Summary Introduction: several studies have evaluated the utilization of lipid biomarkers in an attempt to correlate them with clinical cardiovascular events. Nevertheless, the investigation of clinical conditions under specific plasmatic levels of lipoproteins for long periods presents limitations due to inherent difficulties that are related to the follow-up of individuals throughout their lives. Better understanding of the clinical response and occasional resistance to the action of hypolipidemic drugs in several clinic scenarios is also necessary. Objectives: to determine the role of evaluation of single-nucleotide polymorphisms (SNPs) related to the metabolism of lipids, and its implications in different clinical scenarios. Methods: ...
Coronary artery disease is among the leading causes of death worldwide. Clinical trials show a prote...
Statins effectively lower total and plasma LDL-cholesterol, but the magnitude of decrease varies amo...
The identification of DNA sequence variants underlying human complex phenotypes remains a significan...
Background: Common single-nucleotide polymorphisms (SNPs) that are associated with blood low-density...
GENERAL AIM: To investigate how common single-nucleotide-polymorphisms (SNPs) that associate with ca...
BackgroundAlthough largely preventable, cardiovascular diseases (CVDs) are the biggest cause of deat...
AIMS: The aim of this study was to quantify the collective effect of common lipid-associated single ...
International audienceThe number of nutrigenetic studies dedicated to the identification of single n...
Aims: The aim of this study was to quantify the collective effect of common lipid-associated single ...
Statins are efficacious lipid-lowering drugs used for prevention of cardiovascular complications in ...
Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low densit...
Cardiovascular drugs are abundantly prescribed to reduce risk of cardiovascular disease. Treatment w...
International audienceScope Cholesterol bioavailability displays a high interindividual variability,...
Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low densit...
Abstract Dyslipidemia is a leading cause of cardiovascular disease. At present, studies have shown ...
Coronary artery disease is among the leading causes of death worldwide. Clinical trials show a prote...
Statins effectively lower total and plasma LDL-cholesterol, but the magnitude of decrease varies amo...
The identification of DNA sequence variants underlying human complex phenotypes remains a significan...
Background: Common single-nucleotide polymorphisms (SNPs) that are associated with blood low-density...
GENERAL AIM: To investigate how common single-nucleotide-polymorphisms (SNPs) that associate with ca...
BackgroundAlthough largely preventable, cardiovascular diseases (CVDs) are the biggest cause of deat...
AIMS: The aim of this study was to quantify the collective effect of common lipid-associated single ...
International audienceThe number of nutrigenetic studies dedicated to the identification of single n...
Aims: The aim of this study was to quantify the collective effect of common lipid-associated single ...
Statins are efficacious lipid-lowering drugs used for prevention of cardiovascular complications in ...
Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low densit...
Cardiovascular drugs are abundantly prescribed to reduce risk of cardiovascular disease. Treatment w...
International audienceScope Cholesterol bioavailability displays a high interindividual variability,...
Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low densit...
Abstract Dyslipidemia is a leading cause of cardiovascular disease. At present, studies have shown ...
Coronary artery disease is among the leading causes of death worldwide. Clinical trials show a prote...
Statins effectively lower total and plasma LDL-cholesterol, but the magnitude of decrease varies amo...
The identification of DNA sequence variants underlying human complex phenotypes remains a significan...