What is he best known for?
The fields of study he is best known for:
- Immune system
- Antibody
- Cytokine
Yasuhiro Suzuki mainly investigates Immunology, Toxoplasma gondii, Toxoplasmosis, Necrosis and Interferon.
His Immunology study typically links adjacent topics like Genetic marker.
His Toxoplasma gondii research also works with subjects such as
- Cytokine together with CD8,
- Interferon gamma that connect with fields like Virology.
His Toxoplasmosis research also works with subjects such as
- Immunity together with Monoclonal antibody,
- Antibody, which have a strong connection to Lymphokine.
Much of his study explores Necrosis relationship to Small intestine.
His work focuses on many connections between Interferon and other disciplines, such as Tumor necrosis factor alpha, that overlap with his field of interest in Nitric oxide, B cell, Interleukin 10 and Polyclonal antibodies.
His most cited work include:
- Interferon-gamma: the major mediator of resistance against Toxoplasma gondii. (916 citations)
- Success and virulence in Toxoplasma as the result of sexual recombination between two distinct ancestries. (291 citations)
- Success and virulence in Toxoplasma as the result of sexual recombination between two distinct ancestries. (291 citations)
What are the main themes of his work throughout his whole career to date?
Yasuhiro Suzuki spends much of his time researching Toxoplasma gondii, Immunology, Immune system, Toxoplasmosis and Virology.
His research in Toxoplasma gondii intersects with topics in Necrosis, Chronic infection, CD8 and Interferon gamma.
His studies link Pathology with Immunology.
His Immune system research is multidisciplinary, relying on both Molecular biology and Microglia.
His Toxoplasmosis research includes elements of Agglutination, Titer, Atopy, Microbiology and Ratón.
He has researched Virology in several fields, including Recombinant DNA, Antigen and Virulence.
He most often published in these fields:
- Toxoplasma gondii (103.88%)
- Immunology (96.12%)
- Immune system (63.11%)
What were the highlights of his more recent work (between 2012-2021)?
- Immune system (63.11%)
- Toxoplasma gondii (103.88%)
- CD8 (28.16%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Immune system, Toxoplasma gondii, CD8, Immunology and Microglia.
His Immune system research incorporates elements of Cyst and Microbiology.
Yasuhiro Suzuki works mostly in the field of Toxoplasma gondii, limiting it down to concerns involving Innate immune system and, occasionally, Cell culture.
His research integrates issues of Epitope, T cell, Phagocyte and Virology in his study of CD8.
Yasuhiro Suzuki integrates Immunology with Preclinical imaging in his research.
Yasuhiro Suzuki combines subjects such as Toxoplasmosis, Antibody and Sulfadiazine with his study of Chronic infection.
Between 2012 and 2021, his most popular works were:
- IL-2 produced by CD8+ immune T cells can augment their IFN-γ production independently from their proliferation in the secondary response to an intracellular pathogen. (32 citations)
- Adjuvanted multi-epitope vaccines protect HLA-A*11:01 transgenic mice against Toxoplasma gondii (26 citations)
- CXCL9 is important for recruiting immune T cells into the brain and inducing an accumulation of the T cells to the areas of tachyzoite proliferation to prevent reactivation of chronic cerebral infection with Toxoplasma gondii. (25 citations)
In his most recent research, the most cited papers focused on:
- Immune system
- Gene
- Antibody
Yasuhiro Suzuki mainly focuses on Immune system, Toxoplasma gondii, Immunology, CD8 and Microglia.
His study in Immune system is interdisciplinary in nature, drawing from both Epitope, Antigen and Virology.
His work on Toxoplasma gondii is being expanded to include thematically relevant topics such as Major histocompatibility complex.
His CD8 research includes themes of Chronic infection, Toxoplasmosis, CXCL9 and Sulfadiazine.
The study incorporates disciplines such as Cell culture, Innate immune system, Interferon gamma and Bone marrow in addition to Microglia.
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