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2017, Methods in molecular biology, ISBN 1493971131, Volume 1627
This volume describes state-of-the-art protocols that serve as "recipes" for scientists concentrating on fibrosis research. This book is divided into four... 
Fibrosis
Web Resource
2017, Methods in molecular biology, ISBN 1493971131, Volume 1627
This volume describes state-of-the-art protocols that serve as "recipes" for scientists concentrating on fibrosis research. This book is divided into four... 
Fibrosis
Web Resource
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2008, Volume 105, Issue 35, pp. 13051 - 13056
Idiopathic interstitial pneumonias (IIPs) have a progressive and often fatal course, and their enigmatic etiology has complicated approaches to effective... 
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 | DOMINANT DYSKERATOSIS-CONGENITA | REVERSE-TRANSCRIPTASE | LENGTH | IN-SITU HYBRIDIZATION | TERMINAL TRANSFERASE | liver fibrosis | dyskeratosis congenita | telomerase | GENE | interstitial lung disease | FAMILIES | aplastic anemia | MUTATIONS | APLASTIC-ANEMIA | 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 | Tissue | Leucocytes | Pneumonia | Mutation | Chromosomes | Deoxyribonucleic acid--DNA | Epithelial cells | Lung | Lung diseases | Heredity | Leukocytes | Cirrhosis | Etiology | telomerase reverse transcriptase | Alveoli | Age | Index Medicus | Biological Sciences
Journal Article
Journal of Oral Pathology & Medicine, ISSN 0904-2512, 07/2018, Volume 47, Issue 6, pp. 632 - 632
Journal Article
Journal of Oral Pathology & Medicine, ISSN 0904-2512, 07/2018, Volume 47, Issue 6, pp. 630 - 631
Journal Article
Journal of Oral Pathology & Medicine, ISSN 0904-2512, 05/2018, Volume 47, Issue 5, pp. 538 - 538
Journal Article
Value in Health : The Journal of the International Society for Pharmacoeconomics and Outcomes Research, ISSN 1098-3015, 10/2017, Volume 20, Issue 9, p. A854
Journal Article
Clinical and Experimental Pharmacology and Physiology, ISSN 0305-1870, 11/2016, Volume 43, Issue 11, p. 1029
Senescent hearts exhibit defective responses to [beta]-adrenergic receptor ([beta]-AR) over-activation upon stress, leading to more severe pathological cardiac... 
Fibrosis
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2013, Volume 8, Issue 10, pp. e76451 - e76451
Rationale: Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease characterized by progressive scarring and matrix deposition. Recent reports... 
GROWTH-FACTOR-BETA | MESSENGER-RNA | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | PRIMARY GRAFT DYSFUNCTION | IN-VIVO | MYOFIBROBLAST | AUTOREACTIVITY | IDENTIFICATION | FIBROBLASTS | INDUCED LUNG FIBROSIS | T-Lymphocyte Subsets - immunology | Transcription, Genetic - drug effects | Idiopathic Pulmonary Fibrosis - genetics | Collagen Type V - genetics | Autoantibodies - blood | Humans | Collagen Type V - immunology | Pulmonary Fibrosis - genetics | RNA, Messenger - metabolism | Transforming Growth Factor beta - biosynthesis | Collagen Type V - administration & dosage | Idiopathic Pulmonary Fibrosis - metabolism | Lymphocyte Activation - immunology | Inflammation Mediators - metabolism | Female | Pulmonary Fibrosis - metabolism | Collagen Type V - metabolism | Cytokines - genetics | Disease Models, Animal | Gene Expression | RNA, Messenger - genetics | Pulmonary Fibrosis - immunology | Immune Tolerance | Pulmonary Fibrosis - pathology | Bleomycin - adverse effects | Idiopathic Pulmonary Fibrosis - immunology | Collagen Type I - immunology | Gene Expression Regulation - drug effects | Autoantibodies - immunology | Animals | Transforming Growth Factor beta - genetics | T-Lymphocyte Subsets - metabolism | Idiopathic Pulmonary Fibrosis - pathology | Mice | Pulmonary Fibrosis - drug therapy | Cytokines - biosynthesis | Idiopathic Pulmonary Fibrosis - drug therapy | Nebulizers and Vaporizers | Animal models | Disease | Transcription | Pathogenesis | Lung | Antibodies | Immunity | Interleukin 6 | Bleomycin | Consent | Lymphocytes | Smad2 protein | Rodents | Animal tissues | Collagen (type V) | Extracellular matrix | Growth factors | Deposition | NF-κB protein | Lung diseases | Tumor necrosis factor-α | Gene expression | Sp1 protein | Patients | Immunological tolerance | Medicine | Pathology | Signaling | Scars | Pulmonary fibrosis | Lungs | Liquid oxygen | Collagen | γ-Interferon | Fibrosis | Interferon | Binding sites | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2017, Volume 377, Issue 21, pp. 2024 - 2035
Approximately 5% of patients with cystic fibrosis express one allele with some retained CFTR function. In a prospective trial, tezacaftor–ivacaftor had a... 
POPULATION | REGULATOR | MEDICINE, GENERAL & INTERNAL | LUMACAFTOR | EFFICACY | SAFETY | PHENOTYPE | AGED 6-11 YEARS | RANDOMIZED CONTROLLED-TRIAL | F508DEL-CFTR | G551D-CFTR MUTATION | Forced Expiratory Volume - drug effects | Cystic Fibrosis - physiopathology | Humans | Male | Aminophenols - therapeutic use | Quinolones - pharmacology | Aminophenols - adverse effects | Aminophenols - pharmacology | Young Adult | Quinolones - adverse effects | Quinolones - therapeutic use | Cystic Fibrosis Transmembrane Conductance Regulator - pharmacology | Adult | Benzodioxoles - adverse effects | Female | Indoles - pharmacology | Benzodioxoles - therapeutic use | Child | Double-Blind Method | Cross-Over Studies | Cystic Fibrosis Transmembrane Conductance Regulator - therapeutic use | Indoles - adverse effects | Cystic Fibrosis - genetics | Cystic Fibrosis Transmembrane Conductance Regulator - adverse effects | Adolescent | Quality of Life | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Heterozygote | Indoles - therapeutic use | Mutation | Benzodioxoles - pharmacology | Cystic Fibrosis - drug therapy | Drug Combinations | Proteins | Clonal deletion | Clinical trials | Heterozygotes | Cystic fibrosis | Cystic fibrosis transmembrane conductance regulator | Gene deletion | Drug therapy | Patients | Pharmaceuticals | Index Medicus | Abridged Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2014, Volume 9, Issue 6, p. e100407
Following publication, the authors were informed that the Danish Health and Medicines Authority (formerly Danish Medicines Agency) has changed the side effects... 
Fibrosis
Journal Article
Magnetic Resonance in Medicine, ISSN 0740-3194, 02/2014, Volume 71, Issue 2, pp. 823 - 829
Purpose Myocardial T sub(1) mapping is an emerging technique that could improve cardiovascular magnetic resonance diagnostic accuracy. In this study, a... 
Fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 06/2013, Volume 187, Issue 11, pp. 1219 - 1225
Journal Article
2015, ISBN 9781926710341, 79
"Beth Gobeil narrates a poignant story, a mother's journey, beginning at the point her son is diagnosed with Cystic Fibrosis."--Back cover. 
Cystic fibrosis
Book
2004, Lung biology in health and disease, ISBN 9780824740733, Volume 185, xxii, 772
A discussion of the epidemiology, clinical features, and differential diagnoses of idiopathic pulmonary fibrosis (IPF). Key topics include the role of... 
Pulmonary Fibrosis | diagnosis | Treatment | therapy | etiology | Pulmonary Medicine | Pulmonary fibrosis
Book
Journal of Experimental Medicine, ISSN 0022-1007, 07/2011, Volume 208, Issue 7, pp. 1459 - 1471
Journal Article
Nuclear Medicine and Biology, ISSN 0969-8051, 10/2014, Volume 41, Issue 9, p. 728
Fibrosis affecting functionality of vital organs such as liver, lung, heart, and kidney, is involved in many chronic diseases. Positron emission tomography... 
Fibrosis
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 09/2009, Volume 119, Issue 9, pp. 2550 - 2563
Uncontrolled activation of the coagulation cascade contributes to the pathophysiology of several conditions, including acute and chronic lung diseases.... 
MEDICINE, RESEARCH & EXPERIMENTAL | GROWTH-FACTOR-BETA | BLOOD-COAGULATION | THROMBUS FORMATION | GENE-EXPRESSION | IDIOPATHIC PULMONARY-FIBROSIS | PROTEASE-ACTIVATED RECEPTOR-1 | TISSUE FACTOR EXPRESSION | SUSCEPTIBILITY GENES | RESPIRATORY-DISTRESS-SYNDROME | BRONCHOALVEOLAR LAVAGE | Up-Regulation | Lung Injury - pathology | Factor Xa Inhibitors | Receptor, PAR-1 - metabolism | Humans | Middle Aged | Actins - metabolism | Male | Pulmonary Fibrosis - blood | Idiopathic Pulmonary Fibrosis - blood | RNA, Messenger - metabolism | Case-Control Studies | Idiopathic Pulmonary Fibrosis - metabolism | Idiopathic Pulmonary Fibrosis - etiology | Base Sequence | Lung Injury - metabolism | Adult | Female | Cell Differentiation | Pulmonary Fibrosis - metabolism | Receptors, Vitronectin - metabolism | Pulmonary Fibrosis - etiology | Bleomycin - toxicity | Fibroblasts - metabolism | Gene Expression | Factor Xa - genetics | Mice, Inbred C57BL | RNA, Messenger - genetics | Cells, Cultured | Pulmonary Fibrosis - pathology | Fibroblasts - pathology | Factor Xa - metabolism | Animals | Transforming Growth Factor beta - genetics | Models, Biological | Fibroblasts - drug effects | Idiopathic Pulmonary Fibrosis - pathology | Aged | Mice | Transforming Growth Factor beta - metabolism | Transforming growth factors | Lung diseases | Integrins | Index Medicus | Abridged Index Medicus
Journal Article
Nature Medicine, ISSN 1078-8956, 2013, Volume 19, Issue 7, pp. 939 - 945
Journal Article