Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45–>Asn), in a Turkish patient.-Reference-Cited by-同舟云学术

Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45–>Asn), in a Turkish patient.

Published:1994-08 Issue:8 Volume:35 Page:1431-1440
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Lüttmann S,von Eckardstein A,Wei W,Funke H,Köhler E,Mahley R W,Assmann G

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference50 articles.

1. The apolipoprotein multigene family: biosynthesis, structure, structure-function relationships, and evolution;Li;J. Lipid Res.,1988

2. Characterization of the oligosaccharide side chain of apolipoprotein C-III from human plasma very low density lipoproteins;Vaith;Biochim. Biophys. Acta.,1978

3. Characterization of an apolipoprotein C-III mutant by high performance liquid chromatography and time-of-flight secondary ion mass spectrometry;Jabs;J. Chromatogr.,1987

4. Apolipoprotein C-IIIO lacks carbohydrate residues: use of mass spectrometry to study apolipoprotein structure;Ito;J Lipid Res.,1989

5. Inhibition of lipoprotein lipase by an apoprotein of human very low density lipoprotein;Brown;Biochem. Biopkys. Res. Commun.,1972

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