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Volumn 226, Issue 11, 2001, Pages 991-996

Genetics of pathways regulating body weight in the development of obesity in humans

Author keywords

Genetics of obesity; Leptin pathway

Indexed keywords

BETA 3 ADRENERGIC RECEPTOR; LEPTIN; MELANOCORTIN RECEPTOR; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; PROOPIOMELANOCORTIN; UNCOUPLING PROTEIN 1; UNCOUPLING PROTEIN 2; UNCOUPLING PROTEIN 3;

EID: 0035758099     PISSN: 00379727     EISSN: None     Source Type: Journal    
DOI: 10.1177/153537020122601105     Document Type: Conference Paper
Times cited : (43)

References (36)
  • 1
    • 0025740249 scopus 로고
    • Current understanding of aetiology of obesity genetic and non-genetic factors
    • Bouchard C. Current understanding of aetiology of obesity genetic and non-genetic factors. Am J Clin Nutr 53:1561-1565, 1991.
    • (1991) Am J Clin Nutr , vol.53 , pp. 1561-1565
    • Bouchard, C.1
  • 3
    • 0030843960 scopus 로고    scopus 로고
    • Genetic and environmental factors in relative body weight and human adiposity
    • Maes HH, Neale MC, Eaves LJ. Genetic and environmental factors in relative body weight and human adiposity. Behav Genet 27:325-351, 1997.
    • (1997) Behav Genet , vol.27 , pp. 325-351
    • Maes, H.H.1    Neale, M.C.2    Eaves, L.J.3
  • 4
    • 0030830035 scopus 로고    scopus 로고
    • Prader-Willi and other syndromes associated with obesity and mental retardation
    • Gunay-Aygun M, Cassidy SB, Nicholls RD. Prader-Willi and other syndromes associated with obesity and mental retardation. Behav Genet 27:307-324, 1997.
    • (1997) Behav Genet , vol.27 , pp. 307-324
    • Gunay-Aygun, M.1    Cassidy, S.B.2    Nicholls, R.D.3
  • 7
    • 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, Horn R, Brabant G, Gruters A. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nat Genet 19:155-157, 1998.
    • (1998) Nat Genet , vol.19 , pp. 155-157
    • Krude, H.1    Biebermann, H.2    Luck, W.3    Horn, R.4    Brabant, G.5    Gruters, A.6
  • 8
    • 0031662163 scopus 로고    scopus 로고
    • A frameshift mutation in human MC4R is associated with a dominant form of obesity
    • Vaisse C, Clement K, Guy GB, Froguel P. A frameshift mutation in human MC4R is associated with a dominant form of obesity. Nat Genet 20:113-114, 1998.
    • (1998) Nat Genet , vol.20 , pp. 113-114
    • Vaisse, C.1    Clement, K.2    Guy, G.B.3    Froguel, P.4
  • 11
    • 0033927916 scopus 로고    scopus 로고
    • Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity
    • Vaisse C, Clement K, Durand E, Hercberg S, Guy-Grand B, Froguel P. Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity. J Clin Invest 106:253-262, 2000.
    • (2000) J Clin Invest , vol.106 , pp. 253-262
    • Vaisse, C.1    Clement, K.2    Durand, E.3    Hercberg, S.4    Guy-Grand, B.5    Froguel, P.6
  • 12
    • 0033928278 scopus 로고    scopus 로고
    • Haploinsufficiency of the melanocortin-4 receptor deficiency
    • Cone RD. Haploinsufficiency of the melanocortin-4 receptor deficiency. J Clin Invest 106:185-187, 2000.
    • (2000) J Clin Invest , vol.106 , pp. 185-187
    • Cone, R.D.1
  • 14
    • 0028978913 scopus 로고
    • Association of a polymorphism in the β3-adrenergic receptor gene with features of the insulin resistance syndrome in Finns
    • Widen E, Lehto M, Kanninen T, Walston J, Shuldiner AR, Group LC. Association of a polymorphism in the β3-adrenergic receptor gene with features of the insulin resistance syndrome in Finns. N Engl J Med 3331:348-352, 1995.
    • (1995) N Engl J Med , vol.3331 , pp. 348-352
    • Widen, E.1    Lehto, M.2    Kanninen, T.3    Walston, J.4    Shuldiner, A.R.5    Group, L.C.6
  • 22
    • 0031595923 scopus 로고    scopus 로고
    • A Pro12A1a substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
    • Deeb SS, Fajas L, Nemoto M, Pihlajamaki J, Mykkanen L, Kuusisto J, Laakso M, Fujimoto W, Auwerx J. A Pro12A1a substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nat Genet 20:284-287, 1998.
    • (1998) Nat Genet , vol.20 , pp. 284-287
    • Deeb, S.S.1    Fajas, L.2    Nemoto, M.3    Pihlajamaki, J.4    Mykkanen, L.5    Kuusisto, J.6    Laakso, M.7    Fujimoto, W.8    Auwerx, J.9
  • 26
    • 16944362008 scopus 로고    scopus 로고
    • Genome-wide search for genes influencing percent body fat in Pima Indians: Suggestive linkage at chromosome 11q21-q 22
    • Norman RA, Thompson DB, Foroud T, Garvey WT, Bennett PH, Bogardus C, Ravussin E. Genome-wide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Am J Hum Genet 60:166-173, 1997.
    • (1997) Am J Hum Genet , vol.60 , pp. 166-173
    • Norman, R.A.1    Thompson, D.B.2    Foroud, T.3    Garvey, W.T.4    Bennett, P.H.5    Bogardus, C.6    Ravussin, E.7
  • 30
    • 0032972276 scopus 로고    scopus 로고
    • The quantitative trait locus on chromosome 2 for serum leptin levels is confirmed in African-Americans
    • Rotimi CN, Comuzzie AG, Lowe WL, Luke A, Blangero J, Cooper RS. The quantitative trait locus on chromosome 2 for serum leptin levels is confirmed in African-Americans. Diabetes 48:643-644, 1999.
    • (1999) Diabetes , vol.48 , pp. 643-644
    • Rotimi, C.N.1    Comuzzie, A.G.2    Lowe, W.L.3    Luke, A.4    Blangero, J.5    Cooper, R.S.6
  • 34
    • 0033652271 scopus 로고    scopus 로고
    • Genomewide search for type 2 diabetes-susceptibility genes in French whites: Evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independant replication of a type 2-diabetes locus on chromosome 1q21-q 24
    • Vionnet N, Hani El-H, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Lepretre F, Lecoeur C, Gallina P, Zekiri L. Dina C, Froguel P. Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independant replication of a type 2-diabetes locus on chromosome 1q21-q24. Am J Hum Genet 67:1470-1480, 2000.
    • (2000) Am J Hum Genet , vol.67 , pp. 1470-1480
    • Vionnet, N.1    Hani, E.L.-H.2    Dupont, S.3    Gallina, S.4    Francke, S.5    Dotte, S.6    De Matos, F.7    Durand, E.8    Lepretre, F.9    Lecoeur, C.10    Gallina, P.11    Zekiri, L.12    Dina, C.13    Froguel, P.14
  • 35
    • 0035852760 scopus 로고    scopus 로고
    • Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice
    • Fruebis J, Tsao TS, Javorschi S, Ebbets-Reed D, Erickson MR, Yen FT, Bihain BE, Lodish HF. Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice. Proc Natl Acad Sci U S A 98:2005-2010, 2001.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 2005-2010
    • Fruebis, J.1    Tsao, T.S.2    Javorschi, S.3    Ebbets-Reed, D.4    Erickson, M.R.5    Yen, F.T.6    Bihain, B.E.7    Lodish, H.F.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.