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Meenakshi Balganesh

Researcher at AstraZeneca

Publications -  13
Citations -  583

Meenakshi Balganesh is an academic researcher from AstraZeneca. The author has contributed to research in topics: Efflux & Mycobacterium tuberculosis. The author has an hindex of 9, co-authored 13 publications receiving 535 citations.

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Efflux Pumps of Mycobacterium tuberculosis Play a Significant Role in Antituberculosis Activity of Potential Drug Candidates

TL;DR: It is shown that these four efflux pump KO mutants of M. tuberculosis play a vital role in mediating efflux of different chemical scaffolds and inhibitors of one or several of these efflux pumps could have a significant impact in the treatment of tuberculosis.

Efflux Pumps of Mycobacterium tuberculosis play a significant role in anti

TL;DR: In this paper, the authors have shown that four efflux pumps of Mycobacterium tuberculosis play a vital role in mediating efflux of 48 different chemical scaffolds, and that inhibitors of one or several of these pumps could have a significant impact in the treatment for tuberculosis.
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Rv1218c, an ABC Transporter of Mycobacterium tuberculosis with Implications in Drug Discovery

TL;DR: Most of the compound classes had significantly better bactericidal activity in the ΔRv 1218c mutant than in the wild-type H37Rv, suggesting the involvement of Rv1218c gene product in effluxing these compounds from M. tuberculosis.
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Bactericidal Activity and Mechanism of Action of AZD5847, a Novel Oxazolidinone for Treatment of Tuberculosis

TL;DR: AZD5847, a novel oxazolidinone, demonstrates improved in vitro bactericidal activity against both extracellular and intracellular M. tuberculosis compared to that of linezolid, and appears to function similarly to lineZolid through impairment of the mycobacterial 50S ribosomal subunit.
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In Vitro and In Vivo Efficacy of β-Lactams against Replicating and Slowly Growing/Nonreplicating Mycobacterium tuberculosis

TL;DR: Based on pharmacokinetic/pharmacodynamic indexes reported for beta-lactams against other bacterial pathogens, a cumulative percentage of a 24-h period that the drug concentration exceeds the MIC under steady-state pharmacokinetics conditions (%TMIC) of 20 to 40% was achieved in mice using a suitable dosing regimen.