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Cited by in F6Publishing
For: 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. A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy. Cell Rep 2017;21:926-33. [PMID: 29069600 DOI: 10.1016/j.celrep.2017.09.088] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Byers N, Hahm ET, Tsunoda S. Slo2/KNa Channels in Drosophila Protect against Spontaneous and Induced Seizure-like Behavior Associated with an Increased Persistent Na+ Current. J Neurosci 2021;41:9047-63. [PMID: 34544836 DOI: 10.1523/JNEUROSCI.0290-21.2021] [Reference Citation Analysis]
2 Ehinger R, Kuret A, Matt L, Frank N, Wild K, Kabagema-Bilan C, Bischof H, Malli R, Ruth P, Bausch AE, Lukowski R. Slack K+ channels attenuate NMDA-induced excitotoxic brain damage and neuronal cell death. FASEB J 2021;35:e21568. [PMID: 33817875 DOI: 10.1096/fj.202002308RR] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
3 McMillan KJ, Banks PJ, Hellel FL, Carmichael RE, Clairfeuille T, Evans AJ, Heesom KJ, Lewis P, Collins BM, Bashir ZI, Henley JM, Wilkinson KA, Cullen PJ. Sorting nexin-27 regulates AMPA receptor trafficking through the synaptic adhesion protein LRFN2. Elife 2021;10:e59432. [PMID: 34251337 DOI: 10.7554/eLife.59432] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
4 Mohajeri MSA, Eslahi A, Khazaii Z, Moradi MR, Pazhoomand R, Farrokhi S, Feizabadi MH, Alizadeh F, Mojarrad M. TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia. Hum Genomics 2021;15:42. [PMID: 34238371 DOI: 10.1186/s40246-021-00343-2] [Reference Citation Analysis]
5 Gong P, Jiao X, Yu D, Yang Z. Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy. Front Genet 2021;12:649556. [PMID: 34276763 DOI: 10.3389/fgene.2021.649556] [Reference Citation Analysis]
6 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]
7 Nikitin ES, Vinogradova LV. Potassium channels as prominent targets and tools for the treatment of epilepsy. Expert Opin Ther Targets 2021;25:223-35. [PMID: 33754930 DOI: 10.1080/14728222.2021.1908263] [Reference Citation Analysis]
8 Palmer EE, Sachdev R, Macintosh R, Melo US, Mundlos S, Righetti S, Kandula T, Minoche AE, Puttick C, Gayevskiy V, Hesson L, Idrisoglu S, Shoubridge C, Thai MHN, Davis RL, Drew AP, Sampaio H, Andrews PI, Lawson J, Cardamone M, Mowat D, Colley A, Kummerfeld S, Dinger ME, Cowley MJ, Roscioli T, Bye A, Kirk E. Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies. Neurology 2021;96:e1770-82. [PMID: 33568551 DOI: 10.1212/WNL.0000000000011655] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
9 Inuzuka LM, Macedo-Souza LI, Della-Ripa B, Monteiro FP, Ramos L, Kitajima JP, Garzon E, Kok F. Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy. Brain Dev 2020;42:691-5. [PMID: 32773162 DOI: 10.1016/j.braindev.2020.05.003] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
10 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: 6] [Article Influence: 3.5] [Reference Citation Analysis]
11 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: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 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: 8] [Article Influence: 3.5] [Reference Citation Analysis]
13 Bar C, Barcia G, Jennesson M, Le Guyader G, Schneider A, Mignot C, Lesca G, Breuillard D, Montomoli M, Keren B, Doummar D, Billette de Villemeur T, Afenjar A, Marey I, Gerard M, Isnard H, Poisson A, Dupont S, Berquin P, Meyer P, Genevieve D, De Saint Martin A, El Chehadeh S, Chelly J, Guët A, Scalais E, Dorison N, Myers CT, Mefford HC, Howell KB, Marini C, Freeman JL, Nica A, Terrone G, Sekhara T, Lebre A, Odent S, Sadleir LG, Munnich A, Guerrini R, Scheffer IE, Kabashi E, Nabbout R. Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. Human Mutation 2019;41:69-80. [DOI: 10.1002/humu.23915] [Cited by in Crossref: 9] [Cited by in F6Publishing: 15] [Article Influence: 3.0] [Reference Citation Analysis]
14 Yang L, Xu Y, Yan Y, Luo P, Chen S, Zheng B, Yan W, Chen Y, Wang C. Common Nevus and Skin Cutaneous Melanoma: Prognostic Genes Identified by Gene Co-Expression Network Analysis. Genes (Basel) 2019;10:E747. [PMID: 31557882 DOI: 10.3390/genes10100747] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
15 Ambrosino P, Soldovieri MV, Bast T, Turnpenny PD, Uhrig S, Biskup S, Döcker M, Fleck T, Mosca I, Manocchio L, Iraci N, Taglialatela M, Lemke JR. De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy. Ann Neurol 2018;83:1198-204. [PMID: 29740868 DOI: 10.1002/ana.25248] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 6.7] [Reference Citation Analysis]
16 Perucca P, Perucca E. Identifying mutations in epilepsy genes: Impact on treatment selection. Epilepsy Research 2019;152:18-30. [DOI: 10.1016/j.eplepsyres.2019.03.001] [Cited by in Crossref: 40] [Cited by in F6Publishing: 32] [Article Influence: 13.3] [Reference Citation Analysis]
17 Møller RS, Hammer TB, Rubboli G, Lemke JR, Johannesen KM. From next-generation sequencing to targeted treatment of non-acquired epilepsies. Expert Review of Molecular Diagnostics 2019;19:217-28. [DOI: 10.1080/14737159.2019.1573144] [Cited by in Crossref: 22] [Cited by in F6Publishing: 20] [Article Influence: 7.3] [Reference Citation Analysis]
18 Smith CO, Wang YT, Nadtochiy SM, Miller JH, Jonas EA, Dirksen RT, Nehrke K, Brookes PS. Cardiac metabolic effects of KNa1.2 channel deletion and evidence for its mitochondrial localization. FASEB J 2018;:fj201800139R. [PMID: 29863912 DOI: 10.1096/fj.201800139R] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 4.3] [Reference Citation Analysis]