Literature DB >> 32305096

Familial Hypercholesterolemia and Atherosclerosis: Animal Models and Therapeutic Advances.

Suowen Xu1, Jianping Weng2.   

Abstract

Familial hypercholesterolemia (FH), mainly arising from loss-of-function mutation of the low-density lipoprotein receptor (LDLR), is a life-threatening inherited cardiometabolic disorder with limited therapies. In a recent study, Zhao et al. created a new model of FH and demonstrate that LDLR gene editing protects against both FH and atherosclerosis.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  LDL receptor; atherosclerosis; familial hypercholesterolemia; therapy

Mesh:

Substances:

Year:  2020        PMID: 32305096     DOI: 10.1016/j.tem.2020.02.007

Source DB:  PubMed          Journal:  Trends Endocrinol Metab        ISSN: 1043-2760            Impact factor:   12.015


  2 in total

1.  An insertion mutation in the Apoe gene associated with spontaneous hyperlipidemia in mice.

Authors:  Hitoshi Hatakeyama; Ichiro Yoshioka; Takeshi Ohsawa; Yoshibumi Matsushima; Kazuhiko Kotani; Shuichi Tsuchida
Journal:  Arch Med Sci Atheroscler Dis       Date:  2022-08-08

2.  Investigation of the underlying genes and mechanism of familial hypercholesterolemia through bioinformatics analysis.

Authors:  Dinghui Wang; Bin Liu; Tianhua Xiong; Wenlong Yu; Qiang She
Journal:  BMC Cardiovasc Disord       Date:  2020-09-16       Impact factor: 2.298

  2 in total

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