Author

J. P. Singh

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

Biology Disciplines

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Biochemistry· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

C. Jiang· 1 shared D. Bartee· 1 shared D. Brady· 1 shared E. L. Varner· 1 shared E. Rame· 1 shared G. Bagchi· 1 shared G. Dagar· 1 shared H. Jiang· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperBiochemistry

C. Jiang

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Author profile →

2 papers

Recent·Most cited

Direct anabolic three carbon metabolism via propionate to a six carbon metabolite occurs in human heart and in vivo across mouse tissues

M. T. Doan, M. D. Neinast, E. L. Varner, K. Bedi, D. Bartee, H. Jiang, S. Trefely, P. Xu, J. P. Singh, C. Jiang, E. Rame, D. Brady, J. L. Meier, K. Marguiles, Z. Arany, N. W. Snyder

The paper confirms the in vivo synthesis of a six-carbon metabolite from propionate in human heart and mouse tissues through non-oxidative pathways.

bioRxiv · Jun 15, 2020 · PreprintBiochemistry

Activation of GPR56, a novel adhesion GPCR, is necessary for nuclear androgen receptor signaling in prostate cells

G. Bagchi, J. P. Singh, M. Dagar, G. Dagar, S. Rawal, R. D. Sharma, R. K. Tyagi

This study shows that GPR56 activation by androgens enhances AR signaling through Rho and cAMP/PKA pathways, and its expression is higher in prostate tumors, suggesting it as a therapeutic target.

bioRxiv · Nov 21, 2019Cancer Biology