The scientist’s investigation covers issues in Immunology, Antigen, Cell biology, Molecular biology and Immune system. His Immunology study frequently draws parallels with other fields, such as Cytotoxic T cell. His studies in Antigen integrate themes in fields like Rhoptry neck, Antigen presentation and Antigen-presenting cell.
The various areas that Andrew M. Lew examines in his Cell biology study include Cytokine, CD8 and Cellular differentiation. Andrew M. Lew interconnects Surgery, T cell, GATA3 and Spleen in the investigation of issues within CD8. His Molecular biology study incorporates themes from Nucleic Acid Synthesis Inhibitor, Immunoglobulin G, Antiserum, Antibody and Ovalbumin.
Andrew M. Lew spends much of his time researching Immunology, Antigen, Molecular biology, Cell biology and Immune system. Andrew M. Lew has researched Immunology in several fields, including Cytotoxic T cell and Transplantation. His work focuses on many connections between Cytotoxic T cell and other disciplines, such as CD8, that overlap with his field of interest in CD40.
Virology is closely connected to Antibody in his research, which is encompassed under the umbrella topic of Antigen. His research in Molecular biology tackles topics such as DNA which are related to areas like Polymerase chain reaction. His biological study spans a wide range of topics, including Cytokine, Dendritic cell and Cellular differentiation.
Andrew M. Lew mainly investigates Immunology, Cell biology, Immune system, Cell type and Cellular differentiation. His Immunology study frequently links to adjacent areas such as Type 1 diabetes. His Cell biology study combines topics in areas such as Cell, Conventional Dendritic Cell and Antigen presentation.
His Dendritic cell study in the realm of Immune system connects with subjects such as Population and PDE4B. His work investigates the relationship between Cellular differentiation and topics such as Bone marrow that intersect with problems in CCR2 and Immunity. T cell and Antigen are commonly linked in his work.
His primary areas of investigation include Cell biology, Cell, T cell, Immunology and Immune system. His studies deal with areas such as Acquired immune system, Myeloid Cell Leukemia Sequence 1 Protein, Molecular biology, Bcl-2 family and Tissue culture as well as Cell biology. His T cell research incorporates elements of Tumor necrosis factor alpha, Cellular differentiation, Antigen and Tumor antigen, Immunotherapy.
He is interested in Dendritic cell, which is a branch of Antigen. His Immunology research incorporates themes from Secretion and Transgene. His study in Immune system is interdisciplinary in nature, drawing from both Immunopathology, Immunophenotyping, Signal transduction and Transplantation.
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.
Migratory dendritic cells transfer antigen to a lymph node-resident dendritic cell population for efficient CTL priming.
Rhys S. Allan;Jason Waithman;Sammy Bedoui;Claerwen M. Jones.
The dendritic cell subtype restricted C-type lectin Clec9A is a target for vaccine enhancement
Irina Caminschi;Anna I Proietto;Fatma Ahmet;Susie Kitsoulis.
The development, maturation, and turnover rate of mouse spleen dendritic cell populations.
Arun T. Kamath;Joanne Pooley;Meredith A. O’Keeffe;David Vremec.
Journal of Immunology (2000)
The need for IgG2c specific antiserum when isotyping antibodies from C57BL/6 and NOD mice
Roland M. Martin;Jamie L. Brady;Andrew M. Lew.
Journal of Immunological Methods (1998)
Developmental kinetics, turnover and stimulatory capacity of thymic epithelial cells
Daniel Herbert Donald Gray;Natalie Louise Seach;Tomoo Ueno;Morag Kertanya Milton.
Differential development of murine dendritic cells by GM-CSF versus Flt3 ligand has implications for inflammation and trafficking.
Yuekang Xu;Yuekang Xu;Yifan Zhan;Andrew M. Lew;Shalin H. Naik;Shalin H. Naik.
Journal of Immunology (2007)
Enhanced responses to a DNA vaccine encoding a fusion antigen that is directed to sites of immune induction
Boyle Js;Brady Jl;Lew Am;Lew Am.
Cell-associated ovalbumin is cross-presented much more efficiently than soluble ovalbumin in vivo.
Ming Li;Gayle M. Davey;Robyn M. Sutherland;Christian Kurts.
Journal of Immunology (2001)
Secretion of a malarial histidine-rich protein (Pf HRP II) from Plasmodium falciparum-infected erythrocytes.
R J Howard;S Uni;M Aikawa;S B Aley.
Journal of Cell Biology (1986)
CD8 T cell ignorance or tolerance to islet antigens depends on antigen dose
Christian Kurts;Robyn M. Sutherland;Gayle Davey;Ming Li.
Proceedings of the National Academy of Sciences of the United States of America (1999)
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: