CpG and non-CpG methylation in epigenetic gene regulation and brain function
HS Jang, WJ Shin, JE Lee, JT Do - Genes, 2017 - mdpi.com
DNA methylation is a major epigenetic mark with important roles in genetic regulation.
Methylated cytosines are found primarily at CpG dinucleotides, but are also found at non …
Methylated cytosines are found primarily at CpG dinucleotides, but are also found at non …
Developing in 3D: the role of CTCF in cell differentiation
RG Arzate-Mejía, F Recillas-Targa… - Development, 2018 - journals.biologists.com
ABSTRACT CTCF is a highly conserved zinc-finger DNA-binding protein that mediates
interactions between distant sequences in the genome. As a consequence, CTCF regulates …
interactions between distant sequences in the genome. As a consequence, CTCF regulates …
[HTML][HTML] Huntington's disease accelerates epigenetic aging of human brain and disrupts DNA methylation levels
Age of Huntington's disease (HD) motoric onset is strongly related to the number of CAG
trinucleotide repeats in the huntingtin gene, suggesting that biological tissue age plays an …
trinucleotide repeats in the huntingtin gene, suggesting that biological tissue age plays an …
Dynamic regulation of DNA methylation and brain functions
J Xie, L Xie, H Wei, XJ Li, L Lin - Biology, 2023 - mdpi.com
Simple Summary DNA methylation is involved in biological processes including
neurogenesis, aging, and the pathogenesis of brain disorders by the regulation of gene …
neurogenesis, aging, and the pathogenesis of brain disorders by the regulation of gene …
DNA methylation study of Huntington's disease and motor progression in patients and in animal models
AT Lu, P Narayan, MJ Grant, P Langfelder… - Nature …, 2020 - nature.com
Although Huntington's disease (HD) is a well studied Mendelian genetic disorder, less is
known about its associated epigenetic changes. Here, we characterize DNA methylation …
known about its associated epigenetic changes. Here, we characterize DNA methylation …
The contribution of DNA methylation to the (dys) function of oligodendroglia in neurodegeneration
K Fodder, R de Silva, TT Warner… - Acta Neuropathologica …, 2023 - Springer
Neurodegenerative diseases encompass a heterogeneous group of conditions
characterised by the progressive degeneration of the structure and function of the central or …
characterised by the progressive degeneration of the structure and function of the central or …
A systematic review of transcriptional dysregulation in Huntington's disease studied by RNA sequencing
B Malla, X Guo, G Senger, Z Chasapopoulou… - Frontiers in …, 2021 - frontiersin.org
Huntington's disease (HD) is a chronic neurodegenerative disorder caused by an expansion
of polyglutamine repeats in exon 1 of the Huntingtin gene. Transcriptional dysregulation …
of polyglutamine repeats in exon 1 of the Huntingtin gene. Transcriptional dysregulation …
Epigenetic mechanisms of neurodegenerative diseases and acute brain injury
MJ Bertogliat, KC Morris-Blanco… - Neurochemistry …, 2020 - Elsevier
Epigenetic modifications are emerging as major players in the pathogenesis of
neurodegenerative disorders and susceptibility to acute brain injury. DNA and histone …
neurodegenerative disorders and susceptibility to acute brain injury. DNA and histone …
Hierarchical deconvolution for extensive cell type resolution in the human brain using DNA methylation
Introduction The human brain comprises heterogeneous cell types whose composition can
be altered with physiological and pathological conditions. New approaches to discern the …
be altered with physiological and pathological conditions. New approaches to discern the …
Epigenetic changes in prion and prion-like neurodegenerative diseases: Recent advances, potential as biomarkers, and future perspectives
A Hernaiz, JM Toivonen, R Bolea… - International journal of …, 2022 - mdpi.com
Prion diseases are transmissible spongiform encephalopathies (TSEs) caused by a
conformational conversion of the native cellular prion protein (PrPC) to an abnormal …
conformational conversion of the native cellular prion protein (PrPC) to an abnormal …