陳儀莊博士
特聘研究員
- +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
Dysregulation of C/EBPa by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease.
Dr. Chern, Yijuang
Hum Mol Genet., Jan 09, 2007Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by a CAG trinucleotide expansion in the Huntingtin (Htt) gene.