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Vijay Kumar Prajapati

Researcher at Central University of Rajasthan

Publications -  117
Citations -  3698

Vijay Kumar Prajapati is an academic researcher from Central University of Rajasthan. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 31, co-authored 93 publications receiving 2754 citations. Previous affiliations of Vijay Kumar Prajapati include Institute of Medical Sciences, Banaras Hindu University & Banaras Hindu University.

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Efficacy of Miltefosine in the Treatment of Visceral Leishmaniasis in India After a Decade of Use

TL;DR: There is a substantial increase in the failure rate of oral miltefosine for treatment of VL in India as compared to the phase III trial that led to registration of the drug a decade ago.
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Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach.

TL;DR: This study warrants the experimental validation to ensure the immunogenicity and safety profile of presented vaccine construct which may be further helpful to control VL infection.
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Exploring dengue genome to construct a multi-epitope based subunit vaccine by utilizing immunoinformatics approach to battle against dengue infection.

TL;DR: This work used immunoinformatics approaches to develop a multi-epitope based subunit vaccine for dengue which can generate various immune responses inside the host and confirmed the humoral and cell mediated immune response developed by designed vaccine.
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Novel Immunoinformatics Approaches to Design Multi-epitope Subunit Vaccine for Malaria by Investigating Anopheles Salivary Protein

TL;DR: The designed subunit vaccine was found to induce anti-salivary immunity which may have the ability to prevent the entry of Plasmodium sporozoites into the human host.
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Targeted killing of Leishmania donovani in vivo and in vitro with amphotericin B attached to functionalized carbon nanotubes.

TL;DR: The results of these experiments clearly demonstrate that f-CNT-AmB has significantly greater antileishmanial efficacy than AmB and had no significant cytotoxic effects.