| scholarly article | Q13442814 |
| P2093 | author name string | Yucheng Chen | |
| Yu Liu | |||
| Rui Liu | |||
| Huai Bai | |||
| Xian Li | |||
| Yan Qiao | |||
| Ou Qiang | |||
| P2860 | cites work | Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor | Q24319938 |
| The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes | Q28239011 | ||
| A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians | Q28262072 | ||
| Ath-1, a gene determining atherosclerosis susceptibility and high density lipoprotein levels in mice | Q28505210 | ||
| CD4 T cell cytokine differentiation: the B cell activation molecule, OX40 ligand, instructs CD4 T cells to express interleukin 4 and upregulates expression of the chemokine receptor, Blr-1 | Q28508535 | ||
| High-density lipoprotein cholesterol as an independent risk factor in cardiovascular disease: assessing the data from Framingham to the Veterans Affairs High--Density Lipoprotein Intervention Trial | Q30652770 | ||
| Hepatic lipase: new insights from genetic and metabolic studies | Q33702418 | ||
| Natural genetic variation as a tool in understanding the role of CETP in lipid levels and disease | Q35086131 | ||
| The T cell-B cell interaction via OX40-OX40L is necessary for the T cell-dependent humoral immune response | Q36365985 | ||
| Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility | Q45306054 | ||
| Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency | Q46847097 | ||
| Affinity and kinetics of the interaction between soluble trimeric OX40 ligand, a member of the tumor necrosis factor superfamily, and its receptor OX40 on activated T cells. | Q51605911 | ||
| Association of TNFRSF4 gene polymorphisms with essential hypertension. | Q51707239 | ||
| Genetic variants of tumor necrosis factor superfamily, member 4 (TNFSF4), and risk of incident atherothrombosis and venous thromboembolism. | Q51710047 | ||
| Human genetic evidence that OX40 is implicated in myocardial infarction | Q57607674 | ||
| Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males | Q73221058 | ||
| Expression and function of OX40 ligand on human dendritic cells | Q73900124 | ||
| P433 | issue | 3 | |
| P921 | main subject | genetic variation | Q349856 |
| P304 | page(s) | 207-213 | |
| P577 | publication date | 2012-12-07 | |
| P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
| P1476 | title | Genetic variation in the OX40L/OX40 system and plasma lipid and lipoprotein levels in a Chinese hypertriglyceridemic population | |
| P478 | volume | 17 |
| Q37112659 | Lack of Association Between rs17568 Polymorphism in OX40 Gene and Myocardial Infarction, Southern of Iran | cites work | P2860 |
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