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Published in 2019 at "Developmental psychobiology"
DOI: 10.1002/dev.21901
Abstract: The Val158Met rs4680 single-nucleotide polymorphism (SNP) at the catechol-O-methyltransferase (COMT) gene, primarily involved in dopamine breakdown within prefrontal cortex, has shown relations with inhibitory control (IC) in both adults and children. However, little is known…
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Keywords:
comt genotype;
childhood;
catechol methyltransferase;
performance ... See more keywords
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Published in 2021 at "Psychoneuroendocrinology"
DOI: 10.1016/j.psyneuen.2021.105361
Abstract: Women experience different degrees of subjective cognitive changes during pregnancy. The exact mechanism underlying these changes is unknown, although endocrine alterations and genetics may be contributing factors. We investigated whether multiple pregnancy-related hormones were associated…
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Keywords:
related hormones;
working memory;
comt genotype;
pregnancy related ... See more keywords
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Published in 2019 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2019.00092
Abstract: Few studies have been conducted to explore the influence of the catechol-o-methyltransferase (COMT) genotype on the severity of and treatment efficacy on auditory verbal hallucination (AVH) symptoms in healthy individuals with AVHs (Hi-AVHs). We hypothesized…
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Keywords:
comt genotype;
treatment;
genotype;
genotype subjects ... See more keywords
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Published in 2017 at "Frontiers in Human Neuroscience"
DOI: 10.3389/fnhum.2017.00578
Abstract: Evidence suggests that dopamine levels in the prefrontal cortex (PFC) modulate executive functions. A key regulator of PFC dopamine is catechol-O-methyltransferase (COMT). The activity level of the COMT enzyme are influenced by sex and the…
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Keywords:
comt genotype;
val158met polymorphism;
comt;
sex ... See more keywords