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Leishmania donovani triose phosphate isomerase: a potential vaccine target against visceral leishmaniasisOver-expression of 60s ribosomal L23a is associated with cellular proliferation in SAG resistant clinical isolates of Leishmania donovaniTh1-stimulatory polyproteins of soluble Leishmania donovani promastigotes ranging from 89.9 to 97.1 kDa offers long-lasting protection against experimental visceral leishmaniasis.Th1 stimulatory proteins of Leishmania donovani: comparative cellular and protective responses of rTriose phosphate isomerase, rProtein disulfide isomerase and rElongation factor-2 in combination with rHSP70 against visceral leishmaniasis.Comparative Analysis of Cellular Immune Responses in Treated Leishmania Patients and Hamsters against Recombinant Th1 Stimulatory Proteins of Leishmania donovani.Supplementation of host response by targeting nitric oxide to the macrophage cytosol is efficacious in the hamster model of visceral leishmaniasis and adds to efficacy of amphotericin B.Development of Leishmania donovani stably expressing DsRed for flow cytometry-based drug screening using chalcone thiazolyl-hydrazone as a new antileishmanial target.Immunostimulatory potential and proteome profiling of Leishmania donovani soluble exogenous antigens.Development of targeted 1,2-diacyl-sn-glycero-3-phospho-l-serine-coated gelatin nanoparticles loaded with amphotericin B for improved in vitro and in vivo effect in leishmaniasis.Investigations on feasibility of in situ development of amphotericin B liposomes for industrial applications.Immunization with the DNA-encoding N-terminal domain of proteophosphoglycan of Leishmania donovani generates Th1-type immunoprotective response against experimental visceral leishmaniasis.Pro-apoptotic effect of the landrace Bangla Mahoba of Piper betle on Leishmania donovani may be due to the high content of eugenol.Immunoprotective responses of T helper type 1 stimulatory protein-S-adenosyl-L-homocysteine hydrolase against experimental visceral leishmaniasis.Photodynamic vaccination of hamsters with inducible suicidal mutants of Leishmania amazonensis elicits immunity against visceral leishmaniasis.Selective elimination of Leptomonas from the in vitro co-culture with Leishmania.Immunological consequences of stress-related proteins--cytosolic tryparedoxin peroxidase and chaperonin TCP20--identified in splenic amastigotes of Leishmania donovani as Th1 stimulatory, in experimental visceral leishmaniasis.Identification of novel S-adenosyl-L-homocysteine hydrolase inhibitors through homology-model-based virtual screening, synthesis, and biological evaluation.Efficacy of Leishmania donovani trypanothione reductase, identified as a potent Th1 stimulatory protein, for its immunogenicity and prophylactic potential against experimental visceral leishmaniasis.Itch inhibits IL-17-mediated colon inflammation and tumorigenesis by ROR-γt ubiquitination.Induction of Th1-type cellular responses in cured/exposed Leishmania-infected patients and hamsters against polyproteins of soluble Leishmania donovani promastigotes ranging from 89.9 to 97.1 kDa.SUMOylation of ROR-γt inhibits IL-17 expression and inflammation via HDAC2Development and performance evaluation of alginate-capped amphotericin B lipid nanoconstructs against visceral leishmaniasis
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Prashant Khare
@ast
Prashant Khare
@en
Prashant Khare
@es
Prashant Khare
@nl
Prashant Khare
@sl
type
label
Prashant Khare
@ast
Prashant Khare
@en
Prashant Khare
@es
Prashant Khare
@nl
Prashant Khare
@sl
prefLabel
Prashant Khare
@ast
Prashant Khare
@en
Prashant Khare
@es
Prashant Khare
@nl
Prashant Khare
@sl
P1053
O-8447-2017
P106
P21
P31
P3829
P496
0000-0001-5792-3082