Bernard Weisblum focuses on Molecular biology, Biochemistry, Stereochemistry, Antimicrobial and Microbiology. His Molecular biology study incorporates themes from Nucleic acid sequence, Erythromycin, Lincomycin and Plasmid. His Biochemistry research is multidisciplinary, incorporating elements of Derivative, Reagent and Polymer.
His studies deal with areas such as Folding and Structure–activity relationship as well as Stereochemistry. His Antimicrobial research is multidisciplinary, relying on both Amphiphile, Oligomer, Peptide and Bacteria. His research combines 23S ribosomal RNA and Microbiology.
Bernard Weisblum mostly deals with Biochemistry, Molecular biology, Stereochemistry, Peptide and Microbiology. Bernard Weisblum studied Biochemistry and Bacillus subtilis that intersect with Cell wall and Autolysis. He combines subjects such as Plasmid, Nucleic acid sequence, DNA, Messenger RNA and Ribosome with his study of Molecular biology.
His work carried out in the field of Stereochemistry brings together such families of science as Amphiphile, Antimicrobial, Cationic polymerization, Side chain and Structure–activity relationship. His work on Magainin is typically connected to Motif as part of general Peptide study, connecting several disciplines of science. Bernard Weisblum works mostly in the field of Microbiology, limiting it down to concerns involving Staphylococcus aureus and, occasionally, Ribosomal RNA and Antibiotic resistance.
The scientist’s investigation covers issues in Biochemistry, Stereochemistry, Peptide, Microbiology and Structure–activity relationship. The study incorporates disciplines such as Bacillus subtilis and Bacteria in addition to Biochemistry. He interconnects Biological activity, Protein subunit, Sequence, Cationic polymerization and Side chain in the investigation of issues within Stereochemistry.
In general Peptide study, his work on Magainin often relates to the realm of Zipper, thereby connecting several areas of interest. As a part of the same scientific study, Bernard Weisblum usually deals with the Microbiology, concentrating on Staphylococcus aureus and frequently concerns with Antibiotics, Clostridium difficile and Bacillus cereus. His study in Structure–activity relationship is interdisciplinary in nature, drawing from both Folding and Candida albicans.
His primary scientific interests are in Structure–activity relationship, Stereochemistry, Candida albicans, Biochemistry and Cationic polymerization. His Structure–activity relationship research includes themes of Fibroblast, Protein folding, Folding, Protein structure and Biological activity. His biological study spans a wide range of topics, including Peptide sequence, Computational biology and Sequence.
His Stereochemistry research is multidisciplinary, incorporating perspectives in Bacterial cell structure, Membrane, Polymerization and Peptide. Candida albicans is a subfield of Microbiology that Bernard Weisblum investigates. His Cationic polymerization research includes elements of Side chain, Polymer and Protein subunit.
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Erythromycin resistance by ribosome modification.
Bernard Weisblum.
Antimicrobial Agents and Chemotherapy (1995)
Nucleotide sequence and functional map of pC194, a plasmid that specifies inducible chloramphenicol resistance.
S Horinouchi;B Weisblum.
Journal of Bacteriology (1982)
Non-haemolytic β-amino-acid oligomers
Emilie A. Porter;Xifang Wang;Hee-Seung Lee;Bernard Weisblum.
Nature (2000)
Nucleotide sequence and functional map of pE194, a plasmid that specifies inducible resistance to macrolide, lincosamide, and streptogramin type B antibodies.
S Horinouchi;B Weisblum.
Journal of Bacteriology (1982)
Construction of a colicin E1-R factor composite plasmid in vitro: means for amplification of deoxyribonucleic acid.
T Tanaka;B Weisblum.
Journal of Bacteriology (1975)
Mimicry of host-defense peptides by unnatural oligomers: antimicrobial beta-peptides.
Emilie A. Porter;Bernard Weisblum;Samuel H. Gellman.
Journal of the American Chemical Society (2002)
On the role of soluble ribonucleic acid in coding for amino acids.
Francois Chapeville;Fritz Lipmann;Günter von Ehrenstein;Bernard Weisblum.
Proceedings of the National Academy of Sciences of the United States of America (1962)
Mimicry of antimicrobial host-defense peptides by random copolymers.
Brendan P. Mowery;Sarah E. Lee;Denis A. Kissounko;Raquel F. Epand.
Journal of the American Chemical Society (2007)
Antibiotic inhibitors of the bacterial ribosome.
B Weisblum;J Davies.
Bacteriological Reviews (1968)
Quinacrine, A Chromosome Stain Specific for Deoxyadenylate-Deoxythymidylate-Rich Regions in DNA
Bernard Weisblum;Pieter L. De Haseth.
Proceedings of the National Academy of Sciences of the United States of America (1972)
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