Author

S. Sehrawat

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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Immunology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1 Organism:virus· 1

Frequent Co-Authors

R. Sarkar· 3 shared S. Singh· 3 shared A. Dubey· 2 shared A. Jain· 2 shared A. Tehseen· 1 shared C. Shanmugam· 1 shared C. Shekhar· 1 shared D. Kumar· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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3 shared papersImmunology

R. Sarkar

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Glucocorticoid signaling mediates CD8+ T cell memory differentiation

A. Tehseen, D. Kumar, R. Sarkar, S. Singh, A. Dubey, S. Sehrawat

The paper shows glucocorticoids enhance CD8+ T cell memory differentiation by promoting tissue-homing TRM cells and metabolic shifts via AMPK and STAT3/5 signaling.

bioRxiv · Jul 19, 2022 · PreprintImmunology

Targeting conserved viral virulence determinants by single domain antibodies to block SARS-CoV2 infectivity

S. Singh, S. Dahiya, Y. J. Singh, K. Beeton, A. Jain, R. Sarkar, A. Dubey, S. A. Tehseen, S. Sehrawat

This study identifies single domain antibodies that neutralize SARS-CoV2 by targeting the cleavage site and receptor binding domain of the spike protein, showing their stability and effectiveness in blocking infectivity.

bioRxiv · Jan 13, 2021 · PreprintImmunology

Modeling PPRV pathogenesis in mice to assess the contribution of innate cells and anti-viral T cells

Y. Sharma, R. Sarkar, A. Jain, S. Singh, C. Shekhar, C. Shanmugam, M. Dhanavelu, P. Tembure, R. Kaul, S. Sehrawat

This study establishes a mouse model to investigate PPRV pathogenesis, showing that IFNR KO mice succumb to infection regardless of dose, with neutrophils/macrophages transporting virus to CNS and CD8+ T cells providing protection.

bioRxiv · Oct 27, 2020 · PreprintImmunology