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Richard A. Radcliffe

Researcher at University of Montana

Publications -  67
Citations -  2172

Richard A. Radcliffe is an academic researcher from University of Montana. The author has contributed to research in topics: Quantitative trait locus & Gene. The author has an hindex of 25, co-authored 67 publications receiving 1921 citations. Previous affiliations of Richard A. Radcliffe include University of Colorado Boulder & University of Colorado Denver.

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The multiMiR R package and database: integration of microRNA–target interactions along with their disease and drug associations

TL;DR: MultiMiR is presented, a new miRNA–target interaction R package and database, which includes several novel features not available in existing R packages and was used to generate testable hypotheses that were pursued experimentally.
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Quantitative trait locus analysis of contextual fear conditioning in mice

TL;DR: A quantitative trait locus (QTL) analysis of contextual fear conditioning was performed in a B6/D2 F2 intercross population of mice, finding evidence for a substantial genetic component underlying individual differences in general intelligence, specific cognitive abilities and susceptibility to psychopathologies related to fear-inducing events.
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The Role of RNA Editing of Kainate Receptors in Synaptic Plasticity and Seizures

TL;DR: Results suggest that GluR6 Q/R site RNA editing may modulate synaptic plasticity and seizure vulnerability and suggest that NMDA receptor-independent long-term potentiation could be induced at the medial perforant path-dentate gyrus synapse.
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Growth inhibition and regression of lung tumors by silibinin: modulation of angiogenesis by macrophage-associated cytokines and nuclear factor-kappaB and signal transducers and activators of transcription 3.

TL;DR: Therapeutic efficacy of silibinin in lung tumor growth inhibition and regression by antiangiogenic mechanisms seem to be mediated by decreased tumor-associated macrophages and cytokines, inhibition of hypoxia-inducible factor-1α, NF-κB, and STAT-3 activation, and up-regulation of the angiogenic inhibitors, Ang-2 and Tie-2.
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Contextual and cued fear conditioning in C57BL/6J and DBA/2J mice: context discrimination and the effects of retention interval.

TL;DR: Context discrimination and time course studies of contextual fear conditioning revealed strain differences between C57BL/6J (B6) and DBA/2J (D2) mice, which confirmed that B6, but not D2, mice retained contextual memories for at least 60 days.