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ame-miR-5119- Eth axis modulates larval-pupal transition of western honeybee worker.
Published in:
Frontiers in Physiology, 2024, p. 1, doi. 10.3389/fphys.2024.1475306
By:
- Dong, Shunan;
- Li, Kunze;
- Zang, He;
- Song, Yuxuan;
- Kang, Jing;
- Chen, Ying;
- Du, Liting;
- Wang, Ning;
- Chen, Dafu;
- Luo, Qingming;
- Yan, Tizhen;
- Guo, Rui;
- Qiu, Jianfeng
Publication type:
Article
Tandem Mass Spectrometry Screening for Inborn Errors of Metabolism in Newborns and High-Risk Infants in Southern China: Disease Spectrum and Genetic Characteristics in a Chinese Population.
Published in:
Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.631688
By:
- Tan, Jianqiang;
- Chen, Dayu;
- Chang, Rongni;
- Pan, Lizhen;
- Yang, Jinling;
- Yuan, Dejian;
- Huang, Lihua;
- Yan, Tizhen;
- Ning, Haiping;
- Wei, Jiangyan;
- Cai, Ren
Publication type:
Article
A Novel Multi-Exon Deletion of PACS1 in a Three-Generation Pedigree: Supplements to PACS1 Neurodevelopmental Disorder Spectrum.
Published in:
Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.690216
By:
- Liu, Yuan;
- Ding, Hongke;
- Yan, Tizhen;
- Liu, Ling;
- Yu, Lihua;
- Huang, Yanlin;
- Li, Fake;
- Zeng, Yukun;
- Huang, Weiwei;
- Zhang, Yan;
- Yin, Aihua
Publication type:
Article
Rapid detection of non-deletional mutations causing α-thalassemia by multicolor melting curve analysis.
Published in:
Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 3, p. 397, doi. 10.1515/cclm-2015-0173
By:
- Qiuying Huang;
- Xudong Wang;
- Ning Tang;
- Chunjiang Zhu;
- Tizhen Yan;
- Ping Chen;
- Qingge Li
Publication type:
Article
Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing.
Published in:
Molecular Genetics & Genomics, 2020, v. 295, n. 2, p. 505, doi. 10.1007/s00438-019-01637-w
By:
- Li, Zhiming;
- Shang, Xuan;
- Luo, Shiqiang;
- Zhu, Fei;
- Wei, Xiaofeng;
- Zhou, Wanjun;
- Ye, Yuhua;
- Yan, Tizhen;
- Cai, Ren;
- Xu, Xiangmin
Publication type:
Article
Rapid and Reliable Detection of Nonsyndromic Hearing Loss Mutations by Multicolor Melting Curve Analysis.
Published in:
Scientific Reports, 2017, p. 42894, doi. 10.1038/srep42894
By:
- Wang, Xudong;
- Hong, Yongjun;
- Cai, Peihong;
- Tang, Ning;
- Chen, Ying;
- Yan, Tizhen;
- Liu, Yinghua;
- Huang, Qiuying;
- Li, Qingge
Publication type:
Article
Prenatal diagnosis of paternal uniparental disomy for chromosome 2 in two fetuses with intrauterine growth restriction.
Published in:
2023
By:
- Tan, Xuemei;
- Liu, Bailing;
- Yan, Tizhen;
- Wei, Xiaobao;
- Qin, Yanfeng;
- Zeng, Dingyuan;
- Yuan, Dejian
Publication type:
Case Study
Analysis of complex chromosomal rearrangements using a combination of current molecular cytogenetic techniques.
Published in:
Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00597-y
By:
- He, Ping;
- Wei, Xiaoni;
- Xu, Yuchan;
- Huang, Jun;
- Tang, Ning;
- Yan, Tizhen;
- Yang, Chuanchun;
- Lu, Kangmo
Publication type:
Article
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
Published in:
Clinical & Translational Medicine, 2022, v. 12, n. 7, p. 1, doi. 10.1002/ctm2.941
By:
- Hao, Lili;
- Ma, Jing;
- Wu, Feizhen;
- Ma, Xiaojing;
- Qian, Maoxiang;
- Sheng, Wei;
- Yan, Tizhen;
- Tang, Ning;
- Jiang, Xin;
- Zhang, Bowen;
- Xiao, Deyong;
- Qian, Yanyan;
- Zhang, Jin;
- Jiang, Nan;
- Zhou, Wenhao;
- Chen, Weicheng;
- Ma, Duan;
- Huang, Guoying
Publication type:
Article
Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations.
Published in:
Molecular Medicine Reports, 2022, v. 25, n. 2, p. N.PAG
By:
- Yang, Jinling;
- Yuan, Dejian;
- Tan, Xiaohui;
- Zeng, Yexi;
- Tang, Ning;
- Chen, Dayu;
- Tan, Jianqiang;
- Cai, Ren;
- Huang, Jun;
- Yan, Tizhen
Publication type:
Article
MALDI--TOF--MS for Rapid Screening and Typing of β-Globin Variant and β-Thalassemia through Direct Measurements of Intact Globin Chains.
Published in:
Clinical Chemistry, 2022, v. 68, n. 12, p. 1541, doi. 10.1093/clinchem/hvac151
By:
- Qianqian Zhang;
- Ge Wang;
- Dehui Sun;
- Wanying Lin;
- Tizhen Yan;
- Yuanjun Wu;
- Meiying Wu;
- Jianhong Chen;
- Shaomin Zou;
- Wenchun Xie;
- Yuqiu Zhou;
- Yuxi Wang;
- Linlin He;
- Yanhui Liu;
- Zhenxiong Qiu;
- Lingling Hu;
- Bin Lin;
- Xiaoguang Zhou;
- Yan Li;
- Xiangmin Xu
Publication type:
Article
Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
Published in:
2019
By:
- Li, Zhetao;
- Huang, Jiwei;
- Liang, Biao;
- Zeng, Dingyuan;
- Luo, Shiqiang;
- Yan, Tizhen;
- Liao, Fengwen;
- Huang, Jun;
- Li, Jingwen;
- Cai, Ren;
- Deng, Xine;
- Tang, Ning
Publication type:
journal article
ame-miR-5119-Eth axis modulates larval-pupal transition of western honeybee worker.
Published in:
Frontiers in Physiology, 2024, p. 1, doi. 10.3389/fphys.2024.1475306
By:
- Shunan Dong;
- Kunze Li;
- He Zang;
- Yuxuan Song;
- Jing Kang;
- Ying Chen;
- Liting Du;
- Ning Wang;
- Dafu Chen;
- Qingming Luo;
- Tizhen Yan;
- Rui Guo;
- Jianfeng Qiu
Publication type:
Article
Detection of four rare thalassemia variants using Single-molecule realtime sequencing.
Published in:
Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.974999
By:
- Shiqiang Luo;
- Xingyuan Chen;
- Dingyuan Zeng;
- Ning Tang;
- Dejian Yuan;
- Bailing Liu;
- Lizhu Chen;
- Qingyan Zhong;
- Jiaqi Li;
- Yinyin Liu;
- Jianping Chen;
- Xiaoyuan Wang;
- Tizhen Yan
Publication type:
Article
Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia.
Published in:
Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.765503
By:
- Yuan, Dejian;
- Yan, Tizhen;
- Luo, Shiqiang;
- Huang, Jun;
- Tan, Jianqiang;
- Zhang, Jianping;
- Zhang, Victor Wei;
- Lan, Yueyuan;
- Hu, Taobo;
- Guo, Jing;
- Huang, Mingwei;
- Zeng, Dingyuan
Publication type:
Article
Full-Length Transcriptome Construction and Systematic Characterization of Virulence Factor-Associated Isoforms in Vairimorpha (Nosema) Ceranae.
Published in:
Genes, 2024, v. 15, n. 9, p. 1111, doi. 10.3390/genes15091111
By:
- Guo, Sijia;
- Zang, He;
- Liu, Xiaoyu;
- Jing, Xin;
- Liu, Zhitan;
- Zhang, Wende;
- Wang, Mengyi;
- Zheng, Yidi;
- Li, Zhengyuan;
- Qiu, Jianfeng;
- Chen, Dafu;
- Yan, Tizhen;
- Guo, Rui
Publication type:
Article
Application of Copy Number Variation Sequencing in Genetic Analysis of Miscarriages in Early and Middle Pregnancy.
Published in:
Cytogenetic & Genome Research, 2020, v. 160, n. 11/12, p. 634, doi. 10.1159/000512801
By:
- Shiqiang Luo;
- Xingyuan Chen;
- Tizhen Yan;
- Jiaolian Ya;
- Zehui Xu;
- Pengfei Cai;
- Dejian Yuan;
- Ning Tang
Publication type:
Article

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