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426 results

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Page 1
Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.
Hinney A, Hohmann S, Geller F, Vogel C, Hess C, Wermter AK, Brokamp B, Goldschmidt H, Siegfried W, Remschmidt H, Schäfer H, Gudermann T, Hebebrand J. Hinney A, et al. Among authors: remschmidt h. J Clin Endocrinol Metab. 2003 Sep;88(9):4258-67. doi: 10.1210/jc.2003-030233. J Clin Endocrinol Metab. 2003. PMID: 12970296 Free article. Clinical Trial.
Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature.
Wang HJ, Geller F, Dempfle A, Schäuble N, Friedel S, Lichtner P, Fontenla-Horro F, Wudy S, Hagemann S, Gortner L, Huse K, Remschmidt H, Bettecken T, Meitinger T, Schäfer H, Hebebrand J, Hinney A. Wang HJ, et al. Among authors: remschmidt h. J Clin Endocrinol Metab. 2004 Jan;89(1):157-62. doi: 10.1210/jc.2003-031395. J Clin Endocrinol Metab. 2004. PMID: 14715843
Beta 3-adrenergic-receptor allele distributions in children, adolescents and young adults with obesity, underweight or anorexia nervosa.
Hinney A, Lentes KU, Rosenkranz K, Barth N, Roth H, Ziegler A, Hennighausen K, Coners H, Wurmser H, Jacob K, Römer G, Winnikes U, Mayer H, Herzog W, Lehmkuhl G, Poustka F, Schmidt MH, Blum WF, Pirke KM, Schäfer H, Grzeschik KH, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: remschmidt h. Int J Obes Relat Metab Disord. 1997 Mar;21(3):224-30. doi: 10.1038/sj.ijo.0800391. Int J Obes Relat Metab Disord. 1997. PMID: 9080262
Serotonin transporter gene-linked polymorphic region: allele distributions in relationship to body weight and in anorexia nervosa.
Hinney A, Barth N, Ziegler A, von Prittwitz S, Hamann A, Hennighausen K, Pirke KM, Heils A, Rosenkranz K, Roth H, Coners H, Mayer H, Herzog W, Siegfried A, Lehmkuhl G, Poustka F, Schmidt MH, Schäfer H, Grzeschik KH, Lesch KP, Lentes KU, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: remschmidt h. Life Sci. 1997;61(21):PL 295-303. doi: 10.1016/s0024-3205(97)00888-6. Life Sci. 1997. PMID: 9395256
Screening for mutations in the neuropeptide Y Y5 receptor gene in cohorts belonging to different weight extremes.
Rosenkranz K, Hinney A, Ziegler A, von Prittwitz S, Barth N, Roth H, Mayer H, Siegfried W, Lehmkuhl G, Poustka F, Schmidt M, Schäfer H, Remschmidt H, Hebebrand J. Rosenkranz K, et al. Among authors: remschmidt h. Int J Obes Relat Metab Disord. 1998 Feb;22(2):157-63. doi: 10.1038/sj.ijo.0800550. Int J Obes Relat Metab Disord. 1998. PMID: 9504324
Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes.
Hinney A, Becker I, Heibült O, Nottebom K, Schmidt A, Ziegler A, Mayer H, Siegfried W, Blum WF, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: remschmidt h. J Clin Endocrinol Metab. 1998 Oct;83(10):3737-41. doi: 10.1210/jcem.83.10.5298. J Clin Endocrinol Metab. 1998. PMID: 9768693
426 results