Search Results - "Hou, Xiaocan"

Updated frequency analysis of spinocerebellar ataxia in China by Chen, Zhao, Wang, Puzhi, Wang, Chunrong, Peng, Yun, Hou, Xiaocan, Zhou, Xin, Li, Tianjiao, Peng, Huirong, Qiu, Rong, Xia, Kun, Sequeiros, Jorge, Tang, Beisha, Jiang, Hong

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Alterations of the Gut Microbiota in Multiple System Atrophy Patients by Wan, Linlin, Zhou, Xin, Wang, Chunrong, Chen, Zhao, Peng, Huirong, Hou, Xuan, Peng, Yun, Wang, Puzhi, Li, Tianjiao, Yuan, Hongyu, Shi, Yuting, Hou, Xiaocan, Xu, Keqin, Xie, Yue, He, Lang, Xia, Kun, Tang, Beisha, Jiang, Hong

“…Multiple system atrophy (MSA) is a fatal neurodegenerative disease, and the pathogenesis is still quite challenging. Emerging evidence has shown that the…”
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Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins? by Li, Tianjiao, Martins, Sandra, Peng, Yun, Wang, Puzhi, Hou, Xiaocan, Chen, Zhao, Wang, Chunrong, Tang, Zhaoli, Qiu, Rong, Chen, Chao, Hu, Zhengmao, Xia, Kun, Tang, Beisha, Sequeiros, Jorge, Jiang, Hong

“…Machado-Joseph disease (MJD, also known as spinocerebellar ataxia 3 or SCA3) is the most common dominant ataxia worldwide, with an overall average prevalence…”
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Birt-Hogg-Dubé syndrome in two Chinese families with mutations in the FLCN gene by Hou, Xiaocan, Zhou, Yuan, Peng, Yun, Qiu, Rong, Xia, Kun, Tang, Beisha, Zhuang, Wei, Jiang, Hong

“…Birt-Hogg-Dubé syndrome is an autosomal dominant hereditary condition caused by mutations in the folliculin-encoding gene FLCN (NM_144997). It is associated…”
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Identification of a potential exosomal biomarker in spinocerebellar ataxia Type 3/Machado–Joseph disease by Hou, Xiaocan, Gong, Xuan, Zhang, Longbo, Li, Tianjiao, Yuan, Hongyu, Xie, Yue, Peng, Yun, Qiu, Rong, Xia, Kun, Tang, Beisha, Jiang, Hong

“…To identify spinocerebellar ataxia Type 3 (SCA3)-related exosomal biomarkers and the underlying mechanisms. Exosomal RNAs from plasma and cerebrospinal fluid…”
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Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population by Peng, Yun, Ye, Wei, Chen, Zhao, Peng, Huirong, Wang, Puzhi, Hou, Xuan, Wang, Chunrong, Zhou, Xin, Hou, Xiaocan, Li, Tianjiao, Qiu, Rong, Hu, Zhengmao, Tang, Beisha, Jiang, Hong

“…Variants in have been widely reported in ataxia patients in Europe, with highly variable clinical phenotype. Until now, no mutation of ataxia has been reported…”
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RNA Expression Profile and Potential Biomarkers in Patients With Spinocerebellar Ataxia Type 3 From Mainland China by Li, Tianjiao, Hou, Xiaocan, Chen, Zhao, Peng, Yun, Wang, Puzhi, Xie, Yue, He, Lang, Yuan, Hongyu, Peng, Huirong, Qiu, Rong, Xia, Kun, Tang, Beisha, Jiang, Hong

“…Long non-coding RNAs (lncRNAs) play an important role in growth, development, and reproduction and undoubtedly contribute to the pathogenesis and progression…”
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Corrigendum: Alterations of the Gut Microbiota in Multiple System Atrophy Patients by Wan, Linlin, Zhou, Xin, Wang, Chunrong, Chen, Zhao, Peng, Huirong, Hou, Xuan, Peng, Yun, Wang, Puzhi, Li, Tianjiao, Yuan, Hongyu, Shi, Yuting, Hou, Xiaocan, Xu, Keqin, Xie, Yue, He, Lang, Xia, Kun, Tang, Beisha, Jiang, Hong

“…[This corrects the article DOI: 10.3389/fnins.2019.01102.]…”
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Cerebellar lncRNA Expression Profile Analysis of SCA3/MJD Mice by Xie, Yue, He, Lang, Peng, Huirong, Qiu, Rong, Xia, Kun, Tang, Bei-sha, Jiang, Hong, Wang, Puzhi, Yuan, Hongyu, Hou, Xiaocan, Wang, Chunrong, Peng, Yun, Chen, Zhao, Li, Tianjiao, Long, Zhe, Zhou, Xin

“…Spinocerebellar ataxia type 3 (SCA3) or Machado-Joseph disease (MJD) is the most common autosomal dominant spinocerebellar ataxia in China with highly clinical…”
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Mapping cell diversity in human sporadic cerebral cavernous malformations by Hou, Xiaocan, Liang, Feng, Li, Jiaoxing, Yang, Yibing, Wang, Chuhuai, Qi, Tiewei, Sheng, Wenli

“…•We performed in-depth single-cell RNA sequencing and ATAC-seq in SCCM and control patients.•We identified six cell types in the SCCM and control vessels and…”
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Let-7f Regulates the Hypoxic Response in Cerebral Ischemia by Targeting NDRG3 by Yao, Yaobing, Wang, Weiwei, Jing, Lijun, Wang, Yiwen, Li, Mingzhe, Hou, Xiaocan, Wang, Jing, Peng, Tao, Teng, Junfang, Jia, Yanjie

“…microRNAs are a class of non-coding RNAs including approximately 22 nucleotides in length and play a pivotal role in post-transcriptional gene regulation…”
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Investigation on modulation of DNA repair pathways in Chinese MJD patients by Wang, Chunrong, Chen, Zhao, Peng, Huirong, Peng, Yun, Zhou, Xin, Yang, Huihua, Wang, Puzhi, Li, Tianjiao, Hou, Xiaocan, Qiu, Rong, Xia, Kun, Sequeiros, Jorge, Tang, Beisha, Jiang, Hong

“…It has been reported that DNA repair pathways could modify age at onset (AO) in Huntington disease (HD) and spinocerebellar ataxias. We genotyped 22 SNPs from…”
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Polymorphisms in DNA methylation–related genes are linked to the phenotype of Machado-Joseph disease by Ding, Dongxue, Wang, Chunrong, Chen, Zhao, Peng, Huirong, Li, Kai, Zhou, Xin, Peng, Yun, Wang, Puzhi, Hou, Xiaocan, Li, Tianjiao, Qiu, Rong, Xia, Kun, Sequeiros, Jorge, Ashizawa, Tetsuo, Tang, Beisha, Jiang, Hong

“…DNA methylation has been reported as an important regulator of genomic structure stability, including large tandem repeats. To test the modulation effect of…”
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Let-7a inhibits migration of melanoma cells via down-regulation of HMGA2 expression by Hou, Xiaocan, Wan, Wencui, Wang, Jing, Li, Mingzhe, Wang, Yiwen, Yao, Yaobing, Feng, Lihong, Jing, Lijun, Lu, Hong, Jia, Yanjie, Peng, Tao

“…This study aimed to investigate the effects of exosomes derived from BM-MSCs transduced with let-7a on B16f10 cells and BM-MSCs. BM-MSCs were transduced with…”
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