What is he best known for?
The fields of study he is best known for:
James E. Robinson spends much of his time researching Virology, Epitope, Monoclonal antibody, Antibody and Molecular biology.
His study looks at the intersection of Virology and topics like Antigen with Molecular cloning, Virus, L Cells and Gene.
His Epitope study incorporates themes from Peptide library, Phage display, Glycoprotein and Monoclonal.
The concepts of his Antibody study are interwoven with issues in Sulfation, Biochemistry, Binding site, Immune system and Peptide sequence.
The study incorporates disciplines such as Tyrosine sulfation, Tyrosine, Antibody-dependent cell-mediated cytotoxicity and Conformational epitope in addition to Immune system.
His Molecular biology study combines topics in areas such as Receptor, Epstein–Barr virus and COS cells.
His most cited work include:
- Wnt Signaling Gradients Establish Planar Cell Polarity by Inducing Vangl2 Phosphorylation through Ror2 (340 citations)
- Structure of HIV-1 gp120 with gp41-interactive region reveals layered envelope architecture and basis of conformational mobility (290 citations)
- Structural basis of tyrosine sulfation and VH-gene usage in antibodies that recognize the HIV type 1 coreceptor-binding site on gp120 (241 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Virology, Epitope, Monoclonal antibody, Antibody and Antigen.
His work carried out in the field of Virology brings together such families of science as Molecular biology, Gene and Immunology, Lymphocyte.
In his work, Recombinant DNA, Gp41, Antigenicity and Monoclonal is strongly intertwined with Phage display, which is a subfield of Monoclonal antibody.
His biological study spans a wide range of topics, including Immune system, Binding site and Cell biology.
His studies in Immune system integrate themes in fields like Peptide sequence, Biochemistry, Antibody-dependent cell-mediated cytotoxicity and Conformational epitope.
His Antigen course of study focuses on Glycoprotein and Molecular cloning, Antigenic variation, Tyrosine sulfation, Tyrosine and Sulfation.
He most often published in these fields:
- Virology (68.18%)
- Epitope (50.00%)
- Monoclonal antibody (27.27%)
What were the highlights of his more recent work (between 2009-2016)?
- Binding site (13.64%)
- Virology (68.18%)
- Epitope (50.00%)
In recent papers he was focusing on the following fields of study:
His main research concerns Binding site, Virology, Epitope, Key and Loop.
The Binding site study combines topics in areas such as Crystallography, Lipid bilayer fusion, Viral protein and Transmembrane protein.
His Virology research includes themes of Adjuvant, Immunogen and Antigen.
Other disciplines of study, such as Mutation, Trimer and Genetics, are mixed together with his Key studies.
Between 2009 and 2016, his most popular works were:
- Wnt Signaling Gradients Establish Planar Cell Polarity by Inducing Vangl2 Phosphorylation through Ror2 (340 citations)
- Structure of HIV-1 gp120 with gp41-interactive region reveals layered envelope architecture and basis of conformational mobility (290 citations)
- Reproducing SIVΔnef vaccine correlates of protection: trimeric gp41 antibody concentrated at mucosal front lines (7 citations)
In his most recent research, the most cited papers focused on:
ROR2, Binding site, Viral protein, Conformational change and Protein structure are his primary areas of study.
His ROR2 study overlaps with Cell biology, Morphogen, Receptor tyrosine kinase-like orphan receptor, Receptor complex and Phosphorylation.
James E. Robinson merges Cell biology with Cellular polarity in his research.
His research integrates issues of Crystallography, Lipid bilayer fusion and Transmembrane protein in his study of Binding site.
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