MUC5B promoter polymorphism and interstitial lung abnormalities. - Wikidata - awgldk - TriplyDB

MUC5B promoter polymorphism and interstitial lung abnormalities.

MUC5B promoter polymorphism and interstitial lung abnormalities.

http://www.wikidata.org/entity/Q37105760

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Idiopathic pulmonary fibrosis: Diagnosis, epidemiology and natural history Understanding Idiopathic Interstitial Pneumonia: A Gene-Based Review of Stressed Lungs Molecular classification of idiopathic pulmonary fibrosis: personalized medicine, genetics and biomarkers Is there still hope for single therapies: how do we set up experimental systems to efficiently test combination therapies?A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung disease Molecular biomarkers in idiopathic pulmonary fibrosis Genetic susceptibility and pulmonary fibrosis Genome-wide association study of subclinical interstitial lung disease in MESA.Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study.Interstitial lung disease: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.Genetics and early detection in idiopathic pulmonary fibrosis Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries.Anterior Mediastinal Masses in the Framingham Heart Study: Prevalence and CT Image Characteristics.Update in diffuse parenchymal lung disease, 2013 Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease.Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy course.Interstitial lung abnormalities in treatment-naïve advanced non-small-cell lung cancer patients are associated with shorter survival.Paraseptal emphysema: Prevalence and distribution on CT and association with interstitial lung abnormalities Detection of Rheumatoid Arthritis-Interstitial Lung Disease Is Enhanced by Serum Biomarkers.Incorporating genetics into the identification and treatment of Idiopathic Pulmonary Fibrosis A comparison of visual and quantitative methods to identify interstitial lung abnormalities.MUC5B and Idiopathic Pulmonary Fibrosis.Association Between Interstitial Lung Abnormalities and All-Cause Mortality Pulmonary cysts identified on chest CT: are they part of aging change or of clinical significance?CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism Galectin-3 Is Associated with Restrictive Lung Disease and Interstitial Lung Abnormalities.Potential Metabolic Biomarkers to Identify Interstitial Lung Abnormalities Association Between the MUC5B Promoter Polymorphism rs35705950 and Idiopathic Pulmonary Fibrosis: A Meta-analysis and Trial Sequential Analysis in Caucasian and Asian Populations.Subclinical Interstitial Lung Abnormalities: Toward the Early Detection of Idiopathic Pulmonary Fibrosis?IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER.Future directions in idiopathic pulmonary fibrosis research. An NHLBI workshop report.The epithelium in idiopathic pulmonary fibrosis: breaking the barrier.Chlorambucil-induced acute interstitial pneumonitis.Epigenetics of idiopathic pulmonary fibrosis.Role of genetics in lung transplant complications.Facts and promises on lung biomarkers in interstitial lung diseases.Imaging approaches to understand disease complexity: Chronic Obstructive Pulmonary Disease as a clinical model.An Ounce of Prevention… Will This Be the Future for IPF?Serum Matrix Metalloproteinase-7, Respiratory Symptoms, and Mortality in Community-dwelling Adults: The Multi-Ethnic Study of Atherosclerosis.

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MUC5B promoter polymorphism and interstitial lung abnormalities.

http://www.wikidata.org/entity/Q37105760

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 21 May 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

MUC5B promoter polymorphism and interstitial lung abnormalities.

@en

MUC5B promoter polymorphism and interstitial lung abnormalities.

@nl

type

label

MUC5B promoter polymorphism and interstitial lung abnormalities.

@en

MUC5B promoter polymorphism and interstitial lung abnormalities.

@nl

prefLabel

MUC5B promoter polymorphism and interstitial lung abnormalities.

@en

MUC5B promoter polymorphism and interstitial lung abnormalities.

@nl

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The New England Journal of Medicine

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MUC5B promoter polymorphism and interstitial lung abnormalities.

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David A Schwartz

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Elissa Murphy

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Gary M Hunninghake

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George R Washko

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Hiroto Hatabu

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Ivan O Rosas

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James C Ross

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James E Loyd

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Mark P Steele

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Marvin I Schwarz

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P2860

Spirometric reference values from a sample of the general U.S. population

Incidence and mortality of idiopathic pulmonary fibrosis and sarcoidosis in the UK

An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management

Testing for genetic association taking into account phenotypic information of relatives.

Incidence, prevalence, and clinical course of idiopathic pulmonary fibrosis: a population-based study.

Incidence and prevalence of idiopathic pulmonary fibrosis.

Single breath diffusing capacity in a representative sample of the population of Michigan, a large industrial state. Predicted values, lower limits of normal, and frequencies of abnormality by smoking history.

The European Community Respiratory Health Survey: what are the main results so far? European Community Respiratory Health Survey II.

Statins and pulmonary fibrosis: the potential role of NLRP3 inflammasome activation.

Lung volumes and emphysema in smokers with interstitial lung abnormalities

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2192-2200

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scholarly article

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10.1056/NEJMOA1216076

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23

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368

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George T O'Connor

Jeanne C Latourelle

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2013-05-21T00:00:00Z

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23692170

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3747636

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