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Items: 1 to 20 of 87

1.

Apolipoprotein-E-deficient mice exhibit an increased susceptibility to disseminated candidiasis.

Vonk AG, De Bont N, Netea MG, Demacker PN, van der Meer JW, Stalenhoef AF, Kullberg BJ.

Med Mycol. 2004 Aug;42(4):341-8.

PMID:
15473359
2.

Hyperlipoproteinemia enhances susceptibility to acute disseminated Candida albicans infection in low-density-lipoprotein-receptor-deficient mice.

Netea MG, Demacker PN, de Bont N, Boerman OC, Stalenhoef AF, van der Meer JW, Kullberg BJ.

Infect Immun. 1997 Jul;65(7):2663-7.

3.

In the absence of endogenous mouse apolipoprotein E, apolipoprotein E*2(Arg-158 --> Cys) transgenic mice develop more severe hyperlipoproteinemia than apolipoprotein E*3-Leiden transgenic mice.

van Vlijmen BJ, van Dijk KW, van't Hof HB, van Gorp PJ, van der Zee A, van der Boom H, Breuer ML, Hofker MH, Havekes LM.

J Biol Chem. 1996 Nov 29;271(48):30595-602.

5.

Apolipoprotein E knock-out mice are highly susceptible to endotoxemia and Klebsiella pneumoniae infection.

de Bont N, Netea MG, Demacker PN, Verschueren I, Kullberg BJ, van Dijk KW, van der Meer JW, Stalenhoef AF.

J Lipid Res. 1999 Apr;40(4):680-5.

6.

Bone marrow transplantation in apolipoprotein E-deficient mice. Effect of ApoE gene dosage on serum lipid concentrations, (beta)VLDL catabolism, and atherosclerosis.

Van Eck M, Herijgers N, Yates J, Pearce NJ, Hoogerbrugge PM, Groot PH, Van Berkel TJ.

Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):3117-26.

PMID:
9409301
7.
9.

Modulation of very low density lipoprotein production and clearance contributes to age- and gender- dependent hyperlipoproteinemia in apolipoprotein E3-Leiden transgenic mice.

van Vlijmen BJ, van 't Hof HB, Mol MJ, van der Boom H, van der Zee A, Frants RR, Hofker MH, Havekes LM.

J Clin Invest. 1996 Mar 1;97(5):1184-92.

10.

Infusion of lipoproteins into volunteers enhances the growth of Candida albicans.

Netea MG, Curfs JH, Demacker PN, Meis JF, Van der Meer JW, Kullberg BJ.

Clin Infect Dis. 1999 May;28(5):1148-51.

PMID:
10452650
12.

Endogenous interleukin (IL)-1 alpha and IL-1 beta are crucial for host defense against disseminated candidiasis.

Vonk AG, Netea MG, van Krieken JH, Iwakura Y, van der Meer JW, Kullberg BJ.

J Infect Dis. 2006 May 15;193(10):1419-26. Epub 2006 Apr 4.

PMID:
16619190
13.

Apolipoprotein E participates in the regulation of very low density lipoprotein-triglyceride secretion by the liver.

Mensenkamp AR, Jong MC, van Goor H, van Luyn MJ, Bloks V, Havinga R, Voshol PJ, Hofker MH, van Dijk KW, Havekes LM, Kuipers F.

J Biol Chem. 1999 Dec 10;274(50):35711-8.

14.
16.

Comparison of pathogenesis and host immune responses to Candida glabrata and Candida albicans in systemically infected immunocompetent mice.

Brieland J, Essig D, Jackson C, Frank D, Loebenberg D, Menzel F, Arnold B, DiDomenico B, Hare R.

Infect Immun. 2001 Aug;69(8):5046-55.

17.

Uptake by J774 macrophages of very-low-density lipoproteins isolated from apoE-deficient mice is mediated by a distinct receptor and stimulated by lipoprotein lipase.

Hendriks WL, van der Sman-de Beer F, van Vlijmen BJ, van Vark LC, Hofker MH, Havekes LM.

Arterioscler Thromb Vasc Biol. 1997 Mar;17(3):498-504.

PMID:
9102168
18.

Characterization of very low density lipoproteins and intermediate density lipoproteins of normo- and hyperlipidemic apolipoprotein E-2 homozygotes.

Schmitz G, Assmann G, Augustin J, Dirkes-Kersting A, BrennhaĆ¼sen B, Karoff C.

J Lipid Res. 1985 Mar;26(3):316-26.

19.
20.

Apolipoprotein E2 (Lys146-->Gln) causes hypertriglyceridemia due to an apolipoprotein E variant-specific inhibition of lipolysis of very low density lipoproteins-triglycerides.

de Beer F, van Dijk KW, Jong MC, van Vark LC, van der Zee A, Hofker MH, Fallaux FJ, Hoeben RC, Smelt AH, Havekes LM.

Arterioscler Thromb Vasc Biol. 2000 Jul;20(7):1800-6.

PMID:
10894820

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