Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant
Gu, Yu, Mei, Daoqi, Wang, Xiaona, Ma, Ang, Kong, Jinghui, Zhang, Yaodong
Published in Frontiers in neurology (09.05.2023)
Published in Frontiers in neurology (09.05.2023)
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Genomic and biological characterization of a pandemic norovirus variant GII.4 Sydney 2012
Ge, Lili, Chen, Xuhui, Liu, Jinjin, Zheng, Lijun, Chen, Chongfen, Luo, Shuying, Guo, Pengbo, Kong, Jinghui, Song, Yinsen, Huo, Yuqi
Published in Virus genes (01.04.2020)
Published in Virus genes (01.04.2020)
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Gastrodin Rescues Autistic-Like Phenotypes in Valproic Acid-Induced Animal Model
Wang, Xiaona, Tao, Jing, Qiao, Yidan, Luo, Shuying, Zhao, Zhenqin, Gao, Yinbo, Guo, Jisheng, Kong, Jinghui, Chen, Chongfen, Ge, Lili, Zhang, Bo, Guo, Pengbo, Liu, Lei, Song, Yinsen
Published in Frontiers in neurology (07.12.2018)
Published in Frontiers in neurology (07.12.2018)
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H19 suppresses the growth of hepatoblastoma cells by promoting their apoptosis via the signaling pathways of miR‐675/FADD and miR‐138/PTK2
Ge, Lili, Zhang, Xianwei, Hu, Shengnan, Song, Yinsen, Kong, Jinghui, Zhang, Bo, Yang, Xiaoang
Published in Journal of cellular biochemistry (01.04.2019)
Published in Journal of cellular biochemistry (01.04.2019)
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GntR is involved in the expression of virulence in strain Streptococcus suis P1/7
Zhou, Ying, Nie, Ruonan, Liu, Xiaoyue, Kong, Jinghui, Wang, Xiaohong, Li, Jinquan
Published in FEMS microbiology letters (01.07.2018)
Published in FEMS microbiology letters (01.07.2018)
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RETRACTED: H19 suppresses the growth of hepatoblastoma cells by promoting their apoptosis via the signaling pathways of miR‐675/FADD and miR‐138/PTK2
Ge, Lili, Zhang, Xianwei, Hu, Shengnan, Song, Yinsen, Kong, Jinghui, Zhang, Bo, Yang, Xiaoang
Published in Journal of cellular biochemistry (01.04.2019)
Published in Journal of cellular biochemistry (01.04.2019)
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Paternal uniparental disomy of chromosome 16 resulting in homozygosity of a GPT2 mutation causes intellectual and developmental disability
Liu, Jing, Chen, Baiyun, Liu, Yuchun, Kong, Jinghui, Zhang, Bo, Han, Liang, Mei, Daoqi, Ma, Cai Yun, Shang, Qing, Xie, Zhenhua, Xiao, Mengjun, Mei, Shiyue, Zhang, Yaodong, Gao, Chao, Li, Dongxiao
Published in European journal of medical genetics (01.09.2022)
Published in European journal of medical genetics (01.09.2022)
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Comprehensive diagnosis and genetic analysis of two children with ring chromosome 18
Ding, Zhe, Mei, Shiyue, Zhang, Bo, Kong, Jinghui, Liu, Lei, Zhang, Zhenhua, Wang, Chaojie, Zhang, Yaodong
Published in Zhonghua yi xue yi chuan xue za zhi (10.09.2024)
Published in Zhonghua yi xue yi chuan xue za zhi (10.09.2024)
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Clinical phenotype and molecular genetic analysis of seven children with CHARGE syndrome
Ge, Lili, Kong, Jinghui, Chen, Chongfen, Xia, Zhiyi, Mei, Shiyue, Zhang, Yaodong
Published in Zhonghua yi xue yi chuan xue za zhi (10.09.2024)
Published in Zhonghua yi xue yi chuan xue za zhi (10.09.2024)
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Phenotypic and genetic analysis of a child with partial trisomy 7q
Wang, Chaojie, Li, Dongxiao, Zhang, Yaodong, Kong, Jinghui, Li, Rui, Gao, Chao, Shang, Qing, Zhang, Huichun
Published in Zhonghua yi xue yi chuan xue za zhi (10.05.2023)
Published in Zhonghua yi xue yi chuan xue za zhi (10.05.2023)
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Phenotypic and genetic analysis of a boy with partial trisomy of 22q
Zhang, Bo, Xu, Ying, Kong, Jinghui, Song, Yinsen, Li, Dongxiao
Published in Zhonghua yi xue yi chuan xue za zhi (10.05.2020)
Published in Zhonghua yi xue yi chuan xue za zhi (10.05.2020)
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Analysis of a Chinese pedigree with autosomal dominant Charcot-Marie-Tooth disease type 2A2A
Zhao, Ding, Li, Rui, Zhao, Bojie, Kong, Jinghui, Chen, Chongfen, Song, Jijun
Published in Zhonghua yi xue yi chuan xue za zhi (10.02.2021)
Published in Zhonghua yi xue yi chuan xue za zhi (10.02.2021)
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