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Cited by in F6Publishing
For: Shore AN, Colombo S, Tobin WF, Petri S, Cullen ER, Dominguez S, Bostick CD, Beaumont MA, Williams D, Khodagholy D, Yang M, Lutz CM, Peng Y, Gelinas JN, Goldstein DB, Boland MJ, Frankel WN, Weston MC. Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood Epilepsy. Cell Rep 2020;33:108303. [PMID: 33113364 DOI: 10.1016/j.celrep.2020.108303] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Perszyk RE, Kristensen AS, Lyuboslavsky P, Traynelis SF. Three-dimensional missense tolerance ratio analysis. Genome Res 2021;31:1447-61. [PMID: 34301626 DOI: 10.1101/gr.275528.121] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Wang W, Frankel WN. Overlaps, gaps, and complexities of mouse models of Developmental and Epileptic Encephalopathy. Neurobiol Dis 2021;148:105220. [PMID: 33301879 DOI: 10.1016/j.nbd.2020.105220] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 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] [Reference Citation Analysis]
4 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]
5 Reddy HP, Yakubovich D, Keren-Raifman T, Tabak G, Tsemakhovich VA, Pedersen MH, Shalomov B, Colombo S, Goldstein DB, Javitch JA, Bera AK, Dascal N. Encephalopathy-causing mutations in Gβ1 (GNB1) alter regulation of neuronal GIRK channels. iScience 2021;24:103018. [PMID: 34522861 DOI: 10.1016/j.isci.2021.103018] [Reference Citation Analysis]
6 Griffin AM, Kahlig KM, Hatch RJ, Hughes ZA, Chapman ML, Antonio B, Marron BE, Wittmann M, Martinez-Botella G. Discovery of the First Orally Available, Selective KNa1.1 Inhibitor: In Vitro and In Vivo Activity of an Oxadiazole Series. ACS Med Chem Lett 2021;12:593-602. [PMID: 33859800 DOI: 10.1021/acsmedchemlett.0c00675] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
7 Cho JD, Kim YA, Rafikian EE, Yang M, Santa-Maria I. Marked Mild Cognitive Deficits in Humanized Mouse Model of Alzheimer's-Type Tau Pathology. Front Behav Neurosci 2021;15:634157. [PMID: 34093145 DOI: 10.3389/fnbeh.2021.634157] [Reference Citation Analysis]
8 Zhang Y, Ali SR, Nabbout R, Barcia G, Kaczmarek LK. A KCNC1 mutation in epilepsy of infancy with focal migrating seizures produces functional channels that fail to be regulated by PKC phosphorylation. J Neurophysiol 2021;126:532-9. [PMID: 34232791 DOI: 10.1152/jn.00257.2021] [Reference Citation Analysis]
9 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]
10 Döring JH, Schröter J, Jüngling J, Biskup S, Klotz KA, Bast T, Dietel T, Korenke GC, Christoph S, Brennenstuhl H, Rubboli G, Møller RS, Lesca G, Chaix Y, Kölker S, Hoffmann GF, Lemke JR, Syrbe S. Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders. Int J Mol Sci 2021;22:2824. [PMID: 33802230 DOI: 10.3390/ijms22062824] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Imbrici P, Conte E, Blunck R, Stregapede F, Liantonio A, Tosi M, D'Adamo MC, De Luca A, Brankovic V, Zanni G. A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine. Int J Mol Sci 2021;22:9913. [PMID: 34576077 DOI: 10.3390/ijms22189913] [Reference Citation Analysis]
12 Maguire JL. Same Channel, Different Tune. Epilepsy Curr 2021;21:111-3. [PMID: 34025287 DOI: 10.1177/1535759720986837] [Reference Citation Analysis]
13 McCabe MP, Shore AN, Frankel WN, Weston MC. Altered Fast Synaptic Transmission in a Mouse Model of DNM1-Associated Developmental Epileptic Encephalopathy. eNeuro 2021;8:ENEURO. [PMID: 33372033 DOI: 10.1523/ENEURO.0269-20.2020] [Reference Citation Analysis]