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Molecular Metabolism|December 1, 2022
T3 and glucose increase expression of phosphoenolpyruvate carboxykinase (PCK1) leading to increased β-cell proliferationLiora S Katz, Carmen Argmann, Luca Lambertini, et al.Molecular Genetics and Metabolism|January 23, 2021
Glutaric aciduria type 3 is a naturally occurring biochemical trait in inbred mice of 129 substrainsJoão Leandro, Aaron Bender, Tetyana Dodatko, et al.Genome Medicine|February 10, 2016
Inter-tissue coexpression network analysis reveals DPP4 as an important gene in heart to blood communicationQuan Long, Carmen Argmann, Sander M Houten, et al.Genome Research|March 6, 2009
Integrating siRNA and protein-protein interaction data to identify an expanded insulin signaling networkZhidong Tu, Carmen Argmann, Kenny K Wong, et al.Kidney360|October 15, 2021
Peroxisomal L-bifunctional protein (EHHADH) deficiency causes male-specific kidney hypertrophy and proximal tubular injury in micePablo Ranea-Robles, Kensey Portman, Aaron Bender, et al.Cell Metabolism|January 2, 2009
The Pro12Ala PPARgamma2 variant determines metabolism at the gene-environment interfaceSami Heikkinen, Carmen Argmann, Jérôme N Feige, et al.Plos Genetics|December 10, 2009
Ppargamma2 is a key driver of longevity in the mouseCarmen Argmann, Radu Dobrin, Sami Heikkinen, et al.Cellular and Molecular Life Sciences : CMLS|June 10, 2021
Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasisPablo Ranea-Robles, Sara Violante, Carmen Argmann, et al.Scientific Reports|October 20, 2015
Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseasesJialiang Yang, Tao Huang, Francesca Petralia, et al.Pageof 7