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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=CLCN6</id>
	<title>CLCN6 - История изменений</title>
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	<updated>2026-06-20T23:55:54Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=CLCN6&amp;diff=6222&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Chloride transport protein 6 (Chloride channel protein 6) (ClC-6) [KIAA0046]  ==Publications==  {{medline-entry |title=DNA methylation levels at individual age-as...»</title>
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		<updated>2021-05-12T15:17:47Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Chloride transport protein 6 (Chloride channel protein 6) (ClC-6) [KIAA0046]  ==Publications==  {{medline-entry |title=DNA methylation levels at individual age-as...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Chloride transport protein 6 (Chloride channel protein 6) (ClC-6) [KIAA0046]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=DNA methylation levels at individual age-associated CpG sites can be indicative for life expectancy.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26928272&lt;br /&gt;
|abstract=DNA-methylation (DNAm) levels at age-associated CpG sites can be combined into epigenetic aging signatures to estimate donor age. It has been demonstrated that the difference between such epigenetic age-predictions and chronological age is indicative for of all-cause mortality in later life. In this study, we tested alternative epigenetic signatures and followed the hypothesis that even individual age-associated CpG sites might be indicative for life-expectancy. Using a 99-CpG aging model, a five-year higher age-prediction was associated with 11% greater mortality risk in DNAm profiles of the Lothian Birth Cohort 1921 study. However, models based on three CpGs, or even individual CpGs, generally revealed very high offsets in age-predictions if applied to independent microarray datasets. On the other hand, we demonstrate that DNAm levels at several individual age-associated CpGs seem to be associated with life expectancy - e.g., at CpGs associated with the genesPDE4C and [[CLCN6]]. Our results support the notion that small aging signatures should rather be analysed by more quantitative methods, such as site-specific pyrosequencing, as the precision of age-predictions is rather low on independent microarray datasets. Nevertheless, the results hold the perspective that simple epigenetic biomarkers, based on few or individual age-associated CpGs, could assist the estimation of biological age. &lt;br /&gt;
|mesh-terms=* Aged&lt;br /&gt;
* Aging&lt;br /&gt;
* CpG Islands&lt;br /&gt;
* DNA Methylation&lt;br /&gt;
* Epigenesis, Genetic&lt;br /&gt;
* Female&lt;br /&gt;
* Humans&lt;br /&gt;
* Life Expectancy&lt;br /&gt;
* Male&lt;br /&gt;
* Proportional Hazards Models&lt;br /&gt;
|keywords=* CLCN6&lt;br /&gt;
* DNA-methylation&lt;br /&gt;
* PDE4C&lt;br /&gt;
* age&lt;br /&gt;
* aging&lt;br /&gt;
* epigenetic&lt;br /&gt;
* mortality&lt;br /&gt;
* prediction&lt;br /&gt;
* predictor&lt;br /&gt;
* survival&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789590&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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