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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. J Clin Endocrinol Metab. 1998 Oct;83(10):3737-41. doi: 10.1210/jcem.83.10.5298. J Clin Endocrinol Metab. 1998. PMID: 9768693
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. 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
Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults.
Lentes KU, Hinney A, Ziegler A, Rosenkranz K, Wurmser H, Barth N, Jacob K, Coners H, Mayer H, Grzeschik KH, Schäfer H, Remschmidt H, Pirke KM, Hebebrand J. Lentes KU, et al. Among authors: hinney a. Life Sci. 1997;61(1):PL9-16. doi: 10.1016/s0024-3205(97)00361-5. Life Sci. 1997. PMID: 9200673
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. 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: hinney a. 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
293 results