Arama Sonuçları - Zhengmao Hu

Sonuçları Daraltın
  1. 1
    miR‐222 attenuates cisplatin‐induced cell death by targeting the <scp>PPP</scp>2R2A/Akt/<scp>mTOR</scp> Axis in bladder cancer cells

    miR‐222 attenuates cisplatin‐induced cell death by targeting the <scp>PPP</scp>2R2A/Akt/<scp>mTOR</scp> Axis in bladder cancer cells Yazar: Liping Zeng, Zhengmao Hu, Kai Li, Kun Xia

    Baskı/Yayın Bilgisi 2016
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  2. 2
    Suppression of Akt-mTOR pathway rescued the social behavior in Cntnap2-deficient mice

    Suppression of Akt-mTOR pathway rescued the social behavior in Cntnap2-deficient mice Yazar: Xiaoliang Xing, Jing Zhang, Kunyang Wu, Beibei Cao, Xianfeng Li, Fang Jiang, Zhengmao Hu, Kun Xia, Jia‐Da Li

    Baskı/Yayın Bilgisi 2019
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  3. 3
    Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China

    Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China Yazar: Fengzhen Huang, Zhe Long, Chen Zhao, Jia‐Da Li, Zhengmao Hu, Rong Qiu, Wei Zhuang, Beisha Tang, Kun Xia, Hong Jiang

    Baskı/Yayın Bilgisi 2015
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  4. 4
    Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease

    Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease Yazar: Beisha Tang, Hui Xiong, Ping Sun, Yuhu Zhang, Danling Wang, Zhengmao Hu, Zan-Hua Zhu, Hong Ma, Qian Pan, Jiahui Xia, Kun Xia, Zhuohua Zhang

    Baskı/Yayın Bilgisi 2006
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  5. 5
    Homozygous loss‐of‐function mutation of the <i><scp>LEPREL1</scp></i> gene causes severe non‐syndromic high myopia with early‐onset cataract

    Homozygous loss‐of‐function mutation of the <i><scp>LEPREL1</scp></i> gene causes severe non‐syndromic high myopia with early‐onset cataract Yazar: Hui Guo, Ping Tong, Yu Peng, T. Wang, Yong Liu, J. Chen, Y. Li, Qi Tian, Yuantai Hu, Yi-Cong Zheng, Lin Xiao, Wei Xiong, Qian Pan, Zhengmao Hu, Kun Xia

    Baskı/Yayın Bilgisi 2013
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  6. 6
    Association of genetic variants of GRIN2B with autism

    Association of genetic variants of GRIN2B with autism Yazar: Yongcheng Pan, Jingjing Chen, Hui Guo, Jianjun Ou, Yu Peng, Qiong Liu, Yidong Shen, Lijuan Shi, Yalan Liu, Zhimin Xiong, Tengfei Zhu, Sanchuan Luo, Zhengmao Hu, Jingping Zhao, Kun Xia

    Baskı/Yayın Bilgisi 2015
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  7. 7
    Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia

    Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia Yazar: Hui Guo, Ping Tong, Yanling Liu, Lu Xia, Tianyun Wang, Qi Tian, Ying Li, Yiqiao Hu, Zheng Yu, Xuemin Jin, Yun Li, Wei Xiong, Beisha Tang, Yong Feng, Jia‐Da Li, Qian Pan, Zhengmao Hu, Kun Xia

    Baskı/Yayın Bilgisi 2015
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  8. 8
    Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort

    Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort Yazar: Hui Guo, Peng Yu, Zhengmao Hu, Ying Li, Guanglei Xun, Jianjun Ou, Liangdan Sun, Zhimin Xiong, Yanling Liu, Tianyun Wang, Jingjing Chen, Lu Xia, Ting Bai, Yidong Shen, Qi Tian, Yiqiao Hu, Lu Shen, Rongjuan Zhao, Xuejun Zhang, Fengyu Zhang, Jingping Zhao, Xiaobing Zou, Kun Xia

    Baskı/Yayın Bilgisi 2017
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  9. 9
    <scp>CAG</scp> Repeat Expansion in <scp><i>THAP11</i></scp> Is Associated with a Novel Spinocerebellar Ataxia

    <scp>CAG</scp> Repeat Expansion in <scp><i>THAP11</i></scp> Is Associated with a Novel Spinocerebellar Ataxia Yazar: Dandan Tan, Cuijie Wei, Zhao Chen, Yu Huang, Jianwen Deng, Jingjing Li, Yidan Liu, Xinhua Bao, Jin Xu, Zhengmao Hu, Suxia Wang, Yanbin Fan, Yizheng Jiang, Ye Wu, Yuan Wu, Shuang Wang, Panyan Liu, Yuehua Zhang, Zhixian Yang, Yuwu Jiang, Hong Zhang, Daojun Hong, Nanbert Zhong, Hong Jiang, Hui Xiong

    Baskı/Yayın Bilgisi 2023
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  10. 10
    Identification of CHIP as a Novel Causative Gene for Autosomal Recessive Cerebellar Ataxia

    Identification of CHIP as a Novel Causative Gene for Autosomal Recessive Cerebellar Ataxia Yazar: Yuting Shi, Junling Wang, Jia‐Da Li, Haigang Ren, Wenjuan Guan, Miao He, Weiqian Yan, Ying Zhou, Zhengmao Hu, Jianguo Zhang, Jingjing Xiao, Zheng Su, Meizhi Dai, Jun Wang, Hong Jiang, Jifeng Guo, Yafang Zhou, Fufeng Zhang, Nan Li, Juan Du, Qian Xu, Yacen Hu, Qian Pan, Lu Shen, Guanghui Wang, Kun Xia, Zhuohua Zhang, Beisha Tang

    Baskı/Yayın Bilgisi 2013
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  11. 11
    <i>SLC39A5</i>mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia

    <i>SLC39A5</i>mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia Yazar: Hui Guo, Xuemin Jin, Tengfei Zhu, Tianyun Wang, Ping Tong, Lei Tian, Peng Yu, Liangdan Sun, Anran Wan, Jingjing Chen, Yanling Liu, Ying Li, Qi Tian, Lu Xia, Lusi Zhang, Yongcheng Pan, Lina Lu, Qiong Liu, Lu Shen, Yun Li, Wei Xiong, Jia‐Da Li, Beisha Tang, Yong Feng, Xuejun Zhang, Zhuohua Zhang, Qian Pan, Zhengmao Hu, Kun Xia

    Baskı/Yayın Bilgisi 2014
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  12. 12
    Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene

    Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene Yazar: Xiaomeng Yin, Jinghan Lin, Li Cao, Tong-Mei Zhang, Sheng Zeng, Kailin Zhang, Wotu Tian, Zhengmao Hu, Nan Li, Junling Wang, Jifeng Guo, Ruoxi Wang, Kun Xia, Zhuohua Zhang, Fei Yin, Jing Peng, Wei‐Ping Liao, Yong‐Hong Yi, Jingyu Liu, Zhixian Yang, Zhong Chen, Xiao Mao, Xinxiang Yan, Hong Jiang, Lu Shen, Shengdi Chen, Liming Zhang, Beisha Tang

    Baskı/Yayın Bilgisi 2017
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  13. 13
    Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor

    Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor Yazar: Qiying Sun, Qian Xu, Yun Tian, Zhengmao Hu, Lixia Qin, Jinxia Yang, Wen Huang, Jin Xue, Jinchen Li, Sheng Zeng, Ying Wang, Haoxuan Min, Xiaoyu Chen, Junpu Wang, Bin Xie, Fan Liang, Hainan Zhang, Chunyu Wang, Lifang Lei, Xinxiang Yan, Hongwei Xu, Ranhui Duan, Kun Xia, Jingyu Liu, Hong Jiang, Lu Shen, Jifeng Guo, Beisha Tang

    Baskı/Yayın Bilgisi 2019
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  14. 14
    De novo genic mutations among a Chinese autism spectrum disorder cohort

    De novo genic mutations among a Chinese autism spectrum disorder cohort Yazar: Tianyun Wang, Hui Guo, Bo Xiong, Holly A.F. Stessman, Huidan Wu, Bradley P. Coe, Tychele N. Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Long Min, Janice Lin, Zev Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E. Eichler

    Baskı/Yayın Bilgisi 2016
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  15. 15
    Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

    Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders Yazar: Yun Tian, Junling Wang, Wen Huang, Sheng Zeng, Bin Jiao, Zhen Liu, Chen Zhao, Yujing Li, Ying Wang, Haoxuan Min, Xuejing Wang, Yong You, Ruxu Zhang, Xiaoyu Chen, Fang Yi, Yafang Zhou, Hongyu Long, Chaojun Zhou, Xuan Hou, Junpu Wang, Bin Xie, Fan Liang, Zhuanyi Yang, Qiying Sun, Emily G. Allen, Andrew M. Shafik, Ha Eun Kong, Jifeng Guo, Xinxiang Yan, Zhengmao Hu, Kun Xia, Hong Jiang, Hongwei Xu, Ranhui Duan, Peng Jin, Beisha Tang, Lu Shen

    Baskı/Yayın Bilgisi 2019
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  16. 16
    Coding mutations in <i>NUS1</i> contribute to Parkinson’s disease

    Coding mutations in <i>NUS1</i> contribute to Parkinson’s disease Yazar: Jifeng Guo, Lu Zhang, Kai Li, Junpu Mei, Jin Xue, Jia Chen, Xia Tang, Lu Shen, Hong Jiang, Chao Chen, Hui Guo, Xueli Wu, Silong Sun, Qian Xu, Qiying Sun, Piu Chan, Huifang Shang, Tao Wang, Guohua Zhao, Jingyu Liu, Xuefeng Xie, Yiqi Jiang, Zhenhua Liu, Yuwen Zhao, Zuobin Zhu, Jia‐Da Li, Zhengmao Hu, Xinxiang Yan, Xiaodong Fang, Guanghui Wang, Fengyu Zhang, Kun Xia, Chunyu Liu, Xiongwei Zhu, Zhenyu Yue, Shuai Cheng Li, Huaibin Cai, Zhuohua Zhang, Ranhui Duan, Beisha Tang

    Baskı/Yayın Bilgisi 2018
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  17. 17
    GIGYF1 disruption associates with autism and impaired IGF-1R signaling

    GIGYF1 disruption associates with autism and impaired IGF-1R signaling Yazar: Guodong Chen, Bin Yu, Senwei Tan, Jieqiong Tan, Xiangbin Jia, Qiumeng Zhang, Xiaolei Zhang, Qian Jiang, Hua Yue, Yaoling Han, Shengjie Luo, Kendra Hoekzema, Raphael Bernier, Rachel K. Earl, Evangeline C. Kurtz‐Nelson, Michaela J. Idleburg, Suneeta Madan-Khetarpal, Rebecca A. Clark, Jessica Sebastian, Alberto Fernández‐Jaén, Sara Álvarez, Staci D. King, Luiza Ramos, Mara Lúcia Schmitz Ferreira Santos, Donna M. Martin, Dan Brooks, Joseph D. Symonds, Ioana Cutcutache, Qian Pan, Zhengmao Hu, Ling Yuan, Evan E. Eichler, Kun Xia, Hui Guo

    Baskı/Yayın Bilgisi 2022
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  18. 18
    Common genetic variants on 1p13.2 associate with risk of autism

    Common genetic variants on 1p13.2 associate with risk of autism Yazar: Kun Xia, Hui Guo, Zhengmao Hu, Guanglei Xun, Lingjun Zuo, Yu Peng, Keheng Wang, Yijing He, Zhengang Xiong, Linlin Sun, Qian Pan, Z Long, Xiaobing Zou, Xiaoyu Li, Wenjun Li, Xiaojing Xu, Liping Lu, Yukun Liu, Yuantai Hu, Di Tian, Long Liu, Jianjun Ou, Yukun Liu, Xiaoyu Li, Ling Zhang, Yongcheng Pan, Jianxi Chen, Hui Peng, 豊 大根田, Xuerong Luo, Wei Su, Lingqian Wu, Desheng Liang, H Dai, Xin Yan, Yong Feng, Beisha Tang, Jinchen Li, Zosia Miedzybrodzka, Junfeng Xia, Zhiwu Zhang, Xuerong Luo, Xiang Zhang, David St Clair, J. Zhao, Fengyu Zhang

    Baskı/Yayın Bilgisi 2013
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  19. 19
    Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

    Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model Yazar: Hui Guo, Tianyun Wang, Huidan Wu, Long Min, Bradley P. Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan, Ting Bai, Ningxia Zhao, Yidong Shen, Yun Li, Yazhe Wang, Yu Zhang, Carl Baker, Yanling Liu, Nan Pang, Li’an Huang, Lin Han, Xiangbin Jia, Cenying Liu, Hailun Ni, Xinyi Yang, Lu Xia, Jingjing Chen, Lu Shen, Ying Li, Rongjuan Zhao, Wenjing Zhao, Jing Peng, Qian Pan, Zhigao Long, Wei Su, Jieqiong Tan, Xiaogang Du, Xiaoyan Ke, Meiling Yao, Zhengmao Hu, Xiaobing Zou, Jingping Zhao, Raphael Bernier, Evan E. Eichler, Kun Xia

    Baskı/Yayın Bilgisi 2018
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  20. 20
    De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders

    De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders Yazar: Xiangbin Jia, S. Zhang, Senwei Tan, Bing Du, Mei He, Haisong Qin, Jia Chen, Xinyu Duan, Jingsi Luo, Fei Chen, Luping Ouyang, Jian Wang, Guodong Chen, Bin Yu, Ge Zhang, Zimin Zhang, Yongqing Lyu, Yi Huang, Jian Jiao, Jin Yun Chen, Kathryn J. Swoboda, Emanuele Agolini, Antonio Novelli, Chiara Leoni, Giuseppe Zampino, Gerarda Cappuccio, Nicola Brunetti‐Pierri, Bénédicte Gérard, Emmanuelle Ginglinger, Julie Richer, Hugh J. McMillan, Alexandre White‐Brown, Kendra Hoekzema, Raphael Bernier, Evangeline C. Kurtz‐Nelson, Rachel K. Earl, Claartje Meddens, Mariëlle Alders, Meredith Fuchs, Roseline Caumes, Perrine Brunelle, Thomas Smol, Ryan Kuehl, Debra-Lynn Day-Salvatore, Kristin G. Monaghan, Michelle M. Morrow, Evan E. Eichler, Zhengmao Hu, Ling Yuan, Jieqiong Tan, Kun Xia, Yiping Shen, Hui Guo

    Baskı/Yayın Bilgisi 2022
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