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CILP attenuates pulmonary fibrosis through the TGF-β1/SMAD3 pathway

Abstract Idiopathic pulmonary fibrosis (IPF) is a chronic progressive disease with poor survival, which is characterized by abnormal accumulation of fibrotic tissue in the lung parenchyma. Transforming growth factor-β1 (TGF-β) is a central profibrotic mediator, but the related mechanism of the activ...

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Principais autores: Hua Zou, Jiale Dong, Run Zhao, Feng Liu, Jingsong Cheng, Xushan Li, Chengshuo Fei, Peng Li, Chunlei Liu
Formato: Artigo
Idioma:Inglês
Publicado: BMC 2025-12-01
Series:European Journal of Medical Research
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Acceso en liña:https://doi.org/10.1186/s40001-025-03644-7
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