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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=SPTBN1</id>
	<title>SPTBN1 - История изменений</title>
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	<updated>2026-06-24T04:32:18Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=SPTBN1&amp;diff=5711&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Spectrin beta chain, non-erythrocytic 1 (Beta-II spectrin) (Fodrin beta chain) (Spectrin, non-erythroid beta chain 1) [SPTB2]  ==Publications==  {{medline-entry |...»</title>
		<link rel="alternate" type="text/html" href="https://transhumanist.ru/index.php?title=SPTBN1&amp;diff=5711&amp;oldid=prev"/>
		<updated>2021-05-12T13:56:24Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Spectrin beta chain, non-erythrocytic 1 (Beta-II spectrin) (Fodrin beta chain) (Spectrin, non-erythroid beta chain 1) [SPTB2]  ==Publications==  {{medline-entry |...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Spectrin beta chain, non-erythrocytic 1 (Beta-II spectrin) (Fodrin beta chain) (Spectrin, non-erythroid beta chain 1) [SPTB2]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=The influence of the genetic and non-genetic factors on bone mineral density and osteoporotic fractures in Chinese women.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/22798246&lt;br /&gt;
|abstract=To investigate the effects of genetic and non-genetic factors on bone mineral densities (BMDs) and osteoporotic fractures. This was a cross-sectional study to investigate the relationships between 18 SNPs and non-genetic factors with BMDs and osteoporotic fractures in 1012 Chinese Han women. Five SNPs in genes GPR177, [[CTNNB1]], [[MEF2C]], [[SOX6]], and [[TNFRSF11B]] were associated with L1-4 or total hip BMDs. rs11898505 in [[SPTBN1]] gene was associated with osteoporotic fractures. Subjects carrying the largest number of risk alleles (highest 10 %) not only had lower BMD values as compared to those carrying the least number of risk alleles (lowest 10 %), they also had a higher risk of fracture [P = 0.002, OR = 2.252, 95 %CI (1.136, 4.463)]. Results from multivariate stepwise regression analysis revealed that age [P &amp;lt; 0.001, OR = 1.038, 95 % CI (1.018, 1.058)], number of falls in a year [P &amp;lt; 0.001, OR = 2.347, 95 % CI (1.459, 3.774)], the G risk allele in rs11898505 [P = 0.023, OR = 1.559, 95 % CI (1.062, 2.290)], and the L1-4 BMD [P = 0.017, OR = 0.286, 95 % CI (0.102, 0.798)] were associated with the occurrence of osteoporotic fractures. Genetic (rs11898505) and non-genetic factors (age, number of falls in a year and L1-4 BMD) could work in concert to contribute to the risk of osteoporotic fractures.&lt;br /&gt;
|mesh-terms=* Accidental Falls&lt;br /&gt;
* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aging&lt;br /&gt;
* Asian Continental Ancestry Group&lt;br /&gt;
* Bone Density&lt;br /&gt;
* China&lt;br /&gt;
* Cohort Studies&lt;br /&gt;
* Cross-Sectional Studies&lt;br /&gt;
* Female&lt;br /&gt;
* Genetic Association Studies&lt;br /&gt;
* Hip Joint&lt;br /&gt;
* Humans&lt;br /&gt;
* Lumbar Vertebrae&lt;br /&gt;
* MADS Domain Proteins&lt;br /&gt;
* MEF2 Transcription Factors&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Myogenic Regulatory Factors&lt;br /&gt;
* Osteoporosis, Postmenopausal&lt;br /&gt;
* Osteoporotic Fractures&lt;br /&gt;
* Osteoprotegerin&lt;br /&gt;
* Polymorphism, Single Nucleotide&lt;br /&gt;
* Radiography&lt;br /&gt;
* Spectrin&lt;br /&gt;
* Young Adult&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1007/s12020-012-9726-8&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
	</entry>
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