Kazuko Iida

2.3k total citations
36 papers, 1.8k citations indexed

About

Kazuko Iida is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Kazuko Iida has authored 36 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 10 papers in Cell Biology and 9 papers in Plant Science. Recurrent topics in Kazuko Iida's work include Ion channel regulation and function (10 papers), Fungal and yeast genetics research (9 papers) and Plant Stress Responses and Tolerance (8 papers). Kazuko Iida is often cited by papers focused on Ion channel regulation and function (10 papers), Fungal and yeast genetics research (9 papers) and Plant Stress Responses and Tolerance (8 papers). Kazuko Iida collaborates with scholars based in Japan, United States and France. Kazuko Iida's co-authors include Ichiro Yahara, Hidetoshi Iida, Kenji Moriyama, Masataka Nakano, Seiji Matsumoto, Takuya Yamanaka, Kazuo Shinozaki, Yuko Nakagawa, Itaru Kojima and Eisuke Nishida and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Kazuko Iida

36 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Kazuko Iida Japan 20 994 799 558 121 114 36 1.8k
Masaya Yamamoto Japan 15 1.1k 1.1× 216 0.3× 676 1.2× 145 1.2× 82 0.7× 24 1.6k
Isabelle Sagot France 23 2.1k 2.1× 260 0.3× 1.5k 2.7× 91 0.8× 106 0.9× 38 2.7k
Luis Vidali United States 29 2.9k 2.9× 2.6k 3.2× 897 1.6× 56 0.5× 110 1.0× 60 3.7k
Vincent Fraisier France 21 877 0.9× 611 0.8× 645 1.2× 110 0.9× 35 0.3× 27 1.9k
Thomas Egelhoff United States 36 1.6k 1.6× 527 0.7× 1.8k 3.3× 202 1.7× 182 1.6× 62 3.3k
Tina L. Tootle United States 23 1.3k 1.3× 1.2k 1.5× 500 0.9× 52 0.4× 80 0.7× 42 2.6k
Ka Ming Pang United States 17 1.6k 1.6× 384 0.5× 405 0.7× 79 0.7× 28 0.2× 23 2.1k
Chinatsu Otomo United States 11 865 0.9× 128 0.2× 968 1.7× 146 1.2× 88 0.8× 13 1.8k
Elias T. Spiliotis United States 29 2.1k 2.1× 171 0.2× 1.4k 2.5× 137 1.1× 41 0.4× 46 3.0k
David Traynor United Kingdom 26 1.3k 1.3× 106 0.1× 1.2k 2.2× 187 1.5× 76 0.7× 40 2.2k

Countries citing papers authored by Kazuko Iida

Since Specialization
Citations

This map shows the geographic impact of Kazuko Iida's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kazuko Iida with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kazuko Iida more than expected).

Fields of papers citing papers by Kazuko Iida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kazuko Iida. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kazuko Iida. The network helps show where Kazuko Iida may publish in the future.

Co-authorship network of co-authors of Kazuko Iida

This figure shows the co-authorship network connecting the top 25 collaborators of Kazuko Iida. A scholar is included among the top collaborators of Kazuko Iida based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kazuko Iida. Kazuko Iida is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Iwano, Megumi, Noriyuki Suetsugu, Ryuichi Nishihama, et al.. (2024). MID1-COMPLEMENTING ACTIVITY regulates cell proliferation and development via Ca2+ signaling in Marchantia polymorpha. PLANT PHYSIOLOGY. 197(1). 1 indexed citations
2.
Yoshimura, Kenjiro, Kazuko Iida, & Hidetoshi Iida. (2021). MCAs in Arabidopsis are Ca2+-permeable mechanosensitive channels inherently sensitive to membrane tension. Nature Communications. 12(1). 6074–6074. 51 indexed citations
3.
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Hosomi, Akíra, et al.. (2020). The ER-associated protease Ste24 prevents N-terminal signal peptide-independent translocation into the endoplasmic reticulum in Saccharomyces cerevisiae. Journal of Biological Chemistry. 295(30). 10406–10419. 11 indexed citations
5.
Iida, Kazuko, et al.. (2017). Post-translational processing and membrane translocation of the yeast regulatory Mid1 subunit of the Cch1/VGCC/NALCN cation channel family. Journal of Biological Chemistry. 292(50). 20570–20582. 10 indexed citations
6.
Kume, Shinichiro, Kazuko Iida, Kaijian Lei, et al.. (2015). Transmembrane Topologies of Ca2+-permeable Mechanosensitive Channels MCA1 and MCA2 in Arabidopsis thaliana. Journal of Biological Chemistry. 290(52). 30901–30909. 27 indexed citations
7.
Shigematsu, Hideki, Kazuko Iida, Masataka Nakano, et al.. (2014). Structural Characterization of the Mechanosensitive Channel Candidate MCA2 from Arabidopsis thaliana. PLoS ONE. 9(1). e87724–e87724. 26 indexed citations
8.
Miki, Toshiaki, Mizuho Kaneda, Kazuko Iida, et al.. (2013). An anti-sulfatide antibody O4 immunoprecipitates sulfatide rafts including Fyn, Lyn and the G protein α subunit in rat primary immature oligodendrocytes. Glycoconjugate Journal. 30(9). 819–823. 11 indexed citations
9.
Kurusu, Takamitsu, Yukari Yamazaki, Masataka Nakano, et al.. (2012). Plasma membrane protein OsMCA1 is involved in regulation of hypo-osmotic shock-induced Ca2+influx and modulates generation of reactive oxygen species in cultured rice cells. BMC Plant Biology. 12(1). 11–11. 107 indexed citations
10.
Nakano, Masataka, Kazuko Iida, Hiroshi Nyunoya, & Hidetoshi Iida. (2011). Determination of Structural Regions Important for Ca2+ Uptake Activity in Arabidopsis MCA1 and MCA2 Expressed in Yeast. Plant and Cell Physiology. 52(11). 1915–1930. 33 indexed citations
11.
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Nakagawa, Yuko, Takeshi Katagiri, Kazuo Shinozaki, et al.. (2007). Arabidopsis plasma membrane protein crucial for Ca 2+ influx and touch sensing in roots. Proceedings of the National Academy of Sciences. 104(9). 3639–3644. 313 indexed citations
13.
Iida, Kazuko, Jinfeng Teng, Tomoko Tada, et al.. (2007). Essential, Completely Conserved Glycine Residue in the Domain III S2–S3 Linker of Voltage-gated Calcium Channel α1 Subunits in Yeast and Mammals. Journal of Biological Chemistry. 282(35). 25659–25667. 16 indexed citations
14.
Hashimoto, Kenji, et al.. (2004). Functional Analysis of a Rice Putative Voltage-Dependent Ca2+ Channel, OsTPC1, Expressed in Yeast Cells Lacking its Homologous Gene CCH1. Plant and Cell Physiology. 45(4). 496–500. 39 indexed citations
15.
Iida, Kazuko, Tomoko Tada, & Hidetoshi Iida. (2004). Molecular cloning in yeast by in vivo homologous recombination of the yeast putative α1 subunit of the voltage‐gated calcium channel. FEBS Letters. 576(3). 291–296. 30 indexed citations
16.
Aizawa, Hiroyuki, Yoshiro Kishi, Kazuko Iida, Masazumi Sameshima, & Ichiro Yahara. (2001). Cofilin‐2, a novel type of cofilin, is expressed specifically at aggregation stage of Dictyostelium discoideum development. Genes to Cells. 6(10). 913–921. 13 indexed citations
17.
Hirose, Takashi, Kiyotaka Koyama, Shinsaku Natori, et al.. (1990). The effects of new cytochalasins from Phomopsis sp. and the derivatives on cellular structure and actin polymerization.. Chemical and Pharmaceutical Bulletin. 38(4). 971–974. 24 indexed citations
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Yonezawa, Naoto, Eisuke Nishida, Hikoichi Sakai, et al.. (1988). Purification and characterization of the 90-kDa heat-shock protein from mammalian tissues. European Journal of Biochemistry. 177(1). 1–7. 34 indexed citations
20.
Iida, Kazuko, et al.. (1977). . KOBUNSHI RONBUNSHU. 34(4). 287–290. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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