Lpl Gene | List of Frontiers open access articles

Original Research

Published on 17 Aug 2021

A Novel Lipoprotein Lipase Mutation in an Infant With Glycogen Storage Disease Type-Ib and Severe Hypertriglyceridemia

in Genetics of Common and Rare Diseases

Fengyu Wang
Fengli Wang
Xiaojun Zhou
Yingjie Yi
Jie Zhao

Frontiers in Pediatrics

doi 10.3389/fped.2021.671536

3,252 views
2 citations

Original Research

Published on 16 Mar 2022

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

in Genetics of Common and Rare Diseases

Danxia Guo
Yingchun Zheng
Zhongzhi Gan
Yingying Guo
Sijie Jiang
Fang Yang
Fu Xiong
Hua Zheng

Frontiers in Genetics

doi 10.3389/fgene.2022.814295

4,129 views
6 citations

Original Research

Published on 20 May 2022

The Genetic Spectrum of Familial Hypertriglyceridemia in Oman

in Genetics of Common and Rare Diseases

Khalid Al-Waili
Khalid Al-Rasadi
Muna Al-Bulushi
Mohammed Habais
Abdullah Al-Mujaini
Saif Al-Yaarubi
Antoine Rimbert
Razan Zadjali
Pegah Moradi Khaniabadi
Hamida Al-Barwani

Frontiers in Genetics

doi 10.3389/fgene.2022.886182

5,172 views
6 citations

Case Report

Published on 03 Mar 2022

Case Report: Next-Generation Sequencing Identified a Novel Pair of Compound-Heterozygous Mutations of LPL Gene Causing Lipoprotein Lipase Deficiency

in Genetics of Common and Rare Diseases

Yakun Li
Man Hu
Lin Han
Lifang Feng
Luhong Yang
Xiaoqian Chen
Tingting Du
Hui Yao
Xiaohong Chen

Frontiers in Genetics

doi 10.3389/fgene.2022.831133

4,535 views
5 citations

Original Research

Published on 19 Aug 2022

Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon

in Genetics of Common and Rare Diseases

Carine Ayoub
Yara Azar
Dina Maddah
Youmna Ghaleb
Sandy Elbitar
Yara Abou-Khalil
Selim Jambart
Mathilde Varret
Catherine Boileau
Petra El Khoury

Frontiers in Genetics

doi 10.3389/fgene.2022.961028

3,210 views
1 citation

Original Research

Published on 20 Jun 2023

A bidirectional link between metabolic syndrome and elevation in alanine aminotransferase in elderly female: a longitudinal community study

in Cardiovascular Genetics and Systems Medicine

Na Wu
Mofan Feng
Hanhua Zhao
Nan Tang
Yalan Xiong
Xinyu Shi
Dong Li
Hualing Song
Shengfu You
Jianying Wang

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1156123

3,068 views
2 citations

Original Research

Published on 18 Jul 2022

Identification and Characterization of Two Novel Compounds: Heterozygous Variants of Lipoprotein Lipase in Two Pedigrees With Type I Hyperlipoproteinemia

in Systems Endocrinology

Shuping Wang
Yiping Cheng
Yingzhou Shi
Wanyi Zhao
Ling Gao
Li Fang
Xiaolong Jin
Xiaoyan Han
Qiuying Sun
Guimei Li

Frontiers in Endocrinology

doi 10.3389/fendo.2022.874608

4,011 views
6 citations

Articles

A Novel Lipoprotein Lipase Mutation in an Infant With Glycogen Storage Disease Type-Ib and Severe Hypertriglyceridemia

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

The Genetic Spectrum of Familial Hypertriglyceridemia in Oman

Case Report: Next-Generation Sequencing Identified a Novel Pair of Compound-Heterozygous Mutations of LPL Gene Causing Lipoprotein Lipase Deficiency

Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon

A bidirectional link between metabolic syndrome and elevation in alanine aminotransferase in elderly female: a longitudinal community study

Identification and Characterization of Two Novel Compounds: Heterozygous Variants of Lipoprotein Lipase in Two Pedigrees With Type I Hyperlipoproteinemia