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A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation.
Chen J, Lambo ME, Ge X, Dearborn JT, Liu Y, McCullough KB, Swift RG, Tabachnick DR, Tian L, Noguchi K, Garbow JR, Constantino JN, Gabel HW, Hengen KB, Maloney SE, Dougherty JD. Chen J, et al. Among authors: swift rg. Neuron. 2021 Dec 1;109(23):3775-3792.e14. doi: 10.1016/j.neuron.2021.09.009. Epub 2021 Oct 5. Neuron. 2021. PMID: 34614421 Free PMC article.
Extensive characterization of a Williams Syndrome murine model shows Gtf2ird1 -mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior.
Nygaard KR, Maloney SE, Swift RG, McCullough KB, Wagner RE, Fass SB, Garbett K, Mirnics K, Veenstra-VanderWeele J, Dougherty JD. Nygaard KR, et al. Among authors: swift rg. bioRxiv [Preprint]. 2023 Jan 18:2023.01.18.523029. doi: 10.1101/2023.01.18.523029. bioRxiv. 2023. Update in: Genes Brain Behav. 2023 Aug;22(4):e12853. doi: 10.1111/gbb.12853 PMID: 36711815 Free PMC article. Updated. Preprint.
Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits.
Beard DC, Zhang X, Wu DY, Martin JR, Hamagami N, Swift RG, McCullough KB, Ge X, Bell-Hensley A, Zheng H, Lawrence AB, Hill CA, Papouin T, McAlinden A, Garbow JR, Dougherty JD, Maloney SE, Gabel HW. Beard DC, et al. Among authors: swift rg. bioRxiv [Preprint]. 2023 Feb 27:2023.02.27.530041. doi: 10.1101/2023.02.27.530041. bioRxiv. 2023. Update in: Cell Rep. 2023 Nov 28;42(11):113411. doi: 10.1016/j.celrep.2023.113411 PMID: 36909558 Free PMC article. Updated. Preprint.
Extensive characterization of a Williams syndrome murine model shows Gtf2ird1-mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior.
Nygaard KR, Maloney SE, Swift RG, McCullough KB, Wagner RE, Fass SB, Garbett K, Mirnics K, Veenstra-VanderWeele J, Dougherty JD. Nygaard KR, et al. Among authors: swift rg. Genes Brain Behav. 2023 Aug;22(4):e12853. doi: 10.1111/gbb.12853. Epub 2023 Jun 27. Genes Brain Behav. 2023. PMID: 37370259 Free PMC article.
Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits.
Beard DC, Zhang X, Wu DY, Martin JR, Erickson A, Boua JV, Hamagami N, Swift RG, McCullough KB, Ge X, Bell-Hensley A, Zheng H, Palmer CW, Fuhler NA, Lawrence AB, Hill CA, Papouin T, Noguchi KK, McAlinden A, Garbow JR, Dougherty JD, Maloney SE, Gabel HW. Beard DC, et al. Among authors: swift rg. Cell Rep. 2023 Nov 28;42(11):113411. doi: 10.1016/j.celrep.2023.113411. Epub 2023 Nov 11. Cell Rep. 2023. PMID: 37952155 Free PMC article.
A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation.
Chen J, Lambo ME, Ge X, Dearborn JT, Liu Y, McCullough KB, Swift RG, Tabachnick DR, Tian L, Noguchi K, Garbow JR, Constantino JN, Gabel HW, Hengen KB, Maloney SE, Dougherty JD. Chen J, et al. Among authors: swift rg. Neuron. 2024 Jul 3;112(13):2257. doi: 10.1016/j.neuron.2024.06.012. Epub 2024 Jun 20. Neuron. 2024. PMID: 38906150 Free article. No abstract available.
28 results