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81.
Wolf, M.* et al.: Production and release of acylcarnitines by primary myotubes reflect the differences in fasting fat oxidation of the donors. J. Clin. Endocrinol. Metab. 98, E1137-E1142 (2013)
82.
Alkemade, A.* et al.: AgRP and NPY expression in the human hypothalamic infundibular nucleus correlate with body mass index, whereas changes in αMSH are related to type 2 diabetes. J. Clin. Endocrinol. Metab. 97, E925-E933 (2012)
83.
Tong, J.* et al.: Ghrelin stimulation of growth hormone isoforms: Parallel secretion of total and 20-kDag growth hormone and relation to insulin sensitivity in healthy humans. J. Clin. Endocrinol. Metab. 97, 3366-3374 (2012)
84.
Costa-Guda, J.* ; Marinoni, I. ; Molatore, S. ; Pellegata, N.S. & Arnold, A.: Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas. J. Clin. Endocrinol. Metab. 96, E701-E706 (2011)
85.
Kornfeld, J.W.* et al.: Variants in STAT5B associate with serum TC and LDL-C levels. J. Clin. Endocrinol. Metab. 96, E1496-E1501 (2011)
86.
Henopp, T.* et al.: Glucagon cell adenomatosis: A newly recognized disease of the endocrine pancreas. J. Clin. Endocrinol. Metab. 94, 213-217 (2009)
87.
Luotola, K.* et al.: Association of variation in the interleukin-1 gene family with diabetes and glucose homeostasis. J. Clin. Endocrinol. Metab. 94, 4575-4583 (2009)
88.
Reincke, M.* et al.: Risk factors associated with a low glomerular filtration rate in primary aldosteronism. J. Clin. Endocrinol. Metab. 94, 869-875 (2009)
89.
Winkler, C. ; Illig, T. ; Koczwara, K. ; Bonifacio, E.* & Ziegler, A.-G.: HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes. J. Clin. Endocrinol. Metab. 94, 4113-4115 (2009)
90.
Nitz, I.* et al.: Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations. J. Clin. Endocrinol. Metab. 92, 3183-3188 (2007)
91.
Hinney, A.* et al.: Prevalence, spectrum and functional characterization of Melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany. J. Clin. Endocrinol. Metab. 91, 1761-1769 (2006)
92.
Rhoden, K.J.* et al.: RET/papillary thyroid cancer rearrangement in nonneoplastic thyrocytes: Follicular cells of Hashimoto's thyroiditis share low-level recombination events with a subset of papillary carcinoma. J. Clin. Endocrinol. Metab. 91, 2414-2423 (2006)
93.
Illig, T. et al.: Significant association of the interleukin-6 gene polymorphisms C-174G and A-598G with type 2 diabetes. J. Clin. Endocrinol. Metab. 89, 5053-5058 (2004)
94.
Unger, K. et al.: Heterogeneity in the distribution of RET/PTC rearrangements within individual post-Chernobyl papillary thyroid carcinomas. J. Clin. Endocrinol. Metab. 89, 4272-4279 (2004)
95.
Wang, H.J.* et al.: 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. J. Clin. Endocrinol. Metab. 89, 157-162 (2004)
96.
Draper, N.* et al.: Association Studies between Microcatellite Markers within the Gene Encoding Human 11ß-Hydroxysteroid Dehydrogenase Type 1 and Body Mass Index, Waist to Hip Ratio and Glucocorticoid Metabolism. J. Clin. Endocrinol. Metab. 87, 4984-4990 (2002)
97.
Fritz, S.* et al.: Expression of Muscarinic Receptor Types in the Primate Ovary and Evidence for Nonneuronal Acetylcholine Synthesis. J. Clin. Endocrinol. Metab. 86, 349-354 (2001)
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