Update in Interstitial Lung Disease 2019.
暂无分享,去创建一个
F. Martinez | M. Selman | A. Pardo | K. Johannson | J. Fisher | S. Montesi
[1] G. Raghu,et al. Diagnostic accuracy of transbronchial lung cryobiopsy for interstitial lung disease diagnosis (COLDICE): a prospective, comparative study. , 2020, The Lancet. Respiratory medicine.
[2] F. Martinez,et al. Radiographic Honeycombing and Altered Lung Microbiota in Patients with Idiopathic Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[3] J. Harris,et al. Pulmonary Aptamer Signatures in Children's Interstitial and Diffuse Lung Diseases. , 2019, American journal of respiratory and critical care medicine.
[4] F. Martinez,et al. Nintedanib and Sildenafil in Patients with Idiopathic Pulmonary Fibrosis and Right Heart Dysfunction. A Prespecified Subgroup Analysis of a Double-Blind Randomized Clinical Trial (INSTAGE) , 2019, American journal of respiratory and critical care medicine.
[5] R. Summer,et al. Lipid Metabolism: A New Player in the Conundrum of Lung Fibrosis , 2019, American journal of respiratory cell and molecular biology.
[6] K. Tsoyi,et al. Palmitic Acid-Rich High Fat Diet Exacerbates Experimental Pulmonary Fibrosis by Modulating Endoplasmic Reticulum Stress. , 2019, American journal of respiratory cell and molecular biology.
[7] L. Wain,et al. Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[8] P. Reyfman,et al. Idiopathic Pulmonary Fibrosis and Lung Cancer: Finding Similarities within Differences , 2019, American Journal of Respiratory Cell and Molecular Biology.
[9] G. Han,et al. Overexpression of TIM-3 in macrophages aggravates pathogenesis of pulmonary fibrosis in mice. , 2019, American journal of respiratory cell and molecular biology.
[10] A. Günther,et al. The oncogene ECT2 contributes to a hyperplastic, proliferative lung epithelial cell phenotype in IPF. , 2019, American journal of respiratory cell and molecular biology.
[11] M. Selman,et al. The leading role of epithelial cells in the pathogenesis of idiopathic pulmonary fibrosis. , 2019, Cellular signalling.
[12] Ø. Molberg,et al. Tracking Impact of Interstitial Lung Disease in Systemic Sclerosis in a Complete Nationwide Cohort. , 2019, American journal of respiratory and critical care medicine.
[13] K. Korach,et al. microRNA let-7 Downregulates Ligand Independent Estrogen Receptor Mediated Male Predominant Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[14] F. Martinez,et al. Diagnostic Likelihood Thresholds that Define a Working Diagnosis of Idiopathic Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[15] R. Summer,et al. Activated Fibroblasts: Gluttonous for Glutamine , 2019, American journal of respiratory cell and molecular biology.
[16] V. Thannickal,et al. Modeling Fibrosis in Three-Dimensional Organoids Reveals New Epithelial Restraints on Fibroblasts , 2019, American journal of respiratory cell and molecular biology.
[17] G. Ligresti,et al. Nascent Lung Organoids Reveal Epithelium- and BMP-Mediated Suppression of Fibroblast Activation. , 2019, American journal of respiratory cell and molecular biology.
[18] R. Hamanaka,et al. Glutamine Metabolism is Required for Collagen Protein Synthesis in Lung Fibroblasts. , 2019, American journal of respiratory cell and molecular biology.
[19] Biao Hu,et al. Role of B7H3/IL-33 Signaling in Pulmonary Fibrosis-induced Profibrogenic Alterations in Bone Marrow. , 2019, American journal of respiratory and critical care medicine.
[20] M. Glassberg,et al. Trends in IPF-related Mortality in the United States: 2000-2017. , 2019, American journal of respiratory and critical care medicine.
[21] Yutong Zhao,et al. Preventing Glutaminolysis: A Potential Therapy for Pulmonary Fibrosis , 2019, American journal of respiratory cell and molecular biology.
[22] Gang Liu,et al. Inhibition of Glutaminase 1 Attenuates Experimental Pulmonary Fibrosis. , 2019, American journal of respiratory cell and molecular biology.
[23] S. Walsh,et al. Nintedanib in Progressive Fibrosing Interstitial Lung Diseases. , 2019, The New England journal of medicine.
[24] J. Chao,et al. CircRNA-012091/PPP1R13B-Mediated Lung Fibrotic Response in Silicosis via ER Stress and Autophagy. , 2019, American journal of respiratory cell and molecular biology.
[25] B. Barna,et al. PPARγ Deficiency Exacerbates Fibrotic Response to Mycobacteria Peptide in Murine Sarcoidosis Model. , 2019, American journal of respiratory cell and molecular biology.
[26] S. Digumarthy,et al. Type I Collagen-Targeted PET Imaging in Idiopathic Pulmonary Fibrosis: First-in-Human Studies. , 2019, American Journal of Respiratory and Critical Care Medicine.
[27] Darshak M Sanghavi,et al. Clinical Effectiveness of the Anti-Fibrotic Medications for Idiopathic Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[28] T. Maher,et al. The Transferrin Receptor CD71 Delineates Functionally Distinct Airway Macrophage Subsets during Idiopathic Pulmonary Fibrosis , 2019, American journal of respiratory and critical care medicine.
[29] Ivana V. Yang,et al. Resequencing Study Confirms Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[30] E. Mickler,et al. Familial Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Rare Missense Mutations In Context. , 2019, American journal of respiratory and critical care medicine.
[31] R. Hubbard,et al. The Mortality Burden of Idiopathic Pulmonary Fibrosis in the United Kingdom. , 2019, American journal of respiratory and critical care medicine.
[32] B. Stripp,et al. XBP1S Regulates MUC5B in a Promoter Variant-Dependent Pathway in IPF Airway Epithelia. , 2019, American journal of respiratory and critical care medicine.
[33] A. Günther,et al. The Long Non-Coding RNA DNM3OS is a Reservoir of FibromiRs with Major Functions in Lung Fibroblast Response to TGF-β and Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[34] A. Verma,et al. Attenuation of Allergen, IL-13- and TGF-α-Induced Lung Fibrosis Following the Treatment of IL-15 in Mice. , 2019, American journal of respiratory cell and molecular biology.
[35] A. Shilatifard,et al. Single-Cell Transcriptomic Analysis of Human Lung Provides Insights into the Pathobiology of Pulmonary Fibrosis , 2019, American journal of respiratory and critical care medicine.
[36] Jonathan H. Chung,et al. Use of a molecular classifier to identify usual interstitial pneumonia in conventional transbronchial lung biopsy samples: a prospective validation study. , 2019, The Lancet. Respiratory medicine.
[37] Madeleine K. D. Scott,et al. Increased monocyte count as a cellular biomarker for poor outcomes in fibrotic diseases: a retrospective, multicentre cohort study , 2019, The Lancet. Respiratory medicine.
[38] G. Budinger,et al. Proteostasis Takes Center Stage in Pulmonary Fibrosis , 2019, American journal of respiratory cell and molecular biology.
[39] G. Raghu,et al. Idiopathic Pulmonary Fibrosis Guideline Recommendations. Need for Adherence to Institute of Medicine Methodology? , 2019, Annals of the American Thoracic Society.
[40] K. Veraldi,et al. Intracellular Heat Shock Protein 70 Deficiency in Pulmonary Fibrosis. , 2019, American journal of respiratory cell and molecular biology.
[41] G. Raghu,et al. Nintedanib for Systemic Sclerosis-Associated Interstitial Lung Disease. , 2019, The New England journal of medicine.
[42] S. Nava,et al. Poor Concordance between Sequential Transbronchial Lung Cryobiopsy and Surgical Lung Biopsy in the Diagnosis of Diffuse Interstitial Lung Diseases. , 2019, American journal of respiratory and critical care medicine.
[43] K. Brown,et al. Increasing Hypersensitivity Pneumonitis-related Mortality in the United States from 1988 to 2016. , 2019, American journal of respiratory and critical care medicine.
[44] B. Yaspan,et al. Rare Protein-altering Telomere-related Gene Variants in Patients with Chronic Hypersensitivity Pneumonitis. , 2019, American journal of respiratory and critical care medicine.
[45] Meilan K. Han,et al. Lung Microbiota Contribute to Pulmonary Inflammation and Disease Progression in Pulmonary Fibrosis , 2019, American journal of respiratory and critical care medicine.
[46] G. Washko,et al. Imaging Patterns are Associated with Interstitial Lung Abnormality Progression and Mortality. , 2019, American journal of respiratory and critical care medicine.
[47] Jonathan H. Chung,et al. Computed Tomography Honeycombing Identifies a Progressive Fibrotic Phenotype with Increased Mortality across Diverse Interstitial Lung Diseases , 2019, Annals of the American Thoracic Society.
[48] C. Ryerson,et al. YouTube Videos as a Source of Misinformation on Idiopathic Pulmonary Fibrosis , 2019, Annals of the American Thoracic Society.
[49] Steven K. Huang,et al. “Yap”-ing about the Antifibrotic Benefits of Prostacyclin , 2019, American journal of respiratory cell and molecular biology.
[50] O. Nayler,et al. The Antifibrotic Activity of Prostacyclin Receptor Agonism Is Mediated through Inhibition of YAP/TAZ , 2019, American journal of respiratory cell and molecular biology.
[51] J. Leipsic,et al. Role of a Regional Multidisciplinary Conference in the Diagnosis of Interstitial Lung Disease , 2019, Annals of the American Thoracic Society.
[52] Raúl San José Estépar,et al. Increased Airway Wall Thickness in Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis , 2019, Annals of the American Thoracic Society.
[53] C. Hung,et al. Another Weapon in the Battle against Idiopathic Pulmonary Fibrosis? , 2019, American journal of respiratory cell and molecular biology.
[54] Seidai Sato,et al. The Tyrosine Kinase Inhibitor TAS‐115 Attenuates Bleomycin‐induced Lung Fibrosis in Mice , 2019, American journal of respiratory cell and molecular biology.
[55] K. Batra,et al. Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis , 2019, American journal of respiratory and critical care medicine.
[56] Jonathan H. Chung,et al. Prognosticating Outcomes in Interstitial Lung Disease by Mediastinal Lymph Node Assessment. An Observational Cohort Study with Independent Validation , 2019, American journal of respiratory and critical care medicine.
[57] S. Orlov,et al. Sustained Smad2 Phosphorylation Is Required for Myofibroblast Transformation in Response to TGF-β. , 2019, American journal of respiratory cell and molecular biology.
[58] J. Hagood,et al. Outsourcing Invasion, a Novel Function for Extracellular Vesicles in the Lung. , 2019, American journal of respiratory cell and molecular biology.
[59] T. Betsuyaku,et al. Deficiency of CRTH2, a Prostaglandin D2 Receptor, Aggravates Bleomycin‐induced Pulmonary Inflammation and Fibrosis , 2019, American journal of respiratory cell and molecular biology.
[60] R. Sanderson,et al. Fibronectin on the Surface of Extracellular Vesicles Mediates Fibroblast Invasion , 2019, American journal of respiratory cell and molecular biology.
[61] M. Peters-Golden,et al. Special Delivery: A New Package for an Old Antifibrotic Mediator. , 2019, American journal of respiratory cell and molecular biology.
[62] T. Thatcher,et al. Activated Human Lung Fibroblasts Produce Extracellular Vesicles with Antifibrotic Prostaglandins , 2019, American journal of respiratory cell and molecular biology.
[63] G. Kayser,et al. BAL Cell Gene Expression Is Indicative of Outcome and Airway Basal Cell Involvement in Idiopathic Pulmonary Fibrosis , 2019, American journal of respiratory and critical care medicine.
[64] C. Owen,et al. Dusting Off IL-9 as a New Therapeutic Target for Pulmonary Fibrosis. , 2019, American journal of respiratory cell and molecular biology.
[65] D. Lagares. P311 in Scar Wars: Myofibroblasts Lost without Transforming Growth Factor β Translation. , 2019, American journal of respiratory cell and molecular biology.
[66] K. Ohta,et al. IL‐9 Blockade Suppresses Silica‐induced Lung Inflammation and Fibrosis in Mice , 2019, American journal of respiratory cell and molecular biology.
[67] G. Mutlu,et al. P311 Promotes Lung Fibrosis via Stimulation of Transforming Growth Factor‐&bgr;1, ‐&bgr;2, and ‐&bgr;3 Translation , 2019, American journal of respiratory cell and molecular biology.
[68] F. Martinez,et al. Why Does an Aging Smoker's Lung Develop Idiopathic Pulmonary Fibrosis and Not Chronic Obstructive Pulmonary Disease? , 2019, American journal of respiratory and critical care medicine.
[69] S. Kritchevsky,et al. Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study , 2019, EBioMedicine.
[70] P. Caravan,et al. Molecular imaging of fibrosis: recent advances and future directions , 2019, The Journal of clinical investigation.
[71] M. Rojas,et al. Quercetin in Idiopathic Pulmonary Fibrosis: Another Brick in the Senolytic Wall. , 2019, American journal of respiratory cell and molecular biology.
[72] G. Ligresti,et al. Survivin IPF: Targeting Cellular Metabolism to Promote Apoptosis in IPF Fibroblasts. , 2019, American journal of respiratory cell and molecular biology.
[73] Y. Geng,et al. Mitogen‐activated Protein Kinase‐activated Protein Kinase 2 Inhibition Attenuates Fibroblast Invasion and Severe Lung Fibrosis , 2019, American journal of respiratory cell and molecular biology.
[74] J. Horowitz,et al. Glutaminolysis Epigenetically Regulates Antiapoptotic Gene Expression in Idiopathic Pulmonary Fibrosis Fibroblasts , 2019, American journal of respiratory cell and molecular biology.
[75] C. Hogaboam,et al. Quercetin Enhances Ligand‐induced Apoptosis in Senescent Idiopathic Pulmonary Fibrosis Fibroblasts and Reduces Lung Fibrosis In Vivo , 2019, American journal of respiratory cell and molecular biology.
[76] F. Martinez,et al. Telomere Length and Use of Immunosuppressive Medications in Idiopathic Pulmonary Fibrosis. , 2019, American journal of respiratory and critical care medicine.
[77] D. Schwartz. Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways. , 2018, Annals of the American Thoracic Society.
[78] G. Raghu,et al. Nintedanib plus Sildenafil in Patients with Idiopathic Pulmonary Fibrosis , 2018, The New England journal of medicine.
[79] Takeshi Johkoh,et al. Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline , 2018, American journal of respiratory and critical care medicine.
[80] R. Borie,et al. Pulmonary phenotypes associated with genetic variation in telomere-related genes , 2018, Current opinion in pulmonary medicine.
[81] T. Blackwell,et al. Endoplasmic reticulum stress in pulmonary fibrosis. , 2018, Matrix biology : journal of the International Society for Matrix Biology.
[82] D. Lynch,et al. A Standardized Diagnostic Ontology for Fibrotic Interstitial Lung Disease. An International Working Group Perspective , 2017, American journal of respiratory and critical care medicine.
[83] M. Selman,et al. Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease , 2017, Nature Reviews Drug Discovery.
[84] F. Martinez,et al. A Comparative Analysis of Pulmonary and Critical Care Medicine Guideline Development Methodologies , 2017, American journal of respiratory and critical care medicine.
[85] Jin Ock Kim,et al. Tauroursodeoxycholic acid (TUDCA) attenuates pressure overload-induced cardiac remodeling by reducing endoplasmic reticulum stress , 2017, PloS one.
[86] Harry J de Koning,et al. Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis , 2017, Nature Genetics.
[87] M. Mino‐Kenudson,et al. Type I collagen–targeted PET probe for pulmonary fibrosis detection and staging in preclinical models , 2017, Science Translational Medicine.
[88] Athol U. Wells,et al. Idiopathic pulmonary fibrosis , 2012, Nature Reviews Disease Primers.
[89] B. Stripp,et al. Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. , 2016, JCI insight.
[90] J. Roman,et al. Pulmonary Fibrosis in Hermansky-Pudlak Syndrome. , 2016, Annals of the American Thoracic Society.
[91] K. Batra,et al. Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive , 2016, European Respiratory Journal.
[92] R. Homer,et al. The Airway in Idiopathic Pulmonary Fibrosis: Protecting the Lung or Promoting Disease? , 2016, American journal of respiratory and critical care medicine.
[93] Dustin J Maly,et al. Allosteric Inhibition of the IRE1α RNase Preserves Cell Viability and Function during Endoplasmic Reticulum Stress , 2014, Cell.
[94] H. Collard,et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. , 2014, The New England journal of medicine.
[95] M. Selman,et al. Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. , 2014, American journal of respiratory and critical care medicine.
[96] Shandra L. Protzko,et al. An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. , 2013, American journal of respiratory and critical care medicine.
[97] Kevin J Anstrom,et al. Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosis. , 2012, The New England journal of medicine.
[98] Luis Fernandez-Luque,et al. HealthTrust: A Social Network Approach for Retrieving Online Health Videos , 2012, Journal of medical Internet research.
[99] K. Dahlman-Wright,et al. Estrogen Signaling via Estrogen Receptor β* , 2010, The Journal of Biological Chemistry.
[100] Oliver Eickelberg,et al. Inhibition and role of let-7d in idiopathic pulmonary fibrosis. , 2010, American journal of respiratory and critical care medicine.
[101] Christoph Lange,et al. Variants in FAM13A are associated with chronic obstructive pulmonary disease , 2010, Nature Genetics.
[102] F. Martinez,et al. Variable prostaglandin E2 resistance in fibroblasts from patients with usual interstitial pneumonia. , 2008, American journal of respiratory and critical care medicine.