His main research concerns Cell biology, Osteoclast, Bone resorption, Immunology and Haematopoiesis. His studies in Cell biology integrate themes in fields like Cell culture, Cell, Potassium channel, Pathology and Receptor. The subject of his Osteoclast research is within the realm of Biochemistry.
Masaru Ishii combines subjects such as Preclinical imaging, Macrophage colony-stimulating factor, Bisphosphonate, Monocyte and Cartilage with his study of Bone resorption. His Immunology study combines topics in areas such as Positive chemotaxis, Chemotaxis, Macrophage and Bone remodeling. The Haematopoiesis study combines topics in areas such as Cell migration, T lymphocyte, Inflammation, Intravital microscopy and Giant cell.
Masaru Ishii mainly focuses on Cell biology, Lightning, Osteoclast, Electrical engineering and In vivo. His research in Cell biology intersects with topics in Immunology, Bone marrow and Cell. His study looks at the relationship between Lightning and fields such as Transmission line, as well as how they intersect with chemical problems.
His Osteoclast research incorporates themes from Osteoporosis, Cellular differentiation, Bone remodeling and Bone resorption. Masaru Ishii combines subjects such as Impulse and Electronic engineering with his study of Electrical engineering. His work in In vivo addresses issues such as Pathology, which are connected to fields such as Haematopoiesis.
Masaru Ishii focuses on Cell biology, In vivo, Osteoclast, Intravital Imaging and Bone marrow. Masaru Ishii does research in Cell biology, focusing on Homeostasis specifically. His work deals with themes such as Two-photon excitation microscopy, Dynamics, Cellular dynamics, Bone resorption and Pathology, which intersect with In vivo.
His Osteoclast study incorporates themes from Paracrine signalling, Arthritis, Transcription factor, Folliculin and Pharmacology. His studies deal with areas such as Intravital microscopy and Biomedical engineering as well as Intravital Imaging. His Bone marrow research integrates issues from Haematopoiesis, Stem cell, Cancer research, Leukemia and Mesenchymal stem cell.
His primary areas of investigation include Cell biology, Osteoclast, In vivo, Bone resorption and Cell. Cell biology and Purinergic signalling are two areas of study in which Masaru Ishii engages in interdisciplinary research. His Osteoclast research includes themes of Multiphoton fluorescence microscope, Bone remodeling and Fluorescence-lifetime imaging microscopy.
Masaru Ishii interconnects Process, Cell type and Two-photon excitation microscopy in the investigation of issues within In vivo. The various areas that he examines in his Bone resorption study include Osteoporosis, Molecular imaging, Cellular differentiation and Osteoblast. Masaru Ishii has researched Cell in several fields, including Biophysics, Fluorescence, Function and Dynamics.
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Layer V cortical neurons require microglial support for survival during postnatal development
Masaki Ueno;Yuki Fujita;Tatsuhide Tanaka;Tatsuhide Tanaka;Yuka Nakamura.
Nature Neuroscience (2013)
Sphingosine-1-phosphate mobilizes osteoclast precursors and regulates bone homeostasis
Masaru Ishii;Jackson G. Egen;Frederick Klauschen;Martin Meier-Schellersheim.
Nature (2009)
The sphingosine-1-phosphate transporter Spns2 expressed on endothelial cells regulates lymphocyte trafficking in mice
Shigetomo Fukuhara;Szandor Simmons;Shunsuke Kawamura;Asuka Inoue.
Journal of Clinical Investigation (2012)
Plexin-A1 and its interaction with DAP12 in immune responses and bone homeostasis.
Noriko Takegahara;Hyota Takamatsu;Toshihiko Toyofuku;Tohru Tsujimura.
Nature Cell Biology (2006)
Expression and Clustered Distribution of an Inwardly Rectifying Potassium Channel, KAB-2/Kir4.1, on Mammalian Retinal Müller Cell Membrane: Their Regulation by Insulin and Laminin Signals
Masaru Ishii;Yoshiyuki Horio;Yoshihiko Tada;Hiroshi Hibino.
The Journal of Neuroscience (1997)
PDGFRα-positive cells in bone marrow are mobilized by high mobility group box 1 (HMGB1) to regenerate injured epithelia
Katsuto Tamai;Takehiko Yamazaki;Takenao Chino;Masaru Ishii.
Proceedings of the National Academy of Sciences of the United States of America (2011)
Chemorepulsion by blood S1P regulates osteoclast precursor mobilization and bone remodeling in vivo
Masaru Ishii;Masaru Ishii;Junichi Kikuta;Yutaka Shimazu;Martin Meier-Schellersheim.
Journal of Experimental Medicine (2010)
Muscarinic acetylcholine receptors.
Masaru Ishii;Yoshihisa Kurachi.
Current Pharmaceutical Design (2006)
Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene
Masakatsu Watanabe;Motoko Iwashita;Masaru Ishii;Yoshihisa Kurachi.
EMBO Reports (2006)
Dynamic visualization of RANKL and Th17-mediated osteoclast function
Junichi Kikuta;Yoh Wada;Toshiyuki Kowada;Ze Wang.
Journal of Clinical Investigation (2013)
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