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Items: 1 to 20 of 120

1.

HCN channelopathy and cardiac electrophysiologic dysfunction in genetic and acquired rat epilepsy models.

Powell KL, Jones NC, Kennard JT, Ng C, Urmaliya V, Lau S, Tran A, Zheng T, Ozturk E, Dezsi G, Megatia I, Delbridge LM, Pinault D, Reid CA, White PJ, O'Brien TJ.

Epilepsia. 2014 Apr;55(4):609-20. doi: 10.1111/epi.12563. Epub 2014 Mar 4.

2.

LQT, HCN, and epilepsy model.

Kodirov SA.

Epilepsia. 2015 Nov;56(11):1855. doi: 10.1111/epi.13188. No abstract available.

PMID:
26513214
3.

In response: LQT, HCN, and epilepsy model.

Powell KL, O'Brien TJ.

Epilepsia. 2015 Nov;56(11):1855-6. doi: 10.1111/epi.13206. No abstract available.

PMID:
26513215
4.

Neuron-restrictive silencer factor-mediated hyperpolarization-activated cyclic nucleotide gated channelopathy in experimental temporal lobe epilepsy.

McClelland S, Flynn C, Dubé C, Richichi C, Zha Q, Ghestem A, Esclapez M, Bernard C, Baram TZ.

Ann Neurol. 2011 Sep;70(3):454-64. doi: 10.1002/ana.22479.

5.

Progressive dendritic HCN channelopathy during epileptogenesis in the rat pilocarpine model of epilepsy.

Jung S, Jones TD, Lugo JN Jr, Sheerin AH, Miller JW, D'Ambrosio R, Anderson AE, Poolos NP.

J Neurosci. 2007 Nov 21;27(47):13012-21.

6.

Functional stabilization of weakened thalamic pacemaker channel regulation in rat absence epilepsy.

Kuisle M, Wanaverbecq N, Brewster AL, Frère SG, Pinault D, Baram TZ, Lüthi A.

J Physiol. 2006 Aug 15;575(Pt 1):83-100. Epub 2006 May 25.

7.

Mechanisms of seizure-induced 'transcriptional channelopathy' of hyperpolarization-activated cyclic nucleotide gated (HCN) channels.

Richichi C, Brewster AL, Bender RA, Simeone TA, Zha Q, Yin HZ, Weiss JH, Baram TZ.

Neurobiol Dis. 2008 Feb;29(2):297-305. Epub 2007 Sep 22.

8.

Thalamocortical neurons display suppressed burst-firing due to an enhanced Ih current in a genetic model of absence epilepsy.

Cain SM, Tyson JR, Jones KL, Snutch TP.

Pflugers Arch. 2015 Jun;467(6):1367-82. doi: 10.1007/s00424-014-1549-4. Epub 2014 Jun 24.

9.

Decreases in HCN mRNA expression in the hippocampus after kindling and status epilepticus in adult rats.

Powell KL, Ng C, O'Brien TJ, Xu SH, Williams DA, Foote SJ, Reid CA.

Epilepsia. 2008 Oct;49(10):1686-95. doi: 10.1111/j.1528-1167.2008.01593.x. Epub 2008 Apr 7.

10.

The role of the inherited genetic background on the consequences of lithium-pilocarpine status epilepticus: study in Genetic Absence Epilepsy Rats from Strasbourg and Wistar audiogenic rats.

Hanaya R, Koning E, Ferrandon A, Nehlig A.

Neurobiol Dis. 2008 Sep;31(3):451-8. doi: 10.1016/j.nbd.2008.06.006. Epub 2008 Jun 26.

PMID:
18638555
11.

HCN-related channelopathies.

Baruscotti M, Bottelli G, Milanesi R, DiFrancesco JC, DiFrancesco D.

Pflugers Arch. 2010 Jul;460(2):405-15. doi: 10.1007/s00424-010-0810-8. Epub 2010 Mar 8. Review.

PMID:
20213494
12.

The effect of amygdala kindling on neuronal firing patterns in the lateral thalamus in the GAERS model of absence epilepsy.

Carçak N, Zheng T, Ali I, Abdullah A, French C, Powell KL, Jones NC, van Raay L, Rind G, Onat F, O'Brien TJ.

Epilepsia. 2014 May;55(5):654-65. doi: 10.1111/epi.12592. Epub 2014 Mar 27.

13.
14.

Intra-amygdaloid injection of kainic acid in rats with genetic absence epilepsy: the relationship of typical absence epilepsy and temporal lobe epilepsy.

Gurbanova AA, Aker RG, Sirvanci S, Demiralp T, Onat FY.

J Neurosci. 2008 Jul 30;28(31):7828-36. doi: 10.1523/JNEUROSCI.1097-08.2008.

15.

In vitro characterization of HCN channel kinetics and frequency dependence in myocytes predicts biological pacemaker functionality.

Zhao X, Bucchi A, Oren RV, Kryukova Y, Dun W, Clancy CE, Robinson RB.

J Physiol. 2009 Apr 1;587(Pt 7):1513-25. doi: 10.1113/jphysiol.2008.163444. Epub 2009 Jan 26.

16.
17.

Dendritic ion channelopathy in acquired epilepsy.

Poolos NP, Johnston D.

Epilepsia. 2012 Dec;53 Suppl 9:32-40. doi: 10.1111/epi.12033. Review.

18.

Impaired regulation of thalamic pacemaker channels through an imbalance of subunit expression in absence epilepsy.

Budde T, Caputi L, Kanyshkova T, Staak R, Abrahamczik C, Munsch T, Pape HC.

J Neurosci. 2005 Oct 26;25(43):9871-82.

19.

Mislocalization of h channel subunits underlies h channelopathy in temporal lobe epilepsy.

Shin M, Brager D, Jaramillo TC, Johnston D, Chetkovich DM.

Neurobiol Dis. 2008 Oct;32(1):26-36. doi: 10.1016/j.nbd.2008.06.013. Epub 2008 Jul 3.

20.

HCN channelopathies: pathophysiology in genetic epilepsy and therapeutic implications.

Reid CA, Phillips AM, Petrou S.

Br J Pharmacol. 2012 Jan;165(1):49-56. doi: 10.1111/j.1476-5381.2011.01507.x. Review.

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