2022
DOI: 10.1016/j.neurop.2022.01.002
|View full text |Cite
|
Sign up to set email alerts
|

New insights into epigenetics as an influencer: An associative study between maternal prenatal factors in Autism Spectrum Disorder (ASD)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
3
0
2

Year Published

2022
2022
2024
2024

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 7 publications
(5 citation statements)
references
References 91 publications
0
3
0
2
Order By: Relevance
“…The significant relationship between ageing and DNA methylation can be used to explain the maternal age contribution to ASD. As the mother's age rises, she is exposed to a wider range of environmental chemicals that cause DNA damage, hypermethylation, and germline mutations, which may have contributed to the development of ASD in offspring (Vellingiri et al, 2022).…”
Section: -Results Of the Arabic Preschool Language Scale (Pls4)mentioning
confidence: 99%
“…The significant relationship between ageing and DNA methylation can be used to explain the maternal age contribution to ASD. As the mother's age rises, she is exposed to a wider range of environmental chemicals that cause DNA damage, hypermethylation, and germline mutations, which may have contributed to the development of ASD in offspring (Vellingiri et al, 2022).…”
Section: -Results Of the Arabic Preschool Language Scale (Pls4)mentioning
confidence: 99%
“…Epigenetics include DNA methylation, histone modifications, and noncoding RNA (ncRNA) molecules such as microRNA (miRNA). [ 5 ] Specifically, aberrant DNA methylation and histone acetylation are involved in gene regulation, synaptic plasticity, neuroinflammation, and oxidative stress. [ 6 ] Furthermore, studies have shown that miRNAs are involved in gene expression which is critical for the maintenance of cognitive function.…”
Section: Introductionmentioning
confidence: 99%
“…[ 48 ] Cd induced significant death of cholinergic neurons which led to tau and Aβ production. [ 49 ] Cd‐treatment led to a deficit in memory and learning with an increase in plaque depositions and Aβ [ 1–42 ] accumulation. [ 38,47 ] Similarly, Cd treatment stimulated an aggregation of the third repeat binding fragment of tau thereby resulting in partial loss of R3 conformation leading to α‐helix structure followed by tau aggregation.…”
Section: Introductionmentioning
confidence: 99%
“…Un síndrome asociado a una etiología en común es el síndrome de X frágil (SXF). Es la causa hereditaria de un solo gen más común de discapacidad intelectual y TEA [6][7][8]. Su prevalencia es de 1 por cada 4.000-6.000 varones y de 1 por cada 8.000-12.000 mujeres [8].…”
Section: Introductionunclassified
“…Es la causa hereditaria de un solo gen más común de discapacidad intelectual y TEA [6][7][8]. Su prevalencia es de 1 por cada 4.000-6.000 varones y de 1 por cada 8.000-12.000 mujeres [8]. Este síndrome se debe a una alteración en el gen FMR1, situado en el brazo largo del cromosoma X, que provoca un bloqueo en la síntesis de la proteína FMRP, que se encarga de la activación y desactivación de otros genes que sintetizan proteínas encargadas de los procesos de sinaptogenia y dendrogenia [9][10][11].…”
Section: Introductionunclassified