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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=FMC1</id>
	<title>FMC1 - История изменений</title>
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	<updated>2026-08-30T08:23:34Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=FMC1&amp;diff=5488&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «FMC1 homolog (ATP synthase assembly factor FMC1, mitochondrial) (Formation of mitochondrial complex V assembly factor 1 homolog) [C7orf55] [HSPC268]  ==Publicatio...»</title>
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		<updated>2021-05-12T13:46:19Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «FMC1 homolog (ATP synthase assembly factor FMC1, mitochondrial) (Formation of mitochondrial complex V assembly factor 1 homolog) [C7orf55] [HSPC268]  ==Publicatio...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;FMC1 homolog (ATP synthase assembly factor FMC1, mitochondrial) (Formation of mitochondrial complex V assembly factor 1 homolog) [C7orf55] [HSPC268]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Monoclonal antibody-defined B cell subsets in aging humans and Down&amp;#039;s syndrome.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/6240431&lt;br /&gt;
|abstract=Peripheral blood from aging and young humans and patients with Down&amp;#039;s syndrome, and from age- and sex-matched controls, was studied for the proportions of surface immunoglobulin (SIg ) bearing and monoclonal antibodies [[FMC1]], and FMC7 defined B lymphocytes and B lymphocyte subsets using fluorescent-activated cell sorter. In aging humans, the proportion of SIg  and [[FMC1]]  (that detect all B lymphocytes) were comparable to simultaneously studied healthy young controls. However, FMC7  (that detects a subset of B cells) B cells were significantly (p less than 0.05) increased when compared to young subjects. In aging subjects, the proportions of FMC7  B cells were comparable to their [[FMC1]]  B cells, whereas in young subjects FMC7  B cells were a subset of [[FMC1]]  B cells. In Down&amp;#039;s syndrome, a phenomenon similar to aging humans was observed, that is the proportions of FMC7  were increased when compared to age- and sex-matched controls and were comparable to their own [[FMC1]]  B cells. This study demonstrates the abnormality of B lymphocytes in human aging and Down&amp;#039;s syndrome. The significance of these findings is discussed.&lt;br /&gt;
|mesh-terms=* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aging&lt;br /&gt;
* Antibodies, Monoclonal&lt;br /&gt;
* B-Lymphocytes&lt;br /&gt;
* Child&lt;br /&gt;
* Child, Preschool&lt;br /&gt;
* Down Syndrome&lt;br /&gt;
* Female&lt;br /&gt;
* Humans&lt;br /&gt;
* Male&lt;br /&gt;
* Receptors, Antigen, B-Cell&lt;br /&gt;
* Reference Values&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1159/000212661&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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