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Craig McCormick

Researcher at Dalhousie University

Publications -  70
Citations -  8974

Craig McCormick is an academic researcher from Dalhousie University. The author has contributed to research in topics: Viral replication & Lytic cycle. The author has an hindex of 25, co-authored 67 publications receiving 7983 citations. Previous affiliations of Craig McCormick include Halifax & University of British Columbia.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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The Putative Tumor Suppressors EXT1 and EXT2 Form a Stable Complex That Accumulates in the Golgi Apparatus and Catalyzes the Synthesis of Heparan Sulfate

TL;DR: It appears that EXT1 and EXT2 form a hetero-oligomeric complex in vivo that leads to the accumulation of both proteins in the Golgi apparatus, which suggests that the complex represents the biologically relevant form of the enzyme(s).
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The Putative Tumor Suppressors EXT1 and EXT2 Are Glycosyltransferases Required for the Biosynthesis of Heparan Sulfate

TL;DR: McCormick et al. as mentioned in this paper reported the purification of a protein from bovine serum that harbored the D-glucuronyl (GlcA) and N-acetyl-Dglucosaminyl(GlcNAc) transferase activities required for biosynthesis of the glycosaminoglycan, heparan sulfate.
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The putative tumour suppressor EXT1 alters the expression of cell-surface heparan sulfate

TL;DR: It is shown that EXT1 is an ER-resident type II transmembrane glycoprotein whose expression in cells results in the alteration of the synthesis and display of cell surface heparan sulfate glycosaminoglycans (GAGs).
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Translation inhibition and stress granules in the antiviral immune response

TL;DR: This Review focuses on recent advances in the understanding of the role of translation inhibition and stress granules in antiviral immune responses.