Resultados da pesquisa - Song, Zhijian
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Diffusion tensor imaging fiber tracking with reliable tracking orientation and flexible step size☆ Por Yao, Xufeng, Wang, Manning, Chen, Xinrong, Nie, Shengdong, Li, Zhexu, Xu, Xiaoping, Zhang, Xuelong, Song, Zhijian
Publicado em 2013Text -
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Alteration of the Intra- and Cross- Hemisphere Posterior Default Mode Network in Frontal Lobe Glioma Patients Por Zhang, Haosu, Shi, Yonghong, Yao, Chengjun, Tang, Weijun, Yao, Demin, Zhang, Chenxi, Wang, Manning, Wu, Jinsong, Song, Zhijian
Publicado em 2016Text -
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Novel Insights Into Triple-Negative Breast Cancer Prognosis by Comprehensive Characterization of Aberrant Alternative Splicing Por Gong, Shasha, Song, Zhijian, Spezia-Lindner, David, Meng, Feilong, Ruan, Tingting, Ying, Guangzhi, Lai, Changhong, Wu, Qianqian, Liang, Yong
Publicado em 2020Text -
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Whole genomic DNA sequencing and comparative genomic analysis of Arthrospira platensis: high genome plasticity and genetic diversity Por Xu, Teng, Qin, Song, Hu, Yongwu, Song, Zhijian, Ying, Jianchao, Li, Peizhen, Dong, Wei, Zhao, Fangqing, Yang, Huanming, Bao, Qiyu
Publicado em 2016Text -
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Clinically significant genomic alterations in the Chinese and Western patients with intrahepatic cholangiocarcinoma Por Xu, Shifeng, Guo, Yuan, Zeng, Yanwu, Song, Zhijian, Zhu, Xiaodan, Fan, Ning, Zhang, Zhilei, Ren, Guibing, Zang, Yunjin, Rao, Wei
Publicado em 2021Text -
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Identification of a novel autophagy signature for predicting survival in patients with lung adenocarcinoma Por Duan, Jin, Lei, Youming, Lv, Guoli, Liu, Yinqiang, Zhao, Wei, Yang, Qingmei, Su, Xiaona, Song, Zhijian, Lu, Leilei, Shi, Yunfei
Publicado em 2021Text -
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Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review Por Zhou, Zhaowei, Ma, Lidan, Zhou, Juan, Song, Zhijian, Zhang, Jinmai, Wang, Ke, Chen, Boyu, Pan, Dun, Li, Zhiqiang, Li, Changgui, Shi, Yongyong
Publicado em 2018Text -
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SLC39A8 is a risk factor for schizophrenia in Uygur Chinese: a case-control study Por Jian, Xuemin, Chen, Jianhua, Li, Zhiqiang, Song, Zhijian, Zhou, Juan, Xu, Wei, Liu, Yahui, Shen, Jiawei, Wang, Yonggang, Yi, Qizhong, Shi, Yongyong
Publicado em 2019Text -
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Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population Por Xu, Wei, Liu, Yahui, Chen, Jianhua, Guo, Qingli, Liu, Ke, Wen, Zujia, Zhou, Zhaowei, Song, Zhijian, Zhou, Juan, He, Lin, Yi, Qizhong, Shi, Yongyong
Publicado em 2017Text -
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Association study of 15q14 and 15q25 with high myopia in the Han Chinese population Por Qiang, Yu, Li, Wenjin, Wang, Qingzhong, He, Kuanjun, Li, Zhiqiang, Chen, Jianhua, Song, Zhijian, Qu, Jia, Zhou, Xiangtian, Qin, Shengying, Shen, Jiawei, Wen, Zujia, Ji, Jue, Shi, Yongyong
Publicado em 2014Text -
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Germline Mutations in CDH23, Encoding Cadherin-Related 23, Are Associated with Both Familial and Sporadic Pituitary Adenomas Por Zhang, Qilin, Peng, Cheng, Song, Jianping, Zhang, Yichao, Chen, Jianhua, Song, Zhijian, Shou, Xuefei, Ma, Zengyi, Peng, Hong, Jian, Xuemin, He, Wenqiang, Ye, Zhao, Li, Zhiqiang, Wang, Yongfei, Ye, Hongying, Zhang, Zhaoyun, Shen, Ming, Tang, Feng, Chen, Hong, Shi, Zhifeng, Chen, Chunjui, Chen, Zhengyuan, Shen, Yue, Wang, Ye, Lu, Shaoyong, Zhang, Jian, Li, Yiming, Li, Shiqi, Mao, Ying, Zhou, Liangfu, Yan, Hai, Shi, Yongyong, Huang, Chuanxin, Zhao, Yao
Publicado em 2017Text -
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Identification of recurrent USP48 and BRAF mutations in Cushing’s disease Por Chen, Jianhua, Jian, Xuemin, Deng, Siyu, Ma, Zengyi, Shou, Xuefei, Shen, Yue, Zhang, Qilin, Song, Zhijian, Li, Zhiqiang, Peng, Hong, Peng, Cheng, Chen, Min, Luo, Cheng, Zhao, Dan, Ye, Zhao, Shen, Ming, Zhang, Yichao, Zhou, Juan, Fahira, Aamir, Wang, Yongfei, Li, Shiqi, Zhang, Zhaoyun, Ye, Hongying, Li, Yiming, Shen, Jiawei, Chen, Hong, Tang, Feng, Yao, Zhenwei, Shi, Zhifeng, Chen, Chunjui, Xie, Lu, Wang, Ye, Fu, Chaowei, Mao, Ying, Zhou, Liangfu, Gao, Daming, Yan, Hai, Zhao, Yao, Huang, Chuanxin, Shi, Yongyong
Publicado em 2018Text