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1.
Frankó, A. et al.: Epigallocatechin gallate (EGCG) reduces the intensity of pancreatic amyloid fibrils in human islet amyloid polypeptide (hIAPP) transgenic mice. Sci. Rep. 8:1116 (2018)
2.
Frankó, A. et al.: cGMP-dependent protein kinase I (cGKI) modulates human hepatic stellate cell activation. Metab.-Clin. Exp. 88, 22-30 (2018)
3.
Frankó, A. et al.: Dissociation of fatty liver and insulin resistance in I148M PNPLA3 carriers: Differences in diacylglycerol (DAG) FA18:1 lipid species as a possible explanation. Nutrients 10:1314 (2018)
4.
Rodriguez Camargo, D.C. et al.: hIAPP forms toxic oligomers in plasma. Chem. Commun. 54, 5426-5429 (2018)
5.
Frankó, A. et al.: Bezafibrate ameliorates diabetes via reduced steatosis and improved hepatic insulin sensitivity in diabetic TallyHo mice. Mol. Metab. 6, 256-266 (2017)
6.
Rodriguez Camargo, D.C. et al.: The redox environment triggers conformational changes and aggregation of hIAPP in Type II Diabetes. Sci. Rep. 7:44041 (2017)
7.
Frankó, A. et al.: Bezafibrate improves insulin sensitivity and metabolic flexibility in STZ-treated diabetic mice. Diabetes 65, 2540-2552 (2016)
8.
Frankó, A. ; Hrabě de Angelis, M. & Wiesner, R.J.*: Mitochondrial function, dysfunction, and adaption in the liver during the development of diabetes. In: Han, D.* ; Kaplowitz, N.* [Eds.]: Mitochondria in Liver Disease. Boca Raton, FL: CRC Press, 2015. 383-412
9.
Frankó, A. et al.: Liver adapts mitochondrial function to insulin resistant and diabetic states in mice. J. Hepatol. 60, 816-823 (2014)
10.
Frankó, A. et al.: Efficient isolation of pure and functional mitochondria from mouse tissues using automated tissue disruption and enrichment with anti-TOM22 magnetic beads. PLoS ONE 8:e82392 (2013)
11.
Fuchs, H. et al.: Mouse genetics and metabolic mouse phenotyping. In: Suhre, K.* [Eds.]: Genetics Meets Metabolomics: from Experiment to Systems Biology. Springer, 2012. 85-106