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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=TMEM135</id>
	<title>TMEM135 - История изменений</title>
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	<updated>2026-04-23T05:57:27Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=TMEM135&amp;diff=4223&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Transmembrane protein 135 (Peroxisomal membrane protein 52) (PMP52)  ==Publications==  {{medline-entry |title=Mouse [i]Tmem135[/i] mutation reveals a mechanism in...»</title>
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		<updated>2021-04-29T19:07:07Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Transmembrane protein 135 (Peroxisomal membrane protein 52) (PMP52)  ==Publications==  {{medline-entry |title=Mouse [i]Tmem135[/i] mutation reveals a mechanism in...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Transmembrane protein 135 (Peroxisomal membrane protein 52) (PMP52)&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Mouse [i]Tmem135[/i] mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27863209&lt;br /&gt;
|abstract=While the aging process is central to the pathogenesis of age-dependent diseases, it is poorly understood at the molecular level. We identified a mouse mutant with accelerated aging in the retina as well as pathologies observed in age-dependent retinal diseases, suggesting that the responsible gene regulates retinal aging, and its impairment results in age-dependent disease. We determined that a mutation in the transmembrane 135 ([i]Tmem135[/i]) is responsible for these phenotypes. We observed localization of [[TMEM135]] on mitochondria, and imbalance of mitochondrial fission and fusion in mutant [i]Tmem135[/i] as well as [i]Tmem135[/i] overexpressing cells, indicating that [[TMEM135]] is involved in the regulation of mitochondrial dynamics. Additionally, mutant retina showed higher sensitivity to oxidative stress. These results suggest that the regulation of mitochondrial dynamics through [[TMEM135]] is critical for protection from environmental stress and controlling the progression of retinal aging. Our study identified [[TMEM135]] as a critical link between aging and age-dependent diseases.&lt;br /&gt;
|mesh-terms=* Adaptor Proteins, Signal Transducing&lt;br /&gt;
* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Mice&lt;br /&gt;
* Mitochondria&lt;br /&gt;
* Mitochondrial Dynamics&lt;br /&gt;
* Mutant Proteins&lt;br /&gt;
* Nuclear Proteins&lt;br /&gt;
* Retinal Diseases&lt;br /&gt;
|keywords=* ENU&lt;br /&gt;
* age-dependent retinal diseases&lt;br /&gt;
* aging&lt;br /&gt;
* cell biology&lt;br /&gt;
* mitochondrial dynamics&lt;br /&gt;
* mouse&lt;br /&gt;
* neuroscience&lt;br /&gt;
* retina&lt;br /&gt;
* retinal pigment epithelium&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117855&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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