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Patricia M. Ingleton

Researcher at University of Sheffield

Publications -  45
Citations -  1453

Patricia M. Ingleton is an academic researcher from University of Sheffield. The author has contributed to research in topics: Parathyroid hormone-related protein & Prolactin receptor. The author has an hindex of 26, co-authored 45 publications receiving 1420 citations.

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Journal ArticleDOI

Effect of maternal nutrition on brown adipose tissue and its prolactin receptor status in the fetal lamb.

TL;DR: Increasing the quantity of feed provided in late gestation acts to promote fetal weight and BAT maturation, the combination of which will enhance neonatal viability.
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Cloning, characterization, and tissue distribution of prolactin receptor in the sea bream (Sparus aurata).

TL;DR: Immunohistochemistry using specific polyclonal antibodies raised against an oligopeptide from the extracellular domain of sbPRLR detected PRLR in several epithelial tissues of juvenile sea bream, including the anterior gut, renal tubule, choroid membrane of the third ventricle, saccus vasculosus, branchial chloride cells, and branchial cartilage.
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Detection of Prolactin Receptor Gene Expression in the Sheep Pituitary Gland and Visualization of the Specific Translation of the Signal in Gonadotrophs

TL;DR: The hypothesis that PRL may be involved in the regulation of gonadotropin secretion through a paracrine mechanism within the pituitary gland and that this action does not seem to be mediated by changes in PRL-R mRNA expression is supported.
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The effect of stocking density on growth in the gilthead sea‐bream, Sparus aurata (L.)

TL;DR: It was concluded that growth in gilthead sea-bream, although negatively correlated to stocking density, did not seem to be related to intraspecific competition as assessed by changes in size variability.
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Cloning, expression, and tissue localisation of prolactin in adult sea bream (Sparus aurata).

TL;DR: Pituitary prolactin cDNA has been cloned and sequenced from sea bream, a marine teleost, and Reverse transcription and polymerase chain reaction techniques coupled with Southern blot analysis resulted in the detection of PRL in the pituitary but also in the intestine, liver, ovary, and testes.