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A.A. Ritchie

Researcher at University of Nottingham

Publications -  47
Citations -  1672

A.A. Ritchie is an academic researcher from University of Nottingham. The author has contributed to research in topics: In vivo & Medicine. The author has an hindex of 18, co-authored 39 publications receiving 1428 citations. Previous affiliations of A.A. Ritchie include Western General Hospital.

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In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer.

TL;DR: High activity coupled to non cross-resistance in cisplatin resistant models merit further development of this novel group of anticancer compounds.
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Does age matter? The impact of rodent age on study outcomes

TL;DR: It is highlighted that choice of age is inconsistent across the research community and often not based on the development or cellular ageing of the system being studied, which could potentially result in decreased scientific validity and increased experimental variability.
Journal Article

Broad Spectrum Neuropeptide Antagonists Inhibit the Growth of Small Cell Lung Cancer in Vivo

TL;DR: The results indicate that broad spectrum neuropeptide antagonists can inhibit the growth of SCLC in vivo and suggest that these antagonists could be useful in the treatment of S CLC.
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Targeting the EGF receptor in ovarian cancer with the tyrosine kinase inhibitor ZD 1839 (‘Iressa’)

TL;DR: The modulating effects of the orally active epidermal growth factor receptor-specific tyrosine kinase inhibitor ZD 1839 (‘Iressa’) on cell growth and signalling were evaluated in four ovarian cancer cell lines and lend further support to the view that targeting the epidersmal growthFactor receptor in ovarian cancer could have therapeutic benefit.
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Association of c-Raf expression with survival and its targeting with antisense oligonucleotides in ovarian cancer.

TL;DR: Antisense oligodeoxynucleotides (ODNs) reduced c-Raf protein levels and inhibited cell proliferation in vitro and in vivo and use of antisense ODNs targeted to c- Raf could provide a strategy for the treatment of this disease.