Select Publications:

Wagner, N.W.⁺, Siththanandan, V.B.⁺, Sinha, A.⁺, Kowalchuk, A.M., MacDonald, J.L.^§ and Tharin, S^§. (2022) miR-409-3p represses Cited2 to refine neocortical layer V projection neuron identity. Frontiers in Neuroscience. 16:931333 ⁺Co-first authors; ^§Co-senior and corresponding authors. DOI: 10.3389/fnins.2022.931333/full

Ribeiro, M.C. and MacDonald, J.L. (2022) Vitamin D modulates cortical transcriptome and and behavioral phenotypes in an Mecp2 heterozygous Rett syndrome mouse model. Neurobiology of Disease. 165: 105636. DOI: https://doi.org/10.1016/j.nbd.2022.105636

MacDonald, J.L., Tharin, S., Hall, S.E. (2022) Epigenetic regulation of nervous system development and function. Neurochemistry International. 152:105249. DOI: https://doi.org/10.1016/j.neuint.2021.105249

Marballi, K.K. and MacDonald, J.L. (2021) Proteomic and transcriptional changes associated with MeCP2 dysfunction reveal nodes for therapeutic intervention in Rett syndrome. Neurochemistry International. 148:105076. DOI: https://doi.org/10.1016/j.neuint.2021.105076

Wagner, N.R., and MacDonald, J.L. (2021) Atypical neocortical development in the Cited2 conditional knockout leads to behavioral deficits association with neurodevelopmental disorders. Neuroscience, 455:65-78. https://doi.org/10.1016/j.neuroscience.2020.12.009

Ribeiro, M.C., Moore, S.M., Kishi, N., Macklis, J.D. and MacDonald, J.L. (2020) Vitamin D supplementation rescues aberrant NF-kappa B activation and partially ameliorates Rett syndrome phenotypes in Mecp2-mutant mice. eNeuro, 7(3):1-18. https://doi.org/10.1523/ENEURO.0167-20.2020

Ribeiro, M.C. and MacDonald, J.L. (2020) Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development. Brain Research, 1729:146644. DOI:1016/j.brainres.2019.146644

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