Functionally inactive apolipoprotein E3in a type III hyperlipoproteinaemic patient
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.1984.tb00696.x/fullpdf
Reference23 articles.
1. Regulation of Plasma Cholesterol by Lipoprotein Receptors
2. Rapid hepatic clearance of the canine lipoproteins containing only the E apoprotein by a high affinity receptor. Identity with the chylomicron remnant transport process.
3. Polymorphism of apolipoprotein E and occurrence of dysbetalipoproteinaemia in man
4. Human very low density lipoprotein apolipoprotein E isoprotein polymorphism is explained by genetic variation and posttranslational modification
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1. Phenotyping apolipoprotein E*3-Leiden transgenic mice by two-dimensional polyacrylamide gel electrophoresis and mass spectrometric identification;ELECTROPHORESIS;2000
2. Phenotyping apolipoprotein E*3-Leiden transgenic mice by two-dimensional polyacrylamide gel electrophoresis and mass spectrometric identification;Electrophoresis;2000-07-01
3. Effects of family history of heart disease, apolipoprotein E phenotype, and lipoprotein(a) on the response of children’s plasma lipids to change in dietary lipids;The American Journal of Clinical Nutrition;1997-11-01
4. Compound Heterozygote for Both Rare Apolipoprotein E1(Gly127→Asp, Arg158→Cys) and E3(Cys112 → Arg, Arg251 → Gly) Alleles in a Multigeneration Pedigree with Hyperlipoproteinaemia;Clinical Science;1997-07-01
5. Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers.;Journal of Clinical Investigation;1994-09-01
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