Search Results - "Feng, Guoyin"

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    Sclerostin Mediates Bone Response to Mechanical Unloading Through Antagonizing Wnt/β‐Catenin Signaling by Lin, Chuwen, Jiang, Xuan, Dai, Zhongquan, Guo, Xizhi, Weng, Tujun, Wang, Jun, Li, Yinghui, Feng, Guoyin, Gao, Xiang, He, Lin

    Published in Journal of bone and mineral research (01-10-2009)
    “…Reduced mechanical stress leads to bone loss, as evidenced by disuse osteoporosis in bedridden patients and astronauts. Osteocytes have been identified as…”
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    CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population by He, Kuanjun, An, Zhiguo, Wang, Qingzhong, Li, Tao, Li, Zhiqiang, Chen, Jianhua, Li, Wenjin, Wang, Ti, Ji, Jue, Feng, Guoyin, Lin, He, Yi, Qizhong, Shi, Yongyong

    Published in British journal of psychiatry (01-01-2014)
    “…Common psychiatric disorders are highly heritable, indicating that genetic factors play an important role in their aetiology. The CACNA1C gene, which codes for…”
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    Metabolomic Profiling to Identify Potential Serum Biomarkers for Schizophrenia and Risperidone Action by Xuan, Jiekun, Pan, Guihua, Qiu, Yunping, Yang, Lun, Su, Mingming, Liu, Yumin, Chen, Jian, Feng, Guoyin, Fang, Yiru, Jia, Wei, Xing, Qinghe, He, Lin

    Published in Journal of proteome research (02-12-2011)
    “…Despite recent advances in understanding the pathophysiology of schizophrenia and the mechanisms of antipsychotic drug action, the development of biomarkers…”
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    Rates of Adult Schizophrenia Following Prenatal Exposure to the Chinese Famine of 1959-1961 by St Clair, David, Xu, Mingqing, Wang, Peng, Yu, Yaqin, Fang, Yourong, Zhang, Feng, Zheng, Xiaoying, Gu, Niufan, Feng, Guoyin, Sham, Pak, He, Lin

    “…CONTEXT Schizophrenia is a common major mental disorder. Intrauterine nutritional deficiency may increase the risk of schizophrenia. The main evidence comes…”
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    Exploring off-targets and off-systems for adverse drug reactions via chemical-protein interactome--clozapine-induced agranulocytosis as a case study by Yang, Lun, Wang, Kejian, Chen, Jian, Jegga, Anil G, Luo, Heng, Shi, Leming, Wan, Chunling, Guo, Xizhi, Qin, Shengying, He, Guang, Feng, Guoyin, He, Lin

    Published in PLoS computational biology (01-03-2011)
    “…In the era of personalized medical practice, understanding the genetic basis of patient-specific adverse drug reaction (ADR) is a major challenge. Clozapine…”
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    Wls is expressed in the epidermis and regulates embryonic hair follicle induction in mice by Huang, Sixia, Zhu, Xuming, Liu, Yanfang, Tao, Yixin, Feng, Guoyin, He, Lin, Guo, Xizhi, Ma, Gang

    Published in PloS one (24-09-2012)
    “…Wnt proteins are secreted molecules that play multiple roles during hair follicle development and postnatal hair cycling. Wntless (Wls) is a cargo protein…”
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    Rare CNVs and Tag SNPs at 15q11.2 Are Associated With Schizophrenia in the Han Chinese Population by QIAN ZHAO, TAO LI, GUOYIN FENG, ST CLAIR, David, LIN HE, YONGYONG SHI, XINZHI ZHAO, KE HUANG, TI WANG, ZHIQIANG LI, JUE JI, ZHEN ZENG, ZHAO ZHANG, KAN LI

    Published in Schizophrenia bulletin (01-05-2013)
    “…Rare copy number variations (CNVs) were involved in the etiology of neuropsychiatric disorders, and some of them appeared to be shared risk factors for several…”
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    Common Variants in Major Histocompatibility Complex Region and TCF4 Gene Are Significantly Associated with Schizophrenia in Han Chinese by Li, Tao, Li, Zhiqiang, Chen, Peng, Zhao, Qian, Wang, Ti, Huang, Ke, Li, JunYan, Li, You, Liu, Jie, Zeng, Zhen, Feng, GuoYin, He, Lin, Shi, YongYong

    Published in Biological psychiatry (1969) (01-10-2010)
    “…Background Schizophrenia is a complex major psychiatric disorder affecting ∼1% of the world population. Recently, in a genome-wide association study and a…”
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    CNTNAP2 is significantly associated with schizophrenia and major depression in the Han Chinese population by Ji, Weidong, Li, Tao, Pan, Yaosheng, Tao, Hua, Ju, Kang, Wen, Zujia, Fu, Yingchun, An, Zhiguo, Zhao, Qian, Wang, Ti, He, Lin, Feng, Guoyin, Yi, Qizhong, Shi, Yongyong

    Published in Psychiatry research (30-05-2013)
    “…Abstract CNTNAP2 , located on 7q35–36.1, encodes a single-pass transmembrane protein mediating cell–cell interactions in the nervous system. CNTNAP2 has been…”
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    Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels by Ma, Gang, Yu, Jiang, Xiao, Yue, Chan, Danny, Gao, Bo, Hu, Jianxin, He, Yongxing, Guo, Shengzhen, Zhou, Jian, Zhang, Lingling, Gao, Linghan, Zhang, Wenjuan, Kang, Yan, Cheah, Kathryn SE, Feng, Guoyin, Guo, Xizhi, Wang, Yujiong, Zhou, Cong-zhao, He, Lin

    Published in Cell research (01-09-2011)
    “…Brachydactyly type A1 (BDAI), the first recorded Mendelian autosomal dominant disorder in humans, is characterized by a shortening or absence of the middle…”
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    Altered Levels of Acute Phase Proteins in the Plasma of Patients with Schizophrenia by Yang, Yifeng, Wan, Chunling, Li, Huafang, Zhu, Hui, La, Yujuan, Xi, Zhengrui, Chen, Yongshuo, Jiang, Lei, Feng, Guoyin, He, Lin

    Published in Analytical chemistry (Washington) (01-06-2006)
    “…Schizophrenia is a relatively common psychiatric syndrome that affects virtually all brain functions. We investigated the plasma proteome of 22 schizophrenia…”
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    The PstI/RsaI and DraI polymorphisms of CYP2E1 and head and neck cancer risk: a meta-analysis based on 21 case-control studies by Tang, Kefu, Li, Yang, Zhang, Zhao, Gu, Yunmin, Xiong, Yuyu, Feng, Guoyin, He, Lin, Qin, Shengying

    Published in BMC cancer (22-10-2010)
    “…CYP2E1 encodes a member of the cytochrome P450 superfamily of enzymes which play a central role in activating and detoxifying many carcinogens and endogenous…”
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    Common SNPs in myelin transcription factor 1-like (MYT1L): association with major depressive disorder in the Chinese Han population by Wang, Ti, Zeng, Zhen, Li, Tao, Liu, Jie, Li, Junyan, Li, You, Zhao, Qian, Wei, Zhiyun, Wang, Yang, Li, Baojie, Feng, Guoyin, He, Lin, Shi, Yongyong

    Published in PloS one (27-10-2010)
    “…Myelin transcription factor 1-like (MYT1L) is a member of the myelin transcription factor 1 (MYT1) gene family, and the neural specific,…”
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    A systematic genetic polymorphism analysis of the CYP2C9 gene in four different geographical Han populations in mainland China by Xiong, Yuyu, Wang, Ming, Fang, Ke, Xing, Qinghe, Feng, Guoyin, Shen, Lu, He, Lin, Qin, Shengying

    Published in Genomics (San Diego, Calif.) (01-05-2011)
    “…While many studies have been focused on CYP2C9*2 and *3 there was a lack of large full gene sequencing on CYP2C9, and this study was designed to fill this gap…”
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    Systematic functional characterization of cytochrome P450 2E1 promoter variants in the Chinese Han population by Huang, Xunyi, Chen, Lili, Song, Wenlong, Chen, Ling, Niu, Jiamin, Han, Xia, Feng, Guoyin, He, Lin, Qin, Shengying

    Published in PloS one (17-07-2012)
    “…CYP2E1 promoter polymorphisms can lead to significant interindividual differences in expression of CYP2E1. Using a database of CYP2E1 gene polymorphisms…”
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