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American journal of respiratory cell and molecular biology, ISSN 1044-1549, 09/2017, Volume 57, Issue 3, pp. 294 - 306
Journal Article
American journal of respiratory cell and molecular biology, ISSN 1044-1549, 01/2018, Volume 58, Issue 1, pp. 66 - 78
Idiopathic pulmonary fibrosis is a progressive lung disease with complex pathophysiology and fatal prognosis. Macrophages (MΦ) contribute to the development of... 
C-FLIP | RNA-seq | IPF | Fibrosis | Macrophage | Gene deletion | Macrophages | Proteins | FADD protein | Bleomycin | Clonal deletion | Rodents | FLIP protein | Fibroblasts | Alveoli | Growth factors | Enzymes | CD11b antigen | Lung diseases | c-FLIP protein | Inflammation | IL-1β | Ribonucleic acid--RNA | Asthma | Monocytes | Pulmonary fibrosis | Cell death | Medical prognosis | Ligands | Chemokines | Apoptosis
Journal Article
American journal of respiratory and critical care medicine, ISSN 1073-449X, 05/2019, Volume 199, Issue 10, pp. 1284 - 1287
Journal Article
American journal of physiology. Lung cellular and molecular physiology, ISSN 1522-1504, 01/2018, Volume 314, Issue 1, pp. L69 - L82
Journal Article
British journal of radiology, ISSN 0007-1285, 01/2019, Volume 92, Issue 1099, pp. 20181003 - 20181003
Radiologists have a critical role in the evaluation and diagnosis of suspected idiopathic pulmonary fibrosis (IPF). Accurate pattern identification on imaging... 
Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Index Medicus | Abridged Index Medicus | Review
Journal Article
American journal of respiratory cell and molecular biology, ISSN 1044-1549, 01/2018, Volume 58, Issue 1, pp. 66 - 78
Idiopathic pulmonary fibrosis is a progressive lung disease with complex pathophysiology and fatal prognosis. Macrophages (M Phi) contribute to the development... 
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Respiratory System | Science & Technology | Cell Biology
Journal Article
6/2018, ISBN 3319671987
Book Chapter
12/2018, Respiratory Medicine, ISBN 9783319999746
Idiopathic pulmonary fibrosis (IPF) was once thought to be a rare disease and has been classically described as a disease that progresses in a “relentless and... 
Clinical course | Prevalence | Idiopathic pulmonary fibrosis | Mortality | Epidemiology | Natural history | Risk factors | Incidence
Book Chapter
The American journal of physiology, ISSN 0002-9513, 01/2018, Volume 314, Issue 1, p. L69
Microparticles are a newly recognized class of mediators in the pathophysiology of lung inflammation and injury, but little is known about the factors that... 
Physiological aspects | Macrophages | Observations | Lung diseases | Phagocytosis
Journal Article
The American journal of physiology, ISSN 0002-9513, 07/2016, Volume 311, Issue 1
During homeostasis two distinct macrophage (M[empty set]) populations inhabit the lungs: tissue M[empty set] (often called interstitial M[empty set]) and... 
Phagocytes | Genetic aspects | Lungs | Health aspects
Journal Article
American journal of respiratory and critical care medicine, ISSN 1535-4970, 08/2019, Volume 200, Issue 4, pp. 518 - 519
[...]of ethnicity/race confounding bias by workplace exposure, genetic variation (which can be related to and differ by race) is likely one of the many risk... 
Alveolitis, Extrinsic Allergic | United States | Humans | Occupations | Pulmonary fibrosis | Epidemiology | Mortality | Race | Index Medicus | Abridged Index Medicus | Correspondence
Journal Article
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