Targeting Proteases in Cystic Fibrosis Lung Disease. Paradigms, Progress, and Potential-Reference-Cited by-同舟云学术

Targeting Proteases in Cystic Fibrosis Lung Disease. Paradigms, Progress, and Potential

Published:2020-01-15 Issue:2 Volume:201 Page:141-147
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

McKelvey Michael C.¹,Weldon Sinéad¹,McAuley Daniel F.²,Mall Marcus A.³⁴⁵,Taggart Clifford C.¹

Affiliation:

1. Airway Innate Immunity Research Group

2. Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen’s University Belfast, Belfast, United Kingdom

3. Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine, Charité – Universitätsmedizin Berlin, Berlin, Germany

4. Berlin Institute of Health, Berlin, Germany; and

5. German Center for Lung Research, Berlin, Germany

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Link

https://www.atsjournals.org/doi/pdf/10.1164/rccm.201906-1190PP

Reference70 articles.

1. CFTR: cystic fibrosis and beyond

2. VX-659–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

3. VX-445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

4. Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections

5. Protease-antiprotease imbalance in the lungs of children with cystic fibrosis.

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