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UnknownRecent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.
Not available
S-EPMC1226098 | biostudies-literature
UnknownCorrelation between coronary artery calcification by non-cardiac CT and Framingham score in young patients.
Not available
S-EPMC5874063 | biostudies-literature
UnknownRefinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries.
Not available
S-EPMC4892342 | biostudies-literature
UnknownIdentification of bile acid precursors as endogenous ligands for the nuclear xenobiotic pregnane X receptor.
Not available
S-EPMC140933 | biostudies-literature
UnknownAssociation of Lipoprotein(a) With Risk of Recurrent Ischemic Events Following Acute Coronary Syndrome: Analysis of the dal-Outcomes Randomized Clinical Trial.
Not available
S-EPMC5838593 | biostudies-literature
UnknownCETP genotype and changes in lipid levels in response to weight-loss diet intervention in the POUNDS LOST and DIRECT randomized trials.
Not available
S-EPMC4340318 | biostudies-literature
UnknownIn search of a genetic explanation for LDLc variability in an FH family: common SNPs and a rare mutation in MTTP explain only part of LDL variability in an FH family.
Not available
S-EPMC6795082 | biostudies-literature
UnknownDalcetrapib Reduces Risk of New-Onset Diabetes in Patients With Coronary Heart Disease.
Not available
S-EPMC7171952 | biostudies-literature
UnknownCharacterization of LTBP2 mutation causing mitral valve prolapse.
Not available
S-EPMC11775471 | biostudies-literature
UnknownWhole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations.
Not available
S-EPMC4112429 | biostudies-literature
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