What is he best known for?
The fields of study he is best known for:
Yoshihide Tsujimoto mainly investigates Cell biology, Apoptosis, Programmed cell death, Cytochrome c and Mitochondrial apoptosis-induced channel.
His Cell biology research is multidisciplinary, relying on both Mitochondrial permeability transition pore, Bcl-2 family, Bcl-2-associated X protein and Voltage-dependent anion channel.
His Apoptosis study combines topics in areas such as Proteases, Membrane potential and Mitochondrion.
His studies deal with areas such as Molecular biology, Cytoplasm, Calcium and Phosphorylation as well as Mitochondrion.
His research integrates issues of Necrosis, Cell, Signal transduction and Immunology in his study of Programmed cell death.
His Mitochondrial apoptosis-induced channel study deals with Apoptosome intersecting with VDAC2, VDAC1 and Cyclosporin a.
His most cited work include:
- Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC (1954 citations)
- Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell death (1349 citations)
- Role of Bcl-2 family proteins in a non-apoptotic programmed cell death dependent on autophagy genes. (1153 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Apoptosis, Cell biology, Programmed cell death, Molecular biology and Mitochondrion.
His Apoptosis research includes themes of Cell culture and Cancer research.
His Cell biology research is multidisciplinary, incorporating elements of Proteases and Voltage-dependent anion channel.
The study incorporates disciplines such as Cell, Immunology, Intracellular, Necrosis and Neuroscience in addition to Programmed cell death.
His Molecular biology research incorporates themes from Genetics, Gene expression, Chromosomal translocation, Transfection and Gene.
The concepts of his Mitochondrial apoptosis-induced channel study are interwoven with issues in Bcl-2 family, Apoptosome and Mitochondrial permeability transition pore.
He most often published in these fields:
- Apoptosis (53.11%)
- Cell biology (52.63%)
- Programmed cell death (37.32%)
What were the highlights of his more recent work (between 2009-2019)?
- Cell biology (52.63%)
- Programmed cell death (37.32%)
- Apoptosis (53.11%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Cell biology, Programmed cell death, Apoptosis, Molecular biology and Mitochondrion.
Yoshihide Tsujimoto studies Intracellular which is a part of Cell biology.
His work carried out in the field of Programmed cell death brings together such families of science as Embryonic stem cell, Neuroscience, Immunology and Homeostasis.
Yoshihide Tsujimoto has included themes like Necrosis, Knockout mouse and Cell growth in his Apoptosis study.
Yoshihide Tsujimoto interconnects Small hairpin RNA, Gene, Blot, RNA interference and Stimulation in the investigation of issues within Molecular biology.
His Mitochondrion research incorporates elements of Mitochondrial permeability transition pore, Infantile neuroaxonal dystrophy, Neurodegeneration and Pathology.
Between 2009 and 2019, his most popular works were:
- Essential versus accessory aspects of cell death: recommendations of the NCCD 2015 (591 citations)
- Involvement of JNK in the regulation of autophagic cell death (129 citations)
- Neuroaxonal Dystrophy in Calcium-Independent Phospholipase A2β Deficiency Results from Insufficient Remodeling and Degeneration of Mitochondrial and Presynaptic Membranes (87 citations)
In his most recent research, the most cited papers focused on:
Yoshihide Tsujimoto spends much of his time researching Programmed cell death, Apoptosis, Cell biology, ATG5 and Autophagy.
He has researched Programmed cell death in several fields, including SH-SY5Y, Lipid peroxidation, Disease and Protein kinase A.
Yoshihide Tsujimoto interconnects Phosphorylation and Osteoblast in the investigation of issues within Apoptosis.
His work deals with themes such as Caenorhabditis elegans and Mitochondrial permeability transition pore, which intersect with Cell biology.
His ATG5 research is multidisciplinary, incorporating elements of Embryonic stem cell, Homeostasis, Embryo, Embryogenesis and Growth factor receptor.
The concepts of his Autophagy study are interwoven with issues in Cell cycle, Kinase, Paraptosis and Protein degradation.
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