What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Biochemistry, Cell biology, Biophysics, Calprotectin and Protein structure.
His Cell biology research includes themes of RAGE, Replication protein A and Apoptosis, Programmed cell death.
The Biophysics study combines topics in areas such as Crystallography, Molecular biology, Protein subunit and Mutant.
The various areas that Walter J. Chazin examines in his Calprotectin study include Pathogenesis, Antimicrobial, Microbiology, Acinetobacter baumannii and Immune system.
The study incorporates disciplines such as Calcium-binding protein, Calmodulin, DNA-binding protein and Structural motif in addition to Protein structure.
In the field of Calmodulin, his study on EF hand overlaps with subjects such as NAV1.5 Voltage-Gated Sodium Channel.
His most cited work include:
- Metal Chelation and Inhibition of Bacterial Growth in Tissue Abscesses (599 citations)
- Nutrient Metal Sequestration by Calprotectin Inhibits Bacterial Superoxide Defense, Enhancing Neutrophil Killing of Staphylococcus aureus (249 citations)
- Calmodulin mutations associated with recurrent cardiac arrest in infants (242 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Biochemistry, Biophysics, Crystallography, Cell biology and Calmodulin.
His Biochemistry study integrates concerns from other disciplines, such as Calcium-binding protein and Calprotectin.
His Biophysics research incorporates themes from Plasma protein binding, Binding domain, Binding site, Primase and DNA replication.
His Crystallography study combines topics from a wide range of disciplines, such as Dihedral angle, Proton NMR, Nuclear magnetic resonance spectroscopy and Molecular dynamics.
The concepts of his Cell biology study are interwoven with issues in Replication protein A, Ubiquitin, DNA damage, Eukaryotic DNA replication and Molecular biology.
As a member of one scientific family, Walter J. Chazin mostly works in the field of Calmodulin, focusing on Long QT syndrome and, on occasion, Endocrinology.
He most often published in these fields:
- Biochemistry (28.18%)
- Biophysics (21.68%)
- Crystallography (17.89%)
What were the highlights of his more recent work (between 2013-2021)?
- Cell biology (17.62%)
- Microbiology (8.40%)
- Biochemistry (28.18%)
In recent papers he was focusing on the following fields of study:
His main research concerns Cell biology, Microbiology, Biochemistry, Calprotectin and Biophysics.
His Cell biology research incorporates elements of Ubiquitin, Genome instability and Calmodulin.
Walter J. Chazin regularly links together related areas like Calcium-binding protein in his Biochemistry studies.
His study in Calprotectin is interdisciplinary in nature, drawing from both Pathogen, Immunology, Antimicrobial, S100A8 and Innate immune system.
His Biophysics research includes elements of Redox, Primase and DNA, DNA replication.
Walter J. Chazin combines subjects such as Replication protein A and Molecular biology with his study of DNA replication.
Between 2013 and 2021, his most popular works were:
- ETAA1 acts at stalled replication forks to maintain genome integrity (130 citations)
- Nutritional Immunity: S100 Proteins at the Host-Pathogen Interface (114 citations)
- Novel calmodulin mutations associated with congenital arrhythmia susceptibility. (113 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Microbiology, Calprotectin, Cell biology, Long QT syndrome and Mutation.
His work deals with themes such as Immune system, Immunology, Acinetobacter baumannii, Staphylococcus aureus and S100A8, which intersect with Microbiology.
The concepts of his Calprotectin study are interwoven with issues in In vitro, Secretion, Antimicrobial, Innate immune system and Virulence.
His work carried out in the field of Cell biology brings together such families of science as DNA damage, DNA, Genome instability and Molecular biology.
His Long QT syndrome research integrates issues from Missense mutation, Endocrinology and Calmodulin.
His Peptide sequence research is under the purview of Biochemistry.
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