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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=FGF1</id>
	<title>FGF1 - История изменений</title>
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	<updated>2026-06-15T17:45:41Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=FGF1&amp;diff=5387&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Fibroblast growth factor 1 precursor (FGF-1) (Acidic fibroblast growth factor) (aFGF) (Endothelial cell growth factor) (ECGF) (Heparin-binding growth factor 1) (H...»</title>
		<link rel="alternate" type="text/html" href="https://transhumanist.ru/index.php?title=FGF1&amp;diff=5387&amp;oldid=prev"/>
		<updated>2021-05-12T13:41:47Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Fibroblast growth factor 1 precursor (FGF-1) (Acidic fibroblast growth factor) (aFGF) (Endothelial cell growth factor) (ECGF) (Heparin-binding growth factor 1) (H...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Fibroblast growth factor 1 precursor (FGF-1) (Acidic fibroblast growth factor) (aFGF) (Endothelial cell growth factor) (ECGF) (Heparin-binding growth factor 1) (HBGF-1) [FGFA]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Attenuation of FGF signalling in mouse beta-cells leads to diabetes.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/11130726&lt;br /&gt;
|abstract=Fibroblast growth factor (FGF) signalling has been implicated in patterning, proliferation and cell differentiation in many organs, including the developing pancreas. Here we show that the FGF receptors (FGFRs) 1 and 2, together with the ligands [[FGF1]], [[FGF2]], [[FGF4]], [[FGF5]], [[FGF7]] and [[[[FGF1]]0]], are expressed in adult mouse beta-cells, indicating that FGF signalling may have a role in differentiated beta-cells. When we perturbed signalling by expressing dominant-negative forms of the receptors, [[FGFR1]]c and FGFR2b, in the pancreas, we found that that mice with attenuated [[FGFR1]]c signalling, but not those with reduced FGFR2b signalling, develop diabetes with age and exhibit a decreased number of beta-cells, impaired expression of glucose transporter 2 and increased proinsulin content in beta-cells owing to impaired expression of prohormone convertases 1/3 and 2. These defects are all characteristic of patients with type-2 diabetes. Mutations in the homeobox gene Ipf1/Pdx1 are linked to diabetes in both mouse and human. We also show that Ipf1/Pdx1 is required for the expression of [[FGFR1]] signalling components in beta-cells, indicating that Ipf1/Pdx1 acts upstream of [[FGFR1]] signalling in beta-cells to maintain proper glucose sensing, insulin processing and glucose homeostasis.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Blood Glucose&lt;br /&gt;
* Diabetes Mellitus, Experimental&lt;br /&gt;
* Diabetes Mellitus, Type 2&lt;br /&gt;
* Fibroblast Growth Factors&lt;br /&gt;
* Glucose Transporter Type 1&lt;br /&gt;
* Glucose Transporter Type 2&lt;br /&gt;
* Homeodomain Proteins&lt;br /&gt;
* Humans&lt;br /&gt;
* Insulin&lt;br /&gt;
* Islets of Langerhans&lt;br /&gt;
* Mice&lt;br /&gt;
* Mice, Transgenic&lt;br /&gt;
* Monosaccharide Transport Proteins&lt;br /&gt;
* Pancreas&lt;br /&gt;
* Receptor Protein-Tyrosine Kinases&lt;br /&gt;
* Receptor, Fibroblast Growth Factor, Type 1&lt;br /&gt;
* Receptor, Fibroblast Growth Factor, Type 2&lt;br /&gt;
* Receptors, Fibroblast Growth Factor&lt;br /&gt;
* Signal Transduction&lt;br /&gt;
* Trans-Activators&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1038/35048589&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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