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Aswini K. Panigrahi

Researcher at Seattle Biomed

Publications -  43
Citations -  3207

Aswini K. Panigrahi is an academic researcher from Seattle Biomed. The author has contributed to research in topics: RNA editing & Trypanosoma brucei. The author has an hindex of 30, co-authored 39 publications receiving 3039 citations. Previous affiliations of Aswini K. Panigrahi include King Abdullah University of Science and Technology & University of Washington.

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Journal ArticleDOI

Complex management: RNA editing in trypanosomes

TL;DR: A picture of highly organized complexes is emerging that shows that the complex that catalyzes the central steps of editing is partitioned into distinct insertion and deletion editing subcomplexes.
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Chromerid genomes reveal the evolutionary path from photosynthetic algae to obligate intracellular parasites

Yong H. Woo, +53 more
- 15 Jul 2015 - 
TL;DR: Insight is provided into how obligate parasites with diverse life strategies arose from a once free-living phototrophic marine alga, and co-regulated with genes encoding the flagellar apparatus supporting the functional contribution of flagella to the evolution of invasion machinery.
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An RNA ligase essential for RNA editing and survival of the bloodstream form of Trypanosoma brucei.

TL;DR: Regulated repression of TbMP52 blocks editing, which shows that it is a functional component of the editing complex, indicating that editing is essential in the mammalian stage of the life cycle.
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A comprehensive analysis of Trypanosoma brucei mitochondrial proteome.

TL;DR: A total of 2897 proteins representing a substantial proportion of procyclic form cellular proteome were identified, which confirmed the validity of the vast majority of gene predictions and showed that the genes annotated as hypothetical (species specific) were overpredicted.
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Identification of novel components of Trypanosoma brucei editosomes.

TL;DR: Nine novel editosome proteins in Trypanosoma brucei are identified by mass spectrometric analysis of functional editosomes that were purified by serial ion exchange/gel permeation chromatography, immunoaffinity chromatography specific to the TbMP63 editosomal protein, or tandem affinity purification based on a tagged RNA editing ligase.