Author

H. Srinivasan

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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Physiology· 3 Microbiology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Research Focus:differential expression· 3 Organism:human· 3 Organism:mouse· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

C. Jacobs· 2 shared L. Tsai· 2 shared A. Courcoulas· 1 shared A. De Vincenzo· 1 shared A. Felton· 1 shared A. Giordano· 1 shared A. Gulko· 1 shared A. Kar· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersPhysiology

C. Jacobs

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

A CRISPR screen of HIV dependency factors reveals CCNT1 is non-essential in T cells but required for HIV-1 reactivation from latency

T. L. Hafer, A. Felton, Y. Delgado, H. Srinivasan, M. Emerman

This study uses a CRISPR screen to identify HIV-1 latency reversal factors, finding that CCNT1 is non-essential for T cell activation but critical for HIV reactivation from latency.

bioRxiv · Jul 28, 2023 · PreprintMicrobiology

Hypoxia-inducible factor 1 signaling drives placental aging and can provoke preterm labor

E. J. Ciampa, P. Flahardy, H. Srinivasan, C. Jacobs, L. Tsai, S. A. Karumanchi, S. M. Parikh

This study identifies HIF-1 signaling as a driver of placental aging and preterm labor in mice, with similar effects observed in human placenta.

bioRxiv · Mar 14, 2022Physiology

A single cell atlas of human and mouse white adipose tissue

M. P. Emont, C. Jacobs, A. L. Essene, D. Pant, D. Tenen, G. Colleluori, A. De Vincenzo, A. M. Jorgensen, H. Dashti, A. Stefek, E. McGonagle, S. Strobel, S. Laber, S. Agrawal, G. P. Westcott, , E. D. Rosen

This study creates single-cell atlases of human and mouse white adipose tissue, identifying cell types and their roles in metabolic disease across different body weights and diets.

bioRxiv · Nov 9, 2021Physiology

HGFAC is a ChREBP Regulated Hepatokine that Enhances Glucose and Lipid Homeostasis

A. Sargsyan, L. Doridot, S. A. Hannou, W. Tong, H. Srinivasan, R. Ivison, R. Monn, H. H. Kou, J. M. Haldeman, M. Arlotto, P. J. White, P. A. Grimsrud, I. Astapova, L. Tsai, M. A. Herman

The paper identifies HGFAC as a ChREBP-regulated hepatokine that improves glucose and lipid homeostasis through activation of PPARγ in mice.

bioRxiv · Jul 29, 2021Physiology