Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice

The gain-of-function MUC5B promoter variant rs35705950 is the dominant risk factor for developing idiopathic pulmonary fibrosis (IPF). Here we show in humans that MUC5B, a mucin thought to be restricted to conducting airways, is co-expressed with surfactant protein C (SFTPC) in type 2 alveolar epith...

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Detalles Bibliográficos
Autores principales: Hancock, Laura A., Hennessy, Corinne E., Solomon, George M., Dobrinskikh, Evgenia, Estrella, Alani, Hara, Naoko, Hill, David B., Kissner, William J., Markovetz, Matthew R., Grove Villalon, Diane E., Voss, Matthew E., Tearney, Guillermo J., Carroll, Kate S., Shi, Yunlong, Schwarz, Marvin I., Thelin, William R., Rowe, Steven M., Yang, Ivana V., Evans, Christopher M., Schwartz, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299094/
https://www.ncbi.nlm.nih.gov/pubmed/30560893
http://dx.doi.org/10.1038/s41467-018-07768-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299094/
https://www.ncbi.nlm.nih.gov/pubmed/30560893
http://dx.doi.org/10.1038/s41467-018-07768-9

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