Hyperinflammation and airway surface liquid dehydration in cystic fibrosis: purinergic system as therapeutic target
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology,Immunology
Link
https://link.springer.com/content/pdf/10.1007/s00011-021-01464-z.pdf
Reference167 articles.
1. Rafeeq MM, Murad HAS. Cystic fibrosis: current therapeutic targets and future approaches. J Transl Med. 2017;15:1–9.
2. Rogers GB, Bruce KD, Hoffman LR. How can the cystic fibrosis respiratory microbiome influence our clinical decision-making? Curr Opin Pulm Med. 2017;23:536–43.
3. Ooi CY, Durie PR. Cystic fibrosis from the gastroenterologist’s perspective. Nat Rev Gastroenterol Hepatol. 2016;13:175–85.
4. Kamal N, Surana P, Koh C. Liver disease in patients with cystic fibrosis. Curr Opin Gastroenterol. 2018;34:146–51.
5. Roesch EA, Nichols DP, Chmiel JF. Inflammation in cystic fibrosis: an update. Pediatr Pulmonol. 2018;53:S30-50.
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3. Pancreatic Insufficiency in a Child with p.Gly542* and c.2657+5G>A Heterozygote CFTR: A Case Report;Clinical Medicine & Research;2022-02-07
4. Role of the Purinergic P2Y2 Receptor in Pulmonary Hypertension;International Journal of Environmental Research and Public Health;2021-10-20
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