【Reviewed Original Papers】
48) Takagi K, Yokoyama M, Beppu T, Uemori H, Ohno H, Murakami T, Ifuku O, Tada Y, Yoshida S (2024) High productivity of oxylipin KODA using E. coli with lipoxygenase and allene oxide synthase of Lemna paucicostata introduced. Plant Biotechnol. Oct 12, 2024 doi.org/10.5511/plantbiotechnology.24.0721a
47) Yokoyama M, Kaida R, Miyamoto K, Tada Y, Fujii Y (2024) Characteristics of the systemic activation of the growth by 9,10-ketol-12(Z),15(Z)-octadecadienoic acid (KODA) in Populus alba cultured in vitro. Plant Biotechnol. Oct 12, 2024 doi.org/10.5511/plantbiotechnology.24.0721b
46) Tada Y, Kochiya R, Toyoizumi M, Takano Y (2023) Salt tolerance and regulation of Na+, K+, and proline contents in different wild turfgrasses under salt stress. Plant Biotechnology 40: 301–309, DOI: https://doi.org/10.5511/plantbiotechnology.23.0721a
45) Noike Y, Okamoto I, Tada Y (2023) Root epidermis-specific expression of a phosphate transporter TaPT2 enhances the growth of transgenic Arabidopsis under Pi-replete and Pi-depleted conditions. Plant Sci. 327: 111540, https://doi.org/10.1016/j.plantsci.2022.111540
44) Kato Y, Tada Y (2021) Comparative analysis of various root active promoters by evaluation of GUS expression in transgenic Arabidopsis. Plant Biotechnology 38: 443-448; https://doi.org/10.5511/plantbiotechnology.21.1011a
41) Tada Y (2019) The HKT transporter gene from Arabidopsis, AtHKT1;1, is dominantly expressed in shoot vascular tissue and root tips and is mild salt stress-responsive. Plants 8: 204; https://doi.org/10.3390/plants8070204, [IF 2.632/2018]
40) Tada Y, Kawano R, Komatsubara S, Nishimura H, Katsuhara M, Ozaki O, Terashima S, Yano K, Endo C, Sato M, Okamoto M, Sawada Y, Yokota-Hirai M, Kurusu T (2019) Functional screening of salt tolerance genes from a halophyte Sporobolus virginicus and transcriptomic and metabolomic analysis of salt tolerant plants expressing glycine-rich RNA-binding protein. Plant Sci 278: 54-63 https://doi.org/10.1016/j.plantsci.2018.10.019
39) Tada Y, Endo C, Katsuhara M, Horie T, Shibasaka M, Nakahara Y, Kurusu T (2019) High-affinity K+ transporters from a halophyte, Sporobolus virginicus, mediate both K+ and Na+ transport in transgenic Arabidopsis, X. laevis oocytes, and yeast. Plant Cell Physiol 60:176–187, https://doi.org/10.1093/pcp/pcy202
38) Mansouri M, Naghavi MR, Alizadeh H, Mohammadi-Nejad G, Mousavi SA, Salekdeh GH, Tada Y (2019) Transcriptomic analysis of Aegilops tauschii during long term salinity stress. Funct. Integr. Genomics 19: 13 doi.org/10.1007/s10142-018-0623-y
37) Yamamoto N, Garcia R, Suzuki T, Solis CA, Tada Y, Venuprasad R, Kohli A(2018)Comparative whole genome re-sequencing analysis in upland New Rice for Africa: insights into the breeding history and respective genome compositions. Rice 11:33 doi.org/10.1186/s12284-018-0224-3
36) Endo C, Yamamoto N, Kobayashi M, Nakamura Y, Yokoyama Y, Kurusu T, Yano K, Tada Y (2017) Development of simple sequence repeat markers in the halophytic turf grass Sporobolus virginicus and transferable genotyping across multiple grass genera/species/genotypes Euphytica 213:56 DOI: 10.1007/s10681-017-1846-z
32) Kazama D, Kurusu T, Mitsuda N, Ohme-Takagi M, Tada Y (2014) Involvement of elevated proline accumulation in enhanced osmotic stress tolerance in Arabidopsis conferred by chimeric repressor gene silencing technology. Plant Signal. Behav. 9: e28211; http://dx.doi.org/10.4161/psb.28211 Abstract
31) Kazama D, Itakura M, Kurusu T, Mitsuda N, Ohme-Takagi M, Tada Y (2013) Identification of Chimeric Repressors that Confer Salt and Osmotic Stress Tolerance in Arabidopsis. Plants. 2(4):769-785. doi:10.3390/plants2040769 (5)
30) Tada Y, Tashiro T, Tsuboi S (2013) Thermal Environment Improvement by Using Kudzu (Pueraria lobata (Willd.) Ohwi)in Rooftop Gardening. Journal of Heat Island Institute International 8: 1-6 (In Japanese)
28) Miyama M, Tada Y (2011) Expression of Bruguiera gymnorhiza BgARP1 enhances salt tolerance in transgenic Arabidopsis plants. Euphytica 177:383-392, DOI 10.1007/s10681-010-0264-2 Abstract
26) Matsumoto K, Tada Y, Shimizu H, Shibusawa S (2009) Effect of temperature on the growth and antioxidative activity of Raphanus sativus L. “Kaiwaredaikon (Japanese radish sprout)”. Shokubutsu Kankyo Kogaku 21:117-122 (In Japanese)
25) Matsumoto K, Tada Y, Shimizu H, Shibusawa S (2009) Effect of water supply levels on growth and antioxidative activity of Raphanus sativus L. “Kaiwaredaikon (Japanese radish sprout)”. Shokubutsu Kankyo Kogaku 21:79-85 (In Japanese)
24) Tada Y, Kashimura, T (2009) Proteomic analysis of salt-responsive proteins in mangrove plant, Bruguiera gymnorhiza. Plant Cell Physiol. 50: 439-446, DOI: 10.1093/pcp/pcp002 Abstract
23) Matsumoto K, Tada Y, Shimizu H, Shibusawa S (2009) Effect of temperature on growth and antioxidative activity of Raphanus sativus L. “Kaiwaredaikon (Japanese radish sprout)”. Shokubutsu Kankyo Kogaku 21:29-34 (In Japanese)
21) Ezawa S, Tada Y (2009) Identification of salt tolerance genes from the mangrove plant Bruguiera gymnorhiza using Agrobacterium functional screening. Plant Sci.176: 272-278, DOI: 10.1016/j.plantsci.2008.11.005 Abstract
20) Kotsuka K, Tada Y (2008) Genetic Transformation of Golden Pothos (Epipremnum aureum) mediated by Agrobacterium tumefaciens. Plant Cell Tiss. Organ Cult. 95:305-311, DOI: 10.1007/s11240-008-9444-3 Abstract
19) Miyama M, Tada Y (2008) Transcriptional and physiological study of the response of Burma mangrove (Bruguiera gymnorhiza) to salt and osmotic stress. Plant Mol. Biol. 68:119-129, DOI: 10.1007/s11103-008-9356-y Abstract
14) Sakamoto K, Tada Y, Yokozeki Y, Akagi H, Hayashi N, Fujimura T, Ichikawa N(1999) Chemical induction of disease resistance in rice is associated with the expression of a gene encording a nucleotide binding site and leucine-rich repeats. Plant Mol. Biol. 40:847-855
13) Tada Y, Harada J, Matsumura T, Yamada M, Matsuda T, Adachi T, Nakamura R, Takahashi M, Fujimura T, Shimada H (1997) Environmental Risk Evaluation of Transgenic Rice Expressing an Antisense Gene for 16kDa Albumin(II)Breeding Science 47:77-81 (In Japanese)
12) Tada Y, Yamada M, Sawada R, Samoto S, Matsuda T, Adachi T, Nakamura R, Takahashi M, Fujimura T, Shimada H (1997) Environmental Risk Evaluation of Transgenic Rice Expressing an Antisense Gene for 16kDa Albumin(I)Breeding Science 46:403-407 (In Japanese)
11) Tada Y, Nakase M, Adachi T, Nakamura R, Shimada H, Takahashi M, Fujimura T, Matsuda T.(1996) Reduction of 14-16 kDa allergenic proteins in transgenic rice plants by antisense gene. FEBS Lett. 391:341-345
10) Matsuoka M, Tamaoki M, Tada Y, Fujimura T, Tagiri A, Yamamoto N,. Kanno-Murakami Y (1995) Expression of rice OSH1 gene is localized in developing vascular strands and its ectopic expression in transgenic rice causes altered morphology of leaf. Plant Cell. Rep. 14:555-559
9) Yamamoto N, Tada Y, Fujimura T (1994) The promoter of a pine photosynthetic gene allows expression of a β-glucronidase reporter gene in transgenic rice plants in a light-independent but tissue-specific manner. Plant Cell Physiol. 35:773-778
8) Shimada H, Tada Y, Kawasaki T, Fujimura T (1993) Antisense regulation of the rice waxy gene expression using a PCR-amplified fragment of the rice genome reduces the amylose content in grain starch. Theor.Appl.Genet. 86:665-672
7) Matsuoka M, Tada Y, Fujimura T, Kanno-Murakami. Y (1993) Tissue-specific light-regulated expression directed by the promoter of a C4 gene, maize pyruvate, orthophosphate dikinase, in a C3 plant, rice. Proc.Natl.Acad. Sci.USA 90:9586-9590
6) Matsuoka M, Ichikawa H, Saito A, Tada Y, Fujimura T Kanno-Murakami. Y (1993) Expression of a rice homeobox gene causes altered morphology of transgenic plants. Plant Cell 5:1039-1048
5) Shimada H, Tada Y (1991) Rapid isolation of rice waxy sequence: a simple PCR method for the analysis of recombinant plasmids from intact Escherichia coli cells. Gene 98, 243-248
4) Kato T, Shirano Y, Kawazu T, Tada Y, Itoh E, Shibata D (1991) A modified beta-glucronidase gene: sensitive detection of plant promoter activities in suspension-cultured cell of tobacco and rice. Plant Mol. Biol. Rep. 9, 333-339
3)Tada Y, Sakamoto M, Matsuoka M, Fujimura T (1991) Efficient transformation of rice cells and production of transgenic rice plants. In Rice Genetics II. Proc 2nd Int. Rice Genet. Symp., edited by. IRRI, Manila, pp.575-583
2) Tada Y, Sakamoto M, Matsuoka M, Fujimura T (1991) Expression of a monocot LHCP promoter in transgenic rice. EMBO J. 10, 1803-1808
1) Tada Y, Sakamoto M, Fujimura T (1990) Efficient gene introduction into rice by electroporation and analysis of transgenic plants: use of electroporation buffer lacking chloride ions. Theor. Appl. Genet. 80:475-480
[Review and Book chapters]
T. Kurusu, S. Kimura, Y. Tada, H. Kaya, K. Kuchitsu (2013) “Plant Signaling Networks Involving Reactive Oxygen Species and Ca2+” in “Handbook on Reactive Oxygen Species (ROS): Formation Mechanisms, Physiological Roles and Common Harmful Effects” Eds, Suzuki M and Yamamoto S, Nova Science Publishers, Inc., NY, USA, ISBN: 978-1-62948-049-7
Tada Y (2011) Molecular mechanisms of salt tolerance in mangrove plants. In “Agricultural Research Updates, Volume 1, Chapter 3, pp1-26” Ed, Hendricks BP, Nova Science Publishers, Inc., NY, USA, ISBN:978-1-61324-292-6
T. Matsuda, M. Nakase, A. M. Alvarez, H. Izumi, T. Kato, Y. Tada (2005) “Rice seed allergenic proteins and hypo-allergenic rice” In “Neutraceutical Proteins and Peptides in Health and Disease” p491-p509 Macel Dekker NY
Shimada H, Kawasaki T, Ishikawa M, Okumura S, Baba T, Tada Y, Hayashida N, Shinozaki K (1992) Molecular analysis of genies involved in rice grain starch synthesis: Structure of a seed-development specific protein kinase. In: Research in Photosynthesis vol. III p923-p926 (Murata N ed.) Kluwer Academic Publishers, Dordrecht, the Netherlands
【Non-reviewed papers】
7)Tada Y, Yamanaka T, Miyama M (2008) gene expression profilings of the mangrove plant Bruguiera gymnorhiza under salt stress and identification of salt tolerance genes. Tokyo Kokadaigaku Kenkyu Houkoku 3:77-84 (In Japanese)
6) Tada Y (2005) Fertility restoration in rice with WA- and BT-type cytoplasmic male sterility crossed with near isogenic lines deferring at Rf loci. Proceedings of the 10th International Congress of the Society for the Advancement of Breeding Researches in Asia and Oceania, D-15
5) Tada Y (1996) Modification of rice grain components by recombinant DNA technology. Gamma Field Symposia 35:5-17
4) Matsuda T, Nakase M, Adachi T, Nakamura R,Tada Y, Shimada H, Takahashi M and Fujimura T (1996) Allergenic Proteins in rice: Strategies for reduction and evaluation. In : G. Elisenbrand et al. (eds.) Food Allergies and intolerances, Section III. The input of molecular biology: Transgenic foods. VCH verlagsgesellschaft, Weinheim, FRG, pp161-169
3) Tada Y, Shimada H, Fujimura T (1995) Reduction of allergenic protein in rice grain. In: D.D. Jones (ed.) The biosafety results of field test of genetically modified plants and microorganisms, Univ. of California, U.S.A. pp.290
2) Tada Y, Adachi T, Matsuda T, Takahashi M, Fujimura T, Nakamura R,.Shimada H (1995) Reduction of allergenic proteins in transgenic rice by antisense strategy. In: K. Oono, F. Takaiwa (eds.), Modification of gene expression and non-menderian inheritance. Natl. Inst. Agrobiol. Resources, Japan, pp. 313-324
1) Shimada H, Kawasaki T, Ishikawa M, Okumura S, Baba T, Tada Y, Hayashida N, Shinozaki K: Molecular analysis of genes involved in rice grain starch synthesis: Structure of a seed-development specific protein kinase. In: N. Murata (ed.) Research in photosynthesis. Kluwer Academic Publ., The Netherlands, vol. III, pp923-926 (1992)