What is she best known for?
The fields of study she is best known for:
- Gene
- Immune system
- Cytokine
Her primary areas of study are Cell biology, Cellular differentiation, Immunology, Interleukin 12 and Molecular biology.
Her work carried out in the field of Cell biology brings together such families of science as Cytokine, T cell, FGF and mesoderm formation, Gastrulation and Receptor.
Theresa L. Murphy focuses mostly in the field of Cellular differentiation, narrowing it down to topics relating to BATF and, in certain cases, Activator and Interferon regulatory factors.
The Interleukin 12 study combines topics in areas such as STAT4, Immune system, Interleukin 10, Microbiology and Monocyte.
Her studies in STAT4 integrate themes in fields like Signal transduction and Interleukin 4.
She combines subjects such as Interleukin 2 and CTLA-4 with her study of Molecular biology.
Her most cited work include:
- Interleukin 17–producing CD4 + effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages (3778 citations)
- Batf3 Deficiency Reveals a Critical Role for CD8α+ Dendritic Cells in Cytotoxic T Cell Immunity (1245 citations)
- T-bet is a STAT1-induced regulator of IL-12R expression in naïve CD4 + T cells (845 citations)
What are the main themes of her work throughout her whole career to date?
Theresa L. Murphy mostly deals with Cell biology, Immunology, Molecular biology, T cell and Antigen.
Her Cell biology research incorporates themes from Dendritic cell, Transcription factor and Cellular differentiation.
Immunology and Cytotoxic T cell are frequently intertwined in her study.
Within one scientific family, she focuses on topics pertaining to STAT4 under Molecular biology, and may sometimes address concerns connected to Interleukin 12, Signal transduction, STAT1, Interferon and Phosphorylation.
Her research investigates the link between Interleukin 12 and topics such as Interleukin 21 that cross with problems in IL-2 receptor.
Her T cell course of study focuses on Priming and T-cell receptor.
She most often published in these fields:
- Cell biology (46.67%)
- Immunology (34.29%)
- Molecular biology (24.76%)
What were the highlights of her more recent work (between 2014-2021)?
- Cell biology (46.67%)
- Antigen (19.05%)
- Transcription factor (18.10%)
In recent papers she was focusing on the following fields of study:
Her scientific interests lie mostly in Cell biology, Antigen, Transcription factor, Dendritic cell and CD8.
Her work in Cell biology addresses subjects such as Enhancer, which are connected to disciplines such as Chromatin.
Her Antigen study is concerned with the larger field of Immunology.
In general Transcription factor, her work in IRF8 is often linked to Cyclin-dependent kinase 1 linking many areas of study.
Her Dendritic cell research is multidisciplinary, incorporating elements of Regulation of gene expression and Cancer research.
She has researched CD8 in several fields, including Acquired immune system, Cytotoxic T cell, Immunity and Toxoplasma gondii.
Between 2014 and 2021, her most popular works were:
- Transcriptional Control of Dendritic Cell Development (257 citations)
- Klf4 Expression in Conventional Dendritic Cells Is Required for T Helper 2 Cell Responses (205 citations)
- Batf3 maintains autoactivation of Irf8 for commitment of a CD8α(+) conventional DC clonogenic progenitor (196 citations)
In her most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
Theresa L. Murphy focuses on Immunology, Antigen, IRF4, CD8 and IRF8.
The Toxoplasma gondii and Cross-presentation research she does as part of her general Immunology study is frequently linked to other disciplines of science, such as XCR1, therefore creating a link between diverse domains of science.
Her Antigen research includes themes of Cytotoxic T cell, KLF4 and CRISPR.
Her studies deal with areas such as Receptor, Major Histocompatibility Complex Class II, Transcription and Cross-priming as well as CD8.
Theresa L. Murphy works mostly in the field of IRF8, limiting it down to topics relating to Myelopoiesis and, in certain cases, Conventional Dendritic Cell, as a part of the same area of interest.
Her work in Conventional Dendritic Cell tackles topics such as Cellular differentiation which are related to areas like Cell biology.
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