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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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Journal ArticleDOI
In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer.
R E Aird,Jeffrey Cummings,A.A. Ritchie,M. Muir,Morris Robert Edward,Haimei Chen,Peter J. Sadler,Duncan I. Jodrell +7 more
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
Samuel J. Jackson,Nick Andrews,Doug Ball,Ilaria Bellantuono,James Gray,Lamia Hachoumi,Alan Holmes,Judy Latcham,Anja Petrie,Paul Potter,Andrew S.C. Rice,A.A. Ritchie,Michelle Stewart,Carol Strepka,Mark Yeoman,Kathryn Chapman +15 more
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.
Fiona McPhillips,Peter Mullen,Brett P. Monia,A.A. Ritchie,F A Dorr,John F. Smyth,Simon P. Langdon +6 more
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.