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Items: 11

1.

Activation of AMP-activated protein kinase rapidly suppresses multiple pro-inflammatory pathways in adipocytes including IL-1 receptor-associated kinase-4 phosphorylation.

Mancini SJ, White AD, Bijland S, Rutherford C, Graham D, Richter EA, Viollet B, Touyz RM, Palmer TM, Salt IP.

Mol Cell Endocrinol. 2017 Jan 15;440:44-56. doi: 10.1016/j.mce.2016.11.010. Epub 2016 Nov 11.

2.

Apolipoprotein A5 deficiency aggravates high-fat diet-induced obesity due to impaired central regulation of food intake.

van den Berg SA, Heemskerk MM, Geerling JJ, van Klinken JB, Schaap FG, Bijland S, Berbée JF, van Harmelen VJ, Pronk AC, Schreurs M, Havekes LM, Rensen PC, van Dijk KW.

FASEB J. 2013 Aug;27(8):3354-62. doi: 10.1096/fj.12-225367. Epub 2013 May 6.

PMID:
23650188
3.

Role of AMP-activated protein kinase in adipose tissue metabolism and inflammation.

Bijland S, Mancini SJ, Salt IP.

Clin Sci (Lond). 2013 Apr;124(8):491-507. doi: 10.1042/CS20120536. Review.

PMID:
23298225
4.

Treatment of genetically obese mice with the iminosugar N-(5-adamantane-1-yl-methoxy-pentyl)-deoxynojirimycin reduces body weight by decreasing food intake and increasing fat oxidation.

Langeveld M, van den Berg SA, Bijl N, Bijland S, van Roomen CP, Houben-Weerts JH, Ottenhoff R, Houten SM, van Dijk KW, Romijn JA, Groen AK, Aerts JM, Voshol PJ.

Metabolism. 2012 Jan;61(1):99-107. doi: 10.1016/j.metabol.2011.05.013. Epub 2011 Aug 3.

PMID:
21816446
5.

Perfluoroalkyl sulfonates cause alkyl chain length-dependent hepatic steatosis and hypolipidemia mainly by impairing lipoprotein production in APOE*3-Leiden CETP mice.

Bijland S, Rensen PC, Pieterman EJ, Maas AC, van der Hoorn JW, van Erk MJ, Havekes LM, Willems van Dijk K, Chang SC, Ehresman DJ, Butenhoff JL, Princen HM.

Toxicol Sci. 2011 Sep;123(1):290-303. doi: 10.1093/toxsci/kfr142. Epub 2011 Jun 24.

PMID:
21705711
6.

High-fat diets rich in medium- versus long-chain fatty acids induce distinct patterns of tissue specific insulin resistance.

De Vogel-van den Bosch J, van den Berg SA, Bijland S, Voshol PJ, Havekes LM, Romijn HA, Hoeks J, van Beurden D, Hesselink MK, Schrauwen P, van Dijk KW.

J Nutr Biochem. 2011 Apr;22(4):366-71. doi: 10.1016/j.jnutbio.2010.03.004. Epub 2010 Jul 23.

PMID:
20655716
7.

An 8-week high-fat diet induces obesity and insulin resistance with small changes in the muscle transcriptome of C57BL/6J mice.

de Wilde J, Smit E, Mohren R, Boekschoten MV, de Groot P, van den Berg SA, Bijland S, Voshol PJ, van Dijk KW, de Wit NW, Bunschoten A, Schaart G, Hulshof MF, Mariman EC.

J Nutrigenet Nutrigenomics. 2009;2(6):280-91. doi: 10.1159/000308466. Epub 2010 Jun 28.

PMID:
20588053
8.

Fenofibrate increases very low density lipoprotein triglyceride production despite reducing plasma triglyceride levels in APOE*3-Leiden.CETP mice.

Bijland S, Pieterman EJ, Maas AC, van der Hoorn JW, van Erk MJ, van Klinken JB, Havekes LM, van Dijk KW, Princen HM, Rensen PC.

J Biol Chem. 2010 Aug 13;285(33):25168-75. doi: 10.1074/jbc.M110.123992. Epub 2010 May 25.

9.

High levels of whole-body energy expenditure are associated with a lower coupling of skeletal muscle mitochondria in C57Bl/6 mice.

van den Berg SA, Nabben M, Bijland S, Voshol PJ, van Klinken JB, Havekes LM, Romijn JA, Hoeks J, Hesselink MK, Schrauwen P, van Dijk KW.

Metabolism. 2010 Nov;59(11):1612-8. doi: 10.1016/j.metabol.2010.03.008. Epub 2010 May 24.

PMID:
20494374
10.

High levels of dietary stearate promote adiposity and deteriorate hepatic insulin sensitivity.

van den Berg SA, Guigas B, Bijland S, Ouwens M, Voshol PJ, Frants RR, Havekes LM, Romijn JA, van Dijk KW.

Nutr Metab (Lond). 2010 Mar 27;7:24. doi: 10.1186/1743-7075-7-24.

11.

CETP does not affect triglyceride production or clearance in APOE*3-Leiden mice.

Bijland S, van den Berg SA, Voshol PJ, van den Hoek AM, Princen HM, Havekes LM, Rensen PC, Willems van Dijk K.

J Lipid Res. 2010 Jan;51(1):97-102. doi: 10.1194/jlr.M900186-JLR200.

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