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Tomohide Natsuaki

Researcher at Utsunomiya University

Publications -  108
Citations -  2561

Tomohide Natsuaki is an academic researcher from Utsunomiya University. The author has contributed to research in topics: Plant virus & Virus. The author has an hindex of 25, co-authored 104 publications receiving 2213 citations. Previous affiliations of Tomohide Natsuaki include Tokyo University of Agriculture and Technology & Scottish Crop Research Institute.

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Characterization of Silencing Suppressor 2b of Cucumber Mosaic Virus Based on Examination of its Small RNA-Binding Abilities

TL;DR: It is demonstrated that the PTGS suppressor (2b) of a severe strain of cucumber mosaic virus (CMV) can bind to in vitro synthesized siRNAs and even to long dsRNAs to a lesser extent, however, the 2b suppressor weakly bound to a miRNA (miR171) duplex in contrast to another small RNA-binding suppressor, p19 of tombusvirus that can effectively bind miRNAs.
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Sequence variation of the rDNA ITS regions within and between anastomosis groups in Rhizoctonia solani

TL;DR: Results suggest that sequence analysis of ITS rDNA regions of R. solani may be a valuable tool for identifying AG subgroups of biological significance.
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2020 taxonomic update for phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales

Jens H. Kuhn, +234 more
- 31 Aug 2021 - 
TL;DR: The updated taxonomy of Negarnaviricota is presented, as now accepted by the ICTV, after the phylum was amended and emended in March 2020.
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An important determinant of the ability of Turnip mosaic virus to infect Brassica spp. and/or Raphanus sativus is in its P3 protein.

TL;DR: The results suggest that the P3 protein is an important factor in the infection cycle of TuMV and in determining the host range of this and perhaps other potyviruses.
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Analysis of the Spatial Distribution of Identical and Two Distinct Virus Populations Differently Labeled with Cyan and Yellow Fluorescent Proteins in Coinfected Plants

TL;DR: Apple latent spherical virus expressing yellow and cyan fluorescent proteins (ALSV-YFP and ALSV-CFP) was used to investigate the distribution of identical virus populations in coinfected plants and fluorescence from YFP and CFP was always distributed separately in both inoculated and upper uninoculated leaves.