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Journal of Clinical Medicine|December 18, 2020
The Vicious Circle of Hepatic Glucagon Resistance in Non-Alcoholic Fatty Liver DiseaseKatrine D Galsgaard
Biochemical Society Transactions|January 31, 2025
Understanding the release mechanisms and secretion patterns for glucagon-like peptide-1 using the isolated perfused intestine as a modelKatrine D Galsgaard, Ida M Modvig, Jens J Holst
Journal of the Endocrine Society|November 24, 2025
In Vivo Inhibition of Dipeptidyl Peptidase 4 and Neprilysin Activity Enables Measurement of GLP-1 Secretion in Male RatsKatrine D Galsgaard, Valentina Abba, Rune E Kuhre, et al.
Frontiers in Physiology|May 10, 2019
Glucagon Receptor Signaling and Lipid MetabolismKatrine D Galsgaard, Jens Pedersen, Filip K Knop, et al.
Physiological Reports|December 13, 2025
GLP-2 and GIP acutely increase superior mesenteric artery blood flow in male rats, and the effect is independent of nitric oxide and vasoactive intestinal peptideKatrine D Galsgaard, Bolette Hartmann, Mette M Rosenkilde, et al.
Diabetes|January 31, 2024
In Vivo Inhibition of Dipeptidyl Peptidase 4 Allows Measurement of GLP-1 Secretion in MiceMark M Smits, Katrine D Galsgaard, Sara Lind Jepsen, et al.
American Journal of Physiology. Endocrinology and Metabolism|February 11, 2025
Single incretin receptor knockout mice do not compensate by increasing glucose-stimulated secretion of the remaining incretin hormoneKatrine D Galsgaard, Jon Vergara, Sara L Jepsen, et al.
American Journal of Physiology. Endocrinology and Metabolism|April 8, 2020
Alanine, arginine, cysteine, and proline, but not glutamine, are substrates for, and acute mediators of, the liver-α-cell axis in female miceKatrine D Galsgaard, Sara L Jepsen, Sasha A S Kjeldsen, et al.
Cell Metabolism|December 14, 2022
Q-Flux: A method to assess hepatic mitochondrial succinate dehydrogenase, methylmalonyl-CoA mutase, and glutaminase fluxes in vivoBrandon T Hubbard, Traci E LaMoia, Leigh Goedeke, et al.
American Journal of Physiology. Endocrinology and Metabolism|February 27, 2019
Glucose and amino acid metabolism in mice depend mutually on glucagon and insulin receptor signalingKatrine D Galsgaard, Marie Winther-Sørensen, Jens Pedersen, et al.
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