His primary areas of investigation include Cell adhesion molecule, Molecular biology, Cell biology, Antigen and Cell adhesion. His Cell adhesion molecule research includes themes of Endothelial stem cell, E-selectin, Extravasation and Cell–cell interaction. Takashi Kei Kishimoto interconnects Inflammation, Interleukin 8, In vitro and Chinese hamster ovary cell in the investigation of issues within Cell biology.
His Antigen study deals with the bigger picture of Immunology. His Cell adhesion research also works with subjects such as
His main research concerns Immunology, Antigen, Cell biology, Molecular biology and Cell adhesion molecule. His Antigen research is multidisciplinary, incorporating perspectives in Lymphocyte, Adjuvant, Antibody and Extravasation. The study incorporates disciplines such as Inflammation, Human umbilical vein endothelial cell, IL-2 receptor and Integrin in addition to Cell biology.
His research in Molecular biology intersects with topics in Ex vivo, Neutrophil extracellular traps, Peptide sequence, Monoclonal antibody and Cell–cell interaction. His Cell adhesion molecule research incorporates themes from Endothelial stem cell and Lymphocyte homing receptor, Cell adhesion, E-selectin. His T lymphocyte research focuses on COS cells and how it connects with Addressin.
Takashi Kei Kishimoto mostly deals with Immunology, Antigen, Immune system, Antibody and Immune tolerance. His work deals with themes such as Pharmacology and Cell biology, which intersect with Immunology. In his research, Immunogenicity is intimately related to Adjuvant, which falls under the overarching field of Antigen.
Takashi Kei Kishimoto works mostly in the field of Immune system, limiting it down to topics relating to Nanocarriers and, in certain cases, Dosing and Immune checkpoint inhibitors, as a part of the same area of interest. His work carried out in the field of Antibody brings together such families of science as Endothelial stem cell, Human neutrophil, In vitro and Molecular biology. Takashi Kei Kishimoto combines subjects such as Experimental autoimmune encephalomyelitis, Monoclonal antibody, Drug and Immunotherapy with his study of Immune tolerance.
His primary areas of study are Antigen, Immunology, Immune tolerance, Antibody and Immune system. Takashi Kei Kishimoto has researched Antigen in several fields, including Adjuvant, T cell and Virology. His study explores the link between Immune tolerance and topics such as Experimental autoimmune encephalomyelitis that cross with problems in Adoptive cell transfer.
His Antibody research includes elements of Tumor necrosis factor alpha, Cancer research, Transgene and Recombinant DNA. His Immunotherapy study in the realm of Immune system connects with subjects such as Therapeutic protein. The various areas that he examines in his Immunogenicity study include IL-2 receptor and Cell biology.
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Neutrophil Mac-1 and MEL-14 adhesion proteins inversely regulated by chemotactic factors
Takashi Kei Kishimoto;Mark A. Jutila;Ellen Lakey Berg;Eugene C. Butcher.
ELAM-1 is an adhesion molecule for skin-homing T cells
Louis J. Picker;Louis J. Picker;Louis J. Picker;Takashi K. Kishimoto;Takashi K. Kishimoto;C. Wayne Smith;R. Aaron Warnock;R. Aaron Warnock.
Contaminated heparin associated with adverse clinical events and activation of the contact system.
Takashi Kei Kishimoto;Karthik Viswanathan;Tanmoy Ganguly;Subbiah Elankumaran.
The New England Journal of Medicine (2008)
The cutaneous lymphocyte antigen is a skin lymphocyte homing receptor for the vascular lectin endothelial cell-leukocyte adhesion molecule 1
E L Berg;T Yoshino;L S Rott;M K Robinson.
Journal of Experimental Medicine (1991)
Chemotactic factors regulate lectin adhesion molecule 1 (LECAM-1)-dependent neutrophil adhesion to cytokine-stimulated endothelial cells in vitro.
C W Smith;T K Kishimoto;O Abbassi;B Hughes.
Journal of Clinical Investigation (1991)
Identification of a human peripheral lymph node homing receptor: a rapidly down-regulated adhesion molecule
Takashi Kei Kishimoto;Mark A. Jutila;Eugene C. Butcher.
Proceedings of the National Academy of Sciences of the United States of America (1990)
Diverse Cell Surface Protein Ectodomains Are Shed by a System Sensitive to Metalloprotease Inhibitors
Joaquin Arribas;Lavanya Coodly;Petra Vollmer;Takashi Kei Kishimoto.
Journal of Biological Chemistry (1996)
Neutrophil-neutrophil interactions under hydrodynamic shear stress involve L-selectin and PSGL-1. A mechanism that amplifies initial leukocyte accumulation of P-selectin in vitro.
Bruce Walcheck;Kevin L. Moore;Kevin L. Moore;Rodger P. McEver;Rodger P. McEver;Takashi Kei Kishimoto.
Journal of Clinical Investigation (1996)
E-selectin supports neutrophil rolling in vitro under conditions of flow.
Omid Abbassi;T. K. Kishimoto;L. V. Mcintire;D. C. Anderson.
Journal of Clinical Investigation (1993)
Neutrophil rolling altered by inhibition of L-selectin shedding in vitro.
B. Walcheck;J. Kahn;J. M. Fisher;B. B. Wang.
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