Year |
Citation |
Score |
2016 |
Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, Macdonald RL. Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. Plos One. 11: e0162883. PMID 27622563 DOI: 10.1371/Journal.Pone.0162883 |
0.384 |
|
2015 |
Kole MJ, Qian J, Waase MP, Klassen TL, Chen TT, Augustine GJ, Noebels JL. Selective Loss of Presynaptic Potassium Channel Clusters at the Cerebellar Basket Cell Terminal Pinceau in Adam11 Mutants Reveals Their Role in Ephaptic Control of Purkinje Cell Firing. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 11433-44. PMID 26269648 DOI: 10.1523/Jneurosci.1346-15.2015 |
0.419 |
|
2014 |
Klassen TL, Bomben VC, Patel A, Drabek J, Chen TT, Gu W, Zhang F, Chapman K, Lupski JR, Noebels JL, Goldman AM. High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile. Epilepsia. 55: e6-12. PMID 24372310 DOI: 10.1111/Epi.12489 |
0.316 |
|
2013 |
Chen TT, Klassen TL, Goldman AM, Marini C, Guerrini R, Noebels JL. Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 80: 1078-85. PMID 23408874 DOI: 10.1212/Wnl.0B013E31828868E7 |
0.467 |
|
2011 |
Klassen T, Davis C, Goldman A, Burgess D, Chen T, Wheeler D, McPherson J, Bourquin T, Lewis L, Villasana D, Morgan M, Muzny D, Gibbs R, Noebels J. Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 145: 1036-48. PMID 21703448 DOI: 10.1016/J.Cell.2011.05.025 |
0.475 |
|
2010 |
Glasscock E, Yoo JW, Chen TT, Klassen TL, Noebels JL. Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 5167-75. PMID 20392939 DOI: 10.1523/Jneurosci.5591-09.2010 |
0.368 |
|
2009 |
Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL. Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death. Science Translational Medicine. 1: 2ra6. PMID 20368164 DOI: 10.1126/Scitranslmed.3000289 |
0.36 |
|
2008 |
Klassen TL, O'Mara ML, Redstone M, Spencer AN, Gallin WJ. Non-linear intramolecular interactions and voltage sensitivity of a KV1 family potassium channel from Polyorchis penicillatus (Eschscholtz 1829). The Journal of Experimental Biology. 211: 3442-53. PMID 18931317 DOI: 10.1242/Jeb.022608 |
0.64 |
|
2008 |
Klassen TL, Spencer AN, Gallin WJ. A naturally occurring omega current in a Kv3 family potassium channel from a platyhelminth. Bmc Neuroscience. 9: 52. PMID 18565223 DOI: 10.1186/1471-2202-9-52 |
0.642 |
|
2006 |
Klassen TL, Buckingham SD, Atherton DM, Dacks JB, Gallin WJ, Spencer AN. Atypical phenotypes from flatworm Kv3 channels. Journal of Neurophysiology. 95: 3035-46. PMID 16452260 DOI: 10.1152/Jn.00858.2005 |
0.64 |
|
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