Sadr S, Tahermohammadi H, Kaveh S, Khanbabaee G, Tabatabaei S, Choopani R
BMC Pulm Med. 2023; 23(1):488.
PMID: 38053097
PMC: 10696786.
DOI: 10.1186/s12890-023-02787-9.
Oza P, Kashfi K
Pharmacol Ther. 2023; 249:108502.
PMID: 37517510
PMC: 10529678.
DOI: 10.1016/j.pharmthera.2023.108502.
Oza P, Kashfi K
Nitric Oxide. 2022; 128:72-102.
PMID: 36029975
PMC: 9398942.
DOI: 10.1016/j.niox.2022.08.003.
Kamenshchikov N, Berra L, Carroll R
Biomedicines. 2022; 10(2).
PMID: 35203578
PMC: 8962307.
DOI: 10.3390/biomedicines10020369.
Cho S, Hamilos D, Han D, Laidlaw T
J Allergy Clin Immunol Pract. 2020; 8(5):1505-1511.
PMID: 32389275
PMC: 7696652.
DOI: 10.1016/j.jaip.2019.12.021.
Could nasal nitric oxide help to mitigate the severity of COVID-19?.
Martel J, Ko Y, Young J, Ojcius D
Microbes Infect. 2020; 22(4-5):168-171.
PMID: 32387333
PMC: 7200356.
DOI: 10.1016/j.micinf.2020.05.002.
Induced Sputum Nitrite Levels Correlate with Clinical Asthma Parameters in Children Aged 7-18 Years with Mild to Moderate Persistent Asthma.
Nandan D, Kansal P, Patharia N, Goyal P
J Lab Physicians. 2016; 8(2):90-5.
PMID: 27365917
PMC: 4866390.
DOI: 10.4103/0974-2727.180788.
Clinical application of exhaled nitric oxide measurements in a korean population.
Song W, Kwon J, Kim E, Lee S, Kim S, Lee S
Allergy Asthma Immunol Res. 2015; 7(1):3-13.
PMID: 25553257
PMC: 4274466.
DOI: 10.4168/aair.2015.7.1.3.
Reduced nasal nitric oxide production in cystic fibrosis patients with elevated systemic inflammation markers.
Michl R, Hentschel J, Fischer C, Beck J, Mainz J
PLoS One. 2013; 8(11):e79141.
PMID: 24236100
PMC: 3827333.
DOI: 10.1371/journal.pone.0079141.
Ventilatory pattern and energy expenditure are altered in cystic fibrosis mice.
Darrah R, Bederman I, Mitchell A, Hodges C, Campanaro C, Drumm M
J Cyst Fibros. 2013; 12(4):345-51.
PMID: 23290341
PMC: 3620718.
DOI: 10.1016/j.jcf.2012.11.008.
Clinical application of exhaled nitric oxide measurement in pediatric lung diseases.
Manna A, Caffarelli C, Varini M, Dascola C, Montella S, Maglione M
Ital J Pediatr. 2013; 38:74.
PMID: 23273317
PMC: 3545741.
DOI: 10.1186/1824-7288-38-74.
Interferon γ stimulates accumulation of gas phase nitric oxide in differentiated cultures of normal and cystic fibrosis airway epithelial cells.
Ostrowski L, Stewart D, Hazucha M
Lung. 2012; 190(5):563-71.
PMID: 22729230
PMC: 4152005.
DOI: 10.1007/s00408-012-9395-7.
An official ATS clinical practice guideline: interpretation of exhaled nitric oxide levels (FENO) for clinical applications.
Dweik R, Boggs P, Erzurum S, Irvin C, Leigh M, Lundberg J
Am J Respir Crit Care Med. 2011; 184(5):602-15.
PMID: 21885636
PMC: 4408724.
DOI: 10.1164/rccm.9120-11ST.
Biomarkers in exhaled breath condensate: a review of collection, processing and analysis.
Grob N, Aytekin M, Dweik R
J Breath Res. 2011; 2(3):037004.
PMID: 21386165
PMC: 3058888.
DOI: 10.1088/1752-7155/2/3/037004.
Myeloperoxidase-dependent oxidative metabolism of nitric oxide in the cystic fibrosis airway.
Chapman A, Morrissey B, Vasu V, Juarez M, Houghton J, Li C
J Cyst Fibros. 2010; 9(2):84-92.
PMID: 20080069
PMC: 3118565.
DOI: 10.1016/j.jcf.2009.10.001.
Extended nitric oxide measurements in exhaled air of cystic fibrosis and healthy adults.
Hofer M, Mueller L, Rechsteiner T, Benden C, Boehler A
Lung. 2009; 187(5):307-13.
PMID: 19669109
DOI: 10.1007/s00408-009-9160-8.
Airway biomarkers of the oxidant burden in asthma and chronic obstructive pulmonary disease: current and future perspectives.
Louhelainen N, Myllarniemi M, Rahman I, Kinnula V
Int J Chron Obstruct Pulmon Dis. 2009; 3(4):585-603.
PMID: 19281076
PMC: 2650600.
DOI: 10.2147/copd.s3671.
Evidence that CFTR is expressed in rat tracheal smooth muscle cells and contributes to bronchodilation.
Vandebrouck C, Melin P, Norez C, Robert R, Guibert C, Mettey Y
Respir Res. 2006; 7:113.
PMID: 16938132
PMC: 1560124.
DOI: 10.1186/1465-9921-7-113.
Role of epithelial nitric oxide in airway viral infection.
Xu W, Zheng S, Dweik R, Erzurum S
Free Radic Biol Med. 2006; 41(1):19-28.
PMID: 16781449
PMC: 7127628.
DOI: 10.1016/j.freeradbiomed.2006.01.037.
Inducible NO synthase expression is low in airway epithelium from young children with cystic fibrosis.
Moeller A, Horak Jr F, Lane C, Knight D, Kicic A, Brennan S
Thorax. 2006; 61(6):514-20.
PMID: 16517573
PMC: 2111217.
DOI: 10.1136/thx.2005.054643.