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Michael McGregor

Researcher at Gladstone Institutes

Publications -  5
Citations -  3762

Michael McGregor is an academic researcher from Gladstone Institutes. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 2, co-authored 3 publications receiving 2407 citations. Previous affiliations of Michael McGregor include University of California, San Francisco.

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Journal ArticleDOI

A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.

David E. Gordon, +128 more
- 30 Apr 2020 - 
TL;DR: A human–SARS-CoV-2 protein interaction map highlights cellular processes that are hijacked by the virus and that can be targeted by existing drugs, including inhibitors of mRNA translation and predicted regulators of the sigma receptors.
Posted ContentDOI

A SARS-CoV-2-Human Protein-Protein Interaction Map Reveals Drug Targets and Potential Drug-Repurposing

David E. Gordon, +123 more
- 22 Mar 2020 - 
TL;DR: The identification of host dependency factors mediating virus infection may provide key insights into effective molecular targets for developing broadly acting antiviral therapeutics against SARS-CoV-2 and other deadly coronavirus strains.
Journal ArticleDOI

Transcription factor protein interactomes reveal genetic determinants in heart disease

TL;DR: In this paper , the authors proposed that genetic determinants for CHD may lie in the protein interactomes of transcription factors whose mutations cause CHDs, and defined the interactome of two transcription factors haplo-insufficient in CHD, GATA4 and TBX5 within human cardiac progenitors, and integrating the results with nearly 9,000 exomes from proband-parent trios revealed an enrichment of de novo missense variants associated with CHD within the interactomes.
Journal ArticleDOI

A functional map of HIV-host interactions in primary human T cells

TL;DR: In this paper , the authors target 426 genes previously implicated in the HIV lifecycle through protein interaction studies for CRISPR-Cas9-mediated knockout in primary human CD4+ T cells in order to systematically assess their functional roles in HIV replication.