L
Lucas G. Nivón
Researcher at University of Washington
Publications - 15
Citations - 3075
Lucas G. Nivón is an academic researcher from University of Washington. The author has contributed to research in topics: Hairpin ribozyme & Nanopore. The author has an hindex of 12, co-authored 15 publications receiving 2835 citations. Previous affiliations of Lucas G. Nivón include Rowland Institute for Science & Howard Hughes Medical Institute.
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Journal ArticleDOI
Rapid nanopore discrimination between single polynucleotide molecules.
TL;DR: Because nanopores can rapidly discriminate and characterize unlabeled DNA molecules at low copy number, refinements of the experimental approach demonstrated here could eventually provide a low-cost high-throughput method of analyzing DNA polynucleotides.
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Voltage-driven DNA translocations through a nanopore.
TL;DR: Current blockade and time distributions for single-stranded DNA polymers during voltage-driven translocations through a single alpha-hemolysin pore imply that, while polymers longer than the pore are translocated at a constant speed, the velocity of shorter polymers increases with decreasing length.
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Effects of chronic stress on hippocampal long-term potentiation.
TL;DR: The effects of chronic stress on hippocampal physiology and long‐term potentiation (LTP) in the CA3 and dentate gyrus suggest that chronic stress produces changes in the input‐output relationship in the hippocampal trisynaptic circuit which could affect information flow through this structure.
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Prion protein NMR structures of cats, dogs, pigs, and sheep
Dominikus A. Lysek,Christian Schorn,Lucas G. Nivón,Vicent Esteve-Moya,Barbara Christen,Luigi Calzolai,Christine von Schroetter,Francesco Fiorito,Torsten Herrmann,Peter Güntert,Kurt Wüthrich +10 more
TL;DR: Because the five newly determined PrPC structures originate from species with widely different transmissible spongiform encephalopathy records, the present data indicate previously uncharacterized possible correlations between local features in PrPC three-dimensional structures and susceptibility of different mammalian species to transmissible scrofa encephalopathies.
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A Pareto-optimal refinement method for protein design scaffolds.
TL;DR: A protocol using cycles of minimization with combined backbone/sidechain restraints that is Pareto-optimal with respect to RMSD to the native structure and energetic strain reduction is described.