R
Rie Terada
Researcher at Meijo University
Publications - 45
Citations - 3553
Rie Terada is an academic researcher from Meijo University. The author has contributed to research in topics: Gene & Gene targeting. The author has an hindex of 26, co-authored 44 publications receiving 3232 citations. Previous affiliations of Rie Terada include Graduate University for Advanced Studies & National Institute for Basic Biology, Japan.
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Fertile transgenic rice plants regenerated from transformed protoplasts
TL;DR: The production of fertile transgenic rice plants obtained by introducing the bacterial hph gene, encoding hygromycin B resistance12 (Hmr), into protoplasts of Oryza sativa (L.) by electroporation is reported.
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Targeted base editing in rice and tomato using a CRISPR-Cas9 cytidine deaminase fusion
Zenpei Shimatani,Sachiko Kashojiya,Mariko Takayama,Rie Terada,Takayuki Arazoe,Hisaki Ishii,Hiroshi Teramura,Tsuyoshi Yamamoto,Hiroki Komatsu,Kenji Miura,Hiroshi Ezura,Keiji Nishida,Tohru Ariizumi,Akihiko Kondo +13 more
TL;DR: A fusion of CRISPR-Cas9 and activation-induced cytidine deaminase (Target-AID) for point mutagenesis at genomic regions specified by single guide RNAs (sgRNAs) in two crop plants demonstrates the feasibility of base editing for crop improvement.
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Efficient gene targeting by homologous recombination in rice
TL;DR: An efficient and reproducible procedure with a strong positive/negative selection for gene targeting in rice, which feeds more than half of the world's population and is an important model plant is described.
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Expression of CaMV35S-GUS gene in transgenic rice plants
Rie Terada,Ko Shimamoto +1 more
TL;DR: The results indicate that the level of expression of the CaMV 35S promoter in rice is similar to that in tobacco, a dicotyledonous plant, suggesting that it is useful for expression of a variety of foreign genes in rice plants.
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A wheat histone H3 promoter confers cell division-dependent and -independent expression of the gus A gene in transgenic rice plants
TL;DR: The observed expression pattern in different parts of roots suggested that the level of the H3/GUS gene expression is well correlated with activity of cell division in roots, and it was indicated that the proximal promoter region (up to -185) containing the conserved hexamer, octamer and nonamer motifs is sufficient to direct both cell division-dependent and -independent expression.