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Alistair R. R. Forrest

Researcher at Harry Perkins Institute of Medical Research

Publications -  184
Citations -  27204

Alistair R. R. Forrest is an academic researcher from Harry Perkins Institute of Medical Research. The author has contributed to research in topics: Gene & Regulation of gene expression. The author has an hindex of 59, co-authored 175 publications receiving 23544 citations. Previous affiliations of Alistair R. R. Forrest include Griffith University & Centre for Life.

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Expression analysis of the long non-coding RNA antisense to Uchl1 (AS Uchl1) during dopaminergic cells' differentiation in vitro and in neurochemical models of Parkinson's disease.

TL;DR: It is shown that AS Uchl1 expression is under the regulation of Nurr1, a major transcription factor involved in dopaminergic cells' differentiation and maintenance, extending the understanding on the role of antisense transcription in the brain.
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Differential roles of epigenetic changes and Foxp3 expression in regulatory T cell-specific transcriptional regulation

TL;DR: It is found that Treg-specific DNA hypomethylated regions were closely associated with Treg up-regulated transcriptional start site clusters, whereas Foxp3 binding regions had no significant correlation with either up- or down-regulated clusters in nonactivated Treg cells.
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Predicting cell-to-cell communication networks using NATMI

TL;DR: Analysis of the Tabula Muris (organism-wide) atlas confirms the previous prediction that autocrine signalling is a major feature of cell-to-cell communication networks, while also revealing that hundreds of ligands and their cognate receptors are co-expressed in individual cells suggesting a substantial potential for self-signalling.
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A rescue strategy for multimapping short sequence tags refines surveys of transcriptional activity by CAGE

TL;DR: The results suggest that the multimap tags produced by high-throughput, short sequence tag-based approaches can be rescued to augment greatly the transcriptome coverage provided by single-map tags alone.