Search Results - Zu, Bailing

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  1. 1
    Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517]

    Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517] by Zu, Bailing, Zhang, Xiaoqing, You, Guoling, Fu, Qihua

    Published in Stem cell research
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  2. 2
    Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot

    Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot by You, Guoling, Zu, Bailing, Wang, Bo, Fu, Qihua, Li, Fen

    Published in Frontiers in genetics
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  3. 3
    Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene

    Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene by Zu, Bailing, Zhang, Xiaoqing, You, Guoling, Fu, Qihua

    Published in Stem cell research
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  4. 4
    Correction to: ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells

    Correction to: ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells by Zu, Bailing, Shi, Yi, Xu, Min, You, Guoling, Huang, Zhenglan, Gao, Miao, Feng, Wenli

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  5. 5
    Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing

    Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing by Zu, Bailing, Zhang, Xiaoqing, Xu, Yunlan, Xiang, Ying, Wang, Zhigang, Cai, Haiqing, Wang, Bo, You, Guoling, Fu, Qihua

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  6. 6
    Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families

    Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families by Zu, Bailing, Wang, Zhigang, Xu, Yunlan, You, Guoling, Fu, Qihua

    Published in Developmental dynamics
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  7. 7
    Association between ABO Blood Group and Risk of Congenital Heart Disease: A 6-year large cohort study

    Association between ABO Blood Group and Risk of Congenital Heart Disease: A 6-year large cohort study by Zu, Bailing, You, Guoling, Fu, Qihua, Wang, Jing

    Published in Scientific reports
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  8. 8
    A new risk factor for coronary artery disease can be detected by an ApoA1 mAb-based assay

    A new risk factor for coronary artery disease can be detected by an ApoA1 mAb-based assay by Ding, Hui, Wang, Yin, Zhang, Yan, Zhou, Lida, Wang, Dong, Lv, Liangjie, Wan, Qianli, Tong, Minghong, Deng, Chenxia, Xu, Huihong, Zu, Bailing, Zhang, Jie, Qiu, Zhaohui, Sheng, Huiming

    Published in Clinica chimica acta
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  9. 9
    Molecular diagnostics for congenital heart disease: a narrative review of the current technologies and applications

    Molecular diagnostics for congenital heart disease: a narrative review of the current technologies and applications by Zu, Bailing, Zheng, Zhaojing, Fu, Qihua

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  10. 10
    Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly

    Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly by You, Guoling, Zu, Bailing, Wang, Bo, Wang, Zhigang, Xu, Yunlan, Fu, Qihua

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  11. 11
    ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells

    ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells by Zu, Bailing, Shi, Yi, Xu, Min, You, Guoling, Huang, Zhenglan, Gao, Miao, Feng, Wenli

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