Author

D. P. Sarkar

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Microbiology· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:drug response / drug discovery· 2 Research Focus:host-pathogen & immune response· 2 Assay:imaging· 2 Research Focus:cell signaling & trafficking· 1 Approach:experimental assay· 1 Approach:mechanistic / dynamical model· 1 Approach:microscopy & imaging analysis· 1 Organism:mouse· 1

Frequent Co-Authors

N. R. Sharma· 2 shared A. Mohanty· 1 shared D. Mandal· 1 shared D. Pandey· 1 shared K. K. Biligiri· 1 shared M. Kumar· 1 shared N. K. Ganguly· 1 shared P. Vemula· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersMicrobiology

N. R. Sharma

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Chandipura Virus forms cytoplasmic inclusion bodies through phase separation and proviral association of cellular protein Kinase R and stress granules protein TIA-1

S. Sarkar, S. Ganguly, N. K. Ganguly, D. P. Sarkar, N. R. Sharma

This study shows Chandipura virus forms cytoplasmic inclusion bodies through phase separation involving PKR and TIA-1, evading antiviral stress granules and enhancing viral replication.

Viruses · Jun 26, 2024Peer-reviewedMicrobiology

Phase Separation of a Novel form of Euchromatic Histone Methyltransferase1 (EHMT1N/C) into cytoplasmic RNA viral Inclusion bodies facilitates their coalescence, thereby enhancing viral replication

K. K. Biligiri, N. R. Sharma, A. Mohanty, D. P. Sarkar, P. Vemula, S. Rampalli

This study identifies a novel cytoplasmic form of EHMT1 that phase separates into viral inclusion bodies, enhancing viral replication through nucleoprotein methylation.

bioRxiv · Nov 1, 2023 · PreprintCell Biology

Remdesivir, Zidovudine (AZT) and Nevirapine inhibit Chandipura virus replication through high energy interactions with the RdRp domain of the polymerase protein L

D. Mandal, D. Pandey, D. P. Sarkar, M. Kumar

This study investigates the antiviral effects of remdesivir, nevirapine, and AZT on Chandipura virus replication and identifies remdesivir as the most potent inhibitor through molecular docking analysis.

bioRxiv · Mar 2, 2022 · PreprintMicrobiology