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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=PROCR</id>
	<title>PROCR - История изменений</title>
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	<updated>2026-06-23T05:29:58Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=PROCR&amp;diff=5307&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Endothelial protein C receptor precursor (Activated protein C receptor) (APC receptor) (Endothelial cell protein C receptor) (CD201 antigen) [EPCR]  ==Publication...»</title>
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		<updated>2021-05-12T13:38:29Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Endothelial protein C receptor precursor (Activated protein C receptor) (APC receptor) (Endothelial cell protein C receptor) (CD201 antigen) [EPCR]  ==Publication...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Endothelial protein C receptor precursor (Activated protein C receptor) (APC receptor) (Endothelial cell protein C receptor) (CD201 antigen) [EPCR]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=[[PROC]], [[PROC]]R and [[PROS1]] polymorphisms, plasma anticoagulant phenotypes, and risk of cardiovascular disease and mortality in older adults: the Cardiovascular Health Study.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/18680534&lt;br /&gt;
|abstract=Genes encoding protein C anticoagulant pathways are candidates for atherothrombotic and other aging-related disorders. Using a tagSNP approach, and data from the Cardiovascular Health Study (CHS), we assessed associations of common polymorphisms of [[PROC]], [[PROS1]] and [[PROC]]R with: (i) plasma protein C, soluble protein C endothelial receptor (sEPCR) and protein S levels measured in a subsample of 336 participants at study entry; and (ii) risk of incident clinical outcomes [coronary heart disease (CHD), stroke, and mortality] in 4547 participants during follow-up. Secondarily, we explored associations between plasma protein C, protein S and sEPCR levels and other candidate genes involved in thrombosis, inflammation, and aging. The [[PROC]]R Ser219Gly polymorphism (rs867186) was strongly associated with higher sEPCR levels, explaining 75% of the phenotypic variation. The [[PROC]]R Ser219Gly variant was also associated with higher levels of circulating protein C antigen. An [[IL10]] polymorphism was associated with higher free protein S levels. The minor alleles of [[PROC]] rs2069901 and [[PROS1]] rs4857343 were weakly associated with lower protein C and free protein S levels, respectively. There was no association between [[PROC]]R Ser219Gly and risk of CHD, stroke, or mortality. The minor allele of another common [[PROC]]R tagSNP, rs2069948, was associated with lymphoid [[PROC]]R mRNA expression and with increased risk of incident stroke and all-cause mortality, and decreased healthy survival during follow-up. A common [[PROC]]R variant may be associated with decreased healthy survival in older adults. Additional studies are warranted to establish the role of [[PROC]]R variants in ischemic and aging-related disorders.&lt;br /&gt;
|mesh-terms=* Aged&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Aging&lt;br /&gt;
* Antigens, CD&lt;br /&gt;
* Blood Coagulation Factor Inhibitors&lt;br /&gt;
* Cardiovascular Diseases&lt;br /&gt;
* Coronary Disease&lt;br /&gt;
* Endothelial Protein C Receptor&lt;br /&gt;
* Female&lt;br /&gt;
* Humans&lt;br /&gt;
* Inflammation&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Mortality&lt;br /&gt;
* Polymorphism, Genetic&lt;br /&gt;
* Protein C&lt;br /&gt;
* Protein S&lt;br /&gt;
* Receptors, Cell Surface&lt;br /&gt;
* Risk&lt;br /&gt;
* Stroke&lt;br /&gt;
* Thrombosis&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856703&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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