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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=PPP2R2B</id>
	<title>PPP2R2B - История изменений</title>
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	<updated>2026-06-10T01:01:05Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=PPP2R2B&amp;diff=4368&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform (PP2A subunit B isoform B55-beta) (PP2A subunit B isoform PR55-beta) (PP2A subuni...»</title>
		<link rel="alternate" type="text/html" href="https://transhumanist.ru/index.php?title=PPP2R2B&amp;diff=4368&amp;oldid=prev"/>
		<updated>2021-04-29T19:14:34Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform (PP2A subunit B isoform B55-beta) (PP2A subunit B isoform PR55-beta) (PP2A subuni...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform (PP2A subunit B isoform B55-beta) (PP2A subunit B isoform PR55-beta) (PP2A subunit B isoform R2-beta) (PP2A subunit B isoform beta)&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Germline genetics of the p53 pathway affect longevity in a gender specific manner.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24654968&lt;br /&gt;
|abstract=Aging is thought to occur through the accumulation of molecular and cellular damage. A key regulator of the cell&amp;#039;s stress response is p53. In mice, the activity of p53 associates with lifespan. We were therefore interested whether SNPs in members of the p53-pathway are associated with longevity in humans. We genotyped the following SNPs: p53 - rs1042522 (Arg72Pro), [[MDM2]] - rs2279744 (SNP309), [[MDM4]] - rs4245739 (SNP34091), rs1563828 (SNP31826), [[PPP2R2B]] (rs319217) in 155 long-lived individuals (LLIs) who died at the age of 91 and over and in 171 ethnically-matched control subjects. Kaplan-Meier survival curves and log-Rank-test were used to determine the mean and median survival times. In female LLIs, the Pro-allele of rs1042522 (Arg72Pro) and the G-allele of rs2279744 (SNP309) were significantly associated with an increased survival time (P=0.026, P&amp;lt;0.001, respectively, log-Rank-test). In contrast, there was no difference regarding the survival time in male LLIs (rs1042522: P=0.58, rs2279744: P=0.503, log-Rank-test). There was no difference regarding the average age of death for the genotypes of the respective SNPs in the [[MDM4]] gene (rs1563828: P=0.99; rs4245739: P=0.179, respectively). Here we show for the first time that the G-allele of rs2279744 (SNP309) is associated with increased lifespan. Importantly, this effect is gender-specific. Our data support the hypothesis that genetic variants that are associated with lower activity of p53--and therefore increased tumor risk--are associated with prolonged lifespan in a gender-specific manner.&lt;br /&gt;
|mesh-terms=* Age Factors&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Case-Control Studies&lt;br /&gt;
* Cell Cycle Proteins&lt;br /&gt;
* Female&lt;br /&gt;
* Gene Frequency&lt;br /&gt;
* Genotype&lt;br /&gt;
* Humans&lt;br /&gt;
* Kaplan-Meier Estimate&lt;br /&gt;
* Longevity&lt;br /&gt;
* Male&lt;br /&gt;
* Nerve Tissue Proteins&lt;br /&gt;
* Nuclear Proteins&lt;br /&gt;
* Phenotype&lt;br /&gt;
* Polymorphism, Single Nucleotide&lt;br /&gt;
* Protein Phosphatase 2&lt;br /&gt;
* Proto-Oncogene Proteins&lt;br /&gt;
* Proto-Oncogene Proteins c-mdm2&lt;br /&gt;
* Sex Factors&lt;br /&gt;
* Signal Transduction&lt;br /&gt;
* Time Factors&lt;br /&gt;
* Tumor Suppressor Protein p53&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.2174/1874609807666140321150751&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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