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N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer’s disease
Author / Creator:Shafik, Andrew M. ; Zhang, Feiran ; Guo, Zhenxing ; Dai, Qing ; Pajdzik, Kinga ; Li, Yangping ; Kang, Yunhee ; Yao, Bing ; Wu, Hao ; He, Chuan ; Allen, Emily G. ; Duan, Ranhui ; Jin, Peng
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology, 2021-01, Vol.22 (1), p.17-17, Article 17
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A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Author / Creator:Kang, Yunhee ; Zhou, Ying ; Li, Yujing ; Han, Yanfei ; Xu, Jie ; Niu, Weibo ; Li, Ziyi ; Liu, Shiying ; Feng, Hao ; Huang, Wen ; Duan, Ranhui ; Xu, Tianmin ; Raj, Nisha ; Zhang, Feiran ; Dou, Juan ; Xu, Chongchong ; Wu, Hao ; Bassell, Gary J. ; Warren, Stephen T. ; Allen, Emily G. ; Jin, Peng ; Wen, Zhexing
Publisher:New York: Nature Publishing Group US
Journal title:Nature neuroscience, 2021-10, Vol.24 (10), p.1377-1391
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UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia
Author / Creator:Duan, Ranhui ; Shi, Yuting ; Yu, Li ; Zhang, Gehan ; Li, Jia ; Lin, Yunting ; Guo, Jifeng ; Wang, Junling ; Shen, Lu ; Jiang, Hong ; Wang, Guanghui ; Tang, Beisha
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-02, Vol.11 (2), p.e0149039-e0149039
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Eg5 UFMylation promotes spindle organization during mitosis
Author / Creator:Li, Guangxu ; Huang, Yuanjiang ; Han, Wenbo ; Wei, Liyi ; Huang, Hongjing ; Zhu, Yingbao ; Xiao, Qiao ; Wang, Zujia ; Huang, Wen ; Duan, Ranhui
Publisher:London: Nature Publishing Group UK
Journal title:Cell death & disease, 2024-07, Vol.15 (7), p.544-13, Article 544
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Clinical application of polar body-based preimplantation genetic testing for maternal mutations in women with a limited number of oocytes
Author / Creator:Chen, Jia ; Wu, Xingwu ; Xu, Qiang ; Ding, Tao ; Chen, Ge ; Chen, Houyang ; Zou, Yongyi ; Huang, Jialyu ; Zhang, Ziyu ; Tian, Lifeng ; Zhao, Yan ; Duan, Ranhui ; Li, Zengming ; Wu, Qiongfang ; Liu, Yanqiu
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2025-04, Vol.20 (1), p.152-13, Article 152
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Modulating CCTG repeat expansion toxicity in DM2 Drosophila model through TDP1 inhibition
Author / Creator:Zhu, Yingbao ; Xiao, Shengwei ; Guan, Xinxin ; Deng, Haitao ; Ai, Liqiang ; Fan, Kaijing ; Xue, Jin ; Li, Guangxu ; Bi, Xiaoxue ; Xiao, Qiao ; Huang, Yuanjiang ; Jiang, Lin ; Huang, Wen ; Jin, Peng ; Duan, Ranhui
Publisher:London: Nature Publishing Group UK
Journal title:EMBO molecular medicine, 2025-05, Vol.17 (5), p.967-992
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Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells
Author / Creator:Luo, Yuping ; Shan, Ge ; Guo, Weixiang ; Smrt, Richard D. ; Johnson, Eric B. ; Li, Xuekun ; Pfeiffer, Rebecca L. ; Szulwach, Keith E. ; Duan, Ranhui ; Barkho, Basam Z. ; Li, Wendi ; Liu, Changmei ; Jin, Peng ; Zhao, Xinyu
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2010-04, Vol.6 (4), p.e1000898-e1000898
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MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm
Author / Creator:Jiang, Yugang ; Zhang, Mingming ; He, Hua ; Chen, Jia ; Zeng, Hua ; Li, Jia ; Duan, Ranhui
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2013-09, Vol.6 (1), p.36-36, Article 36
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Activation of mTOR Ameliorates Fragile X Premutation rCGG Repeat-Mediated Neurodegeneration
Author / Creator:Lin, Yunting ; Tang, Chengyuan ; He, Hua ; Duan, Ranhui
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-04, Vol.8 (4), p.e62572
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Drosophila Netrin-B controls mushroom body axon extension and regulates courtship-associated learning and memory of a Drosophila fragile X syndrome model
Author / Creator:Kang, Huaixing ; Zhao, Juan ; Jiang, Xuan ; Li, Guangxu ; Huang, Wen ; Cheng, Huili ; Duan, Ranhui
Publisher:England: BioMed Central Ltd
Journal title:Molecular brain, 2019-05, Vol.12 (1), p.52-52, Article 52
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Evaluation of the role of FMR1 CGG repeat allele in Parkinson’s disease from the Chinese population
Author / Creator:Chen, Juan ; Zhao, Yuwen ; Zhou, Xun ; Xue, Jin ; Xiao, Qiao ; Pan, Hongxu ; Zhou, Xiaoxia ; Xiang, Yaqin ; Li, Jian ; Zhu, Liping ; Zhou, Zhou ; Yang, Yang ; Xu, Qian ; Sun, Qiying ; Yan, Xinxiang ; Tan, Jieqiong ; Li, Jinchen ; Guo, Jifeng ; Duan, Ranhui ; Tang, Beisha ; Yu, Qiao ; Liu, Zhenhua
Publisher:Lausanne: Frontiers Research Foundation
Journal title:Frontiers in aging neuroscience, 2023-07, Vol.15, p.1234027-1234027
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Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy
Author / Creator:Gao, Fei ; Huang, Wen ; You, Yanjun ; Huang, Jie ; Zhao, Juan ; Xue, Jin ; Kang, Huaixing ; Zhu, Yingbao ; Hu, Zhengmao ; Allen, Emily G. ; Jin, Peng ; Xia, Kun ; Duan, Ranhui
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-06, Vol.8 (6), p.e1236-n/a
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Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center
Author / Creator:Xi, Hui ; Xie, Wanqin ; Chen, Jing ; Tang, Wanglan ; Deng, Xiuli ; Li, Hua ; Peng, Ying ; Wang, Dan ; Yang, Shuting ; Zhang, Yanan ; Duan, Ranhui ; Fang, Junqun ; Wang, Hua
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2021-07, Vol.9 (7), p.e1711-n/a
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A small molecule enhances RNA interference and promotes microRNA processing
Author / Creator:Shan, Ge ; Li, Yujing ; Zhang, Junliang ; Li, Wendi ; Szulwach, Keith E ; Duan, Ranhui ; Faghihi, Mohammad A ; Khalil, Ahmad M ; Lu, Lianghua ; Paroo, Zain ; Chan, Anthony W S ; Shi, Zhangjie ; Liu, Qinghua ; Wahlestedt, Claes ; He, Chuan ; Jin, Peng
Publisher:New York, NY: Nature Publishing Group
Journal title:Nature biotechnology, 2008-08, Vol.26 (8), p.933-940
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Mitochondrial DNA analysis of human remains from the Yuansha site in Xinjiang, China
Author / Creator:Gao, Shizhu ; Cui, Yinqiu ; Yang, Yidai ; Duan, Ranhui ; Abuduresule, Idelisi ; Mair, Victor H ; Zhu, Hong ; Zhou, Hui
Publisher:Dordrecht: Springer Nature B.V
Journal title:Science China. Life sciences, 2008-03, Vol.51 (3), p.205
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Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease
Author / Creator:Tian, Yun ; Zhou, Lu ; Gao, Jing ; Jiao, Bin ; Zhang, Sizhe ; Xiao, Qiao ; Xue, Jin ; Wang, Ying ; liang, Hui ; Liu, Yaling ; Ji, Guang ; Mao, Chenhui ; Liu, Caiyan ; Dong, Liling ; Zhang, Long ; Zhang, Shugang ; Yi, Jiping ; Zhao, Guohua ; Luo, Yingying ; Sun, Qiying ; Zhou, Yafang ; Yi, Fang ; Chen, Xiaoyu ; Zhou, Chaojun ; Xie, Nina ; Luo, Mengchuan ; Yao, Lingyan ; Hu, Yacen ; Zhang, Mengqi ; Zeng, Qiuming ; Fang, Liangjuan ; Long, Hong-Yu ; Xie, Yuanyuan ; Weng, Ling ; Chen, Si ; Du, Juan ; Xu, Qian ; Feng, Li ; Huang, Qing ; Hou, Xuan ; Wang, Junpu ; Xie, Bin ; Zhou, Lin ; Long, Lili ; Guo, Ji-feng ; Wang, Junling ; Yan, Xinxiang ; Jiang, Hong ; Xu, Hongwei ; Duan, Ranhui ; Tang, Beisha ; Shen, Lu
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 2022-12, Vol.93 (12), p.1289-1298
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The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies
Author / Creator:Wang, Mengli ; Yang, Honglan ; Lin, Zhiqiang ; Li, Xiaobo ; Liu, Lei ; Huang, Shunxiang ; Zhao, Huadong ; Zhu, Xiying ; Xiao, Qiao ; Duan, Ranhui ; Wang, Junling ; Zuchner, Stephan ; Tang, Beisha ; Zhang, Ruxu
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2023-10, Vol.270 (10), p.4959-4967
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GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degeneration
Author / Creator:Liu, Qiong ; Chen, Juan ; Xue, Jin ; Zhou, Xun ; Tian, Yun ; Xiao, Qiao ; Huang, Wen ; Pan, Yongcheng ; Zhou, Xiaoxia ; Li, Jian ; Zhao, Yuwen ; Pan, Hongxu ; Wang, Yige ; He, Runcheng ; Xiang, Yaqin ; Tu, Tian ; Xu, Qian ; Sun, Qiying ; Tan, Jieqiong ; Yan, Xinxiang ; Li, Jinchen ; Guo, Jifeng ; Shen, Lu ; Duan, Ranhui ; Tang, Beisha ; Liu, Zhenhua
Publisher:England: John Wiley & Sons, Inc
Journal title:European journal of neurology, 2024-02, Vol.31 (2), p.e16145-n/a
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Dysregulated CRMP Mediates Circadian Deficits in a Drosophila Model of Fragile X Syndrome
Author / Creator:Zhao, Juan ; Xue, Jin ; Zhu, Tengfei ; He, Hua ; Kang, Huaixing ; Jiang, Xuan ; Huang, Wen ; Duan, Ranhui
Publisher:Singapore: Springer Singapore
Journal title:Neuroscience bulletin, 2021-07, Vol.37 (7), p.973-984
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A small molecule enhances RNA interference and promotes microRNA processing
Author / Creator:Shan, Ge ; Li, Yujing ; Zhang, Junliang ; Li, Wendi ; Szulwach, Keith E ; Duan, Ranhui ; Faghihi, Mohammad A ; Khalil, Ahmad M ; Lu, Lianghua ; Paroo, Zain ; Chan, Anthony W S ; Shi, Zhangjie ; Liu, Qinghua ; Wahlestedt, Claes ; He, Chuan ; Jin, Peng
Publisher:New York: Nature Publishing Group US
Journal title:Nature biotechnology, 2008-08, Vol.26 (8), p.933-940
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Showing 1 to 20 of 30 results

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N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer’s disease

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A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies

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UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia

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Eg5 UFMylation promotes spindle organization during mitosis

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Clinical application of polar body-based preimplantation genetic testing for maternal mutations in women with a limited number of oocytes

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Modulating CCTG repeat expansion toxicity in DM2 Drosophila model through TDP1 inhibition

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Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells

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MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm

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Activation of mTOR Ameliorates Fragile X Premutation rCGG Repeat-Mediated Neurodegeneration

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Drosophila Netrin-B controls mushroom body axon extension and regulates courtship-associated learning and memory of a Drosophila fragile X syndrome model

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Evaluation of the role of FMR1 CGG repeat allele in Parkinson’s disease from the Chinese population

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Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy

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Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center

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A small molecule enhances RNA interference and promotes microRNA processing

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Mitochondrial DNA analysis of human remains from the Yuansha site in Xinjiang, China

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Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease

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The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies

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GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degeneration

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Dysregulated CRMP Mediates Circadian Deficits in a Drosophila Model of Fragile X Syndrome

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A small molecule enhances RNA interference and promotes microRNA processing

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