Search Results - Duan, Fuxi

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  1. 1
    Extraction and analysis of the sea ice parameter dataset of the Bohai Sea from 2011 to 2021 based on GOCI

    Extraction and analysis of the sea ice parameter dataset of the Bohai Sea from 2011 to 2021 based on GOCI by Yan, Ran, Zhang, Xi, Bi, Wenlong, Wang, Ning, Zhao, Yiding, Bi, Luchuan, Guan, Haipeng, Liu, Yunbo, Duan, Fuxi, Liu, Meijie

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  2. 2
    Monolithically Stacked Two Layers of a-IGZO-Based Transistors Upon a-IGZO-Based Analog/Logic Circuits

    Monolithically Stacked Two Layers of a-IGZO-Based Transistors Upon a-IGZO-Based Analog/Logic Circuits by Lu, Wendong, Lu, Congyan, Yang, Guanhua, Liu, Menggan, Chen, Kaifei, Liao, Fuxi, Duan, Xinlv, Lu, Nianduan, Li, Ling

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  3. 3
    A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia

    A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia by Xiang, Mingfei, Wang, Yu, Xu, Weilong, Zheng, Na, Deng, Hongshi, Zhang, Jingjing, Duan, Zongliu, Zha, Xiaomin, Zhang, Wenjun, Song, Gaojie, Shi, Xuanming, Wang, Fengsong, Cao, Yunxia, Zhu, Fuxi

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  4. 4
    A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome

    A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome by Lu, Mengmeng, Kong, Shuai, Xiang, Mingfei, Wang, Yu, Zhang, Jingjing, Duan, Zongliu, Zha, Xiaomin, Wang, Fengsong, Cao, Yunxia, Zhu, Fuxi

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  5. 5
    Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10

    Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10 by Xiang, Mingfei, Wang, Yu, Xu, Weilong, Zheng, Na, Zhang, Jingjing, Duan, Zongliu, Zha, Xiaomin, Shi, Xuanming, Wang, Fengsong, Cao, Yunxia, Zhu, Fuxi

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  6. 6
    A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency

    A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency by Wang, Fengsong, Zhang, Jingjing, Kong, Shuai, Li, Chanjuan, Zhang, Zhiguo, He, Xiaojin, Wu, Huan, Tang, Dongdong, Zha, Xiaomin, Tan, Qing, Duan, Zongliu, Cao, Yunxia, Zhu, Fuxi

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  7. 7
    Unraveling the Impact of the PROCA1 Mutation in Male Infertility: Incorporating Whole Exome Sequencing in Teratozoospermia Patients and Analyzing Proca1 Knockout Mice

    Unraveling the Impact of the PROCA1 Mutation in Male Infertility: Incorporating Whole Exome Sequencing in Teratozoospermia Patients and Analyzing Proca1 Knockout Mice by Zheng, Na, Shen, Yiru, Wang, Yu, Xiang, Mingfei, Yu, Kexin, Zhang, Jingjing, Zha, Xiaomin, Duan, Zongliu, Wang, Fengsong, Zhu, Fuxi, Cao, Yunxia

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  8. 8
    Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa Syndrome

    Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa Syndrome by Xiang, Mingfei, Wang, Yu, Wang, Ke, Kong, Shuai, Lu, Mengmeng, Zhang, Jingjing, Duan, Zongliu, Zha, Xiaomin, Shi, Xuanming, Wang, Fengsong, Cao, Yunxia, Zhu, Fuxi

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  9. 9
    A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans

    A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans by Xiang, Mingfei, Wang, Yu, Jiao, Yuying, Guo, Rui, Zheng, Na, Yu, Kexin, Zhu, Xiaoya, Hu, Pengcheng, Zhang, Jingjing, Zha, Xiaomin, Duan, Zongliu, Wang, Fengsong, Cao, Yunxia, Zhu, Fuxi

    Published in Andrology (Oxford)
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  10. 10
    Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription

    Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription by Wang, Yu, Xiang, Mingfei, Zhou, Yiru, Zheng, Na, Zhang, Jingjing, Zha, Xiaomin, Duan, Zongliu, Wang, Fengsong, Zhang, Ying, Wang, Zhongxin, Cao, Yunxia, Zhu, Fuxi

    Published in Andrology (Oxford)
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  11. 11
    First Demonstration of Dual-Gate IGZO 2T0C DRAM with Novel Read Operation, One Bit Line in Single Cell, ION=1500 μA/μm@VDS=1V and Retention Time>300s

    First Demonstration of Dual-Gate IGZO 2T0C DRAM with Novel Read Operation, One Bit Line in Single Cell, ION=1500 μA/μm@VDS=1V and Retention Time>300s by Lu, Wendong, Zhu, Zhengyong, Chen, Kaifei, Liu, Menggan, Kang, Bok-Moon, Duan, Xinlv, Niu, Jiebin, Liao, Fuxi, Dan, Wang, Wu, Xie-Shuai, Son, Joohwan, Xiao, De-Yuan, Wang, Gui-Lei, Yoo, Abraham, Cao, Kan-Yu, Geng, Di, Lu, Nianduan, Yang, Guanhua, Zhao, Chao, Li, Ling, Liu, Ming

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