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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=C4B</id>
	<title>C4B - История изменений</title>
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	<updated>2026-06-06T15:47:20Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=C4B&amp;diff=4059&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Complement C4-B precursor (Basic complement C4) (C3 and PZP-like alpha-2-macroglobulin domain-containing protein 3) [Contains: Complement C4 beta chain; Complemen...»</title>
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		<updated>2021-04-29T18:58:28Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Complement C4-B precursor (Basic complement C4) (C3 and PZP-like alpha-2-macroglobulin domain-containing protein 3) [Contains: Complement C4 beta chain; Complemen...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Complement C4-B precursor (Basic complement C4) (C3 and PZP-like alpha-2-macroglobulin domain-containing protein 3) [Contains: Complement C4 beta chain; Complement C4-B alpha chain; C4a anaphylatoxin; C4b-B; C4d-B; Complement C4 gamma chain] [CO4] [CPAMD3]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Investigation of complement component C4 copy number variation in human longevity.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24465950&lt;br /&gt;
|abstract=Genetic factors have been estimated to account for about 25% of the variation in an adult&amp;#039;s life span. The complement component C4 with the isotypes [[C4A]] and [[C4B]] is an effector protein of the immune system, and differences in the overall C4 copy number or gene size (long C4L; short C4S) may influence the strength of the immune response and disease susceptibilities. Previously, an association between [[C4B]] copy number and life span was reported for Hungarians and Icelanders, where the [[C4B]]*Q0 genotype, which is defined by [[C4B]] gene deficiency, showed a decrease in frequency with age. Additionally, one of the studies indicated that a low [[C4B]] copy number might be a genetic trait that is manifested only in the presence of the environmental risk factor &amp;quot;smoking&amp;quot;. These observations prompted us to investigate the role of the C4 alleles in our large German longevity sample (∼ 700 cases; 94-110 years and ∼ 900 younger controls). No significant differences in the number of [[C4A]], [[C4B]] and C4S were detected. Besides, the [[C4B]]*Q0 carrier state did not decrease with age, irrespective of smoking as an interacting variable. However, for C4L*Q0 a significantly different carrier frequency was observed in the cases compared with controls (cases: 5.08%; controls: 9.12%; p = 0.003). In a replication sample of 714 German cases (91-108 years) and 890 controls this result was not replicated (p = 0.14) although a similar trend of decreased C4L*Q0 carrier frequency in cases was visible (cases: 7.84%; controls: 10.00%).&lt;br /&gt;
|mesh-terms=* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Alleles&lt;br /&gt;
* Complement C4&lt;br /&gt;
* DNA Copy Number Variations&lt;br /&gt;
* Female&lt;br /&gt;
* Gene Frequency&lt;br /&gt;
* Genotype&lt;br /&gt;
* Germany&lt;br /&gt;
* Humans&lt;br /&gt;
* Longevity&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Risk Factors&lt;br /&gt;
* Young Adult&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899116&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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