What is he best known for?
The fields of study he is best known for:
Scot A. Marsters mainly investigates Molecular biology, Apoptosis, Immunology, Cell biology and Fas receptor.
His work in Molecular biology addresses subjects such as Tumor necrosis factor alpha, which are connected to disciplines such as B-cell activating factor.
The Apoptosis study combines topics in areas such as Mediator and Intracellular.
His Immunology study integrates concerns from other disciplines, such as 5-HT5A receptor, Decoy Receptor 1, Growth factor receptor and Decoy receptors.
His work on Endoplasmic reticulum as part of his general Cell biology study is frequently connected to Tumor Necrosis Factor Decoy Receptors, thereby bridging the divide between different branches of science.
His work focuses on many connections between Fas receptor and other disciplines, such as Receptor, that overlap with his field of interest in Natural killer cell and Decoy receptor 3.
His most cited work include:
- Safety and antitumor activity of recombinant soluble Apo2 ligand (1994 citations)
- Induction of Apoptosis by Apo-2 Ligand, a New Member of the Tumor Necrosis Factor Cytokine Family * (1671 citations)
- Control of TRAIL-induced apoptosis by a family of signaling and decoy receptors (1598 citations)
What are the main themes of his work throughout his whole career to date?
Scot A. Marsters mostly deals with Molecular biology, Antibody, Biochemistry, Cell biology and Apoptosis.
His Molecular biology research includes elements of Tumor necrosis factor alpha, DNA, Receptor, B-cell activating factor and Binding site.
His Tumor necrosis factor alpha study which covers Pharmacology that intersects with Agonist.
He has researched Antibody in several fields, including Antigen and Virology.
His Cell biology study combines topics from a wide range of disciplines, such as XBP1 and Programmed cell death.
His studies examine the connections between Apoptosis and genetics, as well as such issues in Cancer cell, with regards to Tumor microenvironment.
He most often published in these fields:
- Molecular biology (29.09%)
- Antibody (25.45%)
- Biochemistry (20.91%)
What were the highlights of his more recent work (between 2013-2021)?
- Cell biology (20.91%)
- Endoplasmic reticulum (9.09%)
- Apoptosis (19.09%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Cell biology, Endoplasmic reticulum, Apoptosis, Unfolded protein response and Receptor.
His Cell biology research incorporates elements of XBP1 and Programmed cell death.
His research investigates the connection with Endoplasmic reticulum and areas like Transcription factor which intersect with concerns in Kinase, Phosphorylation, Cancer cell and Cancer research.
His study looks at the intersection of Apoptosis and topics like Ectodomain with Cytoprotection.
His studies deal with areas such as Epitope, Antibody, Tissue homeostasis and Cytotoxicity as well as Receptor.
His biological study spans a wide range of topics, including Tumor necrosis factor alpha, Pharmacology and Recombinant DNA.
Between 2013 and 2021, his most popular works were:
- Opposing unfolded-protein-response signals converge on death receptor 5 to control apoptosis. (327 citations)
- Coordination between Two Branches of the Unfolded Protein Response Determines Apoptotic Cell Fate (60 citations)
- E-cadherin couples death receptors to the cytoskeleton to regulate apoptosis. (59 citations)
In his most recent research, the most cited papers focused on:
Scot A. Marsters mainly focuses on Cell biology, Apoptosis, Programmed cell death, Receptor and Unfolded protein response.
His Apoptosis study incorporates themes from Cadherin and Cell fate determination.
His study in Programmed cell death is interdisciplinary in nature, drawing from both Cancer cell, Ectodomain, Cell membrane, Cytotoxicity and Kinase.
The study incorporates disciplines such as Tissue homeostasis, Actin cytoskeleton, Cytoskeleton, Signal transduction and Actin in addition to Receptor.
Scot A. Marsters has included themes like Proteostasis, Transcription factor and Phosphorylation in his Unfolded protein response study.
His research integrates issues of Caspase, Mediator and Intracellular in his study of Endoplasmic reticulum.
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