CareLit · DOI-Nachweis · Pneumologie
Remodelling-related molecular profiles in interstitial pulmonary fibrosis
DOI 10.1055/s-0032-1315510
Bibliografische Angaben
Nachweis in CareLit
Autor:innenD Jonigk, J Rische, L Maegel, H Golpon, N Izykowski, CL Bockmeyer, T Welte, S Janciauskiene, J Gottlieb, G Warnecke, A Haverich, H Kreipe, F Laenger
ZeitschriftPneumologie
Ausgabe05/2012
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Rationale: Idiopathic pulmonary fibrosis (IPF) is the most representative of the idiopathic interstitial pneumonia group (IIP) and is a disease characterized by an overall poor prognosis and unresponsiveness to currently available therapies. Thus elucidation of molecular pathways to gain better insight into the pathogenesis and identify potential therapeutic targets is warranted. Methods: We performed compartment-sp…
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Zitierempfehlung
D Jonigk, J Rische, L Maegel, H Golpon, N Izykowski, CL Bockmeyer, T Welte, S Janciauskiene, J Gottlieb, G Warnecke, A Haverich, H Kreipe, F Laenger (2012) Remodelling-related molecular profiles in interstitial pulmonary fibrosis. Pneumologie (05). https://doi.org/10.1055/s-0032-1315510
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