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DC Field | Value | Language |
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dc.contributor.author | Vieira, Elaine | - |
dc.contributor.author | Burris, Thomas P. | - |
dc.contributor.author | Quesada, Ivan | - |
dc.contributor.other | Departamentos de la UMH::Biología Aplicada | es |
dc.date.accessioned | 2017-11-03T15:52:01Z | - |
dc.date.available | 2017-11-03T15:52:01Z | - |
dc.date.created | 2014-11-05 | - |
dc.date.issued | 2017-11-03 | - |
dc.identifier.uri | http://hdl.handle.net/11000/4230 | - |
dc.description.abstract | Circadian physiology is responsible for the temporal regulation of metabolism to optimize energy homeostasis throughout the day. Disturbances in the light/dark cycle, sleep/wake schedule, or feeding/activity behavior can affect the circadian function of the clocks located in the brain and peripheral tissues. These alterations have been associated with impaired glucose tolerance and type 2 diabetes. Animal models with molecular manipulation of clock genes and genetic studies in humans also support these links. It has been demonstrated that the endocrine pancreas has an intrinsic self-sustained clock, and recent studies have revealed an important role of clock genes in pancreatic β cells, glucose homeostasis, and diabetes. | es |
dc.description.sponsorship | This work was supported by grants from the Ministerio de Economía (BFU2013-42789) | - |
dc.description.sponsorship | This work was supported by grants from Generalitat Valenciana (PROMETEO/2011/080) | - |
dc.format | application/pdf | es |
dc.format.extent | 31 | es |
dc.language.iso | eng | es |
dc.rights | info:eu-repo/semantics/openAccess | es |
dc.subject | clock genes | es |
dc.subject | diabetes | es |
dc.subject | pancreas | es |
dc.subject | β cell | es |
dc.subject | insulin | es |
dc.subject.other | Biología | es |
dc.title | Clock genes, pancreatic function and diabetes | es |
dc.type | info:eu-repo/semantics/article | es |
dc.identifier.doi | 10.1016/j.molmed.2014.10.007 | - |
dc.relation.publisherversion | https://doi.org/10.1016/j.molmed.2014.10.007 | - |
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