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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 17, 2016 - Issue 7-8
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Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

Shi ShuNeuroscience Centre, CAMS, Beijing, ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, and
,
Xiao Ling LiNeuroscience Centre, CAMS, Beijing, ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, and
,
Qing LiuNeuroscience Centre, CAMS, Beijing, ;Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China
,
Fang LiuNeuroscience Centre, CAMS, Beijing, ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, and
,
Bo CuiNeuroscience Centre, CAMS, Beijing, ;Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China
,
Ming Sheng LiuNeuroscience Centre, CAMS, Beijing, ;Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China
,
Li-Ying CuiNeuroscience Centre, CAMS, Beijing, ;Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China
,
Xiao Guang LiNeuroscience Centre, CAMS, Beijing, ;Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, ChinaCorrespondence[email protected]
&
Xue ZhangNeuroscience Centre, CAMS, Beijing, ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, and ;Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, ChinaCorrespondence[email protected]
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Pages 605-607 | Received 09 Feb 2016, Accepted 28 Mar 2016, Published online: 03 Jun 2016

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Yaling Jiang, Bin Jiao, Xuewen Xiao & Lu Shen. (2021) Genetics of frontotemporal dementia in China. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:5-6, pages 321-335.
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Articles from other publishers (13)

Bi Zhao, Qirui Jiang, Junyu Lin, Qianqian Wei, Chunyu Li, Yanbing Hou, Bei Cao, Lingyu Zhang, Ruwei Ou, Kuncheng Liu, Tianmi Yang, Yi Xiao & Huifang Shang. (2023) TBK1 variants in Chinese patients with amyotrophic lateral sclerosis: Genetic analysis and clinical features . European Journal of Neurology.
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Ilaria Giovannelli, Adrian Higginbottom, Janine Kirby, Mimoun Azzouz & Pamela J. Shaw. (2022) Prospects for gene replacement therapies in amyotrophic lateral sclerosis. Nature Reviews Neurology 19:1, pages 39-52.
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Marta Cozzi & Veronica Ferrari. (2022) Autophagy Dysfunction in ALS: from Transport to Protein Degradation. Journal of Molecular Neuroscience 72:7, pages 1456-1481.
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Faheem Arshad, Seena Vengalil, Atchayaram Nalini, Kiran Polavarapu, Uzma Shamim, Shumyla Jabeen, Chandana Nagaraj, Subasree Ramakrishnan, Mohammad Faruq & Suvarna Alladi. (2021) Novel TBK1 variant associated with Frontotemporal Dementia overlap syndrome . Acta Neurologica Scandinavica 145:4, pages 399-406.
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Xiaolu Liu, Ji He, Lu Chen, Nan Zhang, Lu Tang, Xiangyi Liu, Yan Ma & Dongsheng Fan. (2021) TBK1 variants in Chinese patients with amyotrophic lateral sclerosis. Neurobiology of Aging 97, pages 149.e9-149.e15.
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Serena Lattante, Paolo Niccolò Doronzio, Giuseppe Marangi, Amelia Conte, Giulia Bisogni, Daniela Bernardo, Tommaso Russo, Dante Lamberti, Sara Patrizi, Francesco Paolo Apollo, Christian Lunetta, Stefania Scarlino, Laura Pozzi, Marcella Zollino, Nilo Riva & Mario Sabatelli. (2019) Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS. Neurobiology of Aging 84, pages 239.e9-239.e14.
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Huiling Yu, Wenbo Yu, Su‐shan Luo, Yu‐Jie Yang, Feng‐Tao Liu, Yue Zhang, Yan Chen, Yi‐min Sun & Jian‐jun Wu. (2019) Association of the TBK1 mutation p.Ile334Thr with frontotemporal dementia and literature review . Molecular Genetics & Genomic Medicine 7:3, pages e547.
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Bin Jiao, Qiying Sun, Zhenhua Yuan, Junling Wang, Lin Zhou, Xinxiang Yan, Beisha Tang & Lu Shen. (2018) Rare TBK1 variants in patients with frontotemporal dementia and amyotrophic lateral sclerosis in a Chinese cohort. Translational Neurodegeneration 7:1.
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Shi Shu, Xingxing Lei, Fang Liu, Bo Cui, Qing Liu, Qingyun Ding, Ming Sheng Liu, Xiao Guang Li, Liying Cui & Xue Zhang. (2018) Mutation screening of NEK1 in Chinese ALS patients. Neurobiology of Aging 71, pages 267.e1-267.e4.
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Xiaolu Liu, Ji He, Fen-Biao Gao, Aaron D. Gitler & Dongsheng Fan. (2018) The epidemiology and genetics of Amyotrophic lateral sclerosis in China. Brain Research 1693, pages 121-126.
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Hung Phuoc Nguyen, Christine Van Broeckhoven & Julie van der Zee. (2018) ALS Genes in the Genomic Era and their Implications for FTD. Trends in Genetics 34:6, pages 404-423.
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James A. Oakes, Maria C. Davies & Mark O. Collins. (2017) TBK1: a new player in ALS linking autophagy and neuroinflammation. Molecular Brain 10:1.
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Irene Piaceri, Valentina Bessi, Sabrina Matà, Cristina Polito, Andrea Tedde, Valentina Berti, Silvia Bagnoli, Arianna Braccia, Monica Del Mastio, Alberto Moggi Pignone, Alberto Pupi, Sandro Sorbi & Benedetta Nacmias. (2017) Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline. Journal of Alzheimer's Disease 61:1, pages 41-46.
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