Hasil Pencarian - Bobo Xie

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  1. 1
    Genomic structure, expression pattern, and functional characterization of transcription factor E2F-2 from black tiger shrimp (Penaeus monodon).

    Genomic structure, expression pattern, and functional characterization of transcription factor E2F-2 from black tiger shrimp (Penaeus monodon). oleh Bobo Xie, Pengfei Wang, Chao Zhao, Lihua Qiu

    Diterbitkan 2017-01-01
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  2. 2
    Attention-Enhanced Generative Adversarial Network for Hyperspectral Imagery Spatial Super-Resolution

    Attention-Enhanced Generative Adversarial Network for Hyperspectral Imagery Spatial Super-Resolution oleh Baorui Wang, Yifan Zhang, Yan Feng, Bobo Xie, Shaohui Mei

    Diterbitkan 2023-07-01
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  3. 3
    Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome

    Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome oleh Yunting Lin, Xiaohong Chen, Bobo Xie, Bobo Xie, Zhihong Guan, Xiaodan Chen, Xiuzhen Li, Peng Yi, Rong Du, Huifen Mei, Li Liu, Wen Zhang, Chunhua Zeng

    Diterbitkan 2023-03-01
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  4. 4
    Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five‐generation family

    Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five‐generation family oleh Xianda Wei, Guori Huang, Baoheng Gui, Bobo Xie, Shaoke Chen, Xin Fan, Yujun Chen

    Diterbitkan 2022-04-01
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  5. 5
    Genomic structure, expression, and functional characterization of checkpoint kinase 1 from Penaeus monodon.

    Genomic structure, expression, and functional characterization of checkpoint kinase 1 from Penaeus monodon. oleh Lihua Qiu, Chao Zhao, Pengfei Wang, Sigang Fan, Lulu Yan, Bobo Xie, Shigui Jiang, Shu Wang, Heizhao Lin

    Diterbitkan 2018-01-01
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  6. 6
    Impact of Viscoelasticity on Sand-Carrying Ability of Viscous Slickwater and Its Sand-Carrying Threshold in Hydraulic Fractures

    Impact of Viscoelasticity on Sand-Carrying Ability of Viscous Slickwater and Its Sand-Carrying Threshold in Hydraulic Fractures oleh Xianzhu Han, Junlin Wu, Yongjun Ji, Jinjun Liu, Yang Liu, Bobo Xie, Xianjiang Chen, Hui Yin, Tianbo Liang

    Diterbitkan 2024-01-01
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  7. 7
    Study of stress field induced by natural fracture and its influence on hydraulic fracture propagation

    Study of stress field induced by natural fracture and its influence on hydraulic fracture propagation oleh Shanzhi Shi, Mingxing Wang, Wei Tang, Yuting Pan, Haozeng Jin, Jiale He, Lei Hou, Bobo Xie, Xi Chen, Zhao Lv

    Diterbitkan 2024-02-01
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  8. 8
    Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound

    Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound oleh Shiyu Luo, Dahua Meng, Qifei Li, Xuehua Hu, Yuhua Chen, Chun He, Bobo Xie, Shangyang She, Yingfeng Li, Chunyun Fu

    Diterbitkan 2018-08-01
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  9. 9
    Case report: A novel heterozygous synonymous variant in deep exon region of NIPBL gene generating a non-canonical splice donor in a patient with cornelia de lange syndrome

    Case report: A novel heterozygous synonymous variant in deep exon region of NIPBL gene generating a non-canonical splice donor in a patient with cornelia de lange syndrome oleh Meizhen Shi, Meizhen Shi, Yuying Liang, Bobo Xie, Bobo Xie, Xianda Wei, Xianda Wei, Haiyang Zheng, Haiyang Zheng, Chunrong Gui, Chunrong Gui, Rong Huang, Rong Huang, Xin Fan, Xin Fan, Chuan Li, Chuan Li, Xiaojiao Wei, Yunting Ma, Shaoke Chen, Shaoke Chen, Yujun Chen, Yujun Chen, Baoheng Gui, Baoheng Gui

    Diterbitkan 2022-11-01
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  10. 10
    Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations

    Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations oleh Qi Yang, Sheng Yi, Mengting Li, Bobo Xie, Jinsi Luo, Jin Wang, Xiuliang Rong, Qinle Zhang, Zailong Qin, Limei Hang, Shihan Feng, Xin Fan

    Diterbitkan 2019-06-01
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  11. 11
    Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

    Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature oleh Jiasun Su, Huayu Fu, Bobo Xie, Weiliang Lu, Wei Li, Yuan Wei, Qiang Zhang, Shengkai Wei, Qiuli Chen, Yingchi Lu, Tingting Jiang, Jingsi Luo, Zailong Qin

    Diterbitkan 2019-12-01
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  12. 12
    Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism

    Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism oleh Chunyun Fu, Haiyang Zheng, Shujie Zhang, Yun Chen, Jiasun Su, Jin Wang, Bobo Xie, Xuyun Hu, Xin Fan, Jingsi Luo, Chuan Li, Rongyu Chen, Yiping Shen, Shaoke Chen

    Diterbitkan 2016-02-01
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  13. 13
    Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

    Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature oleh Baoheng Gui, Baoheng Gui, Baoheng Gui, Chenxi Yu, Chenxi Yu, Xiaoxin Li, Sen Zhao, Sen Zhao, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Xi Cheng, Xi Cheng, Jiachen Lin, Jiachen Lin, Haiyang Zheng, Haiyang Zheng, Haiyang Zheng, Jiashen Shao, Jiashen Shao, Zhengye Zhao, Zhengye Zhao, Lina Zhao, Yuchen Niu, Zhi Zhao, Huizi Wang, Bobo Xie, Bobo Xie, Bobo Xie, Xianda Wei, Xianda Wei, Chunrong Gui, Chunrong Gui, Chuan Li, Chuan Li, Chuan Li, Shaoke Chen, Shaoke Chen, Shaoke Chen, Yi Wang, Yanning Song, Chunxiu Gong, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang

    Diterbitkan 2021-04-01
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  14. 14
    The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping

    The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping oleh Yunting Ma, Chunrong Gui, Meizhen Shi, Lilin Wei, Junfang He, Bobo Xie, Haiyang Zheng, Xiaoyun Lei, Xianda Wei, Zifeng Cheng, Xu Zhou, Shaoke Chen, Jiefeng Luo, Yan Huang, Baoheng Gui

    Diterbitkan 2024-09-01
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  15. 15
    Complex genotype–phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes

    Complex genotype–phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes oleh Xiaojiao Wei, Yunting Ma, Bobo Xie, Chunrong Gui, Meizhen Shi, Xianda Wei, Yan Huang, Xin Fan, Qiaozhen Wei, Qingmei Huang, Li Deng, Chi Zhang, Xiaoli Deng, Baoheng Gui, Yujun Chen

    Diterbitkan 2024-05-01
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  16. 16
    The incidence of congenital hypothyroidism (CH) in Guangxi, China and the predictors of permanent and transient CH

    The incidence of congenital hypothyroidism (CH) in Guangxi, China and the predictors of permanent and transient CH oleh Chunyun Fu, Shiyu Luo, Yingfeng Li, Qifei Li, Xuehua Hu, Mengting Li, Yue Zhang, Jiasun Su, Xuyun Hu, Yun Chen, Jin Wang, Bobo Xie, Jingsi Luo, Xin Fan, Shaoke Chen, Yiping Shen

    Diterbitkan 2017-11-01
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  17. 17
    Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency

    Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency oleh Xin Fan, Bobo Xie, Jun Zou, Jingsi Luo, Zailong Qin, Alissa M. D'Gama, Jiahai Shi, Shang Yi, Qi Yang, Jin Wang, Shiyu Luo, Shaoke Chen, Pankaj B. Agrawal, Qifei Li, Yiping Shen

    Diterbitkan 2018-09-01
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  18. 18
    Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients

    Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients oleh Chenxi Yu, Chenxi Yu, Chenxi Yu, Bobo Xie, Bobo Xie, Bobo Xie, Zhengye Zhao, Zhengye Zhao, Sen Zhao, Sen Zhao, Lian Liu, Lian Liu, Xi Cheng, Xi Cheng, Xiaoxin Li, Xiaoxin Li, Bingyan Cao, Jiashen Shao, Jiashen Shao, Jiajia Chen, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Chang Su, Yuchen Niu, Yuchen Niu, Yanning Song, Liya Wei, Yi Wang, Xiaoya Ren, Lijun Fan, Beibei Zhang, Chuan Li, Chuan Li, Chuan Li, Baoheng Gui, Baoheng Gui, Baoheng Gui, Yuanqiang Zhang, Lianlei Wang, Shaoke Chen, Shaoke Chen, Shaoke Chen, Jianguo Zhang, Jianguo Zhang, Jianguo Zhang, Zhihong Wu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Chunxiu Gong, Xin Fan, Xin Fan, Xin Fan, Nan Wu, Nan Wu, Nan Wu, Nan Wu

    Diterbitkan 2021-09-01
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  19. 19
    Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese

    Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese oleh Yuanfeng Li, Lanlan Si, Yun Zhai, Yanling Hu, Zhibin Hu, Jin-Xin Bei, Bobo Xie, Qian Ren, Pengbo Cao, Fei Yang, Qingfeng Song, Zhiyu Bao, Haitao Zhang, Yuqing Han, Zhifu Wang, Xi Chen, Xia Xia, Hongbo Yan, Rui Wang, Ying Zhang, Chengming Gao, Jinfeng Meng, Xinyi Tu, Xinqiang Liang, Ying Cui, Ying Liu, Xiaopan Wu, Zhuo Li, Huifen Wang, Zhaoxia Li, Bo Hu, Minghui He, Zhibo Gao, Xiaobing Xu, Hongzan Ji, Chaohui Yu, Yi Sun, Baocai Xing, Xiaobo Yang, Haiying Zhang, Aihua Tan, Chunlei Wu, Weihua Jia, Shengping Li, Yi-Xin Zeng, Hongbing Shen, Fuchu He, Zengnan Mo, Hongxing Zhang, Gangqiao Zhou

    Diterbitkan 2016-05-01
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