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Rachel Young

Researcher at University of Edinburgh

Publications -  30
Citations -  958

Rachel Young is an academic researcher from University of Edinburgh. The author has contributed to research in topics: Gene & Transgene. The author has an hindex of 15, co-authored 29 publications receiving 716 citations. Previous affiliations of Rachel Young include Institut Gustave Roussy & Institut national de la recherche agronomique.

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Chromosome-level assembly of the water buffalo genome surpasses human and goat genomes in sequence contiguity

TL;DR: This new reference genome improves the contig N50 of the previous short-read based buffalo assembly more than a thousand-fold and contains only 383 gaps, which surpasses the human and goat references in sequence contiguity and facilitates the annotation of hard to assemble gene clusters such as the major histocompatibility complex (MHC).
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A high resolution atlas of gene expression in the domestic sheep (Ovis aries).

TL;DR: This high-resolution gene expression atlas for sheep is the largest transcriptomic dataset from any livestock species to date and provides a resource to improve the annotation of the current reference genome for sheep, presenting a model transcriptome for ruminants and insight into gene, cell and tissue function at multiple developmental stages.
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Zinc finger nuclease technology heralds a new era in mammalian transgenesis

TL;DR: This review focuses on the potential of this latter technology to modify mammalian genomes without the need to apply challenging and less-efficient protocols and the complementary aims of these new approaches and the as-yet-unexplored possibilities offered by their combination.
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ADGRE1 (EMR1, F4/80) Is a Rapidly-Evolving Gene Expressed in Mammalian Monocyte-Macrophages.

TL;DR: It is demonstrated that ADGRE1 is a myeloid differentiation marker in pigs, absent from progenitors in bone marrow, highly-expressed in mature granulocytes, monocytes, and tissue macrophages and induced by macrophage colony-stimulating factor (CSF1) treatment in vivo.
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The prion or the related Shadoo protein is required for early mouse embryogenesis

TL;DR: It is reported that the Shadoo‐encoding gene knockdown in PrP‐knockout mouse embryos results in a lethal phenotype, occurring between E8 and E11, not observed on the wild‐type genetic background.