What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Virology, Capsid, Cell biology, Molecular biology and SAMHD1. His Virology research focuses on Coiled coil and how it relates to Tripartite motif family, Function and Zinc finger. His research integrates issues of Retrovirus and Avidity in his study of Capsid.
His Cell biology research includes elements of Apoptosis, Caspase 1 and Proteolysis. Felipe Diaz-Griffero has researched Molecular biology in several fields, including Mutant, CDC2 Protein Kinase, Phosphorylation, RNA-binding protein and Binding site. His research in SAMHD1 intersects with topics in Cell culture, Viral replication, Origin recognition complex and Kinase.
His most cited work include:
- Specific recognition and accelerated uncoating of retroviral capsids by the TRIM5α restriction factor (621 citations)
- Peripheral Blood CCR4 + CCR6 + and CXCR3 + CCR6 + CD4 + T Cells Are Highly Permissive to HIV-1 Infection (226 citations)
- The Retroviral Restriction Ability of SAMHD1, but Not Its Deoxynucleotide Triphosphohydrolase Activity, Is Regulated by Phosphorylation (226 citations)
What are the main themes of his work throughout his whole career to date?
Felipe Diaz-Griffero mainly focuses on Virology, Cell biology, Capsid, SAMHD1 and Molecular biology. The study of Virology is intertwined with the study of Cell culture in a number of ways. Felipe Diaz-Griffero interconnects Jurkat cells, Mutant and TRIM Family in the investigation of issues within Cell biology.
Felipe Diaz-Griffero has included themes like Cyclophilin A, Plasma protein binding, Reverse transcriptase and Avidity in his Capsid study. The various areas that Felipe Diaz-Griffero examines in his SAMHD1 study include Interferon, Restriction factor, Allosteric regulation and Phosphorylation. The study incorporates disciplines such as Cytoplasm, Mutation, Sterile alpha motif, Wild type and Fusion protein in addition to Molecular biology.
He most often published in these fields:
- Virology (42.15%)
- Cell biology (34.71%)
- Capsid (32.23%)
What were the highlights of his more recent work (between 2017-2021)?
- Cell biology (34.71%)
- Capsid (32.23%)
- SAMHD1 (20.66%)
In recent papers he was focusing on the following fields of study:
Cell biology, Capsid, SAMHD1, Reverse transcriptase and Cyclophilin A are his primary areas of study. His biological study spans a wide range of topics, including Autophagy, TRIM5alpha and Fusion protein. His Capsid study incorporates themes from Infectivity, Polyadenylation, Binding ability and Cytosol.
His work carried out in the field of Cytosol brings together such families of science as Nucleus and Virology. His studies deal with areas such as Mutant, Nucleotide, Allosteric regulation, Enzyme and Phosphorylation as well as SAMHD1. His study looks at the relationship between Primary cell and topics such as Specificity factor, which overlap with Molecular biology.
Between 2017 and 2021, his most popular works were:
- Nup153 Unlocks the Nuclear Pore Complex for HIV-1 Nuclear Translocation in Nondividing Cells. (35 citations)
- Infection by Zika viruses requires the transmembrane protein AXL, endocytosis and low pH. (35 citations)
- Cyclophilin A Prevents HIV-1 Restriction in Lymphocytes by Blocking Human TRIM5α Binding to the Viral Core. (24 citations)
In his most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Cell biology, Capsid, Cell cycle, Transmembrane protein and Phosphorylation. His Cell biology research is multidisciplinary, incorporating perspectives in Jurkat cells and Human cytomegalovirus. His Capsid research is multidisciplinary, relying on both Reverse transcriptase, Primary cell, Cypa, Cyclophilin A and Peripheral blood mononuclear cell.
His Phosphorylation research includes themes of Mitosis and Holoenzymes. His Cell study combines topics from a wide range of disciplines, such as SAMHD1 and Virology. His Virology study combines topics in areas such as Receptor tyrosine kinase, Endocytosis and Intracellular.
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