Apolipoprotein B-100-containing lipoprotein metabolism in subjects with lipoprotein lipase gene mutations

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Post-heparin LPL activity measurement using VLDL as a substrate: a new robust method for routine assessment of plasma triglyceride lipolysis defects Diagnosis and treatment of severe hypertriglyceridemia.Homozygous LPL p.Gly188Glu Mutation in a Mexican Girl With Lipoprotein Lipase Deficiency.

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Apolipoprotein B-100-containing lipoprotein metabolism in subjects with lipoprotein lipase gene mutations

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http://www.wikidata.org/entity/Q36509548

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2011 nî lūn-bûn

@nan

2011年の論文

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2011年論文

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2011年論文

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2011年論文

@zh-hk

2011年論文

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2011年論文

@zh-tw

2011年论文

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2011年论文

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2011年论文

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name

Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

@ast

Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

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type

Item

label

Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

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Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

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prefLabel

Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

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Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

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P1476

Apolipoprotein B-100-containin ...... oprotein lipase gene mutations

@en

P2093

Alice H Lichtenstein

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Betsy S Russell

http://www.w3.org/2001/XMLSchema#string

Dennis L Sprecher

http://www.w3.org/2001/XMLSchema#string

Eric Olson

http://www.w3.org/2001/XMLSchema#string

Ernst J Schaefer

http://www.w3.org/2001/XMLSchema#string

Leonard Keilson

http://www.w3.org/2001/XMLSchema#string

Margaret R Diffenderfer

http://www.w3.org/2001/XMLSchema#string

Sam Z Sun

http://www.w3.org/2001/XMLSchema#string

P2860

Activation of lipoprotein lipase by native and synthetic fragments of human plasma apolipoprotein C-II

Inhibition of lipoprotein lipase by an apoprotein of human very low density lipoprotein

Gender-specific differences in the kinetics of nonfasting TRL, IDL, and LDL apolipoprotein B-100 in men and premenopausal women.

Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency.

Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene

Metabolism of apolipoprotein B in large triglyceride-rich very low density lipoproteins of normal and hypertriglyceridemic subjects.

Lipoprotein lipase: genetics, lipid uptake, and regulation.

Apolipoprotein C-III and the metabolic basis for hypertriglyceridemia and the dense low-density lipoprotein phenotype

Lipoprotein lipase bound to apolipoprotein B lipoproteins accelerates clearance of postprandial lipoproteins in humans

Distribution of apolipoprotein(a) in the plasma from patients with lipoprotein lipase deficiency and with type III hyperlipoproteinemia. No evidence for a triglyceride-rich precursor of lipoprotein(a)

P304

459-466

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scholarly article

P356

10.1161/ATVBAHA.111.238493

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English

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P478

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P50

Esther MM. Ooi

Phr Barrett

P577

2011-11-17T00:00:00Z

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P698

22095987

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P921

lipoprotein

P932

4729373

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Apolipoprotein B-100-containing lipoprotein metabolism in subjects with lipoprotein lipase gene mutations

about

P2860

P2860

Apolipoprotein B-100-containing lipoprotein metabolism in subjects with lipoprotein lipase gene mutations

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932