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Shireen A. Davies

Researcher at University of Glasgow

Publications -  98
Citations -  5869

Shireen A. Davies is an academic researcher from University of Glasgow. The author has contributed to research in topics: Malpighian tubule system & Drosophila melanogaster. The author has an hindex of 44, co-authored 96 publications receiving 5345 citations. Previous affiliations of Shireen A. Davies include University of Bordeaux & Life Sciences Institute.

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Normal p21N-ras couples bombesin and other growth factor receptors to inositol phosphate production.

TL;DR: It is shown that the expression of normal p21N–ras in NIH 3T3 fibroblasts leads to the coupling of certain growth factor receptors to stimulated inositol phosphate production, and it is proposed that the N-ras proto-oncogene encodes a protein which couples the receptors for certain growth factors to the stimulation of phospholipase C.
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FlyAtlas 2: a new version of the Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data

TL;DR: Gene coverage has been extended by the inclusion of microRNAs and many of the RNA genes included in Release 6 of the Drosophila reference genome, and the web interface has been modified to accommodate the extra data, but at the same time has been adapted for viewing on small mobile devices.
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Function-informed transcriptome analysis of Drosophila renal tubule

TL;DR: A radically new view of the function of the tubule, emphasizing solute transport rather than fluid secretion, can be obtained from those genes that are identifiable.
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Two nitridergic peptides are encoded by the gene capability in Drosophila melanogaster

TL;DR: The capa gene is the first to be shown to encode neuropeptides that act on renal fluid production through nitric oxide and is shown to be not synergistic, implying that both act on the same pathways in tubules.
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Isolation and characterization of a leucokinin-like peptide of Drosophila melanogaster

TL;DR: The genomic sequence encoding the DLK peptide has been identified, and the gene has been named pp.E3-70F4 of chromosome 3L, and it is suggested that this first Drosophila LK gene in a genetic model permits a genetic analysis of the locus.