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...

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Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: The Rockefeller University Press 2008
Assuntos:
Brief Definitive Reports
Acesso em linha: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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