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Two-Way Conversion between Lipogenic and Myogenic Fibroblastic Phenotypes Marks the Progression and Resolution of Lung Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a form of progressive interstitial lung disease with unknown etiology. Due to a lack of effective treatment, IPF is associated with a high mortality rate. The hallmark feature of this disease is the accumulation of activated myofibroblasts that excessively depo...

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Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:	Cell Stem Cell
Κύριοι συγγραφείς:	Agha, Elie El, Moiseenko, Alena, Kheirollahi, Vahid, De Langhe, Stijn, Crnkovic, Slaven, Kwapiszewska, Grazyna, Kosanovic, Djuro, Schwind, Felix, Schermuly, Ralph T., Henneke, Ingrid, MacKenzie, BreAnne, Quantius, Jennifer, Herold, Susanne, Ntokou, Aglaia, Ahlbrecht, Katrin, Morty, Rory E., Günther, Andreas, Seeger, Werner, Bellusci, Saverio
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	2016
Θέματα:	Article
Διαθέσιμο Online:	https://ncbi.nlm.nih.gov/pmc/articles/PMC5291816/ https://ncbi.nlm.nih.gov/pubmed/27867035 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.stem.2016.10.004
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Two-Way Conversion between Lipogenic and Myogenic Fibroblastic Phenotypes Marks the Progression and Resolution of Lung Fibrosis

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