师资

崔欢欢
研究助理教授
cuihh@sustc.edu.cn

教育经历

2011.9-2016.4    柏林自由大学                  博士

2008.9-2010.7    西北农林科技大学          硕士

2004.9-2008.7    西北农林科技大学        学士

 

工作经历

2018.11-今                南方科技大学                 研究助理教授

2017.9-2018.10     华大基因                          遗传咨询师&讲师

2015.10-2017.5     柏林夏洛蒂医学院        博士后

 

交叉研究领域

1. 染色体重塑在生长发育和疾病发生中的作用

2. 利用干细胞重塑人类疾病

 

所获荣誉:

深圳市海外高层次“C类”人才(孔雀计划C类)

 

代表文章

Cui H, Schlesinger J, Schoenhals S,Tönjes M, Dunkel I, Meierhofer D, Cano E, Schulz K, Berger MF, Haack T, Abdelilah-Seyfried S, Bulyk ML, Sauer S, Sperling SR. Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA. 2016. Nucleic Acids Research.

Cui H, Bansal V, Schulz K, Malecova B, Dall'Agnese A, Latella L, Gatto S, Chen W, Grunert M, Dorn C, Puri PL, and Sperling SR. Muscle-relevant genes marked by stable H3K4me2/3 profiles and enriched MyoD binding during myogenic differentiation. 2017. Plos One.

Grunert M, Dorn C, Cui H, Dunkel I, Schulz K, Schoenhals S, Sun W, Berger F, Chen W, Sperling SR. DNA methylation alterations associated with gene expression changes depict congenital heart disease: Tetralogy of Fallot and ventricular septal defects. 2016. Cardiovascular Research.

Ben Jehuda R, Eisen B, Shemer Y, Mekies L.N, Szantai A, Reiter I, Cui H, Guan K, Haron-Khun S, Freimark D, Sperling S.R, Gherghiceanu M, Arad M, Binah O. CRISPR correction of the PRKAG2 gene mutation in the patient's iPSC-derived cardiomyocytes eliminates the electrophysiological and structural abnormalities. 2017. Heart Rhythm.

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