic pulmonary fibrosis
Q90023673Idiopathic pulmonary fibrosis in West Highland white terriers: An update
Q57762744Idiopathic pulmonary fibrosis: An update
Q42109310Idiopathic pulmonary fibrosis: a paradigm of late-onset, single-gene human disease?
Q54445538Idiopathic pulmonary fibrosis: combating on a new turf.
Q50139812Idiopathic pulmonary fibrosis: idiopathic no more?
Q48129735Idiopathic pulmonary fibrosis: on the move.
Q50326794Idiopathic pulmonary fibrosis: pathogenesis and management.
Q99630566Immunopathobiology of chronic lung disease
Q35786160Incorporating genetics into the identification and treatment of Idiopathic Pulmonary Fibrosis
Q59332980Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis
Q47239342Insights from human genetic studies of lung and organ fibrosis
Q47658743Integrating Patient Perspectives into Personalized Medicine in Idiopathic Pulmonary Fibrosis.
Q100317970Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function
Q52642397Integrative genomics identifies new genes associated with severe COPD and emphysema.
Q97568165Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society
Q52718368Is personalized medicine a realistic goal in idiopathic pulmonary fibrosis?
Q26998459Is there still hope for single therapies: how do we set up experimental systems to efficiently test combination therapies?
Q27301341Linking the genetic architecture of cytosine modifications with human complex traits
Q38924351Living with Fibrosis: From Diagnosis to Future Hope.
Q89582257Loss of Family with Sequence Similarity 13, Member A Exacerbates Pulmonary Fibrosis Potentially by Promoting Epithelial to Mesenchymal Transition
Q89696096Loss of family with sequence similarity 13, member A exacerbates pulmonary hypertension through accelerating endothelial-to-mesenchymal transition
Q52937788Lung Fibroblasts, Aging, and Idiopathic Pulmonary Fibrosis.
Q39335156Lung Manifestations in the Rheumatic Diseases
Q37189462Lung fibrosis-associated surfactant protein A1 and C variants induce latent transforming growth factor β1 secretion in lung epithelial cells
Q30384494Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study
Q57808775MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease
Q42940622MUC5B Promoter Variant rs35705950 Affects MUC5B Expression in the Distal Airways in Idiopathic Pulmonary Fibrosis.
Q36490141MUC5B and Idiopathic Pulmonary Fibrosis
Q36132579MUC5B expression and location in surfactant protein C mutations in children
Q90316654MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis
Q58761750Macrophages: friend or foe in idiopathic pulmonary fibrosis?
Q38981232Microbes Are Associated with Host Innate Immune Response in Idiopathic Pulmonary Fibrosis
Q29248145Mitochondria in the spotlight of aging and idiopathic pulmonary fibrosis
Q64937660Modeling of Fibrotic Lung Disease Using 3D Organoids Derived from Human Pluripotent Stem Cells.
Q60923169Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
Q38220769Molecular biomarkers in interstitial lung diseases.
Q26864836Molecular classification of idiopathic pulmonary fibrosis: personalized medicine, genetics and biomarkers
Q38243943Moving beyond genetics: is FAM13A a major biological contributor in lung physiology and chronic lung diseases?
Q90408307Muc5b Enhances Murine Honeycomb-like Cyst Formation
Q34046860Mucin 5B promoter polymorphism is associated with susceptibility to interstitial lung diseases in Chinese males
Q34471193Nintedanib in the treatment of idiopathic pulmonary fibrosis
Q64957934Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing.
Q36123192Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Q38806251Numericware i: Identical by State Matrix Calculator
Q57101603OUP accepted manuscript
Q57289193Obesity-associated family with sequence similarity 13, member A (FAM13A) is dispensable for adipose development and insulin sensitivity
Q38222245Pathogenesis of idiopathic pulmonary fibrosis and its clinical implications
Q34019921Pathogenesis of idiopathic pulmonary fibrosis: review of recent findings
Q42479603Permanent alveolar collapse is the predominant mechanism in idiopathic pulmonary fibrosis
Q43062778Personalizing Therapy in Idiopathic Pulmonary Fibrosis: A Glimpse of the Future?
Q38851479Pharmacogenetics and interstitial lung disease
Q29248074Phospholipid flippases attenuate LPS-induced TLR4 signaling by mediating endocytic retrieval of Toll-like receptor 4
Q30253065Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis
Q37431872Plasma microRNAs are associated with acute exacerbation in idiopathic pulmonary fibrosis
Q38832472Precision medicine in idiopathic pulmonary fibrosis.
Q91784806Prognostic relevance of telomere length and telomerase reverse transcriptase variant (rs2242652) on the multiple myeloma patients
Q37734892Protein tyrosine phosphatase α mediates profibrotic signaling in lung fibroblasts through TGF-β responsiveness.
Q36062197Proteomic Analysis of the Rat Canalicular Membrane Reveals Expression of a Complex System of P4-ATPases in Liver
Q38995612Pulmonary fibrosis in the era of stratified medicine.
Q40272697Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis
Q35262015Rare variants in RTEL1 are associated with familial interstitial pneumonia
Q36472166Rationale for and design of the Idiopathic Pulmonary Fibrosis-PRospective Outcomes (IPF-PRO) registry
Q26745905Recent advances in understanding idiopathic pulmonary fibrosis
Q48150087Regulation of MUC5B Expression in Idiopathic Pulmonary Fibrosis
Q35171019Regulation of nuclear-cytoplasmic shuttling and function of Family with sequence similarity 13, member A (Fam13a), by B56-containing PP2As and Akt.
Q35044740Relationship of DNA methylation and gene expression in idiopathic pulmonary fibrosis
Q92193223Resequencing to Fine Map Known Idiopathic Pulmonary Fibrosis Risk Genes. Homing in on Causal Variants
Q27687743Respiratory epithelial cells orchestrate pulmonary innate immunity
Q35157806Respiratory microbiome in IPF: cause, effect, or biomarker?
Q50676736Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model.
Q89167691Reversing Mechanoinductive DSP Expression by CRISPR/dCas9-mediated Epigenome Editing
Q90537703Risk factors for the development of idiopathic pulmonary fibrosis: A review
Q46028356Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.
Q95355760Role of Microbial Agents in Pulmonary Fibrosis
Q39296044SH2 Domain-Containing Phosphatase-2 Is a Novel Antifibrotic Regulator in Pulmonary Fibrosis.
Q38930521SIRT3 deficiency promotes lung fibrosis by augmenting alveolar epithelial cell mitochondrial DNA damage and apoptosis
Q28386089Secreted Phosphoprotein 1 and Sex-Specific Differences in Silica-Induced Pulmonary Fibrosis in Mice
Q34692137Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations
Q91235944Shared and distinct mechanisms of fibrosis
Q88875725Short Telomere Syndromes in Clinical Practice: Bridging Bench and Bedside
Q37469191Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis.
Q36095068Six-SOMAmer Index Relating to Immune, Protease and Angiogenic Functions Predicts Progression in IPF.
Q38432028Stem Cell-Based Therapy in Idiopathic Pulmonary Fibrosis
Q92684874Susceptible loci associated with autoimmune disease as potential biomarkers for checkpoint inhibitor-induced immune-related adverse events
Q36516894TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis
Q42580526Taking the "I" out of IPF.
Q89154468Targeted resequencing reveals genetic risks in patients with sporadic idiopathic pulmonary fibrosis
Q27027433Targeting EGFR signalling in chronic lung disease: therapeutic challenges and opportunities
Q38296340Targeting defective Toll-like receptor-3 function and idiopathic pulmonary fibrosis
Q52726708Telomerase Reverse Transcriptase Polymorphism rs2736100: A Balancing Act between Cancer and Non-Cancer Disease, a Meta-Analysis.
Q37277301Telomere dysfunction in alveolar epithelial cells causes lung remodeling and fibrosis
Q28084275Telomere maintenance and the etiology of adult glioma
Q89170883Telomere shortening activates TGF-β/Smads signaling in lungs and enhances both lipopolysaccharide and bleomycin-induced pulmonary fibrosis
Q26795473The Dipeptidyl Peptidase Family, Prolyl Oligopeptidase, and Prolyl Carboxypeptidase in the Immune System and Inflammatory Disease, Including Atherosclerosis
Q47282447The Lung Microbiome in Idiopathic Pulmonary Fibrosis: A Promising Approach for Targeted Therapies
Q40146154The MUC5B promoter polymorphism and telomere length in patients with chronic hypersensitivity pneumonitis: an observational cohort-control study.
Q35041524The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries.
Q47124422The MUC5B promoter polymorphism is associated with specific interstitial lung abnormality subtypes
Q34935466The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population
Q91910333The Possible Pathogenesis of Idiopathic Pulmonary Fibrosis considering MUC5B
Q26786969The Role of Mitochondrial DNA in Mediating Alveolar Epithelial Cell Apoptosis and Pulmonary Fibrosis
Q59801806The Role of TGF-β Signaling in Lung Cancer Associated with Idiopathic Pulmonary Fibrosis
Q93082066The Role of Telomerase and Telomeres in Interstitial Lung Diseases: From Molecules to Clinical Implications
Q98190329The contribution of animal models to understanding the role of the immune system in human idiopathic pulmonary fibrosis
Q38181073The epithelium in idiopathic pulmonary fibrosis: breaking the barrier
Q38809929The expression of proline-specific enzymes in the human lung
Q35785682The future of the development of medicines in idiopathic pulmonary fibrosis
Q40777090The genetic basis of idiopathic pulmonary fibrosis
Q37342804The importance of detailed epigenomic profiling of different cell types within organs
Q38215534The importance of matrix metalloproteinase-3 in respiratory disorders
Q46825127The lung microbiome in idiopathic pulmonary fibrosis. What does it mean and what should we do about it?
Q90950675The relationship between MUC5B promoter, TERT polymorphisms and telomere lengths with radiographic extent and survival in a Chinese IPF cohort
Q88129968The relationship between complement C3 expression and the MUC5B genotype in pulmonary fibrosis
Q33871544The respiratory microbiome in idiopathic pulmonary fibrosis
Q34986902The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis
Q39198820The utility of comprehensive autoantibody testing to differentiate connective tissue disease associated and idiopathic interstitial lung disease subgroup cases
Q50056514Time for a change: is idiopathic pulmonary fibrosis still idiopathic and only fibrotic?
Q39040828Tissue remodelling in pulmonary fibrosis
Q40463304Toll-like receptor 4 activation attenuates profibrotic response in control lung fibroblasts but not in fibroblasts from patients with IPF.
Q89067946Towards genetic reclassification of idiopathic pulmonary fibrosis
Q51764891Trade-offs in aging lung diseases: a review on shared but opposite genetic risk variants in idiopathic pulmonary fibrosis, lung cancer and chronic obstructive pulmonary disease.
Q90628690Transcriptional regulatory model of fibrosis progression in the human lung
Q52648646Transcriptome analysis reveals differential splicing events in IPF lung tissue.
Q50074612Transformation of Summary Statistics from Linear Mixed Model Association on All-or-None Traits to Odds Ratio.
Q91622811Translational research in pulmonary fibrosis
Q39013034Treatment of idiopathic pulmonary fibrosis: a position paper from a Nordic expert group
Q26775753Treatment of rheumatoid arthritis-associated interstitial lung disease: a perspective review
Q54264691Tuberculosis and lung damage: from epidemiology to pathophysiology.
Q26779192Understanding Idiopathic Interstitial Pneumonia: A Gene-Based Review of Stressed Lungs
Q49734357Update in Interstitial Lung Disease 2016.
Q35153423Update in diffuse parenchymal lung disease, 2013
Q92030137Use of precision cut lung slices as a translational model for the study of lung biology
Q38642884Using omics approaches to understand pulmonary diseases
Q47804444Validation of the prognostic value of MMP-7 in idiopathic pulmonary fibrosis
Q29417088Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk
Q50241447What if we made stratified medicine work for patients?
Q64977645Whole-Exome Sequencing Identifies Somatic Mutations Associated With Mortality in Metastatic Clear Cell Kidney Carcinoma.
Q55407487Whole-Exome Sequencing Insights into Adult Pulmonary Fibrosis. Repeating the Telomere Theme.
Q26766313Year in review 2015: Interstitial lung disease, pulmonary vascular disease, pulmonary function, sleep and ventilation, cystic fibrosis and paediatric lung disease
Q42498214mTORC1 activation decreases autophagy in aging and idiopathic pulmonary fibrosis and contributes to apoptosis resistance in IPF fibroblasts.

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