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Baitao Zeng

Showing results (1-10 of 15) with videos related to

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International Journal of Molecular Sciences|August 26, 2022
Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and CardiomyocytesRou Xiao, Miaojin Zhou, Peiyun Wang, et al.
BMC Pregnancy and Childbirth|December 9, 2025
Anaysis of the association between chromosomal abnormalities in early missed abortion embryos and maternal age and AMH levels based on CNV-SeqShuhui Huang, Tingting Huang, Danping Liu, et al.
Life (Basel, Switzerland)|November 27, 2021
An Episomal CRISPR/Cas12a System for Mediating Efficient Gene EditingNannan Duan, Shuqing Tang, Baitao Zeng, et al.
Frontiers in Genetics|January 5, 2024
Identification of two novel and one rare mutation in <i>DYRK1A</i> and prenatal diagnoses in three Chinese families with intellectual Disability-7Cheng Huang, Haiyan Luo, Baitao Zeng, et al.
Frontiers in Genetics|February 27, 2023
Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi provinceBaitao Zeng, Qing Lu, Shaohong Chen, et al.
Scientific Reports|March 8, 2025
Identification of novel COL4A5 variants and prenatal diagnosis in three large familiesBaitao Zeng, Yao Yu, Cong Liu, et al.
Frontiers in Genetics|December 30, 2022
Mutation spectrum of <i>PTS</i> gene in patients with tetrahydrobiopterin deficiency from jiangxi provinceKang Xie, Baitao Zeng, Liuyang Zhang, et al.
Biochemical and Biophysical Research Communications|February 4, 2021
Targeted addition of mini-dystrophin into rDNA locus of Duchenne muscular dystrophy patient-derived iPSCsBaitao Zeng, Miaojin Zhou, Bo Liu, et al.
International Journal of Molecular Sciences|October 14, 2022
Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2<sup>P497H</sup> MutationYiti Zhang, Baitao Zeng, Ao Gu, et al.
Human Gene Therapy|March 31, 2018
Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem CellsMiaojin Zhou, Zhiqing Hu, Liyan Qiu, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
International Journal of Molecular Sciences|August 26, 2022
Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and CardiomyocytesRou Xiao, Miaojin Zhou, Peiyun Wang, et al.
BMC Pregnancy and Childbirth|December 9, 2025
Anaysis of the association between chromosomal abnormalities in early missed abortion embryos and maternal age and AMH levels based on CNV-SeqShuhui Huang, Tingting Huang, Danping Liu, et al.
Life (Basel, Switzerland)|November 27, 2021
An Episomal CRISPR/Cas12a System for Mediating Efficient Gene EditingNannan Duan, Shuqing Tang, Baitao Zeng, et al.
Frontiers in Genetics|January 5, 2024
Identification of two novel and one rare mutation in <i>DYRK1A</i> and prenatal diagnoses in three Chinese families with intellectual Disability-7Cheng Huang, Haiyan Luo, Baitao Zeng, et al.
Frontiers in Genetics|February 27, 2023
Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi provinceBaitao Zeng, Qing Lu, Shaohong Chen, et al.
Scientific Reports|March 8, 2025
Identification of novel COL4A5 variants and prenatal diagnosis in three large familiesBaitao Zeng, Yao Yu, Cong Liu, et al.
Frontiers in Genetics|December 30, 2022
Mutation spectrum of <i>PTS</i> gene in patients with tetrahydrobiopterin deficiency from jiangxi provinceKang Xie, Baitao Zeng, Liuyang Zhang, et al.
Biochemical and Biophysical Research Communications|February 4, 2021
Targeted addition of mini-dystrophin into rDNA locus of Duchenne muscular dystrophy patient-derived iPSCsBaitao Zeng, Miaojin Zhou, Bo Liu, et al.
International Journal of Molecular Sciences|October 14, 2022
Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2<sup>P497H</sup> MutationYiti Zhang, Baitao Zeng, Ao Gu, et al.
Human Gene Therapy|March 31, 2018
Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem CellsMiaojin Zhou, Zhiqing Hu, Liyan Qiu, et al.
Pageof 2