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For: Evely KM, Pryce KD, Bhattacharjee A. The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype. Neuroscience 2017;351:65-70. [PMID: 28366665 DOI: 10.1016/j.neuroscience.2017.03.035] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Gertler TS, Cherian S, DeKeyser JM, Kearney JA, George AL Jr. KNa1.1 gain-of-function preferentially dampens excitability of murine parvalbumin-positive interneurons. Neurobiol Dis 2022;:105713. [PMID: 35346832 DOI: 10.1016/j.nbd.2022.105713] [Reference Citation Analysis]
2 Zhang Q, Liu Y, Xu J, Teng Y, Zhang Z. The Functional Properties, Physiological Roles, Channelopathy and Pharmacological Characteristics of the Slack (KCNT1) Channel. Adv Exp Med Biol 2021;1349:387-400. [PMID: 35138624 DOI: 10.1007/978-981-16-4254-8_18] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Matt L, Pham T, Skrabak D, Hoffmann F, Eckert P, Yin J, Gisevius M, Ehinger R, Bausch A, Ueffing M, Boldt K, Ruth P, Lukowski R. The Na+-activated K+ channel Slack contributes to synaptic development and plasticity. Cell Mol Life Sci 2021;78:7569-87. [PMID: 34664085 DOI: 10.1007/s00018-021-03953-0] [Reference Citation Analysis]
4 Jackson A, Banka S, Stewart H, Robinson H, Lovell S, Clayton-Smith J; Genomics England Research Consortium. Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotype. Am J Med Genet A 2021. [PMID: 34061450 DOI: 10.1002/ajmg.a.62370] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Cole BA, Clapcote SJ, Muench SP, Lippiat JD. Targeting KNa1.1 channels in KCNT1-associated epilepsy. Trends Pharmacol Sci 2021;42:700-13. [PMID: 34074526 DOI: 10.1016/j.tips.2021.05.003] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Specchio N, Pietrafusa N, Perucca E, Cross JH. New paradigms for the treatment of pediatric monogenic epilepsies: Progressing toward precision medicine. Epilepsy Behav 2021;:107961. [PMID: 33867301 DOI: 10.1016/j.yebeh.2021.107961] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kuchenbuch M, Nabbout R, Yochum M, Sauleau P, Modolo J, Wendling F, Benquet P. In silico model reveals the key role of GABA in KCNT1-epilepsy in infancy with migrating focal seizures. Epilepsia 2021;62:683-97. [PMID: 33617692 DOI: 10.1111/epi.16834] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Nabbout R, Kuchenbuch M. Impact of predictive, preventive and precision medicine strategies in epilepsy. Nat Rev Neurol 2020;16:674-88. [PMID: 33077944 DOI: 10.1038/s41582-020-0409-4] [Cited by in Crossref: 10] [Cited by in F6Publishing: 17] [Article Influence: 5.0] [Reference Citation Analysis]
9 Kessi M, Chen B, Peng J, Tang Y, Olatoutou E, He F, Yang L, Yin F. Intellectual Disability and Potassium Channelopathies: A Systematic Review. Front Genet 2020;11:614. [PMID: 32655623 DOI: 10.3389/fgene.2020.00614] [Cited by in Crossref: 7] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
10 Niu LG, Liu P, Wang ZW, Chen B. Slo2 potassium channel function depends on RNA editing-regulated expression of a SCYL1 protein. Elife 2020;9:e53986. [PMID: 32314960 DOI: 10.7554/eLife.53986] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
11 Mao X, Bruneau N, Gao Q, Becq H, Jia Z, Xi H, Shu L, Wang H, Szepetowski P, Aniksztejn L. The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel. Front Cell Neurosci 2020;14:1. [PMID: 32038177 DOI: 10.3389/fncel.2020.00001] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
12 Ali SR, Malone TJ, Zhang Y, Prechova M, Kaczmarek LK. Phactr1 regulates Slack (KCNT1) channels via protein phosphatase 1 (PP1). FASEB J 2020;34:1591-601. [PMID: 31914597 DOI: 10.1096/fj.201902366R] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
13 Demarest ST, Brooks-kayal A. From molecules to medicines: the dawn of targeted therapies for genetic epilepsies. Nat Rev Neurol 2018;14:735-45. [DOI: 10.1038/s41582-018-0099-3] [Cited by in Crossref: 28] [Cited by in F6Publishing: 25] [Article Influence: 7.0] [Reference Citation Analysis]
14 Bausch AE, Ehinger R, Straubinger J, Zerfass P, Nann Y, Lukowski R. Loss of Sodium-Activated Potassium Channel Slack and FMRP Differentially Affect Social Behavior in Mice. Neuroscience 2018;384:361-74. [DOI: 10.1016/j.neuroscience.2018.05.040] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
15 Zhou P, He N, Zhang JW, Lin ZJ, Wang J, Yan LM, Meng H, Tang B, Li BM, Liu XR, Shi YW, Zhai QX, Yi YH, Liao WP. Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies. Genes Brain Behav 2018;17:e12456. [PMID: 29314583 DOI: 10.1111/gbb.12456] [Cited by in Crossref: 28] [Cited by in F6Publishing: 37] [Article Influence: 7.0] [Reference Citation Analysis]
16 Liu P, Wang SJ, Wang ZW, Chen B. HRPU-2, a Homolog of Mammalian hnRNP U, Regulates Synaptic Transmission by Controlling the Expression of SLO-2 Potassium Channel in Caenorhabditis elegans. J Neurosci 2018;38:1073-84. [PMID: 29217678 DOI: 10.1523/JNEUROSCI.1991-17.2017] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]