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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=SCN1A</id>
	<title>SCN1A - История изменений</title>
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	<updated>2026-04-11T05:59:59Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=SCN1A&amp;diff=3919&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Sodium channel protein type 1 subunit alpha (Sodium channel protein brain I subunit alpha) (Sodium channel protein type I subunit alpha) (Voltage-gated sodium cha...»</title>
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		<updated>2021-04-29T18:51:34Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Sodium channel protein type 1 subunit alpha (Sodium channel protein brain I subunit alpha) (Sodium channel protein type I subunit alpha) (Voltage-gated sodium cha...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Sodium channel protein type 1 subunit alpha (Sodium channel protein brain I subunit alpha) (Sodium channel protein type I subunit alpha) (Voltage-gated sodium channel subunit alpha Nav1.1) [NAC1] [SCN1]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Effects of normal aging and [[SCN1A]] risk-gene expression on brain metabolites: evidence for an association between [[SCN1A]] and myo-inositol.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24357141&lt;br /&gt;
|abstract=Previously reported MRS findings in the aging brain include lower N-acetylaspartate (NAA) and higher myo-inositol (mI), total creatine (Cr) and choline-containing compound (Cho) concentrations. Alterations in the sodium channel voltage gated type I, alpha subunit [[SCN1A]] variant rs10930201 have been reported to be associated with several neurological disorders with cognitive deficits. MRS studies in [[SCN1A]]-related diseases have reported striking differences in the mI concentrations between patients and controls. In a study on &amp;#039;healthy aging&amp;#039;, we investigated metabolite spectra in a sample of 83 healthy volunteers and determined their age dependence. We also investigated a potential link between [[SCN1A]] and mI. We observed a significantly negative association of NAA (p = 0.004) and significantly positive associations of mI (p ≤ 0.001), Cr (p ≤ 0.001) and Cho (p = 0.034) with age in frontal white matter. The linear association of Cho ends at the age of about 50 years and is followed by an inverted &amp;#039;U&amp;#039;-shaped curve. Further, mI was higher in C allele carriers of the [[SCN1A]] variant rs10930201. Our results corroborated the age-related changes in metabolite concentrations, and found evidence for a link between [[SCN1A]] and frontal white matter mI in healthy subjects.&lt;br /&gt;
|mesh-terms=* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Brain&lt;br /&gt;
* Evidence-Based Medicine&lt;br /&gt;
* Female&lt;br /&gt;
* Gene Expression Regulation&lt;br /&gt;
* Genetic Association Studies&lt;br /&gt;
* Genetic Markers&lt;br /&gt;
* Humans&lt;br /&gt;
* Inositol&lt;br /&gt;
* Magnetic Resonance Spectroscopy&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* NAV1.1 Voltage-Gated Sodium Channel&lt;br /&gt;
* Polymorphism, Single Nucleotide&lt;br /&gt;
* Risk Factors&lt;br /&gt;
* Tissue Distribution&lt;br /&gt;
* Young Adult&lt;br /&gt;
|keywords=* MRS&lt;br /&gt;
* SCN1A&lt;br /&gt;
* healthy aging&lt;br /&gt;
* myo-inositol&lt;br /&gt;
* white matter&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1002/nbm.3057&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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