Human pulmonary alveolar proteinosis associated with a defect in GM-CSF/IL-3/IL-5 receptor common beta chain expression.

Pulmonary alveolar proteinosis (PAP) is a heterogeneous disorder of genetic or acquired etiologies. In some cases congenital PAP is associated with hereditary surfactant protein (SP)-B deficiency. To date, the molecular defect in the majority of patients with PAP has not been identified. In mice, PA...

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Detaylı Bibliyografya
Yayımlandı:J Clin Invest
Asıl Yazarlar: Dirksen, U, Nishinakamura, R, Groneck, P, Hattenhorst, U, Nogee, L, Murray, R, Burdach, S
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Clinical Investigation 1997
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC508416/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9410898/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI119758
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