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For: Si M, Trosclair K, Hamilton KA, Glasscock E. Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice. Am J Physiol Cell Physiol 2019;316:C154-61. [PMID: 30427720 DOI: 10.1152/ajpcell.00335.2018] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Trosclair K, Si M, Watts M, Gautier NM, Voigt N, Traylor J, Bitay M, Baczko I, Dobrev D, Hamilton KA, Bhuiyan MS, Dominic P, Glasscock E. Kv1.1 potassium channel subunit deficiency alters ventricular arrhythmia susceptibility, contractility, and repolarization. Physiol Rep 2021;9:e14702. [PMID: 33427415 DOI: 10.14814/phy2.14702] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
2 Glasscock E. Kv1.1 channel subunits in the control of neurocardiac function. Channels (Austin) 2019;13:299-307. [PMID: 31250689 DOI: 10.1080/19336950.2019.1635864] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
3 D'Adamo MC, Liantonio A, Rolland JF, Pessia M, Imbrici P. Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches. Int J Mol Sci 2020;21:E2935. [PMID: 32331416 DOI: 10.3390/ijms21082935] [Cited by in Crossref: 13] [Cited by in F6Publishing: 18] [Article Influence: 6.5] [Reference Citation Analysis]
4 Paulhus K, Ammerman L, Glasscock E. Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity. Int J Mol Sci 2020;21:E2802. [PMID: 32316562 DOI: 10.3390/ijms21082802] [Cited by in Crossref: 14] [Cited by in F6Publishing: 26] [Article Influence: 7.0] [Reference Citation Analysis]
5 Trosclair K, Dhaibar HA, Gautier NM, Mishra V, Glasscock E. Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation. Neurobiol Dis 2020;137:104759. [PMID: 31978607 DOI: 10.1016/j.nbd.2020.104759] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 6.0] [Reference Citation Analysis]
6 De Zio R, Gerbino A, Forleo C, Pepe M, Milano S, Favale S, Procino G, Svelto M, Carmosino M. Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome. J Cell Mol Med 2019;23:6331-42. [PMID: 31361068 DOI: 10.1111/jcmm.14521] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
7 Dhaibar H, Gautier NM, Chernyshev OY, Dominic P, Glasscock E. Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy. Neurobiol Dis 2019;127:502-11. [PMID: 30974168 DOI: 10.1016/j.nbd.2019.04.006] [Cited by in Crossref: 21] [Cited by in F6Publishing: 25] [Article Influence: 7.0] [Reference Citation Analysis]