A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency-Reference-Cited by-同舟云学术

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A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency

Published:2022-07 Issue:4 Volume:16 Page:423-433
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Takeda Tadashi,Ide Tsubasa,Okuda Daishi,Kuroda Masayuki^ORCID,Asada Sakiyo,Kirinashizawa Mika,Yamamoto Misato,Miyoshi Junko,Yokote Koutaro,Mizutani Naohiro

Funder

Ministry of Health, Labour and Welfare

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference57 articles.

1. Extreme high high-density lipoprotein cholesterol is paradoxically associated with high mortality in men and women: Two prospective cohort studies;Madsen;Eur Heart J,2017

2. Associations between risk of overall mortality, cause-specific mortality and level of inflammatory factors with extremely low and high high-density lipoprotein cholesterol levels among American adults;Mazidi;Int J Cardiol,2019

3. Apolipoprotein-mediated removal of cellular cholesterol and phospholipids;Oram;J Lipid Res,1997

4. Cholesterol efflux and atheroprotection: Advancing the concept of reverse cholesterol transport;Rosenson;Circulation,2012

5. Macrophages in Atherosclerosis: a dynamic balance;Moore;Nat Rev Immunol,2013

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