Michael I. Nishimura mostly deals with Immunology, T cell, Antigen, T-cell receptor and Molecular biology. As a member of one scientific family, Michael I. Nishimura mostly works in the field of Immunology, focusing on Cancer and, on occasion, Oncology. Michael I. Nishimura has researched T cell in several fields, including Cytotoxic T cell, Major histocompatibility complex and Cell biology.
Epitope and MART-1 Antigen are the core of his Antigen study. His T-cell receptor research integrates issues from Cancer research and Tumor antigen. His Molecular biology study incorporates themes from Interleukin 21 and CTL*.
His primary areas of investigation include T cell, T-cell receptor, Immunology, Antigen and Cancer research. The T cell study combines topics in areas such as CTL*, CD8, Avidity and Effector. His studies deal with areas such as Molecular biology, Adoptive cell transfer, Receptor and Cell biology as well as T-cell receptor.
His Immunology research incorporates elements of Cytotoxic T cell and Cancer. He interconnects Virology, Melanoma and Immunotherapy in the investigation of issues within Antigen. The concepts of his Cancer research study are interwoven with issues in Protein kinase B, Cancer cell, Cancer immunotherapy, MHC class I and Cell therapy.
Michael I. Nishimura mainly investigates T cell, Cancer research, T-cell receptor, Immunotherapy and Adoptive cell transfer. T cell is a primary field of his research addressed under Immunology. His work on Immune system, Umbilical cord and Cord blood as part of general Immunology study is frequently connected to Interleukin 13, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
His research integrates issues of Cell therapy, Receptor, Transgene and Cell biology in his study of T-cell receptor. His studies examine the connections between Immunotherapy and genetics, as well as such issues in Melanoma, with regards to Cancer immunology, Immunologic evaluation, Chemotherapy and Clinical trial. His Adoptive cell transfer research is multidisciplinary, relying on both Tumor microenvironment and Interferon.
Michael I. Nishimura focuses on T cell, Cell biology, Immunotherapy, Cancer research and Adoptive cell transfer. Michael I. Nishimura studies T-cell receptor, a branch of T cell. The various areas that he examines in his Immunotherapy study include Combined Modality Therapy, Melanoma and Oncology.
His Cancer research research incorporates themes from FOXO1, Protein kinase B and Breast cancer, Triple-negative breast cancer. The Adoptive cell transfer study combines topics in areas such as Tumor microenvironment, Interferon, PI3K/AKT/mTOR pathway and Programmed cell death. His Antigen research is multidisciplinary, incorporating elements of Receptor and Plasma protein binding.
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.
Increased circulating myeloid-derived suppressor cells correlate with clinical cancer stage, metastatic tumor burden, and doxorubicin–cyclophosphamide chemotherapy
C. Marcela Diaz-Montero;Mohamed Labib Salem;Michael I. Nishimura;Elizabeth Garrett-Mayer.
Cancer Immunology, Immunotherapy (2009)
Cancer classification using the Immunoscore: a worldwide task force
Jérôme Galon;Franck Pagès;Francesco M Marincola;Francesco M Marincola;Helen K Angell;Helen K Angell.
Journal of Translational Medicine (2012)
Efficient Transfer of a Tumor Antigen-Reactive TCR to Human Peripheral Blood Lymphocytes Confers Anti-Tumor Reactivity
Timothy M. Clay;Mary C. Custer;Jessica Sachs;Patrick Hwu.
Journal of Immunology (1999)
Adoptive transfer of cloned melanoma-reactive T lymphocytes for the treatment of patients with metastatic melanoma
Mark E. Dudley;John Wunderlich;Michael I. Nishimura;David Yu.
Journal of Immunotherapy (2001)
Tim-3 expression on PD-1+ HCV-specific human CTLs is associated with viral persistence, and its blockade restores hepatocyte-directed in vitro cytotoxicity
Rachel H. McMahan;Lucy Golden-Mason;Michael I. Nishimura;Brian J. McMahon.
Journal of Clinical Investigation (2010)
Recognition of host immune activation by Pseudomonas aeruginosa
Licheng Wu;Oscar Estrada;Olga Zaborina;Manjeet Bains.
Science (2005)
Increasing tumor antigen expression overcomes "ignorance" to solid tumors via crosspresentation by bone marrow-derived stromal cells.
Michael T. Spiotto;Ping Yu;Donald A. Rowley;Michael I. Nishimura.
Immunity (2002)
Biochemical Identification of a Mutated Human Melanoma Antigen Recognized by CD4+ T Cells
Rembert Pieper;Robert E. Christian;Monica I. Gonzales;Michael I. Nishimura.
Journal of Experimental Medicine (1999)
Identification of epitope mimics recognized by CTL reactive to the melanoma/melanocyte-derived peptide MART-1((27-35))
Douglas J. Loftus;Chiara Castelli;Timothy M. Clay;Paola Squarcina.
Journal of Experimental Medicine (1996)
Defining the critical hurdles in cancer immunotherapy
Bernard A. Fox;Bernard A. Fox;Dolores J. Schendel;Lisa H. Butterfield;Steinar Aamdal.
Journal of Translational Medicine (2011)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
National Institutes of Health
Duke University
University of Southern California
Earle A. Chiles Research Institute
Johns Hopkins University
Keio University
University of Southern California
National Cancer Institute
Karolinska Institute
University Health Network
Worcester Polytechnic Institute
Lund University
Shanghai Jiao Tong University
University of Arizona
RWTH Aachen University
University of Connecticut
Chinese Academy of Sciences
East China University of Science and Technology
Linköping University
Radboud University Nijmegen
Texas Tech University
University of Technology Sydney
Sorbonne University
Oregon Health & Science University
University of California, Irvine
Chiba University