Author

S. Mishra

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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Microbiology· 10 Cell Biology· 6 Biochemistry· 4 Biophysics· 4 Immunology· 2 Physiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 24 Organism:human· 13 Assay:proteomics· 10 Research Focus:cell type annotation· 9 Research Focus:cell signaling & trafficking· 7 Organism:mouse· 7 Research Focus:host-pathogen & immune response· 6 Approach:statistical model· 6

Frequent Co-Authors

D. A. Kass· 4 shared A. Knupp· 2 shared A. Singh· 2 shared C. U. Oeing· 2 shared D. W. Hailey· 2 shared J. E. Young· 2 shared M. J. Ranek· 2 shared M. Szabo· 2 shared

Activity by Year

2017-2023 · peak 12/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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4 shared papersPhysiology

D. A. Kass

Mutual co-authors in cluster

Author profile →

32 papers

Recent·Most cited

MicrobiologybioRxivNov 26, 2017

Redox-Dependent Condensation Of the Mycobacterial Nucleoid By WhiB4

M. Chawla, M. Mehta, P. Parikh…·A. Singh

This paper identifies WhiB4 as a redox-dependent nucleoid condensing protein in Mtb that links oxidative stress response with genome organization and gene expression.

DOI 10.1016/j.redox.2018.08.006

humanChIP-seq

𝕏 PostBluesky

MicrobiologyeLifePeer-reviewedMay 26, 2017

Efficacy of the β-lactam\β-lactamase inhibitor combination is linked to WhiB4 mediated changes in redox physiology of Mycobacterium tuberculosis

S. Mishra, P. Shukla, A. Bhaskar…·A. Singh

This paper shows that the effectiveness of the β-lactam/β-lactamase inhibitor combination against Mtb depends on WhiB4-regulated redox changes, with higher mycothiol redox potential enhancing drug efficacy.

DOI 10.7554/elife.25624

humanproteomics

𝕏 PostBluesky