For: | Linsdell P. Cystic fibrosis transmembrane conductance regulator chloride channel blockers: Pharmacological, biophysical and physiological relevance. World J Biol Chem 2014; 5(1): 26-39 [PMID: 24600512 DOI: 10.4331/wjbc.v5.i1.26] |
---|---|
URL: | https://www.wjgnet.com/1949-8454/full/v5/i1/26.htm |
Number | Citing Articles |
1 |
Mayuree Rodrat, Walailak Jantarajit, Demi R. S. Ng, Bartholomew S. J. Harvey, Jia Liu, William J. Wilkinson, Narattaphol Charoenphandhu, David N. Sheppard. Carbon monoxide-releasing molecules inhibit the cystic fibrosis transmembrane conductance regulator Cl−channel. American Journal of Physiology-Lung Cellular and Molecular Physiology 2020; 319(6): L997 doi: 10.1152/ajplung.00440.2019
|
2 |
Toshiki Yamada, Eric E. Figueroa, Jerod S. Denton, Kevin Strange. LRRC8A homohexameric channels poorly recapitulate VRAC regulation and pharmacology. American Journal of Physiology-Cell Physiology 2021; 320(3): C293 doi: 10.1152/ajpcell.00454.2020
|
3 |
Steven D. Broadbent, Wuyang Wang, Paul Linsdell. Interaction between 2 extracellular loops influences the activity of the cystic fibrosis transmembrane conductance regulator chloride channel. Biochemistry and Cell Biology 2014; 92(5): 390 doi: 10.1139/bcb-2014-0066
|
4 |
Sumaira Ashraf, Carolina Carrillo-Carrion, Qian Zhang, Mahmoud G Soliman, Raimo Hartmann, Beatriz Pelaz, Pablo del Pino, Wolfgang J Parak. Fluorescence-based ion-sensing with colloidal particles. Current Opinion in Pharmacology 2014; 18: 98 doi: 10.1016/j.coph.2014.09.011
|
5 |
Matthias Zwick, Cinzia Esposito, Manuel Hellstern, Anna Seelig. How Phosphorylation and ATPase Activity Regulate Anion Flux though the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). Journal of Biological Chemistry 2016; 291(28): 14483 doi: 10.1074/jbc.M116.721415
|
6 |
Paul Linsdell. Architecture and functional properties of the CFTR channel pore. Cellular and Molecular Life Sciences 2017; 74(1): 67 doi: 10.1007/s00018-016-2389-5
|
7 |
Tzyh-Chang Hwang, Jiunn-Tyng Yeh, Jingyao Zhang, Ying-Chun Yu, Han-I Yeh, Samantha Destefano. Structural mechanisms of CFTR function and dysfunction. Journal of General Physiology 2018; 150(4): 539 doi: 10.1085/jgp.201711946
|
8 |
Paul Linsdell. Interactions between permeant and blocking anions inside the CFTR chloride channel pore. Biochimica et Biophysica Acta (BBA) - Biomembranes 2015; 1848(7): 1573 doi: 10.1016/j.bbamem.2015.04.004
|
9 |
Xiangrong Cui, Xueqing Wu, Qiang Li, Xuan Jing. Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review). Molecular Medicine Reports 2020; doi: 10.3892/mmr.2020.11456
|
10 |
Yasunobu Okada, Toshiaki Okada, Kaori Sato-Numata, Md. Rafiqul Islam, Yuhko Ando-Akatsuka, Tomohiro Numata, Machiko Kubo, Takahiro Shimizu, Ranohon S. Kurbannazarova, Yoshinori Marunaka, Ravshan Z. Sabirov. Cell Volume-Activated and Volume-Correlated Anion Channels in Mammalian Cells: Their Biophysical, Molecular, and Pharmacological Properties. Pharmacological Reviews 2019; 71(1): 49 doi: 10.1124/pr.118.015917
|
11 |
Paul Linsdell. State-dependent blocker interactions with the CFTR chloride channel: implications for gating the pore. Pflügers Archiv - European Journal of Physiology 2014; 466(12): 2243 doi: 10.1007/s00424-014-1501-7
|
12 |
Paul Linsdell. On the relationship between anion binding and chloride conductance in the CFTR anion channel. Biochimica et Biophysica Acta (BBA) - Biomembranes 2021; 1863(4): 183558 doi: 10.1016/j.bbamem.2021.183558
|
13 |
John Cuppoletti, Danuta H. Malinowska, Ryuji Ueno. Ion Channels and Transporters of Epithelia in Health and Disease. 2016; : 491 doi: 10.1007/978-1-4939-3366-2_15
|
14 |
Hannah L. Simpson, Carol L. Roberts, Louise M. Thompson, Cameron R. Leiper, Nehana Gittens, Ellie Trotter, Carrie A. Duckworth, Stamatia Papoutsopoulou, Fabio Miyajima, Paul Roberts, Niamh O’Kennedy, Jonathan M. Rhodes, Barry J. Campbell. Soluble Non-Starch Polysaccharides From Plantain (Musa x paradisiaca L.) Diminish Epithelial Impact of Clostridioides difficile. Frontiers in Pharmacology 2021; 12 doi: 10.3389/fphar.2021.766293
|
15 |
Paola Rogliani, Luigino Calzetta, Mario Cazzola, Maria Gabriella Matera. Drug safety evaluation of roflumilast for the treatment of COPD: a meta-analysis. Expert Opinion on Drug Safety 2016; 15(8): 1133 doi: 10.1080/14740338.2016.1199683
|
16 |
Hugo R. de Jonge, Maria C. Ardelean, Marcel J. C. Bijvelds, Paola Vergani. Strategies for cystic fibrosis transmembrane conductance regulator inhibition: from molecular mechanisms to treatment for secretory diarrhoeas. FEBS Letters 2020; 594(23): 4085 doi: 10.1002/1873-3468.13971
|
17 |
John Cuppoletti, Danuta H. Malinowska, Ryuji Ueno. Studies of Epithelial Transporters and Ion Channels. Physiology in Health and Disease 2020; : 495 doi: 10.1007/978-3-030-55454-5_13
|
18 |
Jean-Paul Mornon, Brice Hoffmann, Slavica Jonic, Pierre Lehn, Isabelle Callebaut. Full-open and closed CFTR channels, with lateral tunnels from the cytoplasm and an alternative position of the F508 region, as revealed by molecular dynamics. Cellular and Molecular Life Sciences 2015; 72(7): 1377 doi: 10.1007/s00018-014-1749-2
|
19 |
Can Liu, Chao Song, Jiaxi Li, Qing Sun. <p>CFTR Functions as a Tumor Suppressor and Is Regulated by DNA Methylation in Colorectal Cancer</p>. Cancer Management and Research 2020; : 4261 doi: 10.2147/CMAR.S248539
|
20 |
Leo Han, Rebecca Taub, Jeffrey T. Jensen. Cervical mucus and contraception: what we know and what we don't. Contraception 2017; 96(5): 310 doi: 10.1016/j.contraception.2017.07.168
|
21 |
Kerstin Nagel-Wolfrum, Fabian Möller, Inessa Penner, Timor Baasov, Uwe Wolfrum. Targeting Nonsense Mutations in Diseases with Translational Read-Through-Inducing Drugs (TRIDs). BioDrugs 2016; 30(2): 49 doi: 10.1007/s40259-016-0157-6
|
22 |
Paul Linsdell. Protein Reviews. Advances in Experimental Medicine and Biology 2016; 925: 13 doi: 10.1007/5584_2016_33
|
23 |
Isabelle Callebaut, Brice Hoffmann, Pierre Lehn, Jean-Paul Mornon. Molecular modelling and molecular dynamics of CFTR. Cellular and Molecular Life Sciences 2017; 74(1): 3 doi: 10.1007/s00018-016-2385-9
|
24 |
Hussein N. Rubaiy, Paul Linsdell. Location of a permeant anion binding site in the cystic fibrosis transmembrane conductance regulator chloride channel pore. The Journal of Physiological Sciences 2015; 65(3): 233 doi: 10.1007/s12576-015-0359-6
|
25 |
Paul Linsdell, Alexander Negoda, Elizabeth A. Cowley, Yassine El Hiani. Electrostatic Tuning of Anion Attraction from the Cytoplasm to the Pore of the CFTR Chloride Channel. Cell Biochemistry and Biophysics 2020; 78(1): 15 doi: 10.1007/s12013-019-00899-w
|
26 |
Paul Linsdell, Christina L. Irving, Elizabeth A. Cowley, Yassine El Hiani. Two positively charged amino acid side-chains in the inner vestibule of the CFTR channel pore play analogous roles in controlling anion binding and anion conductance. Cellular and Molecular Life Sciences 2021; 78(12): 5213 doi: 10.1007/s00018-021-03859-x
|
27 |
Miri Park, Chiman Song, Hojong Yoon, Kee-Hyun Choi. Double Blockade of Glioma Cell Proliferation and Migration by Temozolomide Conjugated with NPPB, a Chloride Channel Blocker. ACS Chemical Neuroscience 2016; 7(3): 275 doi: 10.1021/acschemneuro.5b00178
|