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The trajectory of gait development in mice.
Akula SK, McCullough KB, Weichselbaum C, Dougherty JD, Maloney SE. Akula SK, et al. Among authors: mccullough kb. Brain Behav. 2020 Jun;10(6):e01636. doi: 10.1002/brb3.1636. Epub 2020 Apr 24. Brain Behav. 2020. PMID: 32333523 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: mccullough kb. 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.
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: mccullough kb. bioRxiv [Preprint]. 2023 Feb 27:2023.02.27.530041. doi: 10.1101/2023.02.27.530041. bioRxiv. 2023. 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: mccullough kb. 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.
40 results