What is he best known for?
The fields of study he is best known for:
David Kabat mainly investigates Molecular biology, Virus, Virology, Gene and Biochemistry.
He performs multidisciplinary study in the fields of Molecular biology and Viral vector via his papers.
His studies deal with areas such as V3 loop, Tyrosine sulfation, C-C chemokine receptor type 6 and CCL21 as well as Virus.
In his study, Infectivity, In vitro and In vivo is inextricably linked to Cell culture, which falls within the broad field of Virology.
David Kabat combines subjects such as Receptor, Friend virus and Glycoprotein with his study of Gene.
His work on Cell surface receptor as part of general Receptor research is often related to Nonsynonymous substitution, thus linking different fields of science.
His most cited work include:
- Effects of CCR5 and CD4 Cell Surface Concentrations on Infections by Macrophagetropic Isolates of Human Immunodeficiency Virus Type 1 (1043 citations)
- HIV-1 Vif protein binds the editing enzyme APOBEC3G and induces its degradation. (725 citations)
- Cell-surface receptors for gibbon ape leukemia virus and amphotropic murine retrovirus are inducible sodium-dependent phosphate symporters. (505 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Virology, Molecular biology, Virus, Glycoprotein and Cell culture.
David Kabat has researched Virology in several fields, including Mutation, Gene and Leukemia.
His Molecular biology research includes elements of Receptor, Biochemistry, Chinese hamster ovary cell, Retrovirus and Complementary DNA.
His Receptor research is multidisciplinary, incorporating perspectives in Cell and Peptide sequence.
His Glycoprotein research is multidisciplinary, relying on both Cell biology, Mutant, Lipid bilayer fusion and Murine leukemia virus.
The study incorporates disciplines such as In vitro, Antibody and Gene expression in addition to Cell culture.
He most often published in these fields:
- Virology (43.59%)
- Molecular biology (39.32%)
- Virus (36.75%)
What were the highlights of his more recent work (between 2001-2016)?
- Virology (43.59%)
- Virus (36.75%)
- Cell biology (17.09%)
In recent papers he was focusing on the following fields of study:
Virology, Virus, Cell biology, Gp41 and APOBEC3G are his primary areas of study.
His Virology study incorporates themes from Cell culture, Antibody and Messenger RNA.
His research in Infectivity and Murine leukemia virus are components of Virus.
His work deals with themes such as Extracellular, Plasma protein binding, Biochemistry, Lipid bilayer fusion and V3 loop, which intersect with Gp41.
His studies in Cytidine deaminase integrate themes in fields like Molecular biology, Cytidine and MAPK/ERK pathway.
His Glycoprotein study integrates concerns from other disciplines, such as Receptor and Chemokine receptor.
Between 2001 and 2016, his most popular works were:
- HIV-1 Vif protein binds the editing enzyme APOBEC3G and induces its degradation. (725 citations)
- Evidence that ecotropic murine leukemia virus contamination in TZM-bl cells does not affect the outcome of neutralizing antibody assays with human immunodeficiency virus type 1. (188 citations)
- The Anti-HIV-1 Editing Enzyme APOBEC3G Binds HIV-1 RNA and Messenger RNAs That Shuttle between Polysomes and Stress Granules (163 citations)
In his most recent research, the most cited papers focused on:
David Kabat mainly focuses on Molecular biology, APOBEC3G, Glycoprotein, Receptor and Cytidine deaminase.
His biological study spans a wide range of topics, including Cell culture, Neutralizing antibody, Viral infectivity factor, APOBEC3A and Mutant.
His APOBEC3G study combines topics from a wide range of disciplines, such as Reverse transcriptase and Kinase, MAPK/ERK pathway.
His Glycoprotein research incorporates themes from Mutagenesis, Syncytium and Gene.
The Chinese hamster ovary cell research he does as part of his general Receptor study is frequently linked to other disciplines of science, such as Endogenous retrovirus, therefore creating a link between diverse domains of science.
David Kabat has researched Cytidine deaminase in several fields, including c-Raf, Protein kinase C, Protein kinase A and Mitogen-activated protein kinase kinase.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
