Suppression of MAPK11 or HIPK3 reduces mutant Huntingtin levels in Huntington's disease models-Reference-Cited by-同舟云学术

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Suppression of MAPK11 or HIPK3 reduces mutant Huntingtin levels in Huntington's disease models

Published:2017-10-13 Issue:12 Volume:27 Page:1441-1465
ISSN:1001-0602
Container-title:Cell Research
language:en
Short-container-title:Cell Res

Author:

Yu Meng,Fu Yuhua,Liang Yijian,Song Haikun,Yao Yao,Wu Peng,Yao Yuwei,Pan Yuyin,Wen Xue,Ma Lixiang,Hexige Saiyin,Ding Yu,Luo Shouqing,Lu Boxun

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/cr2017113.pdf

Reference88 articles.

1. Martin JB . Molecular basis of the neurodegenerative disorders. N Engl J Med 1999; 340:1970–1980.

2. Soto C . Unfolding the role of protein misfolding in neurodegenerative diseases. Nat Rev Neurosci 2003; 4:49–60.

3. The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993; 72:971–983.

4. Rubinsztein DC, Carmichael J . Huntington's disease: molecular basis of neurodegeneration. Expert Rev Mol Med 2003; 5:1–21.

5. Yamamoto A, Lucas JJ, Hen R . Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease. Cell 2000; 101:57–66.

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