8 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 27578112 | Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia. | 2016 Jul-Aug | 1 |
2 | 10619999 | Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a chinese patient with hypertriglyceridemia. | 2000 Jan | 1 |
3 | 11099402 | A compound heterozygote for a novel missense mutation (G105R) in exon 3 and a missense mutation (D204E) in exon 5 of the lipoprotein lipase gene in a Japanese infant with hyperchylomicronaemia. | 2000 Dec | 1 |
4 | 7538426 | Lipoprotein lipase synergizes with interferon gamma to induce macrophage nitric oxide synthetase mRNA expression and nitric oxide production. | 1995 Mar | 2 |
5 | 7627718 | Apolipoprotein B and E basic amino acid clusters influence low-density lipoprotein association with lipoprotein lipase anchored to the subendothelial matrix. | 1995 Aug | 1 |
6 | 7906986 | Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries. | 1994 | 1 |
7 | 1479292 | Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes. | 1992 Dec | 2 |
8 | 6704414 | Retention of apolipoprotein B and cholesterol by perfused heart during lipolysis of very-low-density lipoprotein. | 1984 Mar 27 | 1 |