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dc.creatorRazquin, C. (Cristina)-
dc.creatorMarti-del-Moral, A. (Amelia)-
dc.creatorMartinez, J.A. (José Alfredo)-
dc.date.accessioned2011-02-08T11:19:38Z-
dc.date.available2011-02-08T11:19:38Z-
dc.date.issued2011-01-
dc.identifier.citationRazquin C, Marti A, Martinez JA. Evidences on three relevant obesogenes: MC4R, FTO and PPARgamma. Approaches for personalized nutrition. Mol Nutr Food Res 2011 Jan;55(1):136-149.es_ES
dc.identifier.issn1613-4125-
dc.identifier.urihttps://hdl.handle.net/10171/16312-
dc.description.abstractObesity is a complex disease that results from the interaction between lifestyle (dietary patterns and sedentary habits) and genetic factors. The recognition of a genetic basis for human obesity have driven to identify putative causal genes to understand the pathways that control body mass and fat deposition in humans as well as to provide personalized treatments and prevention strategies to fight against obesity. More than 120 candidate genes have been associated with obesity-related traits. GWAS (genome-wide association study) have so far identified over 20 novel loci convincingly associated with adiposity. This review is specifically focused on the study of the effects of MC4R, PPARγ and FTO gene variants and their interactions with dietary intake, physical activity or drug administration on body weight control. The advances in this field are expected to open new ways in genome-customized diets for obesity prevention and therapy following personalized approaches. 2es_ES
dc.language.isoenges_ES
dc.publisherWiley Blackwelles_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectObesityes_ES
dc.subjectCandidate genees_ES
dc.subjectGene variantes_ES
dc.subjectNutrigeneticses_ES
dc.subjectPhysical activityes_ES
dc.subjectPharmacogeneticses_ES
dc.subjectObesidades_ES
dc.subjectNutrigenómicaes_ES
dc.subjectGenéticaes_ES
dc.subjectNutrición y dietéticaes_ES
dc.titleEvidences on three relevant obesogenes: MC4R, FTO and PPARγ. Approaches for personalized nutrition.es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doihttp://dx.doi.org/10.1002/mnfr.201000445es_ES

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