What is he best known for?
The fields of study he is best known for:
Alan F. Williams mainly investigates Molecular biology, Monoclonal antibody, Antibody, Antigen and Glycoprotein.
His Molecular biology research incorporates themes from Epitope, T cell and T lymphocyte.
His Monoclonal antibody research integrates issues from Bone marrow, Lymphocyte and Virology.
His work deals with themes such as Transferrin receptor, Endothelium and Nanoparticles for drug delivery to the brain, which intersect with Antibody.
His biological study spans a wide range of topics, including Amino acid, Glycosylation and Protein structure.
Alan F. Williams works mostly in the field of Biochemistry, limiting it down to concerns involving Thymocyte and, occasionally, Affinity chromatography, Transmembrane protein, Complementary DNA, Cell membrane and Cell division.
His most cited work include:
- Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens-new tools for genetic analysis. (1697 citations)
- Cell-Surface Anchoring of Proteins via Glycosyl-Phosphatidylinositol Structures (1093 citations)
- Transferrin receptor on endothelium of brain capillaries (819 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Molecular biology, Antigen, Glycoprotein, Antibody and Biochemistry.
His Molecular biology research includes elements of Protein primary structure, Peptide sequence, Complementary DNA, Cytotoxic T cell and Monoclonal antibody.
The various areas that he examines in his Monoclonal antibody study include Epitope and Cell culture.
The concepts of his Antigen study are interwoven with issues in Affinity chromatography and Cell biology.
He interconnects Amino acid, Membrane protein and Virology in the investigation of issues within Glycoprotein.
His Antibody study combines topics from a wide range of disciplines, such as Cell, Receptor, Bone marrow and Spleen.
He most often published in these fields:
- Molecular biology (54.62%)
- Antigen (49.23%)
- Glycoprotein (35.38%)
What were the highlights of his more recent work (between 1990-2016)?
- Molecular biology (54.62%)
- Glycoprotein (35.38%)
- Cell biology (14.62%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Molecular biology, Glycoprotein, Cell biology, Biochemistry and Antigen.
Alan F. Williams performs multidisciplinary study on Molecular biology and CD53 in his works.
His work deals with themes such as Epitope, Peptide sequence, Membrane protein and Mutation, which intersect with Glycoprotein.
His Peptide sequence study incorporates themes from Antibody, Beta sheet and Binding site.
Alan F. Williams combines subjects such as SUPERFAMILY, T cell and Gpi anchored protein with his study of Cell biology.
His Antigen study deals with T-cell receptor intersecting with CD3, Cytotoxic T cell and T lymphocyte.
Between 1990 and 2016, his most popular works were:
- Crystal structure at 2.8 A resolution of a soluble form of the cell adhesion molecule CD2. (268 citations)
- The dimensions of the T lymphocyte glycoprotein leukosialin and identification of linear protein epitopes that can be modified by glycosylation. (234 citations)
- Molecular associations between the T-lymphocyte antigen receptor complex and the surface antigens CD2, CD4, or CD8 and CD5. (193 citations)
In his most recent research, the most cited papers focused on:
Alan F. Williams focuses on Molecular biology, Glycoprotein, Stereochemistry, Antigen and Antibody.
His study in Molecular biology is interdisciplinary in nature, drawing from both Epitope, Antigenicity and CD8.
His Antigenicity research is multidisciplinary, incorporating elements of Glycosylation, Biochemistry and Fusion protein.
His studies deal with areas such as Protein structure, Ligand and Virology as well as Glycoprotein.
Alan F. Williams works in the field of Antigen, focusing on T lymphocyte in particular.
His study looks at the relationship between T lymphocyte and topics such as Protein secondary structure, which overlap with Cytotoxic T cell.
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