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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=DNMBP</id>
	<title>DNMBP - История изменений</title>
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		<id>https://transhumanist.ru/index.php?title=DNMBP&amp;diff=5679&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Dynamin-binding protein (Scaffold protein Tuba) [ARHGEF36] [KIAA1010] [TUBA]  ==Publications==  {{medline-entry |title=Dynamin binding protein gene expression and...»</title>
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		<updated>2021-05-12T13:55:05Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Dynamin-binding protein (Scaffold protein Tuba) [ARHGEF36] [KIAA1010] [TUBA]  ==Publications==  {{medline-entry |title=Dynamin binding protein gene expression and...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Dynamin-binding protein (Scaffold protein Tuba) [ARHGEF36] [KIAA1010] [TUBA]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Dynamin binding protein gene expression and memory performance in aged rats.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/21232816&lt;br /&gt;
|abstract=Previous studies have shown that messenger RNA (mRNA) of the dynamin-binding protein ([[DNMBP]]), a scaffold protein regulating actin cytoskeleton and synaptic vesicle pools, is lower in neuropathologically-confirmed Alzheimer&amp;#039;s brains. Here we investigated whether a deficit in long term memory formation during physiological aging is also associated with lower [[DNMBP]] expression. Hippocampal [[DNMBP]] mRNA was quantified by quantitative real time reverse transcriptase polymerase chain reaction (qRT-PCR) following inhibitory avoidance task in aged (26- to 27-month-old) rats that, according to memory performance, were ranked as good responders (GR) and bad responders (BR), in adult (3-month-old), late-adult (19-month-old), and aged (26-27-month-old) naive animals. We found that [[DNMBP]] mRNA levels were significantly higher in naive adults versus late adult and aged naive rats, in GR versus BR, and in pooled GR and BR versus aged-matched controls. Our data provide the first evidence that hippocampal [[DNMBP]] mRNA expression is reduced during physiological aging, and suggest that the capability to increase the expression of this mRNA may be a requirement for preserving long term memory formation during aging.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Avoidance Learning&lt;br /&gt;
* Carrier Proteins&lt;br /&gt;
* Cytoskeletal Proteins&lt;br /&gt;
* Down-Regulation&lt;br /&gt;
* Female&lt;br /&gt;
* Gene Expression Regulation&lt;br /&gt;
* Hippocampus&lt;br /&gt;
* Memory, Long-Term&lt;br /&gt;
* Protein Binding&lt;br /&gt;
* Rats&lt;br /&gt;
* Rats, Wistar&lt;br /&gt;
* Real-Time Polymerase Chain Reaction&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1016/j.neurobiolaging.2010.11.012&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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