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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=MAP3K5</id>
	<title>MAP3K5 - История изменений</title>
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	<updated>2026-04-07T23:27:46Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=MAP3K5&amp;diff=4683&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Mitogen-activated protein kinase kinase kinase 5 (EC 2.7.11.25) (Apoptosis signal-regulating kinase 1) (ASK-1) (MAPK/ERK kinase kinase 5) (MEK kinase 5) (MEKK 5)...»</title>
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		<updated>2021-04-29T19:29:39Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Mitogen-activated protein kinase kinase kinase 5 (EC 2.7.11.25) (Apoptosis signal-regulating kinase 1) (ASK-1) (MAPK/ERK kinase kinase 5) (MEK kinase 5) (MEKK 5)...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Mitogen-activated protein kinase kinase kinase 5 (EC 2.7.11.25) (Apoptosis signal-regulating kinase 1) (ASK-1) (MAPK/ERK kinase kinase 5) (MEK kinase 5) (MEKK 5) [ASK1] [MAPKKK5] [MEKK5]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Analysis of Polymorphisms in 59 Potential Candidate Genes for Association With Human Longevity.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29300832&lt;br /&gt;
|abstract=Longevity is a polygenic trait in which genetic predisposition is particularly important. We hypothesized that among genes differentially expressed in response to caloric restriction, several may be candidate longevity genes. We tested 459 single-nucleotide polymorphisms (SNPs) in 47 genes differentially expressed in calorically restricted mice and 12 other genes for association with longevity. Subjects were American men of Japanese ancestry, 440 aged ≥95 years and 374 with an average life span. Based on a dominant model of inheritance, an association with longevity at the p &amp;lt; .05 level was seen for SNPs in 13 of the genes. Testing by all possible models increased the number of genes to 18. After correction for multiple testing, four genes retained significance, namely, [[MAP3K5]] (p = .00004), [[SIRT7]] (p = .00004), [[SIRT5]] (p = .0007), and [[PIK3R1]] (p = .01). In a dominant model, association with longevity was seen for multiple adjacent SNPs within two of these genes ([[MAP3K5]] and [[PIK3R1]]), as well as in [[FLT1]], consistent with linkage disequilibrium with a causative variant in the vicinity of each respective SNP set. [[MAP3K5]] and [[FLT1]] haplotypes were associated with longevity. In conclusion, the present study implicates variation in [[MAP3K5]], [[FLT1]], [[PIK3R1]], [[SIRT7]], and [[SIRT5]] in human longevity.&lt;br /&gt;
|mesh-terms=* Aged, 80 and over&lt;br /&gt;
* Asian Continental Ancestry Group&lt;br /&gt;
* Case-Control Studies&lt;br /&gt;
* Class Ia Phosphatidylinositol 3-Kinase&lt;br /&gt;
* Gene Frequency&lt;br /&gt;
* Haplotypes&lt;br /&gt;
* Humans&lt;br /&gt;
* Japan&lt;br /&gt;
* Linkage Disequilibrium&lt;br /&gt;
* Longevity&lt;br /&gt;
* MAP Kinase Kinase Kinase 5&lt;br /&gt;
* Male&lt;br /&gt;
* Phosphatidylinositol 3-Kinases&lt;br /&gt;
* Polymorphism, Single Nucleotide&lt;br /&gt;
* Sirtuins&lt;br /&gt;
* Vascular Endothelial Growth Factor Receptor-1&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175033&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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