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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: ge x. 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: ge x. 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.
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: ge x. 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.
Evaluation of gliovascular functions of Aqp4 readthrough isoforms.
Mueller SM, White KM, Fass SB, Chen S, Shi Z, Ge X, Engelbach JA, Gaines SH, Bice AR, Vasek MJ, Garbow JR, Culver JP, Zila Martinez-Lozada, Cohen-Salmon M, Dougherty JD, Sapkota D. Mueller SM, et al. Among authors: ge x. bioRxiv [Preprint]. 2023 Jul 25:2023.07.21.549379. doi: 10.1101/2023.07.21.549379. bioRxiv. 2023. PMID: 37546949 Free PMC article. Updated. Preprint.
4,706 results