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Dai Yamamoto

Researcher at Sapporo Medical University

Publications -  9
Citations -  171

Dai Yamamoto is an academic researcher from Sapporo Medical University. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 7, co-authored 8 publications receiving 162 citations.

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Whole-genome characterization of human group C rotaviruses: identification of two lineages in the VP3 gene

TL;DR: The presence of obvious genetic diversity only in the VP3 gene among human GCRVs suggested that either the M2 or M3VP3 gene of human GcrVs might have been derived through reassortment from an animal GCRV or from an unidentified human G CRV strain belonging to a novel genogroup.
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Detection and full genomic analysis of G6P[9] human rotavirus in Japan

TL;DR: Findings suggested that the G6P[9] human rotavirus detected in Japan may have occurred through reassortment among uncommon bovine-like human rotAViruses and human/feline AU-1-like rotaviruses.
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Characterization of PVL/ACME-positive methicillin-resistant Staphylococcus aureus (genotypes ST8-MRSA-IV and ST5-MRSA-II) isolated from a university hospital in Japan.

TL;DR: The present study suggested the spread of ST8-MRSA-IV in northern Japan, and a potential significance of ACME-positive ST5- MRSA-II as an emerging MRSA clone in a hospital.
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Whole-genome analysis reveals the complex evolutionary dynamics of Kenyan G2P[4] human rotavirus strains.

TL;DR: The nearly complete genome sequences of two Kenyan G2P[4] strains detected in 1982 and 1989 were analysed and, except for NSP2 of AK26, appeared to originate from or share a common origin with rotavirus genes of artiodactyl (ruminant and camelid) origin.
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Analysis of genetic diversity and molecular evolution of human group B rotaviruses based on whole genome segments.

TL;DR: Divergent or conserved regions in the deduced amino acid sequences of GBR VP1-VP4 and NSP1-NSP5 were similar to those in group A rotaviruses (GARs), and the functionally important motifs and structural characteristics in viral proteins known for GAR were conserved in all of the human GBRs.