Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
Liang, Desheng, Cram, David S., Tan, Hu, Linpeng, Siyuan, Liu, Yingdi, Sun, Huaiyu, Zhang, Yu, Tian, Feng, Zhu, Hongmin, Xu, Mengnan, Wang, Hua, Yu, Fuli, Wu, Lingqian
Published in Genetics in medicine (01.09.2019)
Published in Genetics in medicine (01.09.2019)
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Identification of MicroRNAs in Human Follicular Fluid: Characterization of MicroRNAs That Govern Steroidogenesis in Vitro and Are Associated With Polycystic Ovary Syndrome in Vivo
Sang, Qing, Yao, Zhongyuan, Wang, Huan, Feng, Ruizhi, Wang, Haojue, Zhao, Xinzhi, Xing, Qinghe, Jin, Li, He, Lin, Wu, Lingqian, Wang, Lei
Published in The journal of clinical endocrinology and metabolism (01.07.2013)
Published in The journal of clinical endocrinology and metabolism (01.07.2013)
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Long-read DNA sequencing fully characterized chromothripsis in a patient with Langer-Giedion syndrome and Cornelia de Lange syndrome-4
Lei, Ming, Liang, Desheng, Yang, Yifeng, Mitsuhashi, Satomi, Katoh, Kazutaka, Miyake, Noriko, Frith, Martin C, Wu, Lingqian, Matsumoto, Naomichi
Published in Journal of human genetics (01.08.2020)
Published in Journal of human genetics (01.08.2020)
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Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and Cardiomyocytes
Xiao, Rou, Zhou, Miaojin, Wang, Peiyun, Zeng, Baitao, Wu, Lingqian, Hu, Zhiqing, Liang, Desheng
Published in International journal of molecular sciences (16.08.2022)
Published in International journal of molecular sciences (16.08.2022)
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Targeted-Deletion of a Tiny Sequence via Prime Editing to Restore SMN Expression
Zhou, Miaojin, Tang, Shuqing, Duan, Nannan, Xie, Mi, Li, Zhuo, Feng, Mai, Wu, Lingqian, Hu, Zhiqing, Liang, Desheng
Published in International journal of molecular sciences (19.07.2022)
Published in International journal of molecular sciences (19.07.2022)
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Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing
Liang, Desheng, Lv, Weigang, Wang, Hua, Xu, Liangpu, Liu, Jing, Li, Haoxian, Hu, Liang, Peng, Ying, Wu, Lingqian
Published in Prenatal diagnosis (01.05.2013)
Published in Prenatal diagnosis (01.05.2013)
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Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem Cells
Zhou, Miaojin, Hu, Zhiqing, Qiu, Liyan, Zhou, Tao, Feng, Mai, Hu, Qian, Zeng, Baitao, Li, Zhuo, Sun, Qianru, Wu, Yong, Liu, Xionghao, Wu, Lingqian, Liang, Desheng
Published in Human gene therapy (01.11.2018)
Published in Human gene therapy (01.11.2018)
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O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells
Teng, Hua, Chen, Siyi, Liu, Fang, Teng, Yanling, Li, Yunlong, Liang, Desheng, Wu, Lingqian, Li, Zhuo
Published in International journal of molecular sciences (01.07.2024)
Published in International journal of molecular sciences (01.07.2024)
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Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndrome
Lei, Ming, Mitsuhashi, Satomi, Miyake, Noriko, Ohta, Tohru, Liang, Desheng, Wu, Lingqian, Matsumoto, Naomichi
Published in Journal of human genetics (01.07.2019)
Published in Journal of human genetics (01.07.2019)
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Ectopic Expression of FVIII in HPCs and MSCs Derived from hiPSCs with Site-Specific Integration of ITGA2B Promoter-Driven BDDF8 Gene in Hemophilia A
Zhao, Junya, Zhou, Miaojin, Wang, Zujia, Wu, Lingqian, Hu, Zhiqing, Liang, Desheng
Published in International journal of molecular sciences (06.01.2022)
Published in International journal of molecular sciences (06.01.2022)
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Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A
Xiao, Rou, Chen, Yan, Hu, Zhiqing, Tang, Qiyu, Wang, Peiyun, Zhou, Miaojin, Wu, Lingqian, Liang, Desheng
Published in International journal of molecular sciences (01.04.2024)
Published in International journal of molecular sciences (01.04.2024)
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Gene Therapy for Hemophilia and Duchenne Muscular Dystrophy in China
Liu, Xionghao, Liu, Mujun, Wu, Lingqian, Liang, Desheng
Published in Human gene therapy (01.02.2018)
Published in Human gene therapy (01.02.2018)
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Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)
Lv, Weigang, Wei, Xianda, Guo, Ruolan, Liu, Qin, Zheng, Yu, Chang, Jiazhen, Bai, Ting, Li, Haoxian, Zhang, Jianguang, Song, Zhuo, Cram, David S, Liang, Desheng, Wu, Lingqian
Published in Clinical chemistry (Baltimore, Md.) (01.01.2015)
Published in Clinical chemistry (Baltimore, Md.) (01.01.2015)
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Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism
Li, Menglin, Li, Zhuo, Chen, Miaomiao, Hu, Zhiqing, Zhou, Miaojin, Wu, Lingqian, Zhang, Chunhua, Liang, Desheng
Published in International journal of molecular sciences (02.01.2023)
Published in International journal of molecular sciences (02.01.2023)
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Noninvasive prenatal testing, ultrasonographic findings and poor prenatal diagnosis rates for twin pregnancies: a retrospective study
Yuan, Xiying, Wang, Weinan, Dai, Lei, Yong, Wenjing, Pei, Chenlin, Li, Jingzhi, Wu, Lingqian
Published in BMC pregnancy and childbirth (13.05.2023)
Published in BMC pregnancy and childbirth (13.05.2023)
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ssODN-Mediated In-Frame Deletion with CRISPR/Cas9 Restores FVIII Function in Hemophilia A-Patient-Derived iPSCs and ECs
Hu, Zhiqing, Zhou, Miaojin, Wu, Yong, Li, Zhuo, Liu, Xionghao, Wu, Lingqian, Liang, Desheng
Published in Molecular therapy. Nucleic acids (06.09.2019)
Published in Molecular therapy. Nucleic acids (06.09.2019)
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