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Alexandra K. Bell

Researcher at University of Glasgow

Publications -  13
Citations -  1323

Alexandra K. Bell is an academic researcher from University of Glasgow. The author has contributed to research in topics: Breast cancer & Involution (medicine). The author has an hindex of 11, co-authored 13 publications receiving 1268 citations.

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p53 polymorphism influences response in cancer chemotherapy via modulation of p73-dependent apoptosis.

TL;DR: Polymorphism in p53 may influence individual responsiveness to cancer therapy, and clinical response following cisplatin-based chemo-radiotherapy for advanced head and neck cancer is influenced by this polymorphism, cancers expressing 72R mutants having lower response rates than those expressing 72P mutants.
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Involution of the mouse mammary gland is associated with an immune cascade and an acute-phase response, involving LBP, CD14 and STAT3

TL;DR: Oligonucleotide microarrays are a useful tool for identifying genes that are involved in the complex developmental process of mammary glands involution, with an early acute-phase response that occurs in the mammary gland itself and resembles a wound healing process.
Journal Article

Epigenetic Inactivation of 14-3-3 σ in Oral Carcinoma Association with p16INK4a Silencing and Human Papillomavirus Negativity

TL;DR: Results implicate coincident epigenetic abrogation of function in both sigma and p16(INK4a) in a subset of SCCs of the oral cavity that were more commonly detected in cancers with wild-type p53.
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Concomitant inactivation of p53 and Chk2 in breast cancer.

TL;DR: The results nevertheless reveal that concomitant loss of function in Chk2 (via down-regulation of expression) and p53 (via mutation) occurs in a proportion of sporadic cases, and it is shown that germ-line mutations in ChK2 are unlikely to account for a significant proportion of non BRCA1-, non B RCA2-associated hereditary breast cancers.
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Loss of Reelin Expression in Breast Cancer Is Epigenetically Controlled and Associated with Poor Prognosis

TL;DR: It is concluded that reelin may play an important role in controlling invasiveness and metastatic potential of breast cancer cells and that its expression is controlled by promoter methylation.