Bhaumik R, Aungkur N, Anderson G
Front Cell Infect Microbiol. 2024; 13:1322853.
PMID: 38274738
PMC: 10808757.
DOI: 10.3389/fcimb.2023.1322853.
Li H, Rodrat M, Al-Salmani M, Veselu D, Han S, Raraigh K
J Physiol. 2024; 602(2):333-354.
PMID: 38186087
PMC: 10872379.
DOI: 10.1113/JP285727.
Martin C, Guzior D, Gonzalez C, Okros M, Mielke J, Padillo L
Respir Res. 2023; 24(1):317.
PMID: 38104128
PMC: 10725582.
DOI: 10.1186/s12931-023-02630-z.
Clemente-Suarez V, Martin-Rodriguez A, Redondo-Florez L, Villanueva-Tobaldo C, Yanez-Sepulveda R, Tornero-Aguilera J
Cells. 2023; 12(20).
PMID: 37887299
PMC: 10605148.
DOI: 10.3390/cells12202455.
Martin C, Guzior D, Gonzalez C, Okros M, Mielke J, Padillo L
Res Sq. 2023; .
PMID: 37841851
PMC: 10571617.
DOI: 10.21203/rs.3.rs-3356170/v1.
New Insights and Potential Therapeutic Interventions in Metabolic Diseases.
Clemente-Suarez V, Martin-Rodriguez A, Redondo-Florez L, Lopez-Mora C, Yanez-Sepulveda R, Tornero-Aguilera J
Int J Mol Sci. 2023; 24(13).
PMID: 37445852
PMC: 10342188.
DOI: 10.3390/ijms241310672.
Effect of Different Molecular Weights of Polyacrylic Acid on Rat Lung Following Intratracheal Instillation.
Nishida C, Izumi H, Tomonaga T, Wang K, Higashi H, Takeshita J
Int J Mol Sci. 2022; 23(18).
PMID: 36142256
PMC: 9499135.
DOI: 10.3390/ijms231810345.
Ultrasound-guided placement of long peripheral cannula in children with cystic fibrosis.
Giardina M, Barilla D, Crimi C, Arone A, Benedetto F, Lucanto C
Pediatr Pulmonol. 2022; 57(9):2060-2066.
PMID: 35574730
PMC: 9545099.
DOI: 10.1002/ppul.25978.
Parasite Survival and Disease Persistence in Cystic Fibrosis, Schistosomiasis and Pathogenic Bacterial Diseases: A Role for Universal Stress Proteins?.
Masamba P, Kappo A
Int J Mol Sci. 2021; 22(19).
PMID: 34639223
PMC: 8509486.
DOI: 10.3390/ijms221910878.
Clinical Considerations for Routine Auditory and Vestibular Monitoring in Patients With Cystic Fibrosis.
Garinis A, Poling G, Rubenstein R, Konrad-Martin D, Hullar T, Baguley D
Am J Audiol. 2021; 30(3S):800-809.
PMID: 34549989
PMC: 9126110.
DOI: 10.1044/2021_AJA-21-00031.
A Fragile Balance: Does Neutrophil Extracellular Trap Formation Drive Pulmonary Disease Progression?.
Block H, Zarbock A
Cells. 2021; 10(8).
PMID: 34440701
PMC: 8394734.
DOI: 10.3390/cells10081932.
CFTR targeted therapies: recent advances in cystic fibrosis and possibilities in other diseases of the airways.
Patel S, Bono T, Rowe S, Solomon G
Eur Respir Rev. 2020; 29(156).
PMID: 32554756
PMC: 9131734.
DOI: 10.1183/16000617.0068-2019.
Cryptides Identified in Human Apolipoprotein B as New Weapons to Fight Antibiotic Resistance in Cystic Fibrosis Disease.
Gaglione R, Cesaro A, DellOlmo E, Di Girolamo R, Tartaglione L, Pizzo E
Int J Mol Sci. 2020; 21(6).
PMID: 32192076
PMC: 7139702.
DOI: 10.3390/ijms21062049.
Prenatal genetic testing for cystic fibrosis: a systematic review of clinical effectiveness and an ethics review.
Kessels S, Carter D, Ellery B, Newton S, Merlin T
Genet Med. 2019; 22(2):258-267.
PMID: 31467445
DOI: 10.1038/s41436-019-0641-8.
From gene to treatment: supporting rare disease translational research through model systems.
Hmeljak J, Justice M
Dis Model Mech. 2019; 12(2).
PMID: 30819728
PMC: 6398488.
DOI: 10.1242/dmm.039271.
Knockdown of Gene Expression in Macrophages by microRNA Mimic-Containing Poly (Lactic--glycolic Acid) Microparticles.
McKiernan P, Lynch P, Ramsey J, Cryan S, M Greene C
Medicines (Basel). 2018; 5(4).
PMID: 30558310
PMC: 6313440.
DOI: 10.3390/medicines5040133.
Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis population.
Polineni D, Piccorelli A, Hannah W, Dalrymple S, Pace R, Durie P
PLoS One. 2018; 13(10):e0205257.
PMID: 30307979
PMC: 6181334.
DOI: 10.1371/journal.pone.0205257.
Infections in Cystic Fibrosis Patients: Drug Resistance and Therapeutic Approaches.
Scoffone V, Chiarelli L, Trespidi G, Mentasti M, Riccardi G, Buroni S
Front Microbiol. 2017; 8:1592.
PMID: 28878751
PMC: 5572248.
DOI: 10.3389/fmicb.2017.01592.
Adherence to tobramycin inhaled powder vs inhaled solution in patients with cystic fibrosis: analysis of US insurance claims data.
Hamed K, Conti V, Tian H, Loefroth E
Patient Prefer Adherence. 2017; 11:831-838.
PMID: 28490864
PMC: 5414718.
DOI: 10.2147/PPA.S134759.
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis.
Straniero L, Solda G, Costantino L, Seia M, Melotti P, Colombo C
J Hum Genet. 2016; 61(12):977-984.
PMID: 27488443
DOI: 10.1038/jhg.2016.101.
