-
1
-
-
0025740249
-
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
-
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
-
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
-
5
-
-
0030878110
-
Congenital leptin deficiency is associated with severe early-onset obesity in humans
-
Montague CT, Farooqi IS, Whitehead JP, Soos MA, Rau H, Wareham NJ, Sewter CP, Digby JE, Mohammed SN, Hurst JA, Cheetham CH, Earley AR, Barnett AH, Prins JB, O'Rahilly S. Congenital leptin deficiency is associated with severe early-onset obesity in humans. Nature 387:903-908, 1997.
-
(1997)
Nature
, vol.387
, pp. 903-908
-
-
Montague, C.T.1
Farooqi, I.S.2
Whitehead, J.P.3
Soos, M.A.4
Rau, H.5
Wareham, N.J.6
Sewter, C.P.7
Digby, J.E.8
Mohammed, S.N.9
Hurst, J.A.10
Cheetham, C.H.11
Earley, A.R.12
Barnett, A.H.13
Prins, J.B.14
O'Rahilly, S.15
-
6
-
-
0344450708
-
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
-
Clement K, Vaisse C, Lahlou N, Cabrol S, Pelloux V, Cassuto D, Gourmelen M, Dina C, Chambaz J, Lacorte JM, Basdevant A, Bougneres P, Lebouc Y, Froguel P, Guy GB. A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction. Nature 392:398-401, 1998.
-
(1998)
Nature
, vol.392
, pp. 398-401
-
-
Clement, K.1
Vaisse, C.2
Lahlou, N.3
Cabrol, S.4
Pelloux, V.5
Cassuto, D.6
Gourmelen, M.7
Dina, C.8
Chambaz, J.9
Lacorte, J.M.10
Basdevant, A.11
Bougneres, P.12
Lebouc, Y.13
Froguel, P.14
Guy, G.B.15
-
7
-
-
0031838353
-
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
-
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
-
9
-
-
0030949271
-
Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene
-
Jackson RS, Creemers JW, Ohagi S, Raffin-Sanson ML, Sanders L, Montague CT, Hutton JC, O'Rahilly S. Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene. Nat Genet 16:303-306, 1997.
-
(1997)
Nat Genet
, vol.16
, pp. 303-306
-
-
Jackson, R.S.1
Creemers, J.W.2
Ohagi, S.3
Raffin-Sanson, M.L.4
Sanders, L.5
Montague, C.T.6
Hutton, J.C.7
O'Rahilly, S.8
-
10
-
-
0033575993
-
Effects of recombinant leptin therapy in a child with congenital leptin deficiency
-
Farooqi IS, Jebb SA, Langmack G, Lawrence E, Cheetham CH, Prentice AM, Hughes IA, McCamish MA, O'Rahilly S. Effects of recombinant leptin therapy in a child with congenital leptin deficiency. N Engl J Med 341:879-884, 1999.
-
(1999)
N Engl J Med
, vol.341
, pp. 879-884
-
-
Farooqi, I.S.1
Jebb, S.A.2
Langmack, G.3
Lawrence, E.4
Cheetham, C.H.5
Prentice, A.M.6
Hughes, I.A.7
McCamish, M.A.8
O'Rahilly, S.9
-
11
-
-
0033927916
-
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
-
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
-
13
-
-
0028978910
-
Genetic variation in the β3-adrenergic receptor gene and an increased capacity to gain weight in patients with morbid obesity
-
Clement K, Vaisse C, Manning BS, Basdevant A, Guy-Grand B, Ruiz J, Silver KD, Shuldiner AR, Froguel P, Strosberg AD. Genetic variation in the β3-adrenergic receptor gene and an increased capacity to gain weight in patients with morbid obesity. N Engl J Med 333:352-354, 1995.
-
(1995)
N Engl J Med
, vol.333
, pp. 352-354
-
-
Clement, K.1
Vaisse, C.2
Manning, B.S.3
Basdevant, A.4
Guy-Grand, B.5
Ruiz, J.6
Silver, K.D.7
Shuldiner, A.R.8
Froguel, P.9
Strosberg, A.D.10
-
14
-
-
0028978913
-
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
-
15
-
-
15444347628
-
The Trp64Arg polymorphism of the β3-adrenergic receptor gene is not associated with obesity or type 2 diabetes mellitus in a large population-based Caucasian cohort
-
Buettner R, Schaffler A, Arndt H, Rogler G, Nusser J, Zietz B, Enger I, Hugl S, Cuk A, Scholmerich J, Palitzsch KD. The Trp64Arg polymorphism of the β3-adrenergic receptor gene is not associated with obesity or type 2 diabetes mellitus in a large population-based Caucasian cohort. J Clin Endocrinol Metab 83:2892-2897, 1998.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 2892-2897
-
-
Buettner, R.1
Schaffler, A.2
Arndt, H.3
Rogler, G.4
Nusser, J.5
Zietz, B.6
Enger, I.7
Hugl, S.8
Cuk, A.9
Scholmerich, J.10
Palitzsch, K.D.11
-
16
-
-
0028136536
-
DNA polymorphism in the uncoupling protein (UCP) gene and human body fat
-
Oppert JM, Vohl MC, Chagnon M, Dionne FT, Cassard-Doulcier AM, Ricquier D, Perusse L, Bouchard C. DNA polymorphism in the uncoupling protein (UCP) gene and human body fat. Int J Obes Relat Metab Disord 18:526-531, 1994.
-
(1994)
Int J Obes Relat Metab Disord
, vol.18
, pp. 526-531
-
-
Oppert, J.M.1
Vohl, M.C.2
Chagnon, M.3
Dionne, F.T.4
Cassard-Doulcier, A.M.5
Ricquier, D.6
Perusse, L.7
Bouchard, C.8
-
17
-
-
0029843407
-
Additive effects of polymorphisms in the uncoupling protein gene and the β3-adrenergic receptor gene on gain weight in morbid obesity
-
Clement K, Ruiz J, Cassard-Doulcier AM, Bouillaud F, Ricquier D, Basdevant A, Guy-Grand B, Froguel P. Additive effects of polymorphisms in the uncoupling protein gene and the β3-adrenergic receptor gene on gain weight in morbid obesity. Int J Obes Relat Metab Disord 20:1062-1066, 1996.
-
(1996)
Int J Obes Relat Metab Disord
, vol.20
, pp. 1062-1066
-
-
Clement, K.1
Ruiz, J.2
Cassard-Doulcier, A.M.3
Bouillaud, F.4
Ricquier, D.5
Basdevant, A.6
Guy-Grand, B.7
Froguel, P.8
-
18
-
-
7344220905
-
Association between uncoupling protein polymorphisms (UCP2-UCP3) and energy metabolism obesity in Pima Indians
-
Walder K, Norman RA, Hanson RL, Schrauwen P, Neverova M, Jenkinson CP, Easlick J, Warden CH, Pecqueur C, Raimbault S, Ricquier D, Silver MH, Shuldiner AR, Solanes G, Lowell BB, Chung WK, Leibel RL, Pratley R, Ravussin E. Association between uncoupling protein polymorphisms (UCP2-UCP3) and energy metabolism obesity in Pima Indians. Hum Mol Genet 7:1431-1435, 1998.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1431-1435
-
-
Walder, K.1
Norman, R.A.2
Hanson, R.L.3
Schrauwen, P.4
Neverova, M.5
Jenkinson, C.P.6
Easlick, J.7
Warden, C.H.8
Pecqueur, C.9
Raimbault, S.10
Ricquier, D.11
Silver, M.H.12
Shuldiner, A.R.13
Solanes, G.14
Lowell, B.B.15
Chung, W.K.16
Leibel, R.L.17
Pratley, R.18
Ravussin, E.19
-
19
-
-
0345335191
-
Indication for linkage of the human ob gene region with extreme obesity
-
Clement K. Garner C, Hager J, Philippi A, LeDuc C, Carey A, Harris TJ, Jury C, Cardon LR, Basdevant A, Demenais F, Guy-Grand B, North M, Froguel P. Indication for linkage of the human ob gene region with extreme obesity. Diabetes 45:687-690, 1996.
-
(1996)
Diabetes
, vol.45
, pp. 687-690
-
-
Clement, K.1
Garner, C.2
Hager, J.3
Philippi, A.4
LeDuc, C.5
Carey, A.6
Harris, T.J.7
Jury, C.8
Cardon, L.R.9
Basdevant, A.10
Demenais, F.11
Guy-Grand, B.12
North, M.13
Froguel, P.14
-
20
-
-
19244362737
-
Quantitative variation in obesity-related traits and insulin precursors linked to the ob gene region on human chromosome 7
-
Duggirala R, Stem MP, Mitchell BD, Reinhart LJ, Shipman PA, Uresandi OC, Chung WK, Leibel RL, Hales CN, O'Connell P, Blangero J. Quantitative variation in obesity-related traits and insulin precursors linked to the ob gene region on human chromosome 7. Am J Hum Genet 59:694-703, 1996.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 694-703
-
-
Duggirala, R.1
Stem, M.P.2
Mitchell, B.D.3
Reinhart, L.J.4
Shipman, P.A.5
Uresandi, O.C.6
Chung, W.K.7
Leibel, R.L.8
Hales, C.N.9
O'Connell, P.10
Blangero, J.11
-
21
-
-
2342609965
-
A polymorphism in the 5 [prime]-untranslated region of the human ob gene is associated with low leptin levels
-
Hager J, Clement K, Francke S, Dina C, Raison J, Lahlou N, Rich N, Pelloux V, Basdevant A, Guy-Grand B, North M, Froguel P. A polymorphism in the 5 [prime]-untranslated region of the human ob gene is associated with low leptin levels. Int J Obes Relat Metab Disord 22:200-205, 1998.
-
(1998)
Int J Obes Relat Metab Disord
, vol.22
, pp. 200-205
-
-
Hager, J.1
Clement, K.2
Francke, S.3
Dina, C.4
Raison, J.5
Lahlou, N.6
Rich, N.7
Pelloux, V.8
Basdevant, A.9
Guy-Grand, B.10
North, M.11
Froguel, P.12
-
22
-
-
0031595923
-
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
-
23
-
-
0033624575
-
The common PPARγ Pro12A1a polymorphism is associated with decreased risk of type 2 diabetes
-
Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, Vohl MC, Nemesh J, Lane CR, Schaffner SF, Bolk S, Brewer C, Tuomi T, Gaudet D, Hudson TJ, Daly M, Groop L, Lander ES. The common PPARγ Pro12A1a polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 26:76-80, 2000.
-
(2000)
Nat Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.C.5
Nemesh, J.6
Lane, C.R.7
Schaffner, S.F.8
Bolk, S.9
Brewer, C.10
Tuomi, T.11
Gaudet, D.12
Hudson, T.J.13
Daly, M.14
Groop, L.15
Lander, E.S.16
-
24
-
-
0031017322
-
A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2
-
Comuzzie AG, Hixson JE, Almasy L, Mitchell BD, Mahaney MC, Dyer TD, Stern MP, MacCluer JW, Blangero J. A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2. Nat Genet 15:273-276, 1997.
-
(1997)
Nat Genet
, vol.15
, pp. 273-276
-
-
Comuzzie, A.G.1
Hixson, J.E.2
Almasy, L.3
Mitchell, B.D.4
Mahaney, M.C.5
Dyer, T.D.6
Stern, M.P.7
MacCluer, J.W.8
Blangero, J.9
-
25
-
-
17344371519
-
A genome-wide scan for human obesity genes shows evidence for a major susceptibility locus on chromosome 10
-
Hager J, Dina C, Francke S, Dubois S, Houari M, Vatin V, Vaillant E, Lorentz N, Basdevant A, Clement K, Guy-Grand B, Froguel P. A genome-wide scan for human obesity genes shows evidence for a major susceptibility locus on chromosome 10. Nat Genet 20:304-338, 1998.
-
(1998)
Nat Genet
, vol.20
, pp. 304-338
-
-
Hager, J.1
Dina, C.2
Francke, S.3
Dubois, S.4
Houari, M.5
Vatin, V.6
Vaillant, E.7
Lorentz, N.8
Basdevant, A.9
Clement, K.10
Guy-Grand, B.11
Froguel, P.12
-
26
-
-
16944362008
-
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
-
27
-
-
0032231322
-
An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians
-
Hanson RL, Ehm MG, Pettitt DJ, Prochazka M, Thompson DB, Timberlake D, Foroud T, Kobes S, Baier L, Burns DK, Almasy L, Blangero J, Garvey WT, Bennett PH, Knowler WC. An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. Am J Hum Genet 63:1130-1138, 1998.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1130-1138
-
-
Hanson, R.L.1
Ehm, M.G.2
Pettitt, D.J.3
Prochazka, M.4
Thompson, D.B.5
Timberlake, D.6
Foroud, T.7
Kobes, S.8
Baier, L.9
Burns, D.K.10
Almasy, L.11
Blangero, J.12
Garvey, W.T.13
Bennett, P.H.14
Knowler, W.C.15
-
28
-
-
0033364313
-
Genome scan for human obesity and linkage to markers in 20q13
-
Lee JH, Reed DR, Li WD, Xu W, Joo EJ, Kilker RL, Nanthakumar E, North M, Sakul H, Bell C, Price RA. Genome scan for human obesity and linkage to markers in 20q13. Am J Hum Genet 64:196-209, 1999.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 196-209
-
-
Lee, J.H.1
Reed, D.R.2
Li, W.D.3
Xu, W.4
Joo, E.J.5
Kilker, R.L.6
Nanthakumar, E.7
North, M.8
Sakul, H.9
Bell, C.10
Price, R.A.11
-
29
-
-
14344273991
-
Quantitative trait loci on chromosome 3 and 17 influence phenotypes of the metabolic syndrome
-
Kissebah AH, Sonnenberg GE, Myklebust J, Goldstein M, Broman K, James RG, Marks JA, Krakower GR, Jacob J, Weber J, Martin L, Blangero J, Comuzzie AG. Quantitative trait loci on chromosome 3 and 17 influence phenotypes of the metabolic syndrome. Proc Natl Acad Sci U S A 97:14478-14483, 2000.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 14478-14483
-
-
Kissebah, A.H.1
Sonnenberg, G.E.2
Myklebust, J.3
Goldstein, M.4
Broman, K.5
James, R.G.6
Marks, J.A.7
Krakower, G.R.8
Jacob, J.9
Weber, J.10
Martin, L.11
Blangero, J.12
Comuzzie, A.G.13
-
30
-
-
0032972276
-
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
-
31
-
-
0034434676
-
Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in Caucasian families
-
Delplanque J, Barat-Houari M, Dina C, Gallina P, Clement K, GuyGrand B, Vasseur F, Boutin P, Froguel P. Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in Caucasian families. Diabetologia 43:1554-1557, 2000.
-
(2000)
Diabetologia
, vol.43
, pp. 1554-1557
-
-
Delplanque, J.1
Barat-Houari, M.2
Dina, C.3
Gallina, P.4
Clement, K.5
GuyGrand, B.6
Vasseur, F.7
Boutin, P.8
Froguel, P.9
-
32
-
-
17744395716
-
Independant confirmation of a major locus for obesity on chromosome 10
-
Hinney A, Ziegler A, Oeffner F, Wedewardt C, Vogel M, Wulftange H, Geller F, Stubing K, Siegfried W, Goldschmidt HP, Remschmidt H, Hedebrand J. Independant confirmation of a major locus for obesity on chromosome 10. J Clin Endocrinol Metabol 85:2962-2965, 2000.
-
(2000)
J Clin Endocrinol Metabol
, vol.85
, pp. 2962-2965
-
-
Hinney, A.1
Ziegler, A.2
Oeffner, F.3
Wedewardt, C.4
Vogel, M.5
Wulftange, H.6
Geller, F.7
Stubing, K.8
Siegfried, W.9
Goldschmidt, H.P.10
Remschmidt, H.11
Hedebrand, J.12
-
33
-
-
0035083564
-
A locus affecting obesity in human chromosome region 10p12
-
Price RA, Li WD, Bernstein A, Crystal A, Golding EM, Weisberg SJ, Zuckerman WA. A locus affecting obesity in human chromosome region 10p12. Diabetologia 44:363-366, 2001.
-
(2001)
Diabetologia
, vol.44
, pp. 363-366
-
-
Price, R.A.1
Li, W.D.2
Bernstein, A.3
Crystal, A.4
Golding, E.M.5
Weisberg, S.J.6
Zuckerman, W.A.7
-
34
-
-
0033652271
-
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
-
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
-
36
-
-
0033515761
-
Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity
-
Arita Y, Kihara S, Ouchi N, Takahashi M, Maeda K, Miyagawa J, Hotta K, Shimomura I, Nakamura T, Miyaoka K, Kuriyama H, Nishida M, Yamashita S, Okubo K, Matsubara K, Muraguchi M, Ohmoto Y, Funahashi T, Matsuzawa Y. Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity. Biochem Biophys Res Commun 257:79-83, 1999.
-
(1999)
Biochem Biophys Res Commun
, vol.257
, pp. 79-83
-
-
Arita, Y.1
Kihara, S.2
Ouchi, N.3
Takahashi, M.4
Maeda, K.5
Miyagawa, J.6
Hotta, K.7
Shimomura, I.8
Nakamura, T.9
Miyaoka, K.10
Kuriyama, H.11
Nishida, M.12
Yamashita, S.13
Okubo, K.14
Matsubara, K.15
Muraguchi, M.16
Ohmoto, Y.17
Funahashi, T.18
Matsuzawa, Y.19
|