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Backman, M.* et al.: Multi-omics insights into functional alterations of the liver in insulin-deficient diabetes mellitus. Mol. Metab., accepted (2019)
Hinrichs, A.* et al.: Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liver. Mol. Metab. 11, 113-128 (2018)
Renner, S.* et al.: Metabolic syndrome and extensive adipose tissue inflammation in morbidly obese Göttingen minipigs. Mol. Metab., accepted (2018)
Blutke, A.* et al.: The Munich MIDY Pig Biobank - A unique resource for studying organ crosstalk in diabetes. Mol. Metab. 6, 931-940 (2017)
Deeg, C.A.* et al.: The INSC94Y transgenic pig: A novel model for diabetic retinopathy with macular edema. Invest. Ophthalmol. Vis. Sci. 57 (2016)
Le, M.* et al.: Detailed morphological analyses of a novel mouse model of site-specific glomerular thrombotic microangiopathy. Nephrol. Dial. Transplant. 30:SP045 (2015)
Friedmann Angeli, J.P.F.* et al.: Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice. Nat. Cell Biol. 16, 1180-1191 (2014)
Kemter, E.* et al.: No amelioration of uromodulin maturation and trafficking defect by sodium-4-phenylbutyrate in vivo: Studies in mouse models of uromodulin-associated kidney disease. J. Biol. Chem. 289, 10715-10726 (2014)
Bielohuby, M.* et al.: Impaired glucose tolerance in rats fed low-carbohydrate, high-fat diets. Am. J. Physiol. Endocrinol. Metab. 305, E1059-E1070 (2013)
Kemter, E.* et al.: Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice. Hum. Mol. Genet. 22, 4148-4163 (2013)
Renner, S.* et al.: Permanent neonatal diabetes in INSC94Y transgenic pigs. Diabetes 62, 1505-1511 (2013)
van Buerck, L.* et al.: Enhanced oxidative stress and endocrine pancreas alterations are linked to a novel glucokinase missense mutation in ENU-derived Munich GckD217V mutants. Mol. Cell. Endocrinol. 362, 139-148 (2012)
Kemter, E.* et al.: Mutation of the Na⁺-K⁺-2Cl‾ cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia. Am. J. Physiol.-Renal Physiol. 298, F1405-F1415 (2010)
van Bürck, L.* et al.: Phenotypic and pathomorphological characteristics of a novel mutant mouse model for maturity-onset diabetes of the young type 2 (MODY 2). Am. J. Physiol. Endocrinol. Metab. 298, E512-E523 (2010)
Kemter, E.* et al.: Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism. Am. J. Physiol.-Renal Physiol. 297, F1391-F1398 (2009)
Aigner, B.* et al.: Diabetes models by screen for hyperglycemia in phenotype-driven ENU mouse mutagenesis projects. Am. J. Physiol. Endocrinol. Metab. 294, 232-240 (2008)
Aigner, B.* et al.: Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models. Am. J. Physiol.-Renal Physiol. 292, 1560-1567 (2007)
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)
Rathkolb, B.* et al.: Large-scale albuminuria screen for nephropathy models in chemically induced mouse mutants. Nephron Exp. Nephrol 100, 143-149 (2005)
Schneider, M.R.* et al.: Betacellulin overexpression in transgenic mice causes disproportionate growth, pulmonary hemorrhage syndrome and complex eye pathology. Endocrinology 146, 5237-5246 (2005)