Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Ji, Feng"'
Autor:
Ji-Feng Guo, Xun Zhou, Yuwen Zhao, Jinxia Yang, Runcheng He, Qi-ying Sun, Jinchen Li, Zhou Zhou, Xin-xiang Yan, Qian Xu, Hongxu Pan, Dongxiao Liang, Beisha Tang, Xiaoting Zhou, Yige Wang, Xiaoxia Zhou
Publikováno v:
Annals of Clinical and Translational Neurology
Objective Parkinson’s disease (PD) and essential tremor (ET) are the two most common movement disorders. A significant overlap in clinical features, epidemiology, imaging, and pathology suggests that PD and ET may also share common genetic risk fac
Publikováno v:
The FASEB Journal. 34:15837-15848
Acute ischemic stroke is one of the leading causes of death in developed countries and the most common cause of disability in adults worldwide. Despite advances in the understanding of stroke pathophysiology, therapeutic options remain limited. In th
Autor:
Ping Hou, Ji-Feng Wan, Yan-Shan Liu, Jian-Huan Chen, En-Min Li, Qian-Hao Yao, Jia-Qi Pan, Shao-Qiang Liu, Jia-Li Zhang, Ruo-Nan Gao, Zhou-Heng Xu, Ji-Hong Wang, Jun-Hua Rao, Xu-Bin Pan, Chun-Yan Ren
Publikováno v:
Biochemical and Biophysical Research Communications. 531:172-179
Mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene, are the major cause of X-linked retinitis pigmentosa (RP), in which exon open reading frame 15 (ORF15) of RPGR has been implicated to play a substantial role. We identified a novel h
Autor:
Yuemeng Huang, Jing Liang, Lixian Wang, Yafen Guo, Kui Li, Siran Zhu, Yanjun Wu, Zhe Li, Shuo Wang, Ji-Feng Fei, Xiurong Yang, Ganqiu Lan, Chao Shi, Ruiqiang Li, Zhonglin Tang, Meng Wang, Qun-Jie Zhang, Li Zhang, Wenjing Qi, Jinglei Si
Publikováno v:
iScience
iScience, Vol 19, Iss, Pp 162-176 (2019)
iScience, Vol 19, Iss, Pp 162-176 (2019)
Summary Pig has been proved to be a valuable large animal model used for research on diabetic disease. However, their translational value is limited given their distinct anatomy and physiology. For the last 30 years, we have been developing a laborat
Autor:
Juan Du, Jun-pu Mei, Li Jiang, Xun Zhou, Hong Jiang, Jinchen Li, Jieqiong Tan, Lu Shen, Hainan Zhang, Yangjie Zhou, Qian Xu, Yuwen Zhao, Yacen Hu, Zhenhua Liu, Zhenghuan Fang, Lifang Lei, Rui Zhang, Yige Wang, Qiying Sun, Ji-Feng Guo, Yan He, Chunyu Wang, Ya-Se Chen, Kai-Lin Zhang, Zheng Wang, Qian Zeng, Xinxiang Yan, Yang Yang, Hongxu Pan, Beisha Tang
Publikováno v:
Translational Neurodegeneration
Translational Neurodegeneration, Vol 9, Iss 1, Pp 1-12 (2020)
Translational Neurodegeneration, Vol 9, Iss 1, Pp 1-12 (2020)
Background Common and rare variants of guanosine triphosphate cyclohydrolase 1 (GCH1) gene may play important roles in Parkinson’s disease (PD). However, there is a lack of comprehensive analysis of GCH1 genotypes, especially in non-coding regions.
Preferential Distribution of Boron to Developing Tissues Is Mediated by the Intrinsic Protein OsNIP3
Publikováno v:
Plant Physiology. 176:1739-1750
Boron is especially required for the growth of meristem and reproductive organs, but the molecular mechanisms underlying the preferential distribution of B to these developing tissues are poorly understood. Here, we show evidence that a member of nod
Publikováno v:
Proceedings of the National Academy of Sciences. 114:12501-12506
Salamanders exhibit extensive regenerative capacities and serve as a unique model in regeneration research. However, due to the lack of targeted gene knockin approaches, it has been difficult to label and manipulate some of the cell populations that
Autor:
Yi-Li Feng, Guo-Fang Yan, Hui Lin, Yang Huang, Hao Dan Li, Na Kong, Anyong Xie, Si-Cheng Liu, Tao Guo, Xiujun Cai, Ji-Feng Xiang, Ye Feng
Publikováno v:
Nucleic Acids Research
Phosphorylated histone H2AX, termed ‘γH2AX’, mediates the chromatin response to DNA double strand breaks (DSBs) in mammalian cells. H2AX deficiency increases the numbers of unrepaired DSBs and translocations, which are partly associated with def
Autor:
Yanlong Zhao, Ji-Feng Zhang, Stanley Pounds, Hang Zhang, Fei Zou, Cheng Cheng, Weihua Yue, Wenjian Bi, Sanjay Shete, Guolian Kang
Publikováno v:
Genetics. 205:1049-1062
In many case-control designs of genome-wide association (GWAS) or next generation sequencing (NGS) studies, extensive data on secondary traits that may correlate and share the common genetic variants with the primary disease are available. Investigat
Publikováno v:
Archives of virology. 164(6)
A nidovirus was isolated from crucian carp (Carassius auratus). The complete genome of the crucian carp nidovirus (CCNV) is 25,971 nt long and has five open reading frames, encoding the polyprotein 1ab (pp1ab), spike glycoprotein (S), membrane protei