Shosei Kishida

5.6k total citations
67 papers, 4.7k citations indexed

About

Shosei Kishida is a scholar working on Molecular Biology, Cell Biology and Oral Surgery. According to data from OpenAlex, Shosei Kishida has authored 67 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 13 papers in Cell Biology and 10 papers in Oral Surgery. Recurrent topics in Shosei Kishida's work include Wnt/β-catenin signaling in development and cancer (21 papers), Cancer-related gene regulation (18 papers) and Oral and Maxillofacial Pathology (10 papers). Shosei Kishida is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (21 papers), Cancer-related gene regulation (18 papers) and Oral and Maxillofacial Pathology (10 papers). Shosei Kishida collaborates with scholars based in Japan, United Kingdom and United States. Shosei Kishida's co-authors include Akira Kikuchi, Hideki Yamamoto, Michiko Kishida, Satoshi Ikeda, Shinya Koyama, Kozo Kaibuchi, Shinji Takada, Hiromichi Shirataki, Shin-ichiro Hino and Makoto Asashima and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Shosei Kishida

67 papers receiving 4.6k citations

Peers

Shosei Kishida
Masayuki Komada Japan
Rosanna Dono France
Weilan Ye United States
Bisei Ohkawara Japan
Yoshiharu Kawaguchi Japan
Kryn Stankunas United States
Alexandre Blais Canada
Xingbin Ai United States
Jörg Stappert Germany
Travis L. Biechele United States
Masayuki Komada Japan
Shosei Kishida
Citations per year, relative to Shosei Kishida Shosei Kishida (= 1×) peers Masayuki Komada

Countries citing papers authored by Shosei Kishida

Since Specialization
Citations

This map shows the geographic impact of Shosei Kishida'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 Shosei Kishida with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shosei Kishida more than expected).

Fields of papers citing papers by Shosei Kishida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shosei Kishida. 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 Shosei Kishida. The network helps show where Shosei Kishida may publish in the future.

Co-authorship network of co-authors of Shosei Kishida

This figure shows the co-authorship network connecting the top 25 collaborators of Shosei Kishida. A scholar is included among the top collaborators of Shosei Kishida 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 Shosei Kishida. Shosei Kishida 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.
Ono, Yusuke, Michiko Kishida, Hirofumi Koyama, et al.. (2023). Interleukin‐1α promotes matrix metalloproteinase‐9 expression, cellular motility, and local invasiveness of ameloblastoma cells. Oral Science International. 21(1). 112–120. 1 indexed citations
2.
Koyama, Hirofumi, Yusuke Ono, Mikio Iijima, et al.. (2022). Intercellular signaling between ameloblastoma and osteoblasts. Biochemistry and Biophysics Reports. 30. 101233–101233. 5 indexed citations
3.
Suzuki, Hajime, T Yoshimura, Toshiro Kibe, et al.. (2020). Ameloblastoma cell lines derived from different subtypes demonstrate distinct developmental patterns in a novel animal experimental model. Journal of Applied Oral Science. 28. e20190558–e20190558. 2 indexed citations
4.
Ahmad, Azlina, et al.. (2020). Cytotoxic Effects of Betel Quid and Areca Nut Aqueous Extracts on Mouse Fibroblast, Human Mouth-Ordinary-Epithelium 1 and Human Oral Squamous Cell Carcinoma Cell Lines. Asian Pacific Journal of Cancer Prevention. 21(4). 1005–1009. 7 indexed citations
5.
Chadt, Alexandra, Kate J. Heesom, Shosei Kishida, et al.. (2020). TBC1D1 interacting proteins, VPS13A and VPS13C, regulate GLUT4 homeostasis in C2C12 myotubes. Scientific Reports. 10(1). 17953–17953. 16 indexed citations
6.
Fujii, Shinsuke, Kana Hasegawa, Shinji Matsumoto, et al.. (2019). The TRPV4-AKT axis promotes oral squamous cell carcinoma cell proliferation via CaMKII activation. Laboratory Investigation. 100(2). 311–323. 43 indexed citations
7.
Nonaka, Miki, Nagomi Kurebayashi, Takashi Murayama, et al.. (2017). Effects of Ghrelin and Des-Acyl Ghrelin on Doxorubicin-Induced Cardiac Toxicity. Biophysical Journal. 112(3). 425a–425a. 1 indexed citations
8.
Kishida, Michiko, Toshiro Kibe, Mikio Iijima, et al.. (2010). Wnt‐5a signaling is correlated with infiltrative activity in human glioma by inducing cellular migration and MMP‐2. Cancer Science. 102(3). 540–548. 107 indexed citations
9.
Kikuchi, Akira, Shosei Kishida, & Hideki Yamamoto. (2006). Regulation of Wnt signaling by protein-protein interaction and post-translational modifications. Experimental & Molecular Medicine. 38(1). 1–10. 178 indexed citations
10.
Tsukamoto, Satoshi, et al.. (2006). Oog1, an oocyte-specific protein, interacts with Ras and Ras-signaling proteins during early embryogenesis. Biochemical and Biophysical Research Communications. 343(4). 1105–1112. 12 indexed citations
11.
Sato, Akira, Shosei Kishida, Toshiya Tanaka, et al.. (2004). Sall1, a causative gene for Townes–Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin. Biochemical and Biophysical Research Communications. 319(1). 103–113. 52 indexed citations
12.
Oshita, Akihiko, Shosei Kishida, Hiroki Kobayashi, et al.. (2003). Identification and characterization of a novel Dvl‐binding protein that suppresses Wnt signalling pathway. Genes to Cells. 8(12). 1005–1017. 54 indexed citations
13.
Nagano, Yoshito, Hiroshi Yamashita, Tetsuya Takahashi, et al.. (2003). Siah-1 Facilitates Ubiquitination and Degradation of Synphilin-1. Journal of Biological Chemistry. 278(51). 51504–51514. 89 indexed citations
14.
Kobayashi, Masashi, Shosei Kishida, Akimasa Fukui, et al.. (2002). Nuclear Localization of Duplin, a β-Catenin-binding Protein, Is Essential for Its Inhibitory Activity on the Wnt Signaling Pathway. Journal of Biological Chemistry. 277(8). 5816–5822. 19 indexed citations
15.
Kishida, Michiko, Shin-ichiro Hino, Tatsuo Michiue, et al.. (2001). Synergistic Activation of the Wnt Signaling Pathway by Dvl and Casein Kinase Iε. Journal of Biological Chemistry. 276(35). 33147–33155. 94 indexed citations
16.
Fukui, Akimasa, Shosei Kishida, Akira Kikuchi, & Makoto Asashima. (2000). Effects of rat Axin domains on axis formation in Xenopus embryos. Development Growth & Differentiation. 42(5). 489–498. 12 indexed citations
17.
Kadoya, Takayuki, Shosei Kishida, Akimasa Fukui, et al.. (2000). Inhibition of Wnt Signaling Pathway by a Novel Axin-binding Protein. Journal of Biological Chemistry. 275(47). 37030–37037. 49 indexed citations
18.
Yamamoto, Hideki, Shosei Kishida, Michiko Kishida, et al.. (1999). Phosphorylation of Axin, a Wnt Signal Negative Regulator, by Glycogen Synthase Kinase-3β Regulates Its Stability. Journal of Biological Chemistry. 274(16). 10681–10684. 307 indexed citations
19.
Kishida, Shosei, Shinya Koyama, Kenji Matsubara, et al.. (1997). Colocalization of Ras and Ral on the membrane is required for Ras-dependent Ral activation through Ral GDP dissociation stimulator. Oncogene. 15(24). 2899–2907. 59 indexed citations
20.

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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