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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: The Rockefeller University Press 2008
विषय:
Brief Definitive Reports
ऑनलाइन पहुंच: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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