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Characterization of a Mouse Model of Börjeson-Forssman-Lehmann Syndrome.
Cheng C, Deng PY, Ikeuchi Y, Yuede C, Li D, Rensing N, Huang J, Baldridge D, Maloney SE, Dougherty JD, Constantino J, Jahani-Asl A, Wong M, Wozniak DF, Wang T, Klyachko VA, Bonni A. Cheng C, et al. Among authors: maloney se. Cell Rep. 2018 Nov 6;25(6):1404-1414.e6. doi: 10.1016/j.celrep.2018.10.043. Cell Rep. 2018. PMID: 30403997 Free PMC article.
The trajectory of gait development in mice.
Akula SK, McCullough KB, Weichselbaum C, Dougherty JD, Maloney SE. Akula SK, et al. Among authors: maloney se. 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: maloney se. 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: maloney se. 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.
68 results