Works by Yan, Tizhen

Results: 25

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

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

Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease.

Published in:

Expert Review of Hematology, 2020, v. 13, n. 9, p. 1027, doi. 10.1080/17474086.2020.1803736

By:

Luo, Shiqiang;
Chen, Xingyuan;
Chen, Lizhu;
Zhong, Qingyan;
Wang, Qiuhua;
Xu, Zehui;
Huang, Jun;
Yan, Tizhen;
Tang, Ning

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

Hb H disease associated with compound heterozygosity for --<sup>SEA</sup> deletion and a novel alpha globin chain variant (HBA2:c.175C>A) on the distal histidine in a Chinese family.

Published in:

Hematology, 2024, v. 29, n. 1, p. 1, doi. 10.1080/16078454.2024.2339559

By:

Sun, Manna;
Lou, Jiwu;
Xinghe, Wang;
Zhao, Ying;
Dai, Yunshi;
Liu, Shuangai;
Yan, Tizhen

Publication type:

Article

Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China.

Published in:

2023

By:

Chen, Lizhu;
Tang, Ning;
Huang, Jun;
Wei, Xiaobao;
Zhong, Qingyan;
Yan, Tizhen;
Luo, Shiqiang

Publication type:

Case Study

Analysis of rare thalassemia caused by HS-40 regulatory site deletion.

Published in:

Hematology, 2020, v. 25, n. 1, p. 286, doi. 10.1080/16078454.2020.1799587

By:

Luo, Shiqiang;
Chen, Xingyuan;
Zhong, Qingyan;
Wang, Qiuhua;
Xu, Zehui;
Qin, Liuqun;
Wang, Jingren;
Yuan, Dejian;
Yan, Tizhen;
Tang, Ning

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

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

Global discovery, expression pattern, and regulatory role of miRNA-like RNAs in Ascosphaera apis infecting the Asian honeybee larvae.

Published in:

Frontiers in Microbiology, 2025, p. 1, doi. 10.3389/fmicb.2025.1551625

By:

Liu, Xiaoyu;
Geng, Sihai;
Ye, Daoyou;
Xu, Wenhua;
Zheng, Yidi;
Wang, Fangji;
Lei, Jianpeng;
Wu, Ying;
Jiang, Haibin;
Hu, Ying;
Chen, Dafu;
Yan, Tizhen;
Guo, Rui;
Qiu, Jianfeng

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

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

Free glutaraldehyde gelatin microsphere loaded mesenchymal stem cells alleviate osteoarthritis by promoting Ext1 expression.

Published in:

Theranostics, 2025, v. 15, n. 9, p. 4135, doi. 10.7150/thno.109468

By:

Ye Yuan;
Longsheng Xu;
Yu Zhao;
Tizhen Yan;
Baobiao Zhuo;
Fan Bu;
Qian Cai;
Youjia Xu;
Qing Bi;
Yu Tong;
Dan Xing;
Di Sun;
Jianhao Lin

Publication type:

Article

Analysis of the Expression Patterns of piRNAs in Response to Microsporidian Invasion in Midgut of Workers (Apis cerana cerana).

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 6, p. 2402, doi. 10.3390/ijms26062402

By:

Zhang, Yiqiong;
Wang, Mengyi;
Xu, Wenhua;
Zang, He;
Yan, Tizhen;
Wu, Tao;
Huang, Kaifei;
Chen, Dafu;
Luo, Qingming;
Guo, Rui;
Qiu, Jianfeng

Publication type:

Article

Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation.

Published in:

Hemoglobin, 2020, v. 44, n. 1, p. 51, doi. 10.1080/03630269.2020.1711771

By:

Chen, Xingyuan;
Luo, Shiqiang;
Huang, Jun;
Yuan, Dejian;
Yan, Tizhen;
Cai, Ren;
Tang, Ning

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

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

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

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

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

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

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