MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis - Wikidata - wikimedia - TriplyDB

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

http://www.wikidata.org/entity/Q28472658

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Biomarkers of World Trade Center particulate matter exposure: physiology of distal airway and blood biomarkers that predict FEV1 decline Early elevation of serum MMP-3 and MMP-12 predicts protection from World Trade Center-lung injury in New York City firefighters: a nested case-control study Inhibition and role of let-7d in idiopathic pulmonary fibrosis Gene expression profiles of acute exacerbations of idiopathic pulmonary fibrosis WNT1-inducible signaling protein-1 mediates pulmonary fibrosis in mice and is upregulated in humans with idiopathic pulmonary fibrosis Recent advances in understanding idiopathic pulmonary fibrosis Treatment of rheumatoid arthritis-associated interstitial lung disease: a perspective review Diverse functions of matrix metalloproteinases during fibrosis Molecular classification of idiopathic pulmonary fibrosis: personalized medicine, genetics and biomarkers Personalized medicine: applying 'omics' to lung fibrosis Peripheral blood biomarkers in idiopathic pulmonary fibrosis A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung disease Molecular biomarkers in idiopathic pulmonary fibrosis Evolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genes Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis Update on therapeutic management of idiopathic 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 An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management Validated prediction of pro-invasive growth factors using a transcriptome-wide invasion signature derived from a complex 3D invasion assay Matrix metalloproteinases as therapeutic targets for idiopathic pulmonary fibrosis Matrix metalloproteinase-10: a novel biomarker for idiopathic pulmonary fibrosis MMP-2 and TIMP-1 predict healing of WTC-lung injury in New York City firefighters The peripheral blood transcriptome identifies the presence and extent of disease in idiopathic pulmonary fibrosis Global methylation patterns in idiopathic pulmonary fibrosis Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF).MMP-7 is a predictive biomarker of disease progression in patients with idiopathic pulmonary fibrosis The peripheral blood proteome signature of idiopathic pulmonary fibrosis is distinct from normal and is associated with novel immunological processes Mononuclear phagocytes and airway epithelial cells: novel sources of matrix metalloproteinase-8 (MMP-8) in patients with idiopathic pulmonary fibrosis.The receptor for advanced glycation end products (RAGE) and the lung.Precision Medicine: The New Frontier in Idiopathic Pulmonary Fibrosis Resistance to bleomycin-induced lung fibrosis in MMP-8 deficient mice is mediated by interleukin-10 Analysis of Microarray-Identified Genes and MicroRNAs Associated with Idiopathic Pulmonary Fibrosis.Matrix metalloproteinase-19 is a key regulator of lung fibrosis in mice and humans Genomewide RNA expression profiling in lung identifies distinct signatures in idiopathic pulmonary arterial hypertension and secondary pulmonary hypertension.Microbial Antigens Stimulate Metalloprotease-7 Secretion in Human B-Lymphocytes Using mTOR-Dependent and Independent Pathways.Alveolar epithelial cells express mesenchymal proteins in patients with idiopathic pulmonary fibrosis High throughput determination of TGFβ1/SMAD3 targets in A549 lung epithelial cells The diagnosis of idiopathic pulmonary fibrosis: current and future approaches.

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MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

http://www.wikidata.org/entity/Q28472658

description

2008 nî lūn-bûn

@nan

2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

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2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

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2008年论文

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name

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

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MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

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MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@nl

type

label

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@ast

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@en

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@nl

prefLabel

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@ast

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@en

MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

@nl

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JOURNAL.PMED.0050093

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MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis

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Anna E Lokshin

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Annie Pardo

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Bernadette R Gochuico

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Ivan O Rosas

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James Dauber

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Jose Cisneros

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Kathleen O Lindell

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Kazuhisa Konishi

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Kevin Gibson

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

Moises Selman

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

P2860

Significance analysis of microarrays applied to the ionizing radiation response

Classification and natural history of the idiopathic interstitial pneumonias

Chronic bird fancier's lung: histopathological and clinical correlation. An application of the 2002 ATS/ERS consensus classification of the idiopathic interstitial pneumonias

Up-regulation and profibrotic role of osteopontin in human idiopathic pulmonary fibrosis

Comparison of normalization methods for CodeLink Bioarray data.

Characteristic elevation of matrix metalloproteinase activity in idiopathic interstitial pneumonias

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

Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease. NHLBI/WHO Global Initiative for Chronic Obstructive Lung Disease (GOLD) Workshop summary

Predicting survival in idiopathic pulmonary fibrosis: scoring system and survival model.

Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans.

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10.1371/JOURNAL.PMED.0050093

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Naftali Kaminski

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5404051

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pulmonary fibrosis

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