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Mrinal Kanti Bhattacharyya

Researcher at University of Hyderabad

Publications -  37
Citations -  583

Mrinal Kanti Bhattacharyya is an academic researcher from University of Hyderabad. The author has contributed to research in topics: Plasmodium falciparum & DNA repair. The author has an hindex of 13, co-authored 35 publications receiving 506 citations. Previous affiliations of Mrinal Kanti Bhattacharyya include Johns Hopkins University & Tulane University.

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Telomere dynamics in genome stability

TL;DR: The insights gained from recent studies extend understanding of similar processes in higher eukaryotes and suggest that the recombinational dynamics of telomeres have additional roles that contribute to genomic stability and instability.
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Identification and molecular characterization of a novel protein Saglin as a target of monoclonal antibodies affecting salivary gland infectivity of Plasmodium sporozoites

TL;DR: Biochemical and molecular characterization of the 100 kDa protein showed that this molecule, designated Saglin, exists as a disulphide‐bonded homodimer of 50 kDa subunits, and the ability to form homodimers was retained even in the recombinant Saglin expressed in mammalian cells (HEK293).
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Molecular players of homologous recombination in protozoan parasites: implications for generating antigenic variation

TL;DR: This work provides comprehensive and up-to-date information on Rad51 in these organisms, an eukaryotic homologue of bacterial RecA, and homologous recombination mechanisms and speculate on how might similar DNA repair mechanisms contribute to genetic rearrangement associated with antigenic variation in the apicomplexan Plasmodium parasites, an immune evasion strategy.
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Effect of xanthurenic acid on infectivity of Plasmodium falciparum to Anopheles stephensi.

TL;DR: It is demonstrated that xanthurenic acid not only induces exflagellation of male gametocytes but also promotes infectivity of Plasmodium falciparum to mosquito vectors.
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Plasmodium falciparum protein phosphatase type 1 functionally complements a glc7 mutant in Saccharomyces cerevisiae.

TL;DR: Complementation studies showed that PfPP1 could rescue low glycogen phenotype of Saccharomyces cerevisiae glc7 (PP1) mutant, strongly suggesting functional interaction of Pf PP1 and yeast proteins involved in glycogen metabolism.