Genes de la obesidad monogénica

Autores/as

  • P.E. Miguel-Soca UNIVERSIDAD DE CIENCIAS MÉDICAS DE HOLGUÍN, CUBA
  • L. Curz-Lage
  • I. Edwards-Scringer

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Citas

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https://doi.org/10.4321/S1137-66272012000200010

2. FAWCETT KA, BARROSO I. The genetics of obesity: FTO leads the way. Trends Genet 2010; 26: 266-274.

https://doi.org/10.1016/j.tig.2010.02.006

3. BRADFIELD JP, TAAL HR, TIMPSON NJ, SCHERAG A, LECOEUR C, WARRINGTON NM et al. A genome-wide association meta-analysis identifies new childhood obesity loci. Nat Genet 2012; 44: 526-531.

https://doi.org/10.1038/ng.2247

4. AHMAD T, CHASMAN DI, MORA S, PARÉ G, COOK NG, BURING JE, et al. The Fat-Mass and Obesity-Associated (FTO) Gene, Physical Activity, and Risk of Incident Cardiovascular Events in Caucasian Women. Am Heart J 2010; 160: 1163-1169.

https://doi.org/10.1016/j.ahj.2010.08.002

5. GERKEN T, GIRARD CA, TUNG YCL,3, WEBBY CJ, SAUDEK V, HEWITSON KS, et al. The Obesity-Associated FTO Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase. Science 2007; 318: 1469-1472.

https://doi.org/10.1126/science.1151710

6. TSENG YH, CYPESS AM, KAHN CR. Cellular Bioenergetics as a Target for Obesity Therapy. Nat Rev Drug Discov 2010; 9: 465-482.

https://doi.org/10.1038/nrd3138

7. CHAO PT, YANG L, AJA S, MORAN TH, BI S. Knockdown of NPY expression in the dorsomedial hypothalamus promotes development of brown adipocytes and prevents diet-induced obesity. Cell Metab 2011; 13: 573-583.

https://doi.org/10.1016/j.cmet.2011.02.019

8. CATALETTO M, ANGULO M, HERTZ G, WHITMAN B. Prader-Willi syndrome: A primer for clinicians. Int J Pediatr Endocrinol (revista electrónica) 2011; (consultado 15-12-2012): 12. Disponible en: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3217845/.

https://doi.org/10.1186/1687-9856-2011-12

9. BUTLER MG, BITTEL DC, KIBIRYEVA N, COOLEY LD, YU S. An Interstitial 15q11-q14 Deletion: Expanded Prader-Willi Syndrome Phenotype. Am J Med Genet A 2010; 152A: 404-408.

https://doi.org/10.1002/ajmg.a.33197

10. BUDISTEANU M, BARCA D, CHIRIEAC SM, MAGUREANU S. Cohen syndrome - a rare genetic cause of hypotonia in children. Maedica (Buchar) 2010; 5: 56-61.

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Publicado

04-04-2013

Cómo citar

1.
Miguel-Soca P, Curz-Lage L, Edwards-Scringer I. Genes de la obesidad monogénica. An Sist Sanit Navar [Internet]. 4 de abril de 2013 [citado 13 de noviembre de 2025];36(1):125-7. Disponible en: https://recyt.fecyt.es/index.php/ASSN/article/view/20015

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