Found: 15
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Mutation screening of the LDLR gene and ApoB gene in patients with a phenotype of familial hypercholesterolemia and normal values in a functional LDL receptor/apolipoprotein B assay.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 1, p. 79, doi. 10.1111/j.1399-0004.1998.tb03699.x
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- Publication type:
- Article
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
- Published in:
- Nature Genetics, 2009, v. 41, n. 3, p. 283, doi. 10.1038/ng.314
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- Publication type:
- Article
Lack of association between complement factor H polymorphisms and coronary artery disease or myocardial infarction.
- Published in:
- Journal of Molecular Medicine, 2007, v. 85, n. 7, p. 771, doi. 10.1007/s00109-007-0185-2
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- Publication type:
- Article
Interleukin-6 gene polymorphisms and susceptibility to myocardial infarction: the ECTIM study.
- Published in:
- Journal of Molecular Medicine, 2001, v. 79, n. 5/6, p. 300, doi. 10.1007/s001090100209
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- Publication type:
- Article
Polymorphisms in the genes encoding platelet-derived growth factor A and α receptor.
- Published in:
- Journal of Molecular Medicine, 2000, v. 78, n. 5, p. 287, doi. 10.1007/s001090000111
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- Publication type:
- Article
Overweight induced by chronic risperidone exposure is correlated with overexpression of the SREBP-1c and FAS genes in mouse liver.
- Published in:
- Naunyn-Schmiedeberg's Archives of Pharmacology, 2011, v. 383, n. 4, p. 423, doi. 10.1007/s00210-010-0597-3
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- Publication type:
- Article
Age discrimination in out-of-hospital cardiac arrest care: a case-control study.
- Published in:
- European Journal of Cardiovascular Nursing, 2018, v. 17, n. 6, p. 505, doi. 10.1177/1474515117746329
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- Publication type:
- Article
Adipocytokines and the risk of ischemic stroke: The PRIME Study.
- Published in:
- Annals of Neurology, 2012, v. 71, n. 4, p. 478, doi. 10.1002/ana.22669
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- Publication type:
- Article
Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the APOE p. Leu167del Mutation.
- Published in:
- Human Mutation, 2013, v. 34, n. 1, p. 83, doi. 10.1002/humu.22215
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- Publication type:
- Article
Erratum: Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.
- Published in:
- Human Mutation, 2005, v. 26, n. 6, p. 592, doi. 10.1002/humu.9386
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- Publication type:
- Article
Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.
- Published in:
- Human Mutation, 2005, v. 26, n. 5, p. 497, doi. 10.1002/humu.9383
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- Publication type:
- Article
Family history, longevity, and risk of coronary heart disease: the PRIME Study.
- Published in:
- 2003
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- Publication type:
- journal article
Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations--the ECTIM Study.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 1, p. 57, doi. 10.1093/hmg/9.1.57
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- Publication type:
- Article
Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction<sup>*</sup>.
- Published in:
- American Journal of Hypertension, 1999, v. 12, n. 3, p. 304, doi. 10.1016/S0895-7061(98)00255-6
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- Publication type:
- Article
CONCENTRACIONES BAJAS DE LIPOPROTEÍNAS DE ALTA DENSIDAD (HDL) EN PLASMA Y ENFERMEDAD ARTERIAL CORONARIA.
- Published in:
- Archivos de Cardiología de México, 2000, v. 70, n. 3, p. 312
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- Publication type:
- Article