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Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2009, Volume 119, Issue 4, pp. 772 - 787
Idiopathic pulmonary fibrosis (IPF) is characterized by distorted lung architecture and loss of respiratory function. Enhanced (myo... 
EPITHELIAL-MESENCHYMAL TRANSITION | PATHOGENESIS | MEDICINE, RESEARCH & EXPERIMENTAL | LUNG FIBROSIS | CELLS | APOPTOSIS | TISSUE GROWTH-FACTOR | CCN FAMILY | MECHANISMS | EXPRESSION | INTERSTITIAL PNEUMONIAS | Oncogene Proteins - genetics | Up-Regulation | Idiopathic Pulmonary Fibrosis - genetics | Epithelial Cells - metabolism | Humans | Middle Aged | Male | Pulmonary Fibrosis - genetics | Wnt Proteins - metabolism | Oncogene Proteins - physiology | CCN Intercellular Signaling Proteins | Idiopathic Pulmonary Fibrosis - etiology | Pulmonary Alveoli - metabolism | Adult | Female | Intracellular Signaling Peptides and Proteins - genetics | Pulmonary Fibrosis - etiology | Bleomycin - toxicity | Disease Models, Animal | Pulmonary Alveoli - pathology | Mice, Inbred C57BL | Oncogene Proteins - pharmacology | Epithelial Cells - pathology | Mice, Transgenic | Proto-Oncogene Proteins - genetics | Recombinant Proteins - pharmacology | beta Catenin - metabolism | Animals | Models, Biological | Proto-Oncogene Proteins - physiology | Pulmonary Fibrosis - physiopathology | Cell Proliferation - drug effects | Idiopathic Pulmonary Fibrosis - physiopathology | Mice | Intracellular Signaling Peptides and Proteins - physiology | Cellular proteins | Pulmonary fibrosis | Genes | Physiological aspects | Genetic aspects | Cellular signal transduction | Research | Risk factors | Index Medicus | Abridged Index Medicus
Journal Article
American journal of respiratory and critical care medicine, ISSN 1535-4970, 2014, Volume 189, Issue 2, pp. 214 - 222
Journal Article
The Journal of immunology (1950), ISSN 1550-6606, 2014, Volume 193, Issue 7, pp. 3755 - 3768
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2008, Volume 105, Issue 35, pp. 13051 - 13056
.... Idiopathic pulmonary fibrosis (IPF) is the most common of IIPs and shares with IIPs an increased incidence with age and unexplained scarring in the lung... 
Telomeres | Pulmonary alveoli | Lungs | Interstitial lung diseases | Idiopathic pulmonary fibrosis | Liver | Fibrosis | Dyskeratosis congenita | Genetic mutation | Liver cirrhosis | Liver fibrosis | Interstitial lung disease | Telomerase | Aplastic anemia | RNA | MULTIDISCIPLINARY SCIENCES | REVERSE-TRANSCRIPTASE | LENGTH | IN-SITU HYBRIDIZATION | TERMINAL TRANSFERASE | liver fibrosis | dyskeratosis congenita | telomerase | GENE | interstitial lung disease | FAMILIES | DYSKERATOSIS-CONGENITA | aplastic anemia | COMPONENT | MUTATIONS | Biomarkers - metabolism | Leukocytes, Mononuclear - metabolism | Epithelium - pathology | Pulmonary Alveoli - pathology | Pulmonary Fibrosis - complications | Fibrosis - complications | Humans | Risk Factors | In Situ Hybridization, Fluorescence | Tomography, X-Ray Computed | Pulmonary Fibrosis - genetics | Pulmonary Fibrosis - pathology | Case-Control Studies | RNA - genetics | Fibrosis - diagnostic imaging | Telomerase - genetics | Pulmonary Fibrosis - diagnostic imaging | Germ-Line Mutation | Family | Heterozygote | Telomere - metabolism | Fibrosis - pathology | Genetic aspects | Pulmonary fibrosis | Properties | Health aspects | Risk factors | Pneumonia | Epithelial cells | Lung | Lung diseases | Heredity | Leukocytes | Cirrhosis | Etiology | Mutation | telomerase reverse transcriptase | Alveoli | Age | Biological Sciences
Journal Article
The Journal of experimental medicine, ISSN 1540-9538, 2010, Volume 207, Issue 8, pp. 1589 - 1597
Uncontrolled extracellular matrix production by fibroblasts in response to tissue injury contributes to fibrotic diseases, such as idiopathic pulmonary fibrosis (IPF... 
MEDICINE, RESEARCH & EXPERIMENTAL | PHOSPHATASE | MECHANISMS | GROWTH-FACTOR | IMMUNOLOGY | MYOFIBROBLAST DIFFERENTIATION | EXPRESSION | MICRORNA | Oligonucleotides - genetics | Pulmonary Fibrosis - therapy | Idiopathic Pulmonary Fibrosis - genetics | Gene Expression - drug effects | Gene Expression - genetics | Humans | Actins - metabolism | MicroRNAs - metabolism | Pulmonary Fibrosis - genetics | Idiopathic Pulmonary Fibrosis - metabolism | Actins - genetics | Antisense Elements (Genetics) - therapeutic use | Collagen - genetics | Lung - metabolism | Phosphorylation - drug effects | Smad7 Protein - genetics | Extracellular Matrix Proteins - metabolism | Transforming Growth Factor beta1 - pharmacology | Fibroblasts - metabolism | Smad7 Protein - metabolism | Cell Line | Lung - pathology | Extracellular Matrix Proteins - genetics | Mice, Inbred C57BL | Smad2 Protein - metabolism | Mice, Transgenic | Pulmonary Fibrosis - pathology | Transforming Growth Factor beta1 - genetics | Fibroblasts - pathology | Fibronectins - metabolism | Collagen - metabolism | Animals | Fibroblasts - drug effects | Antisense Elements (Genetics) - genetics | Idiopathic Pulmonary Fibrosis - pathology | Pulmonary Fibrosis - chemically induced | Bleomycin - pharmacology | Fibronectins - genetics | Mice | MicroRNAs - genetics | Brief Definitive Report
Journal Article