2009 - Member of the National Academy of Sciences
2002 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary areas of study are Stereochemistry, Oligonucleotide, Biochemistry, DNA and Binding site. His studies deal with areas such as Antiparallel, Base pair, Thymine and Nucleotide as well as Stereochemistry. His Biochemistry study incorporates themes from Virus and Ligand.
His biological study spans a wide range of topics, including Crystallography, Helix, Crystal structure and Molecule. His Binding site research incorporates elements of Ubiquitin, Biophysics, Aptamer, Conserved sequence and Proteasome. He works mostly in the field of RNA, limiting it down to topics relating to Cell biology and, in certain cases, RNA-binding protein.
Juli Feigon mainly investigates RNA, DNA, Stereochemistry, Crystallography and Biochemistry. His RNA research incorporates themes from Biophysics, Molecular biology, Telomerase, Telomerase reverse transcriptase and Cell biology. His Cell biology study deals with Telomere intersecting with Protein subunit.
Juli Feigon mostly deals with Base pair in his studies of DNA. His Stereochemistry study combines topics from a wide range of disciplines, such as Nucleotide, Molecule, Hoogsteen base pair, Oligonucleotide and Thymine. His Crystallography research integrates issues from Proton NMR, Nuclear magnetic resonance spectroscopy, Two-dimensional nuclear magnetic resonance spectroscopy and Hydrogen bond.
The scientist’s investigation covers issues in Cell biology, Telomerase, Telomerase reverse transcriptase, Tetrahymena and Telomere. Juli Feigon has researched Cell biology in several fields, including Telomerase rna and DNA. The various areas that he examines in his DNA study include Ion, Isoguanine and Nuclear magnetic resonance spectroscopy.
His Telomerase reverse transcriptase research is multidisciplinary, incorporating elements of RNA, Non-coding RNA, Reverse transcriptase and Pseudoknot. His research in Telomere intersects with topics in Replication protein A and Protein subunit. Biochemistry is frequently linked to Stereochemistry in his study.
Juli Feigon focuses on Cell biology, Telomerase, Telomerase reverse transcriptase, Telomerase RNA component and RNA. His study in Telomerase is interdisciplinary in nature, drawing from both Telomere, Protein subunit, Reverse transcriptase and Tetrahymena. His Telomere study contributes to a more complete understanding of Biochemistry.
His Reverse transcriptase research is multidisciplinary, relying on both Base pair and DNA. Juli Feigon works mostly in the field of Telomerase reverse transcriptase, limiting it down to topics relating to Non-coding RNA and, in certain cases, RNA-dependent RNA polymerase, as a part of the same area of interest. Many of his studies involve connections with topics such as Molecular biology and RNA.
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Thrombin-binding DNA aptamer forms a unimolecular quadruplex structure in solution.
Roman F. Macaya;Peter Schultze;Flint W. Smith;James A. Roe.
Proceedings of the National Academy of Sciences of the United States of America (1993)
Quadruplex structure of Oxytricha telomeric DNA oligonucleotides.
Flint W. Smith;Juli Feigon.
Three-dimensional solution structure of the thrombin-binding DNA aptamer d(GGTTGGTGTGGTTGG).
Peter Schultze;Román F. Macaya;Juli Feigon.
Journal of Molecular Biology (1994)
The Selectivity for K+ versus Na+ in DNA Quadruplexes Is Dominated by Relative Free Energies of Hydration: A Thermodynamic Analysis by 1H NMR†
Nicholas V. Hud;Flint W. Smith;Frank A. L. Anet;Juli Feigon.
Interactions of antitumor drugs with natural DNA: 1H NMR study of binding mode and kinetics.
Juli Feigon;William A. Denny;Werner Leupin;David R. Kearns.
Journal of Medicinal Chemistry (1984)
Structure of the human telomerase RNA pseudoknot reveals conserved tertiary interactions essential for function.
Carla A. Theimer;Craig A. Blois;Juli Feigon.
Molecular Cell (2005)
Multistranded DNA structures.
Dara E Gilbert;Juli Feigon.
Current Opinion in Structural Biology (1999)
Solution structure of protegrin-1, a broad-spectrum antimicrobial peptide from porcine leukocytes.
Richard L. Fahrner;Thorsten Dieckmann;Sylvia S.L. Harwig;Robert I. Lehrer.
Chemistry & Biology (1996)
Triple-strand formation in the homopurine:homopyrimidine DNA oligonucleotides d(G-A)4 and d(T-C)4.
Ponni Rajagopal;Juli Feigon.
Solution structure of an ATP-binding RNA aptamer reveals a novel fold.
T Dieckmann;E Suzuki;G K Nakamura;J Feigon.
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