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Simon J. Cook

Researcher at University of Glasgow

Publications -  16
Citations -  1239

Simon J. Cook is an academic researcher from University of Glasgow. The author has contributed to research in topics: Phosphatidylcholine & Protein kinase C. The author has an hindex of 12, co-authored 16 publications receiving 1214 citations. Previous affiliations of Simon J. Cook include Cetus Corporation.

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Molecular phylogeny and evolutionary timescale for the family of mammalian herpesviruses.

TL;DR: A detailed phylogenetic analysis for mammalian members of the family Herpesviridae, based on molecular sequences is reported, finding that major sublineages within subfamilies were probably generated before the mammalian radiation of 80 to 60 million years ago, and that speciations within sub lineages took place in the last 80 million years, probably with a major component of cospeciation with host lineages.
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Molecular phylogeny of the alphaherpesvirinae subfamily and a proposed evolutionary timescale

TL;DR: It was estimated that the two mammalian alphaherpesvirus groups diverged around the period of the mammalian radiation, and that alphaherpeviral genome sequences have evolved faster than those of mammals by a factor of one to two orders of magnitude.
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Analysis of the water-soluble products of phosphatidylcholine breakdown by ion-exchange chromatography. Bombesin and TPA (12-O-tetradecanoylphorbol 13-acetate) stimulate choline generation in Swiss 3T3 cells by a common mechanism.

TL;DR: The results suggest that stimulation of the cells with either bombesin or TPA activates phospholipase D-catalysed phosphatidylcholine breakdown by a common mechanism involving the activation of protein kinase C.
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Multiple sources of sn-1,2-diacylglycerol in platelet-derived-growth-factor-stimulated Swiss 3T3 fibroblasts. Evidence for activation of phosphoinositidase C and phosphatidylcholine-specific phospholipase D.

TL;DR: Platelet-derived growth factor stimulated sn-1,2-diacylglycerol (DAG) mass formation in Swiss 3T3 fibroblasts with a lag time of some 30 s, suggesting that DAG is derived from PtdIns(4,5)P2 hydrolysis at this time point, and down-regulation of protein kinase C by pre-treatment with phorbol 12-myristate 13-acetate abolished both choline
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Epidermal growth factor increases sn-1,2-diacylglycerol levels and activates phospholipase D-catalysed phosphatidylcholine breakdown in Swiss 3T3 cells in the absence of inositol-lipid hydrolysis.

TL;DR: Addition of epidermal growth factor to quiescent Swiss 3T3 cells resulted in a sustained increase in cellular diacylglycerol (DG) content in the absence of inositol-lipid hydrolysis, suggesting a role for a coupled PLD/phosphatidate phosphohydrolase pathway.