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Summary Expression Phenotypes Gene Literature (16) GO Terms (0) Nucleotides (115) Proteins (54) Interactants (30) Wiki

Papers associated with kcnt2

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Advancements in the use of xenopus oocytes for modelling neurological disease for novel drug discovery., O'Connor EC, Kambara K, Bertrand D., Expert Opin Drug Discov. February 1, 2024; 19 (2): 173-187.      

A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy., Gururaj S, Palmer EE, Sheehan GD, Kandula T, Macintosh R, Ying K, Morris P, Tao J, Dias KR, Zhu Y, Dinger ME, Cowley MJ, Kirk EP, Roscioli T, Sachdev R, Duffey ME, Bye A, Bhattacharjee A., Cell Rep. October 24, 2017; 21 (4): 926-933.

Molecular mechanisms of Slo2 K+ channel closure., Giese MH, Gardner A, Hansen A, Sanguinetti MC., J Physiol. April 1, 2017; 595 (7): 2321-2336.

Heteromeric Slick/Slack K+ channels show graded sensitivity to cell volume changes., Tejada MA, Hashem N, Calloe K, Klaerke DA., PLoS One. February 21, 2017; 12 (2): e0169914.        

Hydrophobic interactions between the S5 segment and the pore helix stabilizes the closed state of Slo2.1 potassium channels., Suzuki T, Hansen A, Sanguinetti MC., Biochim Biophys Acta. April 1, 2016; 1858 (4): 783-92.

Identification of the Intracellular Na+ Sensor in Slo2.1 Potassium Channels., Thomson SJ, Hansen A, Sanguinetti MC., J Biol Chem. June 5, 2015; 290 (23): 14528-35.

Intracellular ATP does not inhibit Slo2.1 K+ channels., Garg P, Sanguinetti MC., Physiol Rep. September 11, 2014; 2 (9):         

Cell volume changes regulate slick (Slo2.1), but not slack (Slo2.2) K+ channels., Tejada MA, Stople K, Hammami Bomholtz S, Meinild AK, Poulsen AN, Klaerke DA., PLoS One. January 1, 2014; 9 (10): e110833.        

Structural basis of ion permeation gating in Slo2.1 K+ channels., Garg P, Gardner A, Garg V, Sanguinetti MC., J Gen Physiol. November 1, 2013; 142 (5): 523-42.                          

Structure-activity relationship of fenamates as Slo2.1 channel activators., Garg P, Sanguinetti MC., Mol Pharmacol. November 1, 2012; 82 (5): 795-802.

PIP₂ modulation of Slick and Slack K⁺ channels., de los Angeles Tejada M, Jensen LJ, Klaerke DA., Biochem Biophys Res Commun. July 27, 2012; 424 (2): 208-13.

Activation of Slo2.1 channels by niflumic acid., Dai L, Garg V, Sanguinetti MC., J Gen Physiol. March 1, 2010; 135 (3): 275-95.                                

The N-terminal domain of Slack determines the formation and trafficking of Slick/Slack heteromeric sodium-activated potassium channels., Chen H, Kronengold J, Yan Y, Gazula VR, Brown MR, Ma L, Ferreira G, Yang Y, Bhattacharjee A, Sigworth FJ, Salkoff L, Kaczmarek LK., J Neurosci. April 29, 2009; 29 (17): 5654-65.

Amino-termini isoforms of the Slack K+ channel, regulated by alternative promoters, differentially modulate rhythmic firing and adaptation., Brown MR, Kronengold J, Gazula VR, Spilianakis CG, Flavell RA, von Hehn CA, Bhattacharjee A, Kaczmarek LK., J Physiol. November 1, 2008; 586 (21): 5161-79.

Opposite regulation of Slick and Slack K+ channels by neuromodulators., Santi CM, Ferreira G, Yang B, Gazula VR, Butler A, Wei A, Kaczmarek LK, Salkoff L., J Neurosci. May 10, 2006; 26 (19): 5059-68.

Slick (Slo2.1), a rapidly-gating sodium-activated potassium channel inhibited by ATP., Bhattacharjee A, Joiner WJ, Wu M, Yang Y, Sigworth FJ, Kaczmarek LK., J Neurosci. December 17, 2003; 23 (37): 11681-91.

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