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Year | Number of Results |
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2020 | 1 |
2021 | 1 |
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Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice.
Cell Rep. 2023 Jul 25;42(7):112706. doi: 10.1016/j.celrep.2023.112706. Epub 2023 Jun 28.
Cell Rep. 2023.
PMID: 37389991
Free PMC article.
Molecular and behavioral consequences of Ube3a gene overdosage in mice.
Punt AM, Judson MC, Sidorov MS, Williams BN, Johnson NS, Belder S, den Hertog D, Davis CR, Feygin MS, Lang PF, Jolfaei MA, Curran PJ, van IJcken WF, Elgersma Y, Philpot BD.
Punt AM, et al.
JCI Insight. 2022 Sep 22;7(18):e158953. doi: 10.1172/jci.insight.158953.
JCI Insight. 2022.
PMID: 36134658
Free PMC article.
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Dual-isoform hUBE3A gene transfer improves behavioral and seizure outcomes in Angelman syndrome model mice.
Judson MC, Shyng C, Simon JM, Davis CR, Punt AM, Salmon MT, Miller NW, Ritola KD, Elgersma Y, Amaral DG, Gray SJ, Philpot BD.
Judson MC, et al.
JCI Insight. 2021 Oct 22;6(20):e144712. doi: 10.1172/jci.insight.144712.
JCI Insight. 2021.
PMID: 34676830
Free PMC article.
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Deficits in higher visual area representations in a mouse model of Angelman syndrome.
Townsend LB, Jones KA, Dorsett CR, Philpot BD, Smith SL.
Townsend LB, et al.
J Neurodev Disord. 2020 Oct 19;12(1):28. doi: 10.1186/s11689-020-09329-y.
J Neurodev Disord. 2020.
PMID: 33076843
Free PMC article.
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