Professor | 范亮亮 | 数字化转型顾问

Name	范亮亮
Contact Information	swfanliangliang@csu.edu.cn
Language ability	英语, 汉语
Province	湖南省

Name

范亮亮

Contact Information

swfanliangliang@csu.edu.cn

Language ability

英语, 汉语

Province

湖南省

University/Lab Affiliation and Title	中南大学
Faculty	Life Sciences
Academic Background & Achievements	2009-2013 中南大学生命科学学院/生命科学/本科 2013-2019 中南大学生命科学学院/细胞生物学/硕博连读美国克里夫兰医学中心/联合培养, 美国康涅狄格大学医学院/联合培养
Work Experience	2019-至今中南大学生命科学学院/特聘副教授

University/Lab Affiliation and Title

中南大学

Faculty

Life Sciences

Academic Background & Achievements

2009-2013 中南大学生命科学学院/生命科学/本科
2013-2019 中南大学生命科学学院/细胞生物学/硕博连读
美国克里夫兰医学中心/联合培养, 美国康涅狄格大学医学院/联合培养

Work Experience

2019-至今中南大学生命科学学院/特聘副教授

Areas of Focus	心血管疾病和呼吸系统疾病的遗传致病因素鉴定和致病分子机理探索
Publications	Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5, Xiang R, Fan L L, Huang H, 等., 2018 A de novo mutation of SMYD1 (p. F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient, Fan L L, Ding D B, Huang H, 等., 2019 A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation, Ding D B, Fan L L, Xiao Z, 等., 2018 Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope, Fan L L, Chen Y Q, Huang H, 等., 2019 Whole-exome sequencing identifies a novel mutation of desmocollin 2 in a Chinese family with arrhythmogenic right ventricular cardiomyopathy, Liu J S, Fan L L, Li J J, 等., 2017 Whole exome sequencing identifies a novel mutation (c. 333+ 2T> C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease, Fan L L, Huang H, Jin J Y, 等., 2018 Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia, Fan L L, Lin M, Chen Y, 等., 2015 Whole exome sequencing identified a novel mutation (p. Ala1884Pro) of β‐spectrin in a Chinese family with hereditary spherocytosis, Fan L L, Liu J S, Huang H, 等., 2017 Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy, Liu J S, Fan L L, Zhang H, 等., 2017 Whole Exome Sequencing identifies a Novel Mutation (p.L320R) of Actinin Alpha 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia, Fan L L, Huang H, Jin J Y, 等., 2018

Areas of Focus

心血管疾病和呼吸系统疾病的遗传致病因素鉴定和致病分子机理探索

Publications

Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5, Xiang R, Fan L L, Huang H, 等., 2018
A de novo mutation of SMYD1 (p. F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient, Fan L L, Ding D B, Huang H, 等., 2019
A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation, Ding D B, Fan L L, Xiao Z, 等., 2018
Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope, Fan L L, Chen Y Q, Huang H, 等., 2019
Whole-exome sequencing identifies a novel mutation of desmocollin 2 in a Chinese family with arrhythmogenic right ventricular cardiomyopathy, Liu J S, Fan L L, Li J J, 等., 2017
Whole exome sequencing identifies a novel mutation (c. 333+ 2T> C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease, Fan L L, Huang H, Jin J Y, 等., 2018
Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia, Fan L L, Lin M, Chen Y, 等., 2015
Whole exome sequencing identified a novel mutation (p. Ala1884Pro) of β‐spectrin in a Chinese family with hereditary spherocytosis, Fan L L, Liu J S, Huang H, 等., 2017
Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy, Liu J S, Fan L L, Zhang H, 等., 2017
Whole Exome Sequencing identifies a Novel Mutation (p.L320R) of Actinin Alpha 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia, Fan L L, Huang H, Jin J Y, 等., 2018

心血管疾病呼吸系统疾病遗传因素致病分子机制鉴定研究内质网线粒体细胞器

赵燕 - 南方科技大学

刘剑淼 - 华中科技大学

郑鹏里 - 北京大学

Area of Focus
内质网 | 线粒体 | 膜细胞器 | 动态 | 互作 | 分子机制 | 人类疾病 | 神经退行性疾病 | 形态 | 功能

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