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pro vyhledávání: '"Beatriz Ballester Llobell"'
Autor:
Olivier Burgy, Christoph H. Mayr, Beatriz Ballester Llobell, Arunima Sengupta, Déborah Schenesse, Christina Coughlan, Tanyalak Parimon, Peter Chen, Michael Lindner, Anne Hilgendorff, Matthias Mann, Ali Önder Yildirim, Oliver Eickelberg, Herbert B. Schiller, Mareike Lehmann, Gerald Burgstaller, Melanie Königshoff
Idiopathic pulmonary fibrosis (IPF) is a lethal and chronic lung disease characterized by aberrant intercellular communication, increased extracellular matrix (ECM) deposition, and destruction of functional lung tissue. Extracellular vesicles (EVs) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a31cfb1b5f105c5100b9610805d9cb
https://doi.org/10.1101/2022.12.22.521499
https://doi.org/10.1101/2022.12.22.521499
Autor:
Cristina Estornut Navarro, Ines Roger Laparra, Paula Montero Magalló, Javier Milara Payá, Julio Cortijo Gimeno, Beatriz Ballester Llobell
Publikováno v:
Idiopathic interstitial pneumonias.
Background: Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive and irreversible form of fibrotic intersticial lung disease, characterized by uncontrolled fibroblast proliferative processes and alveolar type II epithelial dysfunction. MUC4,