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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=COL4A2</id>
	<title>COL4A2 - История изменений</title>
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	<updated>2026-06-14T05:09:46Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=COL4A2&amp;diff=5726&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Collagen alpha-2(IV) chain precursor [Contains: Canstatin]  ==Publications==  {{medline-entry |title=Tissue- and developmental stage-specific activation of alpha...»</title>
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		<updated>2021-05-12T13:57:02Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Collagen alpha-2(IV) chain precursor [Contains: Canstatin]  ==Publications==  {{medline-entry |title=Tissue- and developmental stage-specific activation of alpha...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Collagen alpha-2(IV) chain precursor [Contains: Canstatin]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Tissue- and developmental stage-specific activation of alpha 5 and alpha 6(IV) collagen expression in the upper gastrointestinal tract of transgenic mice.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/14592452&lt;br /&gt;
|abstract=Little is known about mechanisms regulating gene expression for the alpha chains of basement membrane type IV collagen, arranged head-to-head in transcription units [[COL4A1]]-[[COL4A2]], [[COL4A3]]-[[COL4A4]], and [[COL4A5]]-[[COL4A6]], and implicated broadly in genetic diseases. To investigate these mechanisms, we generated transgenic mouse lines bearing 5&amp;#039;-flanking sequences of [[COL4A5]] and [[COL4A6]], cloned upstream of a lacZ reporter gene. A 3.8-kb fragment upstream of [[COL4A6]] directs reporter gene expression in the esophagus, stomach, and duodenum, whereas a 13.8-kb fragment directs expression in the esophagus only. A 10.6-kb fragment upstream of [[COL4A5]] directs expression in the esophagus. Coupled with evidence of long-range conservation between human and mouse non-coding sequences, described herein, our findings provide the first indication that highly specialized patterns characteristic of [[COL4A5]]-[[COL4A6]] expression in vivo arise from effects of distributed cis-acting regulatory elements on a bidirectional proximal promoter, itself transcriptionally competent.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Amino Acid Sequence&lt;br /&gt;
* Animals&lt;br /&gt;
* Collagen Type IV&lt;br /&gt;
* Gene Expression Regulation&lt;br /&gt;
* Genes, Regulator&lt;br /&gt;
* Humans&lt;br /&gt;
* Mice&lt;br /&gt;
* Mice, Transgenic&lt;br /&gt;
* Molecular Sequence Data&lt;br /&gt;
* Organ Specificity&lt;br /&gt;
* Protein Subunits&lt;br /&gt;
* Sequence Homology&lt;br /&gt;
* Species Specificity&lt;br /&gt;
* Tissue Distribution&lt;br /&gt;
* Transcriptional Activation&lt;br /&gt;
* Upper Gastrointestinal Tract&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1016/j.bbrc.2003.09.233&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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