Masanobu Deshimaru

1.4k total citations
42 papers, 1.1k citations indexed

About

Masanobu Deshimaru is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Masanobu Deshimaru has authored 42 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 27 papers in Genetics and 9 papers in Cell Biology. Recurrent topics in Masanobu Deshimaru's work include Venomous Animal Envenomation and Studies (27 papers), Ion channel regulation and function (15 papers) and Cellular transport and secretion (9 papers). Masanobu Deshimaru is often cited by papers focused on Venomous Animal Envenomation and Studies (27 papers), Ion channel regulation and function (15 papers) and Cellular transport and secretion (9 papers). Masanobu Deshimaru collaborates with scholars based in Japan, Taiwan and Malaysia. Masanobu Deshimaru's co-authors include Tomohisa Ogawa, Ikuo Nobuhisa, Yasuyuki Fukumaki, Yasuyuki Shimohigashi, Shigeyuki Terada, Motonori Ohno, Kinichi Nakashima, Takahito Chijiwa, Shôsaku Hattori and Yoshiyuki Sakaki and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Chemical Communications.

In The Last Decade

Masanobu Deshimaru

42 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masanobu Deshimaru Japan 19 819 667 241 167 129 42 1.1k
Márcia Helena Borges Brazil 21 816 1.0× 609 0.9× 245 1.0× 142 0.9× 25 0.2× 48 1.2k
Suely G. Figueiredo Brazil 24 837 1.0× 770 1.2× 99 0.4× 247 1.5× 31 0.2× 57 1.4k
Carole Fruchart‐Gaillard France 20 420 0.5× 850 1.3× 106 0.4× 55 0.3× 47 0.4× 36 1.2k
Léa Rodrigues‐Simioni Brazil 28 2.1k 2.5× 1.3k 1.9× 688 2.9× 621 3.7× 119 0.9× 104 2.3k
Marcelo Ribeiro Vasconcelos Diniz Brazil 13 596 0.7× 389 0.6× 194 0.8× 117 0.7× 51 0.4× 23 688
J.R. Giglio Brazil 19 775 0.9× 595 0.9× 197 0.8× 162 1.0× 12 0.1× 27 938
Nobuhiro Murayama Japan 16 436 0.5× 418 0.6× 109 0.5× 52 0.3× 31 0.2× 32 801
Sílvia Helena Andrião-Escarso Brazil 13 759 0.9× 483 0.7× 210 0.9× 196 1.2× 21 0.2× 17 842
Yan Guang-mei China 11 277 0.3× 330 0.5× 89 0.4× 62 0.4× 39 0.3× 29 615
F. Ducancel France 12 371 0.5× 486 0.7× 57 0.2× 41 0.2× 32 0.2× 18 653

Countries citing papers authored by Masanobu Deshimaru

Since Specialization
Citations

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

Fields of papers citing papers by Masanobu Deshimaru

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masanobu Deshimaru

This figure shows the co-authorship network connecting the top 25 collaborators of Masanobu Deshimaru. A scholar is included among the top collaborators of Masanobu Deshimaru 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 Masanobu Deshimaru. Masanobu Deshimaru 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.
Deshimaru, Masanobu, Kaori Kubota, Takuya Watanabe, et al.. (2023). Astrocyte Ca2+ signaling is facilitated in Scn1a+/− mouse model of Dravet syndrome. Biochemical and Biophysical Research Communications. 643. 169–174. 6 indexed citations
2.
Deshimaru, Masanobu, et al.. (2022). Precursor genes of Bowman-Birk-type serine proteinase inhibitors comprise multiple inhibitory domains to promote diversity. Biochimica et Biophysica Acta (BBA) - General Subjects. 1867(1). 130248–130248. 3 indexed citations
3.
Kawano, Hiroyuki, Masanobu Deshimaru, Kaori Kubota, et al.. (2021). Inhibitory synaptic transmission is impaired at higher extracellular Ca2+ concentrations in Scn1a+/− mouse model of Dravet syndrome. Scientific Reports. 11(1). 10634–10634. 11 indexed citations
4.
Deshimaru, Masanobu, et al.. (2016). Retigabine, a Kv7.2/Kv7.3-Channel Opener, Attenuates Drug-Induced Seizures in Knock-In Mice Harboring Kcnq2 Mutations. PLoS ONE. 11(2). e0150095–e0150095. 64 indexed citations
5.
6.
Terada, Shigeyuki, et al.. (2013). Structural Organization and Evolution of a Cluster of Small Serum Protein Genes of Protobothrops Flavoviridis Snake. 43(1). 59–66. 1 indexed citations
7.
Kuroki, Kimiko, et al.. (2008). Serotriflin, a CRISP family protein with binding affinity for small serum protein-2 in snake serum. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1784(4). 621–628. 18 indexed citations
8.
Matsuo, H, et al.. (2008). Accelerated evolution of small serum proteins (SSPs)—The PSP94 family proteins in a Japanese viper. Gene. 426(1-2). 7–14. 15 indexed citations
9.
Deshimaru, Masanobu, et al.. (2007). Identification of novel serum proteins in a Japanese viper: Homologs of mammalian PSP94. Biochemical and Biophysical Research Communications. 359(2). 330–334. 25 indexed citations
10.
Deshimaru, Masanobu, Ayako Tani, Takahito Chijiwa, et al.. (2005). Purification, primary structures and evolution of coagulant proteases from Deinagkistrodon actus venom. Toxicon. 46(8). 907–917. 7 indexed citations
11.
Deshimaru, Masanobu, et al.. (2003). Efficient Purification of an Antihemorrhagic Factor (HSF) in Serum of Japanese Habu (Trimeresurus flavoviridis). 33(2). 45–53. 1 indexed citations
12.
Deshimaru, Masanobu & Shigeyuki Terada. (2003). Chromatographic separation of brevilysins, metalloproteinases in Chinese Mamushi (Gloydius halys brevicaudus) venom. 33(2). 37–43. 3 indexed citations
13.
Ogawa, Tomohisa, et al.. (2003). Interisland Mutation of a Novel Phospholipase A2 from Trimeresurus flavoviridis Venom and Evolution of Crotalinae Group II Phospholipases A2. Journal of Molecular Evolution. 57(5). 546–554. 32 indexed citations
14.
Chijiwa, Takahito, Yoko Yamaguchi, Tomohisa Ogawa, et al.. (2003). Interisland Evolution of Trimeresurus flavoviridis Venom Phospholipase A 2 Isozymes. Journal of Molecular Evolution. 56(3). 286–293. 45 indexed citations
15.
Tani, Ayako, Tomohisa Ogawa, Takeru Nose, et al.. (2002). Characterization, primary structure and molecular evolution of anticoagulant protein from Agkistrodon actus venom. Toxicon. 40(6). 803–813. 29 indexed citations
16.
Higuchi, Shigesada, Nobuhiro Murayama, Ken‐ichi Saguchi, et al.. (1999). Bradykinin-potentiating peptides and C-type natriuretic peptides from snake venom. Immunopharmacology. 44(1-2). 129–135. 64 indexed citations
17.
Nobuhisa, Ikuo, Tomohisa Ogawa, Masanobu Deshimaru, et al.. (1998). Retrotransposable CR1-like elements in crotalinae snake genomes. Toxicon. 36(6). 915–920. 18 indexed citations
18.
Nobuhisa, Ikuo, Masanobu Deshimaru, Takahito Chijiwa, et al.. (1997). Structures of genes encoding phospholipase A2 inhibitors from the serum of Trimeresurus flavoviridis snake. Gene. 191(1). 31–37. 23 indexed citations
19.
Deshimaru, Masanobu, Tomohisa Ogawa, Kinichi Nakashima, et al.. (1996). Accelerated evolution of crotalinae snake venom gland serine proteases. FEBS Letters. 397(1). 83–88. 143 indexed citations
20.
Arimori, Kazuhiko, Masanobu Deshimaru, Eri Furukawa, & Masahiro Nakano. (1993). Adsorption of Mexiletine onto Activated Charcoal in Macrogol-electrolyte Solution.. Chemical and Pharmaceutical Bulletin. 41(4). 766–768. 11 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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