Author

G. Hager

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell signaling & trafficking· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1

Frequent Co-Authors

J. C. Nwachukwu· 2 shared K. W. Nettles· 2 shared N. Bruno· 2 shared S. Srinivasan· 2 shared C. C. Nettles· 1 shared D. Kojetin· 1 shared D. Phinney· 1 shared D. Stavreva· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersPhysiology

J. C. Nwachukwu

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Activation of the Crtc2/Creb1 transcriptional network in skeletal muscle enhances weight loss during intermittent fasting

N. Bruno, J. C. Nwachukwu, S. Srinivasan, D. Sturgill, G. Hager, S. Hurst, S.-S. Sheu, M. Conkright, K. W. Nettles

This study shows that Crtc2/Creb1 overexpression in skeletal muscle enhances mitochondrial function and promotes weight loss during intermittent fasting by improving metabolic flux and reversing fasting-induced mitochondrial downregulation.

bioRxiv · Jun 27, 2020 · PreprintPhysiology

Chemical Systems Biology Reveals Mechanisms of Glucocorticoid Receptor Signaling

N. Bruno, J. C. Nwachukwu, S. Srinivasan, C. C. Nettles, T. Izard, z. Jin, S. Boregowda, D. Phinney, O. Elemento, X. Liu, E. A. Ortlund, R. Houtman, D. Stavreva, G. Hager, T. Kamencka, , K. W. Nettles

The paper uses Ligand Class Analysis to identify target genes and coregulator interactions of glucocorticoid receptor ligands, revealing mechanisms linking ligand structure to physiological outcomes.

bioRxiv · Jun 15, 2020Pharmacology & Toxicology