meta-analysis | Q815382 |
scholarly article | Q13442814 |
P50 | author | Mark Lathrop | Q6768494 |
Moisés Selman | Q87622005 | ||
Annie Pardo Cemo | Q87622008 | ||
Yoichiro Kamatani | Q88032943 | ||
Tasha E Fingerlin | Q89288019 | ||
Kevin F Gibson | Q124694079 | ||
Janet Talbert | Q125264091 | ||
Steve Groshong | Q125264382 | ||
Diana Zelenika | Q30248012 | ||
Naftali Kaminski | Q41048454 | ||
Miriam F Moffatt | Q56959224 | ||
P2093 | author name string | David 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 | |||
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P4510 | describes a project that uses | genome-wide association study | Q1098876 |
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | pulmonary fibrosis | Q32446 |
genome-wide association study | Q1098876 | ||
susceptibility locus | Q62091149 | ||
P304 | page(s) | 613–620 | |
P577 | publication date | 2013-06-01 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis | |
P478 | volume | 45 |
Q41034398 | 13th ERS Lung Science Conference. The most important take home messages: News from the Underground |
Q37213583 | A Chronic Obstructive Pulmonary Disease Susceptibility Gene, FAM13A, Regulates Protein Stability of β-Catenin |
Q42228778 | A Dataset of 26 Candidate Gene and Pro-Inflammatory Cytokine Variants for Association Studies in Idiopathic Pulmonary Fibrosis: Frequency Distribution in Normal Czech Population |
Q43062900 | A Phenome-Wide Association Study Identifies a Novel Asthma Risk Locus Near TERC. |
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Q35826595 | A comparison of visual and quantitative methods to identify interstitial lung abnormalities |
Q43178545 | A first glimpse at the early origins of idiopathic pulmonary fibrosis |
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Q35177444 | A genome-wide pleiotropy scan for prostate cancer risk |
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Q35819457 | Analysis of heat shock protein 70 gene polymorphisms Mexican patients with idiopathic pulmonary fibrosis |
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Q90051408 | Assessing thyroid cancer risk using polygenic risk scores |
Q30253080 | Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study |
Q37149994 | Association Between the MUC5B Promoter Polymorphism rs35705950 and Idiopathic Pulmonary Fibrosis: A Meta-analysis and Trial Sequential Analysis in Caucasian and Asian Populations |
Q37081313 | Association Study for 26 Candidate Loci in Idiopathic Pulmonary Fibrosis Patients from Four European Populations |
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Q36464726 | Association between MUC5B polymorphism and susceptibility and severity of idiopathic pulmonary fibrosis |
Q90654792 | Association 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 |
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Q36105254 | BARD1 mediates TGF-β signaling in pulmonary fibrosis. |
Q38833878 | Basal cells of the human airways acquire mesenchymal traits in idiopathic pulmonary fibrosis and in culture |
Q64262272 | Bioinformatic analysis of next‑generation sequencing data to identify dysregulated genes in fibroblasts of idiopathic pulmonary fibrosis |
Q37094624 | CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism |
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Q26764812 | Candidate genes of idiopathic pulmonary fibrosis: current evidence and research |
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Q35942991 | Cigarette Smoke Enhances the Expression of Profibrotic Molecules in Alveolar Epithelial Cells. |
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Q93216677 | Conditional deletion of Nedd4-2 in lung epithelial cells causes progressive pulmonary fibrosis in adult mice |
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Q92029835 | DSP variants may be associated with longitudinal change in quantitative emphysema |
Q36916067 | Desmoplakin Variants Are Associated with Idiopathic Pulmonary Fibrosis |
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Q47913152 | Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease |
Q55332823 | Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease. |
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Q92003078 | Etiology, Risk Factors, and Biomarkers in Systemic Sclerosis with Interstitial Lung Disease |
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Q34678023 | Familial Interstitial Pneumonia (FIP). |
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Q30388977 | Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia |
Q37563857 | IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER. |
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Q55238602 | Identification of periplakin as a major regulator of lung injury and repair in mice. |
Q57170607 | Idiopathic Pulmonary Fibrosis (IPF): An Overview |
Q93091814 | Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways |
Q64274792 | Idiopathic Pulmonary Fibrosis and Lung Cancer: Mechanisms and Molecular Targets |
Q38821078 | Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways |
Q60496317 | Idiopathic Pulmonary Fibrosis: Epidemiology, Natural History, Phenotypes |
Q87721963 | Idiopathic pulmonary fibrosis |
Q89691744 | Idiopathic pulmonary fibrosis |
Q90023673 | Idiopathic pulmonary fibrosis in West Highland white terriers: An update |
Q57762744 | Idiopathic pulmonary fibrosis: An update |
Q42109310 | Idiopathic pulmonary fibrosis: a paradigm of late-onset, single-gene human disease? |
Q54445538 | Idiopathic pulmonary fibrosis: combating on a new turf. |
Q50139812 | Idiopathic pulmonary fibrosis: idiopathic no more? |
Q48129735 | Idiopathic pulmonary fibrosis: on the move. |
Q50326794 | Idiopathic pulmonary fibrosis: pathogenesis and management. |
Q99630566 | Immunopathobiology of chronic lung disease |
Q35786160 | Incorporating genetics into the identification and treatment of Idiopathic Pulmonary Fibrosis |
Q59332980 | Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis |
Q47239342 | Insights from human genetic studies of lung and organ fibrosis |
Q47658743 | Integrating Patient Perspectives into Personalized Medicine in Idiopathic Pulmonary Fibrosis. |
Q100317970 | Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function |
Q52642397 | Integrative genomics identifies new genes associated with severe COPD and emphysema. |
Q97568165 | Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society |
Q52718368 | Is personalized medicine a realistic goal in idiopathic pulmonary fibrosis? |
Q26998459 | Is there still hope for single therapies: how do we set up experimental systems to efficiently test combination therapies? |
Q27301341 | Linking the genetic architecture of cytosine modifications with human complex traits |
Q38924351 | Living with Fibrosis: From Diagnosis to Future Hope. |
Q89582257 | Loss of Family with Sequence Similarity 13, Member A Exacerbates Pulmonary Fibrosis Potentially by Promoting Epithelial to Mesenchymal Transition |
Q89696096 | Loss of family with sequence similarity 13, member A exacerbates pulmonary hypertension through accelerating endothelial-to-mesenchymal transition |
Q52937788 | Lung Fibroblasts, Aging, and Idiopathic Pulmonary Fibrosis. |
Q39335156 | Lung Manifestations in the Rheumatic Diseases |
Q37189462 | Lung fibrosis-associated surfactant protein A1 and C variants induce latent transforming growth factor β1 secretion in lung epithelial cells |
Q30384494 | Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study |
Q57808775 | MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease |
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Q36490141 | MUC5B and Idiopathic Pulmonary Fibrosis |
Q36132579 | MUC5B expression and location in surfactant protein C mutations in children |
Q90316654 | MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis |
Q58761750 | Macrophages: friend or foe in idiopathic pulmonary fibrosis? |
Q38981232 | Microbes Are Associated with Host Innate Immune Response in Idiopathic Pulmonary Fibrosis |
Q29248145 | Mitochondria in the spotlight of aging and idiopathic pulmonary fibrosis |
Q64937660 | Modeling of Fibrotic Lung Disease Using 3D Organoids Derived from Human Pluripotent Stem Cells. |
Q60923169 | Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study |
Q38220769 | Molecular biomarkers in interstitial lung diseases. |
Q26864836 | Molecular classification of idiopathic pulmonary fibrosis: personalized medicine, genetics and biomarkers |
Q38243943 | Moving beyond genetics: is FAM13A a major biological contributor in lung physiology and chronic lung diseases? |
Q90408307 | Muc5b Enhances Murine Honeycomb-like Cyst Formation |
Q34046860 | Mucin 5B promoter polymorphism is associated with susceptibility to interstitial lung diseases in Chinese males |
Q34471193 | Nintedanib in the treatment of idiopathic pulmonary fibrosis |
Q64957934 | Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing. |
Q36123192 | Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank |
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Q57289193 | Obesity-associated family with sequence similarity 13, member A (FAM13A) is dispensable for adipose development and insulin sensitivity |
Q38222245 | Pathogenesis of idiopathic pulmonary fibrosis and its clinical implications |
Q34019921 | Pathogenesis of idiopathic pulmonary fibrosis: review of recent findings |
Q42479603 | Permanent alveolar collapse is the predominant mechanism in idiopathic pulmonary fibrosis |
Q43062778 | Personalizing Therapy in Idiopathic Pulmonary Fibrosis: A Glimpse of the Future? |
Q38851479 | Pharmacogenetics and interstitial lung disease |
Q29248074 | Phospholipid flippases attenuate LPS-induced TLR4 signaling by mediating endocytic retrieval of Toll-like receptor 4 |
Q30253065 | Plasma Soluble Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis |
Q37431872 | Plasma microRNAs are associated with acute exacerbation in idiopathic pulmonary fibrosis |
Q38832472 | Precision medicine in idiopathic pulmonary fibrosis. |
Q91784806 | Prognostic relevance of telomere length and telomerase reverse transcriptase variant (rs2242652) on the multiple myeloma patients |
Q37734892 | Protein tyrosine phosphatase α mediates profibrotic signaling in lung fibroblasts through TGF-β responsiveness. |
Q36062197 | Proteomic Analysis of the Rat Canalicular Membrane Reveals Expression of a Complex System of P4-ATPases in Liver |
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Q36472166 | Rationale for and design of the Idiopathic Pulmonary Fibrosis-PRospective Outcomes (IPF-PRO) registry |
Q26745905 | Recent advances in understanding idiopathic pulmonary fibrosis |
Q48150087 | Regulation of MUC5B Expression in Idiopathic Pulmonary Fibrosis |
Q35171019 | Regulation of nuclear-cytoplasmic shuttling and function of Family with sequence similarity 13, member A (Fam13a), by B56-containing PP2As and Akt. |
Q35044740 | Relationship of DNA methylation and gene expression in idiopathic pulmonary fibrosis |
Q92193223 | Resequencing to Fine Map Known Idiopathic Pulmonary Fibrosis Risk Genes. Homing in on Causal Variants |
Q27687743 | Respiratory epithelial cells orchestrate pulmonary innate immunity |
Q35157806 | Respiratory microbiome in IPF: cause, effect, or biomarker? |
Q50676736 | Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. |
Q89167691 | Reversing Mechanoinductive DSP Expression by CRISPR/dCas9-mediated Epigenome Editing |
Q90537703 | Risk factors for the development of idiopathic pulmonary fibrosis: A review |
Q46028356 | Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length. |
Q95355760 | Role of Microbial Agents in Pulmonary Fibrosis |
Q39296044 | SH2 Domain-Containing Phosphatase-2 Is a Novel Antifibrotic Regulator in Pulmonary Fibrosis. |
Q38930521 | SIRT3 deficiency promotes lung fibrosis by augmenting alveolar epithelial cell mitochondrial DNA damage and apoptosis |
Q28386089 | Secreted Phosphoprotein 1 and Sex-Specific Differences in Silica-Induced Pulmonary Fibrosis in Mice |
Q34692137 | Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations |
Q91235944 | Shared and distinct mechanisms of fibrosis |
Q88875725 | Short Telomere Syndromes in Clinical Practice: Bridging Bench and Bedside |
Q37469191 | Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. |
Q36095068 | Six-SOMAmer Index Relating to Immune, Protease and Angiogenic Functions Predicts Progression in IPF. |
Q38432028 | Stem Cell-Based Therapy in Idiopathic Pulmonary Fibrosis |
Q92684874 | Susceptible loci associated with autoimmune disease as potential biomarkers for checkpoint inhibitor-induced immune-related adverse events |
Q36516894 | TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis |
Q42580526 | Taking the "I" out of IPF. |
Q89154468 | Targeted resequencing reveals genetic risks in patients with sporadic idiopathic pulmonary fibrosis |
Q27027433 | Targeting EGFR signalling in chronic lung disease: therapeutic challenges and opportunities |
Q38296340 | Targeting defective Toll-like receptor-3 function and idiopathic pulmonary fibrosis |
Q52726708 | Telomerase Reverse Transcriptase Polymorphism rs2736100: A Balancing Act between Cancer and Non-Cancer Disease, a Meta-Analysis. |
Q37277301 | Telomere dysfunction in alveolar epithelial cells causes lung remodeling and fibrosis |
Q28084275 | Telomere maintenance and the etiology of adult glioma |
Q89170883 | Telomere shortening activates TGF-β/Smads signaling in lungs and enhances both lipopolysaccharide and bleomycin-induced pulmonary fibrosis |
Q26795473 | The Dipeptidyl Peptidase Family, Prolyl Oligopeptidase, and Prolyl Carboxypeptidase in the Immune System and Inflammatory Disease, Including Atherosclerosis |
Q47282447 | The Lung Microbiome in Idiopathic Pulmonary Fibrosis: A Promising Approach for Targeted Therapies |
Q40146154 | The MUC5B promoter polymorphism and telomere length in patients with chronic hypersensitivity pneumonitis: an observational cohort-control study. |
Q35041524 | The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries. |
Q47124422 | The MUC5B promoter polymorphism is associated with specific interstitial lung abnormality subtypes |
Q34935466 | The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population |
Q91910333 | The Possible Pathogenesis of Idiopathic Pulmonary Fibrosis considering MUC5B |
Q26786969 | The Role of Mitochondrial DNA in Mediating Alveolar Epithelial Cell Apoptosis and Pulmonary Fibrosis |
Q59801806 | The Role of TGF-β Signaling in Lung Cancer Associated with Idiopathic Pulmonary Fibrosis |
Q93082066 | The Role of Telomerase and Telomeres in Interstitial Lung Diseases: From Molecules to Clinical Implications |
Q98190329 | The contribution of animal models to understanding the role of the immune system in human idiopathic pulmonary fibrosis |
Q38181073 | The epithelium in idiopathic pulmonary fibrosis: breaking the barrier |
Q38809929 | The expression of proline-specific enzymes in the human lung |
Q35785682 | The future of the development of medicines in idiopathic pulmonary fibrosis |
Q40777090 | The genetic basis of idiopathic pulmonary fibrosis |
Q37342804 | The importance of detailed epigenomic profiling of different cell types within organs |
Q38215534 | The importance of matrix metalloproteinase-3 in respiratory disorders |
Q46825127 | The lung microbiome in idiopathic pulmonary fibrosis. What does it mean and what should we do about it? |
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