Miaojin Zhou

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Duchenne Muscular Dystrophy

Top Venues

International journal of molecular sciences

Life (Basel, Switzerland)

This page only lists publications with an associated author ORCID identifier.

Publications

Rou Xiao, Yan Chen, Zhiqing Hu, Qiyu Tang, Peiyun Wang, Miaojin Zhou, Lingqian Wu, Desheng Liang
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A. International journal of molecular sciences 25 (7) (2024)
Rou Xiao, Yan Chen, Zhiqing Hu, Qiyu Tang, Peiyun Wang, Miaojin Zhou, Lingqian Wu, Desheng Liang
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A. International journal of molecular sciences 25 (7) (2024)
Rou Xiao, Yan Chen, Zhiqing Hu, Qiyu Tang, Peiyun Wang, Miaojin Zhou, Lingqian Wu, Desheng Liang
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A. International journal of molecular sciences 25 (7) (2024)
Qiyu Tang, Zhiqing Hu, Junya Zhao, Tao Zhou, Shuqing Tang, Peiyun Wang, Rou Xiao, Yan Chen, Lingqian Wu, Miaojin Zhou, Desheng Liang
CRISPR-Mediated In Situ Introduction or Integration of F9-Padua in Human iPSCs for Gene Therapy of Hemophilia B. International journal of molecular sciences 24 (10) (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Rou Xiao, Miaojin Zhou, Peiyun Wang, Baitao Zeng, Lingqian Wu, Zhiqing Hu, Desheng Liang
Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and Cardiomyocytes. International journal of molecular sciences 23 (16) (2022)
Junya Zhao, Miaojin Zhou, Zujia Wang, Lingqian Wu, Zhiqing Hu, Desheng Liang
Ectopic Expression of FVIII in HPCs and MSCs Derived from hiPSCs with Site-Specific Integration of ITGA2B Promoter-Driven BDDF8 Gene in Hemophilia A. International journal of molecular sciences 23 (2) (2022)
Zhiqing Hu, Miaomiao Chen, Chunhua Zhang, Zhuo Li, Mai Feng, Lingqian Wu, Miaojin Zhou, Desheng Liang
Cas14a1-Mediated Nucleic Acid Diagnostics for Spinal Muscular Atrophy. Biosensors 12 (5) (2022)
Miaojin Zhou, Shuqing Tang, Nannan Duan, Mi Xie, Zhuo Li, Mai Feng, Lingqian Wu, Zhiqing Hu, Desheng Liang
Targeted-Deletion of a Tiny Sequence via Prime Editing to Restore SMN Expression. International journal of molecular sciences 23 (14) (2022)
Yiti Zhang, Baitao Zeng, Ao Gu, Qinyu Kang, Mingri Zhao, Guangnan Peng, Miaojin Zhou, Wanxi Liu, Min Liu, Lingjie Ding, Desheng Liang, Xionghao Liu, Mujun Liu
Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2 P497H Mutation. International journal of molecular sciences 23 (19) (2022)
Nannan Duan, Shuqing Tang, Baitao Zeng, Zhiqing Hu, Qian Hu, Lingqian Wu, Miaojin Zhou, Desheng Liang
An Episomal CRISPR/Cas12a System for Mediating Efficient Gene Editing. Life (Basel, Switzerland) 11 (11) (2021)
Yanchi Wang, Junya Zhao, Nannan Duan, Wei Liu, Yuxuan Zhang, Miaojin Zhou, Zhiqing Hu, Mai Feng, Xionghao Liu, Lingqian Wu, Zhuo Li, Desheng Liang
Paired CRISPR/Cas9 Nickases Mediate Efficient Site-Specific Integration of F9 into rDNA Locus of Mouse ESCs. International journal of molecular sciences 19 (10) (2018)