His primary areas of investigation include Genetics, Biochemistry, Gene, Escherichia coli and Molecular biology. His work in the fields of Genetics, such as Lytic cycle, Bacteriophage, Prophage and DNA, overlaps with other areas such as Population. As part of one scientific family, Amos B. Oppenheim deals mainly with the area of Biochemistry, narrowing it down to issues related to the Biophysics, and often Protein aggregation, MreB, Cell division and CLPB.
His work carried out in the field of Gene brings together such families of science as Superoxide dismutase and Microbiology. In general Escherichia coli study, his work on Lambda phage often relates to the realm of Chemiosmosis, thereby connecting several areas of interest. His Molecular biology research includes themes of Ribosomal binding site, Repressor and lac operon.
Amos B. Oppenheim spends much of his time researching Molecular biology, Gene, Genetics, Bacteriophage and DNA. His Molecular biology research incorporates elements of Plasmid, Ribosomal binding site, Mutant, Promoter and Transcription. His studies in Bacteriophage integrate themes in fields like Virulence and Virology.
His DNA research is multidisciplinary, incorporating perspectives in Cell biology and DNA-binding protein, Integration Host Factors. The Lysogenic cycle study combines topics in areas such as Lysogen, Lytic cycle, Prophage and Temperateness. His Escherichia coli study is concerned with the field of Biochemistry as a whole.
Amos B. Oppenheim mostly deals with Bacteriophage, Lambda phage, Genetics, DNA and Lytic cycle. His biological study spans a wide range of topics, including Molecular biology and Virology. Genetics is represented through his Escherichia coli, Gene and Transcription research.
His work on RNA as part of general Gene research is frequently linked to Negative feedback, bridging the gap between disciplines. Amos B. Oppenheim combines subjects such as Regulation of gene expression and Nucleoid with his study of DNA. His Lytic cycle study integrates concerns from other disciplines, such as Prophage and Lysogenic cycle.
His primary areas of study are Genetics, Bacteriophage, Lytic cycle, Lysogenic cycle and Escherichia coli. His study in Prophage, Gene, Recombineering and DNA are all subfields of Genetics. His DNA study incorporates themes from Molecular biology, Point mutation, Frameshift mutation and Nucleoid.
He has included themes like Biotinylation, Mycobacterium, Pathogenic bacteria, Phage typing and Bacillus anthracis in his Bacteriophage study. His study in Lysogenic cycle is interdisciplinary in nature, drawing from both Regulation of gene expression and DNA-binding protein. His work on Lambda phage and MreB as part of his general Escherichia coli study is frequently connected to Aggregate, thereby bridging the divide between different branches of science.
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Switches in bacteriophage lambda development.
Amos B. Oppenheim;Oren Kobiler;Joel Stavans;Donald L. Court.
Annual Review of Genetics (2005)
Crystal structure of a bacterial chitinase at 2.3 Å resolution
Anastassis Perrakis;Ivo Tews;Zbigniew Dauter;Amos B Oppenheim.
Structure (1994)
The Thylakoid FtsH Protease Plays a Role in the Light-Induced Turnover of the Photosystem II D1 Protein
Marika Lindahl;Cornelia Spetea;Cornelia Spetea;Torill Hundal;Torill Hundal;Amos B. Oppenheim.
The Plant Cell (2000)
Bacterial chitobiase structure provides insight into catalytic mechanism and the basis of Tay-Sachs disease.
Ivo Tews;Anastassis Perrakis;Amos Oppenheim;Zbigniew Dauter.
Nature Structural & Molecular Biology (1996)
High-sensitivity bacterial detection using biotin-tagged phage and quantum-dot nanocomplexes.
Rotem Edgar;Michael McKinstry;Jeeseong Hwang;Amos B. Oppenheim.
Proceedings of the National Academy of Sciences of the United States of America (2006)
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes
M. F. Hammer;A. J. Redd;E. T. Wood;M. R. Bonner.
Proceedings of the National Academy of Sciences of the United States of America (2000)
Recombineering: Genetic Engineering in Bacteria Using Homologous Recombination
Lynn Thomason;Donald L. Court;Mikail Bubunenko;Nina Costantino.
Current protocols in molecular biology (2003)
Differential mRNA stability of the cspA gene in the cold-shock response of Escherichia coli.
Daniel Goldenberg;Idit Azar;Amos B. Oppenheim.
Molecular Microbiology (1996)
Increased bending rigidity of single DNA molecules by H-NS, a temperature and osmolarity sensor.
Roee Amit;Amos B. Oppenheim;Joel Stavans.
Biophysical Journal (2003)
New components of the chitinolytic system of Trichoderma harzianum
Shoshan Haran;Hedva Schickler;Amos Oppenheim;Ilan Chet.
Fungal Biology (1995)
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