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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=USP8</id>
	<title>USP8 - История изменений</title>
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	<updated>2026-08-22T10:32:56Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=USP8&amp;diff=4173&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Ubiquitin carboxyl-terminal hydrolase 8 (EC 3.4.19.12) (Deubiquitinating enzyme 8) (Ubiquitin isopeptidase Y) (hUBPy) (Ubiquitin thioesterase 8) (Ubiquitin-specif...»</title>
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		<updated>2021-04-29T19:04:22Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Ubiquitin carboxyl-terminal hydrolase 8 (EC 3.4.19.12) (Deubiquitinating enzyme 8) (Ubiquitin isopeptidase Y) (hUBPy) (Ubiquitin thioesterase 8) (Ubiquitin-specif...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Ubiquitin carboxyl-terminal hydrolase 8 (EC 3.4.19.12) (Deubiquitinating enzyme 8) (Ubiquitin isopeptidase Y) (hUBPy) (Ubiquitin thioesterase 8) (Ubiquitin-specific-processing protease 8) [KIAA0055] [UBPY]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Inhibition of the deubiquitinase [[USP8]] corrects a Drosophila [[PINK1]] model of mitochondria dysfunction.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30988163&lt;br /&gt;
|abstract=Aberrant mitochondrial dynamics disrupts mitochondrial function and contributes to disease conditions. A targeted RNA interference screen for deubiquitinating enzymes (DUBs) affecting protein levels of multifunctional mitochondrial fusion protein Mitofusin (MFN) identified [[USP8]] prominently influencing MFN levels. Genetic and pharmacological inhibition of [[USP8]] normalized the elevated MFN protein levels observed in [[PINK1]] and Parkin-deficient models. This correlated with improved mitochondrial function, locomotor performance and life span, and prevented dopaminergic neurons loss in [i]Drosophila[/i] [[PINK1]] KO flies. We identified a novel target antagonizing pathologically elevated MFN levels, mitochondrial dysfunction, and dopaminergic neuron loss of a [i]Drosophila[/i] model of mitochondrial dysfunction.&lt;br /&gt;
|mesh-terms=* Animals&lt;br /&gt;
* Cell Line&lt;br /&gt;
* Dimethyl Sulfoxide&lt;br /&gt;
* Dopamine&lt;br /&gt;
* Dopaminergic Neurons&lt;br /&gt;
* Down-Regulation&lt;br /&gt;
* Drosophila&lt;br /&gt;
* Drosophila Proteins&lt;br /&gt;
* Drosophila melanogaster&lt;br /&gt;
* Gene Silencing&lt;br /&gt;
* Longevity&lt;br /&gt;
* Male&lt;br /&gt;
* Membrane Proteins&lt;br /&gt;
* Mitochondria&lt;br /&gt;
* Parkinson Disease&lt;br /&gt;
* Phenotype&lt;br /&gt;
* Protein-Serine-Threonine Kinases&lt;br /&gt;
* Signal Transduction&lt;br /&gt;
* Transfection&lt;br /&gt;
* Ubiquitin-Protein Ligases&lt;br /&gt;
* Ubiquitin-Specific Proteases&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467245&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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