dc.creatorTsang, Anthony H.
dc.creatorAstiz, Mariana
dc.creatorLeinweber, Brinja
dc.creatorOster, Henrik
dc.date2017-02
dc.date2020-09-15T12:30:17Z
dc.date.accessioned2023-07-14T21:57:16Z
dc.date.available2023-07-14T21:57:16Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/104612
dc.identifierhttp://hdl.handle.net/11336/48627
dc.identifierissn:1664-2392
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/7445042
dc.descriptionThe circadian timing system consists on a distributed network of cellular clocks that together coordinate 24-h rhythms of physiology and behavior. Clock function and metabolism are tightly coupled, from the cellular to the organismal level. Genetic and non-genetic approaches in rodents have been employed to study circadian clock function in the living organism. Due to the ubiquitous expression of clock genes and the intricate interaction between the circadian system and energy metabolism, genetic approaches targeting specific tissue clocks have been used to assess their contribution in systemic metabolic processes. However, special requirements regarding specificity and efficiency have to be met to allow for valid conclusions from such studies. In this review, we provide a brief summary of different approaches developed for dissecting tissue clock function in the metabolic context in rodents, compare their strengths and weaknesses, and suggest new strategies in assessing tissue clock output and the consequences of circadian clock disruption in vivo.
dc.descriptionInstituto de Investigaciones Bioquímicas de La Plata
dc.formatapplication/pdf
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by/4.0/
dc.rightsCreative Commons Attribution 4.0 International (CC BY 4.0)
dc.subjectBiología
dc.subjectCiencias Médicas
dc.subjectBmal1
dc.subjectClock genes
dc.subjectConditional knockout
dc.subjectCRE-loxP system
dc.subjectGene targeting
dc.subjectMetabolism
dc.titleRodent models for the analysis of tissue clock function in metabolic rhythms research
dc.typeArticulo
dc.typeArticulo


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