-
1
-
-
0028139089
-
Positional cloning of the mouse obese gene and its human homologue
-
Zhang, Y., R. Proenca, M. Maffei, M. Barone, L. Leopold, J. M. Friedman: Positional cloning of the mouse obese gene and its human homologue. Nature 372: 425-432 (1994)
-
(1994)
Nature
, vol.372
, pp. 425-432
-
-
Zhang, Y.1
Proenca, R.2
Maffei, M.3
Barone, M.4
Leopold, L.5
Friedman, J.M.6
-
2
-
-
0029020677
-
Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity
-
Considine, R. V., E. L. Considine, C. J. Williams, M. R. Nyce, S. A. Magosin, T. L. Bauer, E. L. Rosato, J. F. Caro: Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity. J Clin Invest 95: 2986-2988 (1995)
-
(1995)
J Clin Invest
, vol.95
, pp. 2986-2988
-
-
Considine, R.V.1
Considine, E.L.2
Williams, C.J.3
Nyce, M.R.4
Magosin, S.A.5
Bauer, T.L.6
Rosato, E.L.7
Caro, J.F.8
-
3
-
-
0030467446
-
The OB protein (leptin) pathway-a link between adipose tissue mass and central neural networks
-
Campfield, L. A., F. J. Smith, P. Burn: The OB protein (leptin) pathway-a link between adipose tissue mass and central neural networks. Horm Metab Res 28: 619-632 (1996)
-
(1996)
Horm Metab Res
, vol.28
, pp. 619-632
-
-
Campfield, L.A.1
Smith, F.J.2
Burn, P.3
-
4
-
-
0029048408
-
Recombinant mouse OB protein: Evidence for a peripheral signal linkage adiposity and central neural networks
-
Campfield, L. A., F. J. Smith, Y. Guisez, R. Devos, P. Burn: Recombinant mouse OB protein: evidence for a peripheral signal linkage adiposity and central neural networks. Science 269: 546-549 (1995)
-
(1995)
Science
, vol.269
, pp. 546-549
-
-
Campfield, L.A.1
Smith, F.J.2
Guisez, Y.3
Devos, R.4
Burn, P.5
-
5
-
-
0000927260
-
Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter
-
Prader, A., A. Labhart, H. Willi: Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz Med Wochenschr 86: 1260-1261 (1956)
-
(1956)
Schweiz Med Wochenschr
, vol.86
, pp. 1260-1261
-
-
Prader, A.1
Labhart, A.2
Willi, H.3
-
6
-
-
0017146353
-
Food and children with Prader-Willi syndrome
-
Holm, V. A., P. L. Pipe: Food and children with Prader-Willi syndrome. Am J Dis Child 130: 1063-1067 (1976)
-
(1976)
Am J Dis Child
, vol.130
, pp. 1063-1067
-
-
Holm, V.A.1
Pipe, P.L.2
-
7
-
-
0031031622
-
Effect of regional fat distribution and Prader-Willi syndrome on plasma leptin levels
-
Weigle, D.S., S. L. Ganter, J. L. Kuijper, D. L. Leonetti, E. J. Boyko, W. Y. Fujimoto: Effect of regional fat distribution and Prader-Willi syndrome on plasma leptin levels. J Clin Endocrinol Metab 82: 566-570 (1997)
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 566-570
-
-
Weigle, D.S.1
Ganter, S.L.2
Kuijper, J.L.3
Leonetti, D.L.4
Boyko, E.J.5
Fujimoto, W.Y.6
-
8
-
-
0029978426
-
Nocturnal rise of leptin in lean, obese, and non-insulin-dependent diabetes mellitus subjects
-
Sinha, M. K., J. P. Ohannesian, M. L. Heiman, A. Kriauciunas, T. W. Stephens, S. Magosin, C. Marco, J. F. Caro: Nocturnal rise of leptin in lean, obese, and non-insulin-dependent diabetes mellitus subjects. J Clin Invest 97: 1344-1347 (1996)
-
(1996)
J Clin Invest
, vol.97
, pp. 1344-1347
-
-
Sinha, M.K.1
Ohannesian, J.P.2
Heiman, M.L.3
Kriauciunas, A.4
Stephens, T.W.5
Magosin, S.6
Marco, C.7
Caro, J.F.8
-
9
-
-
0030478339
-
Serum immunoreactive-leptin levels are increased in patients with Cushing's syndrome
-
Leal-Cerro, A., R. V. Considine, R. Peino, E. Venegas, R. Astorga, F. F. Casanueva, C. Dieguez: Serum immunoreactive-leptin levels are increased in patients with Cushing's syndrome. Horm Metab Res 28: 711-713 (1996)
-
(1996)
Horm Metab Res
, vol.28
, pp. 711-713
-
-
Leal-Cerro, A.1
Considine, R.V.2
Peino, R.3
Venegas, E.4
Astorga, R.5
Casanueva, F.F.6
Dieguez, C.7
-
10
-
-
0019377986
-
Deletion of chromosome 15 as a cause of the Prader-Willi syndrome
-
Ledbetter, D. H., V. M. Riccardi, S. D. Airhart, R. J. Strobel, B. S. Keenan, J. D. Crawford: Deletion of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med 304: 325-329 (1981)
-
(1981)
N Engl J Med
, vol.304
, pp. 325-329
-
-
Ledbetter, D.H.1
Riccardi, V.M.2
Airhart, S.D.3
Strobel, R.J.4
Keenan, B.S.5
Crawford, J.D.6
-
11
-
-
0025181455
-
Prader-Willi syndrome: Current understanding of cause and diagnosis
-
Butler, M. G.: Prader-Willi syndrome: current understanding of cause and diagnosis. Am J Med Genet 35: 319-332 (1990)
-
(1990)
Am J Med Genet
, vol.35
, pp. 319-332
-
-
Butler, M.G.1
-
12
-
-
0029941697
-
Radioimmunoassay of leptin in human plasma
-
Zongmin, M. A., R. L. Gingerich, J. V. Santiago, S. Klein, C. H. Smith, M. Landt: Radioimmunoassay of leptin in human plasma. Clinical Chemistry 42: 942-946 (1996)
-
(1996)
Clinical Chemistry
, vol.42
, pp. 942-946
-
-
Zongmin, M.A.1
Gingerich, R.L.2
Santiago, J.V.3
Klein, S.4
Smith, C.H.5
Landt, M.6
-
13
-
-
18744426094
-
Catecholamine turnover in rats with ventromedial hypothalamic lesion
-
Yoshida, T., G. A. Bray: Catecholamine turnover in rats with ventromedial hypothalamic lesion. Am J Physiol 246: 558-565 (1984)
-
(1984)
Am J Physiol
, vol.246
, pp. 558-565
-
-
Yoshida, T.1
Bray, G.A.2
|