Similar articles for PMID: 32414100

Year	Number of Results
1995	1
1998	1
2000	1
2001	2
2002	1
2006	1
2007	1
2009	1
2010	2
2011	2
2012	3
2013	4
2014	2
2015	8
2016	11
2017	6
2018	12
2019	6
2020	5
2021	3
2022	1
2024	0

1

The CFTR Mutation c.3453G > C (D1152H) Confers an Anion Selectivity Defect in Primary Airway Tissue that Can Be Rescued by Ivacaftor.

Laselva O, Moraes TJ, He G, Bartlett C, Szàrics I, Ouyang H, Gunawardena TNA, Strug L, Bear CE, Gonska T. Laselva O, et al. J Pers Med. 2020 May 13;10(2):40. doi: 10.3390/jpm10020040. J Pers Med. 2020. PMID: 32414100 Free PMC article.

2

Non-classic cystic fibrosis associated with D1152H CFTR mutation.

Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D. Burgel PR, et al. Clin Genet. 2010 Apr;77(4):355-64. doi: 10.1111/j.1399-0004.2009.01294.x. Epub 2009 Oct 15. Clin Genet. 2010. PMID: 19843100

3

A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.

Diana A, Tesse R, Polizzi AM, Santostasi T, Manca A, Leonetti G, Seia M, Porcaro L, Cavallo L. Diana A, et al. Gene. 2012 Apr 10;497(1):90-2. doi: 10.1016/j.gene.2012.01.061. Epub 2012 Jan 31. Gene. 2012. PMID: 22310382

4

Cystic fibrosis transmembrane conductance regulator-modifying medications: the future of cystic fibrosis treatment.

Pettit RS. Pettit RS. Ann Pharmacother. 2012 Jul-Aug;46(7-8):1065-75. doi: 10.1345/aph.1R076. Epub 2012 Jun 26. Ann Pharmacother. 2012. PMID: 22739718 Review.

5

Lumacaftor and ivacaftor in the management of patients with cystic fibrosis: current evidence and future prospects.

Kuk K, Taylor-Cousar JL. Kuk K, et al. Ther Adv Respir Dis. 2015 Dec;9(6):313-26. doi: 10.1177/1753465815601934. Epub 2015 Sep 28. Ther Adv Respir Dis. 2015. PMID: 26416827 Free article. Review.

6

Structural mechanisms for defective CFTR gating caused by the Q1412X mutation, a severe Class VI pathogenic mutation in cystic fibrosis.

Yeh JT, Yu YC, Hwang TC. Yeh JT, et al. J Physiol. 2019 Jan;597(2):543-560. doi: 10.1113/JP277042. Epub 2018 Dec 2. J Physiol. 2019. PMID: 30408177 Free PMC article.

7

ORKAMBI-Mediated Rescue of Mucociliary Clearance in Cystic Fibrosis Primary Respiratory Cultures Is Enhanced by Arginine Uptake, Arginase Inhibition, and Promotion of Nitric Oxide Signaling to the Cystic Fibrosis Transmembrane Conductance Regulator Channel.

Wu YS, Jiang J, Ahmadi S, Lew A, Laselva O, Xia S, Bartlett C, Ip W, Wellhauser L, Ouyang H, Gonska T, Moraes TJ, Bear CE. Wu YS, et al. Mol Pharmacol. 2019 Oct;96(4):515-525. doi: 10.1124/mol.119.117143. Epub 2019 Aug 19. Mol Pharmacol. 2019. PMID: 31427400

8

In vivo and in vitro ivacaftor response in cystic fibrosis patients with residual CFTR function: N-of-1 studies.

McGarry ME, Illek B, Ly NP, Zlock L, Olshansky S, Moreno C, Finkbeiner WE, Nielson DW. McGarry ME, et al. Pediatr Pulmonol. 2017 Apr;52(4):472-479. doi: 10.1002/ppul.23659. Epub 2017 Jan 9. Pediatr Pulmonol. 2017. PMID: 28068001 Free PMC article. Clinical Trial.

9

The combination of tezacaftor and ivacaftor in the treatment of patients with cystic fibrosis: clinical evidence and future prospects in cystic fibrosis therapy.

Lommatzsch ST, Taylor-Cousar JL. Lommatzsch ST, et al. Ther Adv Respir Dis. 2019 Jan-Dec;13:1753466619844424. doi: 10.1177/1753466619844424. Ther Adv Respir Dis. 2019. PMID: 31027466 Free PMC article. Review.

10

Therapeutic benefit observed with the CFTR potentiator, ivacaftor, in a CF patient homozygous for the W1282X CFTR nonsense mutation.

Mutyam V, Libby EF, Peng N, Hadjiliadis D, Bonk M, Solomon GM, Rowe SM. Mutyam V, et al. J Cyst Fibros. 2017 Jan;16(1):24-29. doi: 10.1016/j.jcf.2016.09.005. Epub 2016 Oct 1. J Cyst Fibros. 2017. PMID: 27707539 Free PMC article.

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