-
2
-
-
0344450708
-
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
-
(1998)
Nature
, vol.392
, pp. 398-401
-
-
Clément, 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
Bougnères, P.12
Lebouc, Y.13
Froguel, P.14
Guy-Grand, B.15
-
4
-
-
0030949271
-
Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene
-
(1997)
Nature 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
-
5
-
-
0030878110
-
Congenital leptin deficiency is associated with severe early-onset obesity in humans
-
(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
-
7
-
-
0033304576
-
Human leptin deficiency caused by a missense mutation: Multiple endocrine defects, decreased sympathetic tone, and immune system dysfunction indicate new targets for leptin action, greater central than peripheral resistance to the effects of the leptin, and spontaneous correction of leptin-mediated defects
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 3686-3695
-
-
Ozata, M.1
Ozdemir, I.C.2
Licinio, J.3
-
10
-
-
0033343736
-
Several mutations in the melanocortin-4 receptor gene including a non-sense and a frameshift mutation associated with dominantly inherited obesity in humans
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 1483-1486
-
-
Hinney, A.1
Schmidt, A.2
Nottebom, K.3
Heibult, O.4
Becker, I.5
Ziegler, A.6
Gerber, G.7
Sina, M.8
Gorg, T.9
Mayer, H.10
Siegfried, W.11
Fichter, M.12
Remschmidt, H.13
Hebebrand, J.14
-
11
-
-
0026674886
-
Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction
-
(1992)
Science
, vol.257
, pp. 967-971
-
-
Liang, P.1
Pardee, A.B.2
-
13
-
-
15844428981
-
Suppression subtractive hybridization: A method for generating differentially regulated or tissue-specific cDNA probes and libraries
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 6025-6030
-
-
Diatchenko, L.1
Lau, Y.F.2
Campbell, A.P.3
Chenchik, A.4
Moqadam, F.5
Huang, B.6
Lukyanov, S.7
Lukyanov, K.8
Gurskaya, N.9
Sverdlov, E.D.10
Siebert, P.D.11
-
16
-
-
0032833350
-
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
-
(1999)
Nature Genet
, vol.23
, pp. 217-221
-
-
Den Hollander, A.I.1
Ten Brink, J.B.2
De Kok, Y.J.3
Van Soest, S.4
Van den Born, L.I.5
Van Driel, M.A.6
Van de Pol, D.J.7
Payne, A.M.8
Bhattacharya, S.S.9
Kellner, U.10
Hoyng, C.B.11
Westerveld, A.12
Brunner, H.G.13
Bleeker-Wagemakers, E.M.14
Deutman, A.F.15
Heckenlively, J.R.16
Cremers, F.P.17
Bergen, A.A.18
-
17
-
-
0033954043
-
Identification of syntenin and other TNF-inducible genes in human umbilical arterial endothelial cells by suppression subtractive hybridization
-
(2000)
FEBS Lett
, vol.467
, pp. 299-304
-
-
Stier, S.1
Totzke, G.2
Grunewald, E.3
Neuhaus, T.4
Fronhoffs, S.5
Sachinidis, A.6
Vetter, H.7
Schulze-Osthoff, K.8
Ko, Y.9
-
23
-
-
0029658675
-
The Trp64Arg mutation of the beta3 adrenergic receptor gene has no effect on obesity phenotypes in the Quebec Family Study and Swedish Obese Subjects cohorts
-
(1996)
J Clin Invest
, vol.98
, pp. 2086-2093
-
-
Gagnon, J.1
Mauriège, P.2
Roy, S.3
Sjöström, D.4
Chagnon, Y.C.5
Dionne, F.T.6
Oppert, J.M.7
Pérusse, L.8
Sjöström, L.9
Bouchard, C.10
-
26
-
-
0033364313
-
Genome scan for human obesity and linkage to markers in 20q13
-
(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
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