245 related articles for article (PubMed ID: 24513531)
1. On the structural organization of the intracellular domains of CFTR.
Moran O
Int J Biochem Cell Biol; 2014 Jul; 52():7-14. PubMed ID: 24513531
[TBL] [Abstract][Full Text] [Related]
2. The gating of the CFTR channel.
Moran O
Cell Mol Life Sci; 2017 Jan; 74(1):85-92. PubMed ID: 27696113
[TBL] [Abstract][Full Text] [Related]
3. Molecular modelling approaches for cystic fibrosis transmembrane conductance regulator studies.
Odolczyk N; Zielenkiewicz P
Int J Biochem Cell Biol; 2014 Jul; 52():39-46. PubMed ID: 24735712
[TBL] [Abstract][Full Text] [Related]
4. CFTR structure and cystic fibrosis.
Cant N; Pollock N; Ford RC
Int J Biochem Cell Biol; 2014 Jul; 52():15-25. PubMed ID: 24534272
[TBL] [Abstract][Full Text] [Related]
5. Atomic Structure of the Cystic Fibrosis Transmembrane Conductance Regulator.
Zhang Z; Chen J
Cell; 2016 Dec; 167(6):1586-1597.e9. PubMed ID: 27912062
[TBL] [Abstract][Full Text] [Related]
6. The major cystic fibrosis causing mutation exhibits defective propensity for phosphorylation.
Pasyk S; Molinski S; Ahmadi S; Ramjeesingh M; Huan LJ; Chin S; Du K; Yeger H; Taylor P; Moran MF; Bear CE
Proteomics; 2015 Jan; 15(2-3):447-61. PubMed ID: 25330774
[TBL] [Abstract][Full Text] [Related]
7. Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.
Howell LD; Borchardt R; Kole J; Kaz AM; Randak C; Cohn JA
Biochem J; 2004 Feb; 378(Pt 1):151-9. PubMed ID: 14602047
[TBL] [Abstract][Full Text] [Related]
8. Functions of the cystic fibrosis transmembrane conductance regulator protein.
Frizzell RA
Am J Respir Crit Care Med; 1995 Mar; 151(3 Pt 2):S54-8. PubMed ID: 7533606
[TBL] [Abstract][Full Text] [Related]
9. Revisiting cystic fibrosis transmembrane conductance regulator structure and function.
Hanrahan JW; Wioland MA
Proc Am Thorac Soc; 2004; 1(1):17-21. PubMed ID: 16113406
[TBL] [Abstract][Full Text] [Related]
10. Insights into the mechanisms underlying CFTR channel activity, the molecular basis for cystic fibrosis and strategies for therapy.
Kim Chiaw P; Eckford PD; Bear CE
Essays Biochem; 2011 Sep; 50(1):233-48. PubMed ID: 21967060
[TBL] [Abstract][Full Text] [Related]
11. Cystic fibrosis transmembrane conductance regulator (CFTR) nucleotide-binding domain 1 (NBD-1) and CFTR truncated within NBD-1 target to the epithelial plasma membrane and increase anion permeability.
Clancy JP; Hong JS; Bebök Z; King SA; Demolombe S; Bedwell DM; Sorscher EJ
Biochemistry; 1998 Oct; 37(43):15222-30. PubMed ID: 9790686
[TBL] [Abstract][Full Text] [Related]
12. The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability.
Meng X; Clews J; Kargas V; Wang X; Ford RC
Cell Mol Life Sci; 2017 Jan; 74(1):23-38. PubMed ID: 27734094
[TBL] [Abstract][Full Text] [Related]
13. Understanding how cystic fibrosis mutations disrupt CFTR function: from single molecules to animal models.
Wang Y; Wrennall JA; Cai Z; Li H; Sheppard DN
Int J Biochem Cell Biol; 2014 Jul; 52():47-57. PubMed ID: 24727426
[TBL] [Abstract][Full Text] [Related]
14. The structural basis of cystic fibrosis.
Meng X; Clews J; Martin ER; Ciuta AD; Ford RC
Biochem Soc Trans; 2018 Oct; 46(5):1093-1098. PubMed ID: 30154098
[TBL] [Abstract][Full Text] [Related]
15. Cystic fibrosis transmembrane conductance regulator (CFTR): Making an ion channel out of an active transporter structure.
Linsdell P
Channels (Austin); 2018; 12(1):284-290. PubMed ID: 30152709
[TBL] [Abstract][Full Text] [Related]
16. Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): physiological and pathophysiological relevance.
El Khouri E; Touré A
Int J Biochem Cell Biol; 2014 Jul; 52():58-67. PubMed ID: 24530837
[TBL] [Abstract][Full Text] [Related]
17. Attenuation of Phosphorylation-dependent Activation of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) by Disease-causing Mutations at the Transmission Interface.
Chin S; Yang D; Miles AJ; Eckford PDW; Molinski S; Wallace BA; Bear CE
J Biol Chem; 2017 Feb; 292(5):1988-1999. PubMed ID: 28003367
[TBL] [Abstract][Full Text] [Related]
18. Functional architecture of the CFTR chloride channel.
Linsdell P
Mol Membr Biol; 2014 Feb; 31(1):1-16. PubMed ID: 24341413
[TBL] [Abstract][Full Text] [Related]
19. Cytoskeleton and CFTR.
Edelman A
Int J Biochem Cell Biol; 2014 Jul; 52():68-72. PubMed ID: 24685681
[TBL] [Abstract][Full Text] [Related]
20. Multiple membrane-cytoplasmic domain contacts in the cystic fibrosis transmembrane conductance regulator (CFTR) mediate regulation of channel gating.
He L; Aleksandrov AA; Serohijos AW; Hegedus T; Aleksandrov LA; Cui L; Dokholyan NV; Riordan JR
J Biol Chem; 2008 Sep; 283(39):26383-90. PubMed ID: 18658148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
