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Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive and life-threatening interstitial lung disease characterized by excessive extracellular matrix deposition and fibroblast activation
10.1007/s11154-014-9287-7 156
Instead of antibody recognition, it identifies compounds by their mass-to-charge ratio and fragmentation patterns
A mammalian member of a family of theta class glutathione s-transferase-like proteins"
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