Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Lipoprotein lipase mutation S447X associated with pancreatic calcification and steatorrhea in hyperlipidemic pancreatitis.

Journal of clinical gastroenterology - 1 Jul 2009

Chang Yu-Ting, Chang Ming-Chu, Su Ta-Chen, Liang Po-Chin, Su Yi-Ning, Kuo Chun-Hung, Wei Shu-Chen, Wong Jau-Min

Abstract excerpt

BACKGROUND: The factors that whether and how genes involving lipid metabolism including lipoprotein lipase (LPL) and apolipoprotein CII (apo CII) influence occurrence of acute attack of pancreatitis and chronic pancreatitis is not clear. GOALS: The aim of this study was to determine the association of LPL and apo CII genes with acute attack of pancreatitis and chronic pancreatitis in patients with hyperlipidemic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Apolipoprotein C-II
Share to Hyperlipidemias

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypertriglyceridemia

Share to Lipoprotein Lipase

Share to Pancreas

Share to Pancreatitis

Share to Sequence Analysis, DNA

Share to Taiwan

Source

Identifiers

PMID: 19034041
DOI: 10.1097/MCG.0b013e3181734a30

Genes

LPL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lipoprotein lipase mutation S447X associated with pancreatic calcification and steatorrhea in hyperlipidemic pancreatitis.PMID 19034041Read ↗

Compound but non-linked heterozygous p.W14X and p.L279 V LPL gene mutations in a Chinese patient with long-term severe hypertriglyceridemia and recurrent acute pancreatitis.Semantic proximity Read ↗

Association of lipoprotein lipase (LPL) gene variants with hyperlipidemic acute pancreatitis in southeastern Chinese population.Semantic proximity Read ↗

Identification of a novel LPL nonsense variant and further insights into the complex etiology and expression of hypertriglyceridemia-induced acute pancreatitisSemantic proximity Read ↗

Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE.Semantic proximity Read ↗

Mutations in the lipoprotein lipase gene as a cause of hypertriglyceridemia and pancreatitis in Taiwan.Semantic proximity Read ↗

Genetic determinants of pancreatitis: relevance in severe hypertriglyceridemiaSemantic proximity Read ↗

Lipoprotein lipase activity and mass, apolipoprotein C-II mass and polymorphisms of apolipoproteins E and A5 in subjects with prior acute hypertriglyceridaemic pancreatitis.Semantic proximity Read ↗

Identification of a novel and heterozygous LMF1 nonsense mutation in an acute pancreatitis patient with severe hypertriglyceridemia, severe obesity and heavy smokingSemantic proximity Read ↗

Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitisSemantic proximity Read ↗

The familial hyperchylomicronaemia syndrome.Semantic proximity Read ↗

Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.Semantic proximity Read ↗

Genetic and biochemical analysis of severe hypertriglyceridemia complicated with acute pancreatitis or with low post-heparin lipoprotein lipase mass.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.