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Laurence D. Hurst

Researcher at University of Bath

Publications -  310
Citations -  24738

Laurence D. Hurst is an academic researcher from University of Bath. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 76, co-authored 296 publications receiving 22836 citations. Previous affiliations of Laurence D. Hurst include University of Chicago & University of Oxford.

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Evidence for a Trade-Off between Translational Efficiency and Splicing Regulation in Determining Synonymous Codon Usage in Drosophila melanogaster

TL;DR: It is concluded that usage of translationally optimal codons usage is compromised in the vicinity of splice junctions in intron-containing genes, to the effect that higher levels of usage of translated codons at the center of exons are observed.
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Do we understand the evolution of genomic imprinting

TL;DR: The conflict theory is the only hypothesis to have attracted any critical attention for the evolution of genomic imprinting, but although the earliest data appeared supportive, recent systematic analyses have not confirmed the model's predictions.
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The architecture of intra-organism mutation rate variation in plants.

TL;DR: It is concluded that some mutation rate variation between tissues is consistent with selectionist theory but that a mechanistic null of mutational fragility should be considered.
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Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay

TL;DR: For recently evolved exons the noisy splicing model is the better explanation of their properties, while for ancientExons the nonsense-mediated decay regulated gene expression is a viable explanation.
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Causes and consequences of crossing-over evidenced via a high-resolution recombinational landscape of the honey bee

TL;DR: The data are consistent with the view that diversification of worker behavior, but not immune function, is a driver of the high crossing-over rate in bees, and demonstrate that high non-crossover rates are not a necessary consequence of high recombination rates.