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the whole blood samples sequencing of homozygous familial hypercholesterolemia patients

NIAID Data Ecosystem2026-04-25 收录

家族性高胆固醇血症

代谢转录组学

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP200230 数据链接链接失效反馈

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资源简介：

This study was to explore whether other miRNAs or gene expressions are involved in the process of lipid metabolism and atherosclerosis in patients with homozygous FH.

应用场景：

创建时间：

2020-06-27

RNA测序分析

家族性高胆固醇血症

RNA seq reads constituting of FASTQ paired end reads from 5 FHD/FHDL patientsEGA dataset EGAD00001003790

NIAID Data Ecosystem50

Data_Sheet_1_Developing a Hybrid Risk Assessment Tool for Familial Hypercholesterolemia: A Machine Learning Study of Chinese Arteriosclerotic Cardiovascular Disease Patients.docx

家族性高胆固醇血症

机器学习在心血管疾病中的应用

BackgroundFamilial hypercholesterolemia (FH) is an autosomal-dominant genetic disorder with a high risk of premature arteriosclerotic cardiovascular disease (ASCVD). There are many alternative risk as

NIAID Data Ecosystem30

A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia.

家族性高胆固醇血症

基因启动子突变

We have identified a Finnish family with a typical phenotype of heterozygous familial hypercholesterolemia (FH) due to a single-base substitution in the proximal Sp1 binding site of the low density li

PubMed Central1994-10-25 更新10

Statin Treatments And Dosages In Children With Familial Hypercholesterolemia: Meta-Analysis

他汀类药物

家族性高胆固醇血症

Abstract Background: Children with familial hypercholesterolemia may develop early endothelial damage leading to a high risk for the development of cardiovascular disease (CVD). Statins have been show

DataCite Commons2020-08-28 更新40

Functional Characterization of Two Low-Density Lipoprotein Receptor Gene Mutations in Two Chinese Patients with Familial Hypercholesterolemia

家族性高胆固醇血症

LDLR基因

Background Familial hypercholesterolemia (FH) is an autosomal dominant disease that primarily results from mutations in the low-density lipoprotein receptor (LDLR) gene. We investigated two unrelated

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the whole blood samples sequencing of homozygous familial hypercholesterolemia patients

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