The regulation of plasma lipoprotein concentrations as affected in human mutants.

Proceedings of the National Academy of Sciences of the United States of America ·Vol. 64 ·No. 3 ·1969-11-00 ·Pages 1138-46

Fredrickson DS

Abstract

暂无摘要

MeSH Terms

Abetalipoproteinemia/metabolism Biological Transport Blood Protein Disorders/genetics Cholesterol/metabolism Chylomicrons/blood Fatty Acids, Nonesterified/metabolism Humans Hyperlipidemias/genetics Lipid Metabolism, Inborn Errors Lipoproteins/blood Mononuclear Phagocyte System/metabolism Mutation Tendons Triglycerides/metabolism Xanthomatosis

Chemicals

Chylomicrons Fatty Acids, Nonesterified Lipoproteins Triglycerides Cholesterol

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Fredrickson D S

References (18)

18 references, click to expand

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CONGENITAL BETA-LIPOPROTEIN DEFICIENCY: AN HEREDITARY DISORDER INVOLVING A DEFECT IN THE ABSORPTION AND TRANSPORT OF LIPIDS.
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Evidence for separate monoglyceride hydrolase and triglyceride lipase in post-heparin human plasma.
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A comparison of heritable abnormal lipoprotein patterns as defined by two different techniques.
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Article Info

Journal

Proceedings of the National Academy of Sciences of the United States of America

Abbr.

Proc Natl Acad Sci U S A

ISSN

0027-8424

DOI

10.1073/pnas.64.3.1138

Published

1969-11-00

Pages

1138-46

Language

English

Region

United States

NLM ID

7505876

PMCID

PMC223353

Subset

External Links

PubMed source DOI: 10.1073/pnas.64.3.1138 PMC Full Text View journal details

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The regulation of plasma lipoprotein concentrations as affected in human mutants.

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