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Cited by 599

The DOI matches its Crossref record; 131 of the 131 references it cites were found in a registry or an index.

Molecular regulation of HDL metabolism and function: implications for novel therapies

Open access
Rader, Daniel J.·2006·Journal of Clinical Investigation

Abstract

HDL biosynthesisApolipoprotein production.The biosynthesis of HDL (Figure 1) is complex and involves the synthesis and secretion of the major protein components of HDL followed by the largely extracellular acquisition of lipid (phospholipids [PLs] and cholesterol) and the assembly and generation of the mature HDL particle.The major HDL apolipoproteins are apoA-I and apoA-II, and both are required for normal HDL biosynthesis.ApoA-I constitutes approximately 70% of HDL protein and is present on virtually all HDL particles (3).Thus, it is not surprising that gene deletion of Apoa1/ APOA1 results in extremely low levels of HDL-C in mice (8) and in humans (9).Atherosclerosis-prone mice lacking apoA-I develop significantly increased atherosclerosis (10).ApoA-I is synthesized in both the intestine and the liver (Figure 1), but the relative contribution of the intestine and the liver to the plasma apoA-I pool in humans remains unknown.Hepatic overex-Molecular regulation of HDL metabolism and function: implications for novel therapies

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Metadata

Authors
Rader, D. J.
Venue
Journal of Clinical Investigation
Published
2006-12-01
Volume
116
Issue
12
Pages
3090-3100
ISSN
0021-9738 (ISSN-L)
OpenAlex
W1968196140
Cited by
599
References
131
FWCI
51.74
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Molecular regulation of HDL metabolism and function: implications for novel therapies. https://app.cochat.ai/papers/10.1172/jci30163
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Rader, D. J. (2006). Molecular regulation of HDL metabolism and function: implications for novel therapies. Journal of Clinical Investigation. https://doi.org/10.1172/jci30163

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.