(Q34107183)

31 July 2017

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title

Common mutations of the lipoprotein lipase gene and their clinical significance (English)

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31 July 2017

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Gehrisch S

1

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31 July 2017

publication date

1 July 1999

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Current Atherosclerosis Reports

31 July 2017

published in

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31 July 2017

volume

1

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31 July 2017

issue

1

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31 July 2017

page(s)

70-78

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https://scigraph.springernature.com/pub.10.1007/s11883-999-0052-4

31 July 2017

exact match

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cites work

Ethnic variation and in vivo effects of the -93t-->g promoter variant in the lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1007%2FS11883-999-0052-4

A common mutation in the lipoprotein lipase gene promoter, -93T/G, is associated with lower plasma triglyceride levels and increased promoter activity in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-999-0052-4

Common sequence variants of lipoprotein lipase: standardized studies of in vitro expression and catalytic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-999-0052-4

Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: the European Atherosclerosis Research Study (EARS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-999-0052-4

The familial hyperchylomicronaemia syndrome

21 January 2018

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12 December 2020

Structure of the human lipoprotein lipase gene

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12 December 2020

Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels.

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12 December 2020

Lipoprotein lipase gene mutations in coronary artery disease.

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12 December 2020

A heterozygous mutation (the codon for Ser447→ a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type I hyperlipidemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Associations between lipoprotein lipase gene polymorphisms and plasma correlations of lipids, lipoproteins and lipase activities in young myocardial infarction survivors and age-matched healthy individuals from Sweden

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12 December 2020

Defects of lipoprotein metabolism in familial combined hyperlipidaemia

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12 December 2020

Comparison of risk factors for coronary heart disease in Dresden and Münster. Results of the DRECAN (Dresden Cardiovascular Risk and Nutrition) study and the PROCAM (Prospective Cardiovascular Münster) Study

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12 December 2020

Organization of the human lipoprotein lipase gene and evolution of the lipase gene family

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12 December 2020

A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians

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12 December 2020

Regulatory mutations in the human lipoprotein lipase gene in patients with familial combined hyperlipidemia and coronary artery disease

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12 December 2020

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene

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12 December 2020

The low down on lipoprotein lipase.

1 reference

12 December 2020

The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease

1 reference

12 December 2020

Cloning, sequencing and structural analysis of 976 base pairs of the promoter sequence for the rat lipoprotein lipase gene. Comparison with the mouse and human sequences

1 reference

12 December 2020

A missense mutation (Asp250→Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries

1 reference

12 December 2020

Receptors for triglyceride-rich lipoproteins and their role in lipoprotein metabolism.

1 reference

12 December 2020

Lipoprotein lipase activity in patients with combined hyperlipidaemia

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12 December 2020

Human lipoprotein lipase complementary DNA sequence.

1 reference

12 December 2020

The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia.

1 reference

12 December 2020

The emergence of triglycerides as a significant independent risk factor in coronary artery disease.

1 reference

12 December 2020

Lipoprotein lipase: structure, function and mechanism of action

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12 December 2020

Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)

1 reference

12 December 2020

Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group.

1 reference

12 December 2020

Chylomicronemia syndrome.

1 reference

12 December 2020

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

1 reference

12 December 2020

A common substitution (Asn291Ser) in lipoprotein lipase is associated with increased risk of ischemic heart disease

1 reference

12 December 2020

Lipoprotein lipase mutations and Alzheimer's disease.

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12 December 2020

Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.

1 reference

12 December 2020

Molecular screening of the lipoprotein lipase gene in hypertriglyceridemic members of familial noninsulin-dependent diabetes mellitus families

1 reference

12 December 2020

The lipoprotein lipase-encoding human gene: sequence from intron-6 to intron-9 and presence in intron-7 of a 40-million-year-old Alu sequence

1 reference

12 December 2020

Alterations in plasma lipoproteins and apolipoproteins before the age of 40 in heterozygotes for lipoprotein lipase deficiency

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12 December 2020

Clines of nuclear DNA markers suggest a largely neolithic ancestry of the European gene pool

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12 December 2020

Lipoprotein lipase gene variants and risk of coronary disease: a quantitative analysis of population-based studies

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12 December 2020

Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis.

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12 December 2020

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12 December 2020

Incidence of lipoprotein lipase genotype for premature termination codon (Ser447-Ter) in Japanese, and association with dyslipoproteinemia

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12 December 2020

Familial combined hyperlipidemia and abnormal lipoprotein lipase

1 reference

12 December 2020

Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Québec

1 reference

12 December 2020

The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity

1 reference

12 December 2020

Towards a theory of modern human origins: geography, demography, and diversity in recent human evolution

1 reference

12 December 2020

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries

1 reference

12 December 2020

Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family

1 reference

12 December 2020

Molecular genetics of human lipoprotein lipase deficiency

1 reference

12 December 2020

Lipoprotein lipase genotypes for a common premature termination codon mutation detected by PCR-mediated site-directed mutagenesis and restriction digestion

1 reference

12 December 2020

Hypertriglyceridemia, atherogenic dyslipidemia, and the metabolic syndrome

1 reference

12 December 2020

A common mutation in the lipoprotein lipase gene (N291S) alters the lipoprotein phenotype and risk for cardiovascular disease in patients with familial hypercholesterolemia

1 reference

12 December 2020

Lipoprotein lipase gene polymorphisms in ischaemic stroke and carotid stenosis.

1 reference

12 December 2020

The Münster Heart Study (PROCAM). Results of follow-up at 8 years.

1 reference

12 December 2020

Hypertriglyceridemia as a cardiovascular risk factor

1 reference

12 December 2020

DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population

1 reference

12 December 2020

Familial lipoprotein lipase (LPL) deficiency: A catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy

1 reference

12 December 2020

Triglyceride lipases and atherosclerosis.

1 reference

12 December 2020

Relative contribution of low-density lipoprotein receptor and lipoprotein lipase gene mutations to angiographically assessed coronary artery disease among French Canadians.

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12 December 2020

Common genetic variants of lipoprotein lipase and apolipoproteins AI-CIII that relate to coronary artery disease: a study in Chinese and European subjects.

1 reference

12 December 2020

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia

1 reference

12 December 2020

Hepatic and lipoprotein lipases selectively assayed in postheparin plasma

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12 December 2020

Structure, function and role of lipoprotein lipase in lipoprotein metabolism

1 reference

12 December 2020

10.1007/S11883-999-0052-4

Identifiers

DOI

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Dimensions Publication ID

31 July 2017

1031369942

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1 reference