Author

S. P. Srivastava

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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Cell Biology· 3 Physiology· 1

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Research Focus:cancer & tumor microenvironment· 4 Approach:experimental assay· 4 Organism:mouse· 4 Research Focus:development & morphogenesis· 3 Research Focus:host-pathogen & immune response· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

A. Dardik· 2 shared C. Fernandez-Hernando· 2 shared D. Koya· 2 shared H. Zhou· 2 shared J. E. Goodwin· 2 shared J. Goodwin· 2 shared K. Kanasaki· 2 shared O. Setia· 2 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersCell Biology

A. Dardik

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Renal Angptl4 is a key fibrogenic molecule in progressive diabetic kidney disease

S. P. Srivastava, H. Zhou, R. Shenoi, M. Morris, L. Goedeke, B. K. Rajendran, O. Setia, B. Aryal, K. Kanasaki, D. Koya, A. Dardik, T. Bell, C. Fernandez-Hernando, G. Shulman, J. E. Goodwin

This study identifies Angptl4 as a fibrogenic molecule in diabetic kidney disease and shows that targeting its expression in kidneys reduces fibrosis and proteinuria.

bioRxiv · Nov 8, 2023Cell Biology

Loss of endothelial glucocorticoid receptor accelerates organ fibrosis in db/db mice

S. P. Srivastava, J. Goodwin

This study shows that loss of endothelial glucocorticoid receptor worsens fibrosis in db/db mice, which can be mitigated by Wnt inhibitors or metformin.

bioRxiv · Mar 20, 2023 · PreprintPhysiology

Endothelial SIRT3 regulates myofibroblast metabolic shifts in diabetic kidneys

S. P. Srivastava, J. Li, Y. Takagaki, M. Kitada, J. E. Goodwin, K. Kanasaki, D. Koya

This study shows that endothelial SIRT3 regulates metabolic shifts and fibrosis in diabetic kidneys by controlling EndMT and metabolic reprogramming.

bioRxiv · Dec 15, 2020Cell Biology

Loss of endothelial glucocorticoid receptor accelerates diabetic nephropathy

S. P. Srivastava, H. Zhou, O. Setia, A. Dardik, C. Fernandez-Hernando, J. Goodwin

This study shows that loss of endothelial glucocorticoid receptor accelerates diabetic nephropathy by promoting fibrosis through Wnt signaling and EndMT/EMT mechanisms.

bioRxiv · Jun 29, 2020Cell Biology