Dr. Chern, Yijuang
Distinguished Research Fellow
- +886227899028 (Lab) (Room No: N333)
- +886226523913 (Office)
- 02-27829143 (Fax)
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Specialty:
- Signal Transduction
- Gene Regulation
- Neurodegeneration Disease
Education and Positions:
Ph.D. Univ. of Massachusetts
Highlight Detail
The A2A adenosine receptor rescues the urea cycle deficiency of Huntington's disease by enhancing the activity of the ubiquitin-proteasome system
Dr. Chern, Yijuang
Human Molecular Genetics Advance Access, May 14, 2009Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by a CAG trinucleotide expansion in the Huntingtin (Htt) gene. The resultant mutant Htt protein (mHtt) forms