Gene expression profiling of familial and sporadic interstitial pneumonia. - Wikidata - wikimedia - TriplyDB

Gene expression profiling of familial and sporadic interstitial pneumonia.

Gene expression profiling of familial and sporadic interstitial pneumonia.

http://www.wikidata.org/entity/Q35855118

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A micro RNA processing defect in rapidly progressing idiopathic pulmonary fibrosis WNT5A is a regulator of fibroblast proliferation and resistance to apoptosis 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 Roles of transcriptional factor 7 in production of inflammatory factors for lung diseases Epigenomics of idiopathic pulmonary fibrosis Evolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genes Idiopathic pulmonary fibrosis: diagnostic pitfalls and therapeutic challenges 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 MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis Gene expression profiling of pulmonary fibrosis identifies Twist1 as an antiapoptotic molecular "rectifier" of growth factor signaling The peripheral blood transcriptome identifies the presence and extent of disease in idiopathic pulmonary fibrosis Interactions between β-catenin and transforming growth factor-β signaling pathways mediate epithelial-mesenchymal transition and are dependent on the transcriptional co-activator cAMP-response element-binding protein (CREB)-binding protein (CBP).The role of CXC chemokines in pulmonary fibrosis.A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant.Relationship between gene expression and lung function in Idiopathic Interstitial Pneumonias.Functional Wnt signaling is increased in idiopathic pulmonary fibrosis Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF).Lower expression of platelet derived growth factor is associated with better overall survival rate of patients with idiopathic nonspecific interstitial pneumonia Familial interstitial lung disease in four members of one family: a case series.Inhibitory effect of CXC chemokine receptor 4 antagonist AMD3100 on bleomycin induced murine pulmonary fibrosis.Does current knowledge explain the pathogenesis of idiopathic pulmonary fibrosis? A perspective.Genetic predisposition to respiratory diseases: infiltrative lung diseases.Bayesian probit regression model for the diagnosis of pulmonary fibrosis: proof-of-principle The idiopathic pulmonary fibrosis honeycomb cyst contains a mucocilary pseudostratified epithelium.Intratracheal instillation of high dose adenoviral vectors is sufficient to induce lung injury and fibrosis in mice Application of clinico-radiologic-pathologic diagnosis of diffuse parenchymal lung diseases in children in China.Lung tissues in patients with systemic sclerosis have gene expression patterns unique to pulmonary fibrosis and pulmonary hypertension.Angiotensinogen gene G-6A polymorphism influences idiopathic pulmonary fibrosis disease progression.MetaQC: objective quality control and inclusion/exclusion criteria for genomic meta-analysis.Increased ectodomain shedding of cell adhesion molecule 1 as a cause of type II alveolar epithelial cell apoptosis in patients with idiopathic interstitial pneumonia.Role of the SDF-1/CXCR4 axis in the pathogenesis of lung injury and fibrosis Early interstitial lung disease in familial pulmonary fibrosis.Epigenetics in lung fibrosis: from pathobiology to treatment perspective.A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features.Genetic testing in diffuse parenchymal lung disease.High-resolution CT scan findings in familial interstitial pneumonia do not conform to those of idiopathic interstitial pneumonia Overexpression of Sulf2 in idiopathic pulmonary fibrosis Antioxidants as potential therapeutics for lung fibrosis.

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P2860

Gene expression profiling of familial and sporadic interstitial pneumonia.

http://www.wikidata.org/entity/Q35855118

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2006年論文

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2006年论文

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2006年论文

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name

Gene expression profiling of familial and sporadic interstitial pneumonia.

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Gene expression profiling of familial and sporadic interstitial pneumonia.

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type

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Gene expression profiling of familial and sporadic interstitial pneumonia.

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Gene expression profiling of familial and sporadic interstitial pneumonia.

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Gene expression profiling of familial and sporadic interstitial pneumonia.

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Gene expression profiling of familial and sporadic interstitial pneumonia.

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American Journal of Respiratory and Critical Care Medicine

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Gene expression profiling of familial and sporadic interstitial pneumonia.

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David A Schwartz

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Erin McElvania-Tekippe

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Ivana V Yang

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John W Hollingsworth

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Jordan D Savov

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Katherine G Berman

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Kevin K Brown

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Lauranell H Burch

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Marcy C Speer

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Mark P Steele

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P2860

Regulation of pulmonary fibrosis by chemokine receptor CXCR3

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

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

The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations

FAMILIAL INTERSTITIAL PULMONARY FIBROSIS

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

Overview of pulmonary fibrosis.

Bone marrow-derived progenitor cells in pulmonary fibrosis

Role of Eotaxin-1 (CCL11) and CC chemokine receptor 3 (CCR3) in bleomycin-induced lung injury and fibrosis.

Murine candidate bleomycin induced pulmonary fibrosis susceptibility genes identified by gene expression and sequence analysis of linkage regions

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