Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Fu, Feng"'
Autor:
Qi Luo, Jialin Liu, Xiyang Cai, Kaustubh Adhikari, Andres Ruiz-Linares, Yong Zhou, Fan Liu, Fu-Feng Li, Binghua Jiang, Yan Chen, Li Jin, Ke Xu, Zhaohui Yang, Sijia Wang, Yu Liu, Ziyu Yuan, Luis-Miguel Ramirez-Aristeguieta, Yi Li, Xuyang Liu, Fudi Wang
Publikováno v:
Journal of Investigative Dermatology. 142:1223-1227.e14
Autor:
Xinxiang Yan, Yafang Zhou, Lu Shen, Fu-feng Zhang, Beisha Tang, Xiaoyan Liu, Yan-Jiang Wang, Jun Xu, Bin Jiao, Lin Zhou
Publikováno v:
Neurobiology of aging. 35(8)
Mutations of 3 causative genes, namely presenilin 1 (PSEN1), presenilin 2 (PSEN2), and amyloid precursor protein (APP), have been identified as the major causes of early-onset familial Alzheimer's disease (EOFAD). Recently, a GGGGCC repeat expansion
Autor:
Xiao Nong, Zou, Dong Mei, Lin, Xia, Wan, Ann, Chao, Qin Fu, Feng, Zhen, Dai, Gong Huan, Yang, Ning, Lv
Publikováno v:
Biomedical and environmental sciences : BES. 27(1)
To characterize the histological and epidemiological features of male lung cancer patients in China.The demographic and histological information about male lung cancer patients identified from 2000-01-01 to 2012-12-31, was collected from the Cancer H
Autor:
Yue-Yun, Lai, Xiao-Jun, Huang, Zhen, Cai, Xiang-Shan, Cao, Fang-Ping, Chen, Xie-Qun, Chen, Bao-An, Chen, Mei-Yun, Fang, Jia-Fu, Feng, Wei-Ling, Fu, Hai-Ying, Guo, Ming, Hou, Jian, Hou, Yu, Hu, Xiao-Tong, Hu, Xiao-Mei, Hu, Li-Qiang, Huang, Jie, Jin, Jian-Yong, Li, Juan, Li, Wei, Li, Ying-Min, Liang, Ting, Liu, Qi-Fa, Liu, Yan-Hui, Liu, Ping, Mao, Jian, Ouyang, Lu-Gui, Qiu, Lin, Qiu, Chun-Kui, Shao, Bin, Shi, Yong-Ping, Song, Zi-Min, Sun, Qi-Shan, Wang, Chun, Wang, Jian-Ming, Wang, Yun-Shan, Wang, Zhao, Wang, Jian-Bo, Wu, Yin-Xia, Wu, Rui-Xiang, Xia, Yong-Quan, Xue, Bao-Zhen, Yang, Guang, Yang, Zheng-Lin, Yang, Li, Yu, Zhong, Yuan, Sheng, Zhang, Yin, Zhang, Hong-Guo, Zhao, Li, Zhao, Dao-Bin, Zhou, Shan-Hua, Zou, Yun-Feng, Zhu
Publikováno v:
Chinese medical journal. 125(15)
Chromosomal abnormalities have been shown to play an important prognostic role in multiple myeloma (MM). Interphase fluorescence in situ hybridization (i-FISH) has been much more effective to identify cytogenetic aberrations in MM than conventional c
Publikováno v:
Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi. 32(11)
To apply Estimation and Projection Package (EPP) and Spectrum models for the estimation and projection on HIV/AIDS epidemics in areas with relatively low HIV/AIDS prevalence in China, and to explore the influences of antiretroviral therapy (ART) on t
Publikováno v:
BMC Infectious Diseases
BMC Infectious Diseases, Vol 11, Iss 1, p 69 (2011)
BMC Infectious Diseases, Vol 11, Iss 1, p 69 (2011)
Background Herpes simplex virus (HSV) has two types: HSV-1 and HSV-2. Both infect epithelial cells and establish latent infections in neurons causing an infection that persists for life. Information on age- and gender-specific seroprevalence of HSV-1
Autor:
Wei-ming, Zhu, Hai-jiang, Lin, Ya-fu, Zhang, Dan-hong, Qiu, Ji-fu, Feng, Mei-yang, Gao, Na, He
Publikováno v:
Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi. 29(10)
To study the prevalence of human immunodeficiency virus (HIV), sexually transmitted infection (STI), risk behavior and the sexual networks among men who have sex with men (MSM) in Taizhou city, Zhejiang province.A cross-sectional study was applied wi
Autor:
Bin Jiao, Lu Shen, Lin Zhou, Fu-feng Zhang, Jifeng Guo, Yafang Zhou, Xinxiang Yan, Lihua Hou, Beisha Tang, Xiaoyan Liu
Publikováno v:
Neurobiology of Aging. 35:2422.e9-2422.e11
Recently, 3 rare coding variants significantly associated with Alzheimer's disease (AD) risk have been identified in western populations using whole exome sequencing method, including p.R47H in TREM2, p.V232M in PLD3, and p.T835M in UNC5C. To examine
Autor:
Lu Shen, Fu-feng Zhang, Kun Xia, Zhengmao Hu, Wei Luo, Ruxu Zhang, Fang Cai, Guohua Zhao, Beisha Tang, Biao Chen, Hong Jiang, Cheng Zhang, Qian Pan, Xiao-min Liu
Publikováno v:
Archives of neurology. 62(8)
Background Charcot-Marie-Tooth (CMT) disease, the most common hereditary peripheral neuropathy, is highly clinically and genetically heterogeneous, and mutations in at least 18 genes have been identified. Recently, mutations in small heat shock prote
Autor:
Fu-feng, Zhang, Bei-sha, Tang, Guo-hua, Zhao, Biao, Chen, Cheng, Zhang, Wei, Luo, Xiao-min, Liu, Kun, Xia, Fang, Cai, Zheng-mao, Hu, Xin-xiang, Yan, Ru-xu, Zhang, Peng, Guo
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 22(4)
To study the characteristics of the mutation of small heat-shock protein 22 (HSP22) gene in Chinese patients with Charcot-Marie-Tooth (CMT) disease.A CMT2L proband with 423(G--T) mutation in HSP22 gene had been studied and reported by the present aut