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Items: 1 to 20 of 96

2.
3.

The expression of type III hyperlipoproteinemia: involvement of lipolysis genes.

Henneman P, van der Sman-de Beer F, Moghaddam PH, Huijts P, Stalenhoef AF, Kastelein JJ, van Duijn CM, Havekes LM, Frants RR, van Dijk KW, Smelt AH.

Eur J Hum Genet. 2009 May;17(5):620-8. doi: 10.1038/ejhg.2008.202. Epub 2008 Nov 26.

4.

Patients with apoE3 deficiency (E2/2, E3/2, and E4/2) who manifest with hyperlipidemia have increased frequency of an Asn 291-->Ser mutation in the human LPL gene.

Zhang H, Reymer PW, Liu MS, Forsythe IJ, Groenemeyer BE, Frohlich J, Brunzell JD, Kastelein JJ, Hayden MR, Ma Y.

Arterioscler Thromb Vasc Biol. 1995 Oct;15(10):1695-703.

PMID:
7583546
5.

Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.

de Bruin TW, Mailly F, van Barlingen HH, Fisher R, Castro Cabezas M, Talmud P, Dallinga-Thie GM, Humphries SE.

Eur J Clin Invest. 1996 Aug;26(8):631-9.

PMID:
8872057
6.

Diagnostic value of post-heparin lipase testing in detecting common genetic variants in the LPL and LIPC genes.

van Hoek M, Dallinga-Thie GM, Steyerberg EW, Sijbrands EJ.

Eur J Hum Genet. 2009 Nov;17(11):1386-93. doi: 10.1038/ejhg.2009.61. Epub 2009 Apr 15.

7.

Association of pre-eclampsia with common coding sequence variations in the lipoprotein lipase gene.

Hubel CA, Roberts JM, Ferrell RE.

Clin Genet. 1999 Oct;56(4):289-96.

PMID:
10636447
8.

Expression of type III hyperlipoproteinemia in apolipoprotein E2 (Arg158 --> Cys) homozygotes is associated with hyperinsulinemia.

de Beer F, Stalenhoef AF, Hoogerbrugge N, Kastelein JJ, Gevers Leuven JA, van Duijn CM, Havekes LM, Smelt AH.

Arterioscler Thromb Vasc Biol. 2002 Feb 1;22(2):294-9.

PMID:
11834531
9.

Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women.

Kastelein JJ, Ordovas JM, Wittekoek ME, Pimstone SN, Wilson WF, Gagné SE, Larson MG, Schaefer EJ, Boer JM, Gerdes C, Hayden MR.

Clin Genet. 1999 Oct;56(4):297-305.

PMID:
10636448
10.

Genetic variants of the lipoprotein lipase gene and myocardial infarction in the Central Valley of Costa Rica.

Yang Y, Ruiz-Narvaez E, Niu T, Xu X, Campos H.

J Lipid Res. 2004 Nov;45(11):2106-9. Epub 2004 Aug 1.

11.

Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia.

Evans D, Arzer J, Aberle J, Beil FU.

Atherosclerosis. 2011 Feb;214(2):386-90. doi: 10.1016/j.atherosclerosis.2010.11.026. Epub 2010 Nov 26.

PMID:
21159338
12.

Polymorphisms in the apolipoprotein A5 (APOA5) gene and type III hyperlipidemia.

Evans D, Seedorf U, Beil FU.

Clin Genet. 2005 Oct;68(4):369-72.

PMID:
16143024
13.

Studies of familial type III hyperlipoproteinemia using as a genetic marker the apoE phenotype E2/2.

Breslow JL, Zannis VI, SanGiacomo TR, Third JL, Tracy T, Glueck CJ.

J Lipid Res. 1982 Nov;23(8):1224-35.

14.

Lipoprotein lipase (LPL) gene variation and progression of carotid artery plaque.

Spence JD, Ban MR, Hegele RA.

Stroke. 2003 May;34(5):1176-80. Epub 2003 Apr 10.

PMID:
12690214
15.

[Lipoprotein lipase gene mutations and the risk of cardiovascular diseases in children with obesity].

Guan YM, Gui YH, Luo FH, Shen SX, Yang Y.

Zhongguo Dang Dai Er Ke Za Zhi. 2010 Mar;12(3):161-4. Chinese.

16.

Frequency and allelic association of common variants in the lipoprotein lipase gene in different ethnic groups: the Wandsworth Heart and Stroke Study.

Hall S, Talmud PJ, Cook DG, Wicks PD, Rothwell MJ, Strazzullo P, Sagnella GA, Cappuccio FP.

Genet Epidemiol. 2000 Mar;18(3):203-16.

PMID:
10723106
17.

Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-study.

Ariza MJ, Sánchez-Chaparro MA, Barón FJ, Hornos AM, Calvo-Bonacho E, Rioja J, Valdivielso P, Gelpi JA, González-Santos P.

BMC Med Genet. 2010 Apr 29;11:66. doi: 10.1186/1471-2350-11-66.

19.

Lipoprotein lipase mutation S447X associated with pancreatic calcification and steatorrhea in hyperlipidemic pancreatitis.

Chang YT, Chang MC, Su TC, Liang PC, Su YN, Kuo CH, Wei SC, Wong JM.

J Clin Gastroenterol. 2009 Jul;43(6):591-6. doi: 10.1097/MCG.0b013e3181734a30.

PMID:
19034041
20.

Gene polymorphisms in the Quebec population: a risk to develop hypertriglyceridemia.

Garenc C, Aubert S, Laroche J, Bergeron J, Gagné C, Rousseau F, Julien P.

Biochem Biophys Res Commun. 2006 Jun 2;344(2):588-96. Epub 2006 Apr 6.

PMID:
16630553

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