SAT-428 Sex-Specific Risk Gene of Graves’ Disease

por Zhao, Shuangxia, Chen-Yan, Yan
Publicado 2020

Insights into the pathogenesis of hereditary angioedema using genetic sequencing and recombinant protein expression analyses

por Ren, Zhen, Zhao, Shuangxia, Li, Tiandao, Wedner, H. James, Atkinson, John P.
Publicado 2023

Effects of Osteoglycin (OGN) on treating senile osteoporosis by regulating MSCs

por Chen, Xia, Chen, Junsong, Xu, Dongliang, Zhao, Shuangxia, Song, Huaidong, Peng, Yongde
Publicado 2017

Correlation of TSHR and CTLA-4 Single Nucleotide Polymorphisms with Graves Disease

por Sun, Weihua, Zhang, Xiaomei, Wu, Jing, Zhao, Wendi, Zhao, Shuangxia, Li, Minglong
Publicado 2019

SUN-034 Combined CNV, Haplotyping and Whole Exome Sequencing Implicates Inherited Novel SRY Mutations Not Account for Familial 46,XY Sex Reversal

por Qiao, Jie, Wang, Nan, Zhu, Wenjiao, Han, Bing, Zhao, Shuangxia, Song, Huai-Dong
Publicado 2020

Identification of SERPINA1 promoting better prognosis in papillary thyroid carcinoma along with Hashimoto’s thyroiditis through WGCNA analysis

por Zhang, Yihan, Xie, Xin, Zhou, Hong, Li, Bingxin, Ding, Li, Cai, Zhaogen, Song, Huaidong, Zhao, Shuangxia, Xu, Huanbai
Publicado 2023

Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique

por Wang, Hao, Zhu, Hui, Wang, Nan, Cheng, Tong, Han, Bing, Zhao, Shuangxia, Song, Huaidong, Cheng, Kaixiang, Liu, Yang, Qiao, Jie
Publicado 2019

In‐frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance

por Zhu, Wenjiao, Shi, Yuanping, Zhang, Changrun, Peng, Yajie, Wan, Yueyue, Xu, Yue, Liu, Xuemeng, Han, Bing, Zhao, Shuangxia, Kuang, Yanping, Song, Huaidong, Qiao, Jie
Publicado 2023

Polymorphism in the Alternative Donor Site of the Cryptic Exon of LHCGR: Functional Consequences and Associations with Testosterone Level

por Liu, Wei, Han, Bing, Zhu, Wenjiao, Cheng, Tong, Fan, Mengxia, Wu, Jiajun, Yang, Ying, Zhu, Hui, Si, Jiqiang, Lyu, Qifeng, Chai, Weiran, Zhao, Shuangxia, Song, Huaidong, Kuang, Yanping, Qiao, Jie
Publicado 2017

Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants

por Zhu, Hui, Yao, Haijun, Xu, Yue, Chen, Yan, Han, Bing, Wang, Nan, Wang, Hao, Zhang, Qiang, Zhu, Wenjiao, Shi, Yuanping, Sun, Hua, Zhao, Shuangxia, Song, Huaidong, Liu, Yang, Qiao, Jie
Publicado 2021

PARD3 gene variation as candidate cause of nonsyndromic cleft palate only

por Cui, Renjie, Chen, Dingli, Li, Na, Cai, Ming, Wan, Teng, Zhang, Xueqiang, Zhang, Meiqin, Du, Sichen, Ou, Huayuan, Jiao, Jianjun, Jiang, Nan, Zhao, Shuangxia, Song, Huaidong, Song, Xuedong, Ma, Duan, Zhang, Jin, Li, Shouxia
Publicado 2022

Genetic Heterogeneity of Susceptibility Gene in Different Ethnic Populations: Refining Association Study of PTPN22 for Graves’ Disease in a Chinese Han Population

por Xue, Liqiong, Pan, Chunming, Gu, Zhaohui, Zhao, Shuangxia, Han, Bing, Liu, Wei, Yang, Shaoying, Yu, Shasha, Sun, Yixuan, Liang, Jun, Gao, Guanqi, Zhang, Xiaomei, Yuan, Guoyue, Li, Changgui, Du, Wenhua, Chen, Gang, Chen, Jialun, Song, Huaidong
Publicado 2013