[HTML][HTML] Inhibitory dysfunction and social processing difficulties in autism: A comprehensive narrative review
The primary inhibitory neurotransmitter γ-aminobutyric acid (GABA) has a prominent role in
regulating neural development and function, with disruption to GABAergic signalling linked …
regulating neural development and function, with disruption to GABAergic signalling linked …
Biological and therapeutic role of LSD1 in Alzheimer's diseases
Y Li, Y Zhao, X Li, L Zhai, H Zheng, Y Yan… - Frontiers in …, 2022 - frontiersin.org
Alzheimer's disease (AD) is a common chronic neurodegenerative disease characterized by
cognitive learning and memory impairments, however, current treatments only provide …
cognitive learning and memory impairments, however, current treatments only provide …
baz1b loss-of-function in zebrafish produces phenotypic alterations consistent with the domestication syndrome
JV Torres-Pérez, S Anagianni, AM Mech, W Havelange… - Iscience, 2023 - cell.com
BAZ1B is a ubiquitously expressed nuclear protein with roles in chromatin remodeling, DNA
replication and repair, and transcription. Reduced BAZ1B expression disrupts neuronal and …
replication and repair, and transcription. Reduced BAZ1B expression disrupts neuronal and …
GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders
Copy number variations at 7q11. 23 cause neurodevelopmental disorders with shared and
opposite manifestations. Deletion causes Williams-Beuren syndrome featuring …
opposite manifestations. Deletion causes Williams-Beuren syndrome featuring …
7q11. 23 deletion and duplication
LR Osborne, CB Mervis - Current opinion in genetics & development, 2021 - Elsevier
Copy number variation (CNV) at 7q11. 23 causes distinct disorders with both contrasting
and overlapping phenotypic features of some but not all of the genes encompassed by the …
and overlapping phenotypic features of some but not all of the genes encompassed by the …
DLX5/6 GABAergic Expression Affects Social Vocalization: Implications for Human Evolution
G Levi, C de Lombares, C Giuliani… - Molecular Biology …, 2021 - academic.oup.com
DLX5 and DLX6 are two closely related transcription factors involved in brain development
and in GABAergic differentiation. The DLX5/6 locus is regulated by FoxP2, a gene involved …
and in GABAergic differentiation. The DLX5/6 locus is regulated by FoxP2, a gene involved …
Morphine exposure during adolescence induces enduring social changes dependent on adolescent stage of exposure, sex, and social test.
DN King'uyu, EL Edgar, C Figueroa… - Behavioral …, 2024 - psycnet.apa.org
Drug exposure during adolescence, when the “reward” circuitry of the brain is developing,
can permanently impact reward-related behavior into adulthood. Epidemiological studies …
can permanently impact reward-related behavior into adulthood. Epidemiological studies …
Investigating the therapeutic potential of LSD1 enzyme activity-specific inhibition by TAK-418 for social and memory deficits in rodent disease models
R Baba, S Matsuda, R Maeda… - ACS Chemical …, 2022 - ACS Publications
Inhibition of lysine-specific demethylase 1 (LSD1) enzyme activity is a promising approach
to treat diseases associated with epigenetic dysregulation, such as neurodevelopmental …
to treat diseases associated with epigenetic dysregulation, such as neurodevelopmental …
Cellular Organelle-Related Transcriptomic Profile Abnormalities in Neuronopathic Types of Mucopolysaccharidosis: A Comparison with Other Neurodegenerative …
K Wiśniewska, L Gaffke, M Żabińska… - Current Issues in …, 2024 - mdpi.com
Mucopolysaccharidoses (MPS) are a group of diseases caused by mutations in genes
encoding lysosomal enzymes that catalyze reactions of glycosaminoglycan (GAG) …
encoding lysosomal enzymes that catalyze reactions of glycosaminoglycan (GAG) …
[PDF][PDF] Zabi nska, M.; Wegrzyn, G.; Pierzynowska, K. Cellular Organelle-Related Transcriptomic Profile Abnormalities in Neuronopathic Types of …
K Wisniewska, L Gaffke - Curr. Issues Mol. Biol, 2024 - repozytorium.bg.ug.edu.pl
Mucopolysaccharidoses (MPS) are a group of diseases caused by mutations in genes
encoding lysosomal enzymes that catalyze reactions of glycosaminoglycan (GAG) …
encoding lysosomal enzymes that catalyze reactions of glycosaminoglycan (GAG) …