Continuous size-based separation of microparticles in a microchannel with symmetric sharp corner structures

Por Fan, Liang-Liang, He, Xu-Kun, Han, Yu, Du, Li, Zhao, Liang, Zhe, Jiang
Publicado em 2014

A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal...

Por Liu, Ji-jia, Fan, Liang-liang, Chen, Jin-lan, Tan, Zhi-ping, Yang, Yi-feng
Publicado em 2014

Whole‐exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death

Por Huang, Hao, Chen, Ya‐Qin, Fan, Liang‐Liang, Guo, Shuai, Li, Jing‐Jing, Jin, Jie‐Yuan, Xiang, Rong
Publicado no J Cell Mol Med (2017)

Functional properties and structure changes of soybean protein isolate after subcritical water treatment

Por Zhang, Qiu-Ting, Tu, Zong-Cai, Wang, Hui, Huang, Xiao-Qin, Fan, Liang-Liang, Bao, Zhong-Yu, Xiao, Hui
Publicado no J Food Sci Technol (2014)

A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel’s deformity

Por Guo, Shuai, Fan, Xue-Feng, Jin, Jie-Yuan, Fan, Liang-Liang, Zeng, Lei, Zhou, Zheng-Bing, Xiang, Rong, Tang, Ju-Yu
Publicado no Mol Cytogenet (2018)

Mutation detection in Chinese patients with familial hypercholesterolemia

Por Du, Ran, Fan, Liang-Liang, Lin, Min-Jie, He, Zhi-Jian, Huang, Hao, Chen, Ya-Qin, Li, Jing-Jing, Xia, Kun, Zhao, Shui-Ping, Xiang, Rong
Publicado no Springerplus (2016)