Author

Md Nazrul Islam

National Institute of BiotechnologyORCID 0000-0002-8138-0089Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Research Focus:drug response / drug discovery· 3 Approach:experimental assay· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Organism:E. coli· 1 Organism:mouse· 1 Assay:proteomics· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Arittra BhattacharjeeiD· 2 shared Chaman Ara Keya· 2 shared Ishtiaque AhammadiD· 2 shared Keshob Chandra DasiD· 2 shared M. SalimullahiD· 2 shared Md. MoniruzzamaniD· 2 shared Mohammad Uzzal HossainiD· 2 shared Zeshan Mahmud ChowdhuryiD· 2 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersPharmacology & Toxicology

Arittra BhattacharjeeORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Pharmacology & ToxicologybioRxivPreprintNov 8, 2023

In vivo and in silico experiment on Mitragyna speciosa offers new insight of antidiabetic potentials

Mohammad Uzzal Hossain, Md. Shahadat Hossain, Shajib Dey…·M. Salimullah

This study investigates the anti-diabetic potential of Mitragyna speciosa using in vivo and in silico methods, finding that extracts reduce blood glucose levels and four compounds bind effectively to the DPP4 receptor.

2 citations

mousebulk RNA-seq

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BioinformaticsJournal of Genetic Engineering and BiotechnologyPeer-reviewedApr 2, 2021

Novel Mutations in NSP1 and PLPro of SARS-CoV-2 NIB-1 Genome Mount for Effective Therapeutics

Mohammad Uzzal Hossain, Arittra Bhattacharjee, Md. Tabassum Hossain Emon…·M. Salimullah

The paper identifies novel mutations in SARS-CoV-2 NIB-1 genome and analyzes their impact on NSP1 and PLPro proteins for therapeutic development.

30 citations

viruswhole-genome sequencing

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BioinformaticsbioRxivPreprintFeb 14, 2020

In Silico identification of potential drug targets by subtractive genome analysis of Enterococcus faecium DO.

Marwah Karim, Md Nazrul Islam, G. M. Nurnabi Azad Jewel

This paper identifies potential drug targets for Enterococcus faecium DO using genomic and proteomic analysis, prioritizing non-homologous essential proteins and proposing eight ligands for aldehyde-alcohol dehydrogenase as novel antibiotic targets.

4 citations

E. coliproteomics

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