| scholarly article | Q13442814 |
| P2093 | author name string | Qian Dong | |
| Jian-Jun Li | |||
| Ying Gao | |||
| Di Sun | |||
| Geng Liu | |||
| Cheng-Gang Zhu | |||
| Na-Qiong Wu | |||
| Yuan-Lin Guo | |||
| Hui-Wen Zhang | |||
| Jing-Lu Jin | |||
| Qiu-Ting Dong | |||
| Ye-Xuan Cao | |||
| P2860 | cites work | Hypertriglyceridemic acute pancreatitis in emergency department: Typical clinical features and genetic variants. | Q38761752 |
| Rare and common variants in LPL and APOA5 in Thai subjects with severe hypertriglyceridemia: A resequencing approach | Q39748721 | ||
| Clinical characteristics of Japanese patients with severe hypertriglyceridemia | Q40675413 | ||
| Massive hypertriglyceridemia associated with atenolol | Q44466045 | ||
| Human lipoprotein lipase. Analysis of the catalytic triad by site-directed mutagenesis of Ser-132, Asp-156, and His-241 | Q44585592 | ||
| National lipid association recommendations for patient-centered management of dyslipidemia: part 1--full report | Q45012753 | ||
| Pathogenic classification of LPL gene variants reported to be associated with LPL deficiency | Q45884759 | ||
| Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population | Q46262135 | ||
| Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene | Q46715156 | ||
| Genetic screening of the LPL gene in hypertriglyceridaemic patients | Q46859264 | ||
| Genotype-phenotype relationships in patients with type I hyperlipoproteinemia. | Q51142076 | ||
| Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia. | Q51541596 | ||
| Mechanism of hypertriglyceridaemia associated with contraceptive steroids. | Q53755251 | ||
| Clinical assessment of hyperlipidemic pancreatitis | Q70834720 | ||
| Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650) | Q80838569 | ||
| Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia | Q85226885 | ||
| A functional variant in APOA5/A4/C3/A1 gene cluster contributes to elevated triglycerides and severity of CAD by interfering with microRNA 3201 binding efficiency | Q87407557 | ||
| GPIHBP1 is responsible for the entry of lipoprotein lipase into capillaries | Q24338437 | ||
| Biological, clinical and population relevance of 95 loci for blood lipids | Q24622541 | ||
| Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip | Q24657931 | ||
| Triglycerides and cardiovascular disease: a scientific statement from the American Heart Association | Q28235865 | ||
| Apolipoprotein A-V; a potent triglyceride reducer | Q28245263 | ||
| Newly identified loci that influence lipid concentrations and risk of coronary artery disease | Q28264535 | ||
| The familial chylomicronemia syndrome | Q28286373 | ||
| The association of hypertriglyceridemia with cardiovascular events and pancreatitis: a systematic review and meta-analysis. | Q34215047 | ||
| Variant in the glucokinase regulatory protein (GCKR) gene is associated with fatty liver in obese children and adolescents | Q35783993 | ||
| Lipase maturation factor 1: a lipase chaperone involved in lipid metabolism | Q35784094 | ||
| An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia | Q36582772 | ||
| Plasma lipoproteins: genetic influences and clinical implications | Q37367246 | ||
| Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia | Q37613167 | ||
| Genetic bases of hypertriglyceridemic phenotypes | Q37868881 | ||
| P921 | main subject | acute pancreatitis | Q854573 |
| P304 | page(s) | 171-177 | |
| P577 | publication date | 2018-11-09 | |
| P1433 | published in | EBioMedicine | Q24912341 |
| P1476 | title | Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis | |
| P478 | volume | 38 |
| Q90450216 | Genetic and functional studies of the LMF1 gene in Thai patients with severe hypertriglyceridemia |
| Q92999617 | Glycopatterns and Glycoproteins Changes in MCN and SCN: A Prospective Cohort Study |
| Q90389813 | Large triglyceride-rich lipoproteins in hypertriglyceridemia are associated with the severity of acute pancreatitis in experimental mice |
| Q89960461 | Variants of Lipid-Related Genes in Adult Japanese Patients with Severe Hypertriglyceridemia |
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