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1.
Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome.
Proc Natl Acad Sci U S A
; 120(2): e2122467120, 2023 01 10.
Article
in English
| MEDLINE | ID: mdl-36598943
2.
DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons.
Cereb Cortex
; 33(19): 10272-10285, 2023 09 26.
Article
in English
| MEDLINE | ID: mdl-37566909
3.
MMP2 and MMP9 Activity Is Crucial for Adult Visual Cortex Plasticity in Healthy and Stroke-Affected Mice.
J Neurosci
; 42(1): 16-32, 2022 01 05.
Article
in English
| MEDLINE | ID: mdl-34764155
4.
Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective.
Int J Mol Sci
; 23(2)2022 Jan 16.
Article
in English
| MEDLINE | ID: mdl-35055139
5.
Nucleophosmin 1 cooperates with the methyltransferase DOT1L to preserve peri-nucleolar heterochromatin organization by regulating H3K27me3 levels and DNA repeats expression.
Epigenetics Chromatin
; 16(1): 36, 2023 Sep 28.
Article
in English
| MEDLINE | ID: mdl-37759327
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