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Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome.
Proc Natl Acad Sci U S A. 2023 Jan 10;120(2):e2122467120. doi: 10.1073/pnas.2122467120. Epub 2023 Jan 4.
Proc Natl Acad Sci U S A. 2023.
PMID: 36598943
Free PMC article.
Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective.
Akol I, Gather F, Vogel T.
Akol I, et al.
Int J Mol Sci. 2022 Jan 16;23(2):954. doi: 10.3390/ijms23020954.
Int J Mol Sci. 2022.
PMID: 35055139
Free PMC article.
Review.
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DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons.
Cheffer A, Garcia-Miralles M, Maier E, Akol I, Franz H, Srinivasan VSV, Vogel T.
Cheffer A, et al. Among authors: akol i.
Cereb Cortex. 2023 Sep 26;33(19):10272-10285. doi: 10.1093/cercor/bhad281.
Cereb Cortex. 2023.
PMID: 37566909
Free PMC article.
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Nucleophosmin 1 cooperates with the methyltransferase DOT1L to preserve peri-nucleolar heterochromatin organization by regulating H3K27me3 levels and DNA repeats expression.
Izzo A, Akol I, Villarreal A, Lebel S, Garcia-Miralles M, Cheffer A, Bovio P, Heidrich S, Vogel T.
Izzo A, et al. Among authors: akol i.
Epigenetics Chromatin. 2023 Sep 28;16(1):36. doi: 10.1186/s13072-023-00511-9.
Epigenetics Chromatin. 2023.
PMID: 37759327
Free PMC article.
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MMP2 and MMP9 Activity Is Crucial for Adult Visual Cortex Plasticity in Healthy and Stroke-Affected Mice.
Akol I, Kalogeraki E, Pielecka-Fortuna J, Fricke M, Löwel S.
Akol I, et al.
J Neurosci. 2022 Jan 5;42(1):16-32. doi: 10.1523/JNEUROSCI.0902-21.2021. Epub 2021 Nov 11.
J Neurosci. 2022.
PMID: 34764155
Free PMC article.
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