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pro vyhledávání: '"Erica N. LeClair"'
Autor:
Erica N. LeClair, David A. Stoltz, Nicholas D. Gansemer, Katherine N. Gibson-Corley, Paul B. McCray, Michael J. Welsh, Mariah R. Leidinger, Sarah E. Ernst, Carrie K. Barker, Matthew D. Strub, Ryan J. Adam, Daniel P. Cook, Philip H. Karp, David K. Meyerholz
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) function causes cystic fibrosis (CF), predisposing the lungs to chronic infection and inflammation. In young infants with CF, structural airway defects are increasingly recognized bef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd7b924e768383966392ca32bdd8d29
https://doi.org/10.1038/s41374-018-0026-7
https://doi.org/10.1038/s41374-018-0026-7
