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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=PXN</id>
	<title>PXN - История изменений</title>
	<link rel="self" type="application/atom+xml" href="https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=PXN"/>
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	<updated>2026-04-16T19:29:20Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=PXN&amp;diff=4136&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Paxillin  ==Publications==  {{medline-entry |title=pxn-1 and pxn-2 May Interact Negatively during Neuronal Development and Aging in C. elegans. |pubmed-url=https:...»</title>
		<link rel="alternate" type="text/html" href="https://transhumanist.ru/index.php?title=PXN&amp;diff=4136&amp;oldid=prev"/>
		<updated>2021-04-29T19:02:34Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Paxillin  ==Publications==  {{medline-entry |title=pxn-1 and pxn-2 May Interact Negatively during Neuronal Development and Aging in C. elegans. |pubmed-url=https:...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Paxillin&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=pxn-1 and pxn-2 May Interact Negatively during Neuronal Development and Aging in C. elegans.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26194821&lt;br /&gt;
|abstract=C. elegans has two functional peroxidasins ([[PXN]]), [[PXN]]-1 and [[PXN]]-2. [[PXN]]-2 is essential to consolidate the extracellular matrix during development and is suggested to interact with [[PXN]]-1 antagonistically. pxn-1 is involved in neuronal development and possibly maintenance; therefore, we investigated the relationship between pxn-1 and pxn-2 in neuronal development and in aging. During neuronal development, defects caused by pxn-1 overexpression were suppressed by overexpression of both pxn-1 and pxn-2. In neuronal aging process, pxn-1 mutants showed less age-related neuronal defects, such as neuronal outgrowth, neuronal wavy processes, and enhanced short-term memory performance. In addition, pxn-2 overexpressing animals retained an intact neuronal morphology when compared with age-matched controls. Consistent with these results, overexpression of both pxn-1 and pxn-2 restored the severe neuronal defects present with pxn-1 overexpression. These results implied that there is a negative relationship between pxn-1 and pxn-2 via pxn-1 regulating pxn-2. Therefore, pxn-1 may function in neuronal development and age-related neuronal maintenance through pxn-2. &lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Caenorhabditis elegans&lt;br /&gt;
* Caenorhabditis elegans Proteins&lt;br /&gt;
* Models, Animal&lt;br /&gt;
* Neurogenesis&lt;br /&gt;
* Peroxiredoxins&lt;br /&gt;
|keywords=* C. elegans&lt;br /&gt;
* antagonistic relationship&lt;br /&gt;
* neuronal aging&lt;br /&gt;
* neuronal development&lt;br /&gt;
* pxn-1&lt;br /&gt;
* pxn-2&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546945&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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