The mechanism on phosphorylation of Hsp20(Ser16) inhibit GA stress and ER stress during OGD/R

por Lu, Tonglin, Zou, Yongyi, Zhou, Xu, Peng, Wenna, Hu, Zhiping
Publicado 2019

Long noncoding RNA TUG1 is downregulated in sepsis and may sponge miR-27a to downregulate tumor necrosis factor-α

por Wang, Li, Zhong, Qinghua, Feng, Yanli, Tang, Xiaoying, Wang, Qiong, Zou, Yongyi, Duan, Jiang
Publicado 2020

Effects of Commonly Used Pesticides in China on the Mitochondria and Ubiquitin-Proteasome System in Parkinson’s Disease

por Chen, Tingting, Tan, Jieqiong, Wan, Zhengqing, Zou, Yongyi, Kessete Afewerky, Henok, Zhang, Zhuohua, Zhang, Tongmei
Publicado 2017

Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy

por Zou, Yongyi, Luo, Haiyan, Yuan, Huizhen, Xie, Kang, Yang, Yan, Huang, Shuhui, Yang, Bicheng, Liu, Yanqiu
Publicado 2022

Wooden-Tip Electrospray Mass Spectrometry Characterization of Human Hemoglobin in Whole Blood Sample for Thalassemia Screening: A Pilot Study

por Huang, Tingting, Huang, Ting, Zou, Yongyi, Xie, Kang, Shen, Yinqin, Zhang, Wen, Huang, Shuhui, Liu, Yanqiu, Yang, Bicheng
Publicado 2022

Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi province

por Zeng, Baitao, Lu, Qing, Chen, Shaohong, Guan, Huizhen, Xu, Xiaolan, Zou, Yongyi, Wang, Feng, Huang, Shuhui, Liu, Yanqiu, Yang, Bicheng
Publicado 2023

A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family

por Chen, Jia, Yuan, Huizhen, Xie, Kang, Wang, Xinrong, Tan, Linglong, Zou, Yongyi, Yang, Yan, Pan, Lu, Xiao, Junfang, Chen, Ge, Liu, Yanqiu
Publicado 2020

Mutation spectrum of PTS gene in patients with tetrahydrobiopterin deficiency from jiangxi province

por Xie, Kang, Zeng, Baitao, Zhang, Liuyang, Chen, Shaohong, Zou, Yongyi, Yuan, Huizhen, Huang, Shuhui, Wang, Feng, Lu, Qing, Liu, Yanqiu, Yang, Bicheng
Publicado 2022

Analysis of chromosomal structural variations in patients with recurrent spontaneous abortion using optical genome mapping

por Rao, Huihua, Zhang, Haoyi, Zou, Yongyi, Ma, Pengpeng, Huang, Tingting, Yuan, Huizhen, Zhou, Jihui, Lu, Wan, Li, Qiao, Huang, Shuhui, Liu, Yanqiu, Yang, Bicheng
Publicado 2023

Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China

por Zou, Yongyi, Feng, Chuanxin, Qin, Jiawei, Wang, Xinrong, Huang, Tingting, Yang, Yan, Xie, Kang, Yuan, Huizhen, Huang, Shuhui, Yang, Bicheng, Lu, Wan, Liu, Yanqiu
Publicado 2023

Identification of five novel SCN1A variants

por Zeng, Baitao, Zhang, Haoyi, Lu, Qing, Fu, Qingzi, Yan, Yang, Lu, Wan, Ma, Pengpeng, Feng, Chuanxin, Qin, Jiawei, Luo, Laipeng, Yang, Bicheng, Zou, Yongyi, Liu, Yanqiu
Publicado 2023

Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China

por Luo, Haiyan, Huang, Ting, Lu, Qing, Zhang, Liuyang, Xu, Yonghua, Yang, Yan, Guo, Zhen, Yuan, Huizhen, Shen, Yinqin, Huang, Shuhui, Yang, Bicheng, Zou, Yongyi, Liu, Yanqiu
Publicado 2022

Concurrent newborn hearing and genetic screening of common hearing loss variants with bloodspot-based targeted next generation sequencing in Jiangxi province

por Luo, Haiyan, Yang, Yan, Wang, Xinrong, Xu, Fangping, Huang, Cheng, Liu, Danping, Zhang, Liuyang, Huang, Ting, Ma, Pengpeng, Lu, Qing, Huang, Shuhui, Yang, Bicheng, Zou, Yongyi, Liu, Yanqiu
Publicado 2022