Search Results - "Keeling, Suzanne E"

Lamprey (Geotria australis; Agnatha) reddening syndrome in Southland rivers, New Zealand 2011-2013: laboratory findings and epidemiology, including the incidental detection of an atypical Aeromonas salmonicida by Brosnahan, Cara L., Pande, Anjali, Keeling, Suzanne E., van Andel, Mary, Jones, John B.

“…From 2011, lamprey (Geotria australis) populations in Southland, New Zealand have been affected by reddening along the length of the body and increased…”
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Using chemical and DNA marker analysis to authenticate a high-value food, manuka honey by McDonald, Claire M., Keeling, Suzanne E., Brewer, Mark J., Hathaway, Steve C.

“…Ensuring the authenticity of food is a rapidly emerging issue, especially in regard to high-value products that are marketed through increasingly complex…”
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Optimization of Novel Indazoles as Highly Potent and Selective Inhibitors of Phosphoinositide 3‑Kinase δ for the Treatment of Respiratory Disease by Down, Kenneth, Amour, Augustin, Baldwin, Ian R, Cooper, Anthony W. J, Deakin, Angela M, Felton, Leigh M, Guntrip, Stephen B, Hardy, Charlotte, Harrison, Zoë A, Jones, Katherine L, Jones, Paul, Keeling, Suzanne E, Le, Joelle, Livia, Stefano, Lucas, Fiona, Lunniss, Christopher J, Parr, Nigel J, Robinson, Ed, Rowland, Paul, Smith, Sarah, Thomas, Daniel A, Vitulli, Giovanni, Washio, Yoshiaki, Hamblin, J. Nicole

“…Optimization of lead compound 1, through extensive use of structure-based design and a focus on PI3Kδ potency, isoform selectivity, and inhaled PK properties,…”
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The Squalestatins:  Decarboxy and 4-Deoxy Analogues as Potent Squalene Synthase Inhibitors by Chan, Chuen, Andreotti, Daniele, Cox, Brian, Dymock, Brian W, Hutson, Julie L, Keeling, Suzanne E, McCarthy, Alun D, Procopiou, Panayiotis A, Ross, Barry C, Sareen, Meenu, Scicinski, Jan J, Sharratt, Peter J, Snowden, Michael A, Watson, Nigel S

“…Squalestatins without either the hydroxy group at C-4 or the carboxylic acid at C-3 or C-4 were prepared and evaluated for their ability to inhibit rat liver…”
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Inhibitors of cholesterol biosynthesis. 1. 3,5-Dihydroxy-7-(N-imidazolyl)-6-heptenoates and -heptanoates, a novel series of 3-hydroxy-3-methylglutarate-CoA reductase inhibitors by Chan, Chuen, Bailey, Esme J, Hartley, C. David, Hayman, David F, Hutson, Julie L, Inglis, Graham G. A, Jones, Paul S, Keeling, Suzanne E, Kirk, Barrie E

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The discovery and synthesis of highly potent, A 2a receptor agonists by Keeling, Suzanne E., Albinson, F.David, Ayres, Barry E., Butchers, Peter R., Chambers, C.Lynn, Cherry, Peter C., Ellis, Frank, Ewan, George B., Gregson, Michael, Knight, John, Mills, Keith, Ravenscroft, Paul, Reynolds, Linda H., Sanjar, Shahin, Sheehan, Michael J.

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Inhibitors of cholesterol biosynthesis. 1. 3,5-Dihydroxy-7-(N-imidazolyl)-6-heptenoates and -heptanoates, a novel series of HMG-CoA reductase inhibitors by Chan, C, Bailey, E J, Hartley, C D, Hayman, D F, Hutson, J L, Inglis, G G, Jones, P S, Keeling, S E, Kirk, B E, Lamont, R B

“…3,5-Dihydroxy-7-(N-imidazolyl)heptanoates 4 and the corresponding heptenoates 5 were synthesized as novel classes of potent HMG-CoA reductase (HMGR) inhibitors…”
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