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Patrick J. Tranel

Researcher at University of Illinois at Urbana–Champaign

Publications -  157
Citations -  8039

Patrick J. Tranel is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Amaranthus tuberculatus & Population. The author has an hindex of 45, co-authored 146 publications receiving 6824 citations. Previous affiliations of Patrick J. Tranel include Purdue University & Michigan State University.

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Resistance of weeds to ALS-inhibiting herbicides: what have we learned?

TL;DR: Resistance to ALS-inhibiting herbicides has greatly affected weed science by influencing how the authors view the sustainability of their weed management practices, what they consider when developing and marketing new herbicides, and how they train new weed scientists.
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Gene amplification confers glyphosate resistance in Amaranthus palmeri

TL;DR: This work investigated recently discovered glyphosate-resistant Amaranthus palmeri populations from Georgia, in comparison with normally sensitive populations, and revealed that EPSPS genes were present on every chromosome and, therefore, gene amplification was likely not caused by unequal chromosome crossing over.
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Non-target-site herbicide resistance: a family business.

TL;DR: An integrated genomics approach is proposed to dissect systematically the functional genomics of four gene families in economically important weed species to understand the mechanisms of non-target-site resistance.
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Mechanisms of evolved herbicide resistance

TL;DR: The vast array of herbicide-resistance mechanisms for generalist (NTSR) and specialist (TSR and some NTSR) adaptations that have evolved over a few decades illustrate the evolutionary resilience of weed populations to extreme selection pressures.
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A component of the chloroplastic protein import apparatus is targeted to the outer envelope membrane via a novel pathway.

TL;DR: It is proposed that the N‐terminus of the prOEP75 transit peptide acts as a stromal‐targeting domain and a central, hydrophobic region of this transit peptides acts asA stop‐transfer domain in a complex route of insertion and processing of prO EP75 to ensure high fidelity targeting of this import component.