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Alteration of Aging-dependent MicroRNAs in Idiopathic Pulmonary Fibrosis (IPF)

Idiopathic Pulmonary Fibrosis (IPF) is the most severe fibrotic lung disease and characterized by the accumulation of (myo)fibroblasts and collagen within the alveolar wall resulting in obliteration of the gas-exchange surface. Although the detailed pathogenesis is not understood, recent studies hav...

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Publicat a:Drug Dev Res
Autor principal: Nho, Richard Seonghun
Format: Artigo
Idioma:Inglês
Publicat: 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4615542/
https://ncbi.nlm.nih.gov/pubmed/26303294
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ddr.21272
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