a new drug design targeting the adenosinergic system for huntingtons disease一种新药设计目标为亨廷顿氏舞蹈症adenosinergic系统.pdfVIP
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A New Drug Design Targeting the Adenosinergic System
for Huntington’s Disease
1. 2,3,4. 3 5 4 4
Nai-Kuei Huang , Jung-Hsin Lin , Jiun-Tsai Lin , Chia-I Lin , Eric Minwei Liu , Chun-Jung Lin , Wan-
1 1 3 5 3 5
Ping Chen , Yuh-Chiang Shen , Hui-Mei Chen , Jhih-Bin Chen , Hsing-Lin Lai , Chieh-Wen Yang , Ming-
7 3 3 8 5,6 1
Chang Chiang , Yu-Shuo Wu , Chen Chang , Jiang-Fan Chen , Jim-Min Fang *, Yun-Lian Lin *, Yijuang
Chern3*
1 National Research Institute of Chinese Medicine, Taipei, Taiwan, 2 Division of Mechanics, Research Center for Applied Sciences, Academia Sinica, Taipei, Taiwan,
3 Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan, 4 School of Pharmacy, National Taiwan University, Taipei, Taiwan, 5 Department of Chemistry, National
Taiwan University, Taipei, Taiwan, 6 The Genomics Research Center, Academia Sinica, Taipei, Taiwan, 7 Graduate Institute of Biotechnology, Chinese Culture University,
Taipei, Taiwan, 8 Department of Neurology, Boston University School of Medicine, Boston, Massachusetts, United States of America
Abstract
Background: Huntington’s disease (HD) is a neurodegenerative disease caused by a CAG trinucleotide expansion in the
Huntingtin (Htt) gene. The expanded CAG repeats are translated into polyglutamine (polyQ), causing aberrant functions as
well as aggregate formation of mutant Htt. Effective treatments for HD are yet to be developed.
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