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International Journal of Obesity (2005)|May 18, 2021
Serum IGF1 and linear growth in children with congenital leptin deficiency before and after leptin substitutionMarianna Beghini, Stephanie Brandt, Ingrid Körber, et al.International Journal of Obesity (2005)|July 27, 2019
Targeting parental motivation for change in childhood obesity: development and validation of the PURICA-S scaleFlorian Junne, Stefan Ehehalt, Katrin Ziser, et al.Scientific Reports|July 20, 2017
Trail (TNF-related apoptosis-inducing ligand) induces an inflammatory response in human adipocytesVerena Zoller, Jan-Bernd Funcke, Julian Roos, et al.Epigenetics|November 25, 2021
An integrative epi-transcriptomic approach identifies the human cartilage chitinase 3-like protein 2 (CHI3L2) as a potential mediator of B12 deficiency in adipocytesB William Ogunkolade, Antonysunil Adaikalakoteswari, Shirleny Romualdo Cardoso, et al.BMJ Open|November 19, 2016
Development and psychometric validation of the 'Parent Perspective University of Rhode Island Change Assessment-Short' (PURICA-S) Questionnaire for the application in parents of children with overweight and obesityFlorian Junne, Katrin Ziser, Johannes Mander, et al.Obesity Facts|September 18, 2024
Youths with Extreme Obesity: A High-Risk Group for Pain and Mental Health ImpairmentsHannah Schmidt, Ingo Menrath, Susanna Wiegand, et al.Cell Death Discovery|August 5, 2025
Bridging the marrow: a co-culture-platform of leukemia cells and MS5-derived stromal cells or adipocytesJulia Zinngrebe, Elena Dorothea Brenner, Ferdinand Schlichtig, et al.Biochimica Et Biophysica Acta|June 12, 2012
TNF-α inhibits PPARβ/δ activity and SIRT1 expression through NF-κB in human adipocytesLucía Serrano-Marco, Matilde R Chacón, Elsa Maymó-Masip, et al.Genome Medicine|March 16, 2022
Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genesMichael J Gloudemans, Brunilda Balliu, Daniel Nachun, et al.Molecular and Cellular Pediatrics|July 11, 2020
Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyHelmuth-Günther Dörr, Nadja Schulze, Markus Bettendorf, et al.Pageof 41