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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 3 |
2021 | 3 |
2022 | 3 |
2024 | 0 |
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7 results
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Page 1
Epigenetic regulation of nervous system development and function.
Neurochem Int. 2022 Jan;152:105249. doi: 10.1016/j.neuint.2021.105249. Epub 2021 Nov 24.
Neurochem Int. 2022.
PMID: 34826529
Proteomic and transcriptional changes associated with MeCP2 dysfunction reveal nodes for therapeutic intervention in Rett syndrome.
Marballi K, MacDonald JL.
Marballi K, et al.
Neurochem Int. 2021 Sep;148:105076. doi: 10.1016/j.neuint.2021.105076. Epub 2021 May 26.
Neurochem Int. 2021.
PMID: 34048843
Free PMC article.
Review.
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Sex differences in Mecp2-mutant Rett syndrome model mice and the impact of cellular mosaicism in phenotype development.
Ribeiro MC, MacDonald JL.
Ribeiro MC, et al.
Brain Res. 2020 Feb 15;1729:146644. doi: 10.1016/j.brainres.2019.146644. Epub 2020 Jan 2.
Brain Res. 2020.
PMID: 31904347
Free PMC article.
Review.
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miR-409-3p represses Cited2 to refine neocortical layer V projection neuron identity.
Wagner NR, Sinha A, Siththanandan V, Kowalchuk AM, MacDonald JL, Tharin S.
Wagner NR, et al.
Front Neurosci. 2022 Sep 29;16:931333. doi: 10.3389/fnins.2022.931333. eCollection 2022.
Front Neurosci. 2022.
PMID: 36248641
Free PMC article.
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Vitamin D modulates cortical transcriptome and behavioral phenotypes in an Mecp2 heterozygous Rett syndrome mouse model.
Ribeiro MC, MacDonald JL.
Ribeiro MC, et al.
Neurobiol Dis. 2022 Apr;165:105636. doi: 10.1016/j.nbd.2022.105636. Epub 2022 Jan 25.
Neurobiol Dis. 2022.
PMID: 35091041
Free PMC article.
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Atypical Neocortical Development in the Cited2 Conditional Knockout Leads to Behavioral Deficits Associated with Neurodevelopmental Disorders.
Wagner NR, MacDonald JL.
Wagner NR, et al.
Neuroscience. 2021 Feb 10;455:65-78. doi: 10.1016/j.neuroscience.2020.12.009. Epub 2020 Dec 17.
Neuroscience. 2021.
PMID: 33346116
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Vitamin D Supplementation Rescues Aberrant NF-κB Pathway Activation and Partially Ameliorates Rett Syndrome Phenotypes in Mecp2 Mutant Mice.
Ribeiro MC, Moore SM, Kishi N, Macklis JD, MacDonald JL.
Ribeiro MC, et al.
eNeuro. 2020 May 22;7(3):ENEURO.0167-20.2020. doi: 10.1523/ENEURO.0167-20.2020. Print 2020 May/Jun.
eNeuro. 2020.
PMID: 32393583
Free PMC article.
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