Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

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http://www.wikidata.org/entity/Q36723319

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

@zh-hk

2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

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Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

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type

Item

label

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

@ast

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

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prefLabel

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

@ast

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

@en

P1476

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

@en

P2093

Adriaan G Holleboom

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Alinda W Schimmel

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Angeliki Chroni

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Barbara A Hutten

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Erik S G Stroes

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G Kees Hovingh

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Georgios Daniil

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Jan Albert Kuivenhoven

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John J P Kastelein

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Renliang Zhang

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P2860

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes

The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families

Hydrolysis of platelet-activating factor by human serum paraoxonase

THE DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM

Clinical significance of the humoral immune response to modified LDL.

Monoclonal autoantibodies specific for oxidized phospholipids or oxidized phospholipid-protein adducts inhibit macrophage uptake of oxidized low-density lipoproteins.

Immune responses to oxidative neoepitopes on LDL and phospholipids modulate the development of atherosclerosis.

Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease.

Lecithin cholesterol acyltransferase.

P304

3066-3075

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P31

scholarly article

P356

10.1161/ATVBAHA.112.255711

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P407

English

P433

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

P478

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P50

Joseph L Witztum

Sotirios Tsimikas

P577

2012-09-27T00:00:00Z

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P698

23023370

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P932

3610418

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