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Shashank Gupta

Researcher at University of Copenhagen

Publications -  38
Citations -  1526

Shashank Gupta is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Tuberculosis & Mycobacterium tuberculosis. The author has an hindex of 19, co-authored 32 publications receiving 1289 citations. Previous affiliations of Shashank Gupta include Johns Hopkins University School of Medicine & Lund University.

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High-fat diet reprograms the epigenome of rat spermatozoa and transgenerationally affects metabolism of the offspring

TL;DR: Insight is provided into mechanisms by which HFD transgenerationally reprograms the epigenome of sperm cells, thereby affecting metabolic tissues of offspring throughout two generations, and induces a transcriptomic shift of the let-7c predicted targets.
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Acceleration of Tuberculosis Treatment by Adjunctive Therapy with Verapamil as an Efflux Inhibitor

TL;DR: It is found that standard TB chemotherapy plus verapamil accelerates bacterial clearance in C3HeB/FeJ mice with near sterilization, and significantly lowers relapse rates in just 4 months of treatment when compared with mice receiving standard therapy alone.
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Efflux inhibition with verapamil potentiates bedaquiline in Mycobacterium tuberculosis

TL;DR: It is found that verapamil, an efflux inhibitor, profoundly decreases the MIC of bedaquiline and clofazimine to M. tuberculosis by 8- to 16-fold, and efflux may emerge as a resistance mechanism to these drugs.
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Beta-Cell Specific Deletion of Dicer1 Leads to Defective Insulin Secretion and Diabetes Mellitus

TL;DR: It is demonstrated that a β-cell specific disruption of the miRNAs network, although allowing for apparently normal β- cell development, leads to progressive impairment of insulin secretion, glucose homeostasis and diabetes development.
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Aerosol Mycobacterium tuberculosis infection causes rapid loss of diversity in gut microbiota.

TL;DR: It is demonstrated that the mouse gut microbiota significantly changes with M. tuberculosis infection, with all mice showing a loss and then recovery of microbial community diversity, and that pre-infection samples clustered separately from post-infections samples, using ecological beta-diversity measures.