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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=ESRG</id>
	<title>ESRG - История изменений</title>
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	<updated>2026-04-09T08:28:16Z</updated>
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		<id>https://transhumanist.ru/index.php?title=ESRG&amp;diff=6498&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Embryonic stem cell-related gene protein (hES cell-related gene protein) [HESRG]  ==Publications==  {{medline-entry |title=MYC Releases Early Reprogrammed Hum...»</title>
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		<updated>2021-05-12T15:33:48Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Embryonic stem cell-related gene protein (hES cell-related gene protein) [HESRG]  ==Publications==  {{medline-entry |title=&lt;a href=&quot;/index.php?title=MYC&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;MYC (страница не существует)&quot;&gt;MYC&lt;/a&gt; Releases Early Reprogrammed Hum...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Embryonic stem cell-related gene protein (hES cell-related gene protein) [HESRG]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=[[MYC]] Releases Early Reprogrammed Human Cells from Proliferation Pause via Retinoblastoma Protein Inhibition.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29641997&lt;br /&gt;
|abstract=Here, we report that [[MYC]] rescues early human cells undergoing reprogramming from a proliferation pause induced by OCT3/4, [[SOX2]], and [[KLF4]] (OSK). We identified [[ESRG]] as a marker of early reprogramming cells that is expressed as early as day 3 after OSK induction. On day 4, [[ESRG]] positive ( ) cells converted to a [[[[TRA]]]]-1-60 ( ) intermediate state. These early [[ESRG]] ( ) or [[[[TRA]]]]-1-60 ( ) cells showed a proliferation pause due to increased p16INK4A and p21 and decreased endogenous [[MYC]] caused by OSK. Exogenous [[MYC]] did not enhance the appearance of initial reprogramming cells but instead reactivated their proliferation and improved reprogramming efficiency. [[MYC]] increased expression of LIN41, which potently suppressed p21 post-transcriptionally. [[MYC]] suppressed p16 INK4A. These changes inactivated retinoblastoma protein (RB) and reactivated proliferation. The RB-regulated proliferation pause does not occur in immortalized fibroblasts, leading to high reprogramming efficiency even without exogenous [[MYC]].&lt;br /&gt;
|mesh-terms=* Antigens, Surface&lt;br /&gt;
* Cell Line&lt;br /&gt;
* Cell Proliferation&lt;br /&gt;
* Cellular Reprogramming&lt;br /&gt;
* Cyclin-Dependent Kinase Inhibitor p16&lt;br /&gt;
* Humans&lt;br /&gt;
* Induced Pluripotent Stem Cells&lt;br /&gt;
* Phosphorylation&lt;br /&gt;
* Proteoglycans&lt;br /&gt;
* Proto-Oncogene Proteins c-myc&lt;br /&gt;
* RNA Interference&lt;br /&gt;
* RNA, Small Interfering&lt;br /&gt;
* Retinoblastoma Protein&lt;br /&gt;
* Transcription Factors&lt;br /&gt;
* Tripartite Motif Proteins&lt;br /&gt;
* Ubiquitin-Protein Ligases&lt;br /&gt;
|keywords=* LIN41&lt;br /&gt;
* MYC&lt;br /&gt;
* immortalization&lt;br /&gt;
* induced pluripotent stem cell&lt;br /&gt;
* pluripotency&lt;br /&gt;
* post-transcriptional regulation&lt;br /&gt;
* proliferation&lt;br /&gt;
* reprogramming&lt;br /&gt;
* senescence&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1016/j.celrep.2018.03.057&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
	</entry>
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