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A common MUC5B promoter polymorphism and pulmonary fibrosis.

A common MUC5B promoter polymorphism and pulmonary fibrosis.

http://www.wikidata.org/entity/Q36048530

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Genetic interstitial lung disease Asbestosis and environmental causes of usual interstitial pneumonia Recent advances in understanding idiopathic pulmonary fibrosis Candidate genes of idiopathic pulmonary fibrosis: current evidence and research Year in review 2015: Interstitial lung disease, pulmonary vascular disease, pulmonary function, sleep and ventilation, cystic fibrosis and paediatric lung disease Idiopathic pulmonary fibrosis: Diagnosis, epidemiology and natural history Understanding Idiopathic Interstitial Pneumonia: A Gene-Based Review of Stressed Lungs Role of epithelial mucins during airway infection Epigenomics of idiopathic pulmonary fibrosis Molecular classification of idiopathic pulmonary fibrosis: personalized medicine, genetics and biomarkers Personalized medicine: applying 'omics' to lung fibrosis Is there still hope for single therapies: how do we set up experimental systems to efficiently test combination therapies?Cellular mechanisms of tissue fibrosis. 7. New insights into the cellular mechanisms of pulmonary fibrosis A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung disease Oxidative stress and pulmonary fibrosis Molecular biomarkers in idiopathic pulmonary fibrosis Evolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genes Pulmonary fibrosis: patterns and perpetrators Genetic susceptibility and pulmonary fibrosis Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias Secreted Phosphoprotein 1 and Sex-Specific Differences in Silica-Induced Pulmonary Fibrosis in Mice Muc5b is required for airway defence The peripheral blood transcriptome identifies the presence and extent of disease in idiopathic pulmonary fibrosis Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.Genome-wide association study of subclinical interstitial lung disease in MESA.Malfolded protein structure and proteostasis in lung diseases.Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia.Familial and sporadic idiopathic pulmonary fibrosis: making the diagnosis from peripheral blood.Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC.TH17, TH22 and Treg cells are enriched in the healthy human cecum.The next generation of complex lung genetic studies.Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study.The peripheral blood proteome signature of idiopathic pulmonary fibrosis is distinct from normal and is associated with novel immunological processes Fibrosis of two: Epithelial cell-fibroblast interactions in pulmonary fibrosis Precision Medicine: The New Frontier in Idiopathic Pulmonary Fibrosis YKL-40 in pediatric asthma, MUC5B promoter polymorphism in idiopathic pulmonary fibrosis, and esmolol in septic shock.Variants of the ABCA3 gene might contribute to susceptibility to interstitial lung diseases in the Chinese population.Genome-wide association study and admixture mapping identify different asthma-associated loci in Latinos: the Genes-environments & Admixture in Latino Americans study

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A common MUC5B promoter polymorphism and pulmonary fibrosis.

http://www.wikidata.org/entity/Q36048530

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

A common MUC5B promoter polymorphism and pulmonary fibrosis.

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A common MUC5B promoter polymorphism and pulmonary fibrosis.

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type

label

A common MUC5B promoter polymorphism and pulmonary fibrosis.

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A common MUC5B promoter polymorphism and pulmonary fibrosis.

@en

prefLabel

A common MUC5B promoter polymorphism and pulmonary fibrosis.

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A common MUC5B promoter polymorphism and pulmonary fibrosis.

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The New England Journal of Medicine

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A common MUC5B promoter polymorphism and pulmonary fibrosis

@en

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Anastasia L Wise

http://www.w3.org/2001/XMLSchema#string

Anne L Crews

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Aretha Herron

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Cheryl Markin

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Christopher M Evans

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Corinne E Hennessy

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David A Schwartz

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Dolly Kervitsky

http://www.w3.org/2001/XMLSchema#string

Gunnar Gudmundsson

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Ivana V Yang

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Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.

IL-13 and epidermal growth factor receptor have critical but distinct roles in epithelial cell mucin production

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Haploview: analysis and visualization of LD and haplotype maps

A mutation in the surfactant protein C gene associated with familial interstitial lung disease

American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Soci

Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial

Telomerase mutations in families with idiopathic pulmonary fibrosis

Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer.

Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences.

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1503-1512

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10.1056/NEJMOA1013660

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16

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364

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Burton F Dickey

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2011-04-01T00:00:00Z

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51064254

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21506741

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pulmonary fibrosis

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3379886

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