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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=DSG1</id>
	<title>DSG1 - История изменений</title>
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	<updated>2026-04-13T03:41:39Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=DSG1&amp;diff=6419&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Desmoglein-1 precursor (Cadherin family member 4) (Desmosomal glycoprotein 1) (DG1) (DGI) (Pemphigus foliaceus antigen) [CDHF4]  ==Publications==  {{medline-entry...»</title>
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		<updated>2021-05-12T15:29:26Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Desmoglein-1 precursor (Cadherin family member 4) (Desmosomal glycoprotein 1) (DG1) (DGI) (Pemphigus foliaceus antigen) [CDHF4]  ==Publications==  {{medline-entry...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Desmoglein-1 precursor (Cadherin family member 4) (Desmosomal glycoprotein 1) (DG1) (DGI) (Pemphigus foliaceus antigen) [CDHF4]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Genetic effects on information processing speed are moderated by age--converging results from three samples.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24629169&lt;br /&gt;
|abstract=Information processing is a cognitive trait forming the basis of complex abilities like executive function. The Trail Making Test (TMT) is a well-established test of information processing with moderate to high heritability. Age of the individual also plays an important role. A number of genetic association studies with the TMT have been performed, which, however, did not consider age as a moderating factor. We report the results of genome-wide association studies (GWASs) on age-independent and age-dependent TMT performance in two population-representative community samples (Munich Antidepressant Response Signature, MARS: N1 = 540; Ludwig Maximilians University, LMU: N2 = 350). Age-dependent genome-wide findings were then evaluated in a third sample of healthy elderly subjects (Sydney Memory and Ageing Study, Sydney MAS: N3 = 448). While a meta-analysis on the GWAS findings did not reveal age-independent TMT associations withstanding correction for multiple testing, we found a genome-wide significant age-moderated effect between variants in the [[DSG1]] gene region and TMT-A performance predominantly reflecting visual processing speed (rs2199301, P(meta-analysis) = 1.3 × 10(-7)). The direction of the interaction suggests for the minor allele a beneficial effect in younger adults turning into a detrimental effect in older adults. The detrimental effect of the missense single nucleotide polymorphism rs1426310 within the same [[DSG1]] gene region could be replicated in Sydney MAS participants aged 70-79, but not in those aged 80 years and older, presumably a result of survivor bias. Our findings demonstrate opposing effects of [[DSG1]] variants on information processing speed depending on age, which might be related to the complex processes that [[DSG1]] is involved with, including cell adhesion and apoptosis.&lt;br /&gt;
|mesh-terms=* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Aging&lt;br /&gt;
* Desmoglein 1&lt;br /&gt;
* Executive Function&lt;br /&gt;
* Female&lt;br /&gt;
* Genome-Wide Association Study&lt;br /&gt;
* Humans&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Polymorphism, Single Nucleotide&lt;br /&gt;
|keywords=* Age&lt;br /&gt;
* DSG1&lt;br /&gt;
* GWAS&lt;br /&gt;
* Trail Making Test&lt;br /&gt;
* information processing&lt;br /&gt;
* processing speed&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1111/gbb.12132&lt;br /&gt;
}}&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Expression of pemphigus-autoantigen desmoglein 1 in human thymus.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/18331528&lt;br /&gt;
|abstract=Desmoglein (Dsg) 1 is a transmembrane glycoprotein of the desmosome allowing cell-cell adhesion between keratinocytes, whose expression is restricted to stratified squamous epithelia-like epidermis. Dsg1 is the target autoantigen of pathogenic autoantibodies produced by pemphigus foliaceus and 50% of pemphigus vulgaris patients in a Dsg1-specific T-cell-dependent pathway. Herewith, we show that mRNA of the [[DSG1]] gene is present in normal human thymus and show by quantitative real-time polymerase chain reaction analysis that the expression of [[DSG1]] transcript increases with age. Although immunoblot analysis on human thymus extracts using different anti-Dsg1 antibodies did not allow to detect the protein, we show by double-immunofluorescence assay that Dsg1 is expressed at protein level by CD19  CD63  cells located in the medulla. These data provide another illustration of the thymic expression of a tissue-specific autoantigen involved in an organ-specific autoimmune disease, which may participate in the tolerance acquisition and/or regulation of Dsg1-specific T cells.&lt;br /&gt;
|mesh-terms=* Adolescent&lt;br /&gt;
* Adult&lt;br /&gt;
* Aging&lt;br /&gt;
* Autoantigens&lt;br /&gt;
* Autoimmunity&lt;br /&gt;
* Child&lt;br /&gt;
* Child, Preschool&lt;br /&gt;
* Desmoglein 1&lt;br /&gt;
* Epidermal Cells&lt;br /&gt;
* Epidermis&lt;br /&gt;
* Female&lt;br /&gt;
* Humans&lt;br /&gt;
* Infant&lt;br /&gt;
* Infant, Newborn&lt;br /&gt;
* Keratinocytes&lt;br /&gt;
* Male&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Pemphigus&lt;br /&gt;
* Thymus Gland&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1111/j.1399-0039.2008.01020.x&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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