What is he best known for?
The fields of study he is best known for:
Thomas Ruppert mostly deals with Biochemistry, Molecular biology, Proteasome, Major histocompatibility complex and Cytotoxic T cell.
Many of his research projects under Biochemistry are closely connected to Redox and Cysteine synthase complex with Redox and Cysteine synthase complex, tying the diverse disciplines of science together.
His Molecular biology research integrates issues from Muscle tissue, CTL*, In vivo and Enzyme.
His biological study spans a wide range of topics, including Peptide sequence, Antigen presentation and Cleavage.
Much of his study explores Major histocompatibility complex relationship to Epitope.
His study looks at the relationship between Cytotoxic T cell and fields such as Antigen, as well as how they intersect with chemical problems.
His most cited work include:
- The Amyloid Precursor Protein of Alzheimer's Disease in the Reduction of Copper(II) to Copper(I) (580 citations)
- Circumventing tolerance to a human MDM2-derived tumor antigen by TCR gene transfer. (375 citations)
- Circumventing tolerance to a human MDM2-derived tumor antigen by TCR gene transfer. (375 citations)
What are the main themes of his work throughout his whole career to date?
Biochemistry, Cell biology, Molecular biology, Proteasome and Epitope are his primary areas of study.
Biochemistry and Amyloid precursor protein are two areas of study in which Thomas Ruppert engages in interdisciplinary work.
His Cell biology study integrates concerns from other disciplines, such as Cell adhesion and Centrosome.
His Molecular biology study incorporates themes from Amino acid, MHC class I, Major histocompatibility complex, CTL* and In vivo.
His study explores the link between Major histocompatibility complex and topics such as Cytotoxic T cell that cross with problems in Antigen.
The Proteasome study combines topics in areas such as Cleavage, Ubiquitin, Peptide and Enzyme.
He most often published in these fields:
- Biochemistry (42.53%)
- Cell biology (34.48%)
- Molecular biology (22.99%)
What were the highlights of his more recent work (between 2017-2021)?
- Cell biology (34.48%)
- Biochemistry (42.53%)
- Mutant (4.60%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Cell biology, Biochemistry, Mutant, Cadherin and Extracellular.
His Cell biology research includes themes of Acetylation, Centrosome and Actin nucleation.
The study incorporates disciplines such as Degron, Ubiquitin, Ubiquitin ligase, Enzyme and Proteasome in addition to Acetylation.
In his study, Thomas Ruppert carries out multidisciplinary Biochemistry and Oxidizing agent research.
His research in Mutant intersects with topics in Secretion, Quantitative proteomics, Oryzias, Zebrafish and Eye development.
His work carried out in the field of Cadherin brings together such families of science as HEK 293 cells, Signal transduction, Cell adhesion, Matrix and Extracellular matrix.
Between 2017 and 2021, his most popular works were:
- A role for 2-Cys peroxiredoxins in facilitating cytosolic protein thiol oxidation (88 citations)
- Insights into the assembly and activation of the microtubule nucleator γ-TuRC (40 citations)
- SIRT7-Dependent Deacetylation of Fibrillarin Controls Histone H2A Methylation and rRNA Synthesis during the Cell Cycle. (21 citations)
In his most recent research, the most cited papers focused on:
Thomas Ruppert spends much of his time researching Actin, Microtubule, Cell biology, Thiol oxidation and Protein thiol.
His Actin research is multidisciplinary, incorporating perspectives in Cilium, Ciliogenesis, Domain of unknown function, Centrosome and Actin nucleation.
His biological study spans a wide range of topics, including Microtubule nucleation, Xenopus, Biophysics and Cell migration.
The concepts of his Cell biology study are interwoven with issues in Chromatin and Histone H2A.
His Thiol oxidation research is within the category of Biochemistry.
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