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Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a progressive and devastating lung disorder of unknown origin, with very poor prognosis and no effective treatment. The disease is characterized by abnormal activation of alveolar epithelial cells, which secrete numerous mediators involved in the expansion of t...
保存先:
出版年: | Respir Res |
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主要な著者: | , , , |
フォーマット: | Artigo |
言語: | Inglês |
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BioMed Central
2016
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主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4779202/ https://ncbi.nlm.nih.gov/pubmed/26944412 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-016-0343-6 |
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