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John Lunec

Researcher at Newcastle University

Publications -  148
Citations -  6241

John Lunec is an academic researcher from Newcastle University. The author has contributed to research in topics: Neuroblastoma & Gene. The author has an hindex of 43, co-authored 141 publications receiving 5797 citations. Previous affiliations of John Lunec include National Chemical Laboratory & University of Leicester.

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Induction of thymidylate synthase as a 5-fluorouracil resistance mechanism

TL;DR: In patients, TS levels as determined by enzyme activity assays, immunohistochemistry and mRNA expression, were related to a response to 5FU, and the clear retrospective relation between TS levels and response now forms the basis for a prospective study.
Journal Article

Prognostic Significance of HER2 and HER4 Coexpression in Childhood Medulloblastoma

TL;DR: The hypothesis that HER2-HER4 receptor heterodimerization is of particular biological significance in this disease is suggested and the first to demonstrate potential clinical significance of EGFR family heterodimers in human cancer is demonstrated.
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Alternatively spliced mdm2 transcripts with loss of p53 binding domain sequences: transforming ability and frequent detection in human cancer.

TL;DR: Five alternatively spliced mdm2 gene transcripts in a range of human cancers and their absence in normal tissues suggest a reassessment of the transforming mechanisms of mDM2 and its relation to p53.
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Quantification of MYCN, DDX1, and NAG Gene Copy Number in Neuroblastoma Using a Real-Time Quantitative PCR Assay

TL;DR: A real-time quantitative PCR assay is developed and evaluated as an alternative for time-consuming Southern blot analysis (SB), and as a second independent technique in parallel with fluorescence in situ hybridization (FISH) analysis, which pointed out that DDX1 and NAG amplification has no additional adverse effect on prognosis.
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Evidence for the Development of p53 Mutations after Cytotoxic Therapy in a Neuroblastoma Cell Line

TL;DR: If p53 mutations develop frequently in relapsed neuroblastoma, cytotoxic agents more sensitive to mutant p53 might be more effective at relapse.