Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA

Primary pulmonary alveolar proteinosis (PAP) is a rare syndrome characterized by accumulation of surfactant in the lungs that is presumed to be mediated by disruption of granulocyte/macrophage colony-stimulating factor (GM-CSF) signaling based on studies in genetically modified mice. The effects of...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Suzuki, Takuji, Sakagami, Takuro, Rubin, Bruce K., Nogee, Lawrence M., Wood, Robert E., Zimmerman, Sarah L., Smolarek, Teresa, Dishop, Megan K., Wert, Susan E., Whitsett, Jeffrey A., Grabowski, Gregory, Carey, Brenna C., Stevens, Carrie, van der Loo, Johannes C.M., Trapnell, Bruce C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Rockefeller University Press 2008
Aiheet:
Brief Definitive Reports
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2585845/
https://ncbi.nlm.nih.gov/pubmed/18955570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1084/jem.20080990
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