Sort   by:  
 Page size 
UnknownGenetic polymorphisms at SIRT1 and FOXO1 are associated with carotid atherosclerosis in the SAPHIR cohort.
Not available
S-EPMC4411770 | biostudies-literature
UnknownGenetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins.
Not available
S-EPMC2773273 | biostudies-literature
UnknownMaternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations.
Not available
S-EPMC3573202 | biostudies-literature
UnknownGenetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
Not available
S-EPMC2730542 | biostudies-literature
UnknownAssociation of relative telomere length with progression of chronic kidney disease in two cohorts: effect modification by smoking and diabetes.
Not available
S-EPMC4493689 | biostudies-literature
UnknownEcto-5' -Nucleotidase CD73 (NT5E), vitamin D receptor and FGF23 gene polymorphisms may play a role in the development of calcific uremic arteriolopathy in dialysis patients - Data from the German Calciphylaxis Registry.
Not available
S-EPMC5315275 | biostudies-literature
UnknownMitochondrial DNA copy number is associated with all-cause mortality and cardiovascular events in patients with peripheral arterial disease.
Not available
S-EPMC7318579 | biostudies-literature
UnknownA common variant in the adiponutrin gene influences liver enzyme values.
Not available
S-EPMC3759243 | biostudies-literature
UnknownCompetitive interaction between fibroblast growth factor 23 and asymmetric dimethylarginine in patients with CKD.
Not available
S-EPMC4378102 | biostudies-literature
UnknownCandidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.
Not available
S-EPMC3324414 | biostudies-literature
Sort   by:  
 Page size