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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=AKAP17A</id>
	<title>AKAP17A - История изменений</title>
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	<updated>2026-06-14T00:32:01Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=AKAP17A&amp;diff=5848&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «A-kinase anchor protein 17A (AKAP-17A) (721P) (B-lymphocyte antigen) (Protein XE7) (Protein kinase A-anchoring protein 17A) (PRKA17A) (Splicing factor, arginine/s...»</title>
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		<updated>2021-05-12T14:56:11Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «A-kinase anchor protein 17A (AKAP-17A) (721P) (B-lymphocyte antigen) (Protein XE7) (Protein kinase A-anchoring protein 17A) (PRKA17A) (Splicing factor, arginine/s...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;A-kinase anchor protein 17A (AKAP-17A) (721P) (B-lymphocyte antigen) (Protein XE7) (Protein kinase A-anchoring protein 17A) (PRKA17A) (Splicing factor, arginine/serine-rich 17A) [CXYorf3] [DXYS155E] [SFRS17A] [XE7]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=The transcript expression levels of [[HNRNPM]], [[HNRNPA0]] and [[AKAP17A]] splicing factors may be predictively associated with ageing phenotypes in human peripheral blood.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31292793&lt;br /&gt;
|abstract=Dysregulation of splicing factor expression is emerging as a driver of human ageing; levels of transcripts encoding splicing regulators have previously been implicated in ageing and cellular senescence both in vitro and in vivo. We measured the expression levels of an a priori panel of 20 age- or senescence-associated splicing factors by qRT-PCR in peripheral blood samples from the InCHIANTI Study of Aging, and assessed longitudinal relationships with human ageing phenotypes (cognitive decline and physical ability) using multivariate linear regression. [[AKAP17A]], [[HNRNPA0]] and [[HNRNPM]] transcript levels were all predictively associated with severe decline in MMSE score (p = 0.007, 0.001 and 0.008 respectively). Further analyses also found expression of these genes was associated with a performance decline in two other cognitive measures; the Trail Making Test and the Purdue Pegboard Test. [[AKAP17A]] was nominally associated with a decline in mean hand-grip strength (p = 0.023), and further analyses found nominal associations with two other physical ability measures; the Epidemiologic Studies of the Elderly-Short Physical Performance Battery and calculated speed (m/s) during a timed 400 m fast walking test. These data add weight to the hypothesis that splicing dyregulation may contribute to the development of some ageing phenotypes in the human population.&lt;br /&gt;
|mesh-terms=* Aged&lt;br /&gt;
* Aging&lt;br /&gt;
* Antigens&lt;br /&gt;
* Cellular Senescence&lt;br /&gt;
* Cognitive Dysfunction&lt;br /&gt;
* Correlation of Data&lt;br /&gt;
* Female&lt;br /&gt;
* Hand Strength&lt;br /&gt;
* Heterogeneous-Nuclear Ribonucleoprotein Group M&lt;br /&gt;
* Heterogeneous-Nuclear Ribonucleoproteins&lt;br /&gt;
* Humans&lt;br /&gt;
* Male&lt;br /&gt;
* Membrane Glycoproteins&lt;br /&gt;
* Mental Status and Dementia Tests&lt;br /&gt;
* Physical Functional Performance&lt;br /&gt;
* Predictive Value of Tests&lt;br /&gt;
* RNA Splicing Factors&lt;br /&gt;
* Walking Speed&lt;br /&gt;
|keywords=* Biomarkers&lt;br /&gt;
* Cognitive decline&lt;br /&gt;
* Splicing factors&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733819&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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