Zobrazeno 1 - 10 of 12 pro vyhledávání: '"Marshall Biven"'
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Heterozygous GABA
Autor: Shimian, Qu, Laurel G, Jackson, Chengwen, Zhou, DingDing, Shen, Wangzhen, Shen, Gerald, Nwosu, Rachel, Howe, Mackenzie, Caltron, Carson, Flamm, Marshall, Biven, Jing-Qiong, Kang, Robert L, Macdonald
Publikováno v: Epilepsia.
Infantile spasms are anis an epileptic encephalopathy of childhood, and its pathophysiology is largely unknown.We generated a heterozygous knock-in mouse with the human infantile spasms-associated de novo mutation GABRB3(c.A328G, p.N110D) to investig
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::22c98efa4844ddc1c379c35d975ffd61
https://pubmed.ncbi.nlm.nih.gov/36495145
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3
GABAA Receptor β3 Subunit Mutation N328D Heterozygous Knock-in Mice Have Lennox–Gastaut Syndrome
Autor: Gerald Ikemefuna Nwosu, Wangzhen Shen, Kirill Zavalin, Sarah Poliquin, Karishma Randhave, Carson Flamm, Marshall Biven, Katherine Langer, Jing-Qiong Kang
Publikováno v: International Journal of Molecular Sciences; Volume 24; Issue 9; Pages: 8458
Lennox–Gastaut Syndrome (LGS) is a developmental and epileptic encephalopathy (DEE) characterized by multiple seizure types, electroencephalogram (EEG) patterns, and cognitive decline. Its etiology has a prominent genetic component, including varia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b09d617fee98749dfd9bd74e3730cace
https://doi.org/10.3390/ijms24098458
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4
Akademický článek
GABA A Receptor β3 Subunit Mutation N328D Heterozygous Knock-in Mice Have Lennox–Gastaut Syndrome.
Autor: Nwosu, Gerald Ikemefuna1,2,3 (AUTHOR), Shen, Wangzhen2,3 (AUTHOR), Zavalin, Kirill2,3 (AUTHOR), Poliquin, Sarah2,3 (AUTHOR), Randhave, Karishma2,3 (AUTHOR), Flamm, Carson2,3 (AUTHOR), Biven, Marshall2,3 (AUTHOR), Langer, Katherine2,3,4 (AUTHOR), Kang, Jing-Qiong2,3,4 (AUTHOR) jingqiong.kang@vanderbilt.edu
Publikováno v: International Journal of Molecular Sciences. May2023, Vol. 24 Issue 9, p8458. 18p.
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6
Akademický článek
Abstracts.
Publikováno v: Epilepsia (Series 4); Nov2023 Supplement 1, Vol. 64, p7-570, 564p
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