Author

H. Shivram

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 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Organism:bacteria (other)· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

J. A. Doudna· 2 shared A. Qamra· 1 shared A. Regev· 1 shared A. Teterina· 1 shared B. McMahon· 1 shared C. Fellmann· 1 shared C. M. Rosenberger· 1 shared F. Cai· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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Curved chords = mutual co-authorship

2 shared papersMicrobiology

J. A. Doudna

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Tocilizumab treatment leads to early resolution of lymphopenia and myeloid dysregulation in patients hospitalized with COVID-19

H. Shivram, J. A. Hackney, C. M. Rosenberger, A. Teterina, A. Qamra, O. Onabajo, J. McBride, F. Cai, M. Bao, L. Tsai, A. Regev, I. Rosas, R. Bauer

bioRxiv · Oct 27, 2022 · PreprintImmunology

Diverse ATPase proteins in mobilomes constitute a large potential sink for prokaryotic host ATP

H. Shim, H. Shivram, S. Lei, J. A. Doudna, J. Banfield

The paper identifies ATPase proteins in mobilome genomes as potential energy sinks that may suppress host energy consumption during replication.

bioRxiv · Apr 1, 2021Microbiology

Potent CRISPR-Cas9 inhibitors from Staphylococcus genomes

K. E. Watters, H. Shivram, C. Fellmann, R. J. Lew, B. McMahon, J. A. Doudna

This study identifies three new potent CRISPR-Cas9 inhibitors from Staphylococcus genomes, showing they specifically block SauCas9 activity in human cells.

bioRxiv · Oct 9, 2019Biochemistry