Hiroshi Takeshima

22.2k total citations · 4 hit papers
286 papers, 18.3k citations indexed

About

Hiroshi Takeshima is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Hiroshi Takeshima has authored 286 papers receiving a total of 18.3k indexed citations (citations by other indexed papers that have themselves been cited), including 220 papers in Molecular Biology, 116 papers in Cellular and Molecular Neuroscience and 70 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Hiroshi Takeshima's work include Ion channel regulation and function (134 papers), Cardiac electrophysiology and arrhythmias (56 papers) and Neuropeptides and Animal Physiology (42 papers). Hiroshi Takeshima is often cited by papers focused on Ion channel regulation and function (134 papers), Cardiac electrophysiology and arrhythmias (56 papers) and Neuropeptides and Animal Physiology (42 papers). Hiroshi Takeshima collaborates with scholars based in Japan, United States and United Kingdom. Hiroshi Takeshima's co-authors include Miyuki Nishi, Shosaku Numa, Jianjie Ma, Shinji Komazaki, Masamitsu Iino, Hideo Takahashi, Noah Weisleder, Atsushi Mikami, Keiji Imoto and Tadaaki Hirose and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Hiroshi Takeshima

274 papers receiving 18.0k citations

Hit Papers

Primary structure of the receptor for calcium channel blo... 1986 2026 1999 2012 1987 1989 1986 1989 250 500 750 1000

Peers

Hiroshi Takeshima
Gerhard Meissner United States
John P. Adelman United States
Owen P. Hamill United States
Martin Poenie United States
Martin Biel Germany
Hiroshi Takeshima
Citations per year, relative to Hiroshi Takeshima Hiroshi Takeshima (= 1×) peers Thomas J. Jentsch

Countries citing papers authored by Hiroshi Takeshima

Since Specialization
Citations

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

Fields of papers citing papers by Hiroshi Takeshima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroshi Takeshima

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroshi Takeshima. A scholar is included among the top collaborators of Hiroshi Takeshima 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 Hiroshi Takeshima. Hiroshi Takeshima 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.
Ichimura, Atsuhiko, Jianhong Li, Haruki Ishikawa, et al.. (2025). Phosphodiesterase 3 inhibitors boost bone outgrowth. British Journal of Pharmacology. 182(18). 4327–4342.
2.
Venturi, Elisa, et al.. (2023). The biophysical properties of TRIC-A and TRIC-B and their interactions with RyR2. The Journal of General Physiology. 155(11). 1 indexed citations
3.
Sakagami, Hiroshi, Shigeru Amano, Kenjiro Bandow, et al.. (2023). A Comparative Study of Tumor-Specificity and Neurotoxicity between 3-Styrylchromones and Anti-Cancer Drugs. SHILAP Revista de lepidopterología. 10(7). 43–43. 2 indexed citations
4.
Hall, Duane D., Hiroshi Takeshima, & Long‐Sheng Song. (2023). Structure, Function, and Regulation of the Junctophilin Family. Annual Review of Physiology. 86(1). 123–147. 7 indexed citations
5.
Ichimura, Atsuhiko, Naoki Okamoto, Feng Liu, et al.. (2022). C-type natriuretic peptide facilitates autonomic Ca²⁺ entry in growth plate chondrocytes for stimulating bone growth. Kyoto University Research Information Repository (Kyoto University). 15 indexed citations
6.
O’Brien, Fiona, Katja Witschas, Miyuki Nishi, et al.. (2019). Enhanced activity of multiple TRIC‐B channels: an endoplasmic reticulum/sarcoplasmic reticulum mechanism to boost counterion currents. The Journal of Physiology. 597(10). 2691–2705. 8 indexed citations
7.
Qian, Nianchao, Atsuhiko Ichimura, Daisuke Takei, et al.. (2019). TRPM7 channels mediate spontaneous Ca 2+ fluctuations in growth plate chondrocytes that promote bone development. Science Signaling. 12(576). 25 indexed citations
8.
Suzuki, Yoshiaki, et al.. (2019). A junctophilin-caveolin interaction enables efficient coupling between ryanodine receptors and BKCa channels in the Ca2+ microdomain of vascular smooth muscle. Journal of Biological Chemistry. 294(35). 13093–13105. 30 indexed citations
9.
Kato, Daiki, Yoshiaki Suzuki, Hisao Yamamura, et al.. (2018). Negative regulation of cellular Ca2+mobilization by ryanodine receptor type 3 in mouse mesenteric artery smooth muscle. American Journal of Physiology-Cell Physiology. 315(1). C1–C9. 10 indexed citations
10.
Fujii, Takuto, Takahiro Shimizu, Shota Yamamoto, et al.. (2018). Crosstalk between Na+,K+-ATPase and a volume-regulated anion channel in membrane microdomains of human cancer cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(11). 3792–3804. 39 indexed citations
11.
Cao, Chunmei, Yan Zhang, Noah Weisleder, et al.. (2010). MG53 Constitutes a Primary Determinant of Cardiac Ischemic Preconditioning. Circulation. 121(23). 2565–2574. 162 indexed citations
12.
Fukushima, Hiromichi, et al.. (2010). Effects of Olmesartan on Apelin/APJ and Akt/Endothelial Nitric Oxide Synthase Pathway in Dahl Rats With End-stage Heart Failure. Journal of Cardiovascular Pharmacology. 55(1). 83–88. 47 indexed citations
13.
Cai, Chuanxi, Haruko Masumiya, Noah Weisleder, et al.. (2009). MG53 Nucleates Assembly Of Cell Membrane Repair Machinery. Biophysical Journal. 96(3). 361a–361a. 17 indexed citations
14.
Tang, Wei, et al.. (2008). Superoxide-Induced Potentiation in the Hippocampus Requires Activation of Ryanodine Receptor Type 3 and ERK. Journal of Neurophysiology. 99(3). 1565–1571. 57 indexed citations
15.
Yageta, Yuichi, et al.. (2004). Intradermal Nociceptin Elicits Itch-Associated Responses Through Leukotriene B4 in Mice. Journal of Investigative Dermatology. 123(1). 196–201. 58 indexed citations
16.
Pan, Zui, Dongmei Yang, Ramakrishnan Nagaraj, et al.. (2002). Dysfunction of store-operated calcium channel in muscle cells lacking mg29. Nature Cell Biology. 4(5). 379–383. 144 indexed citations
17.
Bhat, Manjunatha B., Salim M. Hayek, Jiying Zhao, et al.. (1999). Expression and Functional Characterization of the Cardiac Muscle Ryanodine Receptor Ca2+ Release Channel in Chinese Hamster Ovary Cells. Biophysical Journal. 77(2). 808–816. 39 indexed citations
18.
Suda, Noriko, Matthias Bödding, Andrea Fleig, et al.. (1996). Slow calcium-induced calcium release (CICR) in Chinese hamster ovary (CHO) cells expressing skeletal ryanodine receptor (RyR) and chimaeric dihydropyridine receptor (DHPR).. Biophysical Journal. 70(2). 2 indexed citations
19.
Takazoe, I, et al.. (1978). Phospholipid-induced agglutination of plaque bacteria.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 19(1). 35–42.
20.
Takazoe, I, et al.. (1975). Local antibody production in guinea pigs by gingival inoculation of bacteroides melaninogenicus.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 16(4). 177–82. 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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