T cell, Cell biology, Immunology, Cytotoxic T cell and Antigen-presenting cell are his primary areas of study. His work in T cell tackles topics such as Apoptosis which are related to areas like Intracellular. His study in Cell biology is interdisciplinary in nature, drawing from both Receptor, Cytokine and T-cell receptor.
His study connects CD40 and Immunology. His Cytotoxic T cell research is multidisciplinary, incorporating perspectives in Priming and CD8. As a part of the same scientific family, he mostly works in the field of Antigen-presenting cell, focusing on Molecular biology and, on occasion, Dendritic cell, Leukotriene E4, Leukotriene D4 and Leukotriene.
The scientist’s investigation covers issues in Immunology, Cell biology, T cell, Cytotoxic T cell and Immune system. His Immunology study frequently draws connections to adjacent fields such as CD40. His Cell biology study incorporates themes from CD28, Receptor and T-cell receptor.
In general T cell study, his work on CD134 and Naive T cell often relates to the realm of Cellular differentiation and Population, thereby connecting several areas of interest. The various areas that Michael Croft examines in his Cytotoxic T cell study include CD8 and Virology. His Antigen-presenting cell research is multidisciplinary, incorporating elements of Molecular biology, Interleukin 12, Priming and Antigen presentation.
His primary areas of study are Cancer research, Immunology, Inflammation, Tumor necrosis factor alpha and Receptor. His study in Allergen, T cell, Hepatitis B, Innate immune system and Hepatitis B virus is carried out as part of his studies in Immunology. His research links CD40 with T cell.
His work deals with themes such as Bronchoalveolar lavage, Signal transduction, Cytokine and Hepatocyte, which intersect with Inflammation. His Receptor research is multidisciplinary, relying on both Intramolecular force and Cell biology. Michael Croft combines subjects such as Transfection and Conditional gene knockout with his study of Cell biology.
Michael Croft mostly deals with Tumor necrosis factor alpha, Immunology, Cancer research, Cytotoxic T cell and Receptor. His work deals with themes such as Liver injury and CD40, which intersect with Immunology. His Cancer research study combines topics in areas such as Cancer, Cytokine, Lymphotoxin, Monoclonal and Inflammation.
Michael Croft interconnects Humanized mouse, Tumor necrosis factor receptor 2, Antibody and Cancer immunotherapy in the investigation of issues within Cytotoxic T cell. His Receptor study combines topics from a wide range of disciplines, such as Protein structure, CD137, Binding site and Protein–protein interaction. His specific area of interest is T cell, where Michael Croft studies IL-2 receptor.
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.
Co-stimulatory members of the TNFR family: keys to effective T-cell immunity?
Michael Croft.
Nature Reviews Immunology (2003)
The role of TNF superfamily members in T-cell function and diseases
Michael Croft.
Nature Reviews Immunology (2009)
Ox-40 Ligand: A Potent Costimulatory Molecule for Sustaining Primary CD4 T Cell Responses
Irene Gramaglia;Andrew D. Weinberg;Michael Lemon;Michael Croft.
Journal of Immunology (1998)
Naive versus memory CD4 T cell response to antigen. Memory cells are less dependent on accessory cell costimulation and can respond to many antigen-presenting cell types including resting B cells.
M Croft;L M Bradley;S L Swain.
Journal of Immunology (1994)
Generation of polarized antigen-specific CD8 effector populations: reciprocal action of interleukin (IL)-4 and IL-12 in promoting type 2 versus type 1 cytokine profiles.
Michael Croft;Laura Carter;Susan L. Swain;Richard W. Dutton.
Journal of Experimental Medicine (1994)
OX40 promotes Bcl-xL and Bcl-2 expression and is essential for long-term survival of CD4 T cells.
Paul R Rogers;Jianxun Song;Irene Gramaglia;Nigel Killeen.
Immunity (2001)
Control of Immunity by the TNFR-Related Molecule OX40 (CD134)
Michael Croft.
Annual Review of Immunology (2010)
The OX40 costimulatory receptor determines the development of CD4 memory by regulating primary clonal expansion.
Irene Gramaglia;Amha Jember;Susanne D. Pippig;Andrew D. Weinberg.
Journal of Immunology (2000)
The Significance of OX40 and OX40L to T cell Biology and Immune Disease
Michael Croft;Takanori So;Wei Duan;Pejman Soroosh.
Immunological Reviews (2009)
Helper T-cell subsets: phenotype, function and the role of lymphokines in regulating their development.
Susan L. Swain;Linda M. Bradley;Michael Croft;Susan Tonkonogy.
Immunological Reviews (1991)
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:
Discovery Institute
University of California, San Diego
University of Massachusetts Medical School
Tulane University
La Jolla Institute For Allergy & Immunology
La Jolla Institute For Allergy & Immunology
La Jolla Institute For Allergy & Immunology
La Jolla Institute For Allergy & Immunology
Columbia University
La Jolla Institute For Allergy & Immunology
Microsoft Research Asia (China)
Carnegie Mellon University
Baqiyatallah University of Medical Sciences
University of Perugia
University of California, Los Angeles
Tsinghua University
Montana State University
University of Pittsburgh
Australian National University
Freie Universität Berlin
Istituto Neurologico Carlo Besta
Mexican Social Security Institute
Montreal Neurological Institute and Hospital
Rush University Medical Center
Catholic University of America
University of British Columbia