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Nature Communications|March 24, 2023
Mena regulates nesprin-2 to control actin-nuclear lamina associations, trans-nuclear membrane signalling and gene expressionFrederic Li Mow Chee, Bruno Beernaert, Billie G C Griffith, 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 Communications|August 25, 2023
Driver gene combinations dictate cutaneous squamous cell carcinoma disease continuum progressionPeter Bailey, Rachel A Ridgway, Patrizia Cammareri, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|April 12, 2019
The Clinical Features of Bronchiectasis Associated with Alpha-1 Antitrypsin Deficiency, Common Variable Immunodeficiency and Primary Ciliary Dyskinesia--Results from the U.S. Bronchiectasis Research RegistryEdward Eden, Radmila Choate, Alan Barker, 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.
Chest|July 6, 2020
Airway Clearance Techniques in Bronchiectasis: Analysis From the United States Bronchiectasis and Non-TB Mycobacteria Research RegistryAshwin Basavaraj, Radmila Choate, Doreen Addrizzo-Harris, et al.
American Journal of Human Genetics|April 3, 2001
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43N A Alam, S Bevan, M Churchman, et al.
Respiratory Medicine|January 5, 2021
Pseudomonas aeruginosa associated with severity of non-cystic fibrosis bronchiectasis measured by the modified bronchiectasis severity score (BSI) and the FACED: The US bronchiectasis and NTM Research Registry (BRR) studyRadmila Choate, Timothy R Aksamit, David Mannino, et al.
Chest|May 9, 2017
Pharmacotherapy for Non-Cystic Fibrosis Bronchiectasis: Results From an NTM Info & Research Patient Survey and the Bronchiectasis and NTM Research RegistryEmily Henkle, Timothy R Aksamit, Alan F Barker, et al.
American Journal of Human Genetics|March 10, 2005
Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosisDavid P Kelsell, Elizabeth E Norgett, Harriet Unsworth, et al.
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