Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Xiaoxuan Song"'
Autor:
Xiaohang Qian, Xiaoying Liu, Zeyu Zhu, Shige Wang, Xiaoxuan Song, Guang Chen, Jingying Wu, Yuwen Cao, Xinghua Luan, Huidong Tang, Li Cao
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Occipital cortical malformation (OCCM) is a disease caused by malformations of cortical development characterized by polymicrogyria and pachygyria of the occipital lobes and childhood-onset seizures. The recessive or complex heterozygous variants of
Externí odkaz:
https://doaj.org/article/93f6065f66e44337b81264b98df9be03
Publikováno v:
Molecules, Vol 27, Iss 6, p 1904 (2022)
Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder frequently accompanied by cognitive impairment. Contributing factors such as modern lifestyle, genetic predisposition, and gene environmental interactions have been postulated, but the p
Externí odkaz:
https://doaj.org/article/a3196c6ade8649e9af47ee9a7d418b3e
Autor:
Jingwen Jiang, Guang Chen, Jingying Wu, Xinghua Luan, Haiyan Zhou, Xiaoli Liu, Zeyu Zhu, Xiaoxuan Song, Shige Wang, Xiaohang Qian, Juanjuan Du, Xiaojun Huang, Mei Zhang, Wei Xu, Li Cao
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundCerebrotendinous xanthomatosis (CTX) is an autosomal recessive disorder of bile acid synthesis caused by mutations in the CYP27A1 gene. CTX is an underdiagnosed and potentially treatable disease, thus a detailed appreciation of the phenotyp
Externí odkaz:
https://doaj.org/article/dc6bf80aaf134ad1888bdf8f047b5232
Biosynthesis Pathways, Transport Mechanisms and Biotechnological Applications of Fungal Siderophores
Autor:
Lorenzo Pecoraro, Xiao Wang, Dawood Shah, Xiaoxuan Song, Vishal Kumar, Abdul Shakoor, Keshawanand Tripathi, Pramod W. Ramteke, Rupa Rani
Publikováno v:
Journal of Fungi, Vol 8, Iss 1, p 21 (2021)
Iron (Fe) is the fourth most abundant element on earth and represents an essential nutrient for life. As a fundamental mineral element for cell growth and development, iron is available for uptake as ferric ions, which are usually oxidized into compl
Externí odkaz:
https://doaj.org/article/1b81b5bf17704166ac091f54d3d3747c
Autor:
Li Cao, Hui-Dong Tang, Guang Chen, Ze-Yu Zhu, Xiaoxuan Song, Xiao-ying Liu, Jingying Wu, Xiao-Hang Qian, Shi-Ge Wang
Publikováno v:
Seizure. 84:47-52
Background Mutations in the IRF2BPL gene can cause neurodevelopmental disorders. We describe the clinical and genetic characteristics of a Chinese patient with a novel abnormality in this gene, explore the potential pathogenic mechanism and summarize
Autor:
Fei-Xia Zhan, Li Cao, Xiaoxuan Song, Jingwen Jiang, Hui-Dong Tang, Ze-Yu Zhu, Wo-Tu Tian, Binyin Li
Publikováno v:
Molecular Medicine Reports
Alexander disease (AxD) is a cerebral white matter disease affecting a wide range of ages, from infants to adults. In the present study, two cases of bulbospinal form AxD were reported, and a preliminary exploration of AxD was conducted thorough clin
Autor:
Guiying He, Juan Huang, Pei Wang, Xiaoxuan Song, Hui-Dong Tang, Jian-Fang Ma, Fuhua Yan, Qi Luo, Yu-Yan Tan, Yumeng Huang, Sheng-Di Chen, Xinxin Xu
Publikováno v:
Therapeutics and Clinical Risk Management
Introduction Cerebral microbleeds (CMBs) are frequently found in the healthy elderly. However, data on the prevalence and risk factors of CMBs in the general population of China are lacking. Methods A cross-sectional study focusing on the prevalence
Autor:
Xiaohang, Qian, Xiaoying, Liu, Zeyu, Zhu, Shige, Wang, Xiaoxuan, Song, Guang, Chen, Jingying, Wu, Yuwen, Cao, Xinghua, Luan, Huidong, Tang, Li, Cao
Publikováno v:
Frontiers in Genetics
Occipital cortical malformation (OCCM) is a disease caused by malformations of cortical development characterized by polymicrogyria and pachygyria of the occipital lobes and childhood-onset seizures. The recessive or complex heterozygous variants of
Autor:
Jiong Hu, Ming-Liang Zhao, Qing Liu, Xiaoxuan Song, Xiaoli Liu, Li Cao, Xiao-Jun Huang, Wo-Tu Tian, Fei-Xia Zhan, Shi-Ge Wang, Hai-Yan Zhou, Guang Chen, Xing-Hua Luan, Binyin Li, Ze-Yu Zhu, Sheng-Di Chen, Hui-Dong Tang, Ying Wang
Publikováno v:
Brain imaging and behavior. 15(3)
CSF1R-related leukoencephalopathy is a rare white-matter encephalopathy characterized by motor and neuropsychiatric symptoms due to colony-stimulating factor 1 receptor (CSF1R) gene mutation. Few studies have investigated the intrinsic brain alternat