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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=KRR1</id>
	<title>KRR1 - История изменений</title>
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	<updated>2026-08-29T07:45:27Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=KRR1&amp;diff=4778&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «KRR1 small subunit processome component homolog (HIV-1 Rev-binding protein 2) (KRR-R motif-containing protein 1) (Rev-interacting protein 1) (Rip-1) [HRB2]  ==Pub...»</title>
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		<updated>2021-04-29T19:34:32Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «KRR1 small subunit processome component homolog (HIV-1 Rev-binding protein 2) (KRR-R motif-containing protein 1) (Rev-interacting protein 1) (Rip-1) [HRB2]  ==Pub...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;KRR1 small subunit processome component homolog (HIV-1 Rev-binding protein 2) (KRR-R motif-containing protein 1) (Rev-interacting protein 1) (Rip-1) [HRB2]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26416764&lt;br /&gt;
|abstract=Polycystic ovary syndrome (PCOS) is the most common reproductive disorder in women, yet there is little consensus regarding its aetiology. Here we perform a genome-wide association study of PCOS in up to 5,184 self-reported cases of White European ancestry and 82,759 controls, with follow-up in a further ∼2,000 clinically validated cases and ∼100,000 controls. We identify six signals for PCOS at genome-wide statistical significance (P&amp;lt;5 × 10(-8)), in/near genes ERBB4/HER4, [[YAP1]], [[THADA]], [[FSHB]], [[RAD50]] and [[KRR1]]. Variants in/near three of the four epidermal growth factor receptor genes (ERBB2/HER2, ERBB3/HER3 and ERBB4/HER4) are associated with PCOS at or near genome-wide significance. Mendelian randomization analyses indicate causal roles in PCOS aetiology for higher BMI (P=2.5 × 10(-9)), higher insulin resistance (P=6 × 10(-4)) and lower serum sex hormone binding globulin concentrations (P=5 × 10(-4)). Furthermore, genetic susceptibility to later menopause is associated with higher PCOS risk (P=1.6 × 10(-8)) and PCOS-susceptibility alleles are associated with higher serum anti-Müllerian hormone concentrations in girls (P=8.9 × 10(-5)). This large-scale study implicates an aetiological role of the epidermal growth factor receptors, infers causal mechanisms relevant to clinical management and prevention, and suggests balancing selection mechanisms involved in PCOS risk. &lt;br /&gt;
|mesh-terms=* Acid Anhydride Hydrolases&lt;br /&gt;
* Adaptor Proteins, Signal Transducing&lt;br /&gt;
* Aging&lt;br /&gt;
* Case-Control Studies&lt;br /&gt;
* DNA Repair Enzymes&lt;br /&gt;
* DNA-Binding Proteins&lt;br /&gt;
* ErbB Receptors&lt;br /&gt;
* European Continental Ancestry Group&lt;br /&gt;
* Female&lt;br /&gt;
* Follicle Stimulating Hormone, beta Subunit&lt;br /&gt;
* Genome-Wide Association Study&lt;br /&gt;
* Humans&lt;br /&gt;
* Neoplasm Proteins&lt;br /&gt;
* Ovary&lt;br /&gt;
* Phosphoproteins&lt;br /&gt;
* Polycystic Ovary Syndrome&lt;br /&gt;
* Selection, Genetic&lt;br /&gt;
* Transcription Factors&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598835&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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