检索结果 - Qinghe Xing

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  1. 1
    SPRINT: an SNP-free toolkit for identifying RNA editing sites

    SPRINT: an SNP-free toolkit for identifying RNA editing sites 由 Feng Zhang, Yulan Lu, Sijia Yan, Qinghe Xing, Weidong Tian

    出版 2017
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  2. 2
    Modulating neuroinflammation and cognitive function in postoperative cognitive dysfunction via <scp>CCR5</scp>‐<scp>GPCRs</scp>‐Ras‐<scp>MAPK</scp> pathway targeting with microglial <scp>EVs</scp>

    Modulating neuroinflammation and cognitive function in postoperative cognitive dysfunction via <scp>CCR5</scp>‐<scp>GPCRs</scp>‐Ras‐<scp>MAPK</scp> pathway targeting with microglia... 由 Qi Zheng, Junlin Peng, Haitao Wang, Li Wang, Yu Su, Lan Ding, Bin Cao, Yingying Zhao, Qinghe Xing, Jian‐jun Yang

    出版 2024
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  3. 3
    Identification of MicroRNAs in Human Follicular Fluid: Characterization of MicroRNAs That Govern Steroidogenesis in Vitro and Are Associated With Polycystic Ovary Syndrome in Vivo

    Identification of MicroRNAs in Human Follicular Fluid: Characterization of MicroRNAs That Govern Steroidogenesis in Vitro and Are Associated With Polycystic Ovary Syndrome in Vivo 由 Qing Sang, Zhongyuan Yao, Huan Wang, Ruizhi Feng, Haojue Wang, Xinzhi Zhao, Qinghe Xing, Jin Li, Lin He, Lingqian Wu, Lei Wang

    出版 2013
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  4. 4
    A Possible New Mechanism in the Pathophysiology of Polycystic Ovary Syndrome (PCOS): The Discovery That Leukocyte Telomere Length Is Strongly Associated With PCOS

    A Possible New Mechanism in the Pathophysiology of Polycystic Ovary Syndrome (PCOS): The Discovery That Leukocyte Telomere Length Is Strongly Associated With PCOS 由 Qiaoli Li, Jing Du, Ruizhi Feng, Yao Xu, Haojue Wang, Qing Sang, Qinghe Xing, Xinzhi Zhao, Jin Li, Lin He, Lei Wang

    出版 2013
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  5. 5
    Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients

    Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients 由 Yongyong Shi, Mo Li, Chuanfu Song, Qingqing Xu, Ran Huo, Lu Shen, Qinghe Xing, Donghong Cui, W Li, Jingping Zhao, Lin He, Shengying Qin

    出版 2017
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  6. 6
    Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population

    Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population 由 Qingqing Xu, Xi Wu, Mo Li, Hailiang Huang, Camelia C. Minică, Zhenghui Yi, G Wang, Lu Shen, Qinghe Xing, Yongyong Shi, Lin He, Shengying Qin

    出版 2015
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  7. 7
    Large-Scale Screens of miRNA-mRNA Interactions Unveiled That the 3′UTR of a Gene Is Targeted by Multiple miRNAs

    Large-Scale Screens of miRNA-mRNA Interactions Unveiled That the 3′UTR of a Gene Is Targeted by Multiple miRNAs 由 Peng Zhou, Weiyi Xu, Xueling Peng, Zhenhua Luo, Qinghe Xing, Xu‐Lin Chen, Chengqian Hou, Weihong Liang, Jianwen Zhou, Xiaoyan Wu, Zhou Songyang, Songshan Jiang

    出版 2013
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  8. 8
    Association of Leukocyte Telomere Length with Type 2 Diabetes in Mainland Chinese Populations

    Association of Leukocyte Telomere Length with Type 2 Diabetes in Mainland Chinese Populations 由 Qin Shen, Xinzhi Zhao, Lan Yu, Zhou Zhang, Daizhan Zhou, Mengyuan Kan, Di Zhang, Lan Cao, Qinghe Xing, Yifeng Yang, He Xu, Lin He, Yun Liu

    出版 2012
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  9. 9
    The association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsy

    The association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsy 由 Dan Bi, Mingjie Chen, Xiaoli Zhang, Honglian Wang, Lei Xia, Qing Shang, Tongchuan Li, Dengna Zhu, Klas Blomgren, Lin He, Xiaoyang Wang, Qinghe Xing, Changlian Zhu

    出版 2014
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  10. 10
    The Effect of microRNAs in the Regulation of Human CYP3A4: a Systematic Study using a Mathematical Model

    The Effect of microRNAs in the Regulation of Human CYP3A4: a Systematic Study using a Mathematical Model 由 Zhiyun Wei, Songshan Jiang, Yiting Zhang, Xiaofei Wang, Xueling Peng, Chunjie Meng, Yichen Liu, Honglian Wang, Luo Guo, Shengying Qin, Lin He, Fengmin Shao, Lirong Zhang, Qinghe Xing

    出版 2014
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  11. 11
    The aberrantly expressed miR-193b-3p contributes to preeclampsia through regulating transforming growth factor-β signaling

    The aberrantly expressed miR-193b-3p contributes to preeclampsia through regulating transforming growth factor-β signaling 由 Xinyao Zhou, Qiaoli Li, Jiawei Xu, Xiaojing Zhang, Huijuan Zhang, Yuqian Xiang, Chuantao Fang, Teng Wang, Shihui Xia, Qiang Zhang, Qinghe Xing, Lin He, Lei Wang, Mingqing Xu, Xinzhi Zhao

    出版 2016
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  12. 12
    A cross-sectional survey of relationship between serum TSH level and blood pressure

    A cross-sectional survey of relationship between serum TSH level and blood pressure 由 Dongbing Liu, Fengwei Jiang, Zhongyan Shan, Boxin Wang, J Wang, Yaxin Lai, Y Chen, M Li, He Liu, C Li, Haibo Xue, N Li, Jin Yu, Liangfeng Shi, Xue Bai, Xin Hou, Linjia Zhu, Li Lu, Shixiang Wang, Qinghe Xing, Weiping Teng

    出版 2009
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  13. 13
    Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

    Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis 由 Yi‐Ling Qiu, Jing‐Yu Gong, Jia‐Yan Feng, Ren‐Xue Wang, Jun Han, Teng Liu, Yi Lu, Liting Li, Meihong Zhang, Jonathan A. Sheps, Neng‐Li Wang, Yanyan Yan, Jiaqi Li, Lian Chen, Christoph H. Borchers, Bence Sipos, A. S. Knisely, Victor Ling, Qinghe Xing, Jian‐She Wang

    出版 2016
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  14. 14
    Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

    Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma 由 Wei Cao, Hayan Lee, Wei Wu, Aubhishek Zaman, S. McCorkle, Ming Yan, Justin Chen, Qinghe Xing, Nasa Sinnott-Armstrong, Hongen Xu, M. Reza Sailani, Wenxue Tang, Yuanbo Cui, Jia Liu, Hongyan Guan, Pengju Lv, Xiaoyan Sun, Lei Sun, Pengli Han, Yanan Lou, Jing Chang, Jinwu Wang, Yuchi Gao, Jiancheng Guo, Gundolf Schenk, A. Hunter Shain, Fred G. Biddle, Eric A. Collisson, M Snyder, Trever G. Bivona

    出版 2020
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  15. 15
    Mutations in <i>TUBB8</i> and Human Oocyte Meiotic Arrest

    Mutations in <i>TUBB8</i> and Human Oocyte Meiotic Arrest 由 Ruizhi Feng, Qing Sang, Yanping Kuang, Xiaoxi Sun, Zheng Yan, Shaozhen Zhang, Juanzi Shi, Guoling Tian, Anna Łuchniak, Yusuke Fukuda, Bin Li, Min Yu, Junling Chen, Yao Xu, Luo Guo, Ronggui Qu, Xueqian Wang, Zhaogui Sun, Miao Liu, Huijuan Shi, Hongyan Wang, Yi Feng, Ruijin Shao, Renjie Chai, Qiaoli Li, Qinghe Xing, Rui Zhang, Eva Nogales, Jin Li, Lin He, Mohan L. Gupta, Nicholas J. Cowan, Lei Wang

    出版 2016
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  16. 16
    Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

    Mutations disrupting neuritogenesis genes confer risk for cerebral palsy 由 Sheng Chih Jin, Sara A. Lewis, Somayeh Bakhtiari, Xue Zeng, Michael C. Sierant, Sheetal Shetty, Sandra M. Nordlie, Aureliane Elie, Mark Corbett, Bethany Y. Norton, Clare L. van Eyk, Shozeb Haider, Brandon S. Guida, Helen Magee, James H. Liu, Stephen F. Pastore, John B. Vincent, Janice Brunstrom-Hernandez, Antigone Papavasileiou, Michael Fahey, Jesia G. Berry, Kelly Harper, Chongchen Zhou, Junhui Zhang, Boyang Li, Hongyu Zhao, Jennifer Heim, Dani L. Webber, Mahalia S. B. Frank, Lei Xia, Yiran Xu, Dengna Zhu, Bohao Zhang, Amar H. Sheth, James Knight, Christopher Castaldi, Irina R. Tikhonova, Francesc López‐Giráldez, Boris Keren, Sandra Whalen, Julien Buratti, Diane Doummar, Megan Cho, Kyle Retterer, Francisca Millan, Yangong Wang, Jeff L. Waugh, Lance H. Rodan, Julie S. Cohen, Ali Fatemi, Angela E. Lin, J. P. Phillips, Timothy Feyma, Suzanna C. MacLennan, Spencer Vaughan, Kylie Crompton, Susan Reid, Dinah Reddihough, Qing Shang, Chao Gao, Iona Novak, Nadia Badawi, Yana A. Wilson, Sarah McIntyre, Shrikant Mane, Xiaoyang Wang, David J. Amor, Daniela C. Zarnescu, Qiongshi Lu, Qinghe Xing, Changlian Zhu, Kaya Bilgüvar, Sergio Padilla-López, Richard P. Lifton, Jozef Gécz, Alastair H. MacLennan, Michael C. Kruer

    出版 2020
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  17. 17
    De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

    De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias 由 Katherine L. Helbig, Robert J. Lauerer, Jacqueline C Bahr, Ivana A. Souza, Candace T. Myers, Betül Seher Uysal, Niklas Schwarz, María A. Gandini, Sun Huang, Boris Keren, Cyril Mignot, Alexandra Afenjar, Thierry Billette de Villemeur, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina Fagerberg, Kristina P. Soerensen, Maria Kibæk, Erik‐Jan Kamsteeg, David A. Koolen, Boudewijn Gunning, Helenius J. Schelhaas, Michael C. Kruer, Jordana Fox, Somayeh Bakhtiari, Randa Jarrar, Sergio Padilla-López, Kristin Lindstrom, Sheng Chih Jin, Xue Zeng, Kaya Bilgüvar, Antigone Papavasileiou, Qinghe Xing, Changlian Zhu, Katja Boysen, Filippo Pinto e Vairo, Brendan C. Lanpher, Eric W. Klee, Jan‐Mendelt Tillema, Eric T. Payne, Margot A. Cousin, Teresa Kruisselbrink, Myra J. Wick, Joshua Baker, Eric Haan, Nicholas Smith, Azita Sadeghpour, Erica E. Davis, Nicholas Katsanis, Mark Corbett, Alastair H. MacLennan, Jozef Gécz, Saskia Biskup, Eva Goldmann, Lance H. Rodan, Elizabeth Kichula, Eric Segal, Kelly E. Jackson, Alexander Asamoah, David Dimmock, Julie McCarrier, Lorenzo D. Botto, Francis Filloux, Tatiana Tvrdik, Gregory D. Cascino, Sherry Klingerman, Catherine M. Neumann, Raymond Wang, Jessie C. Jacobsen, Melinda Nolan, Russell G. Snell, Klaus Lehnert, Lynette G. Sadleir, Britt‐Marie Anderlid, Malin Kvarnung, Renzo Guerrini, Michael J. Friez, Michael J. Lyons, Jennifer Leonhard, Gabriel Kringlen, Kari Casas, Christelle Moufawad El Achkar, Lacey Smith, Alexander Rotenberg, Annapurna Poduri, Alba Sanchis‐Juan, Keren Carss, Julia Rankin, Adam Zeman, F. Lucy Raymond, Moira Blyth, Bronwyn Kerr, Karla Ruiz, Jill Urquhart, Imelda Hughes, Siddharth Banka, Ulrike B. S. Hedrich, Ingrid E. Scheffer

    出版 2018
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