Trouve P, Saint Pierre A, Ferec C
Int J Mol Sci. 2024; 25(17).
PMID: 39273547
PMC: 11394767.
DOI: 10.3390/ijms25179599.
Ferreira F, Buarque C, Lopes-Pacheco M
Molecules. 2024; 29(4).
PMID: 38398574
PMC: 10891718.
DOI: 10.3390/molecules29040821.
Adela A, Kebede A, Zewdneh D, Kifle M, Basso Dias A
Adolesc Health Med Ther. 2024; 15:19-29.
PMID: 38328573
PMC: 10849877.
DOI: 10.2147/AHMT.S451251.
Zhang Q, Bhatia M, Park T, Ott J
Front Genet. 2023; 14:1222517.
PMID: 37693313
PMC: 10483394.
DOI: 10.3389/fgene.2023.1222517.
Lee J, Cho A, Huang E, Xu Y, Quach H, Hu J
J Transl Med. 2021; 19(1):452.
PMID: 34717671
PMC: 8556969.
DOI: 10.1186/s12967-021-03099-4.
Bacterial Subversion of Autophagy in Cystic Fibrosis.
Flores-Vega V, Vargas-Roldan S, Lezana-Fernandez J, Lascurain R, Santos-Preciado J, Rosales-Reyes R
Front Cell Infect Microbiol. 2021; 11:760922.
PMID: 34692569
PMC: 8531276.
DOI: 10.3389/fcimb.2021.760922.
Genetic variations in medical research in the past, at present and in the future.
Kamatani Y, Nakamura Y
Proc Jpn Acad Ser B Phys Biol Sci. 2021; 97(6):324-335.
PMID: 34121043
PMC: 8403528.
DOI: 10.2183/pjab.97.018.
Dissecting polygenic signals from genome-wide association studies on human behaviour.
Abdellaoui A, Verweij K
Nat Hum Behav. 2021; 5(6):686-694.
PMID: 33986517
DOI: 10.1038/s41562-021-01110-y.
Treatment of Cystic Fibrosis: From Gene- to Cell-Based Therapies.
Allan K, Farrow N, Donnelley M, Jaffe A, Waters S
Front Pharmacol. 2021; 12:639475.
PMID: 33796025
PMC: 8007963.
DOI: 10.3389/fphar.2021.639475.
Non-Linear Pharmacokinetics of Oral Roscovitine (Seliciclib) in Cystic Fibrosis Patients Chronically Infected with : A Study on Population Pharmacokinetics with Monte Carlo Simulations.
Leven C, Schutz S, Audrezet M, Nowak E, Meijer L, Montier T
Pharmaceutics. 2020; 12(11).
PMID: 33198319
PMC: 7696167.
DOI: 10.3390/pharmaceutics12111087.
Clinical and Genotypical Features of False-Negative Patients in 26 Years of Cystic Fibrosis Neonatal Screening in Tuscany, Italy.
Taccetti G, Botti M, Terlizzi V, Cavicchi M, Neri A, Galici V
Diagnostics (Basel). 2020; 10(7).
PMID: 32630227
PMC: 7399885.
DOI: 10.3390/diagnostics10070446.
Toothbrushes may convey bacteria to the cystic fibrosis lower airways.
Mantovani R, Sandri A, Boaretti M, Grilli A, Volpi S, Melotti P
J Oral Microbiol. 2019; 11(1):1647036.
PMID: 31489126
PMC: 6713191.
DOI: 10.1080/20002297.2019.1647036.
Lumacaftor-ivacaftor in the treatment of cystic fibrosis: design, development and place in therapy.
Connett G
Drug Des Devel Ther. 2019; 13:2405-2412.
PMID: 31409974
PMC: 6650604.
DOI: 10.2147/DDDT.S153719.
Cholesterol Interaction Directly Enhances Intrinsic Activity of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR).
Chin S, Ramjeesingh M, Hung M, Ereno-Oreba J, Cui H, Laselva O
Cells. 2019; 8(8).
PMID: 31370288
PMC: 6721619.
DOI: 10.3390/cells8080804.
The Sweat Metabolome of Screen-Positive Cystic Fibrosis Infants: Revealing Mechanisms beyond Impaired Chloride Transport.
Macedo A, Mathiaparanam S, Brick L, Keenan K, Gonska T, Pedder L
ACS Cent Sci. 2017; 3(8):904-913.
PMID: 28852705
PMC: 5571457.
DOI: 10.1021/acscentsci.7b00299.
Incorporate gene signature profiling into routine molecular testing.
Chen N
Appl Transl Genom. 2016; 2:28-33.
PMID: 27942443
PMC: 5133336.
DOI: 10.1016/j.atg.2013.03.002.
CFTR-β-catenin interaction regulates mouse embryonic stem cell differentiation and embryonic development.
Liu Z, Guo J, Wang Y, Weng Z, Huang B, Yu M
Cell Death Differ. 2016; 24(1):98-110.
PMID: 27834953
PMC: 5260497.
DOI: 10.1038/cdd.2016.118.
Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives.
Schmidt B, Haaf J, Leal T, Noel S
Clin Pharmacol. 2016; 8():127-140.
PMID: 27703398
PMC: 5036583.
DOI: 10.2147/CPAA.S100759.
Leveraging Epidemiologic and Clinical Collections for Genomic Studies of Complex Traits.
Crawford D, Goodloe R, Farber-Eger E, Boston J, Pendergrass S, Haines J
Hum Hered. 2015; 79(3-4):137-46.
PMID: 26201699
PMC: 4528966.
DOI: 10.1159/000381805.
Physiological impact of abnormal lipoxin A₄ production on cystic fibrosis airway epithelium and therapeutic potential.
Higgins G, Ringholz F, Buchanan P, McNally P, Urbach V
Biomed Res Int. 2015; 2015:781087.
PMID: 25866809
PMC: 4383482.
DOI: 10.1155/2015/781087.