CFTR-mediated monocyte/macrophage dysfunction revealed by cystic fibrosis proband-parent comparisons

Cystic fibrosis (CF) is an inherited disorder caused by biallelic mutations of the CF transmembrane conductance regulator (CFTR) gene. Converging evidence suggests that CF carriers with only 1 defective CFTR copy are at increased risk for CF-related conditions and pulmonary infections, but the molec...

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Detalles Bibliográficos
Autores principales: Zhang, Xi, Moore, Camille M., Harmacek, Laura D., Domenico, Joanne, Rangaraj, Vittobai Rashika, Ideozu, Justin E., Knapp, Jennifer R., Woods, Katherine J., Jump, Stephanie, Jia, Shuang, Prokop, Jeremy W., Bowler, Russell, Hessner, Martin J., Gelfand, Erwin W., Levy, Hara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986072/
https://www.ncbi.nlm.nih.gov/pubmed/35315363
http://dx.doi.org/10.1172/jci.insight.152186

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986072/
https://www.ncbi.nlm.nih.gov/pubmed/35315363
http://dx.doi.org/10.1172/jci.insight.152186

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