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Timothy J. Tschaplinski

Researcher at Oak Ridge National Laboratory

Publications -  219
Citations -  19587

Timothy J. Tschaplinski is an academic researcher from Oak Ridge National Laboratory. The author has contributed to research in topics: Gene & Clostridium thermocellum. The author has an hindex of 54, co-authored 203 publications receiving 16437 citations. Previous affiliations of Timothy J. Tschaplinski include University of Chicago & University of Toronto.

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The resilience of upland-oak forest canopy trees to chronic and acute precipitation manipulations

TL;DR: In this article, the authors evaluated the impact of chronic and acute precipitation change on trees of upland-oak forests of the eastern United States and concluded that the resilience of canopy trees to chronic change was the result of a disconnect between tree growth phenology and late season drought occurrence.
Journal Article

Indices de crecimiento y formación de compuestos orgánicos en Barleria lupulina sometida a dos condiciones de luminosidad

TL;DR: Barleria lupulina Lindl is un arbusto introducido a Venezuela desde Africa with fine ornamentales as discussed by the authors, and it is conocida desde tiempos ancestrales in la cultura popular de paises como India and Pakistan by sus caracteristicas antiofidicas.
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Targeted redox and energy cofactor metabolomics in Clostridium thermocellum and Thermoanaerobacterium saccharolyticum.

TL;DR: These validated protocols demonstrate and validate the extraction and analysis of selected redox and energy-related metabolites from two candidate consolidated biocatalysts, C. thermocellum and T. saccharolyticum, and highlights the important, but often neglected, need to optimize and validate metabolomic protocols when adapting them to new cell or tissue types.
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Genetic dissection of transcript, metabolite, growth and wood property traits in an F2 pseudo-backcross pedigree of Eucalyptus grandis x E. urophylla

TL;DR: To bridge the gap between fine mapping and QTL validation studies, the expression levels of genes and metabolites in individuals from the segregating population can be treated as quantitative traits and used for eQTL and mQTL mapping, respectively.
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Horizontal transfer of a pathway for coumarate catabolism unexpectedly inhibits purine nucleotide biosynthesis.

TL;DR: It is shown that two different pathways for coumarate catabolism failed to function when initially transferred into Escherichia coli, demonstrating how deleterious interactions can limit pathway transfer and how evolution or engineering can alleviate these limitations.