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"soong bing wen"的相關文件
顯示項目 1-12 / 12 (共1頁)
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| 臺大學術典藏 |
2021-08-15T00:08:16Z |
Rare gain-of-function kcnd3 variant associated with cerebellar ataxia, parkinsonism, cognitive dysfunction, and brain iron accumulation
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Hsiao, Cheng Tsung; Tropea, Thomas F.; Fu, Ssu Ju; Bardakjian, Tanya M.; Gonzalez-Alegre, Pedro; Soong, Bing Wen; CHIH-YUNG TANG; Jeng, Chung Jiuan |
| 臺大學術典藏 |
2021-07-15T05:32:16Z |
Novel KCND3 variant underlying nonprogressive congenital ataxia or SCA19/22 disrupt KV4.3 protein expression and K+ currents with variable effects on channel properties
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Zanni, Ginevra; Hsiao, Chen Tsung; Fu, Ssu Ju; CHIH-YUNG TANG; Capuano, Alessandro; Bosco, Luca; Graziola, Federica; Bellacchio, Emanuele; Servidei, Serenella; Primiano, Guido; Soong, Bing Wen; Jeng, Chung Jiuan |
| 臺大學術典藏 |
2020-02-24T03:35:35Z |
Xenografting of human umbilical mesenchymal stem cells from Wharton's jelly ameliorates mouse spinocerebellar ataxia type 1
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MING-YUAN MIN; Fu, Yu-Show; Soong, Bing-Wen; Hsu, Sanford P. C.; Chen, Tien-Hua; Tsai, Pei-Jiun;Yeh, Chang-Ching;Huang, Wan-Jhen;Min, Ming-Yuan;Huang, Tzu-Hao;Ko, Tsui-Ling;Huang, Pei-Yu;Chen, Tien-Hua;Hsu, Sanford P. C.;Soong, Bing-Wen;Fu, Yu-Show; Tsai, Pei-Jiun; Yeh, Chang-Ching; Huang, Wan-Jhen; Min, Ming-Yuan; Huang, Tzu-Hao; Ko, Tsui-Ling; Huang, Pei-Yu |
| 臺大學術典藏 |
2019-04-24T05:59:31Z |
Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
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Chuang, Ching-Yu;Chih-Chao Yang;Soong, Bing-Wen;Yu, Chun-Ying;Chen, Shu-Hwa;Hsiang-Po Huang;Kuo, Hung-Chih;Jang-Ming Lee;Chuhsing Kate Hsiao; Chuang, Ching-Yu; Chih-Chao Yang; Soong, Bing-Wen; Yu, Chun-Ying; Chen, Shu-Hwa; HSIANG-PO HUANG; Kuo, Hung-Chih; JANG-MING LEE; CHUHSING KATE HSIAO |
| 臺大學術典藏 |
2019-01-01 |
Novel SCA19/22-associated KCND3 mutations disrupt human KV4.3 protein biosynthesis and channel gating
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Jeng, Chung Jiuan; Lu, Yi Hsiang; Soong, Bing Wen; CHIH-YUNG TANG; Hsiao, Cheng Tsung; Jeng, Chung Jiuan;Lu, Yi Hsiang;Soong, Bing Wen;CHIH-YUNG TANG;Hsiao, Cheng Tsung;Liu, Yo Tsen;Zhong, Ciao Yu;Fu, Ssu Ju; Fu, Ssu Ju; Zhong, Ciao Yu; Liu, Yo Tsen |
| 國立成功大學 |
2016-01 |
Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy
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Hsiao, Cheng-Tsung; Tsai, Pei-Chien; Lin, Chou-Ching; Liu, Yo-Tsen; Huang, Yen-Hua; Liao, Yi-Chu; Huang, Han-Wei; Lin, Kon-Ping; Soong, Bing-Wen; Lee, Yi-Chung |
| 國立成功大學 |
2014-10 |
Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis
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Soong, Bing-Wen; Lin, Kon-Ping; Guo, Yuh-Cherng; Lin, Chou-Ching K.; Tsai, Pei-Chien; Liao, Yi-Chu; Lu, Yi-Chun; Wang, Shuu-Jiun; Tsai, Ching-Piao; Lee, Yi-Chung |
| 國立成功大學 |
2012-05-15 |
Quantifying cerebellar atrophy in multiple system atrophy of the cerebellar type (MSA-C) using three-dimensional gyrification index analysis
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Wu, Yu-Te; Shyu, Kuo-Kai; Jao, Chii-Wen; Liao, Yuan-Lin; Wang, Tzu-Yun; Wu, Hsiu-Mei; Wang, Po-Shan; Soong, Bing-Wen |
| 淡江大學 |
2010-08 |
Val-9Ala and Ile + 58Thr polymorphism of MnSOD in Parkinson's disease
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Wang, Vinchi; Chen, Shao-yuan; Chuang, Tzu-chao; Shan, Din-e; Soong, Bing-wen; Kao, Ming-ching |
| 淡江大學 |
2009-01-01 |
Octarepeat changes of prion protein in Parkinson's disease
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Wang, Vinchi; Chuang, Tzu-chao; Soong, Bing-wen; Shan, Din-E.; Kao, Ming-ching |
| 東海大學 |
2007-10 |
Asian origin for the worldwide-spread mutational event in Machado-Joseph disease
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謝明麗; Martins, Sandra; Calafell, Francesc; Gaspa, Claudia; Wong, Virginia C.N.; Silveira, Isabel; Garth, A.Nicholson; Ewout, R.Brunt; Tranebjaerg, Lisbeth; Stevanin, Giovanni; Hsieh, Mingli; Soong, Bing-wen; Loureiro, Leal; Dürr, Alexandra; Tsuji, Shoji; Watanabe, Mitsunori; Laura, B.Jardim; Giunti, Paola; Riess, Olaf; Laura, P.W.Ranum; Brice, Alexis; Guy, A.Rouleau; Coutinho, Paula; Amorim, António; Sequeiros, Jorge |
| 淡江大學 |
2001-11 |
Dentatorubropallidoluysian atrophy in Chinese
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Lee, I-hui; Soong, Bing-wen; Lu, Yi-chun; 張玉坤; Chang, Yue-cune |
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