Similar articles for PMID: 12519372

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1978	1
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1989	3
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1998	1
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2024	0

1

Polymorphisms at the SRBI locus are associated with lipoprotein levels in subjects with heterozygous familial hypercholesterolemia.

Tai ES, Adiconis X, Ordovas JM, Carmena-Ramon R, Real J, Corella D, Ascaso J, Carmena R. Tai ES, et al. Clin Genet. 2003 Jan;63(1):53-8. doi: 10.1034/j.1399-0004.2003.630108.x. Clin Genet. 2003. PMID: 12519372

2

Genetic variation at the scavenger receptor class B type I gene locus determines plasma lipoprotein concentrations and particle size and interacts with type 2 diabetes: the framingham study.

Osgood D, Corella D, Demissie S, Cupples LA, Wilson PW, Meigs JB, Schaefer EJ, Coltell O, Ordovas JM. Osgood D, et al. J Clin Endocrinol Metab. 2003 Jun;88(6):2869-79. doi: 10.1210/jc.2002-021664. J Clin Endocrinol Metab. 2003. PMID: 12788901

3

Influence of microsomal triglyceride transfer protein promoter polymorphism -493 GT on fasting plasma triglyceride values and interaction with treatment response to atorvastatin in subjects with heterozygous familial hypercholesterolaemia.

García-García AB, González C, Real JT, Martín de Llano JJ, González-Albert V, Civera M, Chaves FJ, Ascaso JF, Carmena R. García-García AB, et al. Pharmacogenet Genomics. 2005 Apr;15(4):211-8. doi: 10.1097/01213011-200504000-00004. Pharmacogenet Genomics. 2005. PMID: 15864113

4

Oxidative structural modifications of low density lipoprotein in homozygous familial hypercholesterolemia.

Napoli C, Postiglione A, Triggiani M, Corso G, Palumbo G, Carbone V, Ruocco A, Ambrosio G, Montefusco S, Malorni A, Condorelli M, Chiariello M. Napoli C, et al. Atherosclerosis. 1995 Dec;118(2):259-73. doi: 10.1016/0021-9150(95)05612-2. Atherosclerosis. 1995. PMID: 8770320

5

Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrations.

Torres AL, Moorjani S, Vohl MC, Gagné C, Lamarche B, Brun LD, Lupien PJ, Després JP. Torres AL, et al. Atherosclerosis. 1996 Sep 27;126(1):163-71. doi: 10.1016/0021-9150(96)05907-2. Atherosclerosis. 1996. PMID: 8879444

6

Association between the TaqIB polymorphism in the cholesteryl ester transfer protein gene locus and plasma lipoprotein levels in familial hypercholesterolemia.

Carmena-Ramón R, Ascaso JF, Real JT, Nájera G, Ordovás JM, Carmena R. Carmena-Ramón R, et al. Metabolism. 2001 Jun;50(6):651-6. doi: 10.1053/meta.2001.23289. Metabolism. 2001. PMID: 11398140

7

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK. Jensen HK. Dan Med Bull. 2002 Nov;49(4):318-45. Dan Med Bull. 2002. PMID: 12553167 Review.

8

Increased hepatic secretion of very-low-density-lipoprotein apolipoprotein B-100 in heterozygous familial hypercholesterolaemia: a stable isotope study.

Cummings MH, Watts GF, Umpleby M, Hennessy TR, Quiney JR, Sönksen PH. Cummings MH, et al. Atherosclerosis. 1995 Feb;113(1):79-89. doi: 10.1016/0021-9150(94)05430-q. Atherosclerosis. 1995. PMID: 7755658 Clinical Trial.

9

Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population.

Acton S, Osgood D, Donoghue M, Corella D, Pocovi M, Cenarro A, Mozas P, Keilty J, Squazzo S, Woolf EA, Ordovas JM. Acton S, et al. Arterioscler Thromb Vasc Biol. 1999 Jul;19(7):1734-43. doi: 10.1161/01.atv.19.7.1734. Arterioscler Thromb Vasc Biol. 1999. PMID: 10397692

10

Influence of apolipoprotein E genotypes on plasma lipid and lipoprotein concentrations: results from a segregation analysis in pedigrees with molecularly defined familial hypercholesterolemia.

Friedlander Y, Leitersdorf E. Friedlander Y, et al. Genet Epidemiol. 1996;13(2):159-77. doi: 10.1002/(SICI)1098-2272(1996)13:2<159::AID-GEPI3>3.0.CO;2-3. Genet Epidemiol. 1996. PMID: 8722744

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