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Victoria L. Green

Researcher at University of Hull

Publications -  36
Citations -  741

Victoria L. Green is an academic researcher from University of Hull. The author has contributed to research in topics: Head and neck squamous-cell carcinoma & Adenoma. The author has an hindex of 15, co-authored 34 publications receiving 644 citations. Previous affiliations of Victoria L. Green include Castle Hill Hospital & University of Liverpool.

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Expression of cytokine messenger RNA in normal and neoplastic human breast tissue: Identification of interleukin-8 as a potential regulatory factor in breast tumours

TL;DR: Analysis of primary epithelial and stromal cultures derived from both types of tissue showed that increased levels of IL‐8, but not IL‐6, were secreted by cells obtained from tumours, suggesting breast tissue of both normal and neoplastic origin expresses a wide range of cytokines.
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Prognostic value of the neutrophil‐to‐lymphocyte ratio in patients with laryngeal squamous cell carcinoma

TL;DR: The neutrophil/lymphocyte ratio (NLR) has been found to be predictive of survival outcome in a range of tumors and this study investigated the prognostic value of pretreatment in patients with laryngeal squamous cell carcinoma.
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Increased frequency and suppressive activity of CD127low/− regulatory T cells in the peripheral circulation of patients with head and neck squamous cell carcinoma are associated with advanced stage and nodal involvement

TL;DR: Peripheral Treg cells, identified by the CD127low/− phenotype, have been shown to be influenced by a patient's tumour stage and/or nodal status in HNSCC; suggesting a role in tumour progression that could be manipulated by future immunotherapy.
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Cytokine expression in human anterior pituitary adenomas

TL;DR: In this paper, a reverse transcriptase-linked polymerase chain reaction (PCR) was used to identify the presence of cytokine mRNA within human pituitary adenomas.
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Expression and secretion of TGF-beta isoforms and expression of TGF-beta-receptors I, II and III in normal and neoplastic human breast.

TL;DR: TGF- beta and TGF-beta-receptors are widely and differentially expressed by normal and malignant breast and secretion of this peptide by epithelial and stromal cultures, in particular those derived from tumours, confirms its potential as an autocrine/paracrine regulator in breast cancer.