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Katja Stare

Publications -  14
Citations -  436

Katja Stare is an academic researcher. The author has contributed to research in topics: Potato virus Y & Transcriptome. The author has an hindex of 9, co-authored 12 publications receiving 325 citations.

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Salicylic acid is an indispensable component of the Ny-1 resistance-gene-mediated response against Potato virus Y infection in potato

TL;DR: Grafting experiments show that SA has a critical role in the inhibition of PVY spreading in parenchymal tissue, but not in vascular veins, and showed that the absence of SA leads to significant changes at the transcriptome level, including a delay in activation of expression of genes known to participate in defence responses.
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Dynamics of Responses in Compatible Potato - Potato virus Y Interaction Are Modulated by Salicylic Acid

TL;DR: The differential gene expression pattern of the two sensitive genotypes indicates that the outcome of the interaction does not rely simply on one regulatory component, but similar phenotypical features can result from distinct responses at the molecular level.
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Structural basis for the multitasking nature of the potato virus Y coat protein.

TL;DR: The near-atomic structure of PVY’s flexuous virions is determined, revealing a previously unknown lumenal interplay between extended carboxyl-terminal regions of the coat protein units and viral RNA.
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Bimodal dynamics of primary metabolism-related responses in tolerant potato- Potato virus Y interaction

TL;DR: In this paper, a comprehensive analysis of the dynamic changes in primary metabolism was performed, which included whole transcriptome analysis, nontargeted proteomics, and photosynthetic activity measurements in potato cv.
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CCR5-Mediated Signaling Is Involved in Invasion of Glioblastoma Cells in Its Microenvironment.

TL;DR: Autocrine and paracrine cross-talk in glioblastoma and, in particular, gli oblastoma stem cells with its stromal microenvironment, involves CCR5 and CCL5, contributing to gliOBlastoma invasion, suggesting the CCL 5/CCR5 axis as a potential therapeutic target that can be targeted with repositioned drug maraviroc.