McCarty NA - Search Results

1

Alteration of Membrane Cholesterol Content Plays a Key Role in Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Channel Activity.

Cui G, Cottrill KA, Strickland KM, Mashburn SA, Koval M, McCarty NA. Cui G, et al. Among authors: mccarty na. Front Physiol. 2021 Jun 7;12:652513. doi: 10.3389/fphys.2021.652513. eCollection 2021. Front Physiol. 2021. PMID: 34163370 Free PMC article.

2

Inhibition of CFTR channels by a peptide toxin of scorpion venom.

Fuller MD, Zhang ZR, Cui G, Kubanek J, McCarty NA. Fuller MD, et al. Among authors: mccarty na. Am J Physiol Cell Physiol. 2004 Nov;287(5):C1328-41. doi: 10.1152/ajpcell.00162.2004. Epub 2004 Jul 7. Am J Physiol Cell Physiol. 2004. PMID: 15240343 Free article.

3

Determination of the functional unit of the cystic fibrosis transmembrane conductance regulator chloride channel. One polypeptide forms one pore.

Zhang ZR, Cui G, Liu X, Song B, Dawson DC, McCarty NA. Zhang ZR, et al. Among authors: mccarty na. J Biol Chem. 2005 Jan 7;280(1):458-68. doi: 10.1074/jbc.M409626200. Epub 2004 Oct 25. J Biol Chem. 2005. PMID: 15504728 Free article.

4

Time-dependent interactions of glibenclamide with CFTR: kinetically complex block of macroscopic currents.

Zhang ZR, Cui G, Zeltwanger S, McCarty NA. Zhang ZR, et al. Among authors: mccarty na. J Membr Biol. 2004 Oct 1;201(3):139-55. doi: 10.1007/s00232-004-0712-9. J Membr Biol. 2004. PMID: 15711774

5

The block of CFTR by scorpion venom is state-dependent.

Fuller MD, Zhang ZR, Cui G, McCarty NA. Fuller MD, et al. Among authors: mccarty na. Biophys J. 2005 Dec;89(6):3960-75. doi: 10.1529/biophysj.105.060731. Epub 2005 Sep 23. Biophys J. 2005. PMID: 16183882 Free PMC article.

6

Mutations at arginine 352 alter the pore architecture of CFTR.

Cui G, Zhang ZR, O'Brien AR, Song B, McCarty NA. Cui G, et al. Among authors: mccarty na. J Membr Biol. 2008 Mar;222(2):91-106. doi: 10.1007/s00232-008-9105-9. Epub 2008 Apr 18. J Membr Biol. 2008. PMID: 18421494 Free PMC article.

7

Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters.

Jordan IK, Kota KC, Cui G, Thompson CH, McCarty NA. Jordan IK, et al. Among authors: mccarty na. Proc Natl Acad Sci U S A. 2008 Dec 2;105(48):18865-70. doi: 10.1073/pnas.0806306105. Epub 2008 Nov 19. Proc Natl Acad Sci U S A. 2008. PMID: 19020075 Free PMC article.

8

Differential contribution of TM6 and TM12 to the pore of CFTR identified by three sulfonylurea-based blockers.

Cui G, Song B, Turki HW, McCarty NA. Cui G, et al. Among authors: mccarty na. Pflugers Arch. 2012 Mar;463(3):405-18. doi: 10.1007/s00424-011-1035-1. Epub 2011 Dec 13. Pflugers Arch. 2012. PMID: 22160394

9

Two salt bridges differentially contribute to the maintenance of cystic fibrosis transmembrane conductance regulator (CFTR) channel function.

Cui G, Freeman CS, Knotts T, Prince CZ, Kuang C, McCarty NA. Cui G, et al. Among authors: mccarty na. J Biol Chem. 2013 Jul 12;288(28):20758-67. doi: 10.1074/jbc.M113.476226. Epub 2013 May 24. J Biol Chem. 2013. PMID: 23709221 Free PMC article.

10

Modeling the conformational changes underlying channel opening in CFTR.

Rahman KS, Cui G, Harvey SC, McCarty NA. Rahman KS, et al. Among authors: mccarty na. PLoS One. 2013 Sep 27;8(9):e74574. doi: 10.1371/journal.pone.0074574. eCollection 2013. PLoS One. 2013. PMID: 24086355 Free PMC article.

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