What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Cytokine
His scientific interests lie mostly in Cell biology, Molecular biology, Tumor necrosis factor alpha, Receptor and Lymphotoxin beta receptor.
His work deals with themes such as Immunology, Immune system, Lymphotoxin and Programmed cell death, which intersect with Cell biology.
His Molecular biology study incorporates themes from NFKB1, T cell, Cytotoxic T cell and Cell culture.
Carl F. Ware combines subjects such as Cell and Cytokine with his study of Tumor necrosis factor alpha.
His Receptor research incorporates themes from B-cell activating factor and MAPK/ERK pathway.
His work carried out in the field of Lymphotoxin beta receptor brings together such families of science as Central tolerance, Autoimmunity, Autoimmune regulator, Lymphotoxin alpha and Fusion protein.
His most cited work include:
- Cell-autonomous Fas (CD95)/Fas-ligand interaction mediates activation-induced apoptosis in T-cell hybridomas (1218 citations)
- The Epstein-Barr virus transforming protein LMP1 engages signaling proteins for the tumor necrosis factor receptor family (914 citations)
- The Lymphotoxin-β Receptor Induces Different Patterns of Gene Expression via Two NF-κB Pathways (795 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Cell biology, Immunology, Tumor necrosis factor alpha, Receptor and Lymphotoxin.
His Signal transduction and Effector study in the realm of Cell biology connects with subjects such as Herpesvirus entry mediator.
His work in Immunology covers topics such as Cytotoxic T cell which are related to areas like CD8, Antigen and Lymphokine.
His biological study spans a wide range of topics, including Cell, Cancer research, Cytokine, Inflammation and Apoptosis.
Receptor is closely attributed to Molecular biology in his study.
His Lymphotoxin research is multidisciplinary, incorporating elements of Stromal cell and Lymphatic system.
He most often published in these fields:
- Cell biology (41.67%)
- Immunology (36.31%)
- Tumor necrosis factor alpha (26.79%)
What were the highlights of his more recent work (between 2014-2021)?
- Immune system (21.73%)
- Cell biology (41.67%)
- Immunology (36.31%)
In recent papers he was focusing on the following fields of study:
Carl F. Ware spends much of his time researching Immune system, Cell biology, Immunology, Tumor necrosis factor alpha and Cancer research.
The various areas that Carl F. Ware examines in his Immune system study include Antibody, B cell, Antigen and Cytokine.
The Cell biology study combines topics in areas such as BTLA and Innate lymphoid cell.
His study in Lymphotoxin, Lymphotoxin beta receptor, Inflammation, Lymphotoxin beta and Autoimmunity falls under the purview of Immunology.
His Tumor necrosis factor alpha research integrates issues from Cytotoxic T cell, Receptor and Immunotherapy.
Carl F. Ware interconnects CCL5, Chemokine, Bone metastasis, Lung cancer and Programmed cell death in the investigation of issues within Cancer research.
Between 2014 and 2021, his most popular works were:
- The TNF Receptor Superfamily in Co-stimulating and Co-inhibitory Responses (163 citations)
- A signature of circulating inflammatory proteins and development of end-stage renal disease in diabetes. (85 citations)
- Structure of a HOIP/E2~ubiquitin complex reveals RBR E3 ligase mechanism and regulation (84 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
Carl F. Ware mainly investigates Immunology, Cell biology, Immune system, Cancer research and T cell.
Lymphotoxin beta receptor, Lymphotoxin beta, Lymphotoxin, Interferon type I and Spleen are subfields of Immunology in which his conducts study.
Carl F. Ware is studying Signal transduction, which is a component of Cell biology.
The study of Immune system is intertwined with the study of Tumor necrosis factor alpha in a number of ways.
His Cancer research study integrates concerns from other disciplines, such as Fibrosis, Chemokine, Programmed cell death and Tumor initiation.
He has researched T cell in several fields, including Tumor microenvironment, FOXP3 and High endothelial venules.
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