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Yi, C.-X. et al.: Glucocorticoid signaling in the arcuate nucleus modulates hepatic insulin sensitivity. Diabetes 61, 339-345 (2012)
Ziegler, A.-G. et al.: Long-term protective effect of lactation on the development of type 2 diabetes in women with recent gestational diabetes mellitus. Diabetes 61, 3167-3171 (2012)
Bonifacio, E. ; Warncke, K. ; Winkler, C. ; Wallner, M.* & Ziegler, A.-G.: Cesarean section and interferon-induced helicase gene polymorphisms combine to increase childhood type 1 diabetes risk. Diabetes 60, 3300-3306 (2011)
Hivert, M.F.* et al.: Updated genetic score based on 34 confirmed type 2 diabetes loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program. Diabetes 60, 1340-1348 (2011)
Kanoni, S.* et al.: Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: A 14-cohort meta-analysis. Diabetes 60, 2407-2416 (2011)
Pflueger, M. et al.: Age- and islet autoimmunity-associated differences in amino acid and lipid metabolites in children at risk for type 1 diabetes. Diabetes 60, 2740-2747 (2011)
Renström, F.* et al.: Genetic predisposition to long-term nondiabetic deteriorations in glucose homeostasis: Ten-year follow-up of the GLACIER study. Diabetes 60, 345-354 (2011)
Strawbridge, R.J.* et al.: Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes 60, 2624-2634 (2011)
Winkler, C. et al.: An interferon-induced helicase (IFIH1) gene polymorphism associates with different rates of progression from autoimmunity to type 1 diabetes. Diabetes 60, 685-690 (2011)
Soranzo, N.* et al.: Common variants at 10 genomic loci influence hemoglobin A₁C levels via glycemic and nonglycemic pathways. Diabetes 59, 3229-3239 (2010)
Winkler, C. et al.: BMI at age 8 years is influenced by the type 2 diabetes susceptibility genes HHEX-IDE and CDKAL1. Diabetes 59, 2063-2067 (2010)
Laumen, H.* et al.: Functional characterization of promoter variants of the adiponectin gene complemented by epidemiological data. Diabetes 58, 984-991 (2009)
Wiedmann, S.* et al.: Genetic variants within the LPIN1 gene, encoding lipin, are influencing phenotypes of the metabolic syndrome in humans. Diabetes 57, 209-217 (2008)
Herbach, N.* et al.: Dominant-Negative Effects of a Novel Mutated Ins2 Allele Causes Early-Onset Diabetes and Severe ß-Cell Loss in Munich Ins2C95S Mutant Mice. Diabetes 56, 1268-1276 (2007)
Endl, J.* et al.: Co-expression of CD25 and Ox40 (CD134) receptors delineates autoreactive T-cells in type 1 diabetes. Diabetes 55, 50-60 (2006)
Gray, S.L.* et al.: Leptin deficiency unmasks the deleterious effects of impaired peroxisome proliferator-activated receptor gamma function (P465L PPARgamma) in mice. Diabetes 55, 2669-2677 (2006)
Heid, I.M. et al.: Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels anmd parameters of the metabolic syndrome in 1,727 healthy Caucasians. Diabetes 55, 375-384 (2006)
Huth, C. et al.: IL6 gene promoter polymorphisms and type 2 diabetes: Joint analysis of individual participants' data from 21 studies. Diabetes 55, 2915-2921 (2006)
Schoenborn, V.* et al.: The ATGL gene is associated with free fatty acids, triglycerides and type 2 diabetes. Diabetes 55, 1270-1275 (2006)
Baessler, A.* & Döring, A.: Genetic linkage and association of the growth hormone secretagogue receptor (Ghrelin receptor) gene in human obesity. Diabetes 54, 259-267 (2005)