Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia

scientific article published on 01 August 1994

Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.14.8.1250
P698PubMed publication ID8049185

P2093author name stringH Zhang
M R Hayden
J Genest
E Gagné
L A Clarke
P433issue8
P921main subjectfamilial combined hyperlipidemiaQ2242370
P304page(s)1250-1257
P577publication date1994-08-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleAnalysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia
P478volume14

Reverse relations

cites work (P2860)
Q34335556A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity
Q43546731Apolipoprotein E genotype and cardiovascular disease in the Framingham Heart Study
Q33679278Assessment of French patients with LPL deficiency for French Canadian mutations
Q40440943Clustering of cardiovascular risk factors: Targeting high-risk individuals
Q34107183Common mutations of the lipoprotein lipase gene and their clinical significance
Q34452376Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis.
Q35881946Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.
Q37364446Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes
Q74127774Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian population
Q50874132Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia.
Q34107257Genetic predictors of plasma lipid response to diet intervention
Q34107190Genetics of familial combined hyperlipidemia
Q77452737Genetics of lipoprotein disorders
Q34389639Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
Q77164623Incidence of lipoprotein lipase genotype for premature termination codon (Ser447-Ter) in Japanese, and association with dyslipoproteinemia
Q33945290Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6.
Q34089350Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia
Q35767590Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes
Q74502064Structure-function analysis of D9N and N291S mutations in human lipoprotein lipase using molecular modelling
Q41519599The acylation stimulating protein pathway: Clinical implications
Q40964824The genetic determinants of plasma cholesterol and response to diet
Q37983699The genetics of familial combined hyperlipidaemia
Q34974691The lipoprotein lipase gene in combined hyperlipidemia: evidence of a protective allele depletion

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