The geographical pension gap: Understanding the causes of inequality in China’s pension funds

por Zhang, Songbiao, Wang, Xining, Li, Huajin, Wang, Huilin
Publicado 2023

Novel homozygous nonsynonymous variant of CNNM4 gene in a Chinese family with Jalili syndrome

por Li, Huajin, Huang, Yanfeng, Li, Jing, Xie, Maosong
Publicado 2022

Novel ALMS1 mutations in Chinese patients with Alström syndrome

por Liang, Xiaofang, Li, Hui, Li, Huajin, Xu, Fei, Dong, Fangtian, Sui, Ruifang
Publicado 2013

Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities

por Sun, Zixi, Zhou, Qi, Li, Huajin, Yang, Lizhu, Wu, Shijing, Sui, Ruifang
Publicado 2017

A novel small deletion in the NHS gene associated with Nance-Horan syndrome

por Li, Huajin, Yang, Lizhu, Sun, Zixi, Yuan, Zhisheng, Wu, Shijing, Sui, Ruifang
Publicado 2018

Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinism

por Zou, Xuan, Li, Hui, Yang, Lizhu, Sun, Zixi, Yuan, Zhisheng, Li, Huajin, Sui, Ruifang
Publicado 2017

Defining the Pluripotent Marker Genes for Identification of Teleost Fish Cell Pluripotency During Reprogramming

por Li, Huajin, Xu, Wenting, Xiang, Sijia, Tao, Leiting, Fu, Wen, Liu, Jinhui, Liu, Wenbin, Xiao, Yamei, Peng, Liangyue
Publicado 2022

Generation of Stable Induced Pluripotent Stem-like Cells from Adult Zebra Fish Fibroblasts

por Peng, Liangyue, Zhou, Yonghua, Xu, Wenting, Jiang, Minggui, Li, Huajin, Long, Mindi, Liu, Wenbin, Liu, Jinhui, Zhao, Xiaoyang, Xiao, Yamei
Publicado 2019

Fish Pluripotent Stem-Like Cell Line Induced by Small-Molecule Compounds From Caudal Fin and its Developmental Potentiality

por Xu, Wenting, Li, Huajin, Peng, Liangyue, Pu, Liyu, Xiang, Sijia, Li, Yue, Tao, Leiting, Liu, Wenbin, Liu, Jinhui, Xiao, Yamei, Liu, Shaojun
Publicado 2022

The phenotypic variability of HK1-associated retinal dystrophy

por Yuan, Zhisheng, Li, Baiyu, Xu, Mingchu, Chang, Emmanuel Y., Li, Huajin, Yang, Lizhu, Wu, Shijing, Soens, Zachry T., Li, Yumei, Wong, Lee-Jun C., Lewis, Richard A., Sui, Ruifang, Chen, Rui
Publicado 2017

Comprehensive analysis of Stargardt macular dystrophy patients reveals new genotype-phenotype correlations and unexpected diagnostic revisions

por Zaneveld, Jacques, Siddiqui, Sorath, Li, Huajin, Wang, Xia, Wang, Hui, Wang, Keqing, Li, Hui, Ren, Huanan, Lopez, Irma, Dorfman, Allison, Khan, Ayesha, Wang, Feng, Salvo, Jason, Gelowani, Violet, Li, Yumei, Sui, Ruifang, Koenekoop, Robert, Chen, Rui
Publicado 2014