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pro vyhledávání: '"Katri Koli"'
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 48:448-455
Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease with a poor prognosis and very few therapeutic options. On the molecular level, patients with IPF have increased amounts of the bone morphogenetic protein (BMP) inhibitor gremlin in th
Autor:
Ville Pulkkinen, Katri Koli, Kaisa Salmenkivi, Vuokko L. Kinnula, Markku Heikinheimo, Riika Vähätalo, Outi Leppäranta, Marjukka Myllärniemi
Publikováno v:
American journal of respiratory cell and molecular biology. 42(5)
Idiopathic pulmonary fibrosis (IPF) (histopathology of usual interstitial pneumonia [UIP]) is a progressive disease with poor prognosis. Characteristic features of IPF/UIP include fibroblastic foci, which are patchy lesions of focal, disarranged myof