Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Xiao‐Huan Zou"'
Autor:
Qi‐Jie Zhang, Yang Chen, Xiao‐Huan Zou, Wei Hu, Min‐Lu Ye, Qi‐Fu Guo, Xue‐Liang Lin, Shang‐Yuan Feng, Ning Wang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 10, Pp 2010-2018 (2020)
Abstract Objective Amyotrophic lateral sclerosis (ALS) is an adult‐onset fatal neurodegenerative disease which lacks identified biological markers. A label‐free plasma surface‐enhanced Raman spectroscopy (SERS) method was developed to explore a
Externí odkaz:
https://doaj.org/article/48718ea62f514a23bb4ad6f9f460bc7a
Autor:
Yi Xiang, Xiao Juan Lu, Yi Hang Sun, Xia Liu, Yan Yang Wu, Hui Rao, Qiu Yang Que, Qi Xiao, Rui Zhu, Xiao Fei Feng, Wei Ling Lai, Xiao Huan Zou, Ying Wang, Song Qiu, Li Huang, Hua Qiu Shi, Xiang Cai Wang
Publikováno v:
World journal of oncology. 13(5)
Autor:
Ning Wang, Minlu Ye, Wei Hu, Xueliang Lin, Shangyuan Feng, Qi-Fu Guo, Qi-Jie Zhang, Yang Chen, Xiao-Huan Zou
Publikováno v:
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 7, Iss 10, Pp 2010-2018 (2020)
Annals of Clinical and Translational Neurology, Vol 7, Iss 10, Pp 2010-2018 (2020)
Objective Amyotrophic lateral sclerosis (ALS) is an adult‐onset fatal neurodegenerative disease which lacks identified biological markers. A label‐free plasma surface‐enhanced Raman spectroscopy (SERS) method was developed to explore a simple a
Autor:
Xiao-Huan Zou, Dong-Ping Chen, Bing-Cong Hong, Yao-Bin Liu, Lu-Lu Lai, Xin-Xin Guo, Chang-Yun Liu, Ji-Dong Peng, Jing-Hui Lai, Hui-Zhen Su, Qing-Yang Yao, Hua-Song Lin, Yu-Ying Zhao, Xiao-Pei Lu, Hong-Xia Fu, Yao Xiangping, Dan-Qin Huang, Wan-Jin Chen, Pan Lin, Chong Wang, Yu-Chun Deng, Xiao-Qun Zhu, Hai-Liang Lin, Yan-Fang Niu, Xue-Jiao Chen, Yong-Kun Li, Ning Wang, Hai-Ting Chen, Gen-Bin Huang
Publikováno v:
Human Mutation. 40:392-403
Primary familial brain calcification (PFBC) is a rare neurodegenerative disorder with four causative genes (SLC20A2, PDGFRB, PDGFB, and XPR1) that have been identified. Here, we aim to describe the mutational spectrum of four causative genes in a ser
Autor:
Xiao-Huan Zou, Xin-Xin Guo, Hui-Zhen Su, Chong Wang, En-Lin Dong, Ning Wang, Wan-Jin Chen, Qi-Jie Zhang
Publikováno v:
Journal of molecular neuroscience : MN. 70(4)
The original version of this article unfortunately contained mistakes in the affiliation section.
Autor:
Wan-Jin Chen, Xueliang Lin, Fa Chen, Yang Chen, Wei Hu, Ning Wang, Liu-Qing Xu, Qi-Jie Zhang, Xiao-Huan Zou, Shangyuan Feng
Publikováno v:
Journal of Biophotonics. 12
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with a wide range of survival times. We aimed to explore prognostic factors related to short survival based on clinical features and plasma metabolic signatures using surface-en
Autor:
Lu-Lu Lai, Jie Lin, Jing-Mei Hong, Yun-Lu Li, Kun-Xin Lin, Chong Wang, Ying-Qian Lu, Miao Zhao, Wan-Jin Chen, Ning Wang, Yao Xiangping, Hui-Zhen Su, Xiao-Huan Zou, Xin-Xin Guo, Yi-Heng Zeng
Publikováno v:
Clinical genetics. 96(1)
Primary familial brain calcification (PFBC) is a rare neurological disorder. Mutations in five genes (SLC20A2, PDGFRB, PDGFB, XPR1, and MYORG) have been linked to PFBC. Here, we used SYBR green-based real-time quantitative polymerase chain reaction (
Autor:
En-Lin Dong, Xiao-Huan Zou, Xin-Xin Guo, Qi-Jie Zhang, Chong Wang, Ning Wang, Hui-Zhen Su, Wan-Jin Chen
Publikováno v:
Journal of molecular neuroscience : MN. 68(4)
Autosomal recessive optic neuropathies (IONs) are extremely rare disorders affecting retinal ganglion cells and the nervous system. RTN4IP1 has recently been identified as the third known gene associated with the autosomal recessive ION optic atrophy
Autor:
Yao Xiangping, Shuang Wu, Xue-Jiao Chen, Hui-Zhen Su, Ning Wang, Wan-Jin Chen, Lu-Lu Lai, Xiaojuan Li, Yu-Ying Zhao, Chong Wang, Xuewen Cheng, Hongjie Yu, Miao Zhao, Jianfeng Xu, Zhi-Qi Xiong, Xin-Xin Guo, Xiao-Huan Zou, Ying-Qian Lu, En-Lin Dong, Gaofeng Fan
Publikováno v:
Neuron. 98(6)
Summary Primary familial brain calcification (PFBC) is a genetically heterogeneous disorder characterized by bilateral calcifications in the basal ganglia and other brain regions. The genetic basis of this disorder remains unknown in a significant po
Publikováno v:
Bing du xue bao = Chinese journal of virology. 26(1)
The plaque-forming characteristics of Newcastle disease viruses of chickens and geese source were compared on various cells. The result showed that there were obvious differences of plaque formation between F48E9 and NA-1 on Vero cells, chicken embry