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Items where Author is "Currie, J"

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Number of items: 8.

Article

Tan, GD, Neville, MJ, Liverani, E, Humphreys, SM, Currie, JM, Dennis, L, Fielding, BA and Karpe, F (2006) The in vivo effects of the Pro12Ala PPAR gamma 2 polymorphism on adipose tissue NEFA metabolism: the first use of the Oxford Biobank DIABETOLOGIA, 49 (1). pp. 158-168.

Moffitt, JH, Fielding, BA, Evershed, R, Berstan, R, Currie, JM and Clark, A (2005) Adverse physicochemical properties of tripalmitin in beta cells lead to morphological changes and lipotoxicity in vitro DIABETOLOGIA, 48 (9). pp. 1819-1829.

Riserus, U, Tan, GD, Fielding, BA, Neville, MJ, Currie, J, Savage, DB, Chatterjee, VK, Frayn, KN, O'Rahilly, S and Karpe, F (2005) Rosiglitazone increases indexes of stearoyl-CoA desaturase activity in humans - Link to insulin sensitization and the role of dominant-negative mutation in peroxisome proliferator-activated receptor-gamma DIABETES, 54 (5). pp. 1379-1384.

Tan, GD, Fielding, BA, Currie, JM, Humphreys, SM, Desage, M, Frayn, K, Laville, M, Vidal, H and Karpe, F (2005) The effects of rosiglitazone on fatty acid and triglyceride metabolism in type 2 diabetes DIABETOLOGIA, 48 (1). pp. 83-95.

Ardilouze, JL, Karpe, F, Currie, JM, Frayn, KN and Fielding, BA (2004) Subcutaneous adipose tissue blood flow varies between superior and inferior levels of the anterior abdominal wall INTERNATIONAL JOURNAL OF OBESITY, 28 (2). pp. 228-233.

Ardilouze, JL, Fielding, BA, Currie, JM, Frayn, KN and Karpe, F (2004) Nitric oxide and beta-adrenergic stimulation are major regulators of preprandial and postprandial subcutaneous adipose tissue blood flow in humans CIRCULATION, 109 (1). pp. 47-52.

Robertson, MD, Currie, JM, Morgan, LM, Jewell, DP and Frayn, KN (2003) Prior short-term consumption of resistant starch enhances postprandial insulin sensitivity in healthy subjects DIABETOLOGIA, 46 (5). pp. 659-665.

Conference or Workshop Item

Moffitt, JH, Fielding, B, Currie, J and Clark, A (2004) Triacylglycerol formed in islet beta cells exposed to fatty acids do not contribute to decreased viability except in cells forming predominantly tripalmitin In: 40th Annual Meeting of the European-Association-for-the-Study-of-Diabetes, 2004-09-05 - 2004-09-09, Munich, GERMANY.

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