Liu Y - Search Results

1

Direct fluorescent labeling of NF186 and NaV1.6 in living primary neurons using bioorthogonal click chemistry.

Stajković N, Liu Y, Arsić A, Meng N, Lyu H, Zhang N, Grimm D, Lerche H, Nikić-Spiegel I. Stajković N, et al. Among authors: liu y. J Cell Sci. 2023 Jun 15;136(12):jcs260600. doi: 10.1242/jcs.260600. Epub 2023 Jun 28. J Cell Sci. 2023. PMID: 37288813 Free PMC article.

2

Impaired action potential initiation in GABAergic interneurons causes hyperexcitable networks in an epileptic mouse model carrying a human Na(V)1.1 mutation.

Hedrich UB, Liautard C, Kirschenbaum D, Pofahl M, Lavigne J, Liu Y, Theiss S, Slotta J, Escayg A, Dihné M, Beck H, Mantegazza M, Lerche H. Hedrich UB, et al. Among authors: liu y. J Neurosci. 2014 Nov 5;34(45):14874-89. doi: 10.1523/JNEUROSCI.0721-14.2014. J Neurosci. 2014. PMID: 25378155 Free PMC article.

3

Activity of Na_V1.2 promotes neurodegeneration in an animal model of multiple sclerosis.

Schattling B, Fazeli W, Engeland B, Liu Y, Lerche H, Isbrandt D, Friese MA. Schattling B, et al. Among authors: liu y. JCI Insight. 2016 Nov 17;1(19):e89810. doi: 10.1172/jci.insight.89810. JCI Insight. 2016. PMID: 27882351 Free PMC article.

4

Relationship of electrophysiological dysfunction and clinical severity in SCN2A-related epilepsies.

Lauxmann S, Verbeek NE, Liu Y, Zaichuk M, Müller S, Lemke JR, van Kempen MJA, Lerche H, Hedrich UBS. Lauxmann S, et al. Among authors: liu y. Hum Mutat. 2018 Dec;39(12):1942-1956. doi: 10.1002/humu.23619. Epub 2018 Sep 13. Hum Mutat. 2018. PMID: 30144217

5

Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.

Liu Y, Schubert J, Sonnenberg L, Helbig KL, Hoei-Hansen CE, Koko M, Rannap M, Lauxmann S, Huq M, Schneider MC, Johannesen KM, Kurlemann G, Gardella E, Becker F, Weber YG, Benda J, Møller RS, Lerche H. Liu Y, et al. Brain. 2019 Feb 1;142(2):376-390. doi: 10.1093/brain/awy326. Brain. 2019. PMID: 30615093

6

Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature.

Lauxmann S, Sonnenberg L, Koch NA, Bosselmann C, Winter N, Schwarz N, Wuttke TV, Hedrich UBS, Liu Y, Lerche H, Benda J, Kegele J. Lauxmann S, et al. Among authors: liu y. Front Neurol. 2021 Sep 9;12:703970. doi: 10.3389/fneur.2021.703970. eCollection 2021. Front Neurol. 2021. PMID: 34566847 Free PMC article.

7

A SCN8A variant associated with severe early onset epilepsy and developmental delay: Loss- or gain-of-function?

Liu Y, Koko M, Lerche H. Liu Y, et al. Epilepsy Res. 2021 Dec;178:106824. doi: 10.1016/j.eplepsyres.2021.106824. Epub 2021 Nov 23. Epilepsy Res. 2021. PMID: 34847423

8

Reply: Genotype-phenotype correlations in SCN8A-related epilepsy: a cohort study of Chinese children in southern China.

Johannesen KM, Liu Y, Gardella E, Lerche H, Møller RS. Johannesen KM, et al. Among authors: liu y. Brain. 2022 May 24;145(4):e28-e30. doi: 10.1093/brain/awac039. Brain. 2022. PMID: 35231099 No abstract available.

9

In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders.

Bayraktar E, Liu Y, Sonnenberg L, Hedrich UBS, Sara Y, Eltokhi A, Lyu H, Lerche H, Wuttke TV, Lauxmann S. Bayraktar E, et al. Among authors: liu y. Br J Pharmacol. 2023 Apr;180(8):1038-1055. doi: 10.1111/bph.15981. Epub 2022 Dec 19. Br J Pharmacol. 2023. PMID: 36321697 Free article.

10

Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype.

Knierim E, Vogt J, Kintscher M, Ponomarenko A, Baumgart J, Beed P, Korotkova T, Trimbuch T, Panzer A, Steinlein OK, Stephani U, Escayg A, Koko M, Liu Y, Lerche H, Schmitz D, Nitsch R, Schuelke M. Knierim E, et al. Among authors: liu y. Cereb Cortex. 2023 Jun 8;33(12):7454-7467. doi: 10.1093/cercor/bhad051. Cereb Cortex. 2023. PMID: 36977636

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