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Shailja Singh

Researcher at Jawaharlal Nehru University

Publications -  175
Citations -  2570

Shailja Singh is an academic researcher from Jawaharlal Nehru University. The author has contributed to research in topics: Plasmodium falciparum & Biology. The author has an hindex of 21, co-authored 139 publications receiving 2001 citations. Previous affiliations of Shailja Singh include Shiv Nadar University & University of Delhi.

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Receptor-binding residues lie in central regions of Duffy-binding-like domains involved in red cell invasion and cytoadherence by malaria parasites.

TL;DR: Using biochemical and molecular methods, it is demonstrated that the receptor-binding residues of parasite ligands that bind sialic acid on glycophorin A for invasion as well as complement receptor-1 and chondroitin sulfate A for cytoadherence map to central regions of DBL domains.
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Synthesis and in vitro antiplasmodial activities of fluoroquinolone analogs.

TL;DR: Screening of either known or unknown quinolone/fluoroquinolone analogs are worthwhile to find more potent antimalarial drugs which might prove useful in the treatment of mild or severe malaria in human either alone or in combination with existing antimalaria drugs.
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Plasmodium falciparum signal recognition particle components and anti-parasitic effect of ivermectin in blocking nucleo-cytoplasmic shuttling of SRP

TL;DR: The evaluation of the effect of known SRP and nuclear import/export inhibitors on P. falciparum revealed that ivermectin, an inhibitor of importin α/β mediated nuclear import inhibited the nuclear import of PfSRP polypeptides at submicromolar concentration, thereby killing the parasites.
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Role of exchange protein directly activated by cAMP (EPAC1) in breast cancer cell migration and apoptosis

TL;DR: This study reports that inhibition of EPAC1 activity using pharmacological modulators leads to inhibition of cell migration and induces cell death, and suggests for the first time the mechanistic insights of mode of action of a primary cAMP-dependent sensor, Exchange protein activated by cAMP 1 (EPAC1), via its interaction with A-kinase anchoring protein 9 (AKAP9).
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A thrombospondin structural repeat containing rhoptry protein from Plasmodium falciparum mediates erythrocyte invasion.

TL;DR: Observations suggest that targeting multiple conserved parasite ligands involved in different steps of invasion may provide an effective strategy for the development of vaccines against blood stage malaria parasites.