D-Index & Metrics Best Publications

Masaki Inagaki

Mie University
Japan

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Molecular Biology D-index 83 Citations 25,107 243 World Ranking 551 National Ranking 43

Overview

What is he best known for?

The fields of study Masaki Inagaki is best known for:

Gene
Mitosis
Cytoskeleton

His research on Cell biology often connects related topics like Microtubule. His research ties Cell biology and Microtubule together. Many of his studies on Biochemistry apply to Rho-associated protein kinase as well. His study in Biochemistry extends to Rho-associated protein kinase with its themes. His research brings together the fields of Aurora B kinase and Cell. Masaki Inagaki regularly ties together related areas like Cell in his Aurora B kinase studies. He connects Phosphorylation with Signal transduction in his research. He undertakes multidisciplinary investigations into Signal transduction and Phosphorylation in his work. Kinase and Protein kinase A are two areas of study in which he engages in interdisciplinary work.

His most cited work include:

Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide-dependent protein kinase and protein kinase C (2699 citations)
Biochemical and Cellular Effects of Roscovitine, a Potent and Selective Inhibitor of the Cyclin-Dependent Kinases cdc2, cdk2 and cdk5 (1242 citations)
Phosphorylation of Myosin-Binding Subunit (Mbs) of Myosin Phosphatase by Rho-Kinase in Vivo (521 citations)

What are the main themes of his work throughout his whole career to date

Much of his study explores Cell biology relationship to Signal transduction. Signal transduction is closely attributed to Cell biology in his work. Masaki Inagaki integrates Biochemistry with Enzyme in his study. He merges Enzyme with Biochemistry in his research. His study brings together the fields of Cytokinesis and Cell. His Cytokinesis study often links to related topics such as Cell division. His research links Cell with Cell division. He conducts interdisciplinary study in the fields of Phosphorylation and Cytoskeleton through his works. In his works, he performs multidisciplinary study on Cytoskeleton and Phosphorylation.

Masaki Inagaki most often published in these fields:

Cell biology (84.92%)
Biochemistry (72.63%)
Cell (55.31%)

What were the highlights of his more recent work (between 2016-2021)?

Cell biology (94.44%)
Genetics (66.67%)
Gene (50.00%)

In recent works Masaki Inagaki was focusing on the following fields of study:

Cell biology and Molecular biology are two areas of study in which Masaki Inagaki engages in interdisciplinary research. While working on this project, Masaki Inagaki studies both Molecular biology and Cell biology. His research on Genetics frequently links to adjacent areas such as Microtubule. Microtubule is often connected to Genetics in his work. His multidisciplinary approach integrates Gene and Chromosome in his work. He undertakes multidisciplinary studies into Chromosome and Gene in his work. He incorporates Signal transduction and Protein kinase B in his studies. Masaki Inagaki performs multidisciplinary study on Protein kinase B and Signal transduction in his works. He performs multidisciplinary study on Cilium and Centrosome in his works.

Between 2016 and 2021, his most popular works were:

Mechanisms of ciliogenesis suppression in dividing cells (54 citations)
Primary Cilia as Signaling Hubs in Health and Disease (46 citations)
EGF receptor kinase suppresses ciliogenesis through activation of USP8 deubiquitinase (45 citations)

In his most recent research, the most cited works focused on:

Gene
Cell cycle
DNA

His Genetics study frequently involves adjacent topics like Morphogen. His Cell biology study frequently draws connections between related disciplines such as Kinase. Kinase and Signal transduction are two areas of study in which Masaki Inagaki engages in interdisciplinary research. In his works, he performs multidisciplinary study on Signal transduction and Morphogen. Borrowing concepts from Phosphorylation, Masaki Inagaki weaves in ideas under Gene. The study of Phosphorylation is intertwined with the study of Cell biology in a number of ways. Cilium is often connected to Motile cilium in his work. His Motile cilium study often links to related topics such as Cilium. His research combines Function (biology) and Ciliogenesis.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide dependent protein kinase and protein kinase C.

Hiroyoshi Hidaka;Masaki Inagaki;Sachiyo Kawamoto;Yasuharu Sasaki.
Biochemistry (1984)

4545 Citations

Biochemical and Cellular Effects of Roscovitine, a Potent and Selective Inhibitor of the Cyclin‐Dependent Kinases cdc2, cdk2 and cdk5

Laurent Meijer;Annie Borgne;Odile Mulner;James P.J. Chong.
FEBS Journal (1997)

1579 Citations

Phosphorylation of Myosin-Binding Subunit (Mbs) of Myosin Phosphatase by Rho-Kinase in Vivo

Yoji Kawano;Yuko Fukata;Noriko Oshiro;Mutsuki Amano.
Journal of Cell Biology (1999)

709 Citations

Identification of a novel phosphorylation site on histone H3 coupled with mitotic chromosome condensation.

Hidemasa Goto;Yasuko Tomono;Kozo Ajiro;Hidetaka Kosako.
Journal of Biological Chemistry (1999)

622 Citations

Site-specific phosphorylation induces disassembly of vimentin filaments in vitro.

Masaki Inagaki;Yoshimi Nishi;Kimiko Nishizawa;Mutsushi Matsuyama.
Nature (1987)

602 Citations

Tissue-specific expression of three distinct types of rabbit protein kinase C

Shigeo Ohno;Hiroshi Kawasaki;Shinobu Imajoh;Koichi Suzuki.
Nature (1987)

538 Citations

Requirement of phosphatidylinositol 4,5-bisphosphate for alpha-actinin function.

Kiyoko Fukami;Kiyoshi Furuhashi;Masaki Inagaki;Takeshi Endo.
Nature (1992)

448 Citations

Aurora-B phosphorylates Histone H3 at serine28 with regard to the mitotic chromosome condensation.

Hidemasa Goto;Yoshihiro Yasui;Erich A. Nigg;Masaki Inagaki.
Genes to Cells (2002)

405 Citations

Phosphorylation by Aurora B Converts MgcRacGAP to a RhoGAP during Cytokinesis

Yukinori Minoshima;Toshiyuki Kawashima;Koichi Hirose;Koichi Hirose;Yukio Tonozuka.
Developmental Cell (2003)

371 Citations

PKCε‐mediated phosphorylation of vimentin controls integrin recycling and motility

Johanna Ivaska;Karoliina Vuoriluoto;Tuomas Huovinen;Ichiro Izawa.
The EMBO Journal (2005)

312 Citations

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