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SLC6A14 Impacts Cystic Fibrosis Lung Disease Severity via mTOR and Epithelial Repair Modulation.
Front Mol Biosci. 2022 Mar 9;9:850261. doi: 10.3389/fmolb.2022.850261. eCollection 2022.
Front Mol Biosci. 2022.
PMID: 35372502
Free PMC article.
SLC26A9 Gene Is Associated With Lung Function Response to Ivacaftor in Patients With Cystic Fibrosis.
Corvol H, Mésinèle J, Douksieh IH, Strug LJ, Boëlle PY, Guillot L.
Corvol H, et al. Among authors: mesinele j.
Front Pharmacol. 2018 Jul 26;9:828. doi: 10.3389/fphar.2018.00828. eCollection 2018.
Front Pharmacol. 2018.
PMID: 30140228
Free PMC article.
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[SLC6A14, a modifier gene in cystic fibrosis].
Ruffin M, Mercier J, Calmel C, Mésinèle J, Corvol H, Guillot L.
Ruffin M, et al. Among authors: mesinele j.
Rev Mal Respir. 2020 Mar;37(3):218-221. doi: 10.1016/j.rmr.2020.02.008. Epub 2020 Mar 4.
Rev Mal Respir. 2020.
PMID: 32146055
Free article.
Review.
French.
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Update on SLC6A14 in lung and gastrointestinal physiology and physiopathology: focus on cystic fibrosis.
Ruffin M, Mercier J, Calmel C, Mésinèle J, Bigot J, Sutanto EN, Kicic A, Corvol H, Guillot L.
Ruffin M, et al. Among authors: mesinele j.
Cell Mol Life Sci. 2020 Sep;77(17):3311-3323. doi: 10.1007/s00018-020-03487-x. Epub 2020 Mar 12.
Cell Mol Life Sci. 2020.
PMID: 32166393
Free PMC article.
Review.
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Risk factors for Pseudomonas aeruginosa airway infection and lung function decline in children with cystic fibrosis.
Mésinèle J, Ruffin M, Kemgang A, Guillot L, Boëlle PY, Corvol H.
Mésinèle J, et al.
J Cyst Fibros. 2022 Jan;21(1):45-51. doi: 10.1016/j.jcf.2021.09.017. Epub 2021 Oct 8.
J Cyst Fibros. 2022.
PMID: 34629287
Free article.
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Factors Predisposing the Response to Lumacaftor/Ivacaftor in People with Cystic Fibrosis.
Mésinèle J, Ruffin M, Guillot L, Boëlle PY, Corvol H, On Behalf Of The French Cf Modifier Gene Study Investigators.
Mésinèle J, et al.
J Pers Med. 2022 Feb 10;12(2):252. doi: 10.3390/jpm12020252.
J Pers Med. 2022.
PMID: 35207740
Free PMC article.
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Modifier Factors of Cystic Fibrosis Phenotypes: A Focus on Modifier Genes.
Mésinèle J, Ruffin M, Guillot L, Corvol H.
Mésinèle J, et al.
Int J Mol Sci. 2022 Nov 17;23(22):14205. doi: 10.3390/ijms232214205.
Int J Mol Sci. 2022.
PMID: 36430680
Free PMC article.
Review.
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Airway infections as a risk factor for Pseudomonas aeruginosa acquisition and chronic colonisation in children with cystic fibrosis.
Mésinèle J, Ruffin M, Guillot L, Boëlle PY, Corvol H.
Mésinèle J, et al.
J Cyst Fibros. 2023 Sep;22(5):901-908. doi: 10.1016/j.jcf.2023.06.007. Epub 2023 Jul 6.
J Cyst Fibros. 2023.
PMID: 37422431
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