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Volumn 51, Issue SUPPL. 3, 2010, Pages

Mechanisms of appetite regulation

Author keywords

[No Author keywords available]

Indexed keywords

AGOUTI RELATED PROTEIN; CHOLECYSTOKININ; CORTICOTROPIN RELEASING FACTOR; GHRELIN; GLUCAGON LIKE PEPTIDE 1; LEPTIN; MELANOCORTIN; NEUROMEDIN U; NEUROPEPTIDE Y; OXYTOCIN; PEPTIDE YY [3-36]; PROOPIOMELANOCORTIN; PROTIRELIN;

EID: 78650431885     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPG.0b013e3181f84208     Document Type: Article
Times cited : (14)

References (10)
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  • 2
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    • Monogenic human obesity
    • Farooqi IS. Monogenic human obesity. Front Horm Res 2008;36:1-11.
    • (2008) Front Horm Res , vol.36 , pp. 1-11
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  • 3
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    • Effects of recombinant leptin therapy in a child with congenital leptin deficiency
    • Farooqi IS, Jebb SA, Langmack G, et al. Effects of recombinant leptin therapy in a child with congenital leptin deficiency. N Engl J Med 1999;341:879-84.
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    • Farooqi, I.S.1    Jebb, S.A.2    Langmack, G.3
  • 4
    • 0031838353 scopus 로고    scopus 로고
    • Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
    • Krude H, Biebermann H, Luck W, et al. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nat Genet 1998;19:155-7.
    • (1998) Nat Genet , vol.19 , pp. 155-157
    • Krude, H.1    Biebermann, H.2    Luck, W.3
  • 5
    • 0344450708 scopus 로고    scopus 로고
    • A mutation in the human leptin receptor gene causes obesity and pituitary dysfuntion
    • Clément K, Vaisse C, Lahlou N, et al. A mutation in the human leptin receptor gene causes obesity and pituitary dysfuntion. Nature 1998;392:398-401.
    • (1998) Nature , vol.392 , pp. 398-401
    • Clément, K.1    Vaisse, C.2    Lahlou, N.3
  • 6
    • 0030949271 scopus 로고    scopus 로고
    • Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene
    • Jackson RS, Creemers JWM, Ohagi S, et al. Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene. Nat Genet 1997;16:303-6.
    • (1997) Nat Genet , vol.16 , pp. 303-306
    • Jackson, R.S.1    Creemers, J.W.M.2    Ohagi, S.3
  • 7
    • 0343953074 scopus 로고    scopus 로고
    • Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor defficiency
    • Farooqi IS, Yeo GS, Keogh JM, et al. Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor defficiency. J Clin Invest 2000;106:271-9.
    • (2000) J Clin Invest , vol.106 , pp. 271-279
    • Farooqi, I.S.1    Yeo, G.S.2    Keogh, J.M.3
  • 8
    • 34548797260 scopus 로고    scopus 로고
    • Melanocortin 4 receptor mutations in obese Czech children: Studies of prevalence, phenotype development, weight reduction response and functional analysis
    • Hainerová I, Larsen LH, Holst B, et al. Melanocortin 4 receptor mutations in obese Czech children: Studies of prevalence, phenotype development, weight reduction response and functional analysis. J Clin Endocrinol Metab 2007;92:3689-96.
    • (2007) J Clin Endocrinol Metab , vol.92 , pp. 3689-3696
    • Hainerová, I.1    Larsen, L.H.2    Holst, B.3
  • 9
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    • Neuromedin U has a novel anorexigenic effect independent of the leptin signaling pathway
    • Hanada R, Teranishi H, Pearson JT, et al. Neuromedin U has a novel anorexigenic effect independent of the leptin signaling pathway. Nat Med 2004;10:1067-73.
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  • 10
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    • Association between Neuromedin U gene variants and overweight and obesity
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    • Hainerová, I.1    Torekov, S.S.2    Ek, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.