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Biorxiv : the Preprint Server for Biology|August 30, 2024
Dysregulated Airway Host Defense in Hyper IgE Syndrome due to STAT3 MutationsLing Sun, Samantha A Walls, Hong Dang, et al.American Journal of Respiratory and Critical Care Medicine|April 16, 2024
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and BronchiectasisGerard W Dougherty, Lawrence E Ostrowski, Tabea Nöthe-Menchen, et al.American Journal of Human Genetics|December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesiaMichael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.Nature Medicine|January 31, 2020
Author Correction: A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearanceRaghu R Chivukula, Daniel T Montoro, Hui Min Leung, et al.Nature Medicine|January 22, 2020
A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearanceRaghu R Chivukula, Daniel T Montoro, Hui Min Leung, et al.American Journal of Respiratory and Critical Care Medicine|December 15, 2020
Secretory Cells Dominate Airway CFTR Expression and Function in Human Airway Superficial EpitheliaKenichi Okuda, Hong Dang, Yoshihiko Kobayashi, et al.American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.Pageof 6