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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=SULT1B1</id>
	<title>SULT1B1 - История изменений</title>
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	<updated>2026-06-23T11:21:39Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=SULT1B1&amp;diff=5469&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Sulfotransferase family cytosolic 1B member 1 (EC 2.8.2.-) (ST1B1) (Sulfotransferase 1B1) (Sulfotransferase 1B2) (ST1B2) (Thyroid hormone sulfotransferase) [ST1B2...»</title>
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		<updated>2021-05-12T13:45:21Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Sulfotransferase family cytosolic 1B member 1 (EC 2.8.2.-) (ST1B1) (Sulfotransferase 1B1) (Sulfotransferase 1B2) (ST1B2) (Thyroid hormone sulfotransferase) [ST1B2...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Sulfotransferase family cytosolic 1B member 1 (EC 2.8.2.-) (ST1B1) (Sulfotransferase 1B1) (Sulfotransferase 1B2) (ST1B2) (Thyroid hormone sulfotransferase) [ST1B2] [SULT1B2]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Postnatal ontogeny and hormonal regulation of sulfotransferase [[SULT1B1]] in male and female rats.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/10381794&lt;br /&gt;
|abstract=The ontogenic and hormonal regulation of a sulfotransferase, [[SULT1B1]], was examined. Hepatic RNA was isolated from rats of various ages from 1 to 90 days. The mRNA for [[SULT1B1]] is low for both sexes until a dramatic increase ( approximately 6-fold) occurs between 15 and 30 days of age in male rats. [[SULT1B1]] expression then decreases to half of the maximal level by 90 days of age. The increase in [[SULT1B1]] mRNA in female rats is less dramatic and occurs between 30 and 45 days of age. [[SULT1B1]] mRNA expression plateaus from 45 to 90 days in female rats. Expression of [[SULT1B1]] mRNA is comparable in adult male and female rats. RNA was isolated from hypophysectomized (HX) animals and HX animals treated with growth hormone [by either male (injection) or female (infusion) pattern], estradiol, progesterone, or testosterone. HX and HX plus growth hormone, or HX plus steroid replacement, did not alter [[SULT1B1]] mRNA expression. Pituitary-intact rats were treated with steroidal compounds dexamethasone (DEX) and pregnenolone-16alpha-carbonitrile (PCN). Both DEX and PCN increased expression of [[SULT1B1]] mRNA in male rats (4- and 3-fold, respectively). However, in female rats, only PCN induced [[SULT1B1]] mRNA (2-fold), whereas DEX did not induce [[SULT1B1]] in female rats. Analysis of [[SULT1B1]] protein expression indicated that only when [[SULT1B1]] mRNA was markedly increased, that is in DEX-treated male rats, was [[SULT1B1]] protein increased. Thus, although adult male and female rats have similar [[SULT1B1]] mRNA expressions, the patterns develop ontogenically differently. [[SULT1B1]] is not regulated by pituitary hormones and DEX induces [[SULT1B1]] protein in male rats.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Animals, Newborn&lt;br /&gt;
* Antibody Specificity&lt;br /&gt;
* Blotting, Northern&lt;br /&gt;
* Blotting, Western&lt;br /&gt;
* Dexamethasone&lt;br /&gt;
* Enzyme-Linked Immunosorbent Assay&lt;br /&gt;
* Female&lt;br /&gt;
* Glucocorticoids&lt;br /&gt;
* Hormones&lt;br /&gt;
* Hypophysectomy&lt;br /&gt;
* Male&lt;br /&gt;
* Organ Specificity&lt;br /&gt;
* Pregnenolone Carbonitrile&lt;br /&gt;
* RNA, Messenger&lt;br /&gt;
* Rabbits&lt;br /&gt;
* Rats&lt;br /&gt;
* Rats, Sprague-Dawley&lt;br /&gt;
* Sulfotransferases&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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