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Journal Abstract Search

448 related items for PubMed ID: 11148335

  • 1. [Monogenic forms of obesity: from mice to human].
    Clément K.
    Ann Endocrinol (Paris); 2000 Dec; 61 Suppl 6():39-49. PubMed ID: 11148335
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  • 2. [Monogenic obesity in human].
    Onigata K.
    Nihon Rinsho; 2013 Feb; 71(2):297-302. PubMed ID: 23631210
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  • 3. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.
    Krude H, Biebermann H, Luck W, Horn R, Brabant G, Grüters A.
    Nat Genet; 1998 Jun; 19(2):155-7. PubMed ID: 9620771
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  • 4. Binge eating as a major phenotype of melanocortin 4 receptor gene mutations.
    Branson R, Potoczna N, Kral JG, Lentes KU, Hoehe MR, Horber FF.
    N Engl J Med; 2003 Mar 20; 348(12):1096-103. PubMed ID: 12646666
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  • 5. Monogenic disorders of obesity and body fat distribution.
    Chen D, Garg A.
    J Lipid Res; 1999 Oct 20; 40(10):1735-46. PubMed ID: 10508193
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  • 11. Rare genetic forms of obesity: From gene to therapy.
    Clément K, Mosbah H, Poitou C.
    Physiol Behav; 2020 Dec 01; 227():113134. PubMed ID: 32805220
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  • 12. [Screening of mutations in genes of pro-opiomelanocortin in patients with constitutional exogenous obesity].
    Pankov IuA, Iatsyshina SB, Karpova SK, Chekhranova MK, Popova IuP, Grigorian ON, Rogaev EI.
    Vopr Med Khim; 2002 Dec 01; 48(1):121-30. PubMed ID: 12068494
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  • 15. Melanocortin activation of nucleus of the solitary tract avoids anorectic tachyphylaxis and induces prolonged weight loss.
    Li G, Zhang Y, Rodrigues E, Zheng D, Matheny M, Cheng KY, Scarpace PJ.
    Am J Physiol Endocrinol Metab; 2007 Jul 01; 293(1):E252-8. PubMed ID: 17389713
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  • 17. Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain.
    Dubern B, Lubrano-Berthelier C, Mencarelli M, Ersoy B, Frelut ML, Bouglé D, Costes B, Simon C, Tounian P, Vaisse C, Clement K.
    Pediatr Res; 2008 Feb 01; 63(2):211-6. PubMed ID: 18091355
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