Background: Idiopathic interstitial pneumonia is characterized by fibroblast proliferation and extracellular matrix (ECM) accumulation. Matrix metalloproteases (MMPs) and tissue inhibitors of metalloproteases (TIMPs) have been shown to regulate remodeling of the ECM, which indicates that they are important factors in the process of lung fibrosis. Therefore, we evaluated the expres-sion of MMPs and TIMPs in tissues obtained from patients with idiopathic interstitial pneumonia and control tissues. Methods: Thirty-seven patients who were diagnosed with IIP (22: IPF, 13: NSIP, 2: COP) and 5 controls were enrolled in this study. The MMP-2 and-9 activity in lung tissue ob-tained from these patients was analyzed using gelatin zymography and the le...
To investigate simultaneously localization and relative activity of MMPs during extracellular matrix...
Abstract Background Matrix metalloproteinases (MMPs) ...
Acute lung injury is characterized by a severe disruption of alveolo-capillary structures and includ...
Rationale: Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposit...
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extr...
Background: Idiopathic pulmonary fibrosis (IPF) is characterized by fibroblast expansion and extrace...
Fibroblast proliferation and extracellular matrix accumulation characterize idiopathic pulmonary fib...
Matrix metalloproteinases (MMPs) are zinc-endopeptidases responsible for degradation of the extracel...
AbstractBackgroundPulmonary fibrosis, the final result of a large variety of interstitial lung disea...
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extr...
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extr...
Idiopathic pulmonary fibrosis (IPF), a progressive fibrosing lung condition is a ther-apeutic medica...
Background: Pulmonary fibrosis, the final result of a large variety of interstitial lung diseases, i...
To investigate simultaneously localization and relative activity of MMPs during extracellular matrix...
IntroductionIdiopathic pulmonary fibrosis (IPF) is a progressively fibrotic lung condition with poor...
To investigate simultaneously localization and relative activity of MMPs during extracellular matrix...
Abstract Background Matrix metalloproteinases (MMPs) ...
Acute lung injury is characterized by a severe disruption of alveolo-capillary structures and includ...
Rationale: Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposit...
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extr...
Background: Idiopathic pulmonary fibrosis (IPF) is characterized by fibroblast expansion and extrace...
Fibroblast proliferation and extracellular matrix accumulation characterize idiopathic pulmonary fib...
Matrix metalloproteinases (MMPs) are zinc-endopeptidases responsible for degradation of the extracel...
AbstractBackgroundPulmonary fibrosis, the final result of a large variety of interstitial lung disea...
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extr...
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extr...
Idiopathic pulmonary fibrosis (IPF), a progressive fibrosing lung condition is a ther-apeutic medica...
Background: Pulmonary fibrosis, the final result of a large variety of interstitial lung diseases, i...
To investigate simultaneously localization and relative activity of MMPs during extracellular matrix...
IntroductionIdiopathic pulmonary fibrosis (IPF) is a progressively fibrotic lung condition with poor...
To investigate simultaneously localization and relative activity of MMPs during extracellular matrix...
Abstract Background Matrix metalloproteinases (MMPs) ...
Acute lung injury is characterized by a severe disruption of alveolo-capillary structures and includ...